Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
C |
A |
5: 8,949,677 (GRCm39) |
T79K |
probably damaging |
Het |
Ackr3 |
G |
T |
1: 90,142,558 (GRCm39) |
G339V |
probably damaging |
Het |
Agpat4 |
G |
T |
17: 12,429,186 (GRCm39) |
R146L |
probably damaging |
Het |
Ampd1 |
C |
T |
3: 102,998,936 (GRCm39) |
R364C |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,645,660 (GRCm39) |
T507A |
probably benign |
Het |
Cand2 |
C |
G |
6: 115,768,923 (GRCm39) |
R578G |
probably benign |
Het |
Capg |
C |
T |
6: 72,532,869 (GRCm39) |
P111L |
probably damaging |
Het |
Carm1 |
C |
T |
9: 21,494,350 (GRCm39) |
T289I |
probably damaging |
Het |
Ccr6 |
A |
G |
17: 8,474,965 (GRCm39) |
I57V |
probably benign |
Het |
Cdk5rap2 |
T |
C |
4: 70,255,583 (GRCm39) |
I434V |
possibly damaging |
Het |
Chrdl2 |
C |
T |
7: 99,655,743 (GRCm39) |
|
probably benign |
Het |
Cntnap5a |
A |
G |
1: 116,220,109 (GRCm39) |
T640A |
probably benign |
Het |
Ctsd |
T |
C |
7: 141,937,280 (GRCm39) |
|
probably null |
Het |
D17H6S53E |
G |
T |
17: 35,346,536 (GRCm39) |
R149L |
possibly damaging |
Het |
Dync1i1 |
A |
G |
6: 5,769,706 (GRCm39) |
T77A |
probably benign |
Het |
Emc2 |
T |
C |
15: 43,358,639 (GRCm39) |
M100T |
probably benign |
Het |
Esrra |
A |
G |
19: 6,889,863 (GRCm39) |
V290A |
probably benign |
Het |
Fbl |
T |
C |
7: 27,876,620 (GRCm39) |
I207T |
probably benign |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Gcc1 |
T |
A |
6: 28,420,375 (GRCm39) |
N314I |
possibly damaging |
Het |
Gzmm |
A |
T |
10: 79,530,354 (GRCm39) |
D175V |
probably damaging |
Het |
Heatr1 |
G |
A |
13: 12,448,806 (GRCm39) |
M1840I |
probably benign |
Het |
Helz |
T |
C |
11: 107,523,153 (GRCm39) |
L779P |
probably damaging |
Het |
Impg1 |
T |
A |
9: 80,289,064 (GRCm39) |
N331I |
probably damaging |
Het |
Inmt |
C |
T |
6: 55,150,270 (GRCm39) |
|
probably null |
Het |
Inpp5a |
C |
T |
7: 139,061,634 (GRCm39) |
T102M |
probably damaging |
Het |
Lamc3 |
A |
G |
2: 31,788,323 (GRCm39) |
Y161C |
probably benign |
Het |
Lpin2 |
A |
G |
17: 71,553,966 (GRCm39) |
*932W |
probably null |
Het |
Lrp3 |
C |
T |
7: 34,901,934 (GRCm39) |
R649H |
probably benign |
Het |
Madd |
G |
A |
2: 90,973,949 (GRCm39) |
T1464I |
probably damaging |
Het |
Nceh1 |
C |
A |
3: 27,293,777 (GRCm39) |
Y178* |
probably null |
Het |
Or5ae2 |
A |
T |
7: 84,506,086 (GRCm39) |
K172* |
probably null |
Het |
Or5b96 |
T |
A |
19: 12,867,989 (GRCm39) |
|
probably benign |
Het |
Pramel39-ps |
G |
T |
5: 94,451,001 (GRCm39) |
P375H |
probably damaging |
Het |
Ptchd4 |
A |
T |
17: 42,627,604 (GRCm39) |
R22* |
probably null |
Het |
Ralgapb |
G |
T |
2: 158,277,386 (GRCm39) |
R250L |
probably benign |
Het |
Rcor1 |
T |
A |
12: 111,076,228 (GRCm39) |
Y395* |
probably null |
Het |
Slc35f6 |
G |
T |
5: 30,805,410 (GRCm39) |
|
probably benign |
Het |
Slc40a1 |
A |
G |
1: 45,950,129 (GRCm39) |
V441A |
probably benign |
Het |
Slc6a13 |
T |
A |
6: 121,295,228 (GRCm39) |
F77Y |
probably damaging |
Het |
Slc6a15 |
T |
A |
10: 103,229,406 (GRCm39) |
C148* |
probably null |
Het |
Sox10 |
T |
C |
15: 79,040,640 (GRCm39) |
Y300C |
probably damaging |
Het |
Tomm70a |
T |
A |
16: 56,958,383 (GRCm39) |
|
probably benign |
Het |
Tor4a |
A |
G |
2: 25,085,537 (GRCm39) |
V122A |
probably benign |
Het |
Tpi1 |
T |
C |
6: 124,791,138 (GRCm39) |
Q33R |
probably benign |
Het |
Unk |
T |
C |
11: 115,940,184 (GRCm39) |
V179A |
probably benign |
Het |
Ush2a |
G |
T |
1: 188,365,787 (GRCm39) |
G2214C |
probably damaging |
Het |
Vmn1r159 |
T |
A |
7: 22,542,912 (GRCm39) |
Y40F |
probably benign |
Het |
Wbp2nl |
T |
C |
15: 82,192,748 (GRCm39) |
V144A |
probably benign |
Het |
Wdpcp |
A |
G |
11: 21,835,040 (GRCm39) |
E681G |
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 |
R8416:Ptpru
|
UTSW |
4 |
131,535,783 (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 |
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 |
|