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
Orthologs
SpeciesHumanMouse
Entrez

25802

93689

Ensembl

ENSG00000163431

ENSMUSG00000048096

UniProt

P29536

Q8BVA4

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

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

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000163431 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000048096 - Ensembl, 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

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


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