Gene Gene information from NCBI Gene database.
Entrez ID 147463
Gene name Ankyrin repeat domain 29
Gene symbol ANKRD29
Synonyms (NCBI Gene)
-
Chromosome 18
Chromosome location 18q11.2
miRNA miRNA information provided by mirtarbase database.
38
miRTarBase ID miRNA Experiments Reference
MIRT002779 hsa-miR-1-3p Microarray 15685193
MIRT018603 hsa-miR-335-5p Microarray 18185580
MIRT019593 hsa-miR-340-5p Sequencing 20371350
MIRT020251 hsa-miR-130b-3p Sequencing 20371350
MIRT021843 hsa-miR-132-3p Microarray 17612493
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
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.
Q8N6D5
Protein name Ankyrin repeat domain-containing protein 29
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12796 Ank_2 5 76 Ankyrin repeats (3 copies) Repeat
PF12796 Ank_2 75 142 Ankyrin repeats (3 copies) Repeat
PF12796 Ank_2 134 207 Ankyrin repeats (3 copies) Repeat
PF12796 Ank_2 182 273 Ankyrin repeats (3 copies) Repeat
Sequence
MCRMSFKKETPLANAAFWAARRGNLALLKLLLNSGRVDVDCRDSHGTTLLMVAAYAGHID
CVRELVLQGADINL
QRESGTTALFFAAQQGHNDVVRFLFGFGASTEFRTKDGGTALLAAS
QYGHMQVVETLLKHGANIHDQLYDGATALFLAAQGGYLDVIRLLLASGAKVNQPRQDGTA
PLWIASQMGHSEVVRVMLLRGADRDAARNDGTTALLKAANKGYNDVIKELLKFSPTLGIL
KNGTSALHAAVLSGNIKTVALLLEAGADPSLRN
KANELPAELTKNERILRLLRSKEGPRK
S
Sequence length 301
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
DIGESTIVE SYSTEM INFECTIOUS DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SPORADIC AMYOTROPHIC LATERAL SCLEROSIS 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
Epilepsy Epilepsy Pubtator 37192718 Associate
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 37192718 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer UNIPROT_DG
★☆☆☆☆
Found in Text Mining only