Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
199692
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 627
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF627
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT726027 hsa-miR-27a-3p HITS-CLIP 22473208
MIRT726026 hsa-miR-27b-3p HITS-CLIP 22473208
MIRT1532925 hsa-miR-103a CLIP-seq
MIRT1532926 hsa-miR-107 CLIP-seq
MIRT1532927 hsa-miR-1262 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IBA 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
GO:0005515 Function Protein binding IPI 25416956, 28514442, 32296183
GO:0005634 Component Nucleus IBA 21873635
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612248 30570 ENSG00000198551
Protein
UniProt ID Q7L945
Protein name Zinc finger protein 627
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 3 44 KRAB box Family
PF00096 zf-C2H2 167 189 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 195 217 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 335 357 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 391 413 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 419 441 Zinc finger, C2H2 type Domain
Sequence
MDSVAFEDVAVNFTLEEWALLDPSQKNLYRDVMRETFRNLASVGKQWEDQNIEDPFKIPR
RNISHIPERLCESKEGGQGEETFSQIPDGILNKKTPGVKPCESSVCGEVGMGPSSLNRHI
RDHTGREPNEYQEYGKKSYTRNQCGRALSYHRSFPVRERTHPGGKPYDCKECGETFISLV
SIRRHMLTH
RGGVPYKCKVCGKAFDYPSLFRIHERSHTGEKPYECKQCGKAFSCSSYIRI
HERTHTGDKPYECKQCGKAFSCSKYIRIHERTHTGEKPYECKQCGKAFRCASSVRSHERT
HTGEKLFECKECGKALTCLASVRRHMIKHTGNGPYKCKVCGKAFDFPSSFRIHERTHTGE
KPYDCKQCGKAFSCSSSFRKHERIHTGEKPYKCTKCGKAFSRSSYFRIHERTHTGEKPYE
CKQCGKAFSRSTYFRVHEKIH
TGEKPYENPNPNASVVPVLS
Sequence length 461
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Spondyloenchondrodysplasia with immune dysregulation SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION rs387906668, rs387906669, rs387906670, rs781199182, rs781050795, rs879255600, rs878853218, rs1025967277, rs761798208, rs1599634435, rs747619825 21217752
Unknown
Disease term Disease name Evidence References Source
Alzheimer disease Alzheimer disease GWAS
Oligodendroglioma Oligodendroglioma GWAS
Associations from Text Mining
Disease Name Relationship Type References
Coronary Disease Associate 22042884