Entity Details

Primary name ILDR1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ86SU0
EntryNameILDR1_HUMAN
FullNameImmunoglobulin-like domain-containing receptor 1
TaxID9606
Evidenceevidence at protein level
Length546
SequenceStatuscomplete
DateCreated2006-07-11
DateModified2021-06-02

Ontological Relatives

GenesILDR1

GO terms

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GOName
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
GO:0032991 protein-containing complex
GO:0042802 identical protein binding
GO:0061689 tricellular tight junction
GO:0070506 high-density lipoprotein particle receptor activity
GO:0090277 positive regulation of peptide hormone secretion
GO:1990830 cellular response to leukemia inhibitory factor

Subcellular Location

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Subcellular Location
Cell membrane
Cytoplasm

Domains

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DomainNameCategoryType
IPR003599 Immunoglobulin subtypeDomainDomain
IPR008664 LISCH7DomainDomain
IPR036179 Immunoglobulin-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
609646 OMIMDeafness, autosomal recessive, 42 (DFNB42)A prelingual, non-progressive form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry.

Interactions

0 interactions

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