Bos taurus Gene: AMMECR1
Summary
InnateDB Gene IDBG-634679.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol AMMECR1
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000022288
Encoded Proteins
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000101935:
The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome X:63076962-63193217
Strand Reverse strand
Band
Transcripts
ENSBTAT00000030123 ENSBTAP00000030108
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL F1N4T8
UniProt Splice Variant
Entrez Gene 615842
UniGene
RefSeq
HUGO HGNC:467
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02071553 DAAA02071554
GenPept
RNA Seq Atlas 615842