Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,844,379 (GRCm39) |
D884V |
probably damaging |
Het |
Acvr2a |
C |
T |
2: 48,789,628 (GRCm39) |
T457M |
probably damaging |
Het |
Akr1b10 |
C |
T |
6: 34,369,394 (GRCm39) |
T208I |
probably benign |
Het |
Aldh16a1 |
G |
T |
7: 44,796,674 (GRCm39) |
T275K |
possibly damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Asgr1 |
T |
G |
11: 69,946,923 (GRCm39) |
C56W |
probably benign |
Het |
Atp11b |
T |
C |
3: 35,860,918 (GRCm39) |
I335T |
probably damaging |
Het |
BC061237 |
A |
G |
14: 44,741,762 (GRCm39) |
|
probably benign |
Het |
Bdh1 |
G |
T |
16: 31,275,720 (GRCm39) |
K280N |
probably benign |
Het |
Bmp1 |
C |
T |
14: 70,729,906 (GRCm39) |
C466Y |
probably damaging |
Het |
Ccdc181 |
A |
G |
1: 164,108,172 (GRCm39) |
E285G |
probably benign |
Het |
Ces1f |
C |
T |
8: 94,006,277 (GRCm39) |
G18R |
probably damaging |
Het |
Cfap43 |
T |
A |
19: 47,824,045 (GRCm39) |
I109L |
possibly damaging |
Het |
Edc4 |
A |
G |
8: 106,617,382 (GRCm39) |
|
probably benign |
Het |
F3 |
T |
C |
3: 121,526,159 (GRCm39) |
C241R |
probably damaging |
Het |
Fhdc1 |
T |
A |
3: 84,352,310 (GRCm39) |
S972C |
probably damaging |
Het |
Heatr1 |
T |
G |
13: 12,432,513 (GRCm39) |
I1086R |
possibly damaging |
Het |
Hsh2d |
A |
T |
8: 72,950,738 (GRCm39) |
|
probably benign |
Het |
Ice1 |
T |
C |
13: 70,744,340 (GRCm39) |
Y2081C |
probably damaging |
Het |
Il1rl1 |
A |
G |
1: 40,481,873 (GRCm39) |
N194D |
probably damaging |
Het |
Ip6k1 |
G |
A |
9: 107,923,022 (GRCm39) |
V385M |
probably damaging |
Het |
Lig1 |
G |
A |
7: 13,022,611 (GRCm39) |
R147Q |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 40,537,165 (GRCm39) |
V41I |
probably damaging |
Het |
Macroh2a2 |
A |
T |
10: 61,585,112 (GRCm39) |
D177E |
possibly damaging |
Het |
Mst1r |
T |
A |
9: 107,794,424 (GRCm39) |
V1201E |
probably damaging |
Het |
Myof |
T |
C |
19: 37,892,116 (GRCm39) |
|
probably benign |
Het |
Nbas |
G |
T |
12: 13,532,379 (GRCm39) |
|
probably benign |
Het |
Ndst1 |
A |
G |
18: 60,840,719 (GRCm39) |
I321T |
possibly damaging |
Het |
Nek10 |
G |
A |
14: 14,850,983 (GRCm38) |
G343R |
probably damaging |
Het |
Or2a7 |
A |
T |
6: 43,151,234 (GRCm39) |
T105S |
probably benign |
Het |
Or2y1 |
T |
A |
11: 49,385,650 (GRCm39) |
C97S |
probably damaging |
Het |
Or4d2b |
A |
T |
11: 87,780,122 (GRCm39) |
I200N |
probably damaging |
Het |
Pde4d |
T |
C |
13: 109,253,595 (GRCm39) |
S141P |
probably benign |
Het |
Pigm |
A |
T |
1: 172,204,381 (GRCm39) |
Q39L |
probably damaging |
Het |
Prl7a2 |
T |
A |
13: 27,846,750 (GRCm39) |
I88F |
probably benign |
Het |
Prss16 |
T |
A |
13: 22,192,856 (GRCm39) |
|
probably benign |
Het |
Psmc4 |
G |
A |
7: 27,742,222 (GRCm39) |
|
probably benign |
Het |
Ptger3 |
T |
A |
3: 157,273,365 (GRCm39) |
C237* |
probably null |
Het |
Recql |
G |
A |
6: 142,318,601 (GRCm39) |
T214M |
probably damaging |
Het |
Rfx7 |
T |
A |
9: 72,526,857 (GRCm39) |
V1349D |
probably damaging |
Het |
Ros1 |
A |
G |
10: 51,964,041 (GRCm39) |
S1740P |
probably damaging |
Het |
Rrm2b |
A |
T |
15: 37,947,053 (GRCm39) |
S83T |
probably benign |
Het |
Sall4 |
A |
G |
2: 168,598,394 (GRCm39) |
Y149H |
probably benign |
Het |
Smad1 |
A |
G |
8: 80,076,207 (GRCm39) |
|
probably benign |
Het |
Snrnp70 |
T |
C |
7: 45,030,129 (GRCm39) |
|
probably benign |
Het |
Spef2 |
C |
A |
15: 9,725,194 (GRCm39) |
|
probably benign |
Het |
Sptlc1 |
T |
C |
13: 53,505,660 (GRCm39) |
T253A |
probably benign |
Het |
Zbbx |
T |
C |
3: 74,959,784 (GRCm39) |
Y595C |
possibly damaging |
Het |
Zfp382 |
T |
C |
7: 29,833,114 (GRCm39) |
V255A |
probably benign |
Het |
|
Other mutations in Cma2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01870:Cma2
|
APN |
14 |
56,211,194 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03139:Cma2
|
APN |
14 |
56,211,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Cma2
|
UTSW |
14 |
56,211,135 (GRCm39) |
splice site |
probably benign |
|
R0545:Cma2
|
UTSW |
14 |
56,210,570 (GRCm39) |
missense |
probably benign |
0.01 |
R0558:Cma2
|
UTSW |
14 |
56,210,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1187:Cma2
|
UTSW |
14 |
56,210,280 (GRCm39) |
missense |
probably benign |
0.07 |
R1292:Cma2
|
UTSW |
14 |
56,211,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R1575:Cma2
|
UTSW |
14 |
56,210,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Cma2
|
UTSW |
14 |
56,210,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R5198:Cma2
|
UTSW |
14 |
56,209,532 (GRCm39) |
missense |
probably benign |
0.03 |
R5601:Cma2
|
UTSW |
14 |
56,211,246 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6222:Cma2
|
UTSW |
14 |
56,210,649 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6505:Cma2
|
UTSW |
14 |
56,211,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R7387:Cma2
|
UTSW |
14 |
56,210,505 (GRCm39) |
missense |
probably benign |
0.03 |
R8222:Cma2
|
UTSW |
14 |
56,210,727 (GRCm39) |
missense |
probably benign |
0.00 |
R8860:Cma2
|
UTSW |
14 |
56,210,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R8997:Cma2
|
UTSW |
14 |
56,210,201 (GRCm39) |
missense |
probably benign |
0.00 |
R9429:Cma2
|
UTSW |
14 |
56,210,276 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9548:Cma2
|
UTSW |
14 |
56,211,256 (GRCm39) |
missense |
probably damaging |
0.99 |
|