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Gene: FAM230I (family with sequence similarity 230 member I) Homo sapiens
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Symbol: FAM230I
Name: family with sequence similarity 230 member I
RGD ID: 1603239
Description: ASSOCIATED WITH schizophrenia; INTERACTS WITH aflatoxin B2; rotenone
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LINC01658; LOC388882; long intergenic non-protein coding RNA 1658; uncharacterized LOC388882
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2223,462,086 - 23,486,980 (-)EnsemblGRCh38hg38GRCh38
GRCh382223,462,086 - 23,486,980 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372223,804,477 - 23,829,167 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362222,134,273 - 22,159,167 (-)NCBINCBI36hg18NCBI36
Celera227,619,209 - 7,644,118 (-)NCBI
Cytogenetic Map22q11.23NCBI
HuRef226,772,120 - 6,796,817 (-)NCBIHuRef
CHM1_12223,816,470 - 23,841,332 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM230I
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1603239
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2020-09-16
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.