Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 109,992,813 (GRCm39) |
L1617P |
probably damaging |
Het |
Abhd16b |
T |
C |
2: 181,135,947 (GRCm39) |
V283A |
probably damaging |
Het |
Adamts19 |
G |
T |
18: 58,971,040 (GRCm39) |
R208L |
possibly damaging |
Het |
Adamts4 |
T |
C |
1: 171,078,584 (GRCm39) |
I56T |
possibly damaging |
Het |
Alpk1 |
A |
C |
3: 127,473,684 (GRCm39) |
V773G |
possibly damaging |
Het |
Arhgap10 |
G |
T |
8: 78,177,336 (GRCm39) |
Q100K |
possibly damaging |
Het |
Arhgef18 |
T |
A |
8: 3,489,439 (GRCm39) |
|
probably null |
Het |
Asb15 |
A |
T |
6: 24,564,377 (GRCm39) |
H277L |
probably benign |
Het |
Ascc3 |
T |
A |
10: 50,514,074 (GRCm39) |
V291E |
probably damaging |
Het |
Cnot6l |
A |
C |
5: 96,234,024 (GRCm39) |
V329G |
probably benign |
Het |
Col14a1 |
A |
G |
15: 55,286,908 (GRCm39) |
T910A |
unknown |
Het |
Dhdds |
G |
A |
4: 133,724,141 (GRCm39) |
L58F |
probably damaging |
Het |
Dsc2 |
A |
G |
18: 20,165,567 (GRCm39) |
I846T |
probably benign |
Het |
Evc |
A |
T |
5: 37,483,914 (GRCm39) |
S129T |
probably damaging |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,623,898 (GRCm39) |
V1377A |
probably damaging |
Het |
Haus6 |
C |
T |
4: 86,519,500 (GRCm39) |
A203T |
possibly damaging |
Het |
Hkdc1 |
T |
G |
10: 62,253,712 (GRCm39) |
D23A |
probably damaging |
Het |
Hpdl |
C |
T |
4: 116,677,775 (GRCm39) |
V229M |
probably damaging |
Het |
Hspa12a |
T |
C |
19: 58,810,518 (GRCm39) |
Y175C |
probably damaging |
Het |
Hyal1 |
C |
T |
9: 107,454,866 (GRCm39) |
P59S |
probably damaging |
Het |
Itpr1 |
G |
A |
6: 108,487,699 (GRCm39) |
C2374Y |
probably benign |
Het |
Kmt2a |
A |
T |
9: 44,759,139 (GRCm39) |
Y114* |
probably null |
Het |
Mc2r |
A |
T |
18: 68,540,468 (GRCm39) |
I275K |
probably damaging |
Het |
Mc2r |
A |
T |
18: 68,540,466 (GRCm39) |
Y276N |
possibly damaging |
Het |
Mlycd |
A |
G |
8: 120,137,019 (GRCm39) |
Y413C |
probably damaging |
Het |
Mocs2 |
T |
G |
13: 114,957,455 (GRCm39) |
S86R |
probably damaging |
Het |
Msx2 |
C |
A |
13: 53,626,644 (GRCm39) |
A35S |
probably benign |
Het |
Or6c201 |
A |
T |
10: 128,969,016 (GRCm39) |
L207H |
probably damaging |
Het |
Pla2g4f |
C |
A |
2: 120,135,504 (GRCm39) |
S390I |
probably damaging |
Het |
Plcl1 |
C |
T |
1: 55,735,148 (GRCm39) |
A163V |
possibly damaging |
Het |
Rbmxl1 |
G |
A |
8: 79,232,270 (GRCm39) |
|
probably benign |
Het |
Recql |
G |
T |
6: 142,311,344 (GRCm39) |
|
probably null |
Het |
Rev3l |
T |
A |
10: 39,699,089 (GRCm39) |
N1195K |
probably benign |
Het |
Rfwd3 |
G |
A |
8: 111,999,716 (GRCm39) |
T754M |
probably benign |
Het |
Sctr |
A |
G |
1: 119,959,350 (GRCm39) |
T98A |
probably damaging |
Het |
Sdk1 |
T |
A |
5: 141,921,803 (GRCm39) |
D6E |
probably benign |
Het |
Smpdl3a |
T |
A |
10: 57,684,034 (GRCm39) |
I264K |
possibly damaging |
Het |
Spag6 |
A |
G |
2: 18,736,804 (GRCm39) |
I154V |
probably benign |
Het |
Tbc1d12 |
A |
C |
19: 38,871,127 (GRCm39) |
T297P |
probably benign |
Het |
Tgfb1 |
A |
G |
7: 25,396,385 (GRCm39) |
D226G |
probably benign |
Het |
Ubr3 |
G |
T |
2: 69,846,588 (GRCm39) |
|
probably null |
Het |
Ubr4 |
T |
C |
4: 139,195,407 (GRCm39) |
Y1210H |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 38,006,785 (GRCm39) |
T1157A |
probably benign |
Het |
Vmn2r120 |
T |
G |
17: 57,831,938 (GRCm39) |
T284P |
probably benign |
Het |
Vps13b |
G |
T |
15: 35,794,181 (GRCm39) |
A2286S |
probably damaging |
Het |
Zcchc14 |
A |
T |
8: 122,331,332 (GRCm39) |
|
probably benign |
Het |
Zfr2 |
T |
A |
10: 81,079,547 (GRCm39) |
V362E |
probably benign |
Het |
|
Other mutations in Pnn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02267:Pnn
|
APN |
12 |
59,116,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0350:Pnn
|
UTSW |
12 |
59,113,903 (GRCm39) |
critical splice donor site |
probably null |
|
R1853:Pnn
|
UTSW |
12 |
59,118,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R1854:Pnn
|
UTSW |
12 |
59,118,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R4287:Pnn
|
UTSW |
12 |
59,118,956 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4792:Pnn
|
UTSW |
12 |
59,118,991 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4812:Pnn
|
UTSW |
12 |
59,118,404 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4933:Pnn
|
UTSW |
12 |
59,117,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Pnn
|
UTSW |
12 |
59,118,716 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5716:Pnn
|
UTSW |
12 |
59,118,658 (GRCm39) |
missense |
probably benign |
0.00 |
R5963:Pnn
|
UTSW |
12 |
59,114,617 (GRCm39) |
nonsense |
probably null |
|
R6877:Pnn
|
UTSW |
12 |
59,115,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R6999:Pnn
|
UTSW |
12 |
59,117,085 (GRCm39) |
critical splice donor site |
probably null |
|
R7372:Pnn
|
UTSW |
12 |
59,115,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R7458:Pnn
|
UTSW |
12 |
59,119,200 (GRCm39) |
missense |
unknown |
|
R7535:Pnn
|
UTSW |
12 |
59,118,923 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:Pnn
|
UTSW |
12 |
59,117,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Pnn
|
UTSW |
12 |
59,119,363 (GRCm39) |
missense |
unknown |
|
R9246:Pnn
|
UTSW |
12 |
59,116,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R9404:Pnn
|
UTSW |
12 |
59,118,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R9579:Pnn
|
UTSW |
12 |
59,117,030 (GRCm39) |
missense |
possibly damaging |
0.72 |
Z1177:Pnn
|
UTSW |
12 |
59,119,585 (GRCm39) |
missense |
probably benign |
0.02 |
|