Version: 8.1.0Date: Fri Apr 18 2025
Category
Comp
(Rattus norvegicus)Gene
Name: cartilage oligomeric matrix protein
Synonyms: Not Available
Source: RGD:2378
Biotype: protein coding gene
Symbol: Comp (Rno)
Symbol: Comp
Gene Synopsis: Orthologous to human COMP (cartilage oligomeric matrix protein); PARTICIPATES IN cell-extracellular matrix
Automated Gene Synopsis: Orthologous to human COMP (cartilage oligomeric matrix protein).
Strict Orthology Symbols: comp
Comp
(Mus musculus)Gene
Name: cartilage oligomeric matrix protein
Synonyms: TSP5, thrombospondin-5
Source: MGI:88469
Biotype: protein coding gene
Symbol: Comp (Mmu)
Symbol: Comp
Automated Gene Synopsis: Orthologous to human COMP (cartilage oligomeric matrix protein).
Strict Orthology Symbols: comp
Alleles: Comp
COMP
(Homo sapiens)Gene
Name: cartilage oligomeric matrix protein
Synonyms: EDM1, TSP5, cartilage oligomeric matrix protein (pseudoachondroplasia, epiphyseal dysplasia 1, multiple), pseudoachondroplasia (epiphyseal dysplasia 1, multiple), MED, PSACH, CTS2, THBS5, MGC149768, cartilage oligomeric matrix protein(pseudoachondroplasia, epiphyseal dysplasia 1, multiple), MGC131819, EPD1, thrombospondin-5, multiple epiphyseal dysplasia, TSP-5
Source: HGNC:2227
Biotype: protein coding gene
Symbol: COMP (Hsa)
Symbol: COMP
Strict Orthology Symbols: comp
comp
(Danio rerio)Gene
Name: cartilage oligomeric matrix protein
Synonyms: thbs5, Tsp-4b, thrombospondin 5, im:7154332, wu:fb78h09
Source: ZFIN:ZDB-GENE-060606-1
Biotype: protein coding gene
Symbol: comp (Dre)
Symbol: comp
Automated Gene Synopsis: Orthologous to human COMP (cartilage oligomeric matrix protein).
Strict Orthology Symbols: comp
comp
(Xenopus tropicalis)Gene
Name: cartilage oligomeric matrix protein
Synonyms: comp, thbs5, psach, cartilage oligomeric matrix protein, epd1, edm1, med
Source: Xenbase:XB-GENE-994160
Biotype: gene
Symbol: comp
Symbol: comp (Xtr)
Automated Gene Synopsis: Orthologous to human COMP (cartilage oligomeric matrix protein).
Synonyms: comp...comp...comp
Strict Orthology Symbols: comp
comp.L
(Xenopus laevis)Gene
Name: cartilage oligomeric matrix protein
Synonyms: comp.L, psach, thbs5, cartilage oligomeric matrix protein, epd1, edm1, med
Source: Xenbase:XB-GENE-17333742
Biotype: gene
Symbol: comp.L (Xla)
Automated Gene Synopsis: Orthologous to human COMP (cartilage oligomeric matrix protein).
Strict Orthology Symbols: comp
Symbol: comp.L
comp.S
(Xenopus laevis)Gene
Name: cartilage oligomeric matrix protein
Synonyms: thbs5, psach, cartilage oligomeric matrix protein, epd1, comp.S, edm1, med
Source: Xenbase:XB-GENE-6486400
Biotype: gene
Symbol: comp.S (Xla)
Automated Gene Synopsis: Orthologous to human COMP (cartilage oligomeric matrix protein).
Strict Orthology Symbols: comp
Symbol: comp.S
comp-1
(Caenorhabditis elegans)Gene
Name: sperm COMPetition 1
Synonyms: CELE_F37E3.3, F37E3.3
Source: WB:WBGene00018158
Biotype: protein coding gene
Symbol: comp-1 (Cel)
Symbol: comp-1
compas
(Mus musculus)Gene
Name: compass
Synonyms: Not Available
Source: MGI:3522284
Biotype: heritable phenotypic marker
Symbol: compas (Mmu)
Alleles: compas (Mmu)
Symbol: compas
compressed
(Drosophila melanogaster)Gene
Name: compressed
Synonyms: com
Source: FB:FBgn0000344
Biotype: gene
Symbol: compressed (Dme)
Alleles: compressed<1> (Dme)
Symbol: compressed
compas
(Mus musculus)Allele/Variant
Source: MGI:3522304
Genes: compas (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: compas (Mmu)
Genes: compas (Mmu)
Symbol: compas
Comptm1Aol
(Mus musculus)Allele/Variant
Source: MGI:2180787
Genes: Comp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Comp
Genes: Comp (Mmu)
Symbol: Comptm1Aol
Compem1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7297306
Genes: Comp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Comp
Genes: Comp (Mmu)
Symbol: Compem1Gpt
Compem2Bgao
(Mus musculus)Allele/Variant
Source: MGI:7411334
Genes: Comp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Comp
Genes: Comp (Mmu)
Symbol: Compem2Bgao
compressed1
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0001753
Genes: compressed (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: compressed<1> (Dme)
Genes: compressed (Dme)
Symbol: compressed1
Compem2Cya
(Mus musculus)Allele/Variant
Source: MGI:7792814
Genes: Comp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Comp
Genes: Comp (Mmu)
Symbol: Compem2Cya
Compem1Cya
(Mus musculus)Allele/Variant
Source: MGI:7792812
Genes: Comp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Comp
Genes: Comp (Mmu)
Symbol: Compem1Cya
Compem3Cya
(Mus musculus)Allele/Variant
Source: MGI:7792813
Genes: Comp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Comp
Genes: Comp (Mmu)
Symbol: Compem3Cya
Model
Id: MGI:3758815
Synonyms: Not Available
Symbol: Comp/Comp<+> [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 (Mmu)
Genes: Comp (Mmu)
Alleles: Comp
Name: Comp/Comp<+> [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Model
Id: MGI:5763182
Synonyms: Not Available
Symbol: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ (Mmu)
Genes: Comp (Mmu)
Alleles: Comp
Name: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ
Model
Id: MGI:3037836
Synonyms: Not Available
Symbol: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 (Mmu)
Genes: Comp (Mmu)
Alleles: Comp
Name: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6
compas/compas [background:] C57BL/6J-compas
(Mus musculus)Model
Id: MGI:3522343
Synonyms: Not Available
Symbol: compas/compas [background:] C57BL/6J-compas (Mmu)
Genes: compas (Mmu)
Alleles: compas (Mmu)
Model
Id: MGI:5550572
Synonyms: Not Available
Symbol: Comp/Comp<+> [background:] involves: 129S1/Sv * 129X1/SvJ (Mmu)
Genes: Comp (Mmu)
Alleles: Comp
Name: Comp/Comp<+> [background:] involves: 129S1/Sv * 129X1/SvJ
Model
Id: MGI:5550573
Synonyms: Not Available
Symbol: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ (Mmu)
Genes: Comp (Mmu)
Alleles: Comp
Name: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ
Model
Id: MGI:4417874
Synonyms: Not Available
Symbol: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ (Mmu)
Genes: Comp (Mmu)
Alleles: Comp
Name: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ
Id: MGI:3758814
Synonyms: Not Available
Symbol: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 (Mmu)
Genes: Comp (Mmu)
Alleles: Comp
Name: Comp/Comp [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6
compzf3751/+ (KOLN)
(Danio rerio)Model
Id: ZFIN:ZDB-FISH-240325-24
Synonyms: Not Available
Symbol: comp
Genes: comp (Dre)
Name: comp (KOLN)
compzf3751/zf3751 (KOLN)
(Danio rerio)Model
Id: ZFIN:ZDB-FISH-240325-23
Synonyms: Not Available
Symbol: comp
Genes: comp (Dre)
Name: comp (KOLN)
Source: DOID:0060298
Definition: A complement deficiency that is characterized by recurrent bacterial infections, caused by C4B deficiency.
Symbol: complement component 4b deficiency
Source: DOID:0090137
Definition: A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta 3 class III (TUBB3) gene on chromosome 16q24.3.
Symbol: complex cortical dysplasia with other brain malformations 1
Source: DOID:0060297
Definition: A complement deficiency that is characterized by recurrent bacterial infections, caused by C4A deficiency.
Symbol: complement component 4a deficiency
Source: DOID:0080298
Definition: A lipodystrophy that is characterized by complete loss of adipose tissue.
Symbol: complete generalized lipodystrophy
Source: DOID:0080101
Definition: A congenital myopathy that has_material_basis_in homozygous mutation in the CNTN1 gene on chromosome 12q12 and that is characterized antenatally, by fetal akinesia, intrauterine growth restriction and polyhydramnios, and, following birth, by severe neonatal hypotonia, severe generalized skeletal, bulbar and respiratory muscle weakness, multiple flexion contractures, and normal creatine kinase serum levels.
Symbol: Compton-North congenital myopathy
Source: DOID:0050419
Definition: A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.
Symbol: complement factor I deficiency
Source: DOID:8158
Definition: A complement deficiency that is characterized by susceptibility to recurrent bacterial infections especially to infections of enveloped organisms, and has_material_basis_in mutation in the complement component 5 (C5) gene on chromosome 9q33.2 that encodes the fifth component of complenent, a part of the innate immune system.
Symbol: complement component 5 deficiency
Source: DOID:8354
Definition: A complement deficiency that is characterized by deficiency of complement component 3 that increases susceptibility to infection and autoimmune diseases and has_material_basis_in autosomal recessive inheritance of mutation in the C3 gene on chromosome 19p13.3, has_symptom recurrent bacterial infections.
Symbol: complement component 3 deficiency
Source: DOID:0090134
Definition: A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the kinesin family member 2A (KIF2A) gene on chromosome 5q12.
Symbol: complex cortical dysplasia with other brain malformations 3
Disease
Source: DOID:10031
Definition: A pulmonary emphysema that is characterized by overinflation of part of a lung in response to either removal by surgery of another part of the lung or deceased size of another part of the lung.
Symbol: compensatory emphysema
Disease
Source: DOID:626
Definition: A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation.
Symbol: complement deficiency
Source: DOID:0090138
Definition: A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin gamma 1 gene on chromosome 17q21.
Symbol: complex cortical dysplasia with other brain malformations 4
Source: DOID:0090135
Definition: A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta 2A class IIa (TUBB2A) gene on chromosome 6p25.
Symbol: complex cortical dysplasia with other brain malformations 5
Source: DOID:3223
Definition: Not Available
Symbol: complex regional pain syndrome
Disease
Source: DOID:5820
Definition: A lymphoma that begins in cells of the immune system in which different types of lymphoma cells occur at the same time.
Symbol: composite lymphoma
Disease
Source: DOID:0111719
Definition: An isolated cryptophthalmia characterized by failure of formation of the lid folds and globe results in skin extending from the brow to the cheek without identifiable adnexal structures and often the presence of a vestigial ocular structure or cyst within the socket.
Symbol: complete cryptophthalmia
Gene Ontology
Source: GO:0001856
Synonyms: Not Available
Branch: molecular function
Symbol: complement component C5a binding
Gene Ontology
Source: GO:0001752
Synonyms: Not Available
Branch: biological process
Symbol: compound eye photoreceptor fate commitment
Gene Ontology
Source: GO:0001751
Synonyms: Not Available
Branch: biological process
Symbol: compound eye photoreceptor cell differentiation
Gene Ontology
Source: GO:0001855
Synonyms: Not Available
Branch: molecular function
Symbol: complement component C4b binding
Gene Ontology
Source: GO:0004875
Synonyms:
- anaphylatoxin receptor activity
Branch: molecular function
Symbol: complement receptor activity