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Gene Gene information from NCBI Gene database.
Entrez ID 51281
Gene name Ankyrin repeat and MYND domain containing 1
Gene symbol ANKMY1
Synonyms (NCBI Gene)
ZMYND13
Chromosome 2
Chromosome location 2q37.3
miRNA miRNA information provided by mirtarbase database.
165 Show/Hide all (165)
miRTarBase ID miRNA Experiments Reference
MIRT713597 hsa-miR-4645-5p HITS-CLIP 19536157
MIRT713596 hsa-miR-4673 HITS-CLIP 19536157
MIRT713595 hsa-miR-4667-3p HITS-CLIP 19536157
MIRT713594 hsa-miR-3183 HITS-CLIP 19536157
MIRT713593 hsa-miR-4723-3p HITS-CLIP 19536157
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:0008270 Function Zinc ion binding IEA
GO:0046872 Function Metal ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620842 20987 ENSG00000144504
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P2S6
Protein name Ankyrin repeat and MYND domain-containing protein 1 (Testis-specific ankyrin-like protein 1) (Zinc finger MYND domain-containing protein 13)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00023 Ank 292 → 324 Ankyrin repeat Repeat
PF01753 zf-MYND 880 → 920 MYND finger Domain
PF02493 MORN 25 → 47 MORN repeat Repeat
PF02493 MORN 70 → 92 MORN repeat Repeat
PF02493 MORN 2 → 24 MORN repeat Repeat
PF12796 Ank_2 634 → 724 Ankyrin repeats (3 copies) Repeat
PF12796 Ank_2 520 → 615 Ankyrin repeats (3 copies) Repeat
Sequence
MYQGEFGLNMKLGYGKFSWPTGESYHGQFYRDHCHGLGTYMWPDGSSFTGTFYLSHREGY
GTMYMKTRLFQGLYKADQRFGPGVETYPDGSQDVGLWFREQLIKLCTQIPSGFSLLRYPE
FSSFITHSPARISLSEEEKTEWGLQEGQDPFFYDYKRFLLNDNLTLPPEMYVYSTNSDHL
PMTSSFRKELDARIFLNEIPPFVEDGEPWFIINETPLLVKIQKQTYKFRNKPAHTSWNMG
AILEGKRSGFAPCGPKEQLSMEMILKAEEGNHEWICRILKDNFASADVADAKGYTVLAAA
ATHCHNDIVNLLLDCGADVNKCSD
EGLTALSMCFLLHYPAQSFKPNVAERTIPEPQEPPK
FPVVPILSSSFMDTNLESLYYEVNVPSQGSYELRPPPAPLLLPRVSGSHEGGHFQDTGQC
GGSIDHRSSSLKGDSPLVKGSLGHVESGLEDVLGNTDRGSLCSAETKFESNVCVCDFSIE
LSQAMLERSAQSHSLLKMASPSPCTSSFDKGTMRRMALSMIERRKRWRTIKLLLRRGADP
NLCCVPMQVLFLAVKAGDVDGVRLLLEHGARTDICFPPQLSTLTPLHIAAALPGEEGVQI
VELLLHAITDVDAKA
SDEDDTYKPGKLDLLPSSLKLSNEPGPPQAYYSTDTALPEEGGRT
ALHMACEREDDNKCARDIVRLLLSHGANPNLLWSGHSPLSLSIASGNELVVKELLTQGAD
PNLP
LTKGLGSALCVACDLTYEHQRNMDSKLALIDRLISHGADILKPVMLRQGEKEAVGT
AVDYGYFRFFQDRRIARCPFHTLMPAERETFLARKRLLEYMGLQLRQAVFAKESQWDPTW
LYLCKRAELIPSHRMKKKGPSLPRGLDVKEQGQIPFFKFCYQCGRSIGVRLLPCPRCYGI
LTCSKYCKTKAWTEFHKKDC
GDLVAIVTQLEQVSRRREEFQ
Sequence length 941
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 Reference Evidence Score
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations