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ZIRC
ZFIN ID: ZDB-GENE-040426-1533
Gene Name: Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human)
Gene Symbol: ammecr1
Sequence Ontology ID : SO:0000704

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Previous Names: zgc:66100 (1), zgc:85865

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(Including Attributions)
Location: Chr: 21 Mapping Details/Browsers
Nomenclature History
AUTOMATED DESCRIPTION
Orthologous to several human genes including AMMECR1 (Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1).
GENE EXPRESSION
Directly Submitted Expression Data: 1 figure (1 image) from Thisse et al., 2004 [MGC:85865]
Wild-type Stages, Structures: Zygote:1-cell (0.0h-0.75h) to Hatching:Pec-fin (60.0h-72.0h)
 
Curated Microarray Expression: GEO (1)
DISEASE ASSOCIATED WITH ammecr1 HUMAN ORTHOLOG
Disease Ontology Term OMIM Term OMIM Phenotype ID
Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis 300990
DISEASE ASSOCIATED WITH ammecr1 VIA EXPERIMENTAL MODELS No data available
GENE ONTOLOGY
Ontology GO Term
Biological Process biological_process (more)
Cellular Component cellular_component (more)
Molecular Function molecular_function (more)
GO Terms (all 3)
TRANSCRIPTS
Type Name Length (bp) Analysis
mRNA ammecr1-201 (1) 1325
GENE PRODUCT DESCRIPTION No description available
INTERACTIONS AND PATHWAYS
ANTIBODIESNo data available
PLASMIDSNo data available
CONSTRUCTS WITH SEQUENCES FROM ammecr1 No data available
MARKER RELATIONSHIPS
ammecr1Contained in: [Fosmid] CH1073-167D14 (1) (order this)
ammecr1Encodes: [cDNA] MGC:66100 (1) (order this), MGC:85865 (1) (order this)
SEQUENCE INFORMATION
Type Accession # Length (bp/aa) Analysis
RNA RefSeq:NM_200581 (1) 1264bp
Genomic GenBank:CU550703 (1) 38682bp
Select Tool
Polypeptide UniProtKB:Q6NWA1 (1) 322aa
Sequence Clusters UniGene:77072 (1)
Sequence Information (all 13)
ORTHOLOGY for ammecr1 (Chr: 21)
CITATIONS (18)