NOTUM (notum, palmitoleoyl-protein carboxylesterase)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 147111 |
| Gene name | Notum, palmitoleoyl-protein carboxylesterase |
| Gene symbol | NOTUM |
| Synonyms (NCBI Gene) |
hNOTUM
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| Chromosome | 17 |
| Chromosome location | 17q25.3 |
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miRNA
miRNA information provided by mirtarbase database.
31
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Transcription factors
Transcription factors information provided by TRRUST V2 database.
1
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
23
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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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Q6P988 | ||||||||||
| Protein name | Palmitoleoyl-protein carboxylesterase NOTUM (EC 3.1.1.98) (hNOTUM) | ||||||||||
| Protein function | Carboxylesterase that acts as a key negative regulator of the Wnt signaling pathway by specifically mediating depalmitoleoylation of WNT proteins. Serine palmitoleoylation of WNT proteins is required for efficient binding to frizzled receptors ( | ||||||||||
| PDB | 4UYU , 4UYW , 4UYZ , 4UZ1 , 4UZ5 , 4UZ6 , 4UZ7 , 4UZ9 , 4UZA , 4UZL , 4UZQ , 4WBH , 6R8P , 6R8Q , 6R8R , 6T2H , 6T2K , 6TR5 , 6TR6 , 6TR7 , 6TUZ , 6TV4 , 6YSK , 6YUW , 6YUY , 6YV0 , 6YV2 , 6YV4 , 6YXI , 6ZUV , 6ZVL , 6ZYF , 7ARG , 7B2V , 7B2Y , 7B2Z , 7B37 , 7B3F , 7B3G , 7B3H , 7B3I , 7B3P , 7B3X , 7B45 , 7B4X , 7B50 , 7B7W , 7B7X , 7B7Y , 7B84 , 7B86 | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Rarely expressed in adult normal tissues. {ECO:0000269|PubMed:18429952}. | ||||||||||
| Sequence |
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| Sequence length | 496 | ||||||||||
| 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 (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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