Gene Gene information from NCBI Gene database.
Entrez ID 57567
Gene name Zinc finger protein 319
Gene symbol ZNF319
Synonyms (NCBI Gene)
ZFP319
Chromosome 16
Chromosome location 16q21
miRNA miRNA information provided by mirtarbase database.
65
miRTarBase ID miRNA Experiments Reference
MIRT651180 hsa-miR-130a-5p HITS-CLIP 23824327
MIRT651179 hsa-miR-23c HITS-CLIP 23824327
MIRT651178 hsa-miR-23b-3p HITS-CLIP 23824327
MIRT651177 hsa-miR-23a-3p HITS-CLIP 23824327
MIRT651176 hsa-miR-548c-3p 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:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P2F9
Protein name Zinc finger protein 319
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 202 224 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 230 252 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 258 280 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 315 337 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 343 365 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 371 393 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 428 450 Zinc finger, C2H2 type Domain
PF13465 zf-H2C2_2 500 525 Domain
Sequence
MSESWQQPPQTQPQQPQPPQPQHHAEPPPALAEHTLPPGTAENPLGCAVYGILLQPDPGL
QPPQHAPLQAAGEPGPKCGVCGHDLAHLSSPHEHQCLAGHDRSFQCTQCLKIFHQATDLL
EHQCVQAEQKPFVCGVCKMGFSLLTSLAQHHSSHSGLVKCSICEKTYKPAEAAEPATTAA
PSLPAAPAPSTVTPAEQADKPYSCPICQKPFKHLSELSRHERIHTGEKPYKCTLCDKSFS
QSSHLVHHKRTH
SSERPYKCAVCEKTFKHRSHLVRHMYAHSGEHHLFRCNVCELHFKESS
ELLQHPCTPSGERPFRCGECQKAFKRPSDLRQHERTHSAERPFKCDLCPMGFKQQYALMR
HRRTH
KTEEPFKCGLCEKGFGQPSHLLYHQHVHTLETLFKCPVCQKGFDQSAELLRHKCL
PGAAERPFKCPVCNKAYKRASALQKHQLAHCAAAEKPLRCTLCERRFFSSSEFVQHRCDP
AREKPLKCPDCEKRFKYASDLQRHRRVHTGEKPYKCPNCDKAFKQREHLNKHQGVHAREQ
QFKCVWCGERFLDVALLQEHSAQHSAAAAAAEGAYQVAACLP
Sequence length 582
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CHRONIC OBSTRUCTIVE PULMONARY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations