Gene Gene information from NCBI Gene database.
Entrez ID 79894
Gene name Zinc finger protein 672
Gene symbol ZNF672
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1q44
miRNA miRNA information provided by mirtarbase database.
104
miRTarBase ID miRNA Experiments Reference
MIRT029240 hsa-miR-26b-5p Microarray 19088304
MIRT1534634 hsa-miR-1253 CLIP-seq
MIRT1534635 hsa-miR-1254 CLIP-seq
MIRT1534636 hsa-miR-2110 CLIP-seq
MIRT1534637 hsa-miR-2113 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
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.
Q499Z4
Protein name Zinc finger protein 672
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 14 36 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 42 64 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 163 187 Domain
PF00096 zf-C2H2 199 221 Zinc finger, C2H2 type Domain
PF13894 zf-C2H2_4 227 250 Domain
PF00096 zf-C2H2 255 277 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 283 305 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 311 333 Zinc finger, C2H2 type Domain
PF13894 zf-C2H2_4 339 362 Domain
PF00096 zf-C2H2 367 389 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 396 417 Zinc finger, C2H2 type Domain
Sequence
MFATSGAVAAGKPYSCSECGKSFCYSSVLLRHERAHGGDGRFRCLECGERCARAADLRAH
RRTH
AGQTLYICSECGQSFRHSGRLDLHLGAHRQRCRTCPCRTCGRRFPHLPALLLHRRR
QHLPERPRRCPLCARTFRQSALLFHQARAHPLGTTSDPAAPPHRCAQCPRAFRSGAGLRS
HARIHVS
RSPTRPRVSDAHQCGVCGKCFGKSSTLTRHLQTHSGEKPFKCPECGKGFLESA
TLVRHQRTHT
GEKPYACGDCGRCFSESSTLLRHRRSHQGERPHACATCGKGFGQRSDLVV
HQRIH
TGEKPFACPECGRRFSDRSDLTKHRRTHTGEKPYRCELCGKRFTCVSNLNVHRRN
HA
GHKPHKCPECSKAFSVASKLALHRKTHLGERPAECAECGKCFSHSRSLSQHQRAHTRA
RTAAAVAIQSAVGTALVFEGPAEQEKPGFSVS
Sequence length 452
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OROFACIAL CLEFT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations