SART1 (spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP) - Rat Genome Database

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Gene: SART1 (spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP) Homo sapiens
Analyze
Symbol: SART1
Name: spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP
RGD ID: 736742
HGNC Page HGNC:10538
Description: Enables RNA binding activity. Involved in mRNA splicing, via spliceosome and positive regulation of cytotoxic T cell differentiation. Located in Cajal body; Golgi apparatus; and nuclear speck. Part of U2-type precatalytic spliceosome; U4/U6 x U5 tri-snRNP complex; and catalytic step 2 spliceosome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: Ara1; HAF; HOMS1; hSART-1; hSnu66; hypoxia associated factor; IgE autoantigen; MGC2038; SART-1; SART1(259) protein; SART1(800) protein; SART1, U4/U6.U5 tri-snRNP-associated protein 1; SART1259; small nuclear ribonucleoprotein 110kDa (U4/U6.U5); SNRNP110; Snu66; SNU66 homolog; squamous cell carcinoma antigen recognised by T cells; squamous cell carcinoma antigen recognized by T cells 1; squamous cell carcinoma antigen recognized by T-cells 1; U4/U6.U5 tri-snRNP-associated 110 kDa protein; U4/U6.U5 tri-snRNP-associated protein 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381165,961,734 - 65,980,137 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1165,961,728 - 65,980,137 (+)EnsemblGRCh38hg38GRCh38
GRCh371165,729,205 - 65,747,608 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361165,485,736 - 65,504,183 (+)NCBINCBI36Build 36hg18NCBI36
Build 341165,485,775 - 65,504,183NCBI
Celera1163,052,947 - 63,072,024 (+)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1162,055,564 - 62,073,712 (+)NCBIHuRef
CHM1_11165,613,581 - 65,631,741 (+)NCBICHM1_1
T2T-CHM13v2.01165,954,815 - 65,974,269 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-amino-2,6-dinitrotoluene  (ISO)
acrylamide  (EXP)
Aflatoxin B2 alpha  (EXP)
allethrin  (ISO)
ammonium chloride  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (EXP)
benzo[e]pyrene  (EXP)
bisphenol A  (EXP,ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
caffeine  (EXP)
chlorpyrifos  (ISO)
choline  (ISO)
cisplatin  (EXP)
cocaine  (ISO)
copper(II) chloride  (EXP)
coumarin  (EXP)
cyclosporin A  (EXP)
cyhalothrin  (ISO)
cypermethrin  (ISO)
dextran sulfate  (ISO)
diarsenic trioxide  (EXP)
diazinon  (ISO)
dibutyl phthalate  (ISO)
dieldrin  (ISO)
disodium selenite  (EXP)
elemental selenium  (EXP)
enzyme inhibitor  (EXP)
ethanol  (ISO)
fenvalerate  (ISO)
flutamide  (ISO)
folic acid  (ISO)
FR900359  (EXP)
ionomycin  (EXP)
ivermectin  (EXP)
L-methionine  (ISO)
lead diacetate  (EXP,ISO)
methapyrilene  (EXP)
methidathion  (ISO)
methylparaben  (EXP)
nickel dichloride  (ISO)
ozone  (EXP)
paracetamol  (ISO)
perfluorononanoic acid  (EXP)
phorbol 13-acetate 12-myristate  (EXP)
pyrethrins  (ISO)
pyrrolidine dithiocarbamate  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
selenium atom  (EXP)
sodium arsenite  (EXP)
sunitinib  (EXP)
tamoxifen  (ISO)
thiram  (EXP)
titanium dioxide  (ISO)
triphenyl phosphate  (EXP)
tungsten  (ISO)
valproic acid  (ISO)
vinclozolin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:8889548   PMID:9449708   PMID:9856836   PMID:10209962   PMID:10551332   PMID:10853014   PMID:10929426   PMID:11092984   PMID:11156463   PMID:11350945   PMID:11410364  
PMID:11971955   PMID:11991638   PMID:12032085   PMID:12189166   PMID:12477932   PMID:14702039   PMID:15175327   PMID:15302935   PMID:15489334   PMID:15620657   PMID:16055720   PMID:16158934  
PMID:16344560   PMID:16687569   PMID:16723661   PMID:17000644   PMID:17081983   PMID:17332742   PMID:17643375   PMID:18029348   PMID:18235501   PMID:18374504   PMID:18838541   PMID:19615732  
PMID:20020773   PMID:20056645   PMID:20360068   PMID:20467437   PMID:21145461   PMID:21244100   PMID:21252943   PMID:21614000   PMID:21628590   PMID:21832049   PMID:21873635   PMID:22027693  
PMID:22365833   PMID:22586326   PMID:22658674   PMID:22681889   PMID:22939629   PMID:22944692   PMID:23022380   PMID:23125841   PMID:23398456   PMID:23443559   PMID:23537643   PMID:23602568  
PMID:23726919   PMID:24244333   PMID:24457600   PMID:24711643   PMID:24872507   PMID:24981860   PMID:25092792   PMID:25481564   PMID:25609649   PMID:25693804   PMID:25825154   PMID:25862789  
PMID:25915846   PMID:25921289   PMID:26167880   PMID:26186194   PMID:26344197   PMID:26362536   PMID:26496610   PMID:26527279   PMID:26678539   PMID:26760575   PMID:27025967   PMID:27049334  
PMID:27173435   PMID:27248496   PMID:27437069   PMID:27591049   PMID:27684187   PMID:28077916   PMID:28302793   PMID:28514442   PMID:28515276   PMID:28561026   PMID:28781166   PMID:28878014  
PMID:28977666   PMID:28978906   PMID:29117863   PMID:29180619   PMID:29298432   PMID:29467282   PMID:29478914   PMID:29490077   PMID:29615496   PMID:29802200   PMID:29991511   PMID:30021884  
PMID:30209976   PMID:30415952   PMID:30462309   PMID:30585729   PMID:30705246   PMID:30804502   PMID:30884312   PMID:30890647   PMID:30948266   PMID:30975767   PMID:31010829   PMID:31048545  
PMID:31059266   PMID:31076518   PMID:31180492   PMID:31239290   PMID:31300519   PMID:31553912   PMID:31586073   PMID:31665637   PMID:31753913   PMID:31980649   PMID:32296183   PMID:32416067  
PMID:32538781   PMID:32707033   PMID:32780723   PMID:32786267   PMID:32807901   PMID:32971831   PMID:33022573   PMID:33111431   PMID:33298525   PMID:33306668   PMID:33391530   PMID:33545068  
PMID:33640491   PMID:33658012   PMID:33961781   PMID:34079125   PMID:34189442   PMID:34244482   PMID:34349018   PMID:34672947   PMID:34709727   PMID:34728620   PMID:34795231   PMID:35013218  
PMID:35013556   PMID:35235311   PMID:35253629   PMID:35256949   PMID:35271311   PMID:35439318   PMID:35545047   PMID:35575683   PMID:35627203   PMID:35819319   PMID:35831314   PMID:35844135  
PMID:35850772   PMID:35906200   PMID:35915203   PMID:35944360   PMID:36215168   PMID:36232890   PMID:36273042   PMID:36373674   PMID:36424410   PMID:36526897   PMID:36574265   PMID:36774506  
PMID:37039823   PMID:37059091   PMID:37071682   PMID:37267103   PMID:37827155   PMID:38113892   PMID:38270169   PMID:38697112   PMID:38803224  


Genomics

Comparative Map Data
SART1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381165,961,734 - 65,980,137 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1165,961,728 - 65,980,137 (+)EnsemblGRCh38hg38GRCh38
GRCh371165,729,205 - 65,747,608 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361165,485,736 - 65,504,183 (+)NCBINCBI36Build 36hg18NCBI36
Build 341165,485,775 - 65,504,183NCBI
Celera1163,052,947 - 63,072,024 (+)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1162,055,564 - 62,073,712 (+)NCBIHuRef
CHM1_11165,613,581 - 65,631,741 (+)NCBICHM1_1
T2T-CHM13v2.01165,954,815 - 65,974,269 (+)NCBIT2T-CHM13v2.0
Sart1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39195,427,551 - 5,438,731 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl195,427,551 - 5,438,731 (-)EnsemblGRCm39 Ensembl
GRCm38195,377,523 - 5,388,703 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl195,377,523 - 5,388,703 (-)EnsemblGRCm38mm10GRCm38
MGSCv37195,377,523 - 5,388,703 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36195,380,060 - 5,388,703 (-)NCBIMGSCv36mm8
Celera195,249,908 - 5,261,089 (-)NCBICelera
Cytogenetic Map19ANCBI
cM Map194.31NCBI
Sart1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81212,119,824 - 212,128,517 (-)NCBIGRCr8
mRatBN7.21202,690,472 - 202,699,136 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1202,690,459 - 202,699,136 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1211,043,120 - 211,051,770 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01218,135,893 - 218,144,555 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01210,826,942 - 210,835,604 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01220,762,496 - 220,771,158 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1220,762,349 - 220,771,181 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01227,691,827 - 227,700,489 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41208,026,619 - 208,035,281 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11208,180,071 - 208,188,734 (-)NCBI
Celera1200,225,786 - 200,234,448 (-)NCBICelera
Cytogenetic Map1q43NCBI
Sart1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542219,360,641 - 19,371,105 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495542219,360,641 - 19,370,623 (-)NCBIChiLan1.0ChiLan1.0
SART1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2967,194,567 - 67,211,687 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11168,236,685 - 68,254,507 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01161,326,262 - 61,343,475 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11164,654,470 - 64,670,720 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1164,654,470 - 64,670,720 (+)Ensemblpanpan1.1panPan2
SART1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11851,297,419 - 51,313,804 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1851,297,419 - 51,313,793 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1849,905,958 - 49,922,359 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01852,335,738 - 52,352,155 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1852,335,740 - 52,352,138 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11851,435,710 - 51,452,108 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01851,009,941 - 51,026,329 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01851,799,743 - 51,816,162 (-)NCBIUU_Cfam_GSD_1.0
Sart1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049477,135,211 - 7,145,708 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365993,577,480 - 3,588,706 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365993,577,552 - 3,588,825 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SART1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl26,354,908 - 6,373,272 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.126,355,690 - 6,373,342 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.225,459,382 - 5,477,018 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SART1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.118,279,821 - 8,296,282 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl18,275,123 - 8,296,245 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038105,564,949 - 105,582,326 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Sart1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476720,456,890 - 20,467,641 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476720,456,951 - 20,466,994 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SART1
41 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_152762.2(TSGA10IP):c.1666C>T (p.Pro556Ser) single nucleotide variant Malignant melanoma [RCV000069612] Chr11:65959935 [GRCh38]
Chr11:65727406 [GRCh37]
Chr11:65483982 [NCBI36]
Chr11:11q13.1		 not provided
NM_152762.2(TSGA10IP):c.1667C>T (p.Pro556Leu) single nucleotide variant Malignant melanoma [RCV000069613] Chr11:65959936 [GRCh38]
Chr11:65727407 [GRCh37]
Chr11:65483983 [NCBI36]
Chr11:11q13.1		 not provided
GRCh38/hg38 11q13.1-13.2(chr11:65741431-67705669)x1 copy number loss See cases [RCV000142881] Chr11:65741431..67705669 [GRCh38]
Chr11:65508902..67473140 [GRCh37]
Chr11:65265478..67229716 [NCBI36]
Chr11:11q13.1-13.2		 pathogenic
NM_005146.5(SART1):c.1088G>A (p.Arg363Gln) single nucleotide variant not specified [RCV004317612] Chr11:65966456 [GRCh38]
Chr11:65733927 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11q13.1-13.2(chr11:64501919-67129258)x3 copy number gain See cases [RCV000511632] Chr11:64501919..67129258 [GRCh37]
Chr11:11q13.1-13.2		 likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_005146.5(SART1):c.491G>C (p.Arg164Pro) single nucleotide variant not specified [RCV004327041] Chr11:65965155 [GRCh38]
Chr11:65732626 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11q13.1-13.2(chr11:65138976-67574402) copy number gain not provided [RCV000767601] Chr11:65138976..67574402 [GRCh37]
Chr11:11q13.1-13.2		 pathogenic
NM_005146.5(SART1):c.1844A>G (p.Lys615Arg) single nucleotide variant not specified [RCV004326931] Chr11:65976753 [GRCh38]
Chr11:65744224 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NC_000011.9:g.(?_65633902)_(66115026_?)dup duplication Cutis laxa, autosomal recessive, type 1B [RCV000798155] Chr11:65866431..66347555 [GRCh38]
Chr11:65633902..66115026 [GRCh37]
Chr11:11q13.1-13.2		 uncertain significance
NM_005146.5(SART1):c.2253C>T (p.Asp751=) single nucleotide variant not provided [RCV001200347] Chr11:65978680 [GRCh38]
Chr11:65746151 [GRCh37]
Chr11:11q13.1		 likely benign
NC_000011.9:g.(?_64973914)_(70052579_?)dup duplication Aicardi-Goutieres syndrome 3 [RCV003113322]|FADD-related immunodeficiency [RCV003107753] Chr11:64973914..70052579 [GRCh37]
Chr11:11q13.1-13.3		 uncertain significance
NC_000011.9:g.(?_65633902)_(66115026_?)dup duplication Autosomal recessive cutis laxa type 1B [RCV001305354] Chr11:65633902..66115026 [GRCh37]
Chr11:11q13.1-13.2		 uncertain significance
NC_000011.9:g.(?_59596957)_(68707199_?)dup duplication Familial temporal lobe epilepsy 8 [RCV001372442] Chr11:59596957..68707199 [GRCh37]
Chr11:11q12.1-13.3		 uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh37/hg19 11q13.1-13.2(chr11:64935724-66405514) copy number loss not specified [RCV002052930] Chr11:64935724..66405514 [GRCh37]
Chr11:11q13.1-13.2		 uncertain significance
NC_000011.9:g.(?_64522783)_(66283694_?)del deletion Bardet-Biedl syndrome [RCV002014493]|Glycogen storage disease, type V [RCV002004587] Chr11:64522783..66283694 [GRCh37]
Chr11:11q13.1-13.2		 pathogenic
NM_005146.5(SART1):c.1339G>A (p.Val447Met) single nucleotide variant not specified [RCV004325372] Chr11:65967496 [GRCh38]
Chr11:65734967 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
NM_005146.5(SART1):c.431C>T (p.Ala144Val) single nucleotide variant not specified [RCV004310698] Chr11:65965095 [GRCh38]
Chr11:65732566 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.595G>A (p.Asp199Asn) single nucleotide variant not specified [RCV004331040] Chr11:65965382 [GRCh38]
Chr11:65732853 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1144G>C (p.Val382Leu) single nucleotide variant not specified [RCV004209984] Chr11:65966512 [GRCh38]
Chr11:65733983 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.169C>T (p.Arg57Trp) single nucleotide variant not specified [RCV004200846] Chr11:65961949 [GRCh38]
Chr11:65729420 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1654G>A (p.Val552Met) single nucleotide variant not specified [RCV004169153] Chr11:65976476 [GRCh38]
Chr11:65743947 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.704C>T (p.Thr235Ile) single nucleotide variant not specified [RCV004083238] Chr11:65965745 [GRCh38]
Chr11:65733216 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1228C>G (p.Arg410Gly) single nucleotide variant not specified [RCV004181405] Chr11:65967298 [GRCh38]
Chr11:65734769 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.255G>C (p.Gln85His) single nucleotide variant not specified [RCV004236496] Chr11:65962035 [GRCh38]
Chr11:65729506 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1460C>T (p.Pro487Leu) single nucleotide variant not specified [RCV004157546] Chr11:65967709 [GRCh38]
Chr11:65735180 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.254A>C (p.Gln85Pro) single nucleotide variant not specified [RCV004236494] Chr11:65962034 [GRCh38]
Chr11:65729505 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.360C>G (p.Ile120Met) single nucleotide variant not specified [RCV004157108] Chr11:65964120 [GRCh38]
Chr11:65731591 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1318C>T (p.Arg440Trp) single nucleotide variant not specified [RCV004138505] Chr11:65967475 [GRCh38]
Chr11:65734946 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.221C>T (p.Ala74Val) single nucleotide variant not specified [RCV004081541] Chr11:65962001 [GRCh38]
Chr11:65729472 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.76A>G (p.Thr26Ala) single nucleotide variant not specified [RCV004178775] Chr11:65961856 [GRCh38]
Chr11:65729327 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1479C>G (p.Asp493Glu) single nucleotide variant not specified [RCV004167396] Chr11:65967728 [GRCh38]
Chr11:65735199 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.734G>A (p.Arg245Gln) single nucleotide variant not specified [RCV004242751] Chr11:65965775 [GRCh38]
Chr11:65733246 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.874G>A (p.Val292Met) single nucleotide variant not specified [RCV004242418] Chr11:65966111 [GRCh38]
Chr11:65733582 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.2107G>A (p.Gly703Ser) single nucleotide variant not specified [RCV004203547] Chr11:65977834 [GRCh38]
Chr11:65745305 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1305T>G (p.Phe435Leu) single nucleotide variant not specified [RCV004171809] Chr11:65967375 [GRCh38]
Chr11:65734846 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.271C>T (p.Arg91Trp) single nucleotide variant not specified [RCV004240995] Chr11:65962051 [GRCh38]
Chr11:65729522 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1231A>G (p.Lys411Glu) single nucleotide variant not specified [RCV004107343] Chr11:65967301 [GRCh38]
Chr11:65734772 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1053G>C (p.Leu351Phe) single nucleotide variant not specified [RCV004178938] Chr11:65966421 [GRCh38]
Chr11:65733892 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.476T>C (p.Met159Thr) single nucleotide variant not specified [RCV004163560] Chr11:65965140 [GRCh38]
Chr11:65732611 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.197G>A (p.Gly66Glu) single nucleotide variant not specified [RCV004178393] Chr11:65961977 [GRCh38]
Chr11:65729448 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1334G>A (p.Arg445His) single nucleotide variant not specified [RCV004322857] Chr11:65967491 [GRCh38]
Chr11:65734962 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.2344C>G (p.Pro782Ala) single nucleotide variant not specified [RCV004250373] Chr11:65978874 [GRCh38]
Chr11:65746345 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1229G>T (p.Arg410Leu) single nucleotide variant not specified [RCV004268307] Chr11:65967299 [GRCh38]
Chr11:65734770 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1468C>G (p.Leu490Val) single nucleotide variant not specified [RCV004255513] Chr11:65967717 [GRCh38]
Chr11:65735188 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1547A>C (p.Gln516Pro) single nucleotide variant not specified [RCV004321805] Chr11:65967796 [GRCh38]
Chr11:65735267 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1941C>G (p.Asn647Lys) single nucleotide variant not specified [RCV004270700] Chr11:65977097 [GRCh38]
Chr11:65744568 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1049G>A (p.Arg350His) single nucleotide variant not specified [RCV004287163] Chr11:65966417 [GRCh38]
Chr11:65733888 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1567G>A (p.Glu523Lys) single nucleotide variant not specified [RCV004342032] Chr11:65967816 [GRCh38]
Chr11:65735287 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1165G>A (p.Glu389Lys) single nucleotide variant not specified [RCV004350791] Chr11:65966533 [GRCh38]
Chr11:65734004 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.718G>A (p.Glu240Lys) single nucleotide variant not specified [RCV004339693] Chr11:65965759 [GRCh38]
Chr11:65733230 [GRCh37]
Chr11:11q13.1		 uncertain significance
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3 copy number gain not provided [RCV003484842] Chr11:59923608..76272324 [GRCh37]
Chr11:11q12.2-13.5		 pathogenic
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3 copy number gain not specified [RCV003986944] Chr11:56895955..69295402 [GRCh37]
Chr11:11q12.1-13.3		 likely pathogenic
NM_005146.5(SART1):c.1900G>A (p.Val634Met) single nucleotide variant not specified [RCV004450186] Chr11:65977056 [GRCh38]
Chr11:65744527 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.841G>A (p.Val281Met) single nucleotide variant not specified [RCV004450192] Chr11:65966078 [GRCh38]
Chr11:65733549 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1420A>G (p.Ser474Gly) single nucleotide variant not specified [RCV004450179] Chr11:65967577 [GRCh38]
Chr11:65735048 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.58G>T (p.Ala20Ser) single nucleotide variant not specified [RCV004450189] Chr11:65961838 [GRCh38]
Chr11:65729309 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1204A>G (p.Thr402Ala) single nucleotide variant not specified [RCV004450176] Chr11:65967274 [GRCh38]
Chr11:65734745 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1522C>T (p.Arg508Trp) single nucleotide variant not specified [RCV004450182] Chr11:65967771 [GRCh38]
Chr11:65735242 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1640G>A (p.Arg547Gln) single nucleotide variant not specified [RCV004450184] Chr11:65976462 [GRCh38]
Chr11:65743933 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.140G>A (p.Gly47Asp) single nucleotide variant not specified [RCV004450178] Chr11:65961920 [GRCh38]
Chr11:65729391 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.569T>G (p.Leu190Arg) single nucleotide variant not specified [RCV004450188] Chr11:65965356 [GRCh38]
Chr11:65732827 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.769C>T (p.Leu257Phe) single nucleotide variant not specified [RCV004450191] Chr11:65965917 [GRCh38]
Chr11:65733388 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.722T>C (p.Phe241Ser) single nucleotide variant not specified [RCV004658487] Chr11:65965763 [GRCh38]
Chr11:65733234 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1484C>T (p.Ala495Val) single nucleotide variant not specified [RCV004450181] Chr11:65967733 [GRCh38]
Chr11:65735204 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1667C>T (p.Thr556Met) single nucleotide variant not specified [RCV004450185] Chr11:65976489 [GRCh38]
Chr11:65743960 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.59C>T (p.Ala20Val) single nucleotide variant not specified [RCV004450190] Chr11:65961839 [GRCh38]
Chr11:65729310 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1603C>T (p.Arg535Cys) single nucleotide variant not specified [RCV004450183] Chr11:65976425 [GRCh38]
Chr11:65743896 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1494G>C (p.Glu498Asp) single nucleotide variant not specified [RCV004658486] Chr11:65967743 [GRCh38]
Chr11:65735214 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.1822A>T (p.Thr608Ser) single nucleotide variant not specified [RCV004658485] Chr11:65976731 [GRCh38]
Chr11:65744202 [GRCh37]
Chr11:11q13.1		 uncertain significance
NM_005146.5(SART1):c.181G>A (p.Gly61Ser) single nucleotide variant not specified [RCV004674481] Chr11:65961961 [GRCh38]
Chr11:65729432 [GRCh37]
Chr11:11q13.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2558
Count of miRNA genes:920
Interacting mature miRNAs:1141
Transcripts:ENST00000312397, ENST00000528137, ENST00000528573, ENST00000529532, ENST00000529580, ENST00000530251, ENST00000532333, ENST00000533386
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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
1357380BW64_HBody weight QTL 64 (human)2.2Body weightpercent fat after exercise training116097893786978937Human
406903298GWAS552274_HCOVID-19 QTL GWAS552274 (human)0.000008COVID-19116597495565974956Human
407338437GWAS987413_Hurate measurement QTL GWAS987413 (human)2e-12urate measurementblood uric acid level (CMO:0000501)116597958665979587Human
407165376GWAS814352_Hcardiac troponin T measurement QTL GWAS814352 (human)0.0000007cardiac troponin T measurementblood troponin T level (CMO:0001284)116596347465963475Human
406983941GWAS632917_HBMI-adjusted waist circumference QTL GWAS632917 (human)1e-19BMI-adjusted waist circumference116597679465976795Human
406983946GWAS632922_HBMI-adjusted waist circumference QTL GWAS632922 (human)1e-12BMI-adjusted waist circumference116597481265974813Human
407299711GWAS948687_Hlean body mass QTL GWAS948687 (human)4e-14body lean mass (VT:0010483)total body lean mass (CMO:0003950)116596599465965995Human
407195132GWAS844108_Hcardiac troponin T measurement QTL GWAS844108 (human)0.000003cardiac troponin T measurementblood troponin T level (CMO:0001284)116597299765972998Human
407117434GWAS766410_Hsexual dimorphism measurement QTL GWAS766410 (human)1e-15sexual dimorphism measurement116596599465965995Human
407117386GWAS766362_Hsexual dimorphism measurement QTL GWAS766362 (human)7e-09sexual dimorphism measurement116597679465976795Human
407105868GWAS754844_Hbody height QTL GWAS754844 (human)1e-17body height (VT:0001253)body height (CMO:0000106)116597958665979587Human

Markers in Region
RH92212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,747,072 - 65,747,238UniSTSGRCh37
Build 361165,503,648 - 65,503,814RGDNCBI36
Celera1163,071,489 - 63,071,655RGD
Cytogenetic Map11q13.1UniSTS
HuRef1162,073,177 - 62,073,343UniSTS
GeneMap99-GB4 RH Map11242.84UniSTS
RH16397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,746,107 - 65,746,354UniSTSGRCh37
Build 361165,502,683 - 65,502,930RGDNCBI36
Celera1163,070,524 - 63,070,771RGD
Cytogenetic Map11q13.1UniSTS
HuRef1162,072,212 - 62,072,459UniSTS
GeneMap99-GB4 RH Map11240.12UniSTS
NCBI RH Map11573.2UniSTS
MARC_26072-26073:1032454189:5  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371165,745,281 - 65,746,126UniSTSGRCh37
Build 361165,501,857 - 65,502,702RGDNCBI36
Celera1163,069,698 - 63,070,543RGD
HuRef1162,071,386 - 62,072,231UniSTS


Sequence

Nucleotide Sequences
RefSeq Transcripts NM_005146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011545344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011545345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427856 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_950099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB006198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF109680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF353625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP006287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AU136920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW082868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC018607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM668558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM693243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT006637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y14314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000312397   ⟹   ENSP00000310448
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,961,734 - 65,980,137 (+)Ensembl
Ensembl Acc Id: ENST00000528137
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,978,487 - 65,979,089 (+)Ensembl
Ensembl Acc Id: ENST00000528573
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,961,729 - 65,965,129 (+)Ensembl
Ensembl Acc Id: ENST00000529532
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,961,728 - 65,967,316 (+)Ensembl
Ensembl Acc Id: ENST00000529580
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,977,765 - 65,978,957 (+)Ensembl
Ensembl Acc Id: ENST00000530251   ⟹   ENSP00000436218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,961,729 - 65,965,447 (+)Ensembl
Ensembl Acc Id: ENST00000532333
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,961,728 - 65,964,512 (+)Ensembl
Ensembl Acc Id: ENST00000533386
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1165,976,749 - 65,978,152 (+)Ensembl
RefSeq Acc Id: NM_005146   ⟹   NP_005137
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,961,734 - 65,980,137 (+)NCBI
GRCh371165,729,160 - 65,747,607 (+)ENTREZGENE
Build 361165,485,736 - 65,504,183 (+)NCBI Archive
HuRef1162,055,564 - 62,073,712 (+)ENTREZGENE
CHM1_11165,613,581 - 65,631,741 (+)NCBI
T2T-CHM13v2.01165,954,815 - 65,974,269 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047427856   ⟹   XP_047283812
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,961,734 - 65,976,560 (+)NCBI
RefSeq Acc Id: XM_054370462   ⟹   XP_054226437
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01165,954,815 - 65,970,692 (+)NCBI
RefSeq Acc Id: NP_005137   ⟸   NM_005146
- UniProtKB: A6NDN1 (UniProtKB/Swiss-Prot),   Q53GB5 (UniProtKB/Swiss-Prot),   O43290 (UniProtKB/Swiss-Prot),   B4DDH9 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000436218   ⟸   ENST00000530251
Ensembl Acc Id: ENSP00000310448   ⟸   ENST00000312397
RefSeq Acc Id: XP_047283812   ⟸   XM_047427856
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054226437   ⟸   XM_054370462
- Peptide Label: isoform X1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O43290-F1-model_v2 AlphaFold O43290 1-800 view protein structure

Promoters
RGD ID:6789343
Promoter ID:HG_KWN:13374
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_005146,   UC009YQY.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361165,485,441 - 65,485,941 (+)MPROMDB
RGD ID:7221101
Promoter ID:EPDNEW_H16296
Type:initiation region
Name:SART1_1
Description:squamous cell carcinoma antigen recognized by T-cells 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381165,961,734 - 65,961,794EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:10538 AgrOrtholog
COSMIC SART1 COSMIC
Ensembl Genes ENSG00000175467 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000312397 ENTREZGENE
  ENST00000312397.10 UniProtKB/Swiss-Prot
  ENST00000530251.1 UniProtKB/TrEMBL
GTEx ENSG00000175467 GTEx
HGNC ID HGNC:10538 ENTREZGENE
Human Proteome Map SART1 Human Proteome Map
InterPro HIND UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNU66/SART1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9092 UniProtKB/Swiss-Prot
NCBI Gene 9092 ENTREZGENE
OMIM 605941 OMIM
PANTHER PTHR14152 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  U4/U6.U5 TRI-SNRNP-ASSOCIATED PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam HIND UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SART-1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34947 PharmGKB
UniProt A6NDN1 ENTREZGENE
  B4DDH9 ENTREZGENE, UniProtKB/TrEMBL
  E9PQI8_HUMAN UniProtKB/TrEMBL
  O43290 ENTREZGENE
  Q53GB5 ENTREZGENE
  SNUT1_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A6NDN1 UniProtKB/Swiss-Prot
  Q53GB5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-08-14 SART1  spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP  SART1  SART1, U4/U6.U5 tri-snRNP-associated protein 1  Symbol and/or name change 5135510 APPROVED
2017-06-20 SART1  SART1, U4/U6.U5 tri-snRNP-associated protein 1  SART1  squamous cell carcinoma antigen recognized by T-cells 1  Symbol and/or name change 5135510 APPROVED
2015-12-08 SART1  squamous cell carcinoma antigen recognized by T-cells 1  SART1  squamous cell carcinoma antigen recognized by T cells 1  Symbol and/or name change 5135510 APPROVED
2015-07-07 SART1  squamous cell carcinoma antigen recognized by T cells 1  SART1  squamous cell carcinoma antigen recognized by T cells  Symbol and/or name change 5135510 APPROVED