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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: INTERACTS WITH aflatoxin B1; aflatoxin B2; benzo[a]pyrene
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
GRCh38 Ensembl1598,437,162 - 98,547,728 (-)EnsemblGRCh38hg38GRCh38
GRCh381598,437,162 - 98,514,336 (-)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

Expression

RNA-SEQ Expression

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

CRRD Object Information
CRRD ID: 1602962
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2020-06-18
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.