ARL6IP6 (ADP ribosylation factor like GTPase 6 interacting protein 6) - Rat Genome Database

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Gene: ARL6IP6 (ADP ribosylation factor like GTPase 6 interacting protein 6) Homo sapiens
Analyze
Symbol: ARL6IP6
Name: ADP ribosylation factor like GTPase 6 interacting protein 6
RGD ID: 1347021
HGNC Page HGNC:24048
Description: Predicted to be located in nuclear inner membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: ADP-ribosylation factor GTPase 6 interacting protein 6; ADP-ribosylation factor like GTPase 6 interacting protein 6; ADP-ribosylation factor-like 6 interacting protein 6; ADP-ribosylation factor-like protein 6-interacting protein 6; ADP-ribosylation-like factor 6 interacting protein 6; ADP-ribosylation-like factor 6-interacting protein 6; AIP-6; AIP6; ARL-6-interacting protein 6; MGC33864; PFAAP1; phosphonoformate immuno-associated protein 1; regulated by phosphonoformate
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: LOC100216346  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382152,717,648 - 152,762,396 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2152,717,647 - 152,762,396 (+)EnsemblGRCh38hg38GRCh38
GRCh372153,574,162 - 153,618,910 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362153,283,373 - 153,325,669 (+)NCBINCBI36Build 36hg18NCBI36
Build 342153,400,637 - 153,442,931NCBI
Celera2147,188,879 - 147,232,317 (+)NCBICelera
Cytogenetic Map2q23.3NCBI
HuRef2145,460,777 - 145,504,138 (+)NCBIHuRef
CHM1_12153,580,440 - 153,623,806 (+)NCBICHM1_1
T2T-CHM13v2.02153,170,194 - 153,214,953 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
membrane  (IEA)
nuclear inner membrane  (IEA,ISS)
nucleus  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10508919   PMID:12477932   PMID:14702039   PMID:15342556   PMID:16344560   PMID:17207965   PMID:21832049   PMID:25957586   PMID:26186194   PMID:26496610   PMID:28298427   PMID:28514442  
PMID:29180619   PMID:30804502   PMID:31073040   PMID:32296183   PMID:32353859   PMID:32838362   PMID:33060197   PMID:33961781   PMID:34597346   PMID:35253629   PMID:35271311   PMID:35696571  
PMID:36526897  


Genomics

Comparative Map Data
ARL6IP6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382152,717,648 - 152,762,396 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2152,717,647 - 152,762,396 (+)EnsemblGRCh38hg38GRCh38
GRCh372153,574,162 - 153,618,910 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362153,283,373 - 153,325,669 (+)NCBINCBI36Build 36hg18NCBI36
Build 342153,400,637 - 153,442,931NCBI
Celera2147,188,879 - 147,232,317 (+)NCBICelera
Cytogenetic Map2q23.3NCBI
HuRef2145,460,777 - 145,504,138 (+)NCBIHuRef
CHM1_12153,580,440 - 153,623,806 (+)NCBICHM1_1
T2T-CHM13v2.02153,170,194 - 153,214,953 (+)NCBIT2T-CHM13v2.0
Arl6ip6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39253,082,096 - 53,109,233 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl253,081,738 - 53,109,232 (+)EnsemblGRCm39 Ensembl
GRCm38253,192,084 - 53,219,221 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl253,191,726 - 53,219,220 (+)EnsemblGRCm38mm10GRCm38
MGSCv37253,051,118 - 53,078,255 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36253,014,120 - 53,041,035 (+)NCBIMGSCv36mm8
MGSCv36253,723,963 - 53,751,274 (+)NCBIMGSCv36mm8
Celera254,933,637 - 54,962,312 (+)NCBICelera
Cytogenetic Map2C1.1NCBI
cM Map230.69NCBI
Arl6ip6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8358,098,978 - 58,126,962 (+)NCBIGRCr8
mRatBN7.2337,689,994 - 37,720,358 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl337,690,382 - 37,718,018 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx341,062,985 - 41,088,913 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0349,647,802 - 49,673,731 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0347,432,644 - 47,458,576 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0338,742,072 - 38,768,010 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl338,742,072 - 38,768,008 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0343,839,462 - 43,867,404 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4334,722,398 - 34,748,336 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera335,828,759 - 35,854,697 (+)NCBICelera
Cytogenetic Map3q12NCBI
Arl6ip6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495544018,131,030 - 18,166,804 (+)NCBIChiLan1.0ChiLan1.0
ARL6IP6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21355,401,925 - 55,444,976 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12B55,417,570 - 55,461,583 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02B40,017,540 - 40,061,039 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12B157,255,439 - 157,299,253 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2B157,255,434 - 157,298,857 (+)Ensemblpanpan1.1panPan2
ARL6IP6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11953,711,210 - 53,733,467 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1953,710,992 - 53,732,278 (+)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1953,710,992 - 53,732,278 (+)NCBICanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2627,925,972 - 27,948,172 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01955,223,048 - 55,245,273 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1955,222,176 - 55,244,679 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11953,938,750 - 53,960,956 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01954,008,750 - 54,031,157 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01955,473,743 - 55,496,125 (+)NCBIUU_Cfam_GSD_1.0
Arl6ip6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303116,654,494 - 116,694,501 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493646924,926,597 - 24,963,379 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493646924,928,861 - 24,963,344 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ARL6IP6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1560,440,308 - 60,471,316 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11560,439,588 - 60,472,991 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21567,085,917 - 67,118,921 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ARL6IP6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11038,151,631 - 38,194,800 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1038,152,268 - 38,195,558 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666040161,372,652 - 161,416,164 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Arl6ip6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473213,256,591 - 13,293,337 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473213,260,118 - 13,292,911 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ARL6IP6
16 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q22.3-24.1(chr2:147251948-157856378)x1 copy number loss See cases [RCV000054090] Chr2:147251948..157856378 [GRCh38]
Chr2:148009516..158712890 [GRCh37]
Chr2:147725986..158421136 [NCBI36]
Chr2:2q22.3-24.1		 pathogenic
GRCh38/hg38 2q22.3-23.3(chr2:147590324-153496674)x1 copy number loss See cases [RCV000054091] Chr2:147590324..153496674 [GRCh38]
Chr2:148347892..154353187 [GRCh37]
Chr2:148064362..154061433 [NCBI36]
Chr2:2q22.3-23.3		 pathogenic
GRCh38/hg38 2q23.1-23.3(chr2:148303135-153274626)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054092]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054092]|See cases [RCV000054092] Chr2:148303135..153274626 [GRCh38]
Chr2:149060704..154131140 [GRCh37]
Chr2:148777174..153839386 [NCBI36]
Chr2:2q23.1-23.3		 pathogenic
GRCh38/hg38 2q23.1-24.3(chr2:148917286-163204623)x1 copy number loss See cases [RCV000054093] Chr2:148917286..163204623 [GRCh38]
Chr2:149674855..164061133 [GRCh37]
Chr2:149391325..163769379 [NCBI36]
Chr2:2q23.1-24.3		 pathogenic
GRCh38/hg38 2q22.3-24.1(chr2:143900149-158321624)x3 copy number gain See cases [RCV000135402] Chr2:143900149..158321624 [GRCh38]
Chr2:144657717..159178136 [GRCh37]
Chr2:144374187..158886382 [NCBI36]
Chr2:2q22.3-24.1		 pathogenic
GRCh38/hg38 2q23.3-24.2(chr2:151932344-159419734)x1 copy number loss See cases [RCV000142664] Chr2:151932344..159419734 [GRCh38]
Chr2:152788858..160276245 [GRCh37]
Chr2:152497104..159984491 [NCBI36]
Chr2:2q23.3-24.2		 pathogenic|likely pathogenic
GRCh38/hg38 2q22.3-24.1(chr2:146324191-156219125)x3 copy number gain See cases [RCV000142582] Chr2:146324191..156219125 [GRCh38]
Chr2:147081759..157075637 [GRCh37]
Chr2:146798229..156783883 [NCBI36]
Chr2:2q22.3-24.1		 pathogenic
NM_152522.7(ARL6IP6):c.192G>A (p.Trp64Ter) single nucleotide variant not provided [RCV000412527] Chr2:152718816 [GRCh38]
Chr2:153575330 [GRCh37]
Chr2:2q23.3		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626436] Chr2:104172062..168223828 [GRCh37]
Chr2:2q12.1-24.3		 drug response
GRCh37/hg19 2q23.2-23.3(chr2:150134077-154848282)x1 copy number loss not provided [RCV000682154] Chr2:150134077..154848282 [GRCh37]
Chr2:2q23.2-23.3		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q23.3-31.2(chr2:152409978-179325736)x3 copy number gain not provided [RCV000740654] Chr2:152409978..179325736 [GRCh37]
Chr2:2q23.3-31.2		 pathogenic
NM_152522.7(ARL6IP6):c.605C>G (p.Ser202Cys) single nucleotide variant not specified [RCV004301287] Chr2:152759764 [GRCh38]
Chr2:153616278 [GRCh37]
Chr2:2q23.3		 uncertain significance
GRCh37/hg19 2q22.3-23.3(chr2:147063452-154796058)x1 copy number loss See cases [RCV000448667] Chr2:147063452..154796058 [GRCh37]
Chr2:2q22.3-23.3		 pathogenic
NM_152522.7(ARL6IP6):c.209G>C (p.Arg70Pro) single nucleotide variant not specified [RCV004320539] Chr2:152718833 [GRCh38]
Chr2:153575347 [GRCh37]
Chr2:2q23.3		 uncertain significance
GRCh37/hg19 2q23.3(chr2:153299943-153640839)x3 copy number gain not provided [RCV000740655] Chr2:153299943..153640839 [GRCh37]
Chr2:2q23.3		 benign
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_152522.7(ARL6IP6):c.167G>T (p.Arg56Leu) single nucleotide variant not provided [RCV000966142] Chr2:152718791 [GRCh38]
Chr2:153575305 [GRCh37]
Chr2:2q23.3		 benign
NM_152522.7(ARL6IP6):c.401-8A>G single nucleotide variant not provided [RCV000955970] Chr2:152720525 [GRCh38]
Chr2:153577039 [GRCh37]
Chr2:2q23.3		 benign
GRCh37/hg19 2q22.3-24.1(chr2:147173792-158346266)x1 copy number loss not provided [RCV001005326] Chr2:147173792..158346266 [GRCh37]
Chr2:2q22.3-24.1		 pathogenic
NM_152522.7(ARL6IP6):c.341C>T (p.Ser114Leu) single nucleotide variant not provided [RCV001810617] Chr2:152718965 [GRCh38]
Chr2:153575479 [GRCh37]
Chr2:2q23.3		 uncertain significance
GRCh37/hg19 2q23.3-24.2(chr2:152967964-160089210)x3 copy number gain not provided [RCV001825170] Chr2:152967964..160089210 [GRCh37]
Chr2:2q23.3-24.2		 not provided
NM_152522.7(ARL6IP6):c.536C>T (p.Ser179Phe) single nucleotide variant not specified [RCV004071368] Chr2:152735075 [GRCh38]
Chr2:153591589 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.166C>G (p.Arg56Gly) single nucleotide variant not specified [RCV004219812] Chr2:152718790 [GRCh38]
Chr2:153575304 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.200C>T (p.Pro67Leu) single nucleotide variant not specified [RCV004186229] Chr2:152718824 [GRCh38]
Chr2:153575338 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.361C>A (p.Leu121Ile) single nucleotide variant not specified [RCV004267458] Chr2:152718985 [GRCh38]
Chr2:153575499 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.277G>T (p.Ala93Ser) single nucleotide variant not specified [RCV004256262] Chr2:152718901 [GRCh38]
Chr2:153575415 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.300G>C (p.Gln100His) single nucleotide variant not specified [RCV004325757] Chr2:152718924 [GRCh38]
Chr2:153575438 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.334C>A (p.Leu112Ile) single nucleotide variant not specified [RCV004315714] Chr2:152718958 [GRCh38]
Chr2:153575472 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.163C>G (p.Leu55Val) single nucleotide variant not specified [RCV004272046] Chr2:152718787 [GRCh38]
Chr2:153575301 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.574C>T (p.Pro192Ser) single nucleotide variant not specified [RCV004283385] Chr2:152735113 [GRCh38]
Chr2:153591627 [GRCh37]
Chr2:2q23.3		 uncertain significance
GRCh37/hg19 2q23.3(chr2:151626277-154149348)x1 copy number loss not specified [RCV003986374] Chr2:151626277..154149348 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.296C>T (p.Ala99Val) single nucleotide variant not specified [RCV004417930] Chr2:152718920 [GRCh38]
Chr2:153575434 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.89C>T (p.Ser30Phe) single nucleotide variant not specified [RCV004417935] Chr2:152718713 [GRCh38]
Chr2:153575227 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.5C>T (p.Ser2Leu) single nucleotide variant not specified [RCV004417933] Chr2:152718629 [GRCh38]
Chr2:153575143 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.577G>A (p.Ala193Thr) single nucleotide variant not specified [RCV004417932] Chr2:152735116 [GRCh38]
Chr2:153591630 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.332T>C (p.Ile111Thr) single nucleotide variant not specified [RCV004417931] Chr2:152718956 [GRCh38]
Chr2:153575470 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.263A>C (p.Asn88Thr) single nucleotide variant not specified [RCV004417927] Chr2:152718887 [GRCh38]
Chr2:153575401 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.136G>A (p.Glu46Lys) single nucleotide variant not specified [RCV004417925] Chr2:152718760 [GRCh38]
Chr2:153575274 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.620A>G (p.Tyr207Cys) single nucleotide variant not specified [RCV004417934] Chr2:152759779 [GRCh38]
Chr2:153616293 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.164T>G (p.Leu55Arg) single nucleotide variant not specified [RCV004417926] Chr2:152718788 [GRCh38]
Chr2:153575302 [GRCh37]
Chr2:2q23.3		 uncertain significance
NM_152522.7(ARL6IP6):c.373C>T (p.Leu125Phe) single nucleotide variant Bardet-Biedl syndrome [RCV003224783] Chr2:152718997 [GRCh38]
Chr2:153575511 [GRCh37]
Chr2:2q23.3		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:735
Count of miRNA genes:382
Interacting mature miRNAs:418
Transcripts:ENST00000326446, ENST00000425034, ENST00000455875, ENST00000463690, ENST00000495469
Prediction methods: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
407417920GWAS1066896_Hsystolic blood pressure QTL GWAS1066896 (human)0.000009systolic blood pressuresystolic blood pressure (CMO:0000004)2152762259152762260Human
407415648GWAS1064624_Hpulse pressure measurement QTL GWAS1064624 (human)5e-10pulse pressure measurementpulse pressure (CMO:0000292)2152762259152762260Human
407310011GWAS958987_Hpulse pressure measurement QTL GWAS958987 (human)5e-09pulse pressure measurementpulse pressure (CMO:0000292)2152762259152762260Human

Markers in Region
D2S1676E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372153,584,235 - 153,584,403UniSTSGRCh37
Build 362153,292,481 - 153,292,649RGDNCBI36
Celera2147,198,784 - 147,198,952RGD
Cytogenetic Map2q23.3UniSTS
HuRef2145,470,606 - 145,470,777UniSTS
A009X25  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372153,590,928 - 153,591,193UniSTSGRCh37
Build 362153,299,174 - 153,299,439RGDNCBI36
Celera2147,205,476 - 147,205,741RGD
Cytogenetic Map2q23.3UniSTS
HuRef2145,477,300 - 145,477,565UniSTS
GeneMap99-GB4 RH Map2508.25UniSTS
RH16515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372153,591,085 - 153,591,209UniSTSGRCh37
Build 362153,299,331 - 153,299,455RGDNCBI36
Celera2147,205,633 - 147,205,757RGD
Cytogenetic Map2q23.3UniSTS
HuRef2145,477,457 - 145,477,581UniSTS
GeneMap99-GB4 RH Map2508.25UniSTS
NCBI RH Map21086.5UniSTS
SHGC-30474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372153,584,354 - 153,584,503UniSTSGRCh37
Build 362153,292,600 - 153,292,749RGDNCBI36
Celera2147,198,903 - 147,199,052RGD
Cytogenetic Map2q23.3UniSTS
HuRef2145,470,728 - 145,470,877UniSTS
TNG Radiation Hybrid Map287345.0UniSTS
GeneMap99-GB4 RH Map2508.25UniSTS
Whitehead-RH Map2789.1UniSTS
GeneMap99-G3 RH Map27233.0UniSTS
SHGC-57826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372153,575,904 - 153,576,065UniSTSGRCh37
Build 362153,284,150 - 153,284,311RGDNCBI36
Celera2147,190,360 - 147,190,521RGD
Cytogenetic Map2q23.3UniSTS
HuRef2145,462,274 - 145,462,435UniSTS
TNG Radiation Hybrid Map287331.0UniSTS
G32948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372153,590,928 - 153,591,193UniSTSGRCh37
Celera2147,205,476 - 147,205,741UniSTS
Cytogenetic Map2q23.3UniSTS
HuRef2145,477,300 - 145,477,565UniSTS


Sequence

Nucleotide Sequences
RefSeq Transcripts NG_053091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_152522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_024526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007069661 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA654338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC079344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF530059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094696 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315657 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW967583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC070140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP200063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP265220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX437990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ834436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ834476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA012142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA801290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000326446   ⟹   ENSP00000315357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,620 - 152,762,396 (+)Ensembl
Ensembl Acc Id: ENST00000425034   ⟹   ENSP00000395052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,554 - 152,760,662 (+)Ensembl
Ensembl Acc Id: ENST00000455875   ⟹   ENSP00000399141
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,461 - 152,759,773 (+)Ensembl
Ensembl Acc Id: ENST00000463690
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,719,399 - 152,760,595 (+)Ensembl
Ensembl Acc Id: ENST00000495469
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,732,187 - 152,760,662 (+)Ensembl
Ensembl Acc Id: ENST00000685752   ⟹   ENSP00000510235
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,717,661 - 152,760,028 (+)Ensembl
Ensembl Acc Id: ENST00000686080   ⟹   ENSP00000509648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,597 - 152,761,151 (+)Ensembl
Ensembl Acc Id: ENST00000686839   ⟹   ENSP00000508917
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,717,893 - 152,760,764 (+)Ensembl
Ensembl Acc Id: ENST00000686951
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,461 - 152,724,098 (+)Ensembl
Ensembl Acc Id: ENST00000687504   ⟹   ENSP00000508902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,461 - 152,760,216 (+)Ensembl
Ensembl Acc Id: ENST00000688012   ⟹   ENSP00000508539
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,461 - 152,760,662 (+)Ensembl
Ensembl Acc Id: ENST00000688130
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,726,072 - 152,760,727 (+)Ensembl
Ensembl Acc Id: ENST00000688171
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,958 - 152,724,042 (+)Ensembl
Ensembl Acc Id: ENST00000688293   ⟹   ENSP00000508943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,717,726 - 152,760,662 (+)Ensembl
Ensembl Acc Id: ENST00000689155   ⟹   ENSP00000508418
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,717,932 - 152,760,890 (+)Ensembl
Ensembl Acc Id: ENST00000690119
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,717,726 - 152,718,908 (+)Ensembl
Ensembl Acc Id: ENST00000690703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,717,945 - 152,724,099 (+)Ensembl
Ensembl Acc Id: ENST00000690727   ⟹   ENSP00000510402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,717,647 - 152,760,890 (+)Ensembl
Ensembl Acc Id: ENST00000691523   ⟹   ENSP00000508751
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,324 - 152,760,662 (+)Ensembl
Ensembl Acc Id: ENST00000691702   ⟹   ENSP00000510017
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,002 - 152,760,662 (+)Ensembl
Ensembl Acc Id: ENST00000692124
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,461 - 152,737,363 (+)Ensembl
Ensembl Acc Id: ENST00000692399   ⟹   ENSP00000510087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,510 - 152,760,662 (+)Ensembl
Ensembl Acc Id: ENST00000693573
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2152,718,461 - 152,735,672 (+)Ensembl
RefSeq Acc Id: NM_001350068   ⟹   NP_001336997
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,949 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,171,495 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001371972   ⟹   NP_001358901
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,171,166 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NM_152522   ⟹   NP_689735
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,762,396 (+)NCBI
GRCh372153,574,407 - 153,617,767 (+)NCBI
Build 362153,283,373 - 153,325,669 (+)NCBI Archive
Celera2147,188,879 - 147,232,317 (+)RGD
HuRef2145,460,777 - 145,504,138 (+)NCBI
CHM1_12153,580,440 - 153,623,806 (+)NCBI
T2T-CHM13v2.02153,171,166 - 153,214,953 (+)NCBI
Sequence:
RefSeq Acc Id: NR_024526
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,717,893 - 152,762,385 (+)NCBI
GRCh372153,574,407 - 153,617,767 (+)NCBI
Celera2147,188,879 - 147,232,317 (+)RGD
HuRef2145,460,777 - 145,504,138 (+)NCBI
CHM1_12153,580,440 - 153,623,806 (+)NCBI
T2T-CHM13v2.02153,170,439 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146422
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,717,648 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,170,194 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146423
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,717,893 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,170,439 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146424
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,086 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,170,632 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146425
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,086 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,170,632 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146426
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,324 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,170,870 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146427
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,324 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,170,870 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146428
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,171,166 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146429
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,171,166 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146430
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,171,166 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146431
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,762,385 (+)NCBI
T2T-CHM13v2.02153,171,166 - 153,214,942 (+)NCBI
Sequence:
RefSeq Acc Id: XR_007069661
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,735,080 (+)NCBI
RefSeq Acc Id: XR_008486292
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02153,171,166 - 153,187,621 (+)NCBI
RefSeq Acc Id: NP_689735   ⟸   NM_152522
- Peptide Label: isoform a
- UniProtKB: B2RDS6 (UniProtKB/Swiss-Prot),   Q7Z4G7 (UniProtKB/Swiss-Prot),   Q8N6S5 (UniProtKB/Swiss-Prot),   B3KMZ5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001336997   ⟸   NM_001350068
- Peptide Label: isoform b
- Sequence:
RefSeq Acc Id: NP_001358901   ⟸   NM_001371972
- Peptide Label: isoform c
- UniProtKB: A0A8I5KQ30 (UniProtKB/TrEMBL),   B3KMZ5 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000395052   ⟸   ENST00000425034
Ensembl Acc Id: ENSP00000399141   ⟸   ENST00000455875
Ensembl Acc Id: ENSP00000315357   ⟸   ENST00000326446
Ensembl Acc Id: ENSP00000510087   ⟸   ENST00000692399
Ensembl Acc Id: ENSP00000509648   ⟸   ENST00000686080
Ensembl Acc Id: ENSP00000510235   ⟸   ENST00000685752
Ensembl Acc Id: ENSP00000508902   ⟸   ENST00000687504
Ensembl Acc Id: ENSP00000508943   ⟸   ENST00000688293
Ensembl Acc Id: ENSP00000508418   ⟸   ENST00000689155
Ensembl Acc Id: ENSP00000510017   ⟸   ENST00000691702
Ensembl Acc Id: ENSP00000510402   ⟸   ENST00000690727
Ensembl Acc Id: ENSP00000508917   ⟸   ENST00000686839
Ensembl Acc Id: ENSP00000508539   ⟸   ENST00000688012
Ensembl Acc Id: ENSP00000508751   ⟸   ENST00000691523

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8N6S5-F1-model_v2 AlphaFold Q8N6S5 1-226 view protein structure

Promoters
RGD ID:6861762
Promoter ID:EPDNEW_H4045
Type:initiation region
Name:ARL6IP6_2
Description:ADP ribosylation factor like GTPase 6 interacting protein 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4046  EPDNEW_H4048  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,717,648 - 152,717,708EPDNEW
RGD ID:6861764
Promoter ID:EPDNEW_H4046
Type:initiation region
Name:ARL6IP6_3
Description:ADP ribosylation factor like GTPase 6 interacting protein 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4045  EPDNEW_H4048  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,717,925 - 152,717,985EPDNEW
RGD ID:6861768
Promoter ID:EPDNEW_H4048
Type:initiation region
Name:ARL6IP6_1
Description:ADP ribosylation factor like GTPase 6 interacting protein 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4045  EPDNEW_H4046  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382152,718,620 - 152,718,680EPDNEW
RGD ID:6796803
Promoter ID:HG_KWN:35445
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_152522,   OTTHUMT00000333577,   OTTHUMT00000333578,   OTTHUMT00000333579,   OTTHUMT00000333581
Position:
Human AssemblyChrPosition (strand)Source
Build 362153,282,856 - 153,283,492 (+)MPROMDB
RGD ID:6796804
Promoter ID:HG_KWN:35446
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:UC002TYO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362153,284,156 - 153,285,142 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24048 AgrOrtholog
COSMIC ARL6IP6 COSMIC
Ensembl Genes ENSG00000177917 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000326446 ENTREZGENE
  ENST00000326446.10 UniProtKB/Swiss-Prot
  ENST00000425034.6 UniProtKB/TrEMBL
  ENST00000455875.6 UniProtKB/TrEMBL
  ENST00000463690.2 UniProtKB/TrEMBL
  ENST00000685752.1 UniProtKB/TrEMBL
  ENST00000686080 ENTREZGENE
  ENST00000686080.1 UniProtKB/TrEMBL
  ENST00000686839.1 UniProtKB/TrEMBL
  ENST00000687504.1 UniProtKB/TrEMBL
  ENST00000688012.1 UniProtKB/TrEMBL
  ENST00000688293.1 UniProtKB/TrEMBL
  ENST00000689155.1 UniProtKB/TrEMBL
  ENST00000690727.1 UniProtKB/TrEMBL
  ENST00000691523.1 UniProtKB/TrEMBL
  ENST00000691702.1 UniProtKB/TrEMBL
  ENST00000692399.1 UniProtKB/TrEMBL
GTEx ENSG00000177917 GTEx
HGNC ID HGNC:24048 ENTREZGENE
Human Proteome Map ARL6IP6 Human Proteome Map
InterPro ARL6IP6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:151188 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 151188 ENTREZGENE
OMIM 616495 OMIM
PANTHER ADP-RIBOSYLATION FACTOR-LIKE PROTEIN 6-INTERACTING PROTEIN 6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR28640 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam ARL6IP6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134866669 PharmGKB
UniProt A0A8I5KQ30 ENTREZGENE, UniProtKB/TrEMBL
  A0A8I5KQY4_HUMAN UniProtKB/TrEMBL
  A0A8I5KRB3_HUMAN UniProtKB/TrEMBL
  A0A8I5KU55_HUMAN UniProtKB/TrEMBL
  A0A8I5KYK3_HUMAN UniProtKB/TrEMBL
  A0A8I5QJ95_HUMAN UniProtKB/TrEMBL
  AR6P6_HUMAN UniProtKB/Swiss-Prot
  B2RDS6 ENTREZGENE
  B3KMZ5 ENTREZGENE, UniProtKB/TrEMBL
  H7C0H7_HUMAN UniProtKB/TrEMBL
  H7C192_HUMAN UniProtKB/TrEMBL
  Q7Z4G7 ENTREZGENE
  Q8N6S5 ENTREZGENE
UniProt Secondary B2RDS6 UniProtKB/Swiss-Prot
  Q7Z4G7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 ARL6IP6  ADP ribosylation factor like GTPase 6 interacting protein 6    ADP-ribosylation factor GTPase 6 interacting protein 6  Symbol and/or name change 5135510 APPROVED
2015-11-17 ARL6IP6  ADP-ribosylation factor GTPase 6 interacting protein 6    ADP-ribosylation factor-like 6 interacting protein 6  Symbol and/or name change 5135510 APPROVED
2014-05-21 ARL6IP6  ADP-ribosylation factor-like 6 interacting protein 6    ADP-ribosylation-like factor 6 interacting protein 6  Symbol and/or name change 5135510 APPROVED