AutismKB 2.0

Evidence Details for KCP


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Basic Information Top
Gene Symbol:KCP ( CRIM2,KCP1,NET67 )
Gene Full Name: kielin/chordin-like protein
Band: 7q32.1
Quick LinksEntrez ID:375616; OMIM: 609344; Uniprot ID:KCP_HUMAN; ENSEMBL ID: ENSG00000135253; HGNC ID: 17585
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>KCP|375616|nucleotide
ATGGCCGGGGTCGGGGCCGCTGCGCTGTCCCTTCTCCTGCACCTCGGGGCCCTGGCGCTGGCCGCGGGCGCGGAAGGTGGGGCTGTCCCCAGGGAGCCCCCTGGG
CAGCAGACAACTGCCCATTCCTCAGTCCTTGCTGGGAACTCCCAGGAGCAGTGGCACCCCCTGCGAGAGTGGCTGGGGCGACTGGAGGCTGCAGTGATGGAGCTC
AGAGAACAGAATAAGGACCTGCAGACGAGGGTGAGGCAGCTGGAGTCCTGTGAGTGCCACCCTGCATCTCCCCAGTGCTGGGGGCTGGGGCGTGCCTGGCCCGAG
GGGGCACGCTGGGAGCCTGACGCCTGCACAGCCTGCGTCTGCCAGGATGGGGCCGCTCACTGTGGCCCCCAAGCACACCTGCCCCATTGCAGGGGCTGCAGCCAA
AATGGCCAGACCTACGGCAACGGGGAGACCTTCTCCCCAGATGCCTGCACCACCTGCCGCTGTCTGACAGGAGCCGTGCAGTGCCAGGGGCCCTCGTGTTCAGAG
CTCAACTGCTTGGAGAGCTGCACCCCACCTGGGGAGTGCTGCCCCATCTGCTGCACAGAAGGTGGCTCTCACTGGGAACATGGCCAAGAGTGGACAACACCTGGG
GACCCCTGCCGAATCTGCCGGTGCCTGGAGGGTCACATCCAGTGCCGCCAGCGAGAATGTGCCAGCCTGTGTCCATACCCAGCCCGGCCCCTCCCAGGCACCTGC
TGCCCTGTGTGTGATGGCTGTTTCCTAAACGGGCGGGAGCACCGCAGCGGGGAGCCTGTGGGCTCAGGGGACCCCTGCTCGCACTGCCGCTGTGCTAATGGGAGT
GTCCAGTGTGAGCCTCTGCCCTGCCCGCCAGTGCCCTGCAGACACCCAGGCAAGATCCCTGGGCAGTGCTGCCCTGTCTGCGATGGCTGTGAGTACCAGGGACAC
CAGTATCAGAGCCAGGAGACCTTCAGACTCCAAGAGCGGGGCCTCTGTGTCCGCTGCTCCTGCCAGGCTGGCGAGGTCTCCTGTGAGGAGCAGGAGTGCCCAGTC
ACCCCCTGTGCCCTGCCTGCCTCTGGCCGCCAGCTCTGCCCAGCCTGTGAGCTGGATGGAGAGGAGTTTGCTGAGGGAGTCCAGTGGGAGCCTGATGGTCGGCCC
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>KCP|375616|protein
MAGVGAAALSLLLHLGALALAAGAEGGAVPREPPGQQTTAHSSVLAGNSQEQWHPLREWLGRLEAAVMELREQNKDLQTRVRQLESCECHPASPQCWGLGRAWPE
GARWEPDACTACVCQDGAAHCGPQAHLPHCRGCSQNGQTYGNGETFSPDACTTCRCLTGAVQCQGPSCSELNCLESCTPPGECCPICCTEGGSHWEHGQEWTTPG
DPCRICRCLEGHIQCRQRECASLCPYPARPLPGTCCPVCDGCFLNGREHRSGEPVGSGDPCSHCRCANGSVQCEPLPCPPVPCRHPGKIPGQCCPVCDGCEYQGH
QYQSQETFRLQERGLCVRCSCQAGEVSCEEQECPVTPCALPASGRQLCPACELDGEEFAEGVQWEPDGRPCTACVCQDGVPKCGAVLCPPAPCQHPTQPPGACCP
SCDSCTYHSQVYANGQNFTDADSPCHACHCQDGTVTCSLVDCPPTTCARPQSGPGQCCPRCPDCILEEEVFVDGESFSHPRDPCQECRCQEGHAHCQPRPCPRAP
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Evidence summary Top

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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 (2) 1 (3) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (6)
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
Marshall, 2008 - SNP microarrayASD 427 238 189 - 427 500 927
Sanders, 2011 Simons Simplex Collection SNP microarray--ASD 1127 1127 - - - - -
Linkage Studies Top