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Gene: FAM66E (family with sequence similarity 66 member E) Homo sapiens
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Symbol: FAM66E
Name: family with sequence similarity 66 member E
Description:
Type: ncrna
RefSeq Status: PREDICTED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl87,955,014 - 8,008,755 (+)EnsemblGRCh38hg38GRCh38
GRCh3887,955,013 - 8,008,755 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3787,812,535 - 7,866,277 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3687,849,942 - 7,850,793 (+)NCBINCBI36hg18NCBI36
Cytogenetic Map8p23.1NCBI
HuRef86,853,773 - 6,877,366 (-)NCBIHuRef
CHM1_187,877,801 - 7,931,577 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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 FAM66E
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1605163
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.