NUDT13 (nudix hydrolase 13)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 25961 |
| Gene name | Nudix hydrolase 13 |
| Gene symbol | NUDT13 |
| Synonyms (NCBI Gene) |
-
|
| Chromosome | 10 |
| Chromosome location | 10q22.2 |
|
miRNA
miRNA information provided by mirtarbase database.
15
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Protein
Protein information from UniProt database.
|
|||||||||||||||||||||
|
UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
|
Q86X67 | ||||||||||||||||||||
| Protein name | NAD(P)H pyrophosphatase NUDT13, mitochondrial (EC 3.6.1.22) (Nucleoside diphosphate-linked moiety X motif 13) (Nudix motif 13) (Protein KiSS-16) | ||||||||||||||||||||
| Protein function | NAD(P)H pyrophosphatase that hydrolyzes NADH into NMNH and AMP, and NADPH into NMNH and 2',5'-ADP. Has a marked preference for the reduced pyridine nucleotides. Does not show activity toward NAD-capped RNAs; the NAD-cap is an atypical cap presen | ||||||||||||||||||||
| Family and domains |
Pfam
|
||||||||||||||||||||
| Tissue specificity | TISSUE SPECIFICITY: Highly expressed in metastasis-suppressed chromosome 6 melanoma hybrids. {ECO:0000269|Ref.6}. | ||||||||||||||||||||
| Sequence |
MSLYCGIACRRKFFWCYRLLSTYVTKTRYLFELKEDDDACKKAQQTGAFYLFHSLAPLLQ |
||||||||||||||||||||
| Sequence length | 352 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
|
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
|
|||||||||
|
|||||||||
|
Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
|
|||||||||||||||||||||||||||||||||||||
|
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)
|
|||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||
|
Related Genes
Genes most often co-reported with NUDT13 across shared curated disease and pathway associations.
1
|
|
|
Diseases Linked via Similar Genes
Diseases curated for genes most similar to NUDT13 (see Related Genes above), that are NOT already directly curated for NUDT13 itself -- a lead worth checking, not a confirmed association.
5
|
|