Gene: Ammecr1 (Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1) Rattus norvegicus
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Symbol: Ammecr1
Name: Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Description: Predicted to localize to the nucleus; orthologous to human AMMECR1 (Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1); INTERACTS WITH bisphenol A; (+)-catechin (ortholog); (-)-epigallocatechin 3-gallate (ortholog).
Type: protein-coding
RefSeq Status: MODEL
Also known as: LOC501539; RGD1561004; similar to AMME syndrome candidate gene 1 protein homolog
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.0X114,129,829 - 114,233,013 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0X112,575,812 - 112,679,260 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4X35,588,998 - 35,691,478 (+)NCBIRGSC3.4rn4RGSC3.4
CeleraX105,881,340 - 105,983,582 (-)NCBICelera
Cytogenetic MapXq33NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - curated
References - uncurated

Genomics

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

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome
Promoters

Strain Variation

Strain Sequence Variants (Rnor 5.0)

Additional Information

External Database Links
Nomenclature History
 
More on Ammecr1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1561004
Created: 2006-02-09
Species: Rattus norvegicus
Last Modified: 2019-04-23
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.