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Leiomodin 1

From Wikipedia, the free encyclopedia

LMOD1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLMOD1, 1D, 64kD, D1, SM-LMOD, SMLMOD, leiomodin 1, MMIHS3
External IDsOMIM: 602715; MGI: 2135671; HomoloGene: 8118; GeneCards: LMOD1; OMA:LMOD1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012134

NM_053106

RefSeq (protein)

NP_036266

NP_444336

Location (UCSC)Chr 1: 201.9 – 201.95 MbChr 1: 135.25 – 135.3 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Leiomodin 1 is a protein that in humans is encoded by the LMOD1 gene.[5]

Function

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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].

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000163431Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000048096Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Leiomodin 1". Retrieved 2018-03-12.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.