Evidence Details for KRTAP10-5
Basic Information Top
Gene Symbol: | KRTAP10-5 ( KAP10.5,KAP18-5,KAP18.5,KRTAP10.5,KRTAP18-5,KRTAP18.1,KRTAP18.5 ) |
---|---|
Gene Full Name: | keratin associated protein 10-5 |
Band: | 21q22.3 |
Quick Links | Entrez ID:386680; OMIM: NA; Uniprot ID:KR105_HUMAN; ENSEMBL ID: ENSG00000188155; HGNC ID: 22969 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>KRTAP10-5|386680|nucleotide
ATGGCCGCGTGCACCATGTCCGTCTGCTCCAGCGCTTGCTCTGACTCCTGGCGAGTGGACGACTGCCCAGAGAGCTGCTGTGAGCCCCCCTGCGGCACCGCCCCC
TGCCTGACCCTGGTCTGCACCCCAGTGAGCTGTGTGTCCAGCCCCTGCTGCCAGGCGGCCTGTGAGCCCAGCCCCTGCCAATCAGGCTGCACCAGCTCCTGCACG
CCCTCGTGCTGCCAGCCGGCTTGCTGCGCCTCCTCCCCCTGCCAGCAGGCCTGCTGCGTGCCCGTCTGCTGCAAGCCTGTGTGCTGCCTGCCCACCTGCTCTAAG
GATTCCTCTTCATGCTGCCAGCAGTCTAGCTGCCAGCCAACTTGCTGTGCCTCTTCCTCCTGCCAGCAGTCCTGCTGTGTGCCTGTCTGCTGCAAGCCCGTGTGC
TGTGTGCCCACCTGTTCTGAGGATTCCTCTTCATGCTGCCAGCATTCTAGCTGCCAGCCGACTTGCTGCACCTCCTCCCCCTGCCAGCAGTCCTGCTACGTGCCT
GTCTGTTGCAAGCCTGTCTGCTTCAAACCCATCTGCTGTGTGCCCGTCTGCTCTGGGGCTTCCACTTCATGCTGCCAGCAGTCTAGCTGTCAGCCGGCTTGCTGC
ACCACCTCCTGCTGCAGACCCTCCTCCTCCGTGTCCCTCCTCTGCCGCCCCATATGCAGGCCCGCCTGCTGCGTGCCCATCTCCTCCTGCTGTGCCCCTGCCTCC
TCCTACCAGGCCAGCTGCTGCCGCCCGGCCTCCTGCGTGTCCCTCCTCTGCCGCCCCGCGTGCTCCCGCCTGGCCTGCTGA
Show »
ATGGCCGCGTGCACCATGTCCGTCTGCTCCAGCGCTTGCTCTGACTCCTGGCGAGTGGACGACTGCCCAGAGAGCTGCTGTGAGCCCCCCTGCGGCACCGCCCCC
TGCCTGACCCTGGTCTGCACCCCAGTGAGCTGTGTGTCCAGCCCCTGCTGCCAGGCGGCCTGTGAGCCCAGCCCCTGCCAATCAGGCTGCACCAGCTCCTGCACG
CCCTCGTGCTGCCAGCCGGCTTGCTGCGCCTCCTCCCCCTGCCAGCAGGCCTGCTGCGTGCCCGTCTGCTGCAAGCCTGTGTGCTGCCTGCCCACCTGCTCTAAG
GATTCCTCTTCATGCTGCCAGCAGTCTAGCTGCCAGCCAACTTGCTGTGCCTCTTCCTCCTGCCAGCAGTCCTGCTGTGTGCCTGTCTGCTGCAAGCCCGTGTGC
TGTGTGCCCACCTGTTCTGAGGATTCCTCTTCATGCTGCCAGCATTCTAGCTGCCAGCCGACTTGCTGCACCTCCTCCCCCTGCCAGCAGTCCTGCTACGTGCCT
GTCTGTTGCAAGCCTGTCTGCTTCAAACCCATCTGCTGTGTGCCCGTCTGCTCTGGGGCTTCCACTTCATGCTGCCAGCAGTCTAGCTGTCAGCCGGCTTGCTGC
ACCACCTCCTGCTGCAGACCCTCCTCCTCCGTGTCCCTCCTCTGCCGCCCCATATGCAGGCCCGCCTGCTGCGTGCCCATCTCCTCCTGCTGTGCCCCTGCCTCC
TCCTACCAGGCCAGCTGCTGCCGCCCGGCCTCCTGCGTGTCCCTCCTCTGCCGCCCCGCGTGCTCCCGCCTGGCCTGCTGA
Show »
>KRTAP10-5|386680|protein
MAACTMSVCSSACSDSWRVDDCPESCCEPPCGTAPCLTLVCTPVSCVSSPCCQAACEPSPCQSGCTSSCTPSCCQPACCASSPCQQACCVPVCCKPVCCLPTCSK
DSSSCCQQSSCQPTCCASSSCQQSCCVPVCCKPVCCVPTCSEDSSSCCQHSSCQPTCCTSSPCQQSCYVPVCCKPVCFKPICCVPVCSGASTSCCQQSSCQPACC
TTSCCRPSSSVSLLCRPICRPACCVPISSCCAPASSYQASCCRPASCVSLLCRPACSRLAC
Show »
MAACTMSVCSSACSDSWRVDDCPESCCEPPCGTAPCLTLVCTPVSCVSSPCCQAACEPSPCQSGCTSSCTPSCCQPACCASSPCQQACCVPVCCKPVCCLPTCSK
DSSSCCQQSSCQPTCCASSSCQQSCCVPVCCKPVCCVPTCSEDSSSCCQHSSCQPTCCTSSPCQQSCYVPVCCKPVCFKPICCVPVCSGASTSCCQQSSCQPACC
TTSCCRPSSSVSLLCRPICRPACCVPISSCCAPASSYQASCCRPASCVSLLCRPACSRLAC
Show »
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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (2) |
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 | ||||||
Jacquemont, 2006 | France | aCGH | ASD | - | - | - | - | 29 | - | 29 |
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
Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.