Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700086D15Rik |
A |
G |
11: 65,043,836 (GRCm39) |
M75T |
unknown |
Het |
2700049A03Rik |
T |
G |
12: 71,187,680 (GRCm39) |
N105K |
probably damaging |
Het |
Acvr1c |
A |
T |
2: 58,205,867 (GRCm39) |
V31E |
probably damaging |
Het |
Adra1d |
T |
A |
2: 131,403,170 (GRCm39) |
T307S |
probably benign |
Het |
Akr1c14 |
T |
C |
13: 4,131,051 (GRCm39) |
Y248H |
probably benign |
Het |
Ankub1 |
T |
C |
3: 57,580,406 (GRCm39) |
T84A |
probably benign |
Het |
Asb3 |
C |
A |
11: 30,948,348 (GRCm39) |
S8* |
probably null |
Het |
AU041133 |
G |
A |
10: 81,986,935 (GRCm39) |
G196D |
possibly damaging |
Het |
B4galt7 |
T |
C |
13: 55,756,155 (GRCm39) |
C214R |
probably damaging |
Het |
Chd3 |
A |
G |
11: 69,254,921 (GRCm39) |
S140P |
possibly damaging |
Het |
Ciz1 |
T |
C |
2: 32,254,299 (GRCm39) |
L80P |
probably damaging |
Het |
Col6a4 |
G |
A |
9: 105,949,448 (GRCm39) |
P729L |
possibly damaging |
Het |
Cr2 |
A |
G |
1: 194,845,557 (GRCm39) |
C133R |
probably damaging |
Het |
Dmgdh |
T |
C |
13: 93,828,393 (GRCm39) |
L178P |
probably damaging |
Het |
Dock5 |
C |
A |
14: 68,009,151 (GRCm39) |
E1448* |
probably null |
Het |
Elavl1 |
A |
G |
8: 4,361,767 (GRCm39) |
S2P |
probably benign |
Het |
Flywch1 |
T |
C |
17: 23,980,033 (GRCm39) |
H247R |
possibly damaging |
Het |
Gabpb1 |
A |
T |
2: 126,481,222 (GRCm39) |
I309N |
possibly damaging |
Het |
Glrx3 |
T |
C |
7: 137,066,165 (GRCm39) |
F298L |
possibly damaging |
Het |
Gpc6 |
G |
A |
14: 118,202,268 (GRCm39) |
V493I |
probably benign |
Het |
H2-T13 |
A |
T |
17: 36,391,938 (GRCm39) |
I45N |
possibly damaging |
Het |
Hadha |
C |
T |
5: 30,350,315 (GRCm39) |
E78K |
probably benign |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Ldlrad3 |
G |
T |
2: 101,943,903 (GRCm39) |
F56L |
probably damaging |
Het |
Ldlrad3 |
A |
G |
2: 101,943,905 (GRCm39) |
F56L |
probably damaging |
Het |
Mapk4 |
A |
T |
18: 74,063,990 (GRCm39) |
S411T |
possibly damaging |
Het |
Mcm9 |
A |
G |
10: 53,492,019 (GRCm39) |
M382T |
|
Het |
Muc21 |
TCCTGAGGCAGTGCTGGATACAGGGGTGGTTGGGGTGGGTGAAGAGCCTGAGGCAGTGCTGGAT |
TCCTGAGGCAGTGCTGGAT |
17: 35,933,525 (GRCm39) |
|
probably benign |
Het |
Or2t6 |
A |
T |
14: 14,175,477 (GRCm38) |
C202S |
probably damaging |
Het |
Or5b104 |
T |
C |
19: 13,072,596 (GRCm39) |
T139A |
probably benign |
Het |
Pacs1 |
A |
C |
19: 5,206,441 (GRCm39) |
I248S |
possibly damaging |
Het |
Plekhg1 |
T |
C |
10: 3,906,810 (GRCm39) |
S631P |
|
Het |
Rars2 |
A |
T |
4: 34,645,747 (GRCm39) |
K221N |
probably benign |
Het |
Retsat |
T |
C |
6: 72,583,002 (GRCm39) |
S388P |
possibly damaging |
Het |
Rft1 |
G |
A |
14: 30,404,814 (GRCm39) |
|
probably null |
Het |
Rgsl1 |
A |
G |
1: 153,660,945 (GRCm39) |
V345A |
probably benign |
Het |
Rnf38 |
A |
T |
4: 44,137,620 (GRCm39) |
S320R |
probably benign |
Het |
Sel1l3 |
T |
A |
5: 53,301,451 (GRCm39) |
Y722F |
probably benign |
Het |
Slc13a4 |
T |
C |
6: 35,264,285 (GRCm39) |
E194G |
possibly damaging |
Het |
Spata17 |
G |
A |
1: 186,844,700 (GRCm39) |
R300C |
probably benign |
Het |
Tacc1 |
G |
A |
8: 25,731,656 (GRCm39) |
|
probably benign |
Het |
Tc2n |
T |
G |
12: 101,655,314 (GRCm39) |
I214L |
probably damaging |
Het |
Tet2 |
T |
C |
3: 133,192,953 (GRCm39) |
S494G |
probably benign |
Het |
Tmco5b |
A |
T |
2: 113,121,722 (GRCm39) |
I179L |
probably damaging |
Het |
Triobp |
AGGGACAATCCCAGGGCCTCCTCTCCCAACAGAACTACTCAGCGGGACAA |
AGGGACAA |
15: 78,851,042 (GRCm39) |
|
probably benign |
Het |
Trpv1 |
A |
G |
11: 73,130,412 (GRCm39) |
T173A |
probably damaging |
Het |
Vmn2r56 |
C |
T |
7: 12,444,259 (GRCm39) |
G458R |
probably damaging |
Het |
Vmn2r81 |
T |
G |
10: 79,106,570 (GRCm39) |
|
probably null |
Het |
Wfdc15b |
T |
A |
2: 164,057,037 (GRCm39) |
E80D |
probably benign |
Het |
Wrn |
A |
T |
8: 33,812,376 (GRCm39) |
D423E |
probably benign |
Het |
Zfp775 |
T |
A |
6: 48,597,415 (GRCm39) |
C430S |
possibly damaging |
Het |
|
Other mutations in Pi16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01725:Pi16
|
APN |
17 |
29,545,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02238:Pi16
|
APN |
17 |
29,545,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R0276:Pi16
|
UTSW |
17 |
29,545,917 (GRCm39) |
missense |
probably benign |
0.02 |
R0507:Pi16
|
UTSW |
17 |
29,546,826 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0570:Pi16
|
UTSW |
17 |
29,538,189 (GRCm39) |
start codon destroyed |
possibly damaging |
0.54 |
R1834:Pi16
|
UTSW |
17 |
29,546,419 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1845:Pi16
|
UTSW |
17 |
29,538,361 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5670:Pi16
|
UTSW |
17 |
29,545,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R6223:Pi16
|
UTSW |
17 |
29,546,413 (GRCm39) |
nonsense |
probably null |
|
R7097:Pi16
|
UTSW |
17 |
29,545,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R7122:Pi16
|
UTSW |
17 |
29,545,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Pi16
|
UTSW |
17 |
29,538,072 (GRCm39) |
unclassified |
probably benign |
|
R7219:Pi16
|
UTSW |
17 |
29,538,208 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7220:Pi16
|
UTSW |
17 |
29,538,208 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7278:Pi16
|
UTSW |
17 |
29,538,208 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7318:Pi16
|
UTSW |
17 |
29,538,208 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7822:Pi16
|
UTSW |
17 |
29,538,208 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8254:Pi16
|
UTSW |
17 |
29,538,208 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8265:Pi16
|
UTSW |
17 |
29,545,947 (GRCm39) |
missense |
probably benign |
0.01 |
R8386:Pi16
|
UTSW |
17 |
29,538,208 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9368:Pi16
|
UTSW |
17 |
29,546,852 (GRCm39) |
missense |
probably benign |
0.15 |
R9420:Pi16
|
UTSW |
17 |
29,544,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Pi16
|
UTSW |
17 |
29,538,363 (GRCm39) |
missense |
possibly damaging |
0.89 |
|