RIN1 (Ras and Rab interactor 1) - Rat Genome Database

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Gene: RIN1 (Ras and Rab interactor 1) Homo sapiens
Analyze
Symbol: RIN1
Name: Ras and Rab interactor 1
RGD ID: 1348032
HGNC Page HGNC
Description: Predicted to have small GTPase binding activity. Predicted to be involved in associative learning; memory; and negative regulation of synaptic plasticity. Localizes to cytoplasm and plasma membrane; INTERACTS WITH 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine; 5-aza-2'-deoxycytidine.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: ras inhibitor 1; ras inhibitor JC99; ras inhibitor RIN1; ras interaction/interference protein 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1166,330,241 - 66,336,840 (-)EnsemblGRCh38hg38GRCh38
GRCh381166,330,241 - 66,336,774 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371166,097,712 - 66,104,245 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361165,856,118 - 65,860,576 (-)NCBINCBI36hg18NCBI36
Build 341165,856,128 - 65,860,576NCBI
Celera1163,419,443 - 63,423,901 (-)NCBI
Cytogenetic Map11q13.2NCBI
HuRef1162,424,782 - 62,429,240 (-)NCBIHuRef
CHM1_11165,983,660 - 65,988,118 (-)NCBICHM1_1
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

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:1849280   PMID:3874369   PMID:7862125   PMID:9208849   PMID:10545207   PMID:11703925   PMID:11784866   PMID:11788587   PMID:12477932   PMID:12574403   PMID:12783862   PMID:15031288  
PMID:15489334   PMID:15886098   PMID:15951569   PMID:16273093   PMID:16457816   PMID:16964243   PMID:17390061   PMID:17403676   PMID:18089779   PMID:18729074   PMID:19032933   PMID:19060904  
PMID:19118546   PMID:19570984   PMID:19806790   PMID:21102429   PMID:21209314   PMID:21516116   PMID:21925717   PMID:21926972   PMID:22199357   PMID:22249975   PMID:22562267   PMID:22627834  
PMID:22976291   PMID:25416956   PMID:25814554   PMID:26194865   PMID:26496610   PMID:26871637   PMID:27137893   PMID:27173435   PMID:27184078   PMID:28378594   PMID:28514442   PMID:28612496  
PMID:28656962   PMID:29467282   PMID:31515488   PMID:31741433   PMID:31980649   PMID:32296183   PMID:32572027   PMID:33069695  


Genomics

Comparative Map Data
RIN1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1166,330,241 - 66,336,840 (-)EnsemblGRCh38hg38GRCh38
GRCh381166,330,241 - 66,336,774 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371166,097,712 - 66,104,245 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361165,856,118 - 65,860,576 (-)NCBINCBI36hg18NCBI36
Build 341165,856,128 - 65,860,576NCBI
Celera1163,419,443 - 63,423,901 (-)NCBI
Cytogenetic Map11q13.2NCBI
HuRef1162,424,782 - 62,429,240 (-)NCBIHuRef
CHM1_11165,983,660 - 65,988,118 (-)NCBICHM1_1
Rin1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39195,100,035 - 5,107,100 (+)NCBIGRCm39mm39
GRCm39 Ensembl195,100,509 - 5,107,099 (+)Ensembl
GRCm38195,049,999 - 5,057,071 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl195,050,481 - 5,057,071 (+)EnsemblGRCm38mm10GRCm38
MGSCv37195,050,808 - 5,057,071 (+)NCBIGRCm37mm9NCBIm37
MGSCv36195,050,808 - 5,057,071 (+)NCBImm8
Celera194,919,912 - 4,926,173 (+)NCBICelera
Cytogenetic Map19ANCBI
Rin1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21202,355,729 - 202,362,731 (+)NCBI
Rnor_6.0 Ensembl1220,335,254 - 220,342,297 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl1220,428,481 - 220,433,129 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01220,335,036 - 220,342,319 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01227,359,504 - 227,364,152 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41207,671,502 - 207,676,150 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11207,824,954 - 207,829,599 (+)NCBI
Celera1199,895,635 - 199,900,283 (+)NCBICelera
Cytogenetic Map1q43NCBI
Rin1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542218,990,698 - 18,997,838 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495542218,989,814 - 18,996,570 (+)NCBIChiLan1.0ChiLan1.0
RIN1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11165,023,138 - 65,027,841 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1165,023,138 - 65,027,605 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01161,697,751 - 61,702,501 (-)NCBIMhudiblu_PPA_v0panPan3
RIN1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11850,975,002 - 50,982,052 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1850,975,814 - 50,980,381 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1849,583,999 - 49,591,937 (+)NCBI
ROS_Cfam_1.01852,013,856 - 52,021,793 (+)NCBI
UMICH_Zoey_3.11851,113,972 - 51,121,908 (+)NCBI
UNSW_CanFamBas_1.01850,688,080 - 50,696,013 (+)NCBI
UU_Cfam_GSD_1.01851,478,230 - 51,486,168 (+)NCBI
Rin1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049476,824,947 - 6,831,627 (+)NCBI
SpeTri2.0NW_0049365993,267,223 - 3,274,359 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RIN1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.126,053,875 - 6,061,051 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.225,130,436 - 5,138,504 (+)NCBISscrofa10.2Sscrofa10.2susScr3
RIN1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.117,940,856 - 7,945,419 (+)NCBI
ChlSab1.1 Ensembl17,941,082 - 7,945,206 (+)Ensembl
Rin1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462476720,044,056 - 20,050,868 (+)NCBI

Position Markers
D13S1305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371166,098,188 - 66,098,646UniSTSGRCh37
GRCh371353,175,875 - 53,176,008UniSTSGRCh37
Build 361352,073,876 - 52,074,009RGDNCBI36
Celera1163,418,089 - 63,418,547UniSTS
Celera1334,161,750 - 34,161,883RGD
Cytogenetic Map11q13.2UniSTS
HuRef1162,423,428 - 62,423,886UniSTS
HuRef1333,890,120 - 33,890,253UniSTS
Marshfield Genetic Map1345.55RGD
Marshfield Genetic Map1345.55UniSTS
Genethon Genetic Map1347.6UniSTS
deCODE Assembly Map1355.23UniSTS
Stanford-G3 RH Map131417.0UniSTS
Whitehead-YAC Contig Map13 UniSTS
NCBI RH Map13478.0UniSTS
GeneMap99-G3 RH Map131413.0UniSTS
RIN1__5502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371166,099,512 - 66,100,219UniSTSGRCh37
Build 361165,856,088 - 65,856,795RGDNCBI36
Celera1163,419,413 - 63,420,120RGD
HuRef1162,424,752 - 62,425,459UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4548
Count of miRNA genes:991
Interacting mature miRNAs:1264
Transcripts:ENST00000311320, ENST00000424433, ENST00000524804, ENST00000526246, ENST00000528006, ENST00000530056, ENST00000530745, ENST00000534824
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.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 375 167 318 54 218 22 1735 176 1930 67 685 438 42 266 935
Low 2053 2794 1331 495 1387 370 2620 2007 1770 307 758 1146 131 938 1853 3
Below cutoff 4 25 77 73 327 73 11 24 45 11 27 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001363559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295365 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG163919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ956294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L36463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000311320   ⟹   ENSP00000310406
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,330,241 - 66,336,434 (-)Ensembl
RefSeq Acc Id: ENST00000524804
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,332,590 - 66,333,553 (-)Ensembl
RefSeq Acc Id: ENST00000526246
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,330,242 - 66,336,008 (-)Ensembl
RefSeq Acc Id: ENST00000528006
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,334,999 - 66,335,700 (-)Ensembl
RefSeq Acc Id: ENST00000530056   ⟹   ENSP00000432798
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,332,223 - 66,336,840 (-)Ensembl
RefSeq Acc Id: ENST00000530745   ⟹   ENSP00000431185
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,332,609 - 66,336,436 (-)Ensembl
RefSeq Acc Id: ENST00000534824   ⟹   ENSP00000431550
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,332,210 - 66,335,691 (-)Ensembl
RefSeq Acc Id: ENST00000627248   ⟹   ENSP00000485911
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1166,335,641 - 66,336,402 (-)Ensembl
RefSeq Acc Id: NM_001363559   ⟹   NP_001350488
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381166,330,241 - 66,336,774 (-)NCBI
RefSeq Acc Id: NM_001363560   ⟹   NP_001350489
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381166,330,241 - 66,336,434 (-)NCBI
RefSeq Acc Id: NM_004292   ⟹   NP_004283
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381166,330,241 - 66,336,434 (-)NCBI
GRCh371166,099,535 - 66,104,000 (-)NCBI
Build 361165,856,118 - 65,860,576 (-)NCBI Archive
HuRef1162,424,782 - 62,429,240 (-)ENTREZGENE
CHM1_11165,983,660 - 65,988,118 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017018587   ⟹   XP_016874076
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381166,332,063 - 66,336,434 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_004283   ⟸   NM_004292
- Peptide Label: isoform 1
- UniProtKB: Q13671 (UniProtKB/Swiss-Prot),   A0A0S2Z4U0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016874076   ⟸   XM_017018587
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: NP_001350488   ⟸   NM_001363559
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001350489   ⟸   NM_001363560
- Peptide Label: isoform 3
RefSeq Acc Id: ENSP00000431185   ⟸   ENST00000530745
RefSeq Acc Id: ENSP00000432798   ⟸   ENST00000530056
RefSeq Acc Id: ENSP00000485911   ⟸   ENST00000627248
RefSeq Acc Id: ENSP00000431550   ⟸   ENST00000534824
RefSeq Acc Id: ENSP00000310406   ⟸   ENST00000311320
Protein Domains
Ras-associating   SH2   VPS9

Promoters
RGD ID:6789322
Promoter ID:HG_KWN:13396
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_004292,   UC009YRD.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361165,860,101 - 65,860,937 (-)MPROMDB
RGD ID:7221137
Promoter ID:EPDNEW_H16314
Type:initiation region
Name:RIN1_1
Description:Ras and Rab interactor 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
GRCh381166,336,434 - 66,336,494EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11q13.2(chr11:66193502-67890770)x3 copy number gain See cases [RCV000053623] Chr11:66193502..67890770 [GRCh38]
Chr11:65960973..67658241 [GRCh37]
Chr11:65717549..67414817 [NCBI36]
Chr11:11q13.2
pathogenic
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3
pathogenic
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
GRCh37/hg19 11q13.2(chr11:66024774-67430781)x3 copy number gain See cases [RCV000240374] Chr11:66024774..67430781 [GRCh37]
Chr11:11q13.2
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
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
NM_004292.3(RIN1):c.2211G>A (p.Gly737=) single nucleotide variant not provided [RCV000967214] Chr11:66332417 [GRCh38]
Chr11:66099888 [GRCh37]
Chr11:11q13.2
benign
NM_004292.3(RIN1):c.2098G>A (p.Val700Ile) single nucleotide variant not provided [RCV000967215] Chr11:66332530 [GRCh38]
Chr11:66100001 [GRCh37]
Chr11:11q13.2
benign
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_004292.3(RIN1):c.1636G>A (p.Val546Ile) single nucleotide variant not provided [RCV000893750] Chr11:66333614 [GRCh38]
Chr11:66101085 [GRCh37]
Chr11:11q13.2
benign
NC_000011.9:g.(?_65633902)_(66115026_?)dup duplication Autosomal recessive cutis laxa type 1B [RCV000798155] Chr11:65866431..66347555 [GRCh38]
Chr11:65633902..66115026 [GRCh37]
Chr11:11q13.1-13.2
uncertain significance
NM_004292.3(RIN1):c.1929C>G (p.Thr643=) single nucleotide variant not provided [RCV000955194] Chr11:66332699 [GRCh38]
Chr11:66100170 [GRCh37]
Chr11:11q13.2
benign
NM_004292.3(RIN1):c.2070C>T (p.Ala690=) single nucleotide variant not provided [RCV000956965] Chr11:66332558 [GRCh38]
Chr11:66100029 [GRCh37]
Chr11:11q13.2
benign
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

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:18749 AgrOrtholog
COSMIC RIN1 COSMIC
Ensembl Genes ENSG00000174791 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000310406 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000431185 UniProtKB/TrEMBL
  ENSP00000431550 UniProtKB/TrEMBL
  ENSP00000432798 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000485911 UniProtKB/TrEMBL
Ensembl Transcript ENST00000311320 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000526246 ENTREZGENE
  ENST00000530056 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000530745 UniProtKB/TrEMBL
  ENST00000534824 UniProtKB/TrEMBL
  ENST00000627248 UniProtKB/TrEMBL
Gene3D-CATH 1.20.1050.80 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.505.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000174791 GTEx
HGNC ID HGNC:18749 ENTREZGENE
Human Proteome Map RIN1 Human Proteome Map
InterPro RA_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RIN1_SH2 UniProtKB/TrEMBL
  SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH2_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VPS9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VPS9_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9610 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 9610 ENTREZGENE
OMIM 605965 OMIM
Pfam PF00788 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VPS9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA38671 PharmGKB
PROSITE PS50200 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VPS9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00314 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VPS9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF109993 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF55550 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0S2Z4T3_HUMAN UniProtKB/TrEMBL
  A0A0S2Z4T5_HUMAN UniProtKB/TrEMBL
  A0A0S2Z4U0 ENTREZGENE, UniProtKB/TrEMBL
  E9PMB8_HUMAN UniProtKB/TrEMBL
  E9PNR2_HUMAN UniProtKB/TrEMBL
  H0YCG8_HUMAN UniProtKB/TrEMBL
  Q13671 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary O15010 UniProtKB/Swiss-Prot
  Q00427 UniProtKB/Swiss-Prot
  Q96CC8 UniProtKB/Swiss-Prot