DLX1

Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia

Homeobox protein DLX-1 is a protein that in humans is encoded by the DLX1 gene.[5][6]

AliasesDLX1, Dlx, Dlx-1, distal-less homeobox 1
End172,089,677 bp[1]
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DLX1
Identifiers
AliasesDLX1, Dlx, Dlx-1, distal-less homeobox 1
External IDsOMIM: 600029; MGI: 94901; HomoloGene: 22558; GeneCards: DLX1; OMA:DLX1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001038493
NM_178120

NM_010053

RefSeq (protein)

NP_001033582
NP_835221

NP_034183

Location (UCSC)Chr 2: 172.08 – 172.09 MbChr 2: 71.36 – 71.36 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of a homeobox transcription factor gene family similar to the Drosophila distal-less gene. The encoded protein is localized to the nucleus where it may function as a transcriptional regulator of signals from multiple TGF-β superfamily members. The encoded protein may play a role in the control of craniofacial patterning and the differentiation and survival of inhibitory neurons in the forebrain. This gene is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 2. Alternatively spliced transcript variants encoding different isoforms have been described.[6]

References

Further reading

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