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Gene: FAM169B (family with sequence similarity 169 member B) Homo sapiens
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Symbol: FAM169B
Name: family with sequence similarity 169 member B
Description: null
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: family with sequence similarity 169, member B; FLJ39743; hypothetical protein LOC283777
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381598,437,162 - 98,514,382 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371598,980,391 - 99,057,611 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361596,797,914 - 96,875,134 (-)NCBINCBI36hg18NCBI36
Celera1575,398,171 - 75,475,245 (-)NCBI
Cytogenetic Map15q26.3NCBI
HuRef1575,108,821 - 75,185,983 (-)NCBIHuRef
CHM1_11598,821,961 - 98,899,182 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM169B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1602962
Created: 2007-04-28
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.