Varaico: Literature-Extracted Genetic Variants

Gene:KERA
Variant:p.E88G

KERA

81 papers

RefSeq Summary

The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).[provided by ...

Pfam Domains

LRRNTaa 41–70UCSCLeucine rich repeat N-terminal domain
LRR_8aa 71–133UCSCLeucine rich repeat
LRR_8aa 142–204UCSCLeucine rich repeat
LRR_6aa 281–303UCSCLeucine Rich repeat

Gene Aliases

HGNC Name

keratocan

HGNC Previous Symbol

CNA2

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
2 papers
NM_007035.4
p.E88G
c.263A>G
Surrounding Variants
1 paper
NM_007035.4
p.P87L
c.260C>T
1 paper
NM_007035.4
p.K89K
c.267G>A
1 paper
NM_007035.4
p.E84K
c.250G>A
1 paper
NM_007035.4
p.I83L
c.247A>T
1 paper
NM_007035.4
p.I83V
c.247A>G
1 paper
NM_007035.4
p.I83L
c.247A>C
1 paper
NM_007035.4
p.A94V
c.281C>T
2 papers
NM_007035.4
p.N81S
c.242A>G
1 paper
NM_007035.4
p.N80insFs
c.239_240insCC
1 paper
NM_007035.4
p.N80insFs
c.238_239insCC
1 paper
NM_007035.4
p.N80ins1
c.238_239insCCA
1 paper
NM_007035.4
p.Q79_N80ins1
c.237_238insCCA
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."