Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: FAM230A (family with sequence similarity 230 member A) Homo sapiens
Analyze
Symbol: FAM230A
Name: family with sequence similarity 230 member A
Description: ASSOCIATED WITH autism spectrum disorder; hemorrhagic disease; Neurodevelopmental Disorders
Type: ncrna
RefSeq Status: VALIDATED
Also known as: DGCR15; family with sequence similarity 230, member A; uncharacterized protein LOC653203
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382218,487,127 - 18,500,594 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372220,706,073 - 20,710,680 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362219,022,622 - 19,038,331 (+)NCBINCBI36hg18NCBI36
Cytogenetic Map22q11.21NCBI
CHM1_12220,336,764 - 20,350,053 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics


Expression


Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM230A
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 7207323
Created: 2013-01-29
Species: Homo sapiens
Last Modified: 2019-11-26
Status: ACTIVE



NHLBI Logo

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