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Gene: Fam20a (FAM20A, golgi associated secretory pathway pseudokinase) Rattus norvegicus
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Symbol: Fam20a
Name: FAM20A, golgi associated secretory pathway pseudokinase
Description: Predicted to have protein serine/threonine kinase activator activity. Predicted to be involved in several processes, including odontogenesis; positive regulation of protein phosphorylation; and response to bacterium. Predicted to colocalize with the Golgi apparatus. Human ortholog(s) of this gene implicated in amelogenesis imperfecta type 1G. Orthologous to human FAM20A (FAM20A golgi associated secretory pathway pseudokinase); INTERACTS WITH 6-propyl-2-thiouracil; atrazine; bisphenol A.
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: family with sequence similarity 20, member A; LOC303635; pseudokinase FAM20A; RGD1306364; similar to cDNA sequence BC029169
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.01097,962,467 - 98,017,171 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01097,676,935 - 97,731,346 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41099,113,846 - 99,170,601 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11099,128,215 - 99,184,971 (-)NCBI
Celera1093,301,687 - 93,354,956 (-)NCBICelera
Cytogenetic Map10q32.1NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Rnor_6.0)
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome
Promoters

Strain Variation

Strain Sequence Variants (Rnor 6.0)
Damaging Variants

Additional Information

External Database Links
Nomenclature History
 
More on Fam20a
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1306364
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2019-10-16
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.