Gene Gene information from NCBI Gene database.
Entrez ID 57037
Gene name Ankyrin repeat and MYND domain containing 2
Gene symbol ANKMY2
Synonyms (NCBI Gene)
ZMYND20
Chromosome 7
Chromosome location 7p21.1
miRNA miRNA information provided by mirtarbase database.
217
miRTarBase ID miRNA Experiments Reference
MIRT782398 hsa-miR-1286 CLIP-seq
MIRT782399 hsa-miR-3074-5p CLIP-seq
MIRT782400 hsa-miR-3126-5p CLIP-seq
MIRT782401 hsa-miR-370 CLIP-seq
MIRT782402 hsa-miR-375 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21044950
GO:0005929 Component Cilium IEA
GO:0008270 Function Zinc ion binding IEA
GO:0019899 Function Enzyme binding IEA
GO:0042995 Component Cell projection IEA
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.
Q8IV38
Protein name Ankyrin repeat and MYND domain-containing protein 2
Protein function May be involved in the trafficking of signaling proteins to the cilia.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12796 Ank_2 19 110 Ankyrin repeats (3 copies) Repeat
PF01753 zf-MYND 320 357 MYND finger Domain
Sequence
MVHIKKGELTQEEKELLEVIGKGTVQEAGTLLSSKNVRVNCLDENGMTPLMHAAYKGKLD
MCKLLLRHGADVNCHQHEHGYTALMFAALSGNKDITWVMLEAGAETDVVN
SVGRTAAQMA
AFVGQHDCVTIINNFFPRERLDYYTKPQGLDKEPKLPPKLAGPLHKIITTTNLHPVKIVM
LVNENPLLTEEAALNKCYRVMDLICEKCMKQRDMNEVLAMKMHYISCIFQKCINFLKDGE
NKLDTLIKSLLKGRASDGFPVYQEKIIRESIRKFPYCEATLLQQLVRSIAPVEIGSDPTA
FSVLTQAITGQVGFVDVEFCTTCGEKGASKRCSVCKMVIYCDQTCQKTHWFTHKKICKNL
KDIYEKQQLEAAKEKRQEENHGKLDVNSNCVNEEQPEAEVGISQKDSNPEDSGEGKKESL
ESEAELEGLQDAPAGPQVSEE
Sequence length 441
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
High myopia Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SEVERE MYOPIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations