Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acin1 |
T |
C |
14: 54,881,174 (GRCm39) |
|
probably benign |
Het |
Acot3 |
C |
T |
12: 84,105,484 (GRCm39) |
A317V |
probably benign |
Het |
Ahrr |
T |
C |
13: 74,362,497 (GRCm39) |
D334G |
probably benign |
Het |
Alpk2 |
C |
T |
18: 65,511,108 (GRCm39) |
V30M |
probably damaging |
Het |
Arhgef25 |
G |
T |
10: 127,021,158 (GRCm39) |
H281N |
probably damaging |
Het |
B3gntl1 |
A |
G |
11: 121,521,662 (GRCm39) |
M175T |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,484,295 (GRCm39) |
|
probably benign |
Het |
Cebpzos |
A |
G |
17: 79,225,817 (GRCm39) |
K11E |
probably damaging |
Het |
Col6a6 |
A |
G |
9: 105,655,274 (GRCm39) |
S816P |
probably damaging |
Het |
Cul4a |
A |
G |
8: 13,173,954 (GRCm39) |
R64G |
probably damaging |
Het |
Cul7 |
C |
A |
17: 46,962,748 (GRCm39) |
C126* |
probably null |
Het |
Ercc2 |
T |
C |
7: 19,119,866 (GRCm39) |
Y176H |
probably benign |
Het |
Frem2 |
T |
G |
3: 53,455,144 (GRCm39) |
D2144A |
probably damaging |
Het |
Gabrg3 |
A |
T |
7: 56,384,822 (GRCm39) |
Y246* |
probably null |
Het |
Gpatch2l |
T |
C |
12: 86,303,708 (GRCm39) |
|
probably null |
Het |
Grk1 |
A |
G |
8: 13,455,406 (GRCm39) |
T97A |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,320,799 (GRCm39) |
E4004G |
probably damaging |
Het |
Kcnu1 |
A |
T |
8: 26,339,821 (GRCm39) |
R46S |
probably damaging |
Het |
Lrrfip1 |
T |
C |
1: 91,042,389 (GRCm39) |
S265P |
probably damaging |
Het |
Lyve1 |
A |
G |
7: 110,452,902 (GRCm39) |
|
probably null |
Het |
Mme |
A |
G |
3: 63,272,479 (GRCm39) |
Y659C |
probably damaging |
Het |
Mrs2 |
G |
T |
13: 25,179,393 (GRCm39) |
N299K |
possibly damaging |
Het |
Mtnr1b |
T |
C |
9: 15,774,615 (GRCm39) |
Y148C |
probably damaging |
Het |
Myo5b |
T |
A |
18: 74,846,611 (GRCm39) |
|
probably benign |
Het |
Neb |
A |
G |
2: 52,161,616 (GRCm39) |
Y2059H |
probably damaging |
Het |
Nkain3 |
T |
C |
4: 20,469,528 (GRCm39) |
|
probably benign |
Het |
Peg10 |
A |
T |
6: 4,757,080 (GRCm39) |
|
probably benign |
Het |
Pramel20 |
A |
G |
4: 143,298,537 (GRCm39) |
E160G |
possibly damaging |
Het |
Rufy2 |
A |
G |
10: 62,842,450 (GRCm39) |
T458A |
probably benign |
Het |
Sec14l1 |
G |
A |
11: 117,041,430 (GRCm39) |
V448I |
probably benign |
Het |
Tbx19 |
C |
T |
1: 164,970,136 (GRCm39) |
G251D |
possibly damaging |
Het |
Tcstv7b |
T |
C |
13: 120,702,369 (GRCm39) |
V55A |
probably benign |
Het |
Trappc9 |
G |
A |
15: 72,808,958 (GRCm39) |
Q711* |
probably null |
Het |
Trpm3 |
A |
G |
19: 22,116,519 (GRCm39) |
R13G |
probably benign |
Het |
Usp33 |
G |
T |
3: 152,085,247 (GRCm39) |
A628S |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,643,636 (GRCm39) |
N2080S |
probably benign |
Het |
Wdr45b |
A |
T |
11: 121,221,015 (GRCm39) |
I221N |
probably damaging |
Het |
Zfp119a |
A |
T |
17: 56,175,355 (GRCm39) |
W47R |
possibly damaging |
Het |
Zswim9 |
A |
G |
7: 13,003,497 (GRCm39) |
C118R |
probably damaging |
Het |
|
Other mutations in Ccnj |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01903:Ccnj
|
APN |
19 |
40,834,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02584:Ccnj
|
APN |
19 |
40,833,185 (GRCm39) |
missense |
probably benign |
0.04 |
R0220:Ccnj
|
UTSW |
19 |
40,833,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R0452:Ccnj
|
UTSW |
19 |
40,833,508 (GRCm39) |
splice site |
probably null |
|
R0693:Ccnj
|
UTSW |
19 |
40,825,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R2237:Ccnj
|
UTSW |
19 |
40,834,219 (GRCm39) |
missense |
probably benign |
0.00 |
R2258:Ccnj
|
UTSW |
19 |
40,834,277 (GRCm39) |
missense |
probably benign |
0.00 |
R2879:Ccnj
|
UTSW |
19 |
40,833,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Ccnj
|
UTSW |
19 |
40,833,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R6384:Ccnj
|
UTSW |
19 |
40,834,451 (GRCm39) |
missense |
probably benign |
0.09 |
R6528:Ccnj
|
UTSW |
19 |
40,820,529 (GRCm39) |
splice site |
probably null |
|
R6830:Ccnj
|
UTSW |
19 |
40,833,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R7338:Ccnj
|
UTSW |
19 |
40,825,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Ccnj
|
UTSW |
19 |
40,833,394 (GRCm39) |
missense |
probably benign |
0.28 |
R8472:Ccnj
|
UTSW |
19 |
40,833,608 (GRCm39) |
missense |
probably damaging |
0.97 |
R8977:Ccnj
|
UTSW |
19 |
40,833,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|