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Gene: FAM41AY2 (family with sequence similarity 41 member A, Y-linked 2) Homo sapiens
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Symbol: FAM41AY2
Name: family with sequence similarity 41 member A, Y-linked 2
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblY18,390,994 - 18,405,046 (-)EnsemblGRCh38hg38GRCh38
GRCh38Y18,389,270 - 18,405,046 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37Y20,551,156 - 20,566,932 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic MapYq11.222NCBI
HuRefY14,095,788 - 14,111,585 (+)NCBIHuRef
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM41AY2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 2311620
Created: 2009-07-24
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.