Varaico: Literature-Extracted Genetic Variants

Gene:MNX1
Variant:p.G98delFs

MNX1

151 papers

RefSeq Summary

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....

Pfam Domains

Homeodomainaa 242–298UCSCHomeodomain

Gene Aliases

HGNC Name

motor neuron and pancreas homeobox 1

HGNC Previous Symbol

HLXB9

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_005515.4
p.G98delFs
c.293delC
Surrounding Variants
1 paper
NM_005515.4
p.G98fs
c.292_293fs
1 paper
NM_005515.4
p.G100fs
c.298_299fs
1 paper
NM_005515.4
p.G100delFs
c.298_299delCC
1 paper
NM_005515.4
p.G102G
c.306C>G
2 papers
NM_005515.4
p.G103R
c.307G>C
1 paper
NM_005515.4
p.G103delFs
c.307delC
2 papers
NM_005515.4
p.C88_A89insFs
c.264_265insC
1 paper
NM_005515.4
p.C88*
c.264C>A
1 paper
NM_005515.4
p.G109E
c.326G>A
1 paper
NM_005515.4
p.G112V
c.335G>T
3 papers
NM_005515.4
p.G112insFs
c.336dupG
1 paper
NM_005515.4
p.P113fs
c.337_338fs
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