AutismKB 2.0

Evidence Details for TUBGCP5


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Basic Information Top
Gene Symbol:TUBGCP5 ( GCP5,KIAA1899 )
Gene Full Name: tubulin, gamma complex associated protein 5
Band: 15q11.2
Quick LinksEntrez ID:114791; OMIM: 608147; Uniprot ID:GCP5_HUMAN; ENSEMBL ID: ENSG00000153575; HGNC ID: 18600
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>TUBGCP5|114791|nucleotide
ATGGCGCGGCACGGGCCACCGTGGAGTCGGTTGGACGCGCAGCAGGAGCGCGACGTGCGGGAGCTCGTCCGGGGTGTCGCCGGCCTCCAGGACGAGGCAGACCCC
AACTTCCAGCTCGCCCTAAACTTCGCCTGGTCCAACTTCAGATTTCATCGTTTCTTGGATGTCAACAGCCACAAAATAGAAAAAACAATCGAAGGAATTTATGAA
AAATTTGTCATTCATTCTGATCTAAGCAAAGCTGCTAGTTGGAAGAGATTAACGGAGGAATTTCTAAATGCACCACTTCCCAGTATAAAGGAAATAAAGACAGAT
GCACATTATTCCATACTGTCACTTCTTCTGTGTCTGTCAGACTCTCCTTCAAACAGCAGTTATGTGGAGACACCAAGAAATAAAGAAGTGGAAAAGAAAGATGAT
TTCGACTGGGGAAAATACTTGATGGAAGATGAAGAAATGGACATTGGTCCGTACATGGACACACCAAATTGGTCTGAAGAAAGTGAAGAGGAAAATGATCAACAG
CCCTTAAGCAGAGAGGACTCTGGAATTCAGGTAGACAGGACACCGTTAGAAGAACAAGATCAAAACAGAAAACTGGATCCTTGTATCAGTTGGAAAGATGAGCCA
GATGACCGAAGCTGGCTGGAACATCATGTGGTCCATCAGTACTGGACAGCCAGGCCCTCCCAGTTTCCTCATAGTTTACATTTGCACTCTAATTTAGCTGCTGTC
TGGGACCAACACTTGTACAGCAGTGATCCATTGTATGTTCCAGATGACAGGGTTTTGGTTACTGAGACTCAGGTTATTCGGGAAACCCTATGGTTACTTTCAGGA
GTGAAAAAGCTCTTTATATTTCAGTTGATAGATGGGAAGGTAACTGTGAGAAACAATATTATAGTAACTCATTTAACACATAGCTGTTTACGATCTGTGCTGGAA
CAAATAGCAGCATATGGCCAGGTTGTGTTTCGACTCCAGGAGTTCATTGATGAAGTCATGGGACACAGTTCTGAGAGCATGCTGCCTGGAAGTGGGTCTGTTCCT
AAGAAGTCAACTGAAGCTCCCTTTAGAACCTACCAGGCTTTCATGTGGGCCCTGTACAAATATTTCATTAGTTTCAAAGAGGAACTTGCAGAAATTGAGAAGTGC
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>TUBGCP5|114791|protein
MARHGPPWSRLDAQQERDVRELVRGVAGLQDEADPNFQLALNFAWSNFRFHRFLDVNSHKIEKTIEGIYEKFVIHSDLSKAASWKRLTEEFLNAPLPSIKEIKTD
AHYSILSLLLCLSDSPSNSSYVETPRNKEVEKKDDFDWGKYLMEDEEMDIGPYMDTPNWSEESEEENDQQPLSREDSGIQVDRTPLEEQDQNRKLDPCISWKDEP
DDRSWLEHHVVHQYWTARPSQFPHSLHLHSNLAAVWDQHLYSSDPLYVPDDRVLVTETQVIRETLWLLSGVKKLFIFQLIDGKVTVRNNIIVTHLTHSCLRSVLE
QIAAYGQVVFRLQEFIDEVMGHSSESMLPGSGSVPKKSTEAPFRTYQAFMWALYKYFISFKEELAEIEKCIINNDTTITLAIVVDKLAPRLSQLKVLHKVFSTGV
AEVPPDTRNVVRASHLLNTLYKAILEYDNVGEASEQTVSLLFSLWVETVRPYLQTVDEWIVHGHLWDGAREFIIQRNKNVPVNHRDFWYATYTLYSVSEKTENEE
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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) 3 (21) 0 (0) 0 (1) 2 (2) 0 (1) 0 (0) 0 (0) 0 (0) 8 (25)
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
Wolpert, 2000 - STS mappingautism 3 - 3 - 3 - 3
Wassink, 2001 USA Chromosomal analysis of G-bandautism - - - - 278 - 278
Silva, 2002 - FISHautism - - - - 1 - 1
Keller, 2003 USA FISHASD - - - - 2 - 2
Sahoo, 2005 USA aCGHautism - - - - 9 - 9
Wassink, 2007 USA FISHPDD - - - - 104 - 104
Sebat, 2007 USA aCGHautism 165 118 47 99 195 196 391
Weiss, 2008 USA, Ireland aCGH, SNP microarrayASD 751 - - - 2252 23502 25754
Marshall, 2008 - SNP microarrayASD 427 238 189 - 427 500 927
Christian, 2008 USA aCGHASD 397 35 362 - 397 372 769
Bremer, 2009 - aCGHASD - - - - 148 - 148
van der Zwaag, 2009 Holland SNP microarrayASD 2 - 2 - 3 267 270
Gregory, 2009 USA aCGHASD - - - - 119 54 173
Pinto, 2010 - SNP microarray, qPCRASD - - - - 996 1287 2283
Bremer, 2011 - aCGHASD - - - - 223 - 223
Levy, 2011 Simons Simplex Collection aCGH--ASD 915 915 - - - - -
Sanders, 2011 Simons Simplex Collection SNP microarray--ASD 1127 1127 - - - - -
Laplana M, 2014 - aCGHASD 1 - - - 1 5 6
Zhang Y, 2015 China -autistic 1 - - - 2 - 2
Alvarez-Mora MI, 2016 - MicroarrayASD - - - - 44 - -
Kanduri C, 2016 Finnish -autism 83 - - - 257 288 545
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Family Based Association Studies: 0
Case Control Based Association Studies: 1
Reference Source Platfrom ASD Cases Normal Controls Result
ADI-R ADOS Diagnosis Age
(range)
IQ #Subjects
(% Women)
Age
(range)
ASIAN
Kato, 2008_1 Japan ABI PRISM 7900HT Sequence Detection SystemASD 19.9±9.8
-
- 415
(66.75%)
36±11.5
-
Large Scale Expression Studies Top
Microarray Studies: 2
Reference Source Tissue #Subjects
(% Women)
ADI-R ADOS Endo- pheno Diagnosis Normal Controls
(% Women)
Fold Change Up/ Down P/Q value
Voineagu, 2011_1 Unknown 16 frontal cortex(BA9) and 13 temporal cortex(BA41 16
(25.00%)
-autism 16
(6.25%)
0.758377 Down -
  • Platform: Illumina Ref8 v3 microarrays
  • ProbeSet: ILMN_1803045
  • RefSeq_ID/ EST: -
  • GEO_ID: GSE28521
  • Statistic Method: SAM package and unless otherwise specified the significance threshold was FDR,0.05 and fold changes.1.3.
Voineagu, 2011_2 Unknown frontal, BA44/45 10
(0.00%)
-autism 6
(0.00%)
0.725175 Down 0.00977612
  • Platform: Illumina Ref8 v4 microarrays
  • ProbeSet: ILMN_1803045
  • RefSeq_ID/ EST: -
  • GEO_ID: GSE28521
  • Statistic Method: SAM package and unless otherwise specified the significance threshold was FDR,0.05 and fold changes.1.3.
Proteomics Studies:0
Reference Source Tissue Platform #Subjects
(% Women)
ADI-R ADOS Diagnosis Normal Controls(% Women)
No Evidence.
NGS de novo Mutation Studies Top
Reference Case Number Family Number de novo Number Title
Sanders SJ, 2012 - 238 172 De novo mutations revealed by whole-exome sequencing are strongly associated with 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.

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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