AutismKB 2.0

Evidence Details for GPR144


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Basic Information Top
Gene Symbol:GPR144 ( PGR24 )
Gene Full Name: G protein-coupled receptor 144
Band: 9q33.3
Quick LinksEntrez ID:347088; OMIM: NA; Uniprot ID:GP144_HUMAN; ENSEMBL ID: ENSG00000180264; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>GPR144|347088|nucleotide
ATGGACGCACCTTGGGGAGCAGGGGAAAGGTGGCTGCACGGAGCAGCGGTGGACAGATCAGGAGTCTCTCTGGGACCCCCTCCAACTCCCCAGGTGAATCAAGGA
ACCCTTGGGCCCCAGGTTGCCCCCGTGGCCGCCGGCGAGGTGGTGAAGACTGCAGGTGGGGTGTGCAAGTTCTCTGGACAGCGACTGAGCTGGTGGCAGGCCCAA
GAGTCCTGCGAGCAGCAGTTTGGCCACTTGGCACTGCAGCCCCCTGATGGGGTTCTTGCTTCACGGCTGCGCGATCCGGTCTGGGTGGGCCAAAGAGAGGCCCCT
CTGCGGAGACCCCCACAGAGGCGTGCGCGCACCACCGCCGTGCTGGTGTTCGACGAGAGGACGGCTGACCGGGCGGCGCGGCTGCGGAGCCCTCTGCCTGAGCTG
GCAGCGCTGACCGCGTGTACTCACGTGCAGTGGGACTGTGCCTCGCCCGACCCCGCAGCGCTCTTCTCCGTTGCCGCGCCCGCGCTGCCCAACGCGCTGCAGCTG
CGCGCCTTCGCCGAGCCGGGGGGCGTCGTGCGCGCTGCGCTGGTGGTGCGTGGGCAGCACGCGCCCTTCCTCGCAGCCTTCCGCGCCGACGGCCGCTGGCACCAT
GTGTGCGCCACGTGGGAGCAGCGGGGCGGGCGCTGGGCGCTGTTCTCCGATGGGAGGCGGCGCGCTGGGGCGCGGGGGCTGGGCGCCGGCCACCCGGTGCCGTCC
GGCGGCATCCTGGTGCTGGGCCAGGATCAGGACTCTCTGGGCGGTGGCTTCTCGGTGCGTCACGCCCTCAGCGGCAACCTCACCGACTTCCACCTGTGGGCGCGG
GCGCTGAGCCCCGCTCAGCTGCACCGGGCACGGGCCTGCGCGCCGCCCTCAGAGGGCCTGCTCTTCCGCTGGGACCCGGGCGCCCTGGACGTCACGCCCTCGCTG
CTGCCCACTGTGTGGGTGCGCCTTCTCTGTCCCGTGCCCTCCGAGGAGTGCCCTACGTGGAACCCGGGACCTCGCAGTGAGGGCTCTGAGCTCTGCCTGGAGCCG
CAGCCCTTCCTCTGCTGCTACCGGACAGAGCCCTATCGTCGGCTGCAGGATGCCCAGTCGTGGCCTGGCCAGGATGTTATCAGCCGAGTCAATGCCTTGGCCAAC
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>GPR144|347088|protein
MDAPWGAGERWLHGAAVDRSGVSLGPPPTPQVNQGTLGPQVAPVAAGEVVKTAGGVCKFSGQRLSWWQAQESCEQQFGHLALQPPDGVLASRLRDPVWVGQREAP
LRRPPQRRARTTAVLVFDERTADRAARLRSPLPELAALTACTHVQWDCASPDPAALFSVAAPALPNALQLRAFAEPGGVVRAALVVRGQHAPFLAAFRADGRWHH
VCATWEQRGGRWALFSDGRRRAGARGLGAGHPVPSGGILVLGQDQDSLGGGFSVRHALSGNLTDFHLWARALSPAQLHRARACAPPSEGLLFRWDPGALDVTPSL
LPTVWVRLLCPVPSEECPTWNPGPRSEGSELCLEPQPFLCCYRTEPYRRLQDAQSWPGQDVISRVNALANDIVLLPDPLSEVHGALSPAEASSFLGLLEHVLAME
MAPLGPAALLAVVRFLKRVVALGAGDPELLLTGPWEQLSQGVVSVASLVLEEQVADTWLSLREVIGGPMALVASVQRLAPLLSTSMTSERPRMRIQHRHAGLSGV
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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 (1) 0 (0) 0 (0) 0 (0) 0 (1)
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
Iossifov I, 2014 2508 - 1194 The contribution of de novo coding mutations to autism spectrum disorder.
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