CD300LD - CD300 molecule like family member d Gene

Also Known as CLM-4; CLM-5; CD300D; CMRF35A4; CMRF35-A4

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 100131439

About CD300LD

Cytogenetic location: 17q25.1 Genomic coordinates (GRCh38): 17:74,578,643-74,592,283 (from NCBI)

This gene has 1 transcript (splice variant), 80 orthologues and 13 paralogues. Low expression observed in reference dataset.

Summary

Predicted to enable transmembrane signaling receptor activity and virus receptor activity. Predicted to be involved in immune system process. Predicted to act upstream of or within regulation of interleukin-6 production and regulation of tumor necrosis factor production. Predicted to be integral component of membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

CD300LD Products (1)

mRNA Protein Name
NM_001115152.2 NP_001108624.1 CMRF35-like molecule 5 precursor

Gene Ontology

  • Molecular Function
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
21982860 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CD300LD Protein Structure

V-set

V-set: Immunoglobulin V-set domain (21 - 112)

  • 0
  • 100
  • 194 a.a.
Protein Preferred Names Protein Names

CMRF35-like molecule 5

  • CD300 antigen-like family member D

CD300LD Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CD300LD Q6UXZ3 TFF1 Homo sapiens P04155
Protein Array
21982860
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Ectodermal Dysplasia 11a, Hypohidrotic/Hair/Tooth Type, Autosomal Dominant

  • ECTD11A

  • Hed

  • Ectodermal Dysplasia 11a

  • Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant

  • Ectodermal Dysplasia 11a, Hypohidrotic/Hair/Nail Type, Autosomal Dominant

  • Ectodermal Dysplasia Hypohidrotic Autosomal Dominant

  • Dysplasia, Ectodermal, Type 11a, Hypohidrotic/Hair/Tooth, Autosomal Dominant
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS02230 CD300LD Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus CD300LD RGD RGD:2319739
Others CD300LD NCBI