EIF5A (eukaryotic translation initiation factor 5A) - Rat Genome Database

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Gene: EIF5A (eukaryotic translation initiation factor 5A) Homo sapiens
Analyze
Symbol: EIF5A
Name: eukaryotic translation initiation factor 5A
RGD ID: 1317562
HGNC Page HGNC:3300
Description: Enables U6 snRNA binding activity. Involved in several processes, including cellular response to virus; positive regulation of intrinsic apoptotic signaling pathway by p53 class mediator; and tumor necrosis factor-mediated signaling pathway. Located in annulate lamellae; cytoplasm; and nucleus. Part of nuclear pore. Biomarker of colorectal cancer.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: eIF-4D; EIF-5A; eIF-5A-1; eIF-5A1; EIF5A1; eIF5AI; eukaryotic initiation factor 5A; eukaryotic translation initiation factor 5A-1; FABAS; MGC104255; MGC99547; rev-binding factor
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: EIF5AP2   EIF5AP3   EIF5AP4  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38177,306,999 - 7,312,463 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl177,306,999 - 7,312,463 (+)EnsemblGRCh38hg38GRCh38
GRCh37177,210,318 - 7,215,782 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36177,151,693 - 7,156,498 (+)NCBINCBI36Build 36hg18NCBI36
Build 34177,151,692 - 7,156,496NCBI
Celera177,236,257 - 7,241,723 (+)NCBICelera
Cytogenetic Map17p13.1NCBI
HuRef177,104,783 - 7,109,831 (+)NCBIHuRef
CHM1_1177,219,093 - 7,224,550 (+)NCBICHM1_1
T2T-CHM13v2.0177,210,983 - 7,216,447 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-epigallocatechin 3-gallate  (EXP)
(1->4)-beta-D-glucan  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP,ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP,ISO)
2,3',4,4',5-Pentachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2,4,6-trinitrotoluene  (ISO)
2,4-dinitrotoluene  (ISO)
2,6-dimethoxyphenol  (EXP)
2-bromohexadecanoic acid  (EXP)
3,3',5,5'-tetrabromobisphenol A  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxynon-2-enal  (ISO)
6-propyl-2-thiouracil  (ISO)
acrylamide  (ISO)
actinomycin D  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
amitrole  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
beauvericin  (EXP)
benzo[a]pyrene  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
beta-lapachone  (EXP)
bisphenol A  (EXP,ISO)
bisphenol AF  (EXP)
bleomycin A2  (ISO)
bortezomib  (EXP)
bromobenzene  (ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP,ISO)
caffeine  (EXP)
cannabidiol  (ISO)
carbon nanotube  (ISO)
chlorpyrifos  (ISO)
chromium(6+)  (ISO)
ciguatoxin CTX1B  (ISO)
cisplatin  (EXP)
clofibric acid  (ISO)
cocaine  (EXP,ISO)
CU-O LINKAGE  (ISO)
Cuprizon  (EXP)
dextran sulfate  (ISO)
diarsenic trioxide  (EXP)
diazinon  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
elemental selenium  (EXP)
enzyme inhibitor  (EXP)
ethanol  (ISO)
ethyl methanesulfonate  (EXP)
fenthion  (ISO)
flutamide  (ISO)
folic acid  (ISO)
furfural  (EXP)
genistein  (EXP)
gentamycin  (ISO)
glafenine  (ISO)
haloperidol  (EXP)
heroin  (EXP)
ivermectin  (EXP)
methidathion  (ISO)
methimazole  (ISO)
methotrexate  (EXP)
methyl methanesulfonate  (EXP)
microcystin RR  (EXP)
mitoxantrone  (EXP)
mono(2-ethylhexyl) phthalate  (EXP)
morphine  (EXP)
N-methyl-N'-nitro-N-nitrosoguanidine  (ISO)
N-nitrosodiethylamine  (ISO)
nefazodone  (ISO)
nickel atom  (EXP)
nimesulide  (ISO)
Nutlin-3  (EXP)
paclitaxel  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
PhIP  (ISO)
pioglitazone  (ISO)
propiconazole  (ISO)
raloxifene  (EXP)
resveratrol  (EXP)
SB 431542  (EXP)
selenium atom  (EXP)
sodium arsenate  (ISO)
sodium arsenite  (EXP)
sodium chloride  (EXP)
sodium fluoride  (ISO)
Soman  (ISO)
sulfadimethoxine  (ISO)
sulforaphane  (EXP)
T-2 toxin  (ISO)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
thioacetamide  (ISO)
thiram  (EXP)
titanium dioxide  (ISO)
topotecan  (EXP)
trichloroethene  (ISO)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (EXP)
triptonide  (ISO)
tungsten  (ISO)
urethane  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vitamin E  (EXP)
vorinostat  (EXP)
zinc atom  (ISO)
zinc(0)  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Hypusine Signaling Promotes Pulmonary Vascular Remodeling in Pulmonary Arterial Hypertension. Lemay SE, etal., Am J Respir Crit Care Med. 2024 Jun 1;209(11):1376-1391. doi: 10.1164/rccm.202305-0909OC.
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Upregulation of eIF-5A1 in the paralyzed muscle after spinal cord transection associates with spontaneous hindlimb locomotor recovery in rats by upregulation of the ErbB, MAPK and neurotrophin signal pathways. Shang FF, etal., J Proteomics. 2013 Oct 8;91:188-99. doi: 10.1016/j.jprot.2012.12.002. Epub 2012 Dec 11.
4. Overexpression of CK20, MAP3K8 and EIF5A correlates with poor prognosis in early-onset colorectal cancer patients. Tunca B, etal., J Cancer Res Clin Oncol. 2013 Apr;139(4):691-702. doi: 10.1007/s00432-013-1372-x. Epub 2013 Jan 16.
Additional References at PubMed
PMID:1286667   PMID:1850732   PMID:1900436   PMID:2492279   PMID:3095320   PMID:7545941   PMID:7578077   PMID:7622067   PMID:7759117   PMID:7929297   PMID:7971969   PMID:8125298  
PMID:8253832   PMID:8596953   PMID:9285095   PMID:9285100   PMID:9442029   PMID:9465063   PMID:10229683   PMID:10381392   PMID:10944119   PMID:11161802   PMID:11238447   PMID:11742107  
PMID:11790298   PMID:11870779   PMID:12210765   PMID:12477932   PMID:12562768   PMID:12687616   PMID:12788913   PMID:12894223   PMID:14622290   PMID:15231747   PMID:15303967   PMID:15371445  
PMID:15489334   PMID:16354571   PMID:16371467   PMID:16452303   PMID:16515720   PMID:16519677   PMID:16522190   PMID:16712791   PMID:16842744   PMID:16916647   PMID:16987817   PMID:17008552  
PMID:17187778   PMID:17213197   PMID:17578650   PMID:18067580   PMID:19149558   PMID:19160416   PMID:19322201   PMID:19379712   PMID:19825182   PMID:19946888   PMID:19998337   PMID:20232312  
PMID:20348541   PMID:20360068   PMID:20830705   PMID:20942800   PMID:21145461   PMID:21224998   PMID:21360055   PMID:21565611   PMID:21778671   PMID:21873635   PMID:21942715   PMID:22304920  
PMID:22354994   PMID:22681889   PMID:22771473   PMID:22863883   PMID:22908221   PMID:22927971   PMID:22939629   PMID:22944692   PMID:23132580   PMID:23376485   PMID:23383273   PMID:23402259  
PMID:23403292   PMID:23539416   PMID:23733422   PMID:23991020   PMID:24220243   PMID:24402910   PMID:24491565   PMID:24509416   PMID:24711643   PMID:24778252   PMID:24981860   PMID:24999758  
PMID:25147182   PMID:25218134   PMID:25261239   PMID:25416956   PMID:25468996   PMID:25874870   PMID:25959826   PMID:25963833   PMID:25979826   PMID:26186194   PMID:26282002   PMID:26403856  
PMID:26483550   PMID:26496610   PMID:26618866   PMID:26641092   PMID:26773503   PMID:26979993   PMID:27025967   PMID:27082860   PMID:27114451   PMID:27115996   PMID:27180817   PMID:27306458  
PMID:27371349   PMID:27414022   PMID:27432908   PMID:27609421   PMID:27926873   PMID:28031328   PMID:28330616   PMID:28381547   PMID:28514442   PMID:28515276   PMID:28581483   PMID:28675297  
PMID:28718761   PMID:29128334   PMID:29229926   PMID:29321164   PMID:29428664   PMID:29491746   PMID:29507755   PMID:29509190   PMID:29533498   PMID:29712776   PMID:29791485   PMID:29845934  
PMID:30170728   PMID:30196744   PMID:30206208   PMID:30463901   PMID:30575818   PMID:30761741   PMID:30884312   PMID:30890647   PMID:30948266   PMID:31046837   PMID:31091453   PMID:31558321  
PMID:31586073   PMID:31732153   PMID:31751430   PMID:31801078   PMID:31980649   PMID:31995728   PMID:32296183   PMID:32416067   PMID:32529326   PMID:32605139   PMID:32687490   PMID:32707033  
PMID:32786267   PMID:32807901   PMID:32817651   PMID:32882370   PMID:32929329   PMID:33022573   PMID:33080218   PMID:33188200   PMID:33303756   PMID:33306668   PMID:33545068   PMID:33547280  
PMID:33644029   PMID:33961781   PMID:34273022   PMID:34349018   PMID:34428256   PMID:34597346   PMID:34662580   PMID:34709727   PMID:34901782   PMID:34917906   PMID:34921595   PMID:34947982  
PMID:35013218   PMID:35013556   PMID:35256949   PMID:35271311   PMID:35356984   PMID:35446349   PMID:35562734   PMID:35563538   PMID:35676659   PMID:35831314   PMID:35850772   PMID:35944360  
PMID:35987950   PMID:36057605   PMID:36215168   PMID:36225252   PMID:36232890   PMID:36273042   PMID:36373674   PMID:36610398   PMID:36634849   PMID:36652389   PMID:36762613   PMID:36766751  
PMID:36779763   PMID:36893894   PMID:36973244   PMID:37047039   PMID:37071682   PMID:37137790   PMID:37167062   PMID:37219665   PMID:37314216   PMID:37317656   PMID:37333770   PMID:37448957  
PMID:37653021   PMID:37743008   PMID:37794589   PMID:37827155   PMID:38113892   PMID:38229033   PMID:38245532   PMID:38334954   PMID:38654332   PMID:38862693   PMID:39147351   PMID:39231216  
PMID:39303786   PMID:39358380  


Genomics

Comparative Map Data
EIF5A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38177,306,999 - 7,312,463 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl177,306,999 - 7,312,463 (+)EnsemblGRCh38hg38GRCh38
GRCh37177,210,318 - 7,215,782 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36177,151,693 - 7,156,498 (+)NCBINCBI36Build 36hg18NCBI36
Build 34177,151,692 - 7,156,496NCBI
Celera177,236,257 - 7,241,723 (+)NCBICelera
Cytogenetic Map17p13.1NCBI
HuRef177,104,783 - 7,109,831 (+)NCBIHuRef
CHM1_1177,219,093 - 7,224,550 (+)NCBICHM1_1
T2T-CHM13v2.0177,210,983 - 7,216,447 (+)NCBIT2T-CHM13v2.0
Eif5a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391169,807,538 - 69,812,784 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1169,807,540 - 69,812,784 (-)EnsemblGRCm39 Ensembl
GRCm381169,916,712 - 69,921,958 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1169,916,714 - 69,921,958 (-)EnsemblGRCm38mm10GRCm38
MGSCv371169,730,214 - 69,735,460 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361169,732,917 - 69,737,536 (-)NCBIMGSCv36mm8
Celera1177,464,600 - 77,469,965 (-)NCBICelera
Cytogenetic Map11B3NCBI
cM Map1142.92NCBI
Eif5a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81055,138,821 - 55,143,272 (-)NCBIGRCr8
mRatBN7.21054,640,104 - 54,644,845 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1054,640,024 - 54,644,656 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1059,302,660 - 59,307,064 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01058,791,232 - 58,795,636 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01054,298,539 - 54,302,941 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01056,527,075 - 56,531,615 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1056,527,085 - 56,531,483 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01056,272,194 - 56,276,934 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41056,760,289 - 56,764,689 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11056,773,911 - 56,778,625 (-)NCBI
Celera1053,794,046 - 53,798,461 (-)NCBICelera
Cytogenetic Map10q24NCBI
Eif5a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554679,603,800 - 9,608,490 (-)NCBIChiLan1.0ChiLan1.0
EIF5A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21914,903,844 - 14,909,346 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11716,869,683 - 16,875,178 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0177,341,076 - 7,346,570 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1177,327,363 - 7,333,270 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl177,327,363 - 7,333,270 (+)Ensemblpanpan1.1panPan2
EIF5A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1532,268,103 - 32,272,970 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha532,405,817 - 32,410,703 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0532,373,168 - 32,378,059 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl532,372,977 - 32,378,002 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1532,338,605 - 32,343,491 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0532,297,394 - 32,302,267 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0532,474,419 - 32,479,302 (+)NCBIUU_Cfam_GSD_1.0
Eif5a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560247,129,875 - 47,134,887 (+)NCBIHiC_Itri_2
SpeTri2.0NW_004936595604,268 - 609,075 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
EIF5A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11252,659,040 - 52,664,686 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.23139,934,584 - 139,940,476 (+)NCBISscrofa10.2Sscrofa10.2susScr3
EIF5A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1166,685,908 - 6,691,159 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366605914,719,550 - 14,724,974 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Eif5a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247869,933,325 - 9,938,178 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in EIF5A
26 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17p13.2-13.1(chr17:5732977-8038822)x1 copy number loss See cases [RCV000051043] Chr17:5732977..8038822 [GRCh38]
Chr17:5636297..7942140 [GRCh37]
Chr17:5577021..7882865 [NCBI36]
Chr17:17p13.2-13.1
pathogenic
GRCh38/hg38 17p13.1(chr17:6958978-8335684)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052457]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052457]|See cases [RCV000052457] Chr17:6958978..8335684 [GRCh38]
Chr17:6862297..8239002 [GRCh37]
Chr17:6803021..8179727 [NCBI36]
Chr17:17p13.1
pathogenic
GRCh38/hg38 17p13.2-13.1(chr17:6307904-8842949)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053407]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053407]|See cases [RCV000053407] Chr17:6307904..8842949 [GRCh38]
Chr17:6211224..8746266 [GRCh37]
Chr17:6151948..8686991 [NCBI36]
Chr17:17p13.2-13.1
pathogenic
GRCh38/hg38 17p13.1(chr17:7210345-7496934)x1 copy number loss See cases [RCV000053425] Chr17:7210345..7496934 [GRCh38]
Chr17:7113664..7400253 [GRCh37]
Chr17:7054388..7340977 [NCBI36]
Chr17:17p13.1
pathogenic
GRCh38/hg38 17p13.1(chr17:6958978-7491129)x3 copy number gain See cases [RCV000133763] Chr17:6958978..7491129 [GRCh38]
Chr17:6862297..7394448 [GRCh37]
Chr17:6803021..7335172 [NCBI36]
Chr17:17p13.1
uncertain significance
GRCh38/hg38 17p13.3-13.1(chr17:198748-7491129)x3 copy number gain See cases [RCV000134970] Chr17:198748..7491129 [GRCh38]
Chr17:50690..7394448 [GRCh37]
Chr17:48539..7335172 [NCBI36]
Chr17:17p13.3-13.1
pathogenic
GRCh38/hg38 17p13.2-12(chr17:5732953-12095349)x3 copy number gain See cases [RCV000134851] Chr17:5732953..12095349 [GRCh38]
Chr17:5636273..11998666 [GRCh37]
Chr17:5576997..11939391 [NCBI36]
Chr17:17p13.2-12
pathogenic
GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1 copy number loss See cases [RCV000138214] Chr17:162016..7697012 [GRCh38]
Chr17:45835..7600330 [GRCh37]
Chr17:11807..7541055 [NCBI36]
Chr17:17p13.3-13.1
pathogenic
GRCh38/hg38 17p13.2-13.1(chr17:6361393-7750863)x3 copy number gain See cases [RCV000138220] Chr17:6361393..7750863 [GRCh38]
Chr17:6264713..7654181 [GRCh37]
Chr17:6205437..7594906 [NCBI36]
Chr17:17p13.2-13.1
likely pathogenic
GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3 copy number gain See cases [RCV000138531] Chr17:162016..12343901 [GRCh38]
Chr17:45835..12247218 [GRCh37]
Chr17:11807..12187943 [NCBI36]
Chr17:17p13.3-12
pathogenic
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3 copy number gain See cases [RCV000142236] Chr17:150732..14764202 [GRCh38]
Chr17:525..14667519 [GRCh37]
Chr17:525..14608244 [NCBI36]
Chr17:17p13.3-12
pathogenic
GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3 copy number gain See cases [RCV000511786] Chr17:525..15027737 [GRCh37]
Chr17:17p13.3-12
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NM_001970.5(EIF5A):c.403-4C>T single nucleotide variant not specified [RCV000608599] Chr17:7311574 [GRCh38]
Chr17:7214893 [GRCh37]
Chr17:17p13.1
likely benign
GRCh37/hg19 17p13.1(chr17:6934163-8217978)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626431] Chr17:6934163..8217978 [GRCh37]
Chr17:17p13.1
drug response
GRCh37/hg19 17p13.1(chr17:7094070-7414448)x1 copy number loss See cases [RCV000512276] Chr17:7094070..7414448 [GRCh37]
Chr17:17p13.1
likely pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NC_000017.10:g.7124585_7400253dup duplication Robin sequence [RCV000677112] Chr17:7124585..7400253 [GRCh37]
Chr17:17p13.1
uncertain significance
Single allele duplication Isolated Pierre-Robin syndrome [RCV000677112] Chr17:7124585..7400253 [GRCh37]
Chr17:17p13.1
likely pathogenic
Single allele duplication not provided [RCV000677924] Chr17:7185264..7240701 [GRCh37]
Chr17:17p13.1
uncertain significance
GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3 copy number gain not provided [RCV000683866] Chr17:525..11186432 [GRCh37]
Chr17:17p13.3-12
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.1(chr17:7013365-7265208)x1 copy number loss not provided [RCV000739389] Chr17:7013365..7265208 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.166-10A>G single nucleotide variant not provided [RCV001641287] Chr17:7311008 [GRCh38]
Chr17:7214327 [GRCh37]
Chr17:17p13.1
benign
GRCh37/hg19 17p13.1(chr17:6800893-7304696)x1 copy number loss not provided [RCV001006866] Chr17:6800893..7304696 [GRCh37]
Chr17:17p13.1
pathogenic
GRCh37/hg19 17p13.1(chr17:6826243-7311408)x3 copy number gain not provided [RCV000849961] Chr17:6826243..7311408 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.191_192del (p.Phe64fs) deletion Faundes-Banka syndrome [RCV003110193] Chr17:7311042..7311043 [GRCh38]
Chr17:7214361..7214362 [GRCh37]
Chr17:17p13.1
likely pathogenic
NC_000017.10:g.(?_7123304)_(7606804_?)del deletion Common variable immunodeficiency [RCV003107751] Chr17:7123304..7606804 [GRCh37]
Chr17:17p13.1
uncertain significance
NC_000017.10:g.(?_6589506)_(8151374_?)dup duplication Common variable immunodeficiency [RCV001338841]|Dyskeratosis congenita [RCV001031775] Chr17:6589506..8151374 [GRCh37]
Chr17:17p13.1
uncertain significance
GRCh37/hg19 17p13.1(chr17:6650649-8040151)x3 copy number gain not provided [RCV001259299] Chr17:6650649..8040151 [GRCh37]
Chr17:17p13.1
pathogenic
GRCh37/hg19 17p13.1(chr17:7014481-7283233)x1 copy number loss not provided [RCV001259300] Chr17:7014481..7283233 [GRCh37]
Chr17:17p13.1
pathogenic
NM_001970.5(EIF5A):c.77G>C (p.Arg26Pro) single nucleotide variant Neurodevelopmental disorder [RCV001374964] Chr17:7309712 [GRCh38]
Chr17:7213031 [GRCh37]
Chr17:17p13.1
likely pathogenic
NM_001970.5(EIF5A):c.325C>T (p.Arg109Ter) single nucleotide variant Faundes-Banka syndrome [RCV001509562]|not provided [RCV004728750] Chr17:7311404 [GRCh38]
Chr17:7214723 [GRCh37]
Chr17:17p13.1
pathogenic
NM_001970.5(EIF5A):c.143C>A (p.Thr48Asn) single nucleotide variant Faundes-Banka syndrome [RCV001509560] Chr17:7309778 [GRCh38]
Chr17:7213097 [GRCh37]
Chr17:17p13.1
pathogenic
NM_001970.5(EIF5A):c.325C>G (p.Arg109Gly) single nucleotide variant Faundes-Banka syndrome [RCV001509561] Chr17:7311404 [GRCh38]
Chr17:7214723 [GRCh37]
Chr17:17p13.1
pathogenic
NM_001970.5(EIF5A):c.324dup (p.Arg109fs) duplication Faundes-Banka syndrome [RCV001509563] Chr17:7311402..7311403 [GRCh38]
Chr17:7214721..7214722 [GRCh37]
Chr17:17p13.1
pathogenic
NC_000017.10:g.(?_6328780)_(7606804_?)dup duplication Congenital myasthenic syndrome 2A [RCV003109217]|Very long chain acyl-CoA dehydrogenase deficiency [RCV003119078] Chr17:6328780..7606804 [GRCh37]
Chr17:17p13.2-13.1
uncertain significance
NM_001970.5(EIF5A):c.343C>T (p.Pro115Ser) single nucleotide variant not provided [RCV001794622] Chr17:7311422 [GRCh38]
Chr17:7214741 [GRCh37]
Chr17:17p13.1
likely pathogenic|uncertain significance
GRCh37/hg19 17p13.1(chr17:7020054-8086290) copy number loss not specified [RCV002052585] Chr17:7020054..8086290 [GRCh37]
Chr17:17p13.1
pathogenic
NC_000017.10:g.(?_7120455)_(8151423_?)del deletion Li-Fraumeni syndrome [RCV003111420] Chr17:7120455..8151423 [GRCh37]
Chr17:17p13.1
pathogenic
NC_000017.10:g.(?_7123304)_(8193254_?)del deletion Very long chain acyl-CoA dehydrogenase deficiency [RCV003119081] Chr17:7123304..8193254 [GRCh37]
Chr17:17p13.1
pathogenic
NM_001970.5(EIF5A):c.124G>A (p.Glu42Lys) single nucleotide variant not provided [RCV002265307] Chr17:7309759 [GRCh38]
Chr17:7213078 [GRCh37]
Chr17:17p13.1
likely pathogenic|uncertain significance
NM_001970.5(EIF5A):c.237G>A (p.Met79Ile) single nucleotide variant not provided [RCV004592451] Chr17:7311089 [GRCh38]
Chr17:7214408 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001143760.1(EIF5A):c.37C>T (p.Arg13Cys) single nucleotide variant not specified [RCV004181848] Chr17:7307083 [GRCh38]
Chr17:7210402 [GRCh37]
Chr17:17p13.1
uncertain significance
GRCh37/hg19 17p13.1(chr17:7004894-7766789)x1 copy number loss not provided [RCV003222936] Chr17:7004894..7766789 [GRCh37]
Chr17:17p13.1
pathogenic
NM_001970.5(EIF5A):c.337C>T (p.Arg113Cys) single nucleotide variant not provided [RCV004592003] Chr17:7311416 [GRCh38]
Chr17:7214735 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.270+1G>A single nucleotide variant not provided [RCV003329860] Chr17:7311123 [GRCh38]
Chr17:7214442 [GRCh37]
Chr17:17p13.1
likely pathogenic
GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3 copy number gain Chromosome 17p13.3 duplication syndrome [RCV003327726] Chr17:165730..11404096 [GRCh38]
Chr17:17p13.3-12
pathogenic
NM_001370420.1(EIF5A):c.-52C>A single nucleotide variant not provided [RCV003419598] Chr17:7307083 [GRCh38]
Chr17:7210402 [GRCh37]
Chr17:17p13.1
likely benign
NM_001143760.1(EIF5A):c.69+1G>A single nucleotide variant EIF5A-related disorder [RCV003421054]|Faundes-Banka syndrome [RCV003989843] Chr17:7307116 [GRCh38]
Chr17:7210435 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.333C>A (p.Asp111Glu) single nucleotide variant not provided [RCV004778785] Chr17:7311412 [GRCh38]
Chr17:7214731 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.291dup (p.Tyr98fs) duplication EIF5A-related disorder [RCV003391447] Chr17:7311367..7311368 [GRCh38]
Chr17:7214686..7214687 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.408G>A (p.Thr136=) single nucleotide variant not provided [RCV003428094] Chr17:7311583 [GRCh38]
Chr17:7214902 [GRCh37]
Chr17:17p13.1
likely benign
NM_001970.5(EIF5A):c.37G>A (p.Gly13Arg) single nucleotide variant Faundes-Banka syndrome [RCV003494068] Chr17:7309672 [GRCh38]
Chr17:7212991 [GRCh37]
Chr17:17p13.1
uncertain significance
GRCh37/hg19 17p13.1(chr17:7002380-7469251)x1 copy number loss not specified [RCV003987240] Chr17:7002380..7469251 [GRCh37]
Chr17:17p13.1
pathogenic
GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3 copy number gain not specified [RCV003987215] Chr17:525..21510992 [GRCh37]
Chr17:17p13.3-11.2
pathogenic
NM_001970.5(EIF5A):c.344_345del (p.Pro115fs) deletion not provided [RCV004547133] Chr17:7311423..7311424 [GRCh38]
Chr17:7214742..7214743 [GRCh37]
Chr17:17p13.1
likely pathogenic
NM_001970.5(EIF5A):c.165+1G>A single nucleotide variant not specified [RCV004379986] Chr17:7309801 [GRCh38]
Chr17:7213120 [GRCh37]
Chr17:17p13.1
likely pathogenic
NC_000017.10:g.(?_7123304)_(7360042_?)del deletion Very long chain acyl-CoA dehydrogenase deficiency [RCV004581341] Chr17:7123304..7360042 [GRCh37]
Chr17:17p13.1
pathogenic
NC_000017.10:g.(?_422368)_(8285628_?)dup duplication not provided [RCV004581443] Chr17:422368..8285628 [GRCh37]
Chr17:17p13.3-13.1
uncertain significance
NM_001970.5(EIF5A):c.412C>A (p.Leu138Met) single nucleotide variant not specified [RCV004624678] Chr17:7311587 [GRCh38]
Chr17:7214906 [GRCh37]
Chr17:17p13.1
uncertain significance
Single allele deletion Faundes-Banka syndrome [RCV004577981] Chr17:7004634..7232940 [GRCh37]
Chr17:17p13.1
pathogenic
NM_001970.5(EIF5A):c.415_416delinsAT (p.Ser139Ile) indel Faundes-Banka syndrome [RCV004674040] Chr17:7311590..7311591 [GRCh38]
Chr17:7214909..7214910 [GRCh37]
Chr17:17p13.1
likely pathogenic
NM_001970.5(EIF5A):c.316G>A (p.Gly106Arg) single nucleotide variant not provided [RCV004776200] Chr17:7311395 [GRCh38]
Chr17:7214714 [GRCh37]
Chr17:17p13.1
pathogenic
GRCh37/hg19 17p13.2-12(chr17:4678235-14745263)x3 copy number gain not provided [RCV004819316] Chr17:4678235..14745263 [GRCh37]
Chr17:17p13.2-12
pathogenic
NM_001970.5(EIF5A):c.388G>A (p.Gly130Arg) single nucleotide variant not specified [RCV004912396] Chr17:7311467 [GRCh38]
Chr17:7214786 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.252C>G (p.Ile84Met) single nucleotide variant not provided [RCV005054771] Chr17:7311104 [GRCh38]
Chr17:7214423 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001970.5(EIF5A):c.266T>A (p.Phe89Tyr) single nucleotide variant not provided [RCV005054772] Chr17:7311118 [GRCh38]
Chr17:7214437 [GRCh37]
Chr17:17p13.1
uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:4153
Count of miRNA genes:749
Interacting mature miRNAs:870
Transcripts:ENST00000336452, ENST00000336458, ENST00000355068, ENST00000416016, ENST00000419711, ENST00000571955, ENST00000572815, ENST00000573542, ENST00000573714, ENST00000575001, ENST00000576930
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597399323GWAS1495397_Heducational attainment QTL GWAS1495397 (human)3e-09educational attainment1773122177312218Human
596973181GWAS1092700_Hmajor depressive disorder QTL GWAS1092700 (human)0.000003major depressive disorder1773104547310455Human
597422338GWAS1518412_Halkaline phosphatase measurement QTL GWAS1518412 (human)1e-10alkaline phosphatase measurementblood alkaline phosphatase activity level (CMO:0000576)1773102607310261Human
597126828GWAS1222902_Hmajor depressive disorder QTL GWAS1222902 (human)0.000003major depressive disorder1773104547310455Human
597520803GWAS1616877_Hbody fat percentage QTL GWAS1616877 (human)4e-10body fat mass (VT:0010482)body fat percentage (CMO:0000302)1773073417307342Human
407212202GWAS861178_Hunipolar depression QTL GWAS861178 (human)0.000003unipolar depression1773104547310455Human

Markers in Region
RH67341  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map17p13-p12UniSTS
RH39404  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map17p13-p12UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2437 2788 2253 4971 1725 2350 6 624 1951 465 2269 7303 6470 53 3732 1 850 1741 1616 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001143760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001143761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001143762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001970 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315316 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002957981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC026954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF087992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF376057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK222585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY129319 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY129320 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY129321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY129322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC030160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC080196 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC085015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC107779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG479628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB111036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M23419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U17969 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000336452   ⟹   ENSP00000336702
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,306,999 - 7,312,463 (+)Ensembl
Ensembl Acc Id: ENST00000336458   ⟹   ENSP00000336776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,628 - 7,312,463 (+)Ensembl
Ensembl Acc Id: ENST00000355068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,326 - 7,310,453 (+)Ensembl
Ensembl Acc Id: ENST00000416016   ⟹   ENSP00000396073
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,308,371 - 7,312,455 (+)Ensembl
Ensembl Acc Id: ENST00000419711   ⟹   ENSP00000390677
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,974 - 7,312,455 (+)Ensembl
Ensembl Acc Id: ENST00000571955   ⟹   ENSP00000458269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,974 - 7,312,455 (+)Ensembl
Ensembl Acc Id: ENST00000572815   ⟹   ENSP00000461688
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,582 - 7,311,868 (+)Ensembl
Ensembl Acc Id: ENST00000573542   ⟹   ENSP00000459611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,602 - 7,312,244 (+)Ensembl
Ensembl Acc Id: ENST00000573714   ⟹   ENSP00000460284
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,993 - 7,311,615 (+)Ensembl
Ensembl Acc Id: ENST00000575001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,631 - 7,310,101 (+)Ensembl
Ensembl Acc Id: ENST00000576930   ⟹   ENSP00000459196
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,307,540 - 7,312,455 (+)Ensembl
RefSeq Acc Id: NM_001143760   ⟹   NP_001137232
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,306,999 - 7,312,463 (+)NCBI
GRCh37177,210,318 - 7,215,782 (+)ENTREZGENE
HuRef177,104,783 - 7,109,831 (+)ENTREZGENE
CHM1_1177,219,093 - 7,224,550 (+)NCBI
T2T-CHM13v2.0177,210,983 - 7,216,447 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001143761   ⟹   NP_001137233
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,969 - 7,312,463 (+)NCBI
GRCh37177,210,318 - 7,215,782 (+)ENTREZGENE
HuRef177,104,783 - 7,109,831 (+)ENTREZGENE
CHM1_1177,220,063 - 7,224,550 (+)NCBI
T2T-CHM13v2.0177,211,953 - 7,216,447 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001143762   ⟹   NP_001137234
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,308,373 - 7,312,463 (+)NCBI
GRCh37177,210,318 - 7,215,782 (+)ENTREZGENE
HuRef177,104,783 - 7,109,831 (+)ENTREZGENE
CHM1_1177,220,469 - 7,224,550 (+)NCBI
T2T-CHM13v2.0177,212,357 - 7,216,447 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370420   ⟹   NP_001357349
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,002 - 7,312,463 (+)NCBI
T2T-CHM13v2.0177,210,986 - 7,216,447 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370421   ⟹   NP_001357350
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,984 - 7,312,463 (+)NCBI
T2T-CHM13v2.0177,211,968 - 7,216,447 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001970   ⟹   NP_001961
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,628 - 7,312,463 (+)NCBI
GRCh37177,210,318 - 7,215,782 (+)ENTREZGENE
Build 36177,151,693 - 7,156,498 (+)NCBI Archive
HuRef177,104,783 - 7,109,831 (+)ENTREZGENE
CHM1_1177,219,631 - 7,224,550 (+)NCBI
T2T-CHM13v2.0177,211,612 - 7,216,447 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011523710   ⟹   XP_011522012
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,969 - 7,311,011 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011523711   ⟹   XP_011522013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,308,373 - 7,311,011 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011523712   ⟹   XP_011522014
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,984 - 7,311,011 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011523713   ⟹   XP_011522015
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,308,971 - 7,311,011 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017024301   ⟹   XP_016879790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,002 - 7,311,011 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047435523   ⟹   XP_047291479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,628 - 7,311,011 (+)NCBI
RefSeq Acc Id: XM_047435524   ⟹   XP_047291480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,308,971 - 7,312,463 (+)NCBI
RefSeq Acc Id: XM_054315313   ⟹   XP_054171288
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0177,211,612 - 7,214,995 (+)NCBI
RefSeq Acc Id: XM_054315314   ⟹   XP_054171289
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0177,211,953 - 7,214,995 (+)NCBI
RefSeq Acc Id: XM_054315315   ⟹   XP_054171290
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0177,211,968 - 7,214,995 (+)NCBI
RefSeq Acc Id: XM_054315316   ⟹   XP_054171291
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0177,212,593 - 7,214,995 (+)NCBI
RefSeq Acc Id: XM_054315317   ⟹   XP_054171292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0177,210,986 - 7,214,995 (+)NCBI
RefSeq Acc Id: XM_054315318   ⟹   XP_054171293
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0177,212,357 - 7,214,995 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001137232 (Get FASTA)   NCBI Sequence Viewer  
  NP_001137233 (Get FASTA)   NCBI Sequence Viewer  
  NP_001137234 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357349 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357350 (Get FASTA)   NCBI Sequence Viewer  
  NP_001961 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522012 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522013 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522014 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522015 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879790 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291479 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291480 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171288 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171289 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171290 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171291 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171292 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171293 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188622 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188623 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188624 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188625 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188626 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188627 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA58453 (Get FASTA)   NCBI Sequence Viewer  
  AAA86989 (Get FASTA)   NCBI Sequence Viewer  
  AAH00751 (Get FASTA)   NCBI Sequence Viewer  
  AAH01832 (Get FASTA)   NCBI Sequence Viewer  
  AAH30160 (Get FASTA)   NCBI Sequence Viewer  
  AAH80196 (Get FASTA)   NCBI Sequence Viewer  
  AAH85015 (Get FASTA)   NCBI Sequence Viewer  
  AAI07780 (Get FASTA)   NCBI Sequence Viewer  
  AAL40917 (Get FASTA)   NCBI Sequence Viewer  
  AAN17514 (Get FASTA)   NCBI Sequence Viewer  
  AAN17515 (Get FASTA)   NCBI Sequence Viewer  
  AAN17516 (Get FASTA)   NCBI Sequence Viewer  
  AAN17517 (Get FASTA)   NCBI Sequence Viewer  
  AAN17518 (Get FASTA)   NCBI Sequence Viewer  
  BAF85304 (Get FASTA)   NCBI Sequence Viewer  
  BAH13937 (Get FASTA)   NCBI Sequence Viewer  
  EAW90219 (Get FASTA)   NCBI Sequence Viewer  
  EAW90220 (Get FASTA)   NCBI Sequence Viewer  
  EAW90221 (Get FASTA)   NCBI Sequence Viewer  
  EAW90222 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000336702
  ENSP00000336702.7
  ENSP00000336776
  ENSP00000336776.8
  ENSP00000390677
  ENSP00000390677.2
  ENSP00000396073
  ENSP00000396073.2
  ENSP00000458269.1
  ENSP00000459196.1
  ENSP00000459611.1
  ENSP00000460284
  ENSP00000460284.1
  ENSP00000461688.1
  ENSP00000499855.1
  ENSP00000499995.1
  ENSP00000500228.1
  ENSP00000500414.1
  ENSP00000500543.1
  ENSP00000500624.1
  ENSP00000500669.1
  ENSP00000500717.1
  ENSP00000500847.1
GenBank Protein P63241 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001137232   ⟸   NM_001143760
- Peptide Label: isoform A
- UniProtKB: I3L504 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001961   ⟸   NM_001970
- Peptide Label: isoform B
- UniProtKB: Q7Z4L1 (UniProtKB/Swiss-Prot),   Q7L7L3 (UniProtKB/Swiss-Prot),   Q16182 (UniProtKB/Swiss-Prot),   P10159 (UniProtKB/Swiss-Prot),   D3DTP2 (UniProtKB/Swiss-Prot),   A8K9A0 (UniProtKB/Swiss-Prot),   Q9D0G2 (UniProtKB/Swiss-Prot),   P63241 (UniProtKB/Swiss-Prot),   I3L397 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001137234   ⟸   NM_001143762
- Peptide Label: isoform B
- UniProtKB: Q7Z4L1 (UniProtKB/Swiss-Prot),   Q7L7L3 (UniProtKB/Swiss-Prot),   Q16182 (UniProtKB/Swiss-Prot),   P10159 (UniProtKB/Swiss-Prot),   D3DTP2 (UniProtKB/Swiss-Prot),   A8K9A0 (UniProtKB/Swiss-Prot),   Q9D0G2 (UniProtKB/Swiss-Prot),   P63241 (UniProtKB/Swiss-Prot),   I3L397 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001137233   ⟸   NM_001143761
- Peptide Label: isoform B
- UniProtKB: Q7Z4L1 (UniProtKB/Swiss-Prot),   Q7L7L3 (UniProtKB/Swiss-Prot),   Q16182 (UniProtKB/Swiss-Prot),   P10159 (UniProtKB/Swiss-Prot),   D3DTP2 (UniProtKB/Swiss-Prot),   A8K9A0 (UniProtKB/Swiss-Prot),   Q9D0G2 (UniProtKB/Swiss-Prot),   P63241 (UniProtKB/Swiss-Prot),   I3L397 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522014   ⟸   XM_011523712
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522012   ⟸   XM_011523710
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522013   ⟸   XM_011523711
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522015   ⟸   XM_011523713
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016879790   ⟸   XM_017024301
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001357349   ⟸   NM_001370420
- Peptide Label: isoform B
- UniProtKB: Q7Z4L1 (UniProtKB/Swiss-Prot),   Q7L7L3 (UniProtKB/Swiss-Prot),   Q16182 (UniProtKB/Swiss-Prot),   P63241 (UniProtKB/Swiss-Prot),   P10159 (UniProtKB/Swiss-Prot),   D3DTP2 (UniProtKB/Swiss-Prot),   A8K9A0 (UniProtKB/Swiss-Prot),   Q9D0G2 (UniProtKB/Swiss-Prot),   I3L397 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357350   ⟸   NM_001370421
- Peptide Label: isoform B
- UniProtKB: Q7Z4L1 (UniProtKB/Swiss-Prot),   Q7L7L3 (UniProtKB/Swiss-Prot),   Q16182 (UniProtKB/Swiss-Prot),   P63241 (UniProtKB/Swiss-Prot),   P10159 (UniProtKB/Swiss-Prot),   D3DTP2 (UniProtKB/Swiss-Prot),   A8K9A0 (UniProtKB/Swiss-Prot),   Q9D0G2 (UniProtKB/Swiss-Prot),   I3L397 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000336702   ⟸   ENST00000336452
Ensembl Acc Id: ENSP00000336776   ⟸   ENST00000336458
Ensembl Acc Id: ENSP00000458269   ⟸   ENST00000571955
Ensembl Acc Id: ENSP00000461688   ⟸   ENST00000572815
Ensembl Acc Id: ENSP00000460284   ⟸   ENST00000573714
Ensembl Acc Id: ENSP00000459611   ⟸   ENST00000573542
Ensembl Acc Id: ENSP00000396073   ⟸   ENST00000416016
Ensembl Acc Id: ENSP00000390677   ⟸   ENST00000419711
Ensembl Acc Id: ENSP00000459196   ⟸   ENST00000576930
RefSeq Acc Id: XP_047291479   ⟸   XM_047435523
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047291480   ⟸   XM_047435524
- Peptide Label: isoform X2
- UniProtKB: Q7Z4L1 (UniProtKB/Swiss-Prot),   Q7L7L3 (UniProtKB/Swiss-Prot),   Q16182 (UniProtKB/Swiss-Prot),   P63241 (UniProtKB/Swiss-Prot),   P10159 (UniProtKB/Swiss-Prot),   D3DTP2 (UniProtKB/Swiss-Prot),   A8K9A0 (UniProtKB/Swiss-Prot),   Q9D0G2 (UniProtKB/Swiss-Prot),   I3L397 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171292   ⟸   XM_054315317
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171288   ⟸   XM_054315313
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171289   ⟸   XM_054315314
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171290   ⟸   XM_054315315
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171293   ⟸   XM_054315318
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171291   ⟸   XM_054315316
- Peptide Label: isoform X1
- UniProtKB: B7Z8F1 (UniProtKB/TrEMBL)
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P63241-F1-model_v2 AlphaFold P63241 1-154 view protein structure

Promoters
RGD ID:6793970
Promoter ID:HG_KWN:24864
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001143760,   NM_001143761,   NM_001143762,   OTTHUMT00000220047,   UC002GFS.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36177,151,101 - 7,152,537 (+)MPROMDB
RGD ID:6811162
Promoter ID:HG_ACW:32927
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:EIF5A.IAPR07-UNSPLICED,   EIF5A.JAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 36177,152,821 - 7,154,022 (+)MPROMDB
RGD ID:7233685
Promoter ID:EPDNEW_H22588
Type:initiation region
Name:EIF5A_4
Description:eukaryotic translation initiation factor 5A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22589  EPDNEW_H22590  EPDNEW_H22591  EPDNEW_H22592  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,045 - 7,307,105EPDNEW
RGD ID:7233687
Promoter ID:EPDNEW_H22589
Type:initiation region
Name:EIF5A_5
Description:eukaryotic translation initiation factor 5A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22588  EPDNEW_H22590  EPDNEW_H22591  EPDNEW_H22592  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,299 - 7,307,359EPDNEW
RGD ID:7233689
Promoter ID:EPDNEW_H22590
Type:initiation region
Name:EIF5A_2
Description:eukaryotic translation initiation factor 5A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22588  EPDNEW_H22589  EPDNEW_H22591  EPDNEW_H22592  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,630 - 7,307,690EPDNEW
RGD ID:7233691
Promoter ID:EPDNEW_H22591
Type:initiation region
Name:EIF5A_1
Description:eukaryotic translation initiation factor 5A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22588  EPDNEW_H22589  EPDNEW_H22590  EPDNEW_H22592  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,307,984 - 7,308,044EPDNEW
RGD ID:7233693
Promoter ID:EPDNEW_H22592
Type:initiation region
Name:EIF5A_3
Description:eukaryotic translation initiation factor 5A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22588  EPDNEW_H22589  EPDNEW_H22590  EPDNEW_H22591  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,308,373 - 7,308,433EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3300 AgrOrtholog
COSMIC EIF5A COSMIC
Ensembl Genes ENSG00000132507 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000288145 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000336452 ENTREZGENE
  ENST00000336452.11 UniProtKB/Swiss-Prot
  ENST00000336458 ENTREZGENE
  ENST00000336458.13 UniProtKB/Swiss-Prot
  ENST00000416016 ENTREZGENE
  ENST00000416016.2 UniProtKB/Swiss-Prot
  ENST00000419711 ENTREZGENE
  ENST00000419711.6 UniProtKB/Swiss-Prot
  ENST00000571955.5 UniProtKB/Swiss-Prot
  ENST00000572815.5 UniProtKB/TrEMBL
  ENST00000573542.5 UniProtKB/Swiss-Prot
  ENST00000573714 ENTREZGENE
  ENST00000573714.5 UniProtKB/TrEMBL
  ENST00000576930.5 UniProtKB/Swiss-Prot
  ENST00000672043.1 UniProtKB/TrEMBL
  ENST00000672250.1 UniProtKB/Swiss-Prot
  ENST00000672755.1 UniProtKB/Swiss-Prot
  ENST00000672765.1 UniProtKB/Swiss-Prot
  ENST00000673099.1 UniProtKB/Swiss-Prot
  ENST00000673105.1 UniProtKB/TrEMBL
  ENST00000673210.1 UniProtKB/Swiss-Prot
  ENST00000673259.1 UniProtKB/Swiss-Prot
  ENST00000673304.1 UniProtKB/Swiss-Prot
Gene3D-CATH 2.30.30.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.40.50.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000132507 GTEx
  ENSG00000288145 GTEx
HGNC ID HGNC:3300 ENTREZGENE
Human Proteome Map EIF5A Human Proteome Map
InterPro IF5A-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IF5A-like_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NA-bd_OB-fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Rib_L2_dom2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Trans_elong_IF5A_hypusine_site UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Transl_elong_IF5A_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Translation_prot_SH3-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:1984 UniProtKB/Swiss-Prot
NCBI Gene 1984 ENTREZGENE
OMIM 600187 OMIM
PANTHER PTHR11673 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam eIF-5a UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IF5A-like_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27726 PharmGKB
PIRSF eIF5A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE IF5A_HYPUSINE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART eIF-5a UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50104 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF50249 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K9A0 ENTREZGENE
  B7Z8F1 ENTREZGENE, UniProtKB/TrEMBL
  D3DTP2 ENTREZGENE
  I3L397 ENTREZGENE, UniProtKB/TrEMBL
  I3L504 ENTREZGENE, UniProtKB/TrEMBL
  IF5A1_HUMAN UniProtKB/Swiss-Prot
  P10159 ENTREZGENE
  P63241 ENTREZGENE
  Q16182 ENTREZGENE
  Q7L7L3 ENTREZGENE
  Q7Z4L1 ENTREZGENE
  Q9D0G2 ENTREZGENE
UniProt Secondary A8K9A0 UniProtKB/Swiss-Prot
  D3DTP2 UniProtKB/Swiss-Prot
  P10159 UniProtKB/Swiss-Prot
  Q16182 UniProtKB/Swiss-Prot
  Q7L7L3 UniProtKB/Swiss-Prot
  Q7Z4L1 UniProtKB/Swiss-Prot
  Q9D0G2 UniProtKB/Swiss-Prot