LMO7

LMO7
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
Aliases LMO7, FBX20, FBXO20, LOMP, LIM domain 7
External IDs MGI: 1353586 HomoloGene: 83924 GeneCards: LMO7
Genetically Related Diseases
type 1 diabetes mellitus[1]
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

4008

380928

Ensembl

ENSG00000136153

ENSMUSG00000033060

UniProt

Q8WWI1

n/a

RefSeq (mRNA)

NM_001306080
NM_005358
NM_015842
NM_015843

NM_201529

RefSeq (protein)

NP_001293009.1
NP_005349.3
NP_056667.2
NP_001293009.1

n/a

Location (UCSC) Chr 13: 75.62 – 75.86 Mb Chr 14: 101.73 – 101.93 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

LIM domain only protein 7 is a protein that in humans is encoded by the LMO7 gene.[4][5][6]

This gene encodes a protein containing a calponin homology (CH) domain, a PDZ domain, and a LIM domain. An F-box (FBX) domain is present in alternative splice variants. Members of the LIM protein family carry the LIM domain, a unique cysteine-rich zinc-binding domain. Members of the FBX protein family are involved in protein-protein interactions. The encoded protein may be involved in protein-protein interactions. Multiple alternative splice variants have been described but their full-length sequences have not been determined.[6]

References

  1. "Diseases that are genetically associated with LMO7 view/edit references on wikidata".
  2. "Human PubMed Reference:".
  3. "Mouse PubMed Reference:".
  4. Putilina T, Jaworski C, Gentleman S, McDonald B, Kadiri M, Wong P (Dec 1998). "Analysis of a human cDNA containing a tissue-specific alternatively spliced LIM domain". Biochem Biophys Res Commun. 252 (2): 433–9. doi:10.1006/bbrc.1998.9656. PMID 9826547.
  5. Cenciarelli C, Chiaur DS, Guardavaccaro D, Parks W, Vidal M, Pagano M (Dec 1999). "Identification of a family of human F-box proteins". Curr Biol. 9 (20): 1177–9. doi:10.1016/S0960-9822(00)80020-2. PMID 10531035.
  6. 1 2 "Entrez Gene: LMO7 LIM domain 7".

Further reading


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