Evidence Details for ZNF138
Basic Information Top
| Gene Symbol: | ZNF138 ( pHZ-32 ) |
|---|---|
| Gene Full Name: | zinc finger protein 138 |
| Band: | 7q11.21 |
| Quick Links | Entrez ID:7697; OMIM: 604080; Uniprot ID:A2RRP7_HUMAN; ENSEMBL ID: ENSG00000197008; HGNC ID: 12922 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ZNF138|7697|nucleotide
ATGGGACCACTGACATTTATGGATGTGGCCATAGAGTTCTCTTTGGAGGAGTGGCAGTGCCTGGACACTGCACAGCGGAATGTATATAGGCATGTGATGTTAGAG
AACTACAGAAACCTGGTTTTCTTGGACCTGATTACCTGTCTGGAACAAGGAAAAGAGCCCTGGAATATGAAGAGACATGAGATGGTGGTAGCCAAACATTCAGCT
GTAGCATTTACCTTTGATCTCAGTGGACTCAACATTTTGTCATTCCAAAGTATCCTGCCATTTGTTTCAGCACTTTATGTCATGGGAAACAGAAACCAGTGTCTG
CAAAAGCACCTAGAAGCCAGAAATAAAGATCTCTGTGTTCTCGTTTTGCCCAAGACCTTTGGCTAG
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ATGGGACCACTGACATTTATGGATGTGGCCATAGAGTTCTCTTTGGAGGAGTGGCAGTGCCTGGACACTGCACAGCGGAATGTATATAGGCATGTGATGTTAGAG
AACTACAGAAACCTGGTTTTCTTGGACCTGATTACCTGTCTGGAACAAGGAAAAGAGCCCTGGAATATGAAGAGACATGAGATGGTGGTAGCCAAACATTCAGCT
GTAGCATTTACCTTTGATCTCAGTGGACTCAACATTTTGTCATTCCAAAGTATCCTGCCATTTGTTTCAGCACTTTATGTCATGGGAAACAGAAACCAGTGTCTG
CAAAAGCACCTAGAAGCCAGAAATAAAGATCTCTGTGTTCTCGTTTTGCCCAAGACCTTTGGCTAG
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>ZNF138|7697|protein
MGPLTFMDVAIEFSLEEWQCLDTAQRNVYRHVMLENYRNLVFLDLITCLEQGKEPWNMKRHEMVVAKHSAVAFTFDLSGLNILSFQSILPFVSALYVMGNRNQCL
QKHLEARNKDLCVLVLPKTFG
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MGPLTFMDVAIEFSLEEWQCLDTAQRNVYRHVMLENYRNLVFLDLITCLEQGKEPWNMKRHEMVVAKHSAVAFTFDLSGLNILSFQSILPFVSALYVMGNRNQCL
QKHLEARNKDLCVLVLPKTFG
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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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (2) |
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 | ||||||
| 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 |
|---|---|---|---|---|
| Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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