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Gene: FAM47B (family with sequence similarity 47 member B) Homo sapiens
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Symbol: FAM47B
Name: family with sequence similarity 47 member B
Description: null
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: family with sequence similarity 47, member B; FLJ35782; hypothetical protein LOC170062
Orthologs:
No known orthologs. homologs ...
Related Pseudogenes: FAM47DP  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X34,942,796 - 34,944,917 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X34,960,913 - 34,963,034 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X34,870,852 - 34,872,955 (+)NCBINCBI36hg18NCBI36
Build 34X34,720,587 - 34,722,691NCBI
CeleraX39,088,163 - 39,090,284 (+)NCBI
Cytogenetic MapXp21.1NCBI
HuRefX32,702,357 - 32,704,478 (+)NCBIHuRef
CHM1_1X34,991,454 - 34,993,575 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM47B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1344119
Created: 2005-03-08
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.