AutismKB 2.0

Evidence Details for GTPBP4


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:GTPBP4 ( CRFG,FLJ10686,FLJ10690,FLJ39774,NGB,NOG1 )
Gene Full Name: GTP binding protein 4
Band: 10p15.3
Quick LinksEntrez ID:23560; OMIM: NA; Uniprot ID:NOG1_HUMAN; ENSEMBL ID: ENSG00000107937; HGNC ID: 21535
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>GTPBP4|23560|nucleotide
ATGGCACATTACAACTTCAAGAAAATTACGGTGGTGCCGTCCGCCAAGGACTTCATAGACCTCACGTTGTCGAAGACTCAACGAAAGACTCCAACCGTTATTCAT
AAACATTACCAAATACATCGCATTAGACATTTTTACATGAGAAAAGTCAAATTTACTCAACAGAATTACCATGATAGACTTTCACAAATTCTAACAGATTTCCCC
AAATTGGATGATATTCATCCGTTCTATGCTGATTTGATGAATATTCTCTACGACAAGGATCATTACAAGTTGGCTCTGGGGCAAATAAATATTGCCAAAAATTTA
GTGGACAATGTTGCTAAAGATTATGTGCGACTGATGAAGTATGGCGACTCTCTCTACCGCTGCAAACAGCTGAAGCGTGCGGCCCTGGGACGGATGTGCACAGTG
ATCAAGAGGCAGAAGCAGAGTTTGGAGTATTTGGAGCAAGTGCGTCAGCATTTATCCCGTTTGCCAACCATTGATCCGAATACCAGGACCCTGCTTTTGTGTGGG
TACCCAAATGTTGGGAAGTCCAGCTTCATCAACAAGGTGACGAGAGCAGACGTGGATGTCCAGCCCTATGCGTTCACAACCAAGTCTCTGTTTGTTGGGCACATG
GATTATAAGTATCTACGTTGGCAGGTTGTAGACACTCCTGGGATCCTGGACCACCCTCTGGAGGATAGGAACACCATCGAGATGCAGGCCATCACTGCCCTGGCC
CACCTCCGTGCTGCGGTCCTGTATGTGATGGATTTGTCTGAGCAGTGTGGGCATGGGCTGAGGGAGCAGCTAGAACTCTTCCAGAACATCAGACCTCTCTTCATC
AACAAGCCTCTCATAGTTGTAGCCAACAAATGTGATGTGAAGAGAATAGCTGAACTTTCTGAAGATGATCAGAAAATATTTACAGATTTGCAGTCTGAAGGATTC
CCTGTAATAGAGACCAGCACCCTGACTGAGGAAGGTGTTATTAAAGTTAAAACAGAGGCTTGCGATAGGCTTTTGGCTCATCGAGTGGAAACCAAAATGAAGGGA
AATAAAGTGAATGAGGTGCTGAATAGACTGCACCTGGCTATCCCAACCAGGAGGGACGATAAGGAGAGGCCCCCTTTCATCCCTGAAGGAGTGGTGGCTCGCAGG
Show »

>GTPBP4|23560|protein
MAHYNFKKITVVPSAKDFIDLTLSKTQRKTPTVIHKHYQIHRIRHFYMRKVKFTQQNYHDRLSQILTDFPKLDDIHPFYADLMNILYDKDHYKLALGQINIAKNL
VDNVAKDYVRLMKYGDSLYRCKQLKRAALGRMCTVIKRQKQSLEYLEQVRQHLSRLPTIDPNTRTLLLCGYPNVGKSSFINKVTRADVDVQPYAFTTKSLFVGHM
DYKYLRWQVVDTPGILDHPLEDRNTIEMQAITALAHLRAAVLYVMDLSEQCGHGLREQLELFQNIRPLFINKPLIVVANKCDVKRIAELSEDDQKIFTDLQSEGF
PVIETSTLTEEGVIKVKTEACDRLLAHRVETKMKGNKVNEVLNRLHLAIPTRRDDKERPPFIPEGVVARRKRMETEESRKKRERDLELEMGDDYILDLQKYWDLM
NLSEKHDKIPEIWEGHNIADYIDPAIMKKLEELEKEEELRTAAGEYDSVSESEDEEMLEIRQLAKQIREKKKLKILESKEKNTQGPRMPRTAKKVQRTVLEKEMR
Show »

Evidence summary Top

Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
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) 0 (0) 0 (0) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 10 (3)
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
Pinto, 2010 - SNP microarray, qPCRASD - - - - 996 1287 2283
Levy, 2011 Simons Simplex Collection aCGH--ASD 915 915 - - - - -
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
De Rubeis S, 2014 2270 - 1702 Synaptic, transcriptional and chromatin genes disrupted in autism
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.

Simple Query:


  (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