Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9204
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger MYM-type containing 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZMYM6
Synonyms (NCBI Gene) Gene synonyms aliases
Buster2, MYM, ZBED7, ZNF198L4, ZNF258
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p34.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT626394 hsa-miR-548c-3p HITS-CLIP 23824327
MIRT626393 hsa-miR-4668-3p HITS-CLIP 23824327
MIRT665259 hsa-miR-3065-5p HITS-CLIP 23824327
MIRT626392 hsa-miR-877-3p HITS-CLIP 23824327
MIRT665258 hsa-miR-6845-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding TAS 10486218
GO:0005634 Component Nucleus IEA
GO:0007010 Process Cytoskeleton organization IMP 21834987
GO:0007275 Process Multicellular organism development TAS 10486218
GO:0008270 Function Zinc ion binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613567 13050 ENSG00000163867
Protein
UniProt ID O95789
Protein name Zinc finger MYM-type protein 6 (Transposon-derived Buster2 transposase-like protein) (Zinc finger protein 258)
Protein function Plays a role in the regulation of cell morphology and cytoskeletal organization.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06467 zf-FCS 133 174 MYM-type Zinc finger with FCS sequence motif Domain
PF06467 zf-FCS 426 462 MYM-type Zinc finger with FCS sequence motif Domain
PF06467 zf-FCS 467 500 MYM-type Zinc finger with FCS sequence motif Domain
PF14291 DUF4371 863 992 Domain of unknown function (DUF4371) Family
Tissue specificity TISSUE SPECIFICITY: Expressed at high levels in heart, skeletal muscle, kidney and liver. {ECO:0000269|PubMed:10486218}.
Sequence
MKEPLDGECGKAVVPQQELLDKIKEEPDNAQEYGCVQQPKTQESKLKIGGVSSVNERPIA
QQLNPGFQLSFASSGPSVLLPSVPAVAIKVFCSGCKKMLYKGQTAYHKTGSTQLFCSTRC
ITRHSSPACLPPPPKKTCTNCSKDILNPKDVITTRFENSYPSKDFCSQSCLSSYELKKKP
VVTIYTKSISTKCSMCQKNADTRFEVKYQNVVHGLCSDACFSKFHSTNNLTMNCCENCGS
YCYSSSGPCQSQKVFSSTSVTAYKQNSAQIPPYALGKSLRPSAEMIETTNDSGKTELFCS
INCLSAYRVKTVTSSGVQVSCHSCKTSAIPQYHLAMSNGTIYSFCSSSCVVAFQNVFSKP
KGTNSSAVPLSQGQVVVSPPSSRSAVSIGGGNTSAVSPSSIRGSAAASLQPLAEQSQQVA
LTHTVVKLKCQHCNHLFATKPELLFYKGKMFLFCGKNCSDEYKKKNKVVAMCDYCKLQKI
IKETVRFSGVDKPFCSEVCK
FLSARDFGERWGNYCKMCSYCSQTSPNLVENRLEGKLEEF
CCEDCMSKFTVLFYQMAKCDGCKRQGKLSESIKWRGNIKHFCNLFCVLEFCHQQIMNDCL
PQNKVNISKAKTAVTELPSARTDTTPVITSVMSLAKIPATLSTGNTNSVLKGAVTKEAAK
IIQDESTQEDAMKFPSSQSSQPSRLLKNKGISCKPVTQTKATSCKPHTQHKECQTDLPMP
NEKNDAELDSPPSKKKRLGFFQTYDTEYLKVGFIICPGSKESSPRPQCVICGEILSSENM
KPANLSHHLKTKHSELENKPVDFFEQKSLEMECQNSSLKKCLLVEKSLVKASYLIAFQTA
ASKKPFSIAEELIKPYLVEMCSEVLGSSAGDKMKTIPLSNVTIQHRIDELSADIEDQLIQ
KVRESKWFALQIDESSEISNITLLLCYIRFIDYDCRDVKEELLFCIEMPTQITGFEIFEL
INKYIDSKSLNWKHCVGLCTDGAASMTGRYSG
LKAKIQEVAMNTAAFTHCFIHRERLVAE
KLSPCLHKILLQSAQILSFIKSNALNSRMLTILCEEMGSEHVSLPLHAEVRWISRGRMLK
RLFELRHEIEIFLSQKHSDLAKYFHDEEWVGKLAYLSDIFSLINELNLSLQGTLTTFFNL
CNKIDVFKRKLKMWLKRTQENDYDMFPSFSEFSNSSGLNMTDITRIIFEHLEGLSQVFSD
CFPPEQDLRSGNLWIIHPFMNHQNNNLTDFEEEKLTELSSDLGLQALFKSVSVTQFWINA
KTSYPELHERAMKFLLPFSTVYLCDAAFSALTESKQKNLLGSGPALRLAVTSLIPRIEKL
VKEKE
Sequence length 1325
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Mental retardation Intellectual Disability rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
26350204
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 24098497
Fibrosis Associate 37239897