AutismKB 2.0

Evidence Details for COX4NB


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Basic Information Top
Gene Symbol:COX4NB ( C16orf2,C16orf4,FAM158B,NOC4 )
Gene Full Name: COX4 neighbor
Band: 16q24
Quick LinksEntrez ID:10328; OMIM: 604886; Uniprot ID:CX4NB_HUMAN; ENSEMBL ID: ENSG00000131148; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>COX4NB|10328|nucleotide
ATGCCCGGGGTGAAACTGACCACCCAGGCCTACTGCAAGATGGTGCTGCACGGCGCCAAGTACCCGCACTGCGCCGTCAACGGGCTCCTGGTGGCCGAGAAGCAG
AAGCCGCGTAAGGAGCACCTCCCCCTGGGCGGCCCCGGCGCCCACCACACCCTCTTCGTGGACTGCATCCCCCTCTTCCACGGCACCCTGGCCCTCGCCCCCATG
CTGGAGGTGGCTCTCACCCTGATTGATTCATGGTGCAAAGATCATAGCTACGTGATTGCTGGTTATTATCAAGCTAATGAGCGAGTAAAGGATGCCAGTCCAAAC
CAGGTTGCAGAGAAGGTGGCCTCCAGAATCGCCGAGGGCTTCAGCGACACTGCGCTCATCATGTGA







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>COX4NB|10328|protein
MPGVKLTTQAYCKMVLHGAKYPHCAVNGLLVAEKQKPRKEHLPLGGPGAHHTLFVDCIPLFHGTLALAPMLEVALTLIDSWCKDHSYVIAGYYQANERVKDASPN
QVAEKVASRIAEGFSDTALIM



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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 (2) 0 (0) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 1 (3)
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 - - - - -
Sanders, 2011 Simons Simplex Collection SNP microarray--ASD 1127 1127 - - - - -
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 1
Reference Source Tissue #Subjects
(% Women)
ADI-R ADOS Endo- pheno Diagnosis Normal Controls
(% Women)
Fold Change Up/ Down P/Q value
Hu, 2009_1 mixed lymphoblastoid cell lines 21
(-)
autism with nonaffected sib pairsautism 17
(-)
0.9 Down -
  • Platform: TIGR 40K Human Set
  • ProbeSet: -
  • RefSeq_ID/ EST: AI301207
  • GEO_ID: GSE15402
  • Statistic Method: PCA; SAM by MEV with FDR<0.05
Proteomics Studies:0
Reference Source Tissue Platform #Subjects
(% Women)
ADI-R ADOS Diagnosis Normal Controls(% Women)
No Evidence.
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

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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