LCN1 - lipocalin 1 Gene

Homo sapiens

Also known as TP; TLC; PMFA; VEGP

Gene ID: 3933 | Gene type: protein coding

About LCN1

Cytogenetic location: 9q34.3 Genomic coordinates (GRCh38): 9:135,521,440-135,526,540 (from NCBI)

This gene has 2 transcripts (splice variants), 170 orthologues and 12 paralogues. Low expression observed in reference dataset.

Summary

This gene encodes a member of the lipocalin family of small secretory proteins. Lipocalins are extracellular transport proteins that bind to a variety of hydrophobic ligands. The encoded protein is the primary lipid binding protein in tears and is overproduced in response to multiple stimuli including Infection and stress. The encoded protein may be a marker for chromosome aneuploidy as well as an autoantigen in Sjogren's syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and two pseudogenes of this gene are also located on the long arm of chromosome 9. [provided by RefSeq, Nov 2011]

LCN1 Products(4)

mRNA	Protein	Name
NM_001252617.2	NP_001239546.1	lipocalin-1 isoform 1 precursor
NM_001252618.2	NP_001239547.1	lipocalin-1 isoform 2 precursor
NM_001252619.2	NP_001239548.1	lipocalin-1 isoform 3 precursor
NM_002297.4	NP_002288.1	lipocalin-1 isoform 1 precursor

LCN1 Protein Structure

Lipocalin

0
100
176 a.a.

Protein Preferred Names

Protein Names

lipocalin-1

VEG protein

Recombinant LCN1 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P75905	LCN1/Lipocalin-1 Protein, Human (HEK293, His)	P31025 (H19-D176)	≥95%

Related Diseases

Diseases

Alias

Lateral Displacement Of Eye

Lateral Displacement Of Globe

Pleurisy

Kwashiorkor

Kwashiokor	Nutritional Edema With Dyspigmentation Of Skin And Hair
Nutritional Oedema With Dyspigmentation Of Skin And/Or Hair

Ophthalmia Nodosa

Lacrimal Apparatus Disease

Lacrimal Apparatus Diseases

Apperceptive Agnosia

Dry Eye Syndrome

Dry Eye Syndromes	Dry Eye Disease
Tear Film Insufficiency	Xerophthalmia

Filamentary Keratitis

Excessive Tearing

Epiphora	Lacrimal Apparatus Diseases
Excessive Tear Production	Watering Eye

Blepharitis

Cicatricial Entropion

Pulmonary Large Cell Neuroendocrine Carcinoma

Large Cell Lung Neuroendocrine Carcinoma

Conjunctivochalasis

Background Diabetic Retinopathy

Non Proliferative Diabetic Retinopathy	Non-Proliferative Diabetic Retinopathy
Nonproliferative Diabetic Retinopathy

Eyelid Disease

Eyelid Diseases

Eyelid Disorders

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

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS07554	LCN1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	LCN1	RGD	RGD:619872
Others	LCN1	NCBI