APC membrane recruitment protein 1
The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS). [provided by RefSeq, May 2010]
Gene aliases
FAM123B,
WTX
Chromosome
X
Map location
Xq11.2
Gene type
protein-coding
Gene Ontology (GO) terms enrichment
Database references
Statistics for AMER1
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| PTMs | |
| Protein entries | |
| Sequence variants | |
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| Pathways involved in | |
| Protein-Protein Interactions |
Sequence variants for AMER1
List of cell lines/tissues that have AMER1 sequence variants
List of pathways where AMER1 is involved
| Pathway name | Pathway source |
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Protein-Protein Interaction Network for AMER1
Network key
Number of sequence variations per gene
Protein identification for AMER1
Browse by protein identification methods
| Identification method | Quantitative data available |
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