MNX1
Sign in to saveAlso known as HB9, HLXB9, HOXHB9, SCRA1, motor neuron and pancreas homeobox 1
Motor neuron and pancreas homeobox 1 (MNX1), also known as Homeobox HB9 (HLXB9), is a human protein encoded by the MNX1 gene.
Gene data
MNX1- Name
- motor neuron and pancreas homeobox 1
- Type
- protein-coding
- Aliases
- HB9, HLXB9, HOXHB9, SCRA1
This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009].
via MyGene.info
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 21137
- exact match
- identifiers.org/ncbigene/3110
- genomic end
- 157010663
- genomic start
- 156786745
- cytogenetic location
- 7q36.3
via Wikidata · CC0
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Article
4 sectionsContents
- Clinical significance
- References
- Further reading
- External links
Motor neuron and pancreas homeobox 1 (MNX1), also known as Homeobox HB9 (HLXB9), is a human protein encoded by the MNX1 gene.
== Clinical significance ==
Connections
Q180686
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human chromosome 7
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homeobox
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Ensembl genome database project
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PDX1
Gene
protein
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Wikidata
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gene
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chromosome
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public domain
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digital object identifier
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bibcode
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human genome
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Q229883
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base pair
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Medical Subject Headings
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locus
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gene expression
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Online Mendelian Inheritance in Man
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United States National Library of Medicine
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