InnateDB Protein
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IDBP-176605.7
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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Ammecr1
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Protein Name
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Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human)
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Synonyms
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6230420G18Rik;
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Species
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Mus musculus
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Ensembl Protein
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ENSMUSP00000036085
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InnateDB Gene
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IDBG-176603 (Ammecr1)
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Protein Structure
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Function |
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Subcellular Localization |
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Disease Associations |
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
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Predicted by orthology |
Total |
1 [view]
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
MGI:1860206
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InterPro |
IPR002733
AMMECR1 domain
IPR023473
AMMECR1
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PFAM |
PF01871
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q9JHT5
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PhosphoSite |
PhosphoSite-Q9JHT5
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
56068
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UniGene |
Mm.409950
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RefSeq |
NP_062369
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MGI ID |
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MGI Symbol |
Ammecr1
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OMIM |
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CCDS |
CCDS30452
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HPRD |
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IMGT |
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EMBL |
AJ243485
AK051736
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GenPept |
BAC34745
CAB95767
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