Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84450
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 512
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF512
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p23.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein containing four putative zinc finger motifs. Zinc finger motifs may bind to proteins or nucleic acids. Zinc finger-containing proteins are involved in a variety of processes, including regulation of transcription. Alternative s
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019520 hsa-miR-151a-5p Sequencing 20371350
MIRT043270 hsa-miR-331-3p CLASH 23622248
MIRT1527491 hsa-miR-1 CLIP-seq
MIRT1527492 hsa-miR-1263 CLIP-seq
MIRT1527493 hsa-miR-206 CLIP-seq
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 IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
GO:0046872 Function Metal ion binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620921 29380 ENSG00000243943
Protein
UniProt ID Q96ME7
Protein name Zinc finger protein 512
Protein function May be involved in transcriptional regulation.
PDB 2CTD
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 287 310 Zinc finger, C2H2 type Domain
Sequence
MSSRLGAVPATSGPTTFKQQRSTRIVGAKNSRTQCSIKDNSFQYTIPHDDSLSGSSSASS
CEPVSDFPASFRKSTYWMKMRRIKPAATSHVEGSGGVSAKGKRKPRQEEDEDYREFPQKK
HKLYGRKQRPKTQPNPKSQARRIRKEPPVYAAGSLEEQWYLEIVDKGSVSCPTCQAVGRK
TIEGLKKHMENCKQEMFTCHHCGKQLRSLAGMKYHVMANHNSLPILKAGDEIDEPSERER
LRTVLKRLGKLRCMRESCSSSFTSIMGYLYHVRKCGKGAAELEKMTLKCHHCGKPYRSKA
GLAYHLRSEH
GPISFFPESGQPECLKEMNLESKSGGRVQRRSAKIAVYHLQELASAELAK
EWPKRKVLQDLVPDDRKLKYTRPGLPTFSQEVLHKWKTDIKKYHRIQCPNQGCEAVYSSV
SGLKAHLGSCTLGNFVAGKYKCLLCQKEFVSESGVKYHINSVHAEDWFVVNPTTTKSFEK
LMKIKQRQQEEEKRRQQHRSRRSLRRRQQPGIELPETELSLRVGKDQRRNNEELVVSASC
KEPEQEPVPAQFQKVKPPKTNHKRGRK
Sequence length 567
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Metabolic syndrome Metabolic Syndrome X rs367643250, rs587777380, rs777736953 21386085
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS