AutismKB 2.0

Evidence Details for KRT38


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Basic Information Top
Gene Symbol:KRT38 ( HA8,KRTHA8,hHa8 )
Gene Full Name: keratin 38
Band: 17q21.2
Quick LinksEntrez ID:8687; OMIM: 604542; Uniprot ID:KRT38_HUMAN; ENSEMBL ID: ENSG00000171360; HGNC ID: 6456
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>KRT38|8687|nucleotide
ATGACCTCTTCCTACAGCAGCTCCTCATGCCCTCTGGGTTGCACCATGGCTCCTGGAGCAAGAAATGTCTCTGTCTCTCCCATCGACATTGGGTGCCAGCCTGGG
GCAGAGGCCAACATTGCCCCCATGTGCCTTTTGGCCAACGTGGCACATGCCAACCGAGTCCGTGTGGGGTCCACTCCCCTGGGCCGCCCCAGCCTCTGTCTGCCG
CCTACCTGCCACACTGCTTGTCCCTTGCCAGGGACCTGCCACATTCCTGGCAACATTGGAATCTGTGGGGCCTATGGTGAAAACACCCTGAATGGCCATGAGAAG
GAGACCATGCAGTTCCTGAATGACCGCCTGGCCAACTACCTGGAGAAGGTGCGCCAGCTGGAGCAGGAGAATGCGGAGCTGGAGGCCACACTCCTCGAGAGGAGC
AAGTGCCACGAGTCCACCGTGTGCCCCGACTACCAGTCTTACTTCCACACCATCGAGGAGCTCCAACAGAAGATCCTGTGCAGCAAGGCCGAGAATGCCAGGCTG
ATTGTACAAATTGACAATGCCAAGCTGGCTGCCGATGACTTTAGGATCAAGCTGGAGAGTGAGCGCTCCCTGCGCCAGCTGGTGGAGGCAGACAAGTGTGGGACA
CAGAAGCTCCTGGATGATGCGACCCTGGCCAAGGCCGACCTGGAGGCCCAGCAGGAGTCCCTGAAGGAGGAGCAGCTCTCCCTCAAGAGCAACCACGAGCAGGAA
GTAAAGATTCTGAGGAGTCAGCTGGGGGAGAAGCTCCGGATTGAGCTGGACATTGAGCCCACCATTGACCTGAACAGGGTGCTGGGGGAGATGCGGGCTCAGTAT
GAGGCCATGTTGGAGACCAACCGCCAGGATGTGGAACAGTGGTTCCAAGCCCAGTCTGAAGGCATCAGCCTGCAGGACATGTCCTGCTCCGAGGAGCTGCAGTGC
TGCCAGTCGGAGATCCTGGAGCTGAGATGCACGGTGAATGCCCTGGAGGTGGAGCGCCAAGCCCAGCACACCTTGAAGGACTGTCTGCAGAACTCCCTGTGTGAA
GCCGAGGACCGCTTCGGCACGGAGCTGGCCCAGATGCAGAGCCTCATCAGCAACGTGGAGGAGCAGCTGTCTGAGATCCGGGCCGACCTGGAGCGGCAAAACCAG
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>KRT38|8687|protein
MTSSYSSSSCPLGCTMAPGARNVSVSPIDIGCQPGAEANIAPMCLLANVAHANRVRVGSTPLGRPSLCLPPTCHTACPLPGTCHIPGNIGICGAYGENTLNGHEK
ETMQFLNDRLANYLEKVRQLEQENAELEATLLERSKCHESTVCPDYQSYFHTIEELQQKILCSKAENARLIVQIDNAKLAADDFRIKLESERSLRQLVEADKCGT
QKLLDDATLAKADLEAQQESLKEEQLSLKSNHEQEVKILRSQLGEKLRIELDIEPTIDLNRVLGEMRAQYEAMLETNRQDVEQWFQAQSEGISLQDMSCSEELQC
CQSEILELRCTVNALEVERQAQHTLKDCLQNSLCEAEDRFGTELAQMQSLISNVEEQLSEIRADLERQNQEYQVLLDVKTRLENEIATYRNLLESEDCKLPCNPC
STSPSCVTAPCAPRPSCGPCTTCGPTCGASTTGSRF
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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) 1 (1) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top