Evidence Details for ZNF687
Basic Information Top
Gene Symbol: | ZNF687 ( DKFZp781I1719,KIAA1441 ) |
---|---|
Gene Full Name: | zinc finger protein 687 |
Band: | 1q21.3 |
Quick Links | Entrez ID:57592; OMIM: 610568; Uniprot ID:ZN687_HUMAN; ENSEMBL ID: ENSG00000143373; HGNC ID: 29277 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ZNF687|57592|nucleotide
ATGGGGGATATGAAGACCCCTGATTTTGATGACCTCCTTGCTGCCTTTGACATCCCTGACATTGATGCGAATGAAGCCATCCATTCTGGGCCAGAAGAAAATGAG
GGGCCTGGAGGCCCAGGGAAGCCAGAACCAGGTGTAGGAAGTGAATCTGAAGACACAGCAGCAGCCTCTGCTGGGGATGGCCCTGGAGTTCCAGCCCAGGCCTCT
GACCATGGCCTGCCACCGCCAGACATTTCTGTAGTCAGTGTCATTGTCAAGAACACTGTGTGTCCCGAGCAGTCTGAGGCCCTGGCTGGAGGCTCAGCAGGAGAC
GGGGCCCAGGCTGCTGGGGTAACTAAAGAAGGGCCTGTGGGGCCTCATCGAATGCAGAATGGTTTTGGGAGCCCTGAACCTTCCCTCCCAGGAACTCCCCACTCT
CCTGCTCCTCCCAGTGGGGGCACCTGGAAAGAAAAAGGCATGGAAGGCAAAACTCCCTTGGACCTGTTTGCTCATTTTGGCCCTGAGCCAGGGGACCACTCAGAT
CCGCTGCCTCCCTCTGCACCCTCTCCCACTCGGGAGGGGGCTCTGACCCCGCCTCCTTTCCCCTCTTCCTTTGAGCTGGCCCAGGAGAATGGCCCAGGCATGCAG
CCACCTGTTTCTTCCCCACCATTGGGGGCCTTGAAGCAGGAGAGCTGCAGCCCCCATCATCCCCAGGTCCTAGCCCAACAAGGCTCAGGCTCCAGCCCTAAGGCC
ACGGACATCCCTGCCAGTGCCTCGCCTCCCCCAGTTGCTGGGGTGCCCTTCTTCAAGCAGTCTCCAGGGCACCAGAGCCCTCTTGCCTCCCCCAAAGTGCCCGTC
TGTCAGCCCTTGAAGGAAGAAGATGATGATGAGGGGCCAGTGGACAAGTCTTCCCCAGGAAGTCCCCAGAGTCCCTCTAGTGGGGCCGAGGCTGCAGATGAGGAC
AGCAATGACTCCCCTGCCTCCAGCTCCTCTAGGCCTCTTAAGGTGCGGATCAAGACCATTAAAACATCCTGCGGGAATATCACAAGGACTGTAACTCAGGTCCCC
TCAGATCCTGATCCACCTGCCCCCTTGGCTGAGGGGGCCTTCTTGGCTGAGGCTAGCCTCTTGAAGCTGTCCCCTGCAACACCTACTTCTGAGGGTCCAAAGGTG
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ATGGGGGATATGAAGACCCCTGATTTTGATGACCTCCTTGCTGCCTTTGACATCCCTGACATTGATGCGAATGAAGCCATCCATTCTGGGCCAGAAGAAAATGAG
GGGCCTGGAGGCCCAGGGAAGCCAGAACCAGGTGTAGGAAGTGAATCTGAAGACACAGCAGCAGCCTCTGCTGGGGATGGCCCTGGAGTTCCAGCCCAGGCCTCT
GACCATGGCCTGCCACCGCCAGACATTTCTGTAGTCAGTGTCATTGTCAAGAACACTGTGTGTCCCGAGCAGTCTGAGGCCCTGGCTGGAGGCTCAGCAGGAGAC
GGGGCCCAGGCTGCTGGGGTAACTAAAGAAGGGCCTGTGGGGCCTCATCGAATGCAGAATGGTTTTGGGAGCCCTGAACCTTCCCTCCCAGGAACTCCCCACTCT
CCTGCTCCTCCCAGTGGGGGCACCTGGAAAGAAAAAGGCATGGAAGGCAAAACTCCCTTGGACCTGTTTGCTCATTTTGGCCCTGAGCCAGGGGACCACTCAGAT
CCGCTGCCTCCCTCTGCACCCTCTCCCACTCGGGAGGGGGCTCTGACCCCGCCTCCTTTCCCCTCTTCCTTTGAGCTGGCCCAGGAGAATGGCCCAGGCATGCAG
CCACCTGTTTCTTCCCCACCATTGGGGGCCTTGAAGCAGGAGAGCTGCAGCCCCCATCATCCCCAGGTCCTAGCCCAACAAGGCTCAGGCTCCAGCCCTAAGGCC
ACGGACATCCCTGCCAGTGCCTCGCCTCCCCCAGTTGCTGGGGTGCCCTTCTTCAAGCAGTCTCCAGGGCACCAGAGCCCTCTTGCCTCCCCCAAAGTGCCCGTC
TGTCAGCCCTTGAAGGAAGAAGATGATGATGAGGGGCCAGTGGACAAGTCTTCCCCAGGAAGTCCCCAGAGTCCCTCTAGTGGGGCCGAGGCTGCAGATGAGGAC
AGCAATGACTCCCCTGCCTCCAGCTCCTCTAGGCCTCTTAAGGTGCGGATCAAGACCATTAAAACATCCTGCGGGAATATCACAAGGACTGTAACTCAGGTCCCC
TCAGATCCTGATCCACCTGCCCCCTTGGCTGAGGGGGCCTTCTTGGCTGAGGCTAGCCTCTTGAAGCTGTCCCCTGCAACACCTACTTCTGAGGGTCCAAAGGTG
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>ZNF687|57592|protein
MGDMKTPDFDDLLAAFDIPDIDANEAIHSGPEENEGPGGPGKPEPGVGSESEDTAAASAGDGPGVPAQASDHGLPPPDISVVSVIVKNTVCPEQSEALAGGSAGD
GAQAAGVTKEGPVGPHRMQNGFGSPEPSLPGTPHSPAPPSGGTWKEKGMEGKTPLDLFAHFGPEPGDHSDPLPPSAPSPTREGALTPPPFPSSFELAQENGPGMQ
PPVSSPPLGALKQESCSPHHPQVLAQQGSGSSPKATDIPASASPPPVAGVPFFKQSPGHQSPLASPKVPVCQPLKEEDDDEGPVDKSSPGSPQSPSSGAEAADED
SNDSPASSSSRPLKVRIKTIKTSCGNITRTVTQVPSDPDPPAPLAEGAFLAEASLLKLSPATPTSEGPKVVSVQLGDGTRLKGTVLPVATIQNASTAMLMAASVA
RKAVVLPGGTATSPKMIAKNVLGLVPQALPKADGRAGLGTGGQKVNGASVVMVQPSKTATGPSTGGGTVISRTQSSLVEAFNKILNSKNLLPAYRPNLSPPAEAG
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MGDMKTPDFDDLLAAFDIPDIDANEAIHSGPEENEGPGGPGKPEPGVGSESEDTAAASAGDGPGVPAQASDHGLPPPDISVVSVIVKNTVCPEQSEALAGGSAGD
GAQAAGVTKEGPVGPHRMQNGFGSPEPSLPGTPHSPAPPSGGTWKEKGMEGKTPLDLFAHFGPEPGDHSDPLPPSAPSPTREGALTPPPFPSSFELAQENGPGMQ
PPVSSPPLGALKQESCSPHHPQVLAQQGSGSSPKATDIPASASPPPVAGVPFFKQSPGHQSPLASPKVPVCQPLKEEDDDEGPVDKSSPGSPQSPSSGAEAADED
SNDSPASSSSRPLKVRIKTIKTSCGNITRTVTQVPSDPDPPAPLAEGAFLAEASLLKLSPATPTSEGPKVVSVQLGDGTRLKGTVLPVATIQNASTAMLMAASVA
RKAVVLPGGTATSPKMIAKNVLGLVPQALPKADGRAGLGTGGQKVNGASVVMVQPSKTATGPSTGGGTVISRTQSSLVEAFNKILNSKNLLPAYRPNLSPPAEAG
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
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 |
---|---|---|---|---|
C Yuen RK, 2017 | 1625 | - | 237 | Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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