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Gene: FAM66B (family with sequence similarity 66 member B) Homo sapiens
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Symbol: FAM66B
Name: family with sequence similarity 66 member B
Description: INTERACTS WITH aflatoxin B1
Type: ncrna
RefSeq Status: VALIDATED
Also known as: FAM66E; FLJ53539; RP11-1195F20.2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl87,298,744 - 7,355,359 (-)EnsemblGRCh38hg38GRCh38
GRCh3887,298,744 - 7,355,363 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh3787,159,133 - 7,212,876 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3687,167,578 - 7,170,595 (-)NCBINCBI36hg18NCBI36
Cytogenetic Map8p23.1NCBI
HuRef86,901,656 - 6,902,200 (-)NCBIHuRef
CHM1_187,414,938 - 7,468,660 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM66B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 3398788
Created: 2010-07-04
Species: Homo sapiens
Last Modified: 2020-08-04
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.