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Gene: CUNH9orf16 (chromosome unknown C9orf16 homolog) Ictidomys tridecemlineatus
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Symbol: CUNH9orf16
Name: chromosome unknown C9orf16 homolog
Description: ASSOCIATED WITH congenital disorder of glycosylation Iu (ortholog); early infantile epileptic encephalopathy (ortholog); primary coenzyme Q10 deficiency 7 (ortholog)
Type: protein-coding
RefSeq Status: MODEL
Also known as: chromosome unknown open reading frame, human C9orf16; LOC101964257; UPF0184 protein C9orf16 homolog
Orthologs:
Latest Assembly: SpeTri2.0 - Squirrel SpeTri2.0 Assembly
Position:
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_00493648715,728,776 - 15,732,065 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

Comparative Map Data

Expression


Sequence

Nucleotide Sequences
Protein Sequences

Additional Information

External Database Links
Nomenclature History
 
More on CUNH9orf16
NCBI Gene
Ensembl Gene
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 12440930
Created: 2017-01-27
Species: Ictidomys tridecemlineatus
Last Modified: 2019-01-29
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.