AutismKB 2.0

Evidence Details for ZNF391


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:ZNF391 ( dJ153G14.3 )
Gene Full Name: zinc finger protein 391
Band: 6p22.1
Quick LinksEntrez ID:346157; OMIM: NA; Uniprot ID:ZN391_HUMAN; ENSEMBL ID: ENSG00000124613; HGNC ID: 18779
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZNF391|346157|nucleotide
ATGGAAAGCCTCAGAGGGAATACTGCTCAGGGTCCTACAAATGAAGAAGACTATAAAAACGAAGGCCAATTATCAAGGCAAACAAAATGTCCTGCACAGAAGAAA
TCCTCTTTTGAGAACACAGTGGTCAGAAAAGTGTCAGTGACACTCAAAGAAATTTTCACAGGGGAGGAAGGCCCTGAATCCAGTGAATTTAGTCTAAGCCCAAAC
CTTGACGCACAACAGAAAATTCCAAAGGGACATGGATCCCCAATATCTAGGAAAAACTCCAAAGATAATTCAGACTTAATTAAACACCAAAGACTTTTCTCACAA
AGAAAACCTTGTAAATGCAATGAATGTGAAAAAGCCTTTAGTTACCAATCAGACCTTCTTGTACACAGTAGAATTCATGGTGGAGAAAAGCCTTTTGAATGCAAC
AAATGTGGGAAATCTTTCAGCCGAAGTACACACCTTATTGAACATCAAAGAACTCACACTGGAGAGAAACCTTATGAATGCAATGAATGTGGAAAAGCTTTTAGC
CGGAGCACACATCTTAGTCTACATCAGAGAATCCATACTGGAGAAAAACCATATGAATGTAGTGAATGTGGAAAAGCCTTTAGCCGAAGCACTAACCTTAGTCAG
CATCAGCGAACTCATACTCAAGAAAGGCCTTACAAATGTAATGAATGTGGGAAAGCCTTCGGTGACCGTTCAACCATAATTCAGCATCAACGAATACACACTGGA
GAGAATCCCTATGAATGCAGTAAATGTGGAAAAGCTTTCAGTTGGATCTCATCGCTTACTGAACATCAGAGAACACACACTGGGGAGAACCCCTATGAGTGCAGT
GAATGTGGGAAAGTGTTCAGTCGAAGCTCGTCTCTTACAGAACATCAGAGAATCCACAGTGGAGAAAAGCCTCACGAGTGTAGAGTGTGTGGAAAGGGCTTCAGT
CGAAGCTCATCCCTTATTATTCATCAGAGAACTCATACCGGGGAGAAGCCGTACAAATGTAATGACTGTGGAAAAGCCTTCTGTCAGAGTTCAACTCTGATCAGA
CATCAGCACCTTCATACTAAAGAGTAA
Show »

>ZNF391|346157|protein
MESLRGNTAQGPTNEEDYKNEGQLSRQTKCPAQKKSSFENTVVRKVSVTLKEIFTGEEGPESSEFSLSPNLDAQQKIPKGHGSPISRKNSKDNSDLIKHQRLFSQ
RKPCKCNECEKAFSYQSDLLVHSRIHGGEKPFECNKCGKSFSRSTHLIEHQRTHTGEKPYECNECGKAFSRSTHLSLHQRIHTGEKPYECSECGKAFSRSTNLSQ
HQRTHTQERPYKCNECGKAFGDRSTIIQHQRIHTGENPYECSKCGKAFSWISSLTEHQRTHTGENPYECSECGKVFSRSSSLTEHQRIHSGEKPHECRVCGKGFS
RSSSLIIHQRTHTGEKPYKCNDCGKAFCQSSTLIRHQHLHTKE

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 (0) 1 (1) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 3 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Guerini, 2010 Italy microsatellite-based genomic screen, SNP-based genomic screenASD 61 61 - - 61 149 210
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 0
Reference Source Tissue #Subjects
(% Women)
ADI-R ADOS Endo- pheno Diagnosis Normal Controls
(% Women)
Fold Change Up/ Down P/Q value
No Evidence.
Proteomics Studies:1
Reference Source Tissue Platform #Subjects
(% Women)
ADI-R ADOS Diagnosis Normal Controls(% Women)
Corbett, 2007_1 USA blood liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) 69
(15.94%)
ASD 35
(17.14%)
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.

Simple Query:


  (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