ENSG00000262919


Homo sapiens

Features
Gene ID: ENSG00000262919
  
Biological name :CCNQ
  
Synonyms : CCNQ / cyclin Q / Q8N1B3
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: -1
Band: q28
Gene start: 153587919
Gene end: 153600045
  
Corresponding Affymetrix probe sets: 226466_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000466345
Ensembl peptide - ENSP00000478747
Ensembl peptide - ENSP00000484506
Ensembl peptide - ENSP00000484108
Ensembl peptide - ENSP00000483391
Ensembl peptide - ENSP00000481634
Ensembl peptide - ENSP00000402949
Ensembl peptide - ENSP00000412865
Ensembl peptide - ENSP00000461135
NCBI entrez gene - 92002     See in Manteia.
OMIM - 300708
RefSeq - XM_011531215
RefSeq - NM_001130997
RefSeq - NM_152274
RefSeq - XM_005277920
RefSeq - XM_005277921
RefSeq - XM_011531214
RefSeq Peptide - NP_689487
RefSeq Peptide - NP_001124469
swissprot - A0A087X0G9
swissprot - A0A087WY98
swissprot - A0A087WUL6
swissprot - H7C3N1
swissprot - Q8N1B3
swissprot - K7EM37
swissprot - A0A087X1W3
Ensembl - ENSG00000262919
  
Related genetic diseases (OMIM): 300707 - STAR syndrome, 300707
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 ccnqENSDARG00000037537Danio rerio
 Fam58bENSMUSG00000049489Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
CCNL1 / Q9UK58 / cyclin L1ENSG0000016366028
CCNL2 / Q96S94 / cyclin L2ENSG0000022197827
CCNK / O75909 / cyclin KENSG0000009006125
CCNT2 / O60583 / cyclin T2ENSG0000008225823
CCNT1 / O60563 / cyclin T1ENSG0000012931521
CCNC / P24863 / cyclin CENSG0000011223721


Protein motifs (from Interpro)
Interpro ID Name
 IPR006671  Cyclin, N-terminal
 IPR013763  Cyclin-like
 IPR028759  Cyclin-related protein FAM58
 IPR036915  Cyclin-like superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0045737 positive regulation of cyclin-dependent protein serine/threonine kinase activity IBA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IBA
 biological_processGO:1901409 positive regulation of phosphorylation of RNA polymerase II C-terminal domain IBA
 cellular_componentGO:0000307 cyclin-dependent protein kinase holoenzyme complex IBA
 cellular_componentGO:0005634 nucleus IBA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0016538 cyclin-dependent protein serine/threonine kinase regulator activity IBA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000066 Labial hypoplasia 
Show

 HP:0000076 Vesicoureteral reflux "Abnormal (retrograde) movement of urine from the bladder into ureters or kidneys related to inadequacy of the valvular mechanism at the ureterovesicular junction or other causes." [HPO:curators]
Show

 HP:0000083 Renal failure 
Show

 HP:0000085 Horseshoe kidney 
Show

 HP:0000086 Ectopic kidney "A developmental defect in which a kidney is located in an abnormal anatomic position." [HPO:curators]
Show

 HP:0000104 Renal agenesis 
Show

 HP:0000125 Pelvic kidney "A developmental defect in which a kidney is located in an abnormal anatomic position within the pelvis." [HPO:curators]
Show

 HP:0000143 Rectovaginal fistula "The presence of a fistula between the rectum and the vagina." [HPO:curators]
Show

 HP:0000219 Thin upper lip 
Show

 HP:0000377 Abnormal form of ears "Abnormal form of the out part of the ear (also referred to as the auricle or pinna)." [HPO:curators]
Show

 HP:0000394 Lop ears "The term lop ear refers to excessive protrusion of the ear from the side of the head, that is, the external ear stands away from the head at a greater than normal angle (Normal angle of the auricle to the median plane averages 25 degrees in boys and 18 degrees in girls). Lop ears are usually larger than normal ears." [HPO:curators]
Show

 HP:0000414 Bulbous nose 
Show

 HP:0000431 Broad nasal bridge "Increased horizontal dimension of the upper, bony part of the nose." [HPO:curators]
Show

 HP:0000455 Broad nasal tip 
Show

 HP:0000460 Narrow nose 
Show

 HP:0000506 Telecanthus "An abnormally increased distance between the medial canthi (angle between eyelids) of the eyelids." [HPO:curators]
Show

 HP:0000545 Myopia 
Show

 HP:0000625 Eyelid, cleft "A short discontinuity of the margin of the lower or upper eyelid." [pmid:19125427]
Show

 HP:0000813 Bicornuate uterus 
Show

 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
Show

 HP:0001363 Craniosynostosis "Craniosynostosis refers to the premature closure of the cranial sutures. Primary craniosynostosis refers to the closure of one or more sutures due to abnormalities in skull development, and secondary craniosynostosis results from failure of brain growth." [HPO:curators]
Show

 HP:0001423 X-linked dominant inheritance "A mode of inheritance that is observed for dominant traits related to a gene encoded on the X chromosome. In the context of medical genetics, X-linked dominant disorders tend to manifest very severely in affected males. The severity of manifestation in females may depend on the degree of skewed X inactivation." [HPO:curators]
Show

 HP:0001511 Intrauterine growth retardation 
Show

 HP:0001518 Low birth weight 
Show

 HP:0001647 Bicuspid aortic valve "The presence of a bicuspid `aortic valve` (FMA:7236)." [HPO:probinson]
Show

 HP:0001659 Aortic insufficiency "An insufficiency of the aortic valve, leading to regurgitation (backward flow) of blood from the aorta into the left ventricle." [HPO:curators]
Show

 HP:0001671 Abnormality of the cardiac septa 
Show

 HP:0001770 Toe syndactyly "Webbing or fusion of the toes, involving soft parts only or including bone structure. Bony fusions are revered to as "bony" Syndactyly if the fusion occurs in a radio-ulnar axis. Fusions of bones of the toes in a proximo-distal axis are refered to as "Symphalangism"." [HPO:curators]
Show

 HP:0002023 Anal atresia "Congenital absence of the anus, i.e., the opening at the bottom end of the intestinal tract." [HPO:curators]
Show

 HP:0002025 Anal stenosis "Abnormal narrowing of the anal opening." [HPO:curators]
Show

 HP:0002984 Hypoplasia of the radius "Underdevelopment of the radius." [HPO:curators]
Show

 HP:0003396 Syringomyelia 
Show

 HP:0004209 Clinodactyly of the 5th finger "Clinodactyly refers to a bending or curvature of the `fifth finger` (FMA:24949) in the radial direction (i.e., towards the 4th finger)." [HPO:curators]
Show

 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
Show

 HP:0004415 Pulmonary artery stenosis 
Show

 HP:0004969 peripheral pulmonary artery stenosis 
Show

 HP:0007754 Macular dystrophy 
Show

 HP:0008665 Hypertrophic clitoris 
Show

 HP:0011560 Mitral atresia "A congenital defect with failure to open of the mitral valve orifice." [DDD:dbrown]
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr