| Name |
|---|
METTL11B Genemethyltransferase like 11B Enables N-terminal protein N-methyltransferase activity. Involved in N-terminal protein amino acid methylation. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
CDK11B Genecyclin-dependent kinase 11B This gene encodes a member of the serine/threonine protein kinase family. Members of this kinase family are known to be essential for eukaryotic cell cycle control. Due to a segmental duplication, this gene shares very high sequence identity with a neighboring gene. These two genes are frequently deleted or altered in neuroblastoma. The protein kinase encoded by this gene can be cleaved by caspases and may play a role in cell apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014] |
ZDHHC11B Genezinc finger, DHHC-type containing 11B Predicted to enable protein-cysteine S-palmitoyltransferase activity. Predicted to be involved in several processes, including antiviral innate immune response; peptidyl-L-cysteine S-palmitoylation; and positive regulation of defense response to virus by host. Predicted to be located in endosome membrane. Predicted to be active in Golgi apparatus and endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
SPAG11B Genesperm associated antigen 11B This gene encodes several androgen-dependent, epididymis-specific secretory proteins. The specific functions of these proteins have not been determined, but they are thought to be involved in sperm maturation. Some of the isoforms contain regions of similarity to beta-defensins, a family of antimicrobial peptides. The gene is located on chromosome 8p23 near the defensin gene cluster. Alternative splicing of this gene results in seven transcript variants encoding different isoforms. Two different N-terminal and five different C-terminal protein sequences are encoded by the splice variants. Two additional variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008] |
ZC3H11B Genezinc finger CCCH-type containing 11B pseudogene Predicted to enable metal ion binding activity. Predicted to be involved in poly(A)+ mRNA export from nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ARHGAP11B GeneRho GTPase activating protein 11B Predicted to enable GTPase activator activity. Involved in cerebral cortex development and negative regulation of mitochondrial membrane permeability. Acts upstream of with a positive effect on glutamine catabolic process. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD11B Genesmall nucleolar RNA, C/D box 11B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ATP11B GeneATPase, class VI, type 11B P-type ATPases, such as ATP11B, are phosphorylated in their intermediate state and drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily transports heavy metal ions, such as Cu(2+) or Cd(2+). Another subfamily transports non-heavy metal ions, such as H(+), Na(+), K(+), or Ca(+). A third subfamily transports amphipaths, such as phosphatidylserine.[supplied by OMIM, Feb 2005] |
TMPRSS11B Genetransmembrane protease, serine 11B Enables serine-type peptidase activity. Predicted to be involved in proteolysis. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA11B Genesmall nucleolar RNA, H/ACA box 11B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
BCL11B GeneB-cell CLL/lymphoma 11B (zinc finger protein) This gene encodes a C2H2-type zinc finger protein and is closely related to BCL11A, a gene whose translocation may be associated with B-cell malignancies. Although the specific function of this gene has not been determined, the encoded protein is known to be a transcriptional repressor, and is regulated by the NURD nucleosome remodeling and histone deacetylase complex. Four alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2013] |
TNFRSF11B Genetumor necrosis factor receptor superfamily, member 11b The protein encoded by this gene is a member of the TNF-receptor superfamily. This protein is an osteoblast-secreted decoy receptor that functions as a negative regulator of bone resorption. This protein specifically binds to its ligand, osteoprotegerin ligand, both of which are key extracellular regulators of osteoclast development. Studies of the mouse counterpart also suggest that this protein and its ligand play a role in lymph-node organogenesis and vascular calcification. Alternatively spliced transcript variants of this gene have been reported, but their full length nature has not been determined. [provided by RefSeq, Jul 2008] |
LOC124906741 Genesperm-associated antigen 11B-like |
11b-Hydroxyprogesterone Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 11b-Hydroxyprogesterone metabolite from the curated HMDB Metabolites of Enzymes dataset. |
(1S,6BR,9AS,11R,11BR)-9A,11B-DIMETHYL-1-[(METHYLOXY)METHYL]-3,6,9-TRIOXO-1,6,6B,7,8,9,9A,10,11,11B-DECAHYDRO-3H-FURO[4,3,2-DE]INDENO[4,5-H][2]BENZOPYRAN-11-YL ACETATE Gene Setinteracting proteins for the (1S,6BR,9AS,11R,11BR)-9A,11B-DIMETHYL-1-[(METHYLOXY)METHYL]-3,6,9-TRIOXO-1,6,6B,7,8,9,9A,10,11,11B-DECAHYDRO-3H-FURO[4,3,2-DE]INDENO[4,5-H][2]BENZOPYRAN-11-YL ACETATE drug from the curated DrugBank Drug Targets dataset. |
Peroxisome biogenesis disorder 11B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 11B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
(3b,5b,7a,12a)-7,12-dihydroxy-3-(2-((4-((11b,17b)-17-hydroxy-3-oxo-17-prop-1-ynylestra-4,9-dien-11-yl) phenyl)(methyl)amino)ethoxy)cholan-24-oic acid Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical (3b,5b,7a,12a)-7,12-dihydroxy-3-(2-((4-((11b,17b)-17-hydroxy-3-oxo-17-prop-1-ynylestra-4,9-dien-11-yl) phenyl)(methyl)amino)ethoxy)cholan-24-oic acid from the curated CTD Gene-Chemical Interactions dataset. |
2H-Benzo(a)quinolizin-2-ol, 2-Ethyl-1,3,4,6,7,11b-hexahydro-3-isobutyl-9,10-dimethoxy- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 2H-Benzo(a)quinolizin-2-ol, 2-Ethyl-1,3,4,6,7,11b-hexahydro-3-isobutyl-9,10-dimethoxy- from the curated CTD Gene-Chemical Interactions dataset. |
(6AR,11AS,11BR)-10-ACETYL-9-HYDROXY-7,7-DIMETHYL-2,6,6A,7,11A,11B-HEXAHYDRO-11H-PYRROLO[1',2':2,3]ISOINDOLO[4,5,6-CD]INDOL-11-ONE Gene Setinteracting proteins for the (6AR,11AS,11BR)-10-ACETYL-9-HYDROXY-7,7-DIMETHYL-2,6,6A,7,11A,11B-HEXAHYDRO-11H-PYRROLO[1',2':2,3]ISOINDOLO[4,5,6-CD]INDOL-11-ONE drug from the curated DrugBank Drug Targets dataset. |
11b,21-Dihydroxy-5b-pregnane-3,20-dione Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 11b,21-Dihydroxy-5b-pregnane-3,20-dione metabolite from the curated HMDB Metabolites of Enzymes dataset. |
3a,11b,21-Trihydroxy-20-oxo-5b-pregnan-18-al Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 3a,11b,21-Trihydroxy-20-oxo-5b-pregnan-18-al metabolite from the curated HMDB Metabolites of Enzymes dataset. |
11b-PGF2a Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 11b-PGF2a metabolite from the curated HMDB Metabolites of Enzymes dataset. |
11b,17a,21-Trihydroxypreg-nenolone Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 11b,17a,21-Trihydroxypreg-nenolone metabolite from the curated HMDB Metabolites of Enzymes dataset. |
1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene metabolite from the curated HMDB Metabolites of Enzymes dataset. |
11b-Hydroxyandrost-4-ene-3,17-dione Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 11b-Hydroxyandrost-4-ene-3,17-dione metabolite from the curated HMDB Metabolites of Enzymes dataset. |
11b,21-Dihydroxy-3,20-oxo-5b-pregnan-18-al Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 11b,21-Dihydroxy-3,20-oxo-5b-pregnan-18-al metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Tumour necrosis factor receptor 11B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumour necrosis factor receptor 11B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
peroxisome biogenesis disorder 11b Gene SetFrom OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 11b phenotype from the curated OMIM Gene-Disease Associations dataset. |
Prostate adenocarcinoma_PRAD_TCGA-CH-5767-11B-01R-1789-07 Gene SetFrom TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Prostate adenocarcinoma_PRAD_TCGA-CH-5767-11B-01R-1789-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset. |
increased tumor necrosis factor receptor superfamily member 11b level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased tumor necrosis factor receptor superfamily member 11b level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Immunodeficiency 11B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunodeficiency 11B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ectodermal dysplasia 11B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ectodermal dysplasia 11B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
UM-SCC-11B cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue UM-SCC-11B cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Immunodeficiency 11b Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency 11b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fragile site 11b Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fragile site 11b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
RGS4 INHIBITOR 11B Gene Setinteracting proteins for the RGS4 INHIBITOR 11B drug from theDGIdb Drug Targets 2026 dataset. |