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Gene: FAM226B (family with sequence similarity 226 member B) Homo sapiens
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Symbol: FAM226B
Name: family with sequence similarity 226 member B
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH dorsomorphin; entinostat; methotrexate
Type: ncrna
RefSeq Status: VALIDATED
Also known as: CXorf50B; family with sequence similarity 226 member B (non-protein coding); LINC00246B; NCRNA00246B
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX72,777,608 - 72,779,097 (+)EnsemblGRCh38hg38GRCh38
GRCh38X72,777,073 - 72,779,095 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X71,996,897 - 71,998,919 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X71,905,729 - 71,915,646 (+)NCBINCBI36hg18NCBI36
CeleraX72,340,624 - 72,342,645 (+)NCBI
Cytogenetic MapXq13.1NCBI
HuRefX65,751,248 - 65,753,269 (+)NCBIHuRef
CHM1_1X71,889,316 - 71,890,805 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM226B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1626521
Created: 2007-08-10
Species: Homo sapiens
Last Modified: 2020-03-24
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.