Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
A |
G |
16: 20,369,023 (GRCm39) |
N173S |
probably benign |
Het |
Agps |
A |
G |
2: 75,684,547 (GRCm39) |
I172V |
probably benign |
Het |
Amz1 |
G |
A |
5: 140,737,731 (GRCm39) |
W330* |
probably null |
Het |
Asap1 |
A |
T |
15: 64,002,072 (GRCm39) |
M413K |
possibly damaging |
Het |
Bhmt1b |
T |
C |
18: 87,774,687 (GRCm39) |
V70A |
probably damaging |
Het |
Ccdc83 |
A |
T |
7: 89,885,513 (GRCm39) |
W291R |
unknown |
Het |
Cdh19 |
A |
T |
1: 110,853,610 (GRCm39) |
M277K |
probably benign |
Het |
Clca3a1 |
C |
A |
3: 144,460,914 (GRCm39) |
|
probably null |
Het |
Cnpy1 |
T |
C |
5: 28,408,423 (GRCm39) |
T138A |
probably benign |
Het |
Csnka2ip |
T |
C |
16: 64,300,295 (GRCm39) |
D23G |
|
Het |
Cxcr5 |
A |
T |
9: 44,425,583 (GRCm39) |
F25I |
probably benign |
Het |
Defb33 |
T |
A |
8: 21,387,651 (GRCm39) |
*63R |
probably null |
Het |
Dgkz |
A |
T |
2: 91,770,649 (GRCm39) |
S485T |
possibly damaging |
Het |
Elac1 |
A |
G |
18: 73,871,927 (GRCm39) |
I356T |
probably damaging |
Het |
Fam135a |
C |
T |
1: 24,067,675 (GRCm39) |
D1065N |
probably benign |
Het |
Fbxo10 |
T |
A |
4: 45,058,942 (GRCm39) |
D265V |
possibly damaging |
Het |
Flrt2 |
A |
G |
12: 95,746,331 (GRCm39) |
E223G |
probably benign |
Het |
Gjc2 |
A |
T |
11: 59,068,334 (GRCm39) |
D49E |
probably damaging |
Het |
Hmcn2 |
C |
A |
2: 31,281,088 (GRCm39) |
L1867I |
probably benign |
Het |
Irf2 |
A |
T |
8: 47,271,887 (GRCm39) |
Y158F |
probably benign |
Het |
Jmy |
T |
C |
13: 93,634,949 (GRCm39) |
D289G |
probably damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Limch1 |
T |
G |
5: 67,156,649 (GRCm39) |
I372S |
probably benign |
Het |
Lsm11 |
A |
T |
11: 45,824,730 (GRCm39) |
W266R |
probably benign |
Het |
Mboat2 |
G |
A |
12: 24,984,609 (GRCm39) |
E147K |
probably damaging |
Het |
Mctp2 |
T |
C |
7: 71,852,210 (GRCm39) |
I439V |
probably benign |
Het |
Npc2 |
A |
G |
12: 84,812,131 (GRCm39) |
V37A |
probably damaging |
Het |
Or2t29 |
A |
T |
11: 58,433,778 (GRCm39) |
S188T |
possibly damaging |
Het |
Or5b119 |
A |
T |
19: 13,456,764 (GRCm39) |
M266K |
possibly damaging |
Het |
Parp4 |
T |
C |
14: 56,825,271 (GRCm39) |
|
probably null |
Het |
Pcdhga2 |
A |
T |
18: 37,803,178 (GRCm39) |
N341Y |
probably damaging |
Het |
Pde1b |
G |
A |
15: 103,423,745 (GRCm39) |
|
probably benign |
Het |
Pde1c |
C |
T |
6: 56,128,276 (GRCm39) |
|
probably null |
Het |
Plce1 |
G |
A |
19: 38,761,441 (GRCm39) |
V2098I |
possibly damaging |
Het |
Pou2f2 |
G |
T |
7: 24,815,551 (GRCm39) |
S72* |
probably null |
Het |
Rps15 |
A |
G |
10: 80,128,624 (GRCm39) |
K7E |
probably benign |
Het |
Rtn4rl2 |
C |
T |
2: 84,702,951 (GRCm39) |
G207D |
probably damaging |
Het |
Scn2a |
A |
C |
2: 65,511,345 (GRCm39) |
L130F |
probably benign |
Het |
Sh3tc1 |
G |
A |
5: 35,868,256 (GRCm39) |
R403W |
probably damaging |
Het |
Slc7a9 |
A |
G |
7: 35,152,858 (GRCm39) |
K92R |
probably benign |
Het |
Slit3 |
A |
T |
11: 35,399,062 (GRCm39) |
E142D |
probably benign |
Het |
Srpk1 |
A |
G |
17: 28,813,229 (GRCm39) |
I505T |
probably damaging |
Het |
Sult1c2 |
A |
T |
17: 54,269,580 (GRCm39) |
I216K |
probably benign |
Het |
Susd6 |
T |
A |
12: 80,897,997 (GRCm39) |
M44K |
probably benign |
Het |
Thoc5 |
T |
A |
11: 4,876,068 (GRCm39) |
V607E |
probably benign |
Het |
Tiparp |
A |
G |
3: 65,438,767 (GRCm39) |
R28G |
probably benign |
Het |
Tln1 |
C |
T |
4: 43,540,116 (GRCm39) |
V1498I |
probably benign |
Het |
Tmprss11c |
T |
G |
5: 86,387,276 (GRCm39) |
Q214P |
probably damaging |
Het |
Uck1 |
C |
A |
2: 32,150,153 (GRCm39) |
|
probably benign |
Het |
Wdr11 |
G |
A |
7: 129,232,403 (GRCm39) |
S937N |
possibly damaging |
Het |
Zdhhc23 |
A |
T |
16: 43,791,927 (GRCm39) |
I282K |
probably damaging |
Het |
Zfp488 |
A |
G |
14: 33,693,052 (GRCm39) |
M37T |
probably benign |
Het |
Zmpste24 |
T |
C |
4: 120,940,556 (GRCm39) |
S142G |
probably benign |
Het |
|
Other mutations in Ptpru |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Ptpru
|
APN |
4 |
131,535,546 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00966:Ptpru
|
APN |
4 |
131,499,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01451:Ptpru
|
APN |
4 |
131,496,803 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01453:Ptpru
|
APN |
4 |
131,496,803 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01606:Ptpru
|
APN |
4 |
131,535,792 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02451:Ptpru
|
APN |
4 |
131,504,086 (GRCm39) |
splice site |
probably benign |
|
IGL03135:Ptpru
|
APN |
4 |
131,546,111 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03366:Ptpru
|
APN |
4 |
131,507,178 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4366001:Ptpru
|
UTSW |
4 |
131,527,023 (GRCm39) |
missense |
probably benign |
0.03 |
PIT4576001:Ptpru
|
UTSW |
4 |
131,529,855 (GRCm39) |
nonsense |
probably null |
|
R0299:Ptpru
|
UTSW |
4 |
131,530,698 (GRCm39) |
nonsense |
probably null |
|
R0458:Ptpru
|
UTSW |
4 |
131,526,986 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0502:Ptpru
|
UTSW |
4 |
131,520,954 (GRCm39) |
missense |
probably benign |
0.02 |
R0503:Ptpru
|
UTSW |
4 |
131,520,954 (GRCm39) |
missense |
probably benign |
0.02 |
R0619:Ptpru
|
UTSW |
4 |
131,548,198 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0639:Ptpru
|
UTSW |
4 |
131,498,490 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0843:Ptpru
|
UTSW |
4 |
131,525,259 (GRCm39) |
missense |
probably benign |
0.10 |
R1065:Ptpru
|
UTSW |
4 |
131,535,651 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1170:Ptpru
|
UTSW |
4 |
131,535,838 (GRCm39) |
splice site |
probably benign |
|
R1382:Ptpru
|
UTSW |
4 |
131,535,540 (GRCm39) |
missense |
probably damaging |
0.98 |
R1442:Ptpru
|
UTSW |
4 |
131,535,580 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Ptpru
|
UTSW |
4 |
131,501,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R1624:Ptpru
|
UTSW |
4 |
131,499,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R1688:Ptpru
|
UTSW |
4 |
131,514,656 (GRCm39) |
missense |
probably benign |
0.01 |
R1699:Ptpru
|
UTSW |
4 |
131,506,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Ptpru
|
UTSW |
4 |
131,520,989 (GRCm39) |
splice site |
probably null |
|
R1874:Ptpru
|
UTSW |
4 |
131,497,066 (GRCm39) |
missense |
probably benign |
|
R1959:Ptpru
|
UTSW |
4 |
131,530,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Ptpru
|
UTSW |
4 |
131,546,398 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2200:Ptpru
|
UTSW |
4 |
131,548,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R2281:Ptpru
|
UTSW |
4 |
131,535,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R2304:Ptpru
|
UTSW |
4 |
131,499,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R2411:Ptpru
|
UTSW |
4 |
131,498,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R2845:Ptpru
|
UTSW |
4 |
131,546,972 (GRCm39) |
missense |
probably benign |
0.00 |
R3767:Ptpru
|
UTSW |
4 |
131,535,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R3768:Ptpru
|
UTSW |
4 |
131,535,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R3769:Ptpru
|
UTSW |
4 |
131,535,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R3770:Ptpru
|
UTSW |
4 |
131,535,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R3937:Ptpru
|
UTSW |
4 |
131,501,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R4079:Ptpru
|
UTSW |
4 |
131,526,021 (GRCm39) |
critical splice donor site |
probably null |
|
R4110:Ptpru
|
UTSW |
4 |
131,546,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R4170:Ptpru
|
UTSW |
4 |
131,503,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Ptpru
|
UTSW |
4 |
131,548,279 (GRCm39) |
missense |
probably benign |
|
R4751:Ptpru
|
UTSW |
4 |
131,529,897 (GRCm39) |
missense |
probably damaging |
0.97 |
R4766:Ptpru
|
UTSW |
4 |
131,548,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Ptpru
|
UTSW |
4 |
131,526,914 (GRCm39) |
missense |
probably benign |
|
R4900:Ptpru
|
UTSW |
4 |
131,515,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R4998:Ptpru
|
UTSW |
4 |
131,504,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5279:Ptpru
|
UTSW |
4 |
131,547,334 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5464:Ptpru
|
UTSW |
4 |
131,499,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5625:Ptpru
|
UTSW |
4 |
131,530,691 (GRCm39) |
missense |
probably null |
1.00 |
R5667:Ptpru
|
UTSW |
4 |
131,547,501 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5671:Ptpru
|
UTSW |
4 |
131,547,501 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5735:Ptpru
|
UTSW |
4 |
131,565,401 (GRCm39) |
missense |
probably benign |
0.01 |
R5802:Ptpru
|
UTSW |
4 |
131,515,688 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5809:Ptpru
|
UTSW |
4 |
131,513,067 (GRCm39) |
missense |
probably benign |
0.34 |
R5953:Ptpru
|
UTSW |
4 |
131,504,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R5973:Ptpru
|
UTSW |
4 |
131,546,236 (GRCm39) |
missense |
probably benign |
0.00 |
R6029:Ptpru
|
UTSW |
4 |
131,498,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6072:Ptpru
|
UTSW |
4 |
131,503,539 (GRCm39) |
missense |
probably damaging |
0.99 |
R6089:Ptpru
|
UTSW |
4 |
131,499,941 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6174:Ptpru
|
UTSW |
4 |
131,513,065 (GRCm39) |
missense |
probably benign |
|
R6177:Ptpru
|
UTSW |
4 |
131,520,836 (GRCm39) |
missense |
probably benign |
0.00 |
R6367:Ptpru
|
UTSW |
4 |
131,501,663 (GRCm39) |
missense |
probably benign |
0.18 |
R6682:Ptpru
|
UTSW |
4 |
131,548,093 (GRCm39) |
missense |
probably benign |
|
R6950:Ptpru
|
UTSW |
4 |
131,503,663 (GRCm39) |
missense |
probably damaging |
0.99 |
R7159:Ptpru
|
UTSW |
4 |
131,546,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7736:Ptpru
|
UTSW |
4 |
131,515,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Ptpru
|
UTSW |
4 |
131,515,820 (GRCm39) |
missense |
probably benign |
0.01 |
R8094:Ptpru
|
UTSW |
4 |
131,520,903 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8262:Ptpru
|
UTSW |
4 |
131,522,274 (GRCm39) |
nonsense |
probably null |
|
R8276:Ptpru
|
UTSW |
4 |
131,506,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R8355:Ptpru
|
UTSW |
4 |
131,535,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8377:Ptpru
|
UTSW |
4 |
131,535,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R8858:Ptpru
|
UTSW |
4 |
131,526,825 (GRCm39) |
splice site |
probably benign |
|
R8911:Ptpru
|
UTSW |
4 |
131,503,560 (GRCm39) |
missense |
probably damaging |
0.96 |
R8934:Ptpru
|
UTSW |
4 |
131,546,297 (GRCm39) |
missense |
probably damaging |
0.98 |
R9031:Ptpru
|
UTSW |
4 |
131,515,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Ptpru
|
UTSW |
4 |
131,503,565 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9096:Ptpru
|
UTSW |
4 |
131,499,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9097:Ptpru
|
UTSW |
4 |
131,499,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9151:Ptpru
|
UTSW |
4 |
131,522,278 (GRCm39) |
missense |
probably benign |
|
R9166:Ptpru
|
UTSW |
4 |
131,525,180 (GRCm39) |
missense |
probably benign |
0.00 |
R9174:Ptpru
|
UTSW |
4 |
131,535,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9242:Ptpru
|
UTSW |
4 |
131,530,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R9698:Ptpru
|
UTSW |
4 |
131,547,531 (GRCm39) |
missense |
probably benign |
0.09 |
X0024:Ptpru
|
UTSW |
4 |
131,498,501 (GRCm39) |
missense |
probably benign |
0.15 |
Z1177:Ptpru
|
UTSW |
4 |
131,535,573 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Ptpru
|
UTSW |
4 |
131,527,017 (GRCm39) |
missense |
probably benign |
0.00 |
|