Table 1. Summary of GUCA1A gene known and novel mutations.
Nucleotide change | Exon | Protein change | Region | ExAC | PPhen2 HDIV | PPhen2 HVAR | SIFT | Prov | Mut. taster | Clin. | Ref. |
---|---|---|---|---|---|---|---|---|---|---|---|
c.149C>T |
3 |
p.Pro50Leu |
EF1-EF2 link |
121/121,374 |
BEN |
BEN |
TOL |
DEL |
DIS |
COD, CORD |
[29] |
c.250C>T |
4 |
p.Leu84Phe |
EF2 helix F |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
COD, CORD, MD |
[36] |
c.265G>A |
4 |
p.Glu89Lys |
EF2-EF3 link |
0 |
POS |
BEN |
DAM |
DEL |
DIS |
COD, MD |
[27] |
c.296A>G |
4 |
p.Tyr99Cys |
EF3 helix E |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
COD, CORD, MD |
[33,37] |
c.299A>G |
4 |
p.Asp100Gly |
EF3 loop, Ca2+ binding |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
CORD, MD |
[38] |
c.300T>A |
4 |
p.Asp100Glu |
EF3 loop, Ca2+ binding |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
COD |
[27] |
c.302_304delTAG |
4 |
p.Val101del |
EF3 loop |
0 |
N.A. |
N.A. |
N.A. |
DEL |
DIS |
MD |
Present study |
c.304G>C |
4 |
p.Asp102His |
EF3 loop, Ca2+ binding |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
CORD |
[41] |
c.312C>A |
4 |
p.Asn104Lys |
EF3 loop, Ca2+ binding |
0 |
PRO |
POS |
DAM |
DEL |
DIS |
COD |
[42] |
c.320T>C |
4 |
p.Ile107Thr |
EF3 loop |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
COD, CORD, MD |
[36] |
c.341C>T |
4 |
p.Thr114Ile |
EF3 helix F |
5/121,228 |
BEN |
BEN |
TOL |
NEU |
POL |
Atypical RP |
[30] |
c.428delTinsACAC |
5 |
p.Ile143delinsAsnThr |
EF4 helix E |
0 |
N.A. |
N.A. |
N.A. |
DEL |
POL |
COD |
[30] |
c.444T>A |
5 |
p.Asp148Glu |
EF4 loop |
0 |
POS |
POS |
TOL |
DEL |
DIS |
COD |
Present study |
c.451C>T |
6 |
p.Leu151Phe |
EF4 loop |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
COD |
[27,34] |
c.464A>G |
6 |
p.Glu155Gly |
EF4 loop, Ca2+ binding |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
COD |
[35] |
c.464A>C |
6 |
p.Glu155Ala |
EF4 loop, Ca2+ binding |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
CORD |
[43] |
c.476G>T |
6 |
p.Gly159Val |
EF4 helix F |
0 |
PRO |
PRO |
DAM |
DEL |
DIS |
COD, CORD |
[27] |
c.526C>T | 6 | p.Leu176Phe | C-ter | 0 | PRO | PRO | TOL | NEU | DIS | MD | [39] |
EF, helix E - loop - helix F; Ca2+-binding domain; C-ter, carboxy terminal; ExAC, Exome Aggregation Consortium; COD, cone dystrophy; CORD, cone-rod dystrophy; MD, macular dystrophy; PPhen2, PolyPhen2, POS for possibly damaging, PRO for probably damaging, BEN for benign; SIFT, TOL for tolerated, DAM for damaging Prov; PROVEAN (Prediction with cutoff= -2.5), DEL for deleterious, NEU for neutral; Mut. taster, Mutation taster, POL for Polymorphism and DIS for Disease Causing; N.A., Not applicable; Clin, clinical diagnosis; Ref, reference.s