ENSG00000111678


Homo sapiens

Features
Gene ID: ENSG00000111678
  
Biological name :C12orf57
  
Synonyms : C12orf57 / chromosome 12 open reading frame 57 / Q99622
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 12
Strand: 1
Band: p13.31
Gene start: 6942978
Gene end: 6946003
  
Corresponding Affymetrix probe sets: 224719_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000440602
Ensembl peptide - ENSP00000475422
Ensembl peptide - ENSP00000475635
Ensembl peptide - ENSP00000229281
Ensembl peptide - ENSP00000440937
NCBI entrez gene - 113246     See in Manteia.
OMIM - 615140
RefSeq - NM_001301837
RefSeq - NM_001301834
RefSeq - NM_001301836
RefSeq - NM_001301838
RefSeq - NM_138425
RefSeq Peptide - NP_612434
RefSeq Peptide - NP_001288763
RefSeq Peptide - NP_001288765
RefSeq Peptide - NP_001288766
RefSeq Peptide - NP_001288767
swissprot - U3KQ07
swissprot - Q99622
swissprot - F5GXW5
swissprot - U3KQ85
Ensembl - ENSG00000111678
  
Related genetic diseases (OMIM): 218340 - Temtamy syndrome, 218340
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
 grcc10ENSDARG00000030038Danio rerio
 C1H12ORF57ENSGALG00000014555Gallus gallus
 Grcc10ENSMUSG00000072772Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR026317  Protein C10


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0009791 post-embryonic development IMP
 biological_processGO:0014819 regulation of skeletal muscle contraction IMP
 biological_processGO:0021540 corpus callosum morphogenesis IMP
 biological_processGO:0021678 third ventricle development IMP
 biological_processGO:0036343 psychomotor behavior IMP
 biological_processGO:0048593 camera-type eye morphogenesis IMP
 biological_processGO:0050890 cognition IMP
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0016607 nuclear speck IDA
 molecular_functionGO:0003674 molecular_function ND


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000174 Abnormality of palate "Any abnormality of the `palate` (FMA:54549), i.e., of roof of the mouth)." [HPO:probinson]
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 HP:0000179 Prominent lower lip "Increased thickness of the lower lip, leading to a prominent appearance of the lower lip." [HPO:curators]
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 HP:0000256 Macrocephaly "The presence of an abnormally large `skull` (FMA:46565)." [HPO:probinson]
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 HP:0000268 Dolichocephaly 
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 HP:0000276 Long face 
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 HP:0000280 Coarse facial features 
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 HP:0000316 Hypertelorism 
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 HP:0000324 Facial asymmetry 
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 HP:0000343 Long philtrum 
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000369 Low-set ears "Low-set ears are defined to be set below an arbitrary line drawn between the lateral canthus of the eye and the occipital protruberance." [HPO:curators]
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 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]
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 HP:0000444 Beaked nose 
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 HP:0000494 Downward slanting palpebral fissures 
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 HP:0000506 Telecanthus "An abnormally increased distance between the medial canthi (angle between eyelids) of the eyelids." [HPO:curators]
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 HP:0000545 Myopia 
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 HP:0000567 Chorioretinal coloboma 
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 HP:0000568 Microphthalmos "A developmental anomaly characterized by abnormal smallness of one or both eyes." [HPO:curators]
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 HP:0000612 Iris coloboma "A `coloboma` (HP:0000589) of the `iris` (FMA:58235)." [HPO:probinson]
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 HP:0000678 Dental overcrowding 
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 HP:0000685 Hypoplastic teeth 
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 HP:0001083 Ectopia lentis 
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 HP:0001156 Brachydactyly 
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 HP:0001249 Mental retardation 
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 HP:0001256 Mental retardation, mild "Mild mental retardation is defined as an intelligence quotient (IQ) in the range of 50-69." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001274 Agenesis of corpus callosum "Absence of the corpus callosum as a result of the failure of the corpus callosum to develop, which can be the result of a failure in any one of the multiple steps of callosal development including cellular proliferation and migration, axonal growth or glial patterning at the midline." [HPO:curators]
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 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]
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 HP:0001762 Talipes equinovarus "Also called clubfoot typically has 4 main components: inversion and adduction of the forefoot; inversion of the heel and hindfoot; equinus (limitation of extension) of the ankle and subtalar joint; and internal rotation of the leg. Clubfoot is a complex, multifactorial deformity with genetic and intrauterine factors. One popular theory postulates that a clubfoot is a result of intrauterine maldevelopment of the talus that leads to adduction and plantarflexion of the foot. On radiographic projection a clubfoot can be noted as parallel axes of talus and calcaneus." [HPO:curators]
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 HP:0001763 Pes planus "A condition in which the arch of the foot is flat, with the entire sole of the foot being in near-complete contact with the ground." [HPO:curators]
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 HP:0001831 Brachydactyly (feet) 
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 HP:0001885 Brachydactyly (2nd-5th toes) 
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 HP:0002007 Frontal bossing "The presence of an unusually prominent forehead." [HPO:curators]
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 HP:0002119 Ventriculomegaly 
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 HP:0002553 Arched eyebrows 
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 HP:0002827 Dislocated hips 
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 HP:0002970 Genu varum 
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 HP:0003593 Early onset 
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 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]
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 HP:0004942 Aortic aneurysms 
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 HP:0005692 Joint hyperflexibility 
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 HP:0007370 Aplasia/Hypoplasia of the corpus callosum "Absence or underdevelopment of the corpus callosum." [HPO:curators]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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