Mus musculus

7 known processes

Ccnh

cyclin H

(Aliases: 6330408H09Rik,AI661354,AV102684,AW538719)

Ccnh biological process predictions


Filter by process size:
Biological processGO term IDProcess sizeProbabilityFunc Analog Org
dna metabolic processGO:00062593030.080
divalent inorganic cation transportGO:00725111780.034
histone modificationGO:00165701590.030
cellular ketone metabolic processGO:0042180840.023
cellular amino acid metabolic processGO:00065201030.021
muscle system processGO:00030121410.020
anatomical structure homeostasisGO:00602491450.019
transmembrane receptor protein serine threonine kinase signaling pathwayGO:00071781940.019
dna repairGO:00062811070.019
maintenance of locationGO:0051235890.019
positive regulation of nervous system developmentGO:00519622210.017
divalent metal ion transportGO:00708381720.017
organophosphate catabolic processGO:00464342320.017
multicellular organismal homeostasisGO:00488711640.017
lymphocyte mediated immunityGO:00024491390.017
organic cyclic compound catabolic processGO:19013612950.016
mitochondrial respiratory chain complex assemblyGO:003310820.016
regulation of cellular amino acid metabolic processGO:000652150.016
purine nucleotide metabolic processGO:00061633020.016
transmembrane transportGO:00550854120.015
negative regulation of molecular functionGO:00440922580.015
connective tissue developmentGO:00614481790.014
purine nucleoside triphosphate metabolic processGO:00091442260.014
regulation of cellular amine metabolic processGO:0033238200.014
macromolecule catabolic processGO:00090572810.014
glycosyl compound metabolic processGO:19016572460.014
nucleoside phosphate metabolic processGO:00067533380.013
negative regulation of cell proliferationGO:00082852960.013
regulation of cellular ketone metabolic processGO:0010565660.013
regulation of cell cycleGO:00517262810.013
rna processingGO:00063961050.013
double strand break repairGO:0006302480.013
cytoplasmic transportGO:00164822340.013
regulation of cellular catabolic processGO:00313292420.013
amine metabolic processGO:0009308450.012
cellular amine metabolic processGO:0044106440.012
purine containing compound catabolic processGO:00725232130.012
purine nucleotide catabolic processGO:00061952110.012
positive regulation of cell developmentGO:00107202370.012
striated muscle tissue developmentGO:00147062930.012
cellular protein complex assemblyGO:00436231160.012
cation transportGO:00068123990.012
microtubule cytoskeleton organizationGO:00002261570.012
protein localization to membraneGO:00726571080.011
leukocyte mediated immunityGO:00024431740.011
protein catabolic processGO:00301632210.011
tissue homeostasisGO:00018941150.011
covalent chromatin modificationGO:00165691630.011
immune effector processGO:00022523210.011
cellular homeostasisGO:00197252400.011
positive regulation of cellular amine metabolic processGO:003324050.011
peptidyl amino acid modificationGO:00181933360.011
trna aminoacylationGO:004303910.011
nucleotide metabolic processGO:00091173320.011
ribonucleotide metabolic processGO:00092592910.010
regulation of transmembrane receptor protein serine threonine kinase signaling pathwayGO:00900921120.010
purine containing compound metabolic processGO:00725213110.010
ribonucleoside triphosphate metabolic processGO:00091992200.010
heterocycle catabolic processGO:00467002800.010
g protein coupled receptor signaling pathwayGO:00071862430.010
cation transmembrane transportGO:00986552660.010
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domainsGO:00024601450.010
protein localization to organelleGO:00333651850.010
response to growth factorGO:00708481980.010
gene silencingGO:0016458380.010
response to transforming growth factor betaGO:0071559880.010

Ccnh disease predictions

Disease predictions are made from cross-annotation of human disease genes to the identified functional analogs in mouse and predicted with the mouse functional network.

DiseaseDO term IDSizeProbabilityFunc Analog Org
eye diseaseDOID:561400.020
nervous system diseaseDOID:86300.020
eye and adnexa diseaseDOID:149200.020
disease of anatomical entityDOID:700.020
sensory system diseaseDOID:005015500.020
retinal degenerationDOID:846600.020
retinal diseaseDOID:567900.020