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Gene id 91608
Gene Summary    Protein Summary    Gene ontology    Diseases    PubMed    

Gene Summary

Gene Symbol RASL10B   Gene   UCSC   Ensembl
Aliases RRP17, VTS58635
Gene name RAS like family 10 member B
Alternate names ras-like protein family member 10B, Ras-related protein 17, alternative protein RASL10B, ras-like protein VTS58635,
Gene location 17q12 (35731638: 35743520)     Exons: 6     NC_000017.11
OMIM 605064

Protein Summary

Protein general information Q96S79  

Name: Ras like protein family member 10B (Ras like protein VTS58635) (Ras related protein 17) (RRP17)

Length: 203  Mass: 23229

Tissue specificity: Expressed at high levels in skeletal muscle and, at much lower levels, in heart, brain and pancreas. {ECO

Sequence MVSTYRVAVLGARGVGKSAIVRQFLYNEFSEVCVPTTARRLYLPAVVMNGHVHDLQILDFPPISAFPVNTLQEWA
DTCCRGLRSVHAYILVYDICCFDSFEYVKTIRQQILETRVIGTSETPIIIVGNKRDLQRGRVIPRWNVSHLVRKT
WKCGYVECSAKYNWHILLLFSELLKSVGCARCKHVHAALRFQGALRRNRCAIM
Structural information
Interpro:  IPR027417  IPR001806  IPR020849  
Prosite:   PS51421
MINT:  
STRING:   ENSP00000474230
Other Databases GeneCards:  RASL10B  Malacards:  RASL10B

Gene ontology

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GO accessionTerm nameEvidence codeGo category
GO:0090277 positive regulation of pe
ptide hormone secretion
ISS biological process
GO:0003050 regulation of systemic ar
terial blood pressure by
atrial natriuretic peptid
e
ISS biological process
GO:0003924 GTPase activity
IEA molecular function
GO:0005525 GTP binding
IEA molecular function
GO:0007165 signal transduction
IEA biological process
GO:0016020 membrane
IEA cellular component
GO:0005525 GTP binding
IEA molecular function
GO:0000166 nucleotide binding
IEA molecular function
GO:0005886 plasma membrane
IEA cellular component
GO:0016020 membrane
IEA cellular component
GO:0005515 protein binding
IPI molecular function
GO:0090277 positive regulation of pe
ptide hormone secretion
IEA biological process
GO:0003050 regulation of systemic ar
terial blood pressure by
atrial natriuretic peptid
e
IEA biological process
GO:0005886 plasma membrane
IEA cellular component
Associated diseases References
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Unexplained infertility MIK: 25753583

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract
25753583 Unexplaine
d infertil
ity

46 (17 fertile
men, 29 male pa
tients)
Male infertility Microarray
Show abstract