AutismKB 2.0

Evidence Details for KIN


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Basic Information Top
Gene Symbol:KIN ( BTCD,KIN17 )
Gene Full Name: KIN, antigenic determinant of recA protein homolog (mouse)
Band: 10p14
Quick LinksEntrez ID:22944; OMIM: 601720; Uniprot ID:KIN17_HUMAN; ENSEMBL ID: ENSG00000151657; HGNC ID: 6327
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>KIN|22944|nucleotide
ATGGGGAAGTCGGATTTTCTTACTCCCAAGGCTATCGCCAACAGGATCAAGTCCAAGGGGCTGCAGAAGCTACGCTGGTATTGCCAGATGTGCCAGAAGCAGTGC
CGGGACGAGAATGGCTTTAAGTGTCATTGTATGTCCGAATCTCATCAGAGACAACTATTGCTGGCTTCAGAAAATCCTCAGCAGTTTATGGATTATTTTTCAGAG
GAATTCCGAAATGACTTTCTAGAACTTCTCAGGAGACGCTTTGGCACTAAAAGGGTCCACAACAACATTGTCTACAACGAATACATCAGCCACCGAGAGCACATC
CACATGAATGCCACTCAGTGGGAAACTCTGACTGATTTTACTAAGTGGCTGGGCAGAGAAGGCTTGTGCAAAGTGGACGAGACACCAAAAGGCTGGTATATTCAG
TACATAGACAGGGACCCAGAAACTATCCGCCGGCAACTGGAACTGGAGAAAAAGAAAAAGCAGGACCTTGATGATGAAGAAAAAACTGCCAAATTTATTGAAGAG
CAAGTGAGAAGAGGCCTGGAAGGGAAGGAACAGGAGGTCCCTACTTTTACGGAATTAAGCAGAGAAAATGATGAAGAGAAAGTCACGTTTAATTTGAGTAAAGGA
GCATGTAGCTCATCCGGAGCAACATCTTCCAAGTCAAGTACTCTGGGACCGAGTGCACTGAAGACGATAGGAAGTTCAGCATCAGTGAAACGAAAAGAATCTTCC
CAGAGCTCAACTCAGTCTAAAGAAAAGAAGAAAAAGAAATCTGCACTGGATGAAATCATGGAGATTGAAGAGGAAAAGAAAAGAACTGCCCGAACAGACTACTGG
CTACAGCCTGAAATTATTGTGAAAATTATAACCAAGAAACTGGGAGAGAAATATCATAAGAAAAAGGCTATTGTTAAGGAAGTAATTGACAAATATACAGCTGTT
GTGAAGATGATTGATTCTGGAGACAAGCTGAAACTTGACCAGACTCATTTAGAGACAGTAATTCCAGCACCAGGAAAAAGAATTCTAGTTTTAAATGGAGGCTAC
AGAGGAAATGAAGGTACCCTAGAATCCATCAATGAGAAGACTTTTTCAGCTACTATCGTCATTGAAACTGGCCCTTTAAAAGGACGCAGAGTTGAAGGAATTCAA
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>KIN|22944|protein
MGKSDFLTPKAIANRIKSKGLQKLRWYCQMCQKQCRDENGFKCHCMSESHQRQLLLASENPQQFMDYFSEEFRNDFLELLRRRFGTKRVHNNIVYNEYISHREHI
HMNATQWETLTDFTKWLGREGLCKVDETPKGWYIQYIDRDPETIRRQLELEKKKKQDLDDEEKTAKFIEEQVRRGLEGKEQEVPTFTELSRENDEEKVTFNLSKG
ACSSSGATSSKSSTLGPSALKTIGSSASVKRKESSQSSTQSKEKKKKKSALDEIMEIEEEKKRTARTDYWLQPEIIVKIITKKLGEKYHKKKAIVKEVIDKYTAV
VKMIDSGDKLKLDQTHLETVIPAPGKRILVLNGGYRGNEGTLESINEKTFSATIVIETGPLKGRRVEGIQYEDISKLA

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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 (1) 1 (3) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 2 (4)
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
Levy, 2011 Simons Simplex Collection aCGH--ASD 915 915 - - - - -
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Risch, 1999 USA microsatellite-based genomic screenPDD 90 - 90 - - - -
Lamb, 2005 - microsatellite-based genomic screenautism 207 - 207 - 420 - -
Buxbaum, 2004 USA microsatellite-based genomic screenautism 115 - 115 - - - -
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
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.

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  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018