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This gene encodes a member of the immunoglobulin superfamily. The encoded protein is a ligand of the T lymphocyte CD2 protein, and functions in adhesion and activation of T lymphocytes. The protein is localized to the plasma membrane. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009]
CD58 (CD58 Molecule) is a Protein Coding gene. Diseases associated with CD58 include Oral Lichen Planus and Paroxysmal Nocturnal Hemoglobinuria. Among its related pathways are Cell surface interactions at the vascular wall and Response to elevated platelet cytosolic Ca2+. Gene Ontology (GO) annotations related to this gene include signaling receptor binding.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005102 | signaling receptor binding | IPI | 17344209 |
GO:0005515 | protein binding | IPI | 7544493 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005886 | plasma membrane | TAS | -- |
GO:0005887 | integral component of plasma membrane | NAS | 7544493 |
GO:0009986 | cell surface | IBA,IDA | 15345303 |
GO:0016020 | membrane | IEA,HDA | 19946888 |
GO:0016021 | integral component of membrane | IEA | -- |
SuperPathway | Contained pathways | ||
---|---|---|---|
1 | Innate Immune System |
.61
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2 | Cell adhesion molecules | ||
3 | Measles | ||
4 | Cell surface interactions at the vascular wall | ||
5 | Response to elevated platelet cytosolic Ca2+ |
.44
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GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0032757 | positive regulation of interleukin-8 production | IMP | 19109405 |
GO:0034113 | heterotypic cell-cell adhesion | IDA | 15345303 |
GO:0043312 | neutrophil degranulation | TAS | -- |
GO:0050900 | leukocyte migration | TAS | -- |
GO:0071346 | cellular response to interferon-gamma | IDA | 19109405 |
ExUns: | 1a | · | 1b | · | 1c | ^ | 2a | · | 2b | ^ | 3 | ^ | 4a | · | 4b | ^ | 5a | · | 5b | ^ | 6 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | - | ||||||||||||||||||||
SP2: | - | - | |||||||||||||||||||
SP3: | |||||||||||||||||||||
SP4: | - | - | - |
This gene was present in the common ancestor of mammals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | CD58 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | CD58 30 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | CD58 31 |
|
OneToOne |
SNP ID | Clinical significance and condition | Chr 01 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
rs17426456 | - |
p.Ser15Gly |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
esv1003883 | CNV | deletion | 20482838 |
esv2209199 | CNV | deletion | 18987734 |
esv2512482 | CNV | deletion | 19546169 |
esv2663968 | CNV | deletion | 23128226 |
esv2716607 | CNV | deletion | 23290073 |
esv3303707 | CNV | mobile element insertion | 20981092 |
esv3433 | CNV | loss | 18987735 |
esv3434570 | CNV | insertion | 20981092 |
esv3539978 | CNV | deletion | 23714750 |
esv7455 | CNV | loss | 19470904 |
Disorder | Aliases | PubMed IDs |
---|---|---|
oral lichen planus |
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paroxysmal nocturnal hemoglobinuria |
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psoriatic arthritis |
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actinic prurigo |
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hemoglobinuria |
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