Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alms1 |
C |
A |
6: 85,644,945 (GRCm39) |
|
probably benign |
Het |
Bcorl1 |
T |
A |
X: 47,459,884 (GRCm39) |
M1139K |
probably benign |
Het |
C2cd3 |
T |
C |
7: 100,039,373 (GRCm39) |
S191P |
probably benign |
Het |
Cdc27 |
T |
C |
11: 104,398,026 (GRCm39) |
E778G |
probably damaging |
Het |
Col3a1 |
G |
A |
1: 45,377,913 (GRCm39) |
|
probably benign |
Het |
Cubn |
C |
T |
2: 13,338,319 (GRCm39) |
V2350I |
probably benign |
Het |
Dhodh |
G |
A |
8: 110,330,107 (GRCm39) |
R86* |
probably null |
Het |
Dnhd1 |
C |
T |
7: 105,343,968 (GRCm39) |
Q1771* |
probably null |
Het |
Dpt |
A |
C |
1: 164,624,500 (GRCm39) |
E67A |
probably damaging |
Het |
Eif2ak2 |
A |
G |
17: 79,166,068 (GRCm39) |
|
probably benign |
Het |
Exo1 |
A |
G |
1: 175,733,536 (GRCm39) |
K787E |
possibly damaging |
Het |
Fancm |
T |
C |
12: 65,122,546 (GRCm39) |
S23P |
probably benign |
Het |
Fmn1 |
A |
G |
2: 113,194,693 (GRCm39) |
E131G |
unknown |
Het |
Gm5612 |
A |
T |
9: 18,339,149 (GRCm39) |
|
probably benign |
Het |
Hormad2 |
T |
G |
11: 4,374,302 (GRCm39) |
Q88P |
probably damaging |
Het |
Immp2l |
T |
A |
12: 41,160,846 (GRCm39) |
L48* |
probably null |
Het |
Kcne4 |
C |
T |
1: 78,795,688 (GRCm39) |
A112V |
possibly damaging |
Het |
Lamb1 |
C |
T |
12: 31,337,528 (GRCm39) |
R372C |
probably damaging |
Het |
Lrrc30 |
A |
G |
17: 67,939,175 (GRCm39) |
L135P |
probably damaging |
Het |
Ltn1 |
A |
T |
16: 87,213,103 (GRCm39) |
V486D |
probably damaging |
Het |
Mab21l3 |
C |
A |
3: 101,730,847 (GRCm39) |
V131F |
probably damaging |
Het |
Map3k4 |
A |
T |
17: 12,475,668 (GRCm39) |
F809Y |
probably damaging |
Het |
Mki67 |
T |
A |
7: 135,309,204 (GRCm39) |
T416S |
probably benign |
Het |
Mlst8 |
A |
T |
17: 24,697,099 (GRCm39) |
M56K |
probably benign |
Het |
Mmp9 |
A |
G |
2: 164,791,310 (GRCm39) |
Y160C |
probably damaging |
Het |
Mslnl |
A |
G |
17: 25,965,155 (GRCm39) |
Y507C |
probably damaging |
Het |
Myl12a |
A |
T |
17: 71,301,737 (GRCm39) |
M130K |
probably benign |
Het |
Myrfl |
A |
G |
10: 116,658,770 (GRCm39) |
F396L |
probably damaging |
Het |
Nalf2 |
A |
G |
X: 98,889,109 (GRCm39) |
I325V |
probably benign |
Het |
Ncf2 |
A |
G |
1: 152,701,698 (GRCm39) |
|
probably benign |
Het |
Nlrp9c |
T |
A |
7: 26,084,707 (GRCm39) |
I291F |
probably benign |
Het |
Nrp1 |
T |
A |
8: 129,224,569 (GRCm39) |
Y777* |
probably null |
Het |
Ogdh |
T |
C |
11: 6,299,462 (GRCm39) |
V776A |
probably damaging |
Het |
Pcdh17 |
T |
A |
14: 84,684,062 (GRCm39) |
D176E |
probably damaging |
Het |
Plg |
G |
T |
17: 12,622,096 (GRCm39) |
S472I |
possibly damaging |
Het |
Pnlip |
A |
G |
19: 58,669,191 (GRCm39) |
T397A |
probably benign |
Het |
Rbfox3 |
T |
A |
11: 118,387,283 (GRCm39) |
Q277L |
possibly damaging |
Het |
Senp7 |
T |
A |
16: 56,008,640 (GRCm39) |
W1007R |
probably damaging |
Het |
Stap2 |
A |
T |
17: 56,304,511 (GRCm39) |
W374R |
probably benign |
Het |
Szt2 |
A |
G |
4: 118,251,217 (GRCm39) |
V297A |
probably benign |
Het |
Thada |
A |
T |
17: 84,538,213 (GRCm39) |
|
probably benign |
Het |
Ticrr |
G |
C |
7: 79,344,539 (GRCm39) |
S1468T |
probably benign |
Het |
Uvssa |
G |
T |
5: 33,547,162 (GRCm39) |
G243C |
probably damaging |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vwa8 |
T |
A |
14: 79,401,660 (GRCm39) |
|
probably benign |
Het |
Zfp609 |
A |
T |
9: 65,608,454 (GRCm39) |
M1142K |
possibly damaging |
Het |
|
Other mutations in Gsdma |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01650:Gsdma
|
APN |
11 |
98,564,513 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02573:Gsdma
|
APN |
11 |
98,561,577 (GRCm39) |
splice site |
probably benign |
|
IGL03005:Gsdma
|
APN |
11 |
98,567,085 (GRCm39) |
missense |
probably damaging |
0.97 |
R0143:Gsdma
|
UTSW |
11 |
98,557,080 (GRCm39) |
missense |
probably damaging |
0.96 |
R1337:Gsdma
|
UTSW |
11 |
98,560,533 (GRCm39) |
nonsense |
probably null |
|
R1533:Gsdma
|
UTSW |
11 |
98,567,210 (GRCm39) |
missense |
unknown |
|
R1605:Gsdma
|
UTSW |
11 |
98,557,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R1929:Gsdma
|
UTSW |
11 |
98,562,193 (GRCm39) |
critical splice donor site |
probably null |
|
R1998:Gsdma
|
UTSW |
11 |
98,564,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R2043:Gsdma
|
UTSW |
11 |
98,557,046 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2114:Gsdma
|
UTSW |
11 |
98,563,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Gsdma
|
UTSW |
11 |
98,563,964 (GRCm39) |
splice site |
probably benign |
|
R3406:Gsdma
|
UTSW |
11 |
98,563,964 (GRCm39) |
splice site |
probably benign |
|
R3711:Gsdma
|
UTSW |
11 |
98,557,045 (GRCm39) |
nonsense |
probably null |
|
R3764:Gsdma
|
UTSW |
11 |
98,561,593 (GRCm39) |
missense |
probably damaging |
0.98 |
R4656:Gsdma
|
UTSW |
11 |
98,563,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Gsdma
|
UTSW |
11 |
98,557,275 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5943:Gsdma
|
UTSW |
11 |
98,563,852 (GRCm39) |
missense |
probably benign |
0.30 |
R7620:Gsdma
|
UTSW |
11 |
98,557,429 (GRCm39) |
missense |
probably benign |
0.06 |
R8340:Gsdma
|
UTSW |
11 |
98,557,421 (GRCm39) |
missense |
probably benign |
0.07 |
R9349:Gsdma
|
UTSW |
11 |
98,566,771 (GRCm39) |
missense |
probably benign |
0.36 |
R9736:Gsdma
|
UTSW |
11 |
98,567,169 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Gsdma
|
UTSW |
11 |
98,557,096 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1176:Gsdma
|
UTSW |
11 |
98,560,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|