Entity Details

Primary name Ammecr1
Entity type gene
Source Source Link

Details

PrimaryID56068
RefseqGene
SymbolAmmecr1
NameAlport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
ChromosomeX
LocationX
TaxID10090
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-07-11
ModificationDate2021-06-23

Ontological Relatives

UniProt IDsAMMR1_MOUSE

GO terms

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GOName
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005739 mitochondrion

Diseases

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Interactions

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InteractorPartnerSourcesPublicationsLink