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Gene: FAM230D (family with sequence similarity 230 member D) Homo sapiens
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Symbol: FAM230D
Name: family with sequence similarity 230 member D
Description: ASSOCIATED WITH schizophrenia
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LINC02592; long intergenic non-protein coding RNA 2592
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl2218,178,038 - 18,205,915 (-)EnsemblGRCh38hg38GRCh38
GRCh382218,178,026 - 18,205,909 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372218,660,793 - 18,685,204 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map22q11.21NCBI
HuRef222,473,208 - 2,480,327 (-)NCBIHuRef
CHM1_12218,660,513 - 18,685,592 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM230D
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 13605599
Created: 2018-06-05
Species: Homo sapiens
Last Modified: 2020-06-18
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.