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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: null
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
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

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

CRRD Object Information
CRRD ID: 1626521
Created: 2007-08-10
Species: Homo sapiens
Last Modified: 2019-06-18
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.