Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,349,180 (GRCm39) |
W3585R |
probably null |
Het |
Ajm1 |
G |
T |
2: 25,467,043 (GRCm39) |
S956* |
probably null |
Het |
Babam1 |
G |
C |
8: 71,850,424 (GRCm39) |
E18Q |
probably damaging |
Het |
Bcan |
G |
T |
3: 87,901,519 (GRCm39) |
S394R |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,999,232 (GRCm39) |
F4653L |
probably damaging |
Het |
Camsap2 |
A |
T |
1: 136,209,832 (GRCm39) |
H559Q |
probably benign |
Het |
Cars2 |
G |
T |
8: 11,580,430 (GRCm39) |
|
probably null |
Het |
Ccdc93 |
T |
A |
1: 121,389,712 (GRCm39) |
|
probably benign |
Het |
Ccna2 |
C |
A |
3: 36,624,879 (GRCm39) |
|
probably benign |
Het |
Cdc6 |
T |
A |
11: 98,803,037 (GRCm39) |
L326I |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,255,478 (GRCm39) |
|
probably benign |
Het |
Cenpe |
T |
A |
3: 134,976,661 (GRCm39) |
S2423T |
probably benign |
Het |
Cftr |
A |
G |
6: 18,225,936 (GRCm39) |
M295V |
probably benign |
Het |
Cxcl2 |
A |
G |
5: 91,051,871 (GRCm39) |
H23R |
probably benign |
Het |
Cyp4a12b |
A |
G |
4: 115,291,181 (GRCm39) |
T370A |
probably damaging |
Het |
Daam2 |
A |
G |
17: 49,803,148 (GRCm39) |
|
probably benign |
Het |
Dclk3 |
T |
C |
9: 111,298,276 (GRCm39) |
F607L |
probably damaging |
Het |
Des |
T |
G |
1: 75,337,230 (GRCm39) |
S57A |
probably benign |
Het |
Drd1 |
A |
T |
13: 54,206,964 (GRCm39) |
S410T |
probably damaging |
Het |
Ecm1 |
G |
A |
3: 95,643,275 (GRCm39) |
R342C |
probably damaging |
Het |
Fanci |
T |
C |
7: 79,082,941 (GRCm39) |
L639P |
probably damaging |
Het |
Fancm |
A |
G |
12: 65,140,463 (GRCm39) |
E395G |
probably benign |
Het |
Grik3 |
A |
G |
4: 125,601,790 (GRCm39) |
D889G |
probably benign |
Het |
Heyl |
A |
G |
4: 123,135,192 (GRCm39) |
S62G |
probably damaging |
Het |
Hmox1 |
C |
T |
8: 75,826,577 (GRCm39) |
P267L |
probably damaging |
Het |
Ifi213 |
A |
C |
1: 173,394,784 (GRCm39) |
S584A |
probably benign |
Het |
Il12rb2 |
G |
T |
6: 67,333,576 (GRCm39) |
F234L |
probably benign |
Het |
Il4i1 |
T |
A |
7: 44,488,811 (GRCm39) |
S233T |
probably damaging |
Het |
Itga4 |
A |
G |
2: 79,146,032 (GRCm39) |
S745G |
probably benign |
Het |
Kalrn |
T |
A |
16: 33,830,918 (GRCm39) |
I734F |
possibly damaging |
Het |
Klk1b16 |
T |
C |
7: 43,790,425 (GRCm39) |
I200T |
probably benign |
Het |
Lrrc4c |
T |
A |
2: 97,461,117 (GRCm39) |
M581K |
probably benign |
Het |
M6pr |
A |
T |
6: 122,292,033 (GRCm39) |
I122L |
probably benign |
Het |
Magi3 |
T |
C |
3: 103,954,169 (GRCm39) |
|
probably benign |
Het |
Mybpc2 |
T |
G |
7: 44,163,111 (GRCm39) |
T480P |
probably benign |
Het |
Or1j17 |
A |
G |
2: 36,578,770 (GRCm39) |
Y252C |
probably damaging |
Het |
Or51ab3 |
A |
T |
7: 103,201,372 (GRCm39) |
I127F |
possibly damaging |
Het |
Or8g23 |
T |
C |
9: 38,971,437 (GRCm39) |
N175S |
probably benign |
Het |
Pcx |
T |
A |
19: 4,669,114 (GRCm39) |
I704N |
probably damaging |
Het |
Pde3a |
G |
T |
6: 141,404,824 (GRCm39) |
A350S |
probably damaging |
Het |
Ppox |
A |
T |
1: 171,107,580 (GRCm39) |
|
probably benign |
Het |
Prb1a |
T |
A |
6: 132,185,507 (GRCm39) |
Y42F |
unknown |
Het |
Rsph4a |
T |
A |
10: 33,785,727 (GRCm39) |
V546E |
probably damaging |
Het |
Saxo4 |
T |
C |
19: 10,458,770 (GRCm39) |
T87A |
probably benign |
Het |
Sf3b1 |
C |
G |
1: 55,058,554 (GRCm39) |
E12Q |
possibly damaging |
Het |
Sh3tc1 |
A |
G |
5: 35,860,693 (GRCm39) |
|
probably null |
Het |
Slc22a2 |
T |
C |
17: 12,803,298 (GRCm39) |
F44S |
probably damaging |
Het |
Slco6c1 |
T |
A |
1: 97,026,223 (GRCm39) |
D334V |
probably damaging |
Het |
Smim19 |
T |
C |
8: 22,953,352 (GRCm39) |
D105G |
probably damaging |
Het |
Smpdl3a |
A |
G |
10: 57,683,588 (GRCm39) |
T233A |
probably damaging |
Het |
St8sia5 |
G |
A |
18: 77,299,460 (GRCm39) |
|
probably null |
Het |
Stk32a |
C |
A |
18: 43,376,149 (GRCm39) |
Q73K |
probably benign |
Het |
Tmem129 |
G |
T |
5: 33,815,100 (GRCm39) |
|
probably null |
Het |
Traf3ip3 |
A |
T |
1: 192,860,599 (GRCm39) |
L441Q |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,731,305 (GRCm39) |
|
probably benign |
Het |
Unc45b |
T |
C |
11: 82,808,672 (GRCm39) |
S253P |
possibly damaging |
Het |
Vars2 |
A |
G |
17: 35,977,150 (GRCm39) |
|
probably benign |
Het |
Vmn2r51 |
C |
T |
7: 9,836,372 (GRCm39) |
M136I |
possibly damaging |
Het |
Vmn2r51 |
A |
G |
7: 9,836,373 (GRCm39) |
M136T |
possibly damaging |
Het |
Zfp595 |
T |
C |
13: 67,465,127 (GRCm39) |
I379V |
possibly damaging |
Het |
|
Other mutations in Or14c44 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01015:Or14c44
|
APN |
7 |
86,061,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01459:Or14c44
|
APN |
7 |
86,061,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01538:Or14c44
|
APN |
7 |
86,062,167 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01547:Or14c44
|
APN |
7 |
86,062,079 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0918:Or14c44
|
UTSW |
7 |
86,062,403 (GRCm39) |
missense |
probably benign |
0.01 |
R1651:Or14c44
|
UTSW |
7 |
86,057,078 (GRCm39) |
utr 5 prime |
probably benign |
|
R2411:Or14c44
|
UTSW |
7 |
86,062,290 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3732:Or14c44
|
UTSW |
7 |
86,061,841 (GRCm39) |
missense |
probably damaging |
0.98 |
R3832:Or14c44
|
UTSW |
7 |
86,062,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R5175:Or14c44
|
UTSW |
7 |
86,062,254 (GRCm39) |
missense |
probably benign |
0.00 |
R5372:Or14c44
|
UTSW |
7 |
86,062,176 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5413:Or14c44
|
UTSW |
7 |
86,061,675 (GRCm39) |
missense |
probably benign |
|
R5520:Or14c44
|
UTSW |
7 |
86,062,064 (GRCm39) |
missense |
probably benign |
0.02 |
R5579:Or14c44
|
UTSW |
7 |
86,061,934 (GRCm39) |
nonsense |
probably null |
|
R6037:Or14c44
|
UTSW |
7 |
86,062,478 (GRCm39) |
missense |
probably benign |
0.02 |
R6037:Or14c44
|
UTSW |
7 |
86,062,478 (GRCm39) |
missense |
probably benign |
0.02 |
R7251:Or14c44
|
UTSW |
7 |
86,062,209 (GRCm39) |
missense |
probably benign |
|
R7340:Or14c44
|
UTSW |
7 |
86,061,957 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7860:Or14c44
|
UTSW |
7 |
86,057,119 (GRCm39) |
start gained |
probably benign |
|
R8305:Or14c44
|
UTSW |
7 |
86,061,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Or14c44
|
UTSW |
7 |
86,061,702 (GRCm39) |
missense |
probably benign |
0.14 |
R8487:Or14c44
|
UTSW |
7 |
86,061,647 (GRCm39) |
missense |
probably benign |
0.34 |
R8799:Or14c44
|
UTSW |
7 |
86,061,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R9342:Or14c44
|
UTSW |
7 |
86,062,430 (GRCm39) |
missense |
probably benign |
0.37 |
Z1176:Or14c44
|
UTSW |
7 |
86,061,906 (GRCm39) |
missense |
probably benign |
0.16 |
|