Evidence Details for WFIKKN2
Basic Information Top
Gene Symbol: | WFIKKN2 ( GASP-1,WFIKKNRP,hGASP-1 ) |
---|---|
Gene Full Name: | WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 |
Band: | 17q21.33 |
Quick Links | Entrez ID:124857; OMIM: 610895; Uniprot ID:WFKN2_HUMAN; ENSEMBL ID: ENSG00000173714; HGNC ID: 30916 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>WFIKKN2|124857|nucleotide
ATGTGGGCCCCAAGGTGTCGCCGGTTCTGGTCTCGCTGGGAGCAGGTGGCAGCGCTGCTGCTGCTGCTGCTACTGCTCGGGGTGCCCCCGCGAAGCCTGGCGCTG
CCGCCCATCCGCTATTCCCACGCCGGCATCTGCCCCAACGACATGAATCCCAACCTCTGGGTGGACGCACAGAGCACCTGCAGGCGGGAGTGTGAGACGGACCAG
GAGTGTGAGACCTATGAGAAGTGCTGCCCCAACGTATGTGGGACCAAGAGCTGCGTGGCGGCCCGCTACATGGACGTGAAAGGGAAGAAGGGCCCAGTGGGCATG
CCCAAGGAGGCCACATGTGACCACTTCATGTGTCTGCAGCAGGGCTCTGAGTGTGACATCTGGGATGGCCAGCCCGTGTGTAAGTGCAAAGACCGCTGTGAGAAG
GAGCCCAGCTTTACCTGCGCCTCGGACGGCCTCACCTACTATAACCGCTGCTACATGGATGCCGAGGCCTGCTCCAAAGGCATCACACTGGCCGTTGTAACCTGC
CGCTATCACTTCACCTGGCCCAACACCAGCCCCCCACCACCTGAGACCACCATGCACCCCACCACAGCCTCCCCAGAGACCCCTGAGCTGGACATGGCGGCCCCT
GCGCTGCTCAACAACCCTGTGCACCAGTCGGTCACCATGGGTGAGACAGTGAGCTTCCTCTGTGATGTGGTGGGCCGGCCCCGGCCTGAGATCACCTGGGAGAAG
CAGTTGGAGGATCGGGAGAATGTGGTCATGCGGCCCAACCATGTGCGTGGCAACGTGGTGGTCACCAACATTGCCCAGCTGGTCATCTATAACGCCCAGCTGCAG
GATGCTGGGATCTACACCTGCACGGCCCGGAACGTGGCTGGGGTCCTGAGGGCTGATTTCCCGCTGTCGGTGGTCAGGGGTCATCAGGCTGCAGCCACCTCAGAG
AGCAGCCCCAATGGCACGGCTTTCCCGGCGGCCGAGTGCCTGAAGCCCCCAGACAGTGAGGACTGTGGCGAAGAGCAGACCCGCTGGCACTTCGATGCCCAGGCC
AACAACTGCCTGACCTTCACCTTCGGCCACTGCCACCGTAACCTCAACCACTTTGAGACCTATGAGGCCTGCATGCTGGCCTGCATGAGCGGGCCGCTGGCCGCG
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ATGTGGGCCCCAAGGTGTCGCCGGTTCTGGTCTCGCTGGGAGCAGGTGGCAGCGCTGCTGCTGCTGCTGCTACTGCTCGGGGTGCCCCCGCGAAGCCTGGCGCTG
CCGCCCATCCGCTATTCCCACGCCGGCATCTGCCCCAACGACATGAATCCCAACCTCTGGGTGGACGCACAGAGCACCTGCAGGCGGGAGTGTGAGACGGACCAG
GAGTGTGAGACCTATGAGAAGTGCTGCCCCAACGTATGTGGGACCAAGAGCTGCGTGGCGGCCCGCTACATGGACGTGAAAGGGAAGAAGGGCCCAGTGGGCATG
CCCAAGGAGGCCACATGTGACCACTTCATGTGTCTGCAGCAGGGCTCTGAGTGTGACATCTGGGATGGCCAGCCCGTGTGTAAGTGCAAAGACCGCTGTGAGAAG
GAGCCCAGCTTTACCTGCGCCTCGGACGGCCTCACCTACTATAACCGCTGCTACATGGATGCCGAGGCCTGCTCCAAAGGCATCACACTGGCCGTTGTAACCTGC
CGCTATCACTTCACCTGGCCCAACACCAGCCCCCCACCACCTGAGACCACCATGCACCCCACCACAGCCTCCCCAGAGACCCCTGAGCTGGACATGGCGGCCCCT
GCGCTGCTCAACAACCCTGTGCACCAGTCGGTCACCATGGGTGAGACAGTGAGCTTCCTCTGTGATGTGGTGGGCCGGCCCCGGCCTGAGATCACCTGGGAGAAG
CAGTTGGAGGATCGGGAGAATGTGGTCATGCGGCCCAACCATGTGCGTGGCAACGTGGTGGTCACCAACATTGCCCAGCTGGTCATCTATAACGCCCAGCTGCAG
GATGCTGGGATCTACACCTGCACGGCCCGGAACGTGGCTGGGGTCCTGAGGGCTGATTTCCCGCTGTCGGTGGTCAGGGGTCATCAGGCTGCAGCCACCTCAGAG
AGCAGCCCCAATGGCACGGCTTTCCCGGCGGCCGAGTGCCTGAAGCCCCCAGACAGTGAGGACTGTGGCGAAGAGCAGACCCGCTGGCACTTCGATGCCCAGGCC
AACAACTGCCTGACCTTCACCTTCGGCCACTGCCACCGTAACCTCAACCACTTTGAGACCTATGAGGCCTGCATGCTGGCCTGCATGAGCGGGCCGCTGGCCGCG
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>WFIKKN2|124857|protein
MWAPRCRRFWSRWEQVAALLLLLLLLGVPPRSLALPPIRYSHAGICPNDMNPNLWVDAQSTCRRECETDQECETYEKCCPNVCGTKSCVAARYMDVKGKKGPVGM
PKEATCDHFMCLQQGSECDIWDGQPVCKCKDRCEKEPSFTCASDGLTYYNRCYMDAEACSKGITLAVVTCRYHFTWPNTSPPPPETTMHPTTASPETPELDMAAP
ALLNNPVHQSVTMGETVSFLCDVVGRPRPEITWEKQLEDRENVVMRPNHVRGNVVVTNIAQLVIYNAQLQDAGIYTCTARNVAGVLRADFPLSVVRGHQAAATSE
SSPNGTAFPAAECLKPPDSEDCGEEQTRWHFDAQANNCLTFTFGHCHRNLNHFETYEACMLACMSGPLAACSLPALQGPCKAYAPRWAYNSQTGQCQSFVYGGCE
GNGNNFESREACEESCPFPRGNQRCRACKPRQKLVTSFCRSDFVILGRVSELTEEPDSGRALVTVDEVLKDEKMGLKFLGQEPLEVTLLHVDWACPCPNVTVSEM
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MWAPRCRRFWSRWEQVAALLLLLLLLGVPPRSLALPPIRYSHAGICPNDMNPNLWVDAQSTCRRECETDQECETYEKCCPNVCGTKSCVAARYMDVKGKKGPVGM
PKEATCDHFMCLQQGSECDIWDGQPVCKCKDRCEKEPSFTCASDGLTYYNRCYMDAEACSKGITLAVVTCRYHFTWPNTSPPPPETTMHPTTASPETPELDMAAP
ALLNNPVHQSVTMGETVSFLCDVVGRPRPEITWEKQLEDRENVVMRPNHVRGNVVVTNIAQLVIYNAQLQDAGIYTCTARNVAGVLRADFPLSVVRGHQAAATSE
SSPNGTAFPAAECLKPPDSEDCGEEQTRWHFDAQANNCLTFTFGHCHRNLNHFETYEACMLACMSGPLAACSLPALQGPCKAYAPRWAYNSQTGQCQSFVYGGCE
GNGNNFESREACEESCPFPRGNQRCRACKPRQKLVTSFCRSDFVILGRVSELTEEPDSGRALVTVDEVLKDEKMGLKFLGQEPLEVTLLHVDWACPCPNVTVSEM
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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 |
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Score (No. of Studies) | No | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | (0) |
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 |
---|---|---|---|---|
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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