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Lim homeobox 9

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Protein-coding gene in the species Homo sapiens
LHX9
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2DMQ

Identifiers
AliasesLHX9, LIM homeobox 9
External IDsOMIM: 606066; MGI: 1316721; HomoloGene: 7816; GeneCards: LHX9; OMA:LHX9 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)
Chromosome 1 (human)Genomic location for LHX9Genomic location for LHX9
Band1q31.3Start197,911,902 bp
End197,935,478 bp
Gene location (Mouse)
Chromosome 1 (mouse)
Chr.Chromosome 1 (mouse)
Chromosome 1 (mouse)Genomic location for LHX9Genomic location for LHX9
Band1|1 E4Start138,825,186 bp
End138,848,577 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • germinal epithelium

  • testicle

  • left ovary

  • right ovary

  • stromal cell of endometrium

  • ganglionic eminence

  • gonad

  • tendon of biceps brachii

  • right coronary artery

  • buccal mucosa cell
Top expressed in
  • hand

  • habenula

  • Gonadal ridge

  • fossa

  • coelomic epithelium

  • pineal gland

  • abdominal wall

  • medial dorsal nucleus

  • foot

  • inferior colliculi
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

56956

16876

Ensembl

ENSG00000143355

ENSMUSG00000019230

UniProt

Q9NQ69

Q9WUH2

RefSeq (mRNA)

NM_001014434
NM_020204
NM_001370213

NM_001025565
NM_001042577
NM_010714

RefSeq (protein)

NP_001014434
NP_064589
NP_001357142

NP_001020736
NP_001036042
NP_034844

Location (UCSC)Chr 1: 197.91 – 197.94 MbChr 1: 138.83 – 138.85 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

LIM homeobox 9 is a protein that in humans is encoded by the LHX9 gene.

Function

This gene encodes a member of the LIM homeobox gene family of developmentally expressed transcription factors. The encoded protein contains a homeodomain and two cysteine-rich zinc-binding LIM domains involved in protein-protein interactions. The protein is highly similar to a mouse protein that causes gonadal agenesis when inactivated, suggesting a role in gonadal development. Alternative splicing results in multiple transcript variants.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000143355Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000019230Ensembl, 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: LIM homeobox 9".

Further reading

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


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