1. Gene
  2. LMOD1 - leiomodin 1 Gene

LMOD1 - leiomodin 1 Gene

Homo sapiens

Also known as 1D; D1; 64kD; MMIHS3; SMLMOD; SM-LMOD

Gene ID: 25802 | Gene type: protein coding

About LMOD1

Cytogenetic location: 1q32.1 Genomic coordinates (GRCh38): 1:201,896,456-201,946,548 (from NCBI)

This gene has 2 transcripts (splice variants), 222 orthologues, 6 paralogues and is associated with 2 phenotypes. Broad expression in endometrium (RPKM 75.4), prostate (RPKM 68.0) and 18 other tissues.

Summary

The leiomodin 1 protein has a putative membrane-spanning region and 2 types of tandemly repeated blocks. The transcript is expressed in all tissues tested, with the highest levels in thyroid, eye muscle, skeletal muscle, and ovary. Increased expression of leiomodin 1 may be linked to Graves' disease and thyroid-associated ophthalmopathy. [provided by RefSeq, Jul 2008]

LMOD1 Products(1)

mRNA Protein Name
NM_012134.3 NP_036266.2 leiomodin-1

LMOD1 Protein Structure

Tropomodulin

Tropomodulin: Tropomodulin (2 - 86)

WH2

WH2: WH2 motif (573 - 597)

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Protein Preferred Names Protein Names

leiomodin-1

64 kDa autoantigen 1D

Related Diseases

Diseases Alias
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 3

MMIHS3

Visceral Myopathy 1

Visceral Myopathy

Megaduodenum And/Or Megacystis

VSCM1

Pseudoobstruction, Idiopathic Intestinal

Vscm

Pseudoobstruction Idiopathic Intestinal

Visceral Myopathy Familial

Berdon Syndrome

Idiopathic Intestinal Pseudoobstruction

Infantile Visceral Myopathy

Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome

Mmih

Megacystis Microcolon Intestinal Hypoperistalsis Syndrome

Intestinal Pseudo-Obstruction

Visceral Neuropathy, Familial, Autosomal Dominant

Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 1

Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome

Berdon Syndrome

MMIHS

Megacystis Microcolon Intestinal Hypoperistalsis Syndrome

Megacystis, Microcolon, Hypoperistalsis Syndrome

Visceral Myopathy

Mmih Syndrome

Megacystis-Microcolon-Intestinal Hypoperistalsis-Hydronephrosis Syndrome

MMIHS1

Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome, Mmih

Mmhs

Microcolon
Graves' Disease

Graves Disease

Exophthalmic Goiter

Basedow'S Disease

Grave'S Disease

Basedow Disease

Toxic Diffuse Goiter

Graves' Hyperthyroidism

Parry Disease

Autoimmune Hyperthyroidism

Toxic Multinodular Goiter

Intestinal Pseudo-Obstruction

Chronic Intestinal Pseudoobstruction

Chronic Intestinal Pseudo-Obstruction

Cipo

Neuronal Intestinal Dysplasia

Hollow Visceral Myopathy

Familial Visceral Neuropathy

Paralytic Ileus

Intestinal Pseudoobstruction

Chronic Idiopathic Intestinal Pseudo-Obstruction

Ciip

Congenital Short Bowel Syndrome

Enteric Neuropathy

Familial Visceral Myopathy

Ipo

Pseudo-Obstruction Of Intestine

Pseudointestinal Obstruction Syndrome

Pseudoobstructive Syndrome

Congenital Idiopathic Intestinal Pseudoobstruction

Visceral Myopathy, Familial

Graves Ophthalmopathy

Graves Orbitopathy

Thyroid Associated Ophthalmopathy

Thyroid Eye Disease

Thyroid-Associated Ophthalmopathy

Hyperthyroidism

Overactive Thyroid

Hydronephrosis

Stricture Of Ureteropelvic Junction With Hydronephrosis

Hydronephrosis With Ureteral Stricture, Not Elsewhere Classified

Eye Disease

Eye Diseases

Abnormality Of The Eye

Toxoplasma Oculopathy

Autoimmune Epilepsy
Coronary Restenosis
Prune Belly Syndrome

Eagle-Barrett Syndrome

Abdominal Muscle Deficiency Syndrome

PBS

Abdominal Muscles, Absence Of, With Urinary Tract Abnormality And Cryptorchidism

Egbrs

Eagle-Barret Syndrome

Urethral Obstruction Sequence

Obrinsky Syndrome

Triad Syndrome

Obrisnksy Syndrome

Euos

Early Urethral Obstruction Sequence

Renal Dysplasia Or Hydronephrosis, Oligohydramnios And Subsequent Lung Hypoplasia Due To Urethral Obstruction

Absence Of Abdominal Muscles With Urinary Tract Abnormality And Cryptorchidism

Abdomen Muscle Deficiency Syndrome

Abdomen Muscular Deficiency Syndrome

Abdominal Muscular Deficiency Syndrome

Abdominal Muscle Aplasia Syndrome

Hashimoto Thyroiditis

Autoimmune Thyroiditis

Hashimoto Struma

Hashimoto'S Thyroiditis

Chronic Lymphocytic Thyroiditis

Lymphocytic Thyroiditis

Hashimoto Disease

Ht

Hashimoto'S Disease

Hashimoto'S Syndrome

Hypothyroidism, Autoimmune

Autoimmune Chronic Lymphocytic Thyroiditis

Chronic Lymphocytic Thyroiditides

Hashimoto Syndrome

Hashimotos Thyroiditis

Hashimoto Thyroiditis, Susceptibility To

Thyroiditis, Autoimmune

Lymphomatous Thyroiditis

Lymphoid Thyroiditis

Chronic Lymphadenoid Thyroiditis

Autoimmune Lymphocytic Chronic Thyroiditis

Goitre Lymphomatosa

Hashitoxicosis

Hashimoto Hypothyroidism

Lymphadenoid Goitre

Struma Lymphomatosa

Hyperthyroidism With Hashimoto Disease

Hashimoto Thyrotoxicosis

Thyrotoxicosis Due To Hashimoto Thyroiditis

Struma Lymphomatosis

Lymphadenoid Struma

Myopathy

Muscular Diseases

Myopathies

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 LMOD1 RGD RGD:1307236
Mus musculus LMOD1 MGD MGI:2135671
Bos taurus LMOD1 VGNC VGNC:30938
Macaca mulatta LMOD1 VGNC VGNC:74434
Felis catus LMOD1 VGNC VGNC:68074
Canis familiaris LMOD1 VGNC VGNC:53619