Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6b |
C |
T |
12: 113,453,758 (GRCm39) |
P192S |
possibly damaging |
Het |
Arhgef10 |
A |
G |
8: 14,995,373 (GRCm39) |
T353A |
probably damaging |
Het |
Cabyr |
A |
G |
18: 12,877,828 (GRCm39) |
D55G |
probably damaging |
Het |
Dcaf4 |
T |
C |
12: 83,584,733 (GRCm39) |
V322A |
probably damaging |
Het |
Ephb2 |
T |
A |
4: 136,498,947 (GRCm39) |
E44V |
possibly damaging |
Het |
Fam3c |
T |
C |
6: 22,328,573 (GRCm39) |
I105V |
probably benign |
Het |
Fras1 |
A |
G |
5: 96,900,763 (GRCm39) |
D2994G |
probably damaging |
Het |
Fryl |
C |
T |
5: 73,228,641 (GRCm39) |
D1697N |
probably damaging |
Het |
Gapdh |
A |
T |
6: 125,139,911 (GRCm39) |
Y164* |
probably null |
Het |
Gm4353 |
T |
G |
7: 115,682,998 (GRCm39) |
Q194H |
possibly damaging |
Het |
Ilvbl |
T |
A |
10: 78,413,085 (GRCm39) |
|
probably null |
Het |
Ism2 |
T |
A |
12: 87,333,658 (GRCm39) |
|
probably null |
Het |
Jak2 |
C |
T |
19: 29,254,268 (GRCm39) |
T196I |
probably benign |
Het |
Lcor |
T |
G |
19: 41,547,234 (GRCm39) |
Y273D |
probably benign |
Het |
Ldlrad4 |
G |
T |
18: 68,368,740 (GRCm39) |
A66S |
possibly damaging |
Het |
Lysmd4 |
T |
A |
7: 66,873,446 (GRCm39) |
M27K |
possibly damaging |
Het |
Or11h4b |
A |
T |
14: 50,918,261 (GRCm39) |
Y277N |
probably damaging |
Het |
Or13a25 |
T |
A |
7: 140,247,854 (GRCm39) |
I211N |
probably benign |
Het |
Or5m10 |
A |
G |
2: 85,717,951 (GRCm39) |
E269G |
possibly damaging |
Het |
Oscp1 |
T |
C |
4: 125,958,774 (GRCm39) |
|
probably null |
Het |
Pira2 |
A |
T |
7: 3,844,696 (GRCm39) |
F445Y |
probably benign |
Het |
Pkd2l2 |
C |
A |
18: 34,549,913 (GRCm39) |
P186Q |
probably damaging |
Het |
Plcb1 |
G |
A |
2: 135,062,677 (GRCm39) |
G96R |
possibly damaging |
Het |
Plcd3 |
G |
C |
11: 102,965,481 (GRCm39) |
R535G |
probably benign |
Het |
Plcg1 |
A |
G |
2: 160,596,523 (GRCm39) |
M681V |
possibly damaging |
Het |
Polr1b |
C |
A |
2: 128,967,464 (GRCm39) |
F952L |
probably damaging |
Het |
Polrmt |
A |
T |
10: 79,575,022 (GRCm39) |
D836E |
probably benign |
Het |
Pramel12 |
T |
C |
4: 143,144,331 (GRCm39) |
Y226H |
possibly damaging |
Het |
Prkag1 |
A |
T |
15: 98,712,478 (GRCm39) |
I149N |
probably damaging |
Het |
Prkci |
A |
T |
3: 31,104,362 (GRCm39) |
Q575L |
possibly damaging |
Het |
Prss40 |
C |
T |
1: 34,591,846 (GRCm39) |
W276* |
probably null |
Het |
Ptprn |
T |
C |
1: 75,228,946 (GRCm39) |
D823G |
possibly damaging |
Het |
Radil |
A |
C |
5: 142,529,303 (GRCm39) |
F131C |
probably damaging |
Het |
Rif1 |
A |
G |
2: 52,006,368 (GRCm39) |
I550V |
probably benign |
Het |
Rmnd1 |
T |
C |
10: 4,361,713 (GRCm39) |
E320G |
probably damaging |
Het |
Sec31b |
T |
A |
19: 44,512,212 (GRCm39) |
K561* |
probably null |
Het |
Spata31g1 |
C |
T |
4: 42,970,171 (GRCm39) |
Q53* |
probably null |
Het |
Spata31g1 |
T |
C |
4: 42,971,095 (GRCm39) |
S143P |
probably benign |
Het |
Tbx5 |
A |
C |
5: 120,021,232 (GRCm39) |
T413P |
probably benign |
Het |
Tmprss7 |
A |
G |
16: 45,480,963 (GRCm39) |
|
probably null |
Het |
Tnfaip8l2 |
T |
C |
3: 95,047,307 (GRCm39) |
*185W |
probably null |
Het |
Tpst2 |
A |
G |
5: 112,457,560 (GRCm39) |
E296G |
possibly damaging |
Het |
Ubn2 |
T |
A |
6: 38,467,688 (GRCm39) |
S801T |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,332,638 (GRCm39) |
S1141G |
|
Het |
Uts2r |
A |
G |
11: 121,052,279 (GRCm39) |
N381S |
probably benign |
Het |
Vmn2r44 |
G |
T |
7: 8,381,314 (GRCm39) |
T193K |
possibly damaging |
Het |
Wdr18 |
T |
A |
10: 79,801,884 (GRCm39) |
M223K |
probably benign |
Het |
Wdr64 |
T |
C |
1: 175,617,564 (GRCm39) |
C715R |
possibly damaging |
Het |
Zfp672 |
A |
G |
11: 58,208,081 (GRCm39) |
F80S |
possibly damaging |
Het |
|
Other mutations in Muc17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Muc17
|
APN |
5 |
137,165,971 (GRCm39) |
nonsense |
probably null |
|
R0256:Muc17
|
UTSW |
5 |
137,175,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R0884:Muc17
|
UTSW |
5 |
137,171,146 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1368:Muc17
|
UTSW |
5 |
137,175,674 (GRCm39) |
splice site |
probably benign |
|
R1456:Muc17
|
UTSW |
5 |
137,166,799 (GRCm39) |
missense |
probably benign |
0.01 |
R1670:Muc17
|
UTSW |
5 |
137,172,843 (GRCm39) |
missense |
probably benign |
0.22 |
R2401:Muc17
|
UTSW |
5 |
137,190,980 (GRCm39) |
unclassified |
probably benign |
|
R2698:Muc17
|
UTSW |
5 |
137,175,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R4637:Muc17
|
UTSW |
5 |
137,175,502 (GRCm39) |
missense |
probably damaging |
0.98 |
R5128:Muc17
|
UTSW |
5 |
137,167,034 (GRCm39) |
critical splice donor site |
probably null |
|
R5323:Muc17
|
UTSW |
5 |
137,175,537 (GRCm39) |
nonsense |
probably null |
|
R5601:Muc17
|
UTSW |
5 |
137,166,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5967:Muc17
|
UTSW |
5 |
137,175,485 (GRCm39) |
missense |
probably benign |
0.03 |
R6480:Muc17
|
UTSW |
5 |
137,171,238 (GRCm39) |
missense |
|
|
R7868:Muc17
|
UTSW |
5 |
137,175,625 (GRCm39) |
missense |
|
|
R7974:Muc17
|
UTSW |
5 |
137,175,664 (GRCm39) |
missense |
|
|
R8393:Muc17
|
UTSW |
5 |
137,171,179 (GRCm39) |
missense |
|
|
R8415:Muc17
|
UTSW |
5 |
137,172,798 (GRCm39) |
missense |
|
|
R8419:Muc17
|
UTSW |
5 |
137,175,570 (GRCm39) |
missense |
|
|
R9105:Muc17
|
UTSW |
5 |
137,171,238 (GRCm39) |
missense |
|
|
R9742:Muc17
|
UTSW |
5 |
137,167,127 (GRCm39) |
missense |
|
|
|