Evidence Details for TRIM4
Basic Information Top
Gene Symbol: | TRIM4 ( RNF87 ) |
---|---|
Gene Full Name: | tripartite motif-containing 4 |
Band: | 7q22.1 |
Quick Links | Entrez ID:89122; OMIM: NA; Uniprot ID:TRIM4_HUMAN; ENSEMBL ID: ENSG00000146833; HGNC ID: 16275 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>TRIM4|89122|nucleotide
ATGGAAGCTGAGGACATCCAGGAGGAGTTGACCTGCCCCATCTGCCTGGACTATTTCCAGGACCCGGTGTCCATCGAGTGCGGCCACAACTTCTGCCGCGGCTGC
CTGCACCGCAACTGGGCGCCGGGCGGCGGCCCGTTCCCCTGCCCCGAATGTCGGCACCCATCGGCGCCCGCCGCGCTGCGACCCAACTGGGCCCTGGCCAGGCTG
ACTGAGAAGACGCAGCGCCGGCGCCTGGGCCCCGTGCCCCCGGGCCTGTGCGGCCGCCACTGGGAGCCGCTGCGGCTCTTCTGCGAGGACGACCAGCGGCCAGTG
TGCCTGGTGTGCAGGGAGTCCCAGGAGCACCAGACTCACGCCATGGCACCCATCGACGAGGCCTTCGAGAGCTACCGGACAGGTAACTTTGACATCCACGTGGAT
GAATGGAAGAGAAGACTAATTAGGCTGCTCTTGTACCATTTTAAGCAGGAGGAGAAACTTCTTAAGTCTCAGCGTAATCTCGTGGCCAAGATGAAGAAAGTCATG
CATTTACAGGATGTAGAAGTGAAGAACGCCACACAGTGGAAGGATAAGATAAAGAGTCAGCGAATGAGAATCAGCACGGAGTTTTCAAAGCTGCACAACTTCCTG
GTTGAAGAAGAGGACCTGTTTCTTCAGAGATTGAACAAAGAAGAAGAAGAGACGAAGAAGAAGCTGAATGAGAACACGTTAAAACTCAATCAAACTATCGCTTCA
TTGAAGAAGCTCATCTTAGAGGTGGGGGAGAAGAGCCAGGCTCCCACCCTGGAGCTGCTTCAGAATCCAAAAGAAGTGTTGACCAGGAGTGAGATCCAGGATGTG
AACTATTCTCTTGAAGCTGTAAAGGTGAAGACAGTGTGCCAGATACCATTGATGAAGGAAATGCTAAAGCGATTCCAAGTGGCTGTAAACCTAGCTGAAGACACA
GCTCATCCCAAACTCGTCTTCTCCCAGGAAGGGAGATACGTGAAAAATACAGCATCAGCCAGTTCTTGGCCAGTGTTTTCTTCAGCATGGAACTACTTTGCTGGA
TGGAGGAATCCTCAGAAGACTGCTTTTGTAGAGAGATTTCAGCACTTACCCTGTGTTCTGGGAAAAAACGTTTTCACCTCAGGGAAACATTACTGGGAAGTTGAG
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ATGGAAGCTGAGGACATCCAGGAGGAGTTGACCTGCCCCATCTGCCTGGACTATTTCCAGGACCCGGTGTCCATCGAGTGCGGCCACAACTTCTGCCGCGGCTGC
CTGCACCGCAACTGGGCGCCGGGCGGCGGCCCGTTCCCCTGCCCCGAATGTCGGCACCCATCGGCGCCCGCCGCGCTGCGACCCAACTGGGCCCTGGCCAGGCTG
ACTGAGAAGACGCAGCGCCGGCGCCTGGGCCCCGTGCCCCCGGGCCTGTGCGGCCGCCACTGGGAGCCGCTGCGGCTCTTCTGCGAGGACGACCAGCGGCCAGTG
TGCCTGGTGTGCAGGGAGTCCCAGGAGCACCAGACTCACGCCATGGCACCCATCGACGAGGCCTTCGAGAGCTACCGGACAGGTAACTTTGACATCCACGTGGAT
GAATGGAAGAGAAGACTAATTAGGCTGCTCTTGTACCATTTTAAGCAGGAGGAGAAACTTCTTAAGTCTCAGCGTAATCTCGTGGCCAAGATGAAGAAAGTCATG
CATTTACAGGATGTAGAAGTGAAGAACGCCACACAGTGGAAGGATAAGATAAAGAGTCAGCGAATGAGAATCAGCACGGAGTTTTCAAAGCTGCACAACTTCCTG
GTTGAAGAAGAGGACCTGTTTCTTCAGAGATTGAACAAAGAAGAAGAAGAGACGAAGAAGAAGCTGAATGAGAACACGTTAAAACTCAATCAAACTATCGCTTCA
TTGAAGAAGCTCATCTTAGAGGTGGGGGAGAAGAGCCAGGCTCCCACCCTGGAGCTGCTTCAGAATCCAAAAGAAGTGTTGACCAGGAGTGAGATCCAGGATGTG
AACTATTCTCTTGAAGCTGTAAAGGTGAAGACAGTGTGCCAGATACCATTGATGAAGGAAATGCTAAAGCGATTCCAAGTGGCTGTAAACCTAGCTGAAGACACA
GCTCATCCCAAACTCGTCTTCTCCCAGGAAGGGAGATACGTGAAAAATACAGCATCAGCCAGTTCTTGGCCAGTGTTTTCTTCAGCATGGAACTACTTTGCTGGA
TGGAGGAATCCTCAGAAGACTGCTTTTGTAGAGAGATTTCAGCACTTACCCTGTGTTCTGGGAAAAAACGTTTTCACCTCAGGGAAACATTACTGGGAAGTTGAG
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>TRIM4|89122|protein
MEAEDIQEELTCPICLDYFQDPVSIECGHNFCRGCLHRNWAPGGGPFPCPECRHPSAPAALRPNWALARLTEKTQRRRLGPVPPGLCGRHWEPLRLFCEDDQRPV
CLVCRESQEHQTHAMAPIDEAFESYRTGNFDIHVDEWKRRLIRLLLYHFKQEEKLLKSQRNLVAKMKKVMHLQDVEVKNATQWKDKIKSQRMRISTEFSKLHNFL
VEEEDLFLQRLNKEEEETKKKLNENTLKLNQTIASLKKLILEVGEKSQAPTLELLQNPKEVLTRSEIQDVNYSLEAVKVKTVCQIPLMKEMLKRFQVAVNLAEDT
AHPKLVFSQEGRYVKNTASASSWPVFSSAWNYFAGWRNPQKTAFVERFQHLPCVLGKNVFTSGKHYWEVESRDSLEVAVGVCREDVMGITDRSKMSPDVGIWAIY
WSAAGYWPLIGFPGTPTQQEPALHRVGVYLDRGTGNVSFYSAVDGVHLHTFSCSSVSRLRPFFWLSPLASLVIPPVTDRK
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MEAEDIQEELTCPICLDYFQDPVSIECGHNFCRGCLHRNWAPGGGPFPCPECRHPSAPAALRPNWALARLTEKTQRRRLGPVPPGLCGRHWEPLRLFCEDDQRPV
CLVCRESQEHQTHAMAPIDEAFESYRTGNFDIHVDEWKRRLIRLLLYHFKQEEKLLKSQRNLVAKMKKVMHLQDVEVKNATQWKDKIKSQRMRISTEFSKLHNFL
VEEEDLFLQRLNKEEEETKKKLNENTLKLNQTIASLKKLILEVGEKSQAPTLELLQNPKEVLTRSEIQDVNYSLEAVKVKTVCQIPLMKEMLKRFQVAVNLAEDT
AHPKLVFSQEGRYVKNTASASSWPVFSSAWNYFAGWRNPQKTAFVERFQHLPCVLGKNVFTSGKHYWEVESRDSLEVAVGVCREDVMGITDRSKMSPDVGIWAIY
WSAAGYWPLIGFPGTPTQQEPALHRVGVYLDRGTGNVSFYSAVDGVHLHTFSCSSVSRLRPFFWLSPLASLVIPPVTDRK
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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) | 0 (0) | 1 (1) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 3 (3) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Monaco, 2001 | - | microsatellite-based genomic screen | PDD | 152 | - | 152 | - | - | - | - |
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 1
Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Hu, 2009_1 | mixed | lymphoblastoid cell lines | 21 (-) | autism with nonaffected sib pairs | autism | 17 (-) |
1.07 | Up | - | |||
|
Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | ||||||||
Toma C, 2014 | - | Illumina HiSeq 2000 | - | - | ASD | 10 | - | - | 21 | - |
Low Scale Gene Studies Top
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