Protein family
The protein has not catalytic activity
Protein sequence
Protein function
Catalytic activity
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0000076 | DNA replication checkpoint signaling |
Biological Process | GO:0071163 | DNA replication preinitiation complex assembly |
Biological Process | GO:0051315 | attachment of mitotic spindle microtubules to kinetochore |
Biological Process | GO:0051301 | cell division |
Biological Process | GO:0000278 | mitotic cell cycle |
Biological Process | GO:2000104 | negative regulation of DNA-templated DNA replication |
Biological Process | GO:0045786 | negative regulation of cell cycle |
Biological Process | GO:0045740 | positive regulation of DNA replication |
Biological Process | GO:2000105 | positive regulation of DNA-templated DNA replication |
Biological Process | GO:0035563 | positive regulation of chromatin binding |
Biological Process | GO:1902595 | regulation of DNA replication origin binding |
Biological Process | GO:0030174 | regulation of DNA-templated DNA replication initiation |
Biological Process | GO:0033262 | regulation of nuclear cell cycle DNA replication |
Biological Process | GO:0072708 | response to sorbitol |
Molecular Function | GO:0003677 | DNA binding |
Molecular Function | GO:0070182 | DNA polymerase binding |
Molecular Function | GO:0003682 | chromatin binding |
Cellular Component | GO:0000776 | kinetochore |
Cellular Component | GO:0016604 | nuclear body |
Cellular Component | GO:0005654 | nucleoplasm |
Cellular Component | GO:0005634 | nucleus |
InterPro | InterPro name |
---|---|
IPR014939 | CDT1 Geminin-binding domain-like |
IPR032054 | DNA replication factor Cdt1, C-terminal |
IPR036390 | Winged helix DNA-binding domain superfamily |
IPR038090 | DNA replication factor Cdt1, C-terminal WH domain superfamily |
IPR045173 | DNA replication factor Cdt1 |
Pfam | Pfam name |
---|---|
PF08839 | DNA replication factor CDT1 like |
PF16679 | DNA replication factor Cdt1 C-terminal domain |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-68867 | Assembly of the pre-replicative complex | Internal node | R-HSA-69306 | DNA Replication |
R-HSA-68949 | Orc1 removal from chromatin | Leaf | R-HSA-69306 | DNA Replication |
R-HSA-68962 | Activation of the pre-replicative complex | Leaf | R-HSA-69306 | DNA Replication |
R-HSA-69052 | Switching of origins to a post-replicative state | Internal node | R-HSA-69306 | DNA Replication |
R-HSA-69205 | G1/S-Specific Transcription | Leaf | R-HSA-1640170 | Cell Cycle |
Location | ECO term | Pubmed |
---|---|---|
Chromosome, centromere, kinetochore | ECO:0000269 | PubMed:22581055 |
Nucleus | ECO:0000269 | PubMed:11125146 |
Nucleus | ECO:0000269 | PubMed:26842564 |
HPO ID | HPO name |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000028 | Cryptorchidism |
HP:0000039 | Epispadias |
HP:0000047 | Hypospadias |
HP:0000059 | Hypoplastic labia majora |
HP:0000060 | Clitoral hypoplasia |
HP:0000064 | Hypoplastic labia minora |
HP:0000160 | Narrow mouth |
HP:0000175 | Cleft palate |
HP:0000176 | Submucous cleft hard palate |
HP:0000179 | Thick lower lip vermilion |
HP:0000193 | Bifid uvula |
HP:0000252 | Microcephaly |
HP:0000278 | Retrognathia |
HP:0000327 | Hypoplasia of the maxilla |
HP:0000347 | Micrognathia |
HP:0000356 | Abnormality of the outer ear |
HP:0000358 | Posteriorly rotated ears |
HP:0000365 | Hearing impairment |
HP:0000369 | Low-set ears |
HP:0000413 | Atresia of the external auditory canal |
HP:0000772 | Abnormal rib morphology |
HP:0000895 | Lateral clavicle hook |
HP:0001249 | Intellectual disability |
HP:0001263 | Global developmental delay |
HP:0001328 | Specific learning disability |
HP:0001363 | Craniosynostosis |
HP:0001508 | Failure to thrive |
HP:0001510 | Growth delay |
HP:0001511 | Intrauterine growth retardation |
HP:0002094 | Dyspnea |
HP:0002097 | Emphysema |
HP:0002098 | Respiratory distress |
HP:0002705 | High, narrow palate |
HP:0002750 | Delayed skeletal maturation |
HP:0002816 | Genu recurvatum |
HP:0002878 | Respiratory failure |
HP:0003042 | Elbow dislocation |
HP:0003100 | Slender long bone |
HP:0003187 | Breast hypoplasia |
HP:0003510 | Severe short stature |
HP:0003561 | Birth length less than 3rd percentile |
HP:0003577 | Congenital onset |
HP:0004209 | Clinodactyly of the 5th finger |
HP:0004322 | Short stature |
HP:0005692 | Joint hyperflexibility |
HP:0005930 | Abnormal epiphysis morphology |
HP:0006443 | Patellar aplasia |
HP:0006660 | Aplastic clavicle |
HP:0008551 | Microtia |
HP:0008665 | Clitoral hypertrophy |
HP:0008736 | Hypoplasia of penis |
HP:0009892 | Anotia |
HP:0009939 | Mandibular aplasia |
HP:0011267 | Microtia, third degree |
HP:0011968 | Feeding difficulties |
HP:0012471 | Thick vermilion border |
HP:0100490 | Camptodactyly of finger |
HP:0100783 | Breast aplasia |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
meier-gorlin syndrome 4 | MONDO:0013431 | Q87 | chapter17, Congenital malformations, deformations and chromosomal abnormalities | OMIM:613804 |