Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: FAM226A (family with sequence similarity 226 member A) Homo sapiens
Analyze
Symbol: FAM226A
Name: family with sequence similarity 226 member A
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: CXorf50; family with sequence similarity 226 member A (non-protein coding); LINC00246A; NCRNA00246; NCRNA00246A
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X72,941,728 - 72,943,750 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X72,161,568 - 72,163,589 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X72,078,291 - 72,088,211 (-)NCBINCBI36hg18NCBI36
Build 34X71,944,589 - 71,946,538NCBI
CeleraX72,340,624 - 72,342,645 (+)NCBI
Cytogenetic MapXq13.1NCBI
HuRefX65,751,248 - 65,753,269 (+)NCBIHuRef
CHM1_1X72,054,049 - 72,055,602 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated

Genomics

Position Markers

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM226A
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1354319
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
Status: ACTIVE



NHLBI Logo

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