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Gene: FAM189A2 (family with sequence similarity 189 member A2) Homo sapiens
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Symbol: FAM189A2
Name: family with sequence similarity 189 member A2
Description: Predicted to localize to the integral component of membrane; INTERACTS WITH 17beta-hydroxy-5alpha-androstan-3-one; benzo[e]pyrene; bis(2-ethylhexyl) phthalate.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: C9orf61; chromosome 9 open reading frame 61; family with sequence similarity 189, member A2; Friedreich ataxia region gene X123; MGC142243; MGC142245; RP11-548B3.1; X123
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38969,324,572 - 69,392,473 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37971,939,287 - 72,007,372 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36971,134,061 - 71,197,188 (+)NCBINCBI36hg18NCBI36
Build 34969,173,794 - 69,236,922NCBI
Celera942,529,998 - 42,597,862 (+)NCBI
Cytogenetic Map9q21.12NCBI
HuRef941,778,984 - 41,846,639 (+)NCBIHuRef
CHM1_1972,084,794 - 72,153,792 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM189A2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1316770
Created: 2005-01-12
Species: Homo sapiens
Last Modified: 2019-11-26
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.