Varaico: Literature-Extracted Genetic Variants

Gene:NDN
Variant:p.K284*

NDN

80 papers

RefSeq Summary

This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein e...

Pfam Domains

MAGEaa 157–273UCSCMAGE homology domain

Gene Aliases

HGNC Name

necdin, MAGE family member

HGNC Alias Symbols

HsT16328; PWCR

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_002487.3
p.K284*
c.850A>T
Surrounding Variants
1 paper
NM_002487.3
p.K284T
c.851A>C
3 papers
NM_002487.3
p.D286delFs
c.856delC
1 paper
NM_002487.3
p.D286D
c.858C>T
2 papers
NM_002487.3
p.A280P
c.838G>C
1 paper
NM_002487.3
p.L279L
c.835C>T
1 paper
NM_002487.3
p.F278Y
c.833T>A
1 paper
NM_002487.3
p.M276V
c.826A>G
1 paper
NM_002487.3
p.T271N
c.812C>A
1 paper
NM_002487.3
p.E269K
c.805G>A
1 paper
NM_002487.3
p.R265R
c.795G>T
1 paper
NM_002487.3
p.R265W
c.793C>T
1 paper
NM_002487.3
p.R305W
c.913C>T
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