Gene Gene information from NCBI Gene database.
Entrez ID 7582
Gene name Zinc finger protein 33B
Gene symbol ZNF33B
Synonyms (NCBI Gene)
KOX2KOX31ZNF11B
Chromosome 10
Chromosome location 10q11.21
Summary This gene encodes a member of the zinc finger family of proteins. This gene shows decreased expression in cumulus cells derived from patients undergoing controlled ovarian stimulation. This gene is present in a gene cluster with several related zinc finge
miRNA miRNA information provided by mirtarbase database.
340
miRTarBase ID miRNA Experiments Reference
MIRT1522746 hsa-miR-101 CLIP-seq
MIRT1522747 hsa-miR-105 CLIP-seq
MIRT1522748 hsa-miR-1246 CLIP-seq
MIRT1522749 hsa-miR-1265 CLIP-seq
MIRT1522750 hsa-miR-1273f CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 25416956
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0006355 Process Regulation of DNA-templated transcription IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
194522 13097 ENSG00000196693
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q06732
Protein name Zinc finger protein 33B (Zinc finger protein 11B) (Zinc finger protein KOX2)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 11 52 KRAB box Family
PF00096 zf-C2H2 329 351 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 357 379 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 385 407 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 413 435 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 441 463 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 469 491 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 497 519 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 525 547 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 553 575 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 581 603 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 609 631 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 637 659 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 665 687 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 693 715 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 721 743 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 749 771 Zinc finger, C2H2 type Domain
Sequence
MNKVDQKFQGSVSFKDVTVGFTQEEWQHLDPSQRALYRDVMLENYSNLVSVGYCAHKPEV
IFRLEQGEEPWRLEEEFPSQSFPEVWTADHLKERSQENQSKHLWEVVFINNEMLTKEQGN
VIGIPFNMDVSSFPSRKMFCQYDSRGMSFNTVSELVISKINYLGKKSDEFNACGKLLLNI
KHDETHTREKNEVLKNRNTLSHRENTLQHEKIQTLDHNFEYSICQETLLEKAVFNTRKRE
NAEENNCDYNEFGRTFCDSSSLLFHQIPPSKDSHYEFSDCEKFLCVKSTLSKHDGVPVKH
YDCGESGNNFRRKLCLSQLQKGDKGEKHFECNECGKAFWEKSHLTRHQRVHTGEKHFQCN
QCGKTFWEKSNLTKHQRSH
TGEKPFECNECGKAFSHKSALTLHQRTHTGEKPYQCNACGK
TFYQKSDLTKHQRTH
TGQKPYECYECGKSFCMNSHLTVHQRTHTGEKPFECLECGKSFCQ
KSHLTQHQRTH
IGDKPYECNACGKTFYHKSVLTRHQIIHTGLKPYECYECGKTFCLKSDL
TIHQRTH
TGEKPFACPECGKFFSHKSTLSQHYRTHTGEKPYECHECGKIFYNKSYLTKHN
RTH
TGEKPYECNECGKTFCQKSQLTQHQRIHIGEKPYECNECGKAFCHKSALIVHQRTHT
QEKPYKCNECGKSFCVKSGLILHERKHTGEKPYECNECGKSFSHKSSLTVHHRAHTGEKS
CQCNECGKIFYRKSDLAKHQRSHTGEKPYECNTCRKTFSQKSNLIVHQRTHIGEKPYE
Sequence length 778
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.).
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Asthma Associate 35953101
★☆☆☆☆
Found in Text Mining only
Ige Responsiveness Atopic Associate 35953101
★☆☆☆☆
Found in Text Mining only