Evidence Details for ZNF790


Gene Symbol: | ZNF790 ( FLJ20350,MGC62100 ) |
---|---|
Gene Full Name: | zinc finger protein 790 |
Band: | 19q13.12 |
Quick Links | Entrez ID:388536; OMIM: NA; Uniprot ID:ZN790_HUMAN; ENSEMBL ID: ENSG00000197863; HGNC ID: 33114 |
Relate to Another Database: | SFARIGene; denovo-db |


>ZNF790|388536|nucleotide
ATGGCCCATTTGATGATGTTCAGGGATGTGGCTGTAGATTTCTCTCAGGAGGAGTGGGAGTGCCTGGACCTGGAACAGAGGGATTTATATAGAGATGTGATGTTG
GAGAACTACAGCAACATGGTCTCACTGGGTTTTTGCATTTATCAGCCAGAAGCGTTCTCTTTATTGGAGAAAGGGAAAGAGCCCTGGAAGATTTTGAGGGATGAG
ACAAGAGGACCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTTATTACCAAAAAATGGCATTTTTGAGAGAGAAATAGCCCAATTGGAAATAATGAGA
ATTTGTAAAAACCACAGCCTTGACTGTTTATGTTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACACTTCAAGATAATCAAGAGGAATGCTTCAAGCAG
GTGATACGCACCTGTGAAAAAAGGCCCACTTTTAACCAGCATACAGTGTTTAATCTACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTTAAAGAACTG
GGGAAAGCCTTTATTTCTGGTTCAGATCATACTCAACATCAGTTAATTCACACAAGTGAGAAATTCTGTGGAGATAAAGAATGTGGGAATACCTTTCTTCCTGAT
TCAGAAGTTATTCAATATCAGACAGTTCACACTGTTAAGAAAACATATGAATGTAAAGAATGTGGGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTCATAAG
AGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGGATTGTGGGAAAGCCTTTAGATTTCATTCACAACTTAGTGTCCATAAGCGAATTCATACTGGTGAGAAA
TCTTATGAATGTAAGGAATGTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACATCAGAGAATTCATACTGGTGAAAAACCCTATGAATGTAATGAATGT
AGAAAGGCCTTTAGTCAGCGATCACATCTTATTAAACATCAGAGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTGTGGGAAAGCTTTTACTCGTGGA
TCACACCTAACTCAGCATCAGAGAATTCATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTGGAAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAG
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ATGGCCCATTTGATGATGTTCAGGGATGTGGCTGTAGATTTCTCTCAGGAGGAGTGGGAGTGCCTGGACCTGGAACAGAGGGATTTATATAGAGATGTGATGTTG
GAGAACTACAGCAACATGGTCTCACTGGGTTTTTGCATTTATCAGCCAGAAGCGTTCTCTTTATTGGAGAAAGGGAAAGAGCCCTGGAAGATTTTGAGGGATGAG
ACAAGAGGACCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTTATTACCAAAAAATGGCATTTTTGAGAGAGAAATAGCCCAATTGGAAATAATGAGA
ATTTGTAAAAACCACAGCCTTGACTGTTTATGTTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACACTTCAAGATAATCAAGAGGAATGCTTCAAGCAG
GTGATACGCACCTGTGAAAAAAGGCCCACTTTTAACCAGCATACAGTGTTTAATCTACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTTAAAGAACTG
GGGAAAGCCTTTATTTCTGGTTCAGATCATACTCAACATCAGTTAATTCACACAAGTGAGAAATTCTGTGGAGATAAAGAATGTGGGAATACCTTTCTTCCTGAT
TCAGAAGTTATTCAATATCAGACAGTTCACACTGTTAAGAAAACATATGAATGTAAAGAATGTGGGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTCATAAG
AGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGGATTGTGGGAAAGCCTTTAGATTTCATTCACAACTTAGTGTCCATAAGCGAATTCATACTGGTGAGAAA
TCTTATGAATGTAAGGAATGTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACATCAGAGAATTCATACTGGTGAAAAACCCTATGAATGTAATGAATGT
AGAAAGGCCTTTAGTCAGCGATCACATCTTATTAAACATCAGAGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTGTGGGAAAGCTTTTACTCGTGGA
TCACACCTAACTCAGCATCAGAGAATTCATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTGGAAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAG
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>ZNF790|388536|protein
MAHLMMFRDVAVDFSQEEWECLDLEQRDLYRDVMLENYSNMVSLGFCIYQPEAFSLLEKGKEPWKILRDETRGPCPDMQSRCQTKKLLPKNGIFEREIAQLEIMR
ICKNHSLDCLCFRGDWEGNTQFQTLQDNQEECFKQVIRTCEKRPTFNQHTVFNLHQRLNTGDKLNEFKELGKAFISGSDHTQHQLIHTSEKFCGDKECGNTFLPD
SEVIQYQTVHTVKKTYECKECGKSFSLRSSLTGHKRIHTGEKPFKCKDCGKAFRFHSQLSVHKRIHTGEKSYECKECGKAFSCGSDLTRHQRIHTGEKPYECNEC
RKAFSQRSHLIKHQRIHTGEKPYECKECGKAFTRGSHLTQHQRIHTGEKSHECKECGKAFIRGSNLAQHQNVHVGRKPYKCEKCGKAYIWSSHLARHQRIHTGRK
PYECKQCGKTFTWASYLAQHEKIHNERKSYECKECGKTFLHGSEFNRHQKIHTGERNYECKECGKTFFRGSELNRHQKIHTGKRPYECEECGKAFLWGSQLTRHQ
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MAHLMMFRDVAVDFSQEEWECLDLEQRDLYRDVMLENYSNMVSLGFCIYQPEAFSLLEKGKEPWKILRDETRGPCPDMQSRCQTKKLLPKNGIFEREIAQLEIMR
ICKNHSLDCLCFRGDWEGNTQFQTLQDNQEECFKQVIRTCEKRPTFNQHTVFNLHQRLNTGDKLNEFKELGKAFISGSDHTQHQLIHTSEKFCGDKECGNTFLPD
SEVIQYQTVHTVKKTYECKECGKSFSLRSSLTGHKRIHTGEKPFKCKDCGKAFRFHSQLSVHKRIHTGEKSYECKECGKAFSCGSDLTRHQRIHTGEKPYECNEC
RKAFSQRSHLIKHQRIHTGEKPYECKECGKAFTRGSHLTQHQRIHTGEKSHECKECGKAFIRGSNLAQHQNVHVGRKPYKCEKCGKAYIWSSHLARHQRIHTGRK
PYECKQCGKTFTWASYLAQHEKIHNERKSYECKECGKTFLHGSEFNRHQKIHTGERNYECKECGKTFFRGSELNRHQKIHTGKRPYECEECGKAFLWGSQLTRHQ
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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 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (4) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Gregory, 2009 | USA | aCGH | ![]() | ![]() | ASD | - | - | - | - | 119 | 54 | 173 |
Nord, 2011 | US | aCGH | - | - | ASD | - | - | - | - | 41 | 367 | 408 |








Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Yuen RK, 2016 | 200 | - | 301 | Genome-wide characteristics of de novo mutations in autism. |
C Yuen RK, 2017 | 1625 | - | 237 | Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. |






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