Gene Gene information from NCBI Gene database.
Entrez ID 11179
Gene name Zinc finger protein 277
Gene symbol ZNF277
Synonyms (NCBI Gene)
NRIF4ZNF277P
Chromosome 7
Chromosome location 7q31.1
miRNA miRNA information provided by mirtarbase database.
196
miRTarBase ID miRNA Experiments Reference
MIRT663217 hsa-miR-1197 HITS-CLIP 23824327
MIRT646293 hsa-miR-501-5p HITS-CLIP 23824327
MIRT663216 hsa-miR-4677-3p HITS-CLIP 23824327
MIRT663215 hsa-miR-4751 HITS-CLIP 23824327
MIRT663214 hsa-miR-4316 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IEA
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IEA
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
605465 13070 ENSG00000198839
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NRM2
Protein name Zinc finger protein 277 (Nuclear receptor-interacting factor 4)
Protein function Probable transcription factor. Involved in modulation of cellular senescence; represses transcription of the tumor suppressor gene INK4A/ARF, perhaps acting via the Polycomb group (PcG) complex PRC1.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12756 zf-C2H2_2 58 128 C2H2 type zinc-finger (2 copies) Family
PF12756 zf-C2H2_2 172 269 C2H2 type zinc-finger (2 copies) Family
PF12756 zf-C2H2_2 301 406 C2H2 type zinc-finger (2 copies) Family
Sequence
Sequence length 450
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colon adenocarcinoma Uncertain significance rs146166040 RCV005930853
Sarcoma Uncertain significance rs146166040 RCV005930854
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 24518835
Autistic Disorder Associate 24518835
Specific Language Disorder Associate 24518835