Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9205
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger MYM-type containing 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZMYM5
Synonyms (NCBI Gene) Gene synonyms aliases
HSPC050, MYM, ZNF198L1, ZNF237
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q12.11
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1515100 hsa-miR-3163 CLIP-seq
MIRT1515101 hsa-miR-340 CLIP-seq
MIRT1515102 hsa-miR-362-5p CLIP-seq
MIRT1515103 hsa-miR-4733-5p CLIP-seq
MIRT1515104 hsa-miR-4803 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 17126306
GO:0005515 Function Protein binding IPI 17126306, 25416956
GO:0005634 Component Nucleus IEA
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
616443 13029 ENSG00000132950
Protein
UniProt ID Q9UJ78
Protein name Zinc finger MYM-type protein 5 (Zinc finger protein 198-like 1) (Zinc finger protein 237)
Protein function Functions as a transcriptional regulator.
PDB 2DAS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06467 zf-FCS 240 276 MYM-type Zinc finger with FCS sequence motif Domain
PF06467 zf-FCS 333 369 MYM-type Zinc finger with FCS sequence motif Domain
PF06467 zf-FCS 375 415 MYM-type Zinc finger with FCS sequence motif Domain
Sequence
MEKCSVGGLELTEQTPALLGNMAMATSLMDIGDSFGHPACPLVSRSRNSPVEDDDDDDDV
VFIESIQPPSISAPAIADQRNFIFASSKNEKPQGNYSVIPPSSRDLASQKGNISETIVID
DEEDIETNGGAEKKSSCFIEWGLPGTKNKTNDLDFSTSSLSRSKTKTGVRPFNPGRMNVA
GDLFQNGEFATHHSPDSWISQSASFPSNQKQPGVDSLSPVALLRKQNFQPTAQQQLTKPA
KITCANCKKPLQKGQTAYQRKGSAHLFCSTTCLSSF
SHKRTQNTRSIICKKDASTKKANV
ILPVESSKSFQEFYSTSCLSPCENNWNLKKGVFNKSRCTICSKLAEIRHEVSVNNVTHKL
CSNHCFNKY
RLANGLIMNCCEHCGEYMPSKSTGNNILVIGGQQKRFCCQSCINEYKQMME
TKSKKLTASENRKRNAFREENEKQLYGSSNTLLKKIEGIPEKKEKTSQLQLSVECGTDTL
LIQENVNLPPSSTSTIADTFQEQLEEKNFEDSIVPVVLSADPGTWPRILNIKQRDTLVEN
VPPQVRNFNFPKDNTGRKFSETYYTRILPNGEKTTRSWLLYSTSKDSVFCLYCKLFGEGK
NQLKNENGCKDWQHLSHILSKHEESEMHVNNSVKYSKLKSDLKKNKAIDAAEHRLYENEK
NDGVLLLYT
Sequence length 669
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Multiple Congenital Anomalies multiple congenital anomalies/dysmorphic syndrome GenCC
Alzheimer disease Alzheimer disease GWAS