PCDH11X (protocadherin 11 X-linked)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 27328 |
| Gene name | Protocadherin 11 X-linked |
| Gene symbol | PCDH11X |
| Synonyms (NCBI Gene) |
PCDH-XPCDH-YPCDH11PCDH11YPCDH22PCDHXPPP1R119
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| Chromosome | X |
| Chromosome location | Xq21.31 |
| Summary | This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of th |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9BZA7 | |||||||||||||||||||||||||||||||||||||||||||||
| Protein name | Protocadherin-11 X-linked (Protocadherin-11) (Protocadherin on the X chromosome) (PCDH-X) (Protocadherin-S) | |||||||||||||||||||||||||||||||||||||||||||||
| Protein function | Potential calcium-dependent cell-adhesion protein. | |||||||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed strongly in fetal brain and brain (cortex, amygdala, thalamus, substantia nigra, hippocampus, caudate nucleus and corpus callosum). Expressed at low level in testis. {ECO:0000269|PubMed:10644456, ECO:0000269|PubMed:11003707}. | |||||||||||||||||||||||||||||||||||||||||||||
| Sequence | ||||||||||||||||||||||||||||||||||||||||||||||
| Sequence length | 1347 | |||||||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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