Gene: Whsc1 (Wolf-Hirschhorn syndrome candidate 1) Rattus norvegicus
Symbol: Whsc1
Name: Wolf-Hirschhorn syndrome candidate 1
Description: ENCODES a protein that exhibits chromatin binding (ortholog); histone-lysine N-methyltransferase activity (ortholog); INVOLVED IN atrial septum primum morphogenesis (ortholog); atrial septum secundum morphogenesis (ortholog); bone development (ortholog); PARTICIPATES IN lysine degradation pathway; FOUND IN nuclear membrane (ortholog); nucleolus (ortholog); nucleus (ortholog); INTERACTS WITH thioacetamide; 2,3,7,8-tetrachlorodibenzodioxine (ortholog); 3,4-methylenedioxymethamphetamine (ortholog)
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: LOC305456; LOC680537; probable histone-lysine N-methyltransferase NSD2; RGD1565590; similar to Wolf-Hirschhorn syndrome candidate 1 protein isoform 1; Wolf-Hirschhorn syndrome candidate 1 (human)
Orthologs:
Latest Assembly: RGSC Genome Assembly v3.4
Position:
MapChrPositionStrandSource
Rat Cytogenetic Map14q21 NCBI
RGSC Genome Assembly v5.01482,803,450 - 82,885,540-NCBI
RGSC Genome Assembly v3.41482,528,213 - 82,580,192-NCBI
Rat Celera Assembly1475,757,842 - 75,809,420-NCBI
Genome Assembly 3.11482,532,260 - 82,608,083-NCBI
Model

Launch Genome Browser (GBrowse)


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (RGSC Genome Assembly v3.4)

Sequence

Nucleotide Sequences
Protein Sequences

Strain Variation

Strain Sequence Variants

Additional Information

External Database Links
Nomenclature History
 
More on Whsc1
Entrez Gene
Ensembl Gene
Genome Browser
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1307955
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2014-06-26
Status: ACTIVE