Evidence Details for KRTAP10-2


Gene Symbol: | KRTAP10-2 ( KAP10.2,KAP18-2,KAP18.2,KRTAP10.2,KRTAP18-2,KRTAP18.2 ) |
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Gene Full Name: | keratin associated protein 10-2 |
Band: | 21q22.3 |
Quick Links | Entrez ID:386679; OMIM: NA; Uniprot ID:KR102_HUMAN; ENSEMBL ID: ENSG00000205445; HGNC ID: 22967 |
Relate to Another Database: | SFARIGene; denovo-db |


>KRTAP10-2|386679|nucleotide
ATGGCCGCCTCCACCATGTCCATCTGCTCCAGCGCCTGCACCAACTCCTGGCAGGTGGACGACTGCCCAGAGAGCTGCTGTGAGCTCCCCTGCGGCACCCCCAGC
TGCTGTGCCCCAGCCCCCTGCCTGACCCTGGTCTGCACCCCAGTGAGCTGTGTGTCCAGCCCCTGCTGCCAGGCGGCCTGTGAGCCCAGCGCCTGCCAATCAGGC
TGCACCAGCTCCTGCACGCCCTCGTGCTGCCAGCAGTCTAGCTGCCAGCCGGCTTGCTGCACCTCCTCCCCCTGCCAGCAGGCCTGCTGCGTGCCCGTCTGCTGC
AAGCCTGTGTGCTGTGTGCCCGTCTGCTGTGGGGCTTCTTCATGCTGCCAGCAGTCTAGCTGCCAGCCAGCTTGCTGTGCCTCTTCCTCCTGCCAGCAGTCCTGC
CGTGTGCCTGTCTGCTGCAAAGCTGTGTGCTGCGTGCCCACCTGCTCTGAGTCATCCTCTTCATGCTGCCAGCAGTCTAGCTGCCAGCCGGCTTGCTGCACCTCC
TCCCCGTGTCAGCAGTCCTGCTGTGTGTCCGTCTGCTGCAAGCCTGTCTGCTGCAAGTCCATCTGCTGTGTACCTGTTTGCTCTGGGGCTTCCTCTCCGTGCTGC
CAGCAGTCTAGCTGCCAGCCAGCTTGCTGCACCTCCTCCTGCTGCAGACCCTCCTCCTCTGTGTCCCTCCTCTGCCGCCCCGTGTGCTCCCGCCCAGCCTCCTGC
AGCTTTTCCTCAGGCCAAAAGTCTAGCTGCTGA
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ATGGCCGCCTCCACCATGTCCATCTGCTCCAGCGCCTGCACCAACTCCTGGCAGGTGGACGACTGCCCAGAGAGCTGCTGTGAGCTCCCCTGCGGCACCCCCAGC
TGCTGTGCCCCAGCCCCCTGCCTGACCCTGGTCTGCACCCCAGTGAGCTGTGTGTCCAGCCCCTGCTGCCAGGCGGCCTGTGAGCCCAGCGCCTGCCAATCAGGC
TGCACCAGCTCCTGCACGCCCTCGTGCTGCCAGCAGTCTAGCTGCCAGCCGGCTTGCTGCACCTCCTCCCCCTGCCAGCAGGCCTGCTGCGTGCCCGTCTGCTGC
AAGCCTGTGTGCTGTGTGCCCGTCTGCTGTGGGGCTTCTTCATGCTGCCAGCAGTCTAGCTGCCAGCCAGCTTGCTGTGCCTCTTCCTCCTGCCAGCAGTCCTGC
CGTGTGCCTGTCTGCTGCAAAGCTGTGTGCTGCGTGCCCACCTGCTCTGAGTCATCCTCTTCATGCTGCCAGCAGTCTAGCTGCCAGCCGGCTTGCTGCACCTCC
TCCCCGTGTCAGCAGTCCTGCTGTGTGTCCGTCTGCTGCAAGCCTGTCTGCTGCAAGTCCATCTGCTGTGTACCTGTTTGCTCTGGGGCTTCCTCTCCGTGCTGC
CAGCAGTCTAGCTGCCAGCCAGCTTGCTGCACCTCCTCCTGCTGCAGACCCTCCTCCTCTGTGTCCCTCCTCTGCCGCCCCGTGTGCTCCCGCCCAGCCTCCTGC
AGCTTTTCCTCAGGCCAAAAGTCTAGCTGCTGA
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>KRTAP10-2|386679|protein
MAASTMSICSSACTNSWQVDDCPESCCELPCGTPSCCAPAPCLTLVCTPVSCVSSPCCQAACEPSACQSGCTSSCTPSCCQQSSCQPACCTSSPCQQACCVPVCC
KPVCCVPVCCGASSCCQQSSCQPACCASSSCQQSCRVPVCCKAVCCVPTCSESSSSCCQQSSCQPACCTSSPCQQSCCVSVCCKPVCCKSICCVPVCSGASSPCC
QQSSCQPACCTSSCCRPSSSVSLLCRPVCSRPASCSFSSGQKSSC
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MAASTMSICSSACTNSWQVDDCPESCCELPCGTPSCCAPAPCLTLVCTPVSCVSSPCCQAACEPSACQSGCTSSCTPSCCQQSSCQPACCTSSPCQQACCVPVCC
KPVCCVPVCCGASSCCQQSSCQPACCASSSCQQSCRVPVCCKAVCCVPTCSESSSSCCQQSSCQPACCTSSPCQQSCCVSVCCKPVCCKSICCVPVCSGASSPCC
QQSSCQPACCTSSCCRPSSSVSLLCRPVCSRPASCSFSSGQKSSC
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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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (2) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Jacquemont, 2006 | France | aCGH | ![]() | ![]() | ASD | - | - | - | - | 29 | - | 29 |








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. |






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