Varaico: Literature-Extracted Genetic Variants

Gene:CC2D2A
Variant:p.L1550L

CC2D2A

366 papers

RefSeq Summary

This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert synd...

Pfam Domains

DUF5523aa 131–383UCSCFamily of unknown function (DUF5523)
CC2D2AN-C2aa 645–819UCSCCC2D2A N-terminal C2 domain
CEPT76_peptidaseaa 1349–1465UCSCCEP76 peptidase-like domain
CEP76_Caa 1489–1618UCSCCentrosomal protein of 76 kDa C-terminal domain

Gene Aliases

HGNC Name

coiled-coil and C2 domain containing 2A

HGNC Alias Symbols

KIAA1345; MKS6; JBTS9

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_001378615.1
p.L1550L
c.4650G>T
Surrounding Variants
5 papers
NM_001378615.1
p.L1551P
c.4652T>C
1 paper
NM_001378615.1
p.K1552delFs
c.4656delA
1 paper
NM_001378615.1
p.K1552fs
c.4654_4655fs
18 papers
NM_001378615.1
p.D1556V
c.4667A>T
1 paper
NM_001378615.1
p.R1558_F1559Splc
c.4674+3A>G
1 paper
NM_001378615.1
p.E1540K
c.4618G>A
2 papers
NM_001378615.1
p.L1534V
c.4600T>G
2 papers
NM_001378615.1
p.L1533P
c.4598T>C
9 papers
NM_001378615.1
p.R1528H
c.4583G>A
7 papers
NM_001378615.1
p.R1528C
c.4582C>T
3 papers
NM_001378615.1
p.R1528fs
c.4582_4583fs
3 papers
NM_001378615.1
p.R1528delFs
c.4582_4583delCG
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