Evidence Details for ZNF774
Basic Information Top
| Gene Symbol: | ZNF774 ( MGC75360 ) |
|---|---|
| Gene Full Name: | zinc finger protein 774 |
| Band: | 15q26.1 |
| Quick Links | Entrez ID:342132; OMIM: NA; Uniprot ID:ZN774_HUMAN; ENSEMBL ID: ENSG00000196391; HGNC ID: 33108 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ZNF774|342132|nucleotide
ATGTGGCTGGGGACTTCAGGGAAGAGTGGGTTACCTGGACACTGCTTAGAGAATCCTCTCCAGGAATGCCACCCAGCACAGTTAGAAGAATGGGCTCTCAAAGGA
ATTTCCAGGCCTAGTGTAATCTCCCAGCCGGAGCAGAAAGAAGAGCCATGGGTCCTACCACTCCAAAACTTTGAGGCGAGGAAGATCCCGAGGGAAAGCCACACA
GACTGTGAGCATCAGGTGGCAAAGCTCAATCAGGACAATTCTGAAACAGCAGAACAATGTGGAACATCCTCAGAAAGGACCAATAAAGATCTTTCTCATACTCTT
AGTTGGGGAGGAAACTGGGAGCAAGGCCTAGAATTAGAAGGGCAACATGGAACCCTTCCAGGAGAGGGCCAGCTGGAGTCCTTTTCACAGGAGAGGGATTTAAAC
AAGCTCCTGGATGGATATGTAGGAGAGAAGCCTATGTGTGCAGAATGCGGGAAAAGCTTTAACCAGAGTTCCTATCTCATAAGACACCTAAGAACCCACACTGGC
GAGAGGCCCTATACGTGCATTGAGTGTGGGAAAGGCTTCAAACAGAGCTCAGACCTTGTCACCCATCGCAGAACACACACAGGAGAGAAGCCCTACCAATGCAAG
GGGTGTGAGAAGAAATTCAGCGACAGCTCAACACTCATCAAACATCAGAGAACCCACACAGGGGAGAGACCCTATGAGTGCCCAGAGTGTGGAAAGACTTTTGGG
CGGAAGCCACACCTCATAATGCACCAAAGAACCCACACAGGCGAGAAGCCCTACGCGTGCCTGGAATGTCACAAAAGCTTCAGTCGAAGCTCAAATTTCATCACT
CACCAGAGGACCCACACAGGGGTGAAGCCTTACAGGTGTAATGACTGTGGGGAGAGTTTTAGCCAGAGCTCGGATTTGATTAAGCACCAACGAACCCACACGGGA
GAACGGCCCTTCAAATGCCCGGAGTGCGGGAAGGGCTTCAGAGATAGTTCTCATTTTGTAGCTCACATGAGCACTCATTCAGGAGAGAGGCCTTTCAGTTGTCCT
GACTGCCACAAAAGCTTCAGTCAGAGCTCACATTTGGTCACGCACCAAAGAACACACACAGGTGAGAGACCTTTTAAGTGCGAAAACTGTGGGAAAGGATTCGCC
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ATGTGGCTGGGGACTTCAGGGAAGAGTGGGTTACCTGGACACTGCTTAGAGAATCCTCTCCAGGAATGCCACCCAGCACAGTTAGAAGAATGGGCTCTCAAAGGA
ATTTCCAGGCCTAGTGTAATCTCCCAGCCGGAGCAGAAAGAAGAGCCATGGGTCCTACCACTCCAAAACTTTGAGGCGAGGAAGATCCCGAGGGAAAGCCACACA
GACTGTGAGCATCAGGTGGCAAAGCTCAATCAGGACAATTCTGAAACAGCAGAACAATGTGGAACATCCTCAGAAAGGACCAATAAAGATCTTTCTCATACTCTT
AGTTGGGGAGGAAACTGGGAGCAAGGCCTAGAATTAGAAGGGCAACATGGAACCCTTCCAGGAGAGGGCCAGCTGGAGTCCTTTTCACAGGAGAGGGATTTAAAC
AAGCTCCTGGATGGATATGTAGGAGAGAAGCCTATGTGTGCAGAATGCGGGAAAAGCTTTAACCAGAGTTCCTATCTCATAAGACACCTAAGAACCCACACTGGC
GAGAGGCCCTATACGTGCATTGAGTGTGGGAAAGGCTTCAAACAGAGCTCAGACCTTGTCACCCATCGCAGAACACACACAGGAGAGAAGCCCTACCAATGCAAG
GGGTGTGAGAAGAAATTCAGCGACAGCTCAACACTCATCAAACATCAGAGAACCCACACAGGGGAGAGACCCTATGAGTGCCCAGAGTGTGGAAAGACTTTTGGG
CGGAAGCCACACCTCATAATGCACCAAAGAACCCACACAGGCGAGAAGCCCTACGCGTGCCTGGAATGTCACAAAAGCTTCAGTCGAAGCTCAAATTTCATCACT
CACCAGAGGACCCACACAGGGGTGAAGCCTTACAGGTGTAATGACTGTGGGGAGAGTTTTAGCCAGAGCTCGGATTTGATTAAGCACCAACGAACCCACACGGGA
GAACGGCCCTTCAAATGCCCGGAGTGCGGGAAGGGCTTCAGAGATAGTTCTCATTTTGTAGCTCACATGAGCACTCATTCAGGAGAGAGGCCTTTCAGTTGTCCT
GACTGCCACAAAAGCTTCAGTCAGAGCTCACATTTGGTCACGCACCAAAGAACACACACAGGTGAGAGACCTTTTAAGTGCGAAAACTGTGGGAAAGGATTCGCC
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>ZNF774|342132|protein
MWLGTSGKSGLPGHCLENPLQECHPAQLEEWALKGISRPSVISQPEQKEEPWVLPLQNFEARKIPRESHTDCEHQVAKLNQDNSETAEQCGTSSERTNKDLSHTL
SWGGNWEQGLELEGQHGTLPGEGQLESFSQERDLNKLLDGYVGEKPMCAECGKSFNQSSYLIRHLRTHTGERPYTCIECGKGFKQSSDLVTHRRTHTGEKPYQCK
GCEKKFSDSSTLIKHQRTHTGERPYECPECGKTFGRKPHLIMHQRTHTGEKPYACLECHKSFSRSSNFITHQRTHTGVKPYRCNDCGESFSQSSDLIKHQRTHTG
ERPFKCPECGKGFRDSSHFVAHMSTHSGERPFSCPDCHKSFSQSSHLVTHQRTHTGERPFKCENCGKGFADSSALIKHQRIHTGERPYKCGECGKSFNQSSHFIT
HQRIHLGDRPYRCPECGKTFNQRSHFLTHQRTHTGEKPFHCSKCNKSFRQKAHLLCHQNTHLI
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MWLGTSGKSGLPGHCLENPLQECHPAQLEEWALKGISRPSVISQPEQKEEPWVLPLQNFEARKIPRESHTDCEHQVAKLNQDNSETAEQCGTSSERTNKDLSHTL
SWGGNWEQGLELEGQHGTLPGEGQLESFSQERDLNKLLDGYVGEKPMCAECGKSFNQSSYLIRHLRTHTGERPYTCIECGKGFKQSSDLVTHRRTHTGEKPYQCK
GCEKKFSDSSTLIKHQRTHTGERPYECPECGKTFGRKPHLIMHQRTHTGEKPYACLECHKSFSRSSNFITHQRTHTGVKPYRCNDCGESFSQSSDLIKHQRTHTG
ERPFKCPECGKGFRDSSHFVAHMSTHSGERPFSCPDCHKSFSQSSHLVTHQRTHTGERPFKCENCGKGFADSSALIKHQRIHTGERPYKCGECGKSFNQSSHFIT
HQRIHLGDRPYRCPECGKTFNQRSHFLTHQRTHTGEKPFHCSKCNKSFRQKAHLLCHQNTHLI
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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) | 1 (3) | 1 (1) | 0 (0) | 0 (0) | 2 (2) | 0 (0) | 1 (1) | 0 (0) | 32 (7) |
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 | ||||||
| Bonati, 2005 | - | FISH | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
| Szatmari, 2007 | Europe, North America | SNP microarray | ![]() | ![]() | ASD | 1491 | - | - | - | - | - | 0 |
| Pinto, 2010 | - | SNP microarray, qPCR | ![]() | ![]() | ASD | - | - | - | - | 996 | 1287 | 2283 |
Linkage Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Risch, 1999 | USA | microsatellite-based genomic screen | ![]() | ![]() | PDD | 90 | - | 90 | - | - | - | - |
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 |
| Fromer M, 2014 | - | - | 94 | De novo mutations in schizophrenia implicate synaptic networks. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
| Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | ||||||||
| Yuen RK, 2015 | - | Complete Genomics | ![]() | ![]() | ASD | 85 | - | 85 | 170 | Sanger sequencing |
Low Scale Gene Studies Top
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