Evidence Details for TUBGCP5
Basic Information Top
Gene Symbol: | TUBGCP5 ( GCP5,KIAA1899 ) |
---|---|
Gene Full Name: | tubulin, gamma complex associated protein 5 |
Band: | 15q11.2 |
Quick Links | Entrez 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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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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MARHGPPWSRLDAQQERDVRELVRGVAGLQDEADPNFQLALNFAWSNFRFHRFLDVNSHKIEKTIEGIYEKFVIHSDLSKAASWKRLTEEFLNAPLPSIKEIKTD
AHYSILSLLLCLSDSPSNSSYVETPRNKEVEKKDDFDWGKYLMEDEEMDIGPYMDTPNWSEESEEENDQQPLSREDSGIQVDRTPLEEQDQNRKLDPCISWKDEP
DDRSWLEHHVVHQYWTARPSQFPHSLHLHSNLAAVWDQHLYSSDPLYVPDDRVLVTETQVIRETLWLLSGVKKLFIFQLIDGKVTVRNNIIVTHLTHSCLRSVLE
QIAAYGQVVFRLQEFIDEVMGHSSESMLPGSGSVPKKSTEAPFRTYQAFMWALYKYFISFKEELAEIEKCIINNDTTITLAIVVDKLAPRLSQLKVLHKVFSTGV
AEVPPDTRNVVRASHLLNTLYKAILEYDNVGEASEQTVSLLFSLWVETVRPYLQTVDEWIVHGHLWDGAREFIIQRNKNVPVNHRDFWYATYTLYSVSEKTENEE
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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) | 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 mapping | autism | 3 | - | 3 | - | 3 | - | 3 | ||
Wassink, 2001 | USA | Chromosomal analysis of G-band | autism | - | - | - | - | 278 | - | 278 | ||
Silva, 2002 | - | FISH | autism | - | - | - | - | 1 | - | 1 | ||
Keller, 2003 | USA | FISH | ASD | - | - | - | - | 2 | - | 2 | ||
Sahoo, 2005 | USA | aCGH | autism | - | - | - | - | 9 | - | 9 | ||
Wassink, 2007 | USA | FISH | PDD | - | - | - | - | 104 | - | 104 | ||
Sebat, 2007 | USA | aCGH | autism | 165 | 118 | 47 | 99 | 195 | 196 | 391 | ||
Weiss, 2008 | USA, Ireland | aCGH, SNP microarray | ASD | 751 | - | - | - | 2252 | 23502 | 25754 | ||
Marshall, 2008 | - | SNP microarray | ASD | 427 | 238 | 189 | - | 427 | 500 | 927 | ||
Christian, 2008 | USA | aCGH | ASD | 397 | 35 | 362 | - | 397 | 372 | 769 | ||
Bremer, 2009 | - | aCGH | ASD | - | - | - | - | 148 | - | 148 | ||
van der Zwaag, 2009 | Holland | SNP microarray | ASD | 2 | - | 2 | - | 3 | 267 | 270 | ||
Gregory, 2009 | USA | aCGH | ASD | - | - | - | - | 119 | 54 | 173 | ||
Pinto, 2010 | - | SNP microarray, qPCR | ASD | - | - | - | - | 996 | 1287 | 2283 | ||
Bremer, 2011 | - | aCGH | ASD | - | - | - | - | 223 | - | 223 | ||
Levy, 2011 | Simons Simplex Collection | aCGH | - | - | ASD | 915 | 915 | - | - | - | - | - |
Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Laplana M, 2014 | - | aCGH | ASD | 1 | - | - | - | 1 | 5 | 6 | ||
Zhang Y, 2015 | China | - | autistic | 1 | - | - | - | 2 | - | 2 | ||
Alvarez-Mora MI, 2016 | - | Microarray | ASD | - | - | - | - | 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
Reference | Source | Platform | #Families | Affecteds | Result | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
#Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ (range) |
||||||||
No Evidence. |
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 System | ASD | 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 | - | |||
| ||||||||||||
Voineagu, 2011_2 | Unknown | frontal, BA44/45 | 10 (0.00%) | - | autism | 6 (0.00%) |
0.725175 | Down | 0.00977612 | |||
|
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
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