1. Gene
  2. LCORL - ligand dependent nuclear receptor corepressor like Gene

LCORL - ligand dependent nuclear receptor corepressor like Gene

Homo sapiens

Also known as MLR1

Gene ID: 254251 | Gene type: protein coding

About LCORL

Cytogenetic location: 4p15.31 Genomic coordinates (GRCh38): 4:17,841,187-18,021,875 (from NCBI)

This gene has 15 transcripts (splice variants), 96 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 2.1), small intestine (RPKM 1.8) and 25 other tissues.

Summary

This gene encodes a transcription factor that appears to function in spermatogenesis. Polymorphisms in this gene are associated with measures of skeletal frame size and adult height. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

LCORL Products(10)

mRNA Protein Name
NM_001166139.2 NP_001159611.1 ligand-dependent nuclear receptor corepressor-like protein isoform 1
NM_001365658.1 NP_001352587.1 ligand-dependent nuclear receptor corepressor-like protein isoform 3
NM_001365659.1 NP_001352588.1 ligand-dependent nuclear receptor corepressor-like protein isoform 3
NM_001365660.1 NP_001352589.1 ligand-dependent nuclear receptor corepressor-like protein isoform 4
NM_001365661.1 NP_001352590.1 ligand-dependent nuclear receptor corepressor-like protein isoform 5
NM_001365662.1 NP_001352591.1 ligand-dependent nuclear receptor corepressor-like protein isoform 6
NM_001365663.1 NP_001352592.1 ligand-dependent nuclear receptor corepressor-like protein isoform 7
NM_001365665.1 NP_001352594.1 ligand-dependent nuclear receptor corepressor-like protein isoform 8
NM_001394446.1 NP_001381375.1 ligand-dependent nuclear receptor corepressor-like protein isoform 9
NM_153686.8 NP_710153.2 ligand-dependent nuclear receptor corepressor-like protein isoform 2

LCORL Protein Structure

HTH_psq

HTH_psq: helix-turn-helix, Psq domain (527 - 570)

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  • 602 a.a.
Protein Preferred Names Protein Names

ligand-dependent nuclear receptor corepressor-like protein

LCOR-like protein

Related Diseases

Diseases Alias
Croup

Acute Obstructive Laryngitis

Laryngotracheobronchitis

Acute Laryngotracheobronchitis

Croup Syndrome

Acute Laryngitis With Obstruction

Obstructive Laryngitis

Obstructive Laryngitis Nos

Obstructive Laryngotracheitis Nos

Acromesomelic Dysplasia 2b

Fibular Hypoplasia And Complex Brachydactyly

Du Pan Syndrome

AMD2B

Dupans

Acromesomelic Dysplasia-2b

Fibular Aplasia-Complex Brachydactyly Syndrome

Acromesomelic Dysplasia

Acromesomelic Dwarfism

Dysplasia, Acromesomelic

Acromesomelic Dysplasia Hunter-Thompson Type

Osteochondrosis

Osteochondritis

Apophysitis

Epiphysitis

Osteochondritis Juvenilis

Epiphyseal Necrosis

Juvenile Osteochondrosis Of Tibial Tubercle

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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus LCORL RGD RGD:1561241
Felis catus LCORL VGNC VGNC:78520
Mus musculus LCORL MGD MGI:2651932
Canis familiaris LCORL VGNC VGNC:59023
Macaca mulatta LCORL VGNC VGNC:106624
Bos taurus LCORL VGNC VGNC:30816