Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030458C11Rik |
C |
A |
15: 12,824,615 (GRCm39) |
D7Y |
probably benign |
Het |
Aff1 |
A |
G |
5: 103,981,735 (GRCm39) |
T625A |
possibly damaging |
Het |
Aldh8a1 |
T |
C |
10: 21,265,201 (GRCm39) |
V276A |
probably benign |
Het |
Alkbh3 |
T |
C |
2: 93,831,858 (GRCm39) |
D124G |
probably benign |
Het |
Apob |
T |
A |
12: 8,060,798 (GRCm39) |
N3093K |
possibly damaging |
Het |
Atp13a1 |
C |
T |
8: 70,252,429 (GRCm39) |
R608* |
probably null |
Het |
Bbs7 |
A |
T |
3: 36,648,536 (GRCm39) |
I404K |
probably damaging |
Het |
Cacna2d1 |
A |
T |
5: 16,547,689 (GRCm39) |
T647S |
possibly damaging |
Het |
Carmil1 |
T |
C |
13: 24,220,304 (GRCm39) |
E1140G |
possibly damaging |
Het |
Ccdc158 |
C |
A |
5: 92,796,889 (GRCm39) |
E482D |
probably damaging |
Het |
Ccdc92 |
A |
T |
5: 124,913,090 (GRCm39) |
H146Q |
probably damaging |
Het |
Cntnap4 |
T |
A |
8: 113,480,577 (GRCm39) |
N341K |
probably damaging |
Het |
Cog1 |
A |
G |
11: 113,546,990 (GRCm39) |
D528G |
probably damaging |
Het |
Cttnbp2 |
G |
C |
6: 18,426,092 (GRCm39) |
A762G |
possibly damaging |
Het |
D130043K22Rik |
A |
T |
13: 25,040,685 (GRCm39) |
I36F |
probably damaging |
Het |
Dis3 |
T |
A |
14: 99,314,835 (GRCm39) |
R954W |
possibly damaging |
Het |
Eef1ece2 |
A |
T |
16: 20,461,067 (GRCm39) |
T618S |
probably benign |
Het |
Ext1 |
T |
C |
15: 52,939,283 (GRCm39) |
I589V |
possibly damaging |
Het |
Fam20a |
T |
A |
11: 109,576,332 (GRCm39) |
E142D |
possibly damaging |
Het |
Fars2 |
C |
T |
13: 36,389,068 (GRCm39) |
Q186* |
probably null |
Het |
Fcgbpl1 |
G |
A |
7: 27,836,966 (GRCm39) |
R295H |
probably benign |
Het |
Fhdc1 |
A |
T |
3: 84,381,946 (GRCm39) |
M1K |
probably null |
Het |
Gars1 |
T |
A |
6: 55,050,392 (GRCm39) |
F551Y |
probably benign |
Het |
Gm28363 |
A |
G |
1: 117,654,534 (GRCm39) |
R58G |
probably benign |
Het |
Gm8356 |
A |
T |
14: 17,692,450 (GRCm39) |
N58K |
probably damaging |
Het |
Gpr182 |
T |
C |
10: 127,586,874 (GRCm39) |
T26A |
possibly damaging |
Het |
Gpr19 |
A |
G |
6: 134,846,436 (GRCm39) |
Y416H |
probably damaging |
Het |
Hrob |
A |
G |
11: 102,148,725 (GRCm39) |
N379D |
probably benign |
Het |
Itgb7 |
T |
A |
15: 102,131,087 (GRCm39) |
S322C |
probably damaging |
Het |
Kcnma1 |
T |
A |
14: 23,423,211 (GRCm39) |
I831F |
probably benign |
Het |
Lrba |
A |
T |
3: 86,325,278 (GRCm39) |
D1912V |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,420,619 (GRCm39) |
T212S |
probably benign |
Het |
Map3k4 |
A |
T |
17: 12,489,918 (GRCm39) |
C504* |
probably null |
Het |
Morc2a |
T |
C |
11: 3,627,419 (GRCm39) |
S281P |
probably damaging |
Het |
Muc16 |
T |
C |
9: 18,566,171 (GRCm39) |
H2116R |
unknown |
Het |
Nrp2 |
C |
T |
1: 62,784,567 (GRCm39) |
R239C |
probably damaging |
Het |
Omg |
T |
C |
11: 79,393,729 (GRCm39) |
D43G |
possibly damaging |
Het |
Or13c7 |
T |
A |
4: 43,854,958 (GRCm39) |
F216L |
probably benign |
Het |
Or2ag15 |
C |
T |
7: 106,340,824 (GRCm39) |
V106I |
probably benign |
Het |
Or4c122 |
T |
A |
2: 89,079,343 (GRCm39) |
I220F |
probably damaging |
Het |
Or4c3 |
C |
A |
2: 89,852,087 (GRCm39) |
V108F |
possibly damaging |
Het |
Or5b3 |
A |
T |
19: 13,388,175 (GRCm39) |
T81S |
not run |
Het |
Or5w22 |
A |
T |
2: 87,362,508 (GRCm39) |
M44L |
probably benign |
Het |
Pdia6 |
T |
C |
12: 17,323,966 (GRCm39) |
L66S |
probably damaging |
Het |
Pds5a |
A |
G |
5: 65,785,082 (GRCm39) |
I930T |
possibly damaging |
Het |
Piezo2 |
C |
T |
18: 63,216,271 (GRCm39) |
G1169S |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,579,115 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
A |
T |
10: 3,907,758 (GRCm39) |
R947W |
|
Het |
Ptprs |
A |
C |
17: 56,742,994 (GRCm39) |
S383A |
probably damaging |
Het |
Rin3 |
T |
A |
12: 102,327,630 (GRCm39) |
L193* |
probably null |
Het |
Sgsh |
A |
G |
11: 119,243,521 (GRCm39) |
V67A |
probably damaging |
Het |
Slc16a4 |
A |
G |
3: 107,218,794 (GRCm39) |
Y465C |
probably damaging |
Het |
Stab2 |
C |
A |
10: 86,686,767 (GRCm39) |
S2259I |
possibly damaging |
Het |
Tbc1d24 |
G |
A |
17: 24,401,795 (GRCm39) |
P385S |
possibly damaging |
Het |
Tm4sf1 |
T |
C |
3: 57,200,319 (GRCm39) |
I99V |
probably benign |
Het |
Tmem108 |
A |
T |
9: 103,376,606 (GRCm39) |
I281N |
probably benign |
Het |
Usp31 |
T |
C |
7: 121,248,480 (GRCm39) |
S988G |
probably damaging |
Het |
Usp44 |
G |
T |
10: 93,688,571 (GRCm39) |
|
probably null |
Het |
Zbtb26 |
T |
A |
2: 37,327,013 (GRCm39) |
|
probably null |
Het |
Zfp599 |
A |
G |
9: 22,160,777 (GRCm39) |
Y463H |
probably benign |
Het |
Zfp750 |
T |
A |
11: 121,403,843 (GRCm39) |
D344V |
possibly damaging |
Het |
Zmym5 |
T |
A |
14: 57,031,883 (GRCm39) |
K408N |
possibly damaging |
Het |
|
Other mutations in Gm9758 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Gm9758
|
APN |
5 |
14,963,522 (GRCm39) |
splice site |
probably benign |
|
K3955:Gm9758
|
UTSW |
5 |
14,963,553 (GRCm39) |
missense |
probably benign |
0.05 |
K3955:Gm9758
|
UTSW |
5 |
14,963,522 (GRCm39) |
splice site |
probably benign |
|
R4078:Gm9758
|
UTSW |
5 |
14,961,536 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6269:Gm9758
|
UTSW |
5 |
14,962,274 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7181:Gm9758
|
UTSW |
5 |
14,963,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Gm9758
|
UTSW |
5 |
14,962,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Gm9758
|
UTSW |
5 |
14,964,739 (GRCm39) |
missense |
|
|
Z1088:Gm9758
|
UTSW |
5 |
14,963,553 (GRCm39) |
missense |
probably benign |
0.05 |
Z1176:Gm9758
|
UTSW |
5 |
14,963,553 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Gm9758
|
UTSW |
5 |
14,963,553 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Gm9758
|
UTSW |
5 |
14,961,472 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1177:Gm9758
|
UTSW |
5 |
14,960,599 (GRCm39) |
missense |
|
|
|