Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
4933402D24Rik |
A |
G |
1: 63,795,373 (GRCm39) |
|
probably benign |
Het |
9030612E09Rik |
G |
T |
10: 43,050,796 (GRCm39) |
R30L |
possibly damaging |
Het |
Aadacl2 |
A |
G |
3: 59,924,844 (GRCm39) |
D137G |
possibly damaging |
Het |
Acad11 |
T |
G |
9: 103,963,222 (GRCm39) |
|
probably benign |
Het |
Acap1 |
A |
T |
11: 69,776,311 (GRCm39) |
N229K |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,369,898 (GRCm39) |
T666A |
probably damaging |
Het |
Btbd16 |
T |
C |
7: 130,391,954 (GRCm39) |
F160L |
probably damaging |
Het |
Clock |
A |
C |
5: 76,379,360 (GRCm39) |
H525Q |
probably benign |
Het |
Col6a1 |
G |
T |
10: 76,546,922 (GRCm39) |
Q767K |
unknown |
Het |
Creld1 |
A |
G |
6: 113,466,737 (GRCm39) |
H240R |
probably benign |
Het |
Dlg4 |
G |
A |
11: 69,932,755 (GRCm39) |
|
probably null |
Het |
Fam204a |
A |
T |
19: 60,187,870 (GRCm39) |
*237R |
probably null |
Het |
Filip1 |
T |
A |
9: 79,805,715 (GRCm39) |
N13I |
probably damaging |
Het |
Hddc3 |
A |
T |
7: 79,993,341 (GRCm39) |
Q56L |
probably damaging |
Het |
Hes6 |
A |
C |
1: 91,340,986 (GRCm39) |
|
probably null |
Het |
Hormad1 |
A |
G |
3: 95,487,326 (GRCm39) |
D270G |
probably benign |
Het |
Ifitm1 |
A |
G |
7: 140,549,711 (GRCm39) |
|
probably null |
Het |
Igbp1b |
A |
C |
6: 138,634,871 (GRCm39) |
V191G |
probably damaging |
Het |
Impg2 |
T |
A |
16: 56,072,517 (GRCm39) |
N316K |
probably damaging |
Het |
Kalrn |
C |
T |
16: 33,810,180 (GRCm39) |
D2525N |
possibly damaging |
Het |
Lilra6 |
T |
C |
7: 3,914,453 (GRCm39) |
Y566C |
probably damaging |
Het |
Map4k4 |
A |
G |
1: 40,046,656 (GRCm39) |
D775G |
probably damaging |
Het |
Mtmr10 |
A |
T |
7: 63,947,245 (GRCm39) |
K53N |
probably damaging |
Het |
Mybpc2 |
G |
A |
7: 44,155,662 (GRCm39) |
R864W |
probably damaging |
Het |
Nckap1l |
C |
A |
15: 103,391,995 (GRCm39) |
P810Q |
probably damaging |
Het |
Nsf |
C |
T |
11: 103,821,578 (GRCm39) |
E26K |
possibly damaging |
Het |
Or14c44 |
T |
C |
7: 86,062,290 (GRCm39) |
V281A |
possibly damaging |
Het |
Or1ad1 |
A |
G |
11: 50,875,758 (GRCm39) |
T77A |
probably damaging |
Het |
Or4a27 |
C |
T |
2: 88,559,741 (GRCm39) |
M67I |
probably benign |
Het |
Ppp2r3c |
T |
C |
12: 55,345,269 (GRCm39) |
K73R |
probably benign |
Het |
Ptpru |
A |
T |
4: 131,498,780 (GRCm39) |
F1311Y |
probably damaging |
Het |
Ror2 |
G |
A |
13: 53,284,980 (GRCm39) |
P144L |
possibly damaging |
Het |
Setd2 |
A |
G |
9: 110,379,497 (GRCm39) |
E1104G |
possibly damaging |
Het |
St14 |
G |
A |
9: 31,019,530 (GRCm39) |
T97I |
probably benign |
Het |
Stag3 |
A |
G |
5: 138,281,290 (GRCm39) |
|
probably benign |
Het |
Sytl3 |
T |
C |
17: 7,003,892 (GRCm39) |
S326P |
probably damaging |
Het |
Tor1b |
G |
T |
2: 30,845,824 (GRCm39) |
S167I |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,568,359 (GRCm39) |
E27511D |
probably damaging |
Het |
Uso1 |
T |
A |
5: 92,306,258 (GRCm39) |
|
probably benign |
Het |
Vmn1r10 |
G |
T |
6: 57,091,124 (GRCm39) |
V239F |
probably benign |
Het |
Vps35l |
G |
C |
7: 118,391,818 (GRCm39) |
A410P |
probably damaging |
Het |
Zfp160 |
C |
T |
17: 21,246,007 (GRCm39) |
R186C |
possibly damaging |
Het |
Zfp869 |
A |
G |
8: 70,159,179 (GRCm39) |
C465R |
probably damaging |
Het |
Zfp957 |
T |
C |
14: 79,451,782 (GRCm39) |
K6E |
unknown |
Het |
|
Other mutations in Gm14295 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1623:Gm14295
|
UTSW |
2 |
176,499,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Gm14295
|
UTSW |
2 |
176,502,474 (GRCm39) |
nonsense |
probably null |
|
R2172:Gm14295
|
UTSW |
2 |
176,502,895 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4472:Gm14295
|
UTSW |
2 |
176,501,386 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4949:Gm14295
|
UTSW |
2 |
176,501,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R5082:Gm14295
|
UTSW |
2 |
176,499,210 (GRCm39) |
nonsense |
probably null |
|
R5311:Gm14295
|
UTSW |
2 |
176,502,465 (GRCm39) |
missense |
probably benign |
0.00 |
R5792:Gm14295
|
UTSW |
2 |
176,502,807 (GRCm39) |
missense |
probably benign |
0.10 |
R6170:Gm14295
|
UTSW |
2 |
176,502,937 (GRCm39) |
unclassified |
probably benign |
|
R6267:Gm14295
|
UTSW |
2 |
176,500,782 (GRCm39) |
nonsense |
probably null |
|
R6286:Gm14295
|
UTSW |
2 |
176,501,361 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6743:Gm14295
|
UTSW |
2 |
176,502,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Gm14295
|
UTSW |
2 |
176,500,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7536:Gm14295
|
UTSW |
2 |
176,502,722 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8049:Gm14295
|
UTSW |
2 |
176,500,871 (GRCm39) |
missense |
probably benign |
0.03 |
R8126:Gm14295
|
UTSW |
2 |
176,502,658 (GRCm39) |
missense |
probably benign |
0.04 |
R8209:Gm14295
|
UTSW |
2 |
176,502,970 (GRCm39) |
missense |
unknown |
|
R8292:Gm14295
|
UTSW |
2 |
176,501,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R8356:Gm14295
|
UTSW |
2 |
176,501,307 (GRCm39) |
missense |
probably benign |
0.24 |
R8412:Gm14295
|
UTSW |
2 |
176,501,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R8993:Gm14295
|
UTSW |
2 |
176,501,623 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9459:Gm14295
|
UTSW |
2 |
176,499,165 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9562:Gm14295
|
UTSW |
2 |
176,499,162 (GRCm39) |
missense |
probably benign |
0.34 |
R9565:Gm14295
|
UTSW |
2 |
176,499,162 (GRCm39) |
missense |
probably benign |
0.34 |
|