Gene Gene information from NCBI Gene database.
Entrez ID 30832
Gene name Zinc finger protein 354C
Gene symbol ZNF354C
Synonyms (NCBI Gene)
KID3
Chromosome 5
Chromosome location 5q35.3
miRNA miRNA information provided by mirtarbase database.
34
miRTarBase ID miRNA Experiments Reference
MIRT450085 hsa-miR-548l PAR-CLIP 22100165
MIRT450084 hsa-miR-495-3p PAR-CLIP 22100165
MIRT450083 hsa-miR-5688 PAR-CLIP 22100165
MIRT450082 hsa-miR-7-1-3p PAR-CLIP 22100165
MIRT450081 hsa-miR-7-2-3p PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
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:0001227 Function DNA-binding transcription repressor activity, RNA polymerase II-specific IMP 33154469
GO:0001525 Process Angiogenesis IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619511 16736 ENSG00000177932
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86Y25
Protein name Zinc finger protein 354C (Kidney, ischemia, and developmentally-regulated protein 3) (hKID3)
Protein function Transcriptional repressor that inhibits endothelial angiogenic sprouting (PubMed:15555547, PubMed:33154469). Suppresses osteogenic effects of RUNX2 and may be involved in osteoblastic differentiation (By similarity). Plays a role in postnatal my
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 11 52 KRAB box Family
PF00096 zf-C2H2 216 238 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 244 266 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 272 294 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 300 322 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 356 378 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 384 406 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 412 434 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 440 462 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 468 490 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 496 518 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in kidney and skeletal muscle. Very low expression in brain and heart (PubMed:15555547). Strongly expressed in vascular cells such as umbilical vein endothelial cells, microvascular endothelial cells and aortic smooth muscle
Sequence
MAVDLLSAQEPVTFRDVAVFFSQDEWLHLDSAQRALYREVMLENYSSLVSLGIPFSMPKL
IHQLQQGEDPCMVEREVPSDTRLGFKTWLETEALPHRQDIFIEETSQGMVKKESIKDGHW
DINFEEAVEFESEIEEEQEKKPLRQMIDSHEKTISEDGNHTSLELGKSLFTNTALVTQQS
VPIERIPNMYYTFGKDFKQNFDLMKCFQIYPGGKPHICNECGKSFKQNLHLIEHQRIHTG
EKPYKCNECEKTFSHRSSLLSHQRIHTGEKPYKCNECEKAFSNSSTLIKHLRVHTGEKPY
RCRECGKAFSQCSTLTVHQRIH
TGEKLYKCGECEKAFNCRAKLHRHQRIHTGEKPYKCSE
CGKGYSQFTSLAEHQRFH
TGEQLYTCLECGRTFTRIVTLIEHQRIHTGQKPYQCNECEKA
FNQYSSFNEHRKIH
TGEKLYTCEECGKAFGCKSNLYRHQRIHTGEKPYQCNQCGKAFSQY
SFLTEHERIH
TGEKLYKCMECGKAYSYRSNLCRHKKVHTKEKLYKWKEYGKPFICSSSLT
QYQRFFKGDKAYEV
Sequence length 554
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 27809618
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 27458175
★☆☆☆☆
Found in Text Mining only