AutismKB 2.0

Evidence Details for GPR151


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Basic Information Top
Gene Symbol:GPR151 ( GALR4,GALRL,GPCR,PGR7 )
Gene Full Name: G protein-coupled receptor 151
Band: 5q32
Quick LinksEntrez ID:134391; OMIM: NA; Uniprot ID:GP151_HUMAN; ENSEMBL ID: ENSG00000173250; HGNC ID: 23624
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>GPR151|134391|nucleotide
ATGCTGGCAGCTGCCTTTGCAGACTCTAACTCCAGCAGCATGAATGTGTCCTTTGCTCACCTCCACTTTGCCGGAGGGTACCTGCCCTCTGATTCCCAGGACTGG
AGAACCATCATCCCGGCTCTCTTGGTGGCTGTCTGCCTGGTGGGCTTCGTGGGAAACCTGTGTGTGATTGGCATCCTCCTTCACAATGCTTGGAAAGGAAAGCCA
TCCATGATCCACTCCCTGATTCTGAATCTCAGCCTGGCTGATCTCTCCCTCCTGCTGTTTTCTGCACCTATCCGAGCTACGGCGTACTCCAAAAGTGTTTGGGAT
CTAGGCTGGTTTGTCTGCAAGTCCTCTGACTGGTTTATCCACACATGCATGGCAGCCAAGAGCCTGACAATCGTTGTGGTGGCCAAAGTATGCTTCATGTATGCA
AGTGACCCAGCCAAGCAAGTGAGTATCCACAACTACACCATCTGGTCAGTGCTGGTGGCCATCTGGACTGTGGCTAGCCTGTTACCCCTGCCGGAATGGTTCTTT
AGCACCATCAGGCATCATGAAGGTGTGGAAATGTGCCTCGTGGATGTACCAGCTGTGGCTGAAGAGTTTATGTCGATGTTTGGTAAGCTCTACCCACTCCTGGCA
TTTGGCCTTCCATTATTTTTTGCCAGCTTTTATTTCTGGAGAGCTTATGACCAATGTAAAAAACGAGGAACTAAGACTCAAAATCTTAGAAACCAGATACGCTCA
AAGCAAGTCACAGTGATGCTGCTGAGCATTGCCATCATCTCTGCTCTCTTGTGGCTCCCCGAATGGGTAGCTTGGCTGTGGGTATGGCATCTGAAGGCTGCAGGC
CCGGCCCCACCACAAGGTTTCATAGCCCTGTCTCAAGTCTTGATGTTTTCCATCTCTTCAGCAAATCCTCTCATTTTTCTTGTGATGTCGGAAGAGTTCAGGGAA
GGCTTGAAAGGTGTATGGAAATGGATGATAACCAAAAAACCTCCAACTGTCTCAGAGTCTCAGGAAACACCAGCTGGCAACTCAGAGGGTCTTCCTGACAAGGTT
CCATCTCCAGAATCCCCAGCATCCATACCAGAAAAAGAGAAACCCAGCTCTCCCTCCTCTGGCAAAGGGAAAACTGAGAAGGCAGAGATTCCCATCCTTCCTGAC
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>GPR151|134391|protein
MLAAAFADSNSSSMNVSFAHLHFAGGYLPSDSQDWRTIIPALLVAVCLVGFVGNLCVIGILLHNAWKGKPSMIHSLILNLSLADLSLLLFSAPIRATAYSKSVWD
LGWFVCKSSDWFIHTCMAAKSLTIVVVAKVCFMYASDPAKQVSIHNYTIWSVLVAIWTVASLLPLPEWFFSTIRHHEGVEMCLVDVPAVAEEFMSMFGKLYPLLA
FGLPLFFASFYFWRAYDQCKKRGTKTQNLRNQIRSKQVTVMLLSIAIISALLWLPEWVAWLWVWHLKAAGPAPPQGFIALSQVLMFSISSANPLIFLVMSEEFRE
GLKGVWKWMITKKPPTVSESQETPAGNSEGLPDKVPSPESPASIPEKEKPSSPSSGKGKTEKAEIPILPDVEQFWHERDTVPSVQDNDPIPWEHEDQETGEGVK

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Evidence summary Top

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Evidences Syndromic Gene GWAS CNV Linkage Association Expression NGS de novo NGS Mosaic NGS Other Low-Scale Gene Studies Total
Score (No. of Studies) No 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (2) 0 (0) 0 (0) 0 (0) 0 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference Case Number Family Number de novo Number Title
Yuen RK, 2016 200 - 301 Genome-wide characteristics of de novo mutations in autism.
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

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  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018