Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
282890
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 311
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF311
Synonyms (NCBI Gene) Gene synonyms aliases
zf31
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1521755 hsa-miR-2110 CLIP-seq
MIRT1521756 hsa-miR-216a CLIP-seq
MIRT1521757 hsa-miR-3150a-3p CLIP-seq
MIRT1521758 hsa-miR-342-3p CLIP-seq
MIRT1521759 hsa-miR-3606 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q5JNZ3
Protein name Zinc finger protein 311 (Zinc finger protein zfp-31)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 63 104 KRAB box Family
PF00096 zf-C2H2 275 297 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 303 325 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 387 409 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 415 437 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 443 465 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 499 521 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 527 549 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 583 608 Domain
PF00096 zf-C2H2 611 634 Zinc finger, C2H2 type Domain
Sequence
MQEVVLLDESSGPPSQLLWTRQDTQLPQESALLPAPYPAFTKDGSQGNLPQADITLMSQA
QESVTFEDVAVNFTNREWQCLTYAQRHLYKDVMLENYGNMVSLGFPFPKPPLISHLEREV
DPCVQDPQDRESLSCSYPVSADKMWPENEKASSQQEIFENGEAYWMKFNSLLKVDSRDPK
VREVCVQDVKLENQWETSIREKLREEKEGSEEVTCKKGKNQKVLSKNLNPNSKHSQCNKV
LIAQKLHECARCGKNFSWHSDLILHEQIHSGEKPHVCNECGKAFKTRNQLSMHRIIHTGE
KPFNCTQCGKAFNSRSALCRHKKTHSGEKPHECRDCGKAFKTRNRLCMHQLIHTGEKPYK
CNCCGKAFQFKHSLTIHGRIHTGEKPYECEECGKAFSGSSDLTKHIRIHTGERPYECSKC
GRAFSRSSDLSKHKRIH
TREKHYGCPQCGKDFSIKAELTKHRRIHTEEKRYRCEECGKAF
RHNCKRRAHEREHTGEKPYQCRDCGKTFQDKHCLTIHQRIHTGEKPYKCLECGKAFSGKS
NLTNHRRIH
TGEKPHKCEVCGMAFHHSSVLRQHKRIHTGEKPYTCSECGTSFRQGSALIG
HKRVHTGE
KPYECEECGKAFRVSSNLTGHKKRKHQVWSTHELDGSRKSLSPVTVSQTSVV
SILTSA
Sequence length 666
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Asthma Asthma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Neoplasms Associate 28981872