Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
A |
T |
9: 55,888,147 (GRCm39) |
M390K |
probably benign |
Het |
Bicra |
A |
G |
7: 15,706,257 (GRCm39) |
S1395P |
probably benign |
Het |
Cacnb2 |
G |
A |
2: 14,989,125 (GRCm39) |
D402N |
probably damaging |
Het |
Csmd1 |
T |
A |
8: 16,261,776 (GRCm39) |
D907V |
probably damaging |
Het |
Cstl1 |
T |
A |
2: 148,593,041 (GRCm39) |
Y65* |
probably null |
Het |
Dnajc1 |
T |
C |
2: 18,224,627 (GRCm39) |
I213V |
possibly damaging |
Het |
Emcn |
C |
T |
3: 137,109,772 (GRCm39) |
T138M |
probably damaging |
Het |
F3 |
G |
T |
3: 121,518,689 (GRCm39) |
W51L |
probably damaging |
Het |
Far2 |
A |
G |
6: 148,040,192 (GRCm39) |
Y41C |
probably damaging |
Het |
Flrt1 |
A |
T |
19: 7,073,856 (GRCm39) |
D230E |
probably damaging |
Het |
Gimap7 |
G |
A |
6: 48,700,986 (GRCm39) |
V191M |
probably damaging |
Het |
Gm19402 |
A |
T |
10: 77,526,354 (GRCm39) |
|
probably benign |
Het |
Ipo5 |
A |
C |
14: 121,159,574 (GRCm39) |
K134T |
probably benign |
Het |
Kcnf1 |
T |
C |
12: 17,225,531 (GRCm39) |
E230G |
probably damaging |
Het |
Mad1l1 |
T |
C |
5: 140,247,307 (GRCm39) |
E340G |
probably benign |
Het |
Map4k5 |
T |
C |
12: 69,903,620 (GRCm39) |
I62V |
probably benign |
Het |
Marchf7 |
A |
G |
2: 60,067,244 (GRCm39) |
K588R |
possibly damaging |
Het |
Mctp2 |
T |
A |
7: 71,810,909 (GRCm39) |
K52* |
probably null |
Het |
Nr1h4 |
A |
T |
10: 89,309,756 (GRCm39) |
F310L |
probably damaging |
Het |
Ofcc1 |
G |
A |
13: 40,250,501 (GRCm39) |
S605F |
probably damaging |
Het |
Or2w1b |
A |
T |
13: 21,300,599 (GRCm39) |
T246S |
probably damaging |
Het |
Or5ac25 |
A |
T |
16: 59,181,944 (GRCm39) |
S212R |
possibly damaging |
Het |
Or5b97 |
G |
A |
19: 12,878,679 (GRCm39) |
T155I |
probably benign |
Het |
Pcdh20 |
T |
G |
14: 88,704,672 (GRCm39) |
E876A |
probably benign |
Het |
Plce1 |
C |
T |
19: 38,768,370 (GRCm39) |
A2215V |
probably damaging |
Het |
Sigirr |
A |
G |
7: 140,672,510 (GRCm39) |
L204S |
probably damaging |
Het |
Slc2a12 |
A |
T |
10: 22,540,706 (GRCm39) |
Y187F |
probably damaging |
Het |
Slc31a2 |
A |
T |
4: 62,214,312 (GRCm39) |
R86W |
probably null |
Het |
Smc1b |
T |
C |
15: 84,976,218 (GRCm39) |
K830E |
probably damaging |
Het |
Ssrp1 |
A |
G |
2: 84,872,642 (GRCm39) |
N427D |
possibly damaging |
Het |
Taar9 |
A |
T |
10: 23,985,289 (GRCm39) |
F48L |
probably benign |
Het |
Taok2 |
T |
C |
7: 126,474,272 (GRCm39) |
E319G |
probably damaging |
Het |
Try10 |
T |
C |
6: 41,333,680 (GRCm39) |
S142P |
probably damaging |
Het |
Tsc22d1 |
A |
G |
14: 76,655,644 (GRCm39) |
T626A |
probably benign |
Het |
Zfp101 |
T |
C |
17: 33,599,950 (GRCm39) |
E602G |
possibly damaging |
Het |
|
Other mutations in Ptprg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Ptprg
|
APN |
14 |
12,215,992 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00484:Ptprg
|
APN |
14 |
12,215,220 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL00847:Ptprg
|
APN |
14 |
12,215,265 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01089:Ptprg
|
APN |
14 |
12,215,286 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01382:Ptprg
|
APN |
14 |
12,237,797 (GRCm38) |
missense |
probably benign |
0.16 |
IGL01470:Ptprg
|
APN |
14 |
12,213,702 (GRCm38) |
nonsense |
probably null |
|
IGL01762:Ptprg
|
APN |
14 |
12,037,386 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01886:Ptprg
|
APN |
14 |
12,179,280 (GRCm38) |
missense |
probably benign |
0.22 |
IGL01963:Ptprg
|
APN |
14 |
12,220,661 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02015:Ptprg
|
APN |
14 |
12,237,782 (GRCm38) |
missense |
possibly damaging |
0.46 |
IGL02086:Ptprg
|
APN |
14 |
12,110,080 (GRCm38) |
nonsense |
probably null |
|
IGL02197:Ptprg
|
APN |
14 |
12,220,613 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02341:Ptprg
|
APN |
14 |
12,154,360 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02732:Ptprg
|
APN |
14 |
12,225,617 (GRCm38) |
critical splice donor site |
probably null |
|
IGL03011:Ptprg
|
APN |
14 |
12,219,029 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03261:Ptprg
|
APN |
14 |
12,225,552 (GRCm38) |
missense |
probably damaging |
0.99 |
R0038:Ptprg
|
UTSW |
14 |
12,213,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R0383:Ptprg
|
UTSW |
14 |
12,219,024 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0433:Ptprg
|
UTSW |
14 |
12,220,620 (GRCm38) |
missense |
probably damaging |
1.00 |
R0488:Ptprg
|
UTSW |
14 |
12,220,653 (GRCm38) |
missense |
probably damaging |
1.00 |
R0503:Ptprg
|
UTSW |
14 |
12,237,138 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0520:Ptprg
|
UTSW |
14 |
12,199,783 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0570:Ptprg
|
UTSW |
14 |
12,215,896 (GRCm38) |
missense |
probably damaging |
1.00 |
R0606:Ptprg
|
UTSW |
14 |
12,154,131 (GRCm38) |
missense |
probably benign |
|
R1086:Ptprg
|
UTSW |
14 |
11,952,706 (GRCm38) |
splice site |
probably benign |
|
R1468:Ptprg
|
UTSW |
14 |
12,190,767 (GRCm38) |
missense |
probably benign |
0.02 |
R1468:Ptprg
|
UTSW |
14 |
12,190,767 (GRCm38) |
missense |
probably benign |
0.02 |
R1519:Ptprg
|
UTSW |
14 |
12,220,596 (GRCm38) |
missense |
probably damaging |
1.00 |
R1662:Ptprg
|
UTSW |
14 |
12,207,357 (GRCm38) |
missense |
probably damaging |
1.00 |
R1714:Ptprg
|
UTSW |
14 |
12,213,697 (GRCm38) |
missense |
probably damaging |
1.00 |
R1716:Ptprg
|
UTSW |
14 |
12,154,360 (GRCm38) |
missense |
probably benign |
0.00 |
R1797:Ptprg
|
UTSW |
14 |
12,199,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R1803:Ptprg
|
UTSW |
14 |
12,091,410 (GRCm38) |
splice site |
probably null |
|
R2104:Ptprg
|
UTSW |
14 |
11,952,897 (GRCm38) |
critical splice donor site |
probably null |
|
R2125:Ptprg
|
UTSW |
14 |
12,179,283 (GRCm38) |
missense |
possibly damaging |
0.74 |
R2126:Ptprg
|
UTSW |
14 |
12,154,355 (GRCm38) |
missense |
probably benign |
|
R2133:Ptprg
|
UTSW |
14 |
12,211,637 (GRCm38) |
missense |
probably damaging |
1.00 |
R2571:Ptprg
|
UTSW |
14 |
12,122,135 (GRCm38) |
missense |
probably benign |
|
R3821:Ptprg
|
UTSW |
14 |
12,226,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4196:Ptprg
|
UTSW |
14 |
12,122,002 (GRCm38) |
missense |
possibly damaging |
0.51 |
R4392:Ptprg
|
UTSW |
14 |
12,142,467 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4665:Ptprg
|
UTSW |
14 |
12,215,288 (GRCm38) |
missense |
possibly damaging |
0.90 |
R4730:Ptprg
|
UTSW |
14 |
12,213,713 (GRCm38) |
missense |
probably damaging |
1.00 |
R4737:Ptprg
|
UTSW |
14 |
12,226,314 (GRCm38) |
missense |
probably damaging |
1.00 |
R4764:Ptprg
|
UTSW |
14 |
12,122,068 (GRCm38) |
missense |
probably benign |
0.01 |
R4801:Ptprg
|
UTSW |
14 |
11,554,233 (GRCm38) |
utr 5 prime |
probably benign |
|
R4825:Ptprg
|
UTSW |
14 |
12,220,654 (GRCm38) |
missense |
probably damaging |
1.00 |
R4960:Ptprg
|
UTSW |
14 |
12,237,837 (GRCm38) |
missense |
probably benign |
0.07 |
R4972:Ptprg
|
UTSW |
14 |
12,226,427 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4980:Ptprg
|
UTSW |
14 |
12,154,421 (GRCm38) |
missense |
probably benign |
0.16 |
R5004:Ptprg
|
UTSW |
14 |
12,220,667 (GRCm38) |
missense |
probably damaging |
1.00 |
R5058:Ptprg
|
UTSW |
14 |
12,037,387 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5182:Ptprg
|
UTSW |
14 |
12,154,174 (GRCm38) |
missense |
probably benign |
|
R5258:Ptprg
|
UTSW |
14 |
12,142,431 (GRCm38) |
missense |
probably benign |
0.11 |
R5338:Ptprg
|
UTSW |
14 |
12,154,111 (GRCm38) |
missense |
probably benign |
|
R5353:Ptprg
|
UTSW |
14 |
11,554,235 (GRCm38) |
utr 5 prime |
probably benign |
|
R5373:Ptprg
|
UTSW |
14 |
12,213,665 (GRCm38) |
missense |
probably benign |
0.00 |
R5387:Ptprg
|
UTSW |
14 |
12,153,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R5616:Ptprg
|
UTSW |
14 |
12,122,120 (GRCm38) |
missense |
probably benign |
|
R5623:Ptprg
|
UTSW |
14 |
12,153,857 (GRCm38) |
missense |
probably damaging |
1.00 |
R5976:Ptprg
|
UTSW |
14 |
12,211,625 (GRCm38) |
missense |
probably damaging |
0.96 |
R6027:Ptprg
|
UTSW |
14 |
12,220,613 (GRCm38) |
missense |
possibly damaging |
0.87 |
R6091:Ptprg
|
UTSW |
14 |
12,215,979 (GRCm38) |
missense |
probably damaging |
1.00 |
R6184:Ptprg
|
UTSW |
14 |
12,153,943 (GRCm38) |
missense |
probably benign |
0.00 |
R6234:Ptprg
|
UTSW |
14 |
12,213,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R6318:Ptprg
|
UTSW |
14 |
12,237,118 (GRCm38) |
missense |
probably damaging |
1.00 |
R6324:Ptprg
|
UTSW |
14 |
12,226,314 (GRCm38) |
missense |
probably damaging |
1.00 |
R6334:Ptprg
|
UTSW |
14 |
12,166,832 (GRCm38) |
missense |
probably damaging |
1.00 |
R6646:Ptprg
|
UTSW |
14 |
11,962,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R6647:Ptprg
|
UTSW |
14 |
11,962,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R6992:Ptprg
|
UTSW |
14 |
11,962,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R7088:Ptprg
|
UTSW |
14 |
12,207,365 (GRCm38) |
missense |
probably damaging |
1.00 |
R7250:Ptprg
|
UTSW |
14 |
12,166,767 (GRCm38) |
missense |
probably benign |
0.18 |
R7342:Ptprg
|
UTSW |
14 |
12,237,151 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7358:Ptprg
|
UTSW |
14 |
12,154,198 (GRCm38) |
missense |
possibly damaging |
0.59 |
R7410:Ptprg
|
UTSW |
14 |
11,962,657 (GRCm38) |
missense |
probably damaging |
1.00 |
R7448:Ptprg
|
UTSW |
14 |
12,142,461 (GRCm38) |
missense |
probably benign |
0.12 |
R7514:Ptprg
|
UTSW |
14 |
12,179,342 (GRCm38) |
missense |
possibly damaging |
0.86 |
R7523:Ptprg
|
UTSW |
14 |
12,237,130 (GRCm38) |
missense |
probably damaging |
0.97 |
R7672:Ptprg
|
UTSW |
14 |
12,211,668 (GRCm38) |
missense |
probably benign |
0.04 |
R7709:Ptprg
|
UTSW |
14 |
12,226,452 (GRCm38) |
missense |
probably damaging |
1.00 |
R7720:Ptprg
|
UTSW |
14 |
12,211,703 (GRCm38) |
missense |
probably benign |
0.31 |
R8860:Ptprg
|
UTSW |
14 |
12,213,685 (GRCm38) |
missense |
probably damaging |
1.00 |
R8992:Ptprg
|
UTSW |
14 |
12,154,170 (GRCm38) |
missense |
probably benign |
0.00 |
R9054:Ptprg
|
UTSW |
14 |
12,213,638 (GRCm38) |
missense |
possibly damaging |
0.58 |
R9587:Ptprg
|
UTSW |
14 |
12,215,992 (GRCm38) |
missense |
probably damaging |
1.00 |
R9621:Ptprg
|
UTSW |
14 |
12,237,809 (GRCm38) |
missense |
probably benign |
|
R9625:Ptprg
|
UTSW |
14 |
12,152,027 (GRCm38) |
missense |
probably damaging |
1.00 |
R9773:Ptprg
|
UTSW |
14 |
12,199,806 (GRCm38) |
missense |
probably damaging |
0.97 |
X0020:Ptprg
|
UTSW |
14 |
12,110,070 (GRCm38) |
frame shift |
probably null |
|
X0027:Ptprg
|
UTSW |
14 |
12,110,070 (GRCm38) |
frame shift |
probably null |
|
|