AutismKB 2.0

Evidence Details for GPR158


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Basic Information Top
Gene Symbol:GPR158 ( FLJ37801,KIAA1136,RP11-59G22.1 )
Gene Full Name: G protein-coupled receptor 158
Band: 10p12.1
Quick LinksEntrez ID:57512; OMIM: NA; Uniprot ID:GP158_HUMAN; ENSEMBL ID: ENSG00000151025; HGNC ID: 23689
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>GPR158|57512|nucleotide
ATGGGAGCCATGGCTTACCCCTTACTCCTCTGCCTCCTGCTTGCTCAGCTGGGATTGGGAGCTGTTGGCGCCAGCCGCGACCCCCAAGGACGGCCGGATTCCCCT
CGAGAGAGGACCCCGAAGGGGAAGCCGCACGCCCAGCAGCCGGGTCGAGCCTCTGCCTCGGACTCCTCGGCTCCCTGGAGCCGCTCCACCGATGGCACCATCTTG
GCGCAGAAACTCGCCGAGGAGGTGCCCATGGACGTGGCCTCTTACCTCTACACCGGGGACTCCCACCAGCTGAAGCGAGCCAACTGCTCCGGCCGCTACGAGTTG
GCGGGCCTGCCGGGGAAGTGGCCAGCCCTGGCCAGCGCGCACCCCTCCTTGCACCGGGCGCTGGACACACTGACACACGCCACCAACTTCCTCAACGTGATGCTG
CAGAGCAATAAGTCGCGGGAGCAGAACTTGCAGGACGACCTGGATTGGTACCAGGCGCTGGTGTGGAGCCTTCTGGAGGGCGAGCCCAGCATCTCCCGGGCGGCC
ATCACCTTCAGCACCGATTCGCTGTCCGCACCGGCCCCACAGGTCTTCCTCCAGGCCACGCGCGAGGAGAGCCGCATCCTGCTCCAAGACCTGTCCTCCTCCGCA
CCCCACCTGGCCAACGCCACTCTGGAGACCGAGTGGTTCCACGGCCTCCGGCGCAAGTGGAGGCCCCACTTACACCGCCGCGGCCCCAATCAGGGGCCCCGGGGC
CTGGGCCACAGCTGGCGGCGCAAGGACGGGCTCGGCGGGGACAAGAGCCACTTCAAGTGGTCTCCGCCTTATCTGGAGTGCGAGAACGGGAGTTACAAGCCCGGG
TGGCTGGTTACTCTTTCCTCTGCCATCTACGGGTTGCAGCCTAACCTGGTCCCGGAATTCAGGGGTGTCATGAAAGTTGACATAAATCTTCAGAAAGTGGACATT
GACCAATGCTCAAGTGATGGCTGGTTTTCAGGAACTCATAAATGCCACCTCAACAATTCAGAGTGTATGCCAATTAAAGGCCTAGGATTCGTTCTTGGAGCCTAT
GAGTGCATTTGCAAAGCAGGATTCTATCATCCTGGAGTCTTACCAGTGAACAACTTTCGGAGAAGGGGTCCGGATCAGCATATTTCAGGAAGTACAAAAGATGTG
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>GPR158|57512|protein
MGAMAYPLLLCLLLAQLGLGAVGASRDPQGRPDSPRERTPKGKPHAQQPGRASASDSSAPWSRSTDGTILAQKLAEEVPMDVASYLYTGDSHQLKRANCSGRYEL
AGLPGKWPALASAHPSLHRALDTLTHATNFLNVMLQSNKSREQNLQDDLDWYQALVWSLLEGEPSISRAAITFSTDSLSAPAPQVFLQATREESRILLQDLSSSA
PHLANATLETEWFHGLRRKWRPHLHRRGPNQGPRGLGHSWRRKDGLGGDKSHFKWSPPYLECENGSYKPGWLVTLSSAIYGLQPNLVPEFRGVMKVDINLQKVDI
DQCSSDGWFSGTHKCHLNNSECMPIKGLGFVLGAYECICKAGFYHPGVLPVNNFRRRGPDQHISGSTKDVSEEAYVCLPCREGCPFCADDSPCFVQEDKYLRLAI
ISFQALCMLLDFVSMLVVYHFRKAKSIRASGLILLETILFGSLLLYFPVVILYFEPSTFRCILLRWARLLGFATVYGTVTLKLHRVLKVFLSRTAQRIPYMTGGR
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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) 1 (2) 0 (0) 0 (0) 0 (0) 1 (2) 0 (0) 0 (0) 3 (4)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Bailey, 1998 - microsatellite-based genomic screenPDD 99 - 99 - - - -
Monaco, 2001 - microsatellite-based genomic screenPDD 152 - 152 - - - -
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
Reference Case Number Family Number Mosaic Number Title
Dou Y, 2017 - 2361 230 Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and
Krupp DR, 2017 - 2264 247 Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
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