Gene Gene information from NCBI Gene database.
Entrez ID 55608
Gene name Ankyrin repeat domain 10
Gene symbol ANKRD10
Synonyms (NCBI Gene)
-
Chromosome 13
Chromosome location 13q34
miRNA miRNA information provided by mirtarbase database.
133
miRTarBase ID miRNA Experiments Reference
MIRT023245 hsa-miR-122-5p Microarray 17612493
MIRT031103 hsa-miR-19b-3p Sequencing 20371350
MIRT441229 hsa-miR-218-5p HITS-CLIP 23212916
MIRT441229 hsa-miR-218-5p HITS-CLIP 23212916
MIRT782420 hsa-miR-2861 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183, 33961781
GO:0005654 Component Nucleoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NXR5
Protein name Ankyrin repeat domain-containing protein 10
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12796 Ank_2 26 122 Ankyrin repeats (3 copies) Repeat
PF12796 Ank_2 96 188 Ankyrin repeats (3 copies) Repeat
Sequence
MSAAGAGAGVEAGFSSEELLSLRFPLHRACRDGDLATLCSLLQQTPHAHLASEDSFYGWT
PVHWAAHFGKLECLVQLVRAGATLNVSTTRYAQTP
AHIAAFGGHPQCLVWLIQAGANINK
PD
CEGETPIHKAARSGSLECISALVANGAHVDLRNASGLTAADIAQTQGFQECAQFLLNL
QNCHLNHF
YNNGILNGGHQNVFPNHISVGTNRKRCLEDSEDFGVKKARTEAQSLDSAVPL
TNGDTEDDADKMHVDREFAVVTDMKNSSSVSNTLTNGCVINGHLDFPSTTPLSGMESRNG
QCLTGTNGISSGLAPGQPFPSSQGSLCISGTEEPEKTLRANPELCGSLHLNGSPSSCIAS
RPSWVEDIGDNLYYGHYHGFGDTAESIPELNSVVEHSKSVKVQERYDSAVLGTMHLHHGS
Sequence length 420
Interactions View interactions
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)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CROHN'S DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Triple Negative Breast Neoplasms Triple negative breast cancer Pubtator 33934391 Associate
★☆☆☆☆
Found in Text Mining only