AutismKB 2.0

Evidence Details for ZFYVE19


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Basic Information Top
Gene Symbol:ZFYVE19 ( FLJ14840,MPFYVE )
Gene Full Name: zinc finger, FYVE domain containing 19
Band: 15q15.1
Quick LinksEntrez ID:84936; OMIM: NA; Uniprot ID:ZFY19_HUMAN; ENSEMBL ID: ENSG00000166140; HGNC ID: 20758
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ZFYVE19|84936|nucleotide
ATGAACTACGACTCCCAGCAGCCCCCGTTGCCGCCGCTGCCGTACGCTGGCTGCAGGAGAGCGTCCGGATTCCCTGCTCTAGGTCGCGGCGGGACAGTGCCAGTG
GGCGTGTGGGGCGGGGCAGGGCAGGGAAGGGAAGGGCGGAGCTGGGGTGAGGGTCCAAGGGGCCCAGGACTTGGCCGGCGTGATCTCAGCTCTGCAGACCCTGCG
GTGCTGGGAGCCACCATGGAGAGTAGGTGCTACGGCTGCGCTGTCAAGTTCACCCTCTTCAAGAAGGAGTACGGCTGTAAGAATTGTGGCAGGGCCTTCTGTTCA
GGCTGCCTAAGCTTCAGTGCAGCAGTGCCTCGGACTGGGAACACCCAACAGAAAGTCTGCAAGCAATGCCATGAGGTCCTGACCAGAGGGTCTTCTGCCAATGCC
TCCAAGTGGTCACCACCTCAGAACTATAAGAAGCGTGTGGCAGCCTTGGAAGCCAAGCAAAAGCCCAGCACTTCCCAGAGCCAGGGACTGACACGACAAGACCAG
ATGATTGCTGAGCGCCTAGCACGACTCCGCCAGGAGAACAAGCCCAAGTTAGTCCCCTCACAGGCAGAGATAGAGGCACGGCTGGCTGCCCTAAAGGATGAACGT
CAGGGTTCCATCCCTTCCACCCAGGAAATGGAGGCACGACTTGCAGCGTTGCAGGGCAGAGTTCTACCTTCTCAAACCCCCCAGCCGGCACATCACACACCGGAC
ACCAGGACCCAAGCCCAGCAGACACAGGATCTGCTAACGCAGCTGGCAGCTGAGGTGGCTATCGATGAAAGCTGGAAAGGAGGAGGCCCAGCTGCCTCTCTCCAG
AATGATCTCAACCAGGGTGGCCCAGGGAGCACTAATTCCAAGAGGCAGGCCAACTGGTCCTTGGAGGAGGAGAAGAGCAGACTGCTGGCTGAGGCAGCACTTGAG
TTGCGGGAGGAGAACACGAGGCAGGAACGGATTCTGGCCCTGGCCAAGCGACTAGCCATGCTGCGGGGACAGGACCCCGAGAGAGTGACCCTCCAGGACTATCGC
CTCCCAGACAGTGATGACGACGAGGATGAGGAGACAGCCATCCAAAGAGTCCTGCAGCAGCTCACTGAAGAAGCTTCCCTGGATGAGGCAAGTGGCTTTAACATC
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>ZFYVE19|84936|protein
MNYDSQQPPLPPLPYAGCRRASGFPALGRGGTVPVGVWGGAGQGREGRSWGEGPRGPGLGRRDLSSADPAVLGATMESRCYGCAVKFTLFKKEYGCKNCGRAFCS
GCLSFSAAVPRTGNTQQKVCKQCHEVLTRGSSANASKWSPPQNYKKRVAALEAKQKPSTSQSQGLTRQDQMIAERLARLRQENKPKLVPSQAEIEARLAALKDER
QGSIPSTQEMEARLAALQGRVLPSQTPQPAHHTPDTRTQAQQTQDLLTQLAAEVAIDESWKGGGPAASLQNDLNQGGPGSTNSKRQANWSLEEEKSRLLAEAALE
LREENTRQERILALAKRLAMLRGQDPERVTLQDYRLPDSDDDEDEETAIQRVLQQLTEEASLDEASGFNIPAEQASRPWTQPRGAEPEAQDVDPRPEAEEEELPW
CCICNEDATLRCAGCDGDLFCARCFREGHDAFELKEHQTSAYSPPRAGQEH
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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) 1 (1) 1 (1) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 5 (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
Bucan, 2009 USA SNP microarrayautism, ASD 912 - 912 - - 1488 1488
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Allen-Brady, 2010 USA SNP-based genomic screenASD 40 - 40 - 192 461 653
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
Voineagu, 2011_1 Unknown 16 frontal cortex(BA9) and 13 temporal cortex(BA41 16
(25.00%)
-autism 16
(6.25%)
0.958246 Down 26.4019
  • Platform: Illumina Ref8 v3 microarrays
  • ProbeSet: ILMN_1780698
  • RefSeq_ID/ EST: -
  • GEO_ID: GSE28521
  • Statistic Method: SAM package and unless otherwise specified the significance threshold was FDR,0.05 and fold changes.1.3.
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

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