AutismKB 2.0

Evidence Details for FAM150B


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Basic Information Top
Gene Symbol:FAM150B ( PRO1097,RGPG542 )
Gene Full Name: family with sequence similarity 150, member B
Band: 2p25.3
Quick LinksEntrez ID:285016; OMIM: NA; Uniprot ID:F150B_HUMAN; ENSEMBL ID: ENSG00000189292; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>FAM150B|285016|nucleotide
ATGCGCGGACCCGGGCACCCCCTCCTCCTGGGGCTGCTGCTGGTGCTGGGGGCGGCGGGGCGCGGCCGGGGGGGCGCGGAGCCCCGGGAGCCGGCGGACGGACAG
GCGCTGCTGCGGCTGGTGGTGGAACTCGTCCAGGAGCTGCGGAAGCACCACTCGGCGGAGCACAAGGGCCTGCAGCTCCTCGGGCGGGACTGCGCCCTGGGCCGC
GCGGAGGCGGCGGGGCTGGGGCCTTCGCCGGAGCAGCGAGTGGAAATTGTTCCTCGAGATCTGAGGATGAAGGACAAGTTTCTAAAACACCTTACAGGCCCTCTT
TATTTTAGTCCAAAGTGCAGCAAACACTTCCATAGACTTTATCACAACACCAGAGACTGCACCATTCCTGCATACTATAAAAGATGCGCCAGGCTTCTTACCCGG
CTGGCTGTCAGTCCAGTGTGCATGGAGGATAAGCAGTGA






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>FAM150B|285016|protein
MRGPGHPLLLGLLLVLGAAGRGRGGAEPREPADGQALLRLVVELVQELRKHHSAEHKGLQLLGRDCALGRAEAAGLGPSPEQRVEIVPRDLRMKDKFLKHLTGPL
YFSPKCSKHFHRLYHNTRDCTIPAYYKRCARLLTRLAVSPVCMEDKQ



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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 (2) 1 (2) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (5)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Christian, 2008 USA aCGHASD 397 35 362 - 397 372 769
Gai, 2011 AGRE SNP microarray--autism - - - - 1224 3801 5025
Linkage Studies Top