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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 (Leiomodin 1) is a Protein Coding gene. Diseases associated with LMOD1 include Visceral Myopathy and Graves' Disease. Among its related pathways are Cardiac conduction and Smooth Muscle Contraction. Gene Ontology (GO) annotations related to this gene include actin binding and tropomyosin binding. An important paralog of this gene is LMOD2.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0003779 | actin binding | IEA | -- |
GO:0005523 | tropomyosin binding | IBA,IEA | 21873635 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005737 | cytoplasm | IEA | -- |
GO:0005829 | cytosol | IDA,TAS | -- |
GO:0005856 | cytoskeleton | IEA | -- |
GO:0005865 | striated muscle thin filament | IBA | 21873635 |
GO:0005884 | actin filament | ISS,IEA | -- |
SuperPathway | Contained pathways | ||
---|---|---|---|
1 | Cardiac conduction | ||
2 | Smooth Muscle Contraction |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006936 | muscle contraction | TAS,IEA | -- |
GO:0030239 | myofibril assembly | IBA | 21873635 |
GO:0030838 | positive regulation of actin filament polymerization | IDA | 26370058 |
GO:0045010 | actin nucleation | IDA | 26370058 |
GO:0051694 | pointed-end actin filament capping | IEA | -- |
Name | Status | Disease Links | Group | Role | Mechanism of Action | Clinical Trials |
---|
Name | Synonyms | Role | CAS Number | PubChem IDs | PubMed IDs |
---|
ExUns: | 1a | · | 1b | · | 1c | ^ | 2a | · | 2b |
---|---|---|---|---|---|---|---|---|---|
SP1: | |||||||||
SP2: | - |
This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
chimpanzee (Pan troglodytes) |
Mammalia | LMOD1 33 32 |
|
OneToOne | |
oppossum (Monodelphis domestica) |
Mammalia | LMOD1 33 |
|
OneToOne | |
mouse (Mus musculus) |
Mammalia | Lmod1 17 33 32 |
|
||
rat (Rattus norvegicus) |
Mammalia | Lmod1 32 |
|
||
cow (Bos Taurus) |
Mammalia | LMOD1 33 32 |
|
OneToOne | |
dog (Canis familiaris) |
Mammalia | LMOD1 32 |
|
||
platypus (Ornithorhynchus anatinus) |
Mammalia | LMOD1 33 |
|
OneToOne | |
chicken (Gallus gallus) |
Aves | LMOD1 33 32 |
|
OneToOne | |
lizard (Anolis carolinensis) |
Reptilia | LMOD1 33 |
|
OneToOne | |
tropical clawed frog (Silurana tropicalis) |
Amphibia | lmod1 32 |
|
||
zebrafish (Danio rerio) |
Actinopterygii | CR628365.1 33 |
|
OneToMany | |
lmod1 33 |
|
OneToMany | |||
fruit fly (Drosophila melanogaster) |
Insecta | tmod 33 |
|
OneToMany | |
worm (Caenorhabditis elegans) |
Secernentea | unc-94 33 |
|
ManyToMany | |
tmd-2 33 |
|
ManyToMany | |||
sea squirt (Ciona savignyi) |
Ascidiacea | -- 33 |
|
ManyToMany | |
-- 33 |
|
ManyToMany |
SNP ID | Clin | Chr 01 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
rs777696417 | pathogenic, Visceral myopathy | 201,899,905(-) | G/A/C | coding_sequence_variant, missense_variant, stop_gained | |
rs1000071324 | -- | 201,913,362(-) | T/C | intron_variant | |
rs1000129425 | -- | 201,919,991(-) | G/A | intron_variant | |
rs1000146966 | -- | 201,933,691(-) | G/C | intron_variant | |
rs1000184121 | -- | 201,930,511(-) | A/C | intron_variant |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
nsv1122442 | CNV | deletion | 24896259 |
nsv1144423 | CNV | deletion | 24896259 |
nsv1144424 | CNV | deletion | 24896259 |
nsv1145394 | CNV | deletion | 24896259 |
nsv4088 | CNV | insertion | 18451855 |
nsv521567 | CNV | loss | 19592680 |
Disorder | Aliases | PubMed IDs |
---|---|---|
visceral myopathy |
|
|
graves' disease |
|
|
leukodystrophy, hypomyelinating, 13 |
|
|
leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism |
|
|
cardiomyopathy, familial hypertrophic, 6 |
|
|