Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12b |
C |
A |
12: 70,210,269 (GRCm39) |
N71K |
possibly damaging |
Het |
Adgrl2 |
A |
G |
3: 148,564,854 (GRCm39) |
I242T |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,721,437 (GRCm39) |
S714P |
probably damaging |
Het |
Agap3 |
G |
A |
5: 24,705,184 (GRCm39) |
R704Q |
possibly damaging |
Het |
Ankrd11 |
T |
C |
8: 123,622,509 (GRCm39) |
R448G |
probably damaging |
Het |
Anks1b |
T |
C |
10: 89,909,829 (GRCm39) |
|
probably benign |
Het |
Caml |
A |
T |
13: 55,770,974 (GRCm39) |
Q24L |
possibly damaging |
Het |
Cdc14b |
G |
A |
13: 64,391,497 (GRCm39) |
T124I |
probably benign |
Het |
Clca3a2 |
A |
G |
3: 144,781,571 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,512,610 (GRCm39) |
|
probably null |
Het |
Crispld1 |
T |
C |
1: 17,816,992 (GRCm39) |
V183A |
possibly damaging |
Het |
Cstdc1 |
A |
G |
2: 148,624,092 (GRCm39) |
N22S |
probably benign |
Het |
Dhx40 |
C |
T |
11: 86,695,082 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
T |
A |
18: 50,026,761 (GRCm39) |
D1956E |
probably benign |
Het |
Dsc2 |
A |
G |
18: 20,184,283 (GRCm39) |
V35A |
probably damaging |
Het |
Dync2i2 |
A |
G |
2: 29,921,837 (GRCm39) |
V508A |
probably damaging |
Het |
Elovl2 |
A |
G |
13: 41,345,452 (GRCm39) |
|
probably benign |
Het |
Gapvd1 |
T |
C |
2: 34,615,048 (GRCm39) |
|
probably benign |
Het |
Gnaq |
T |
A |
19: 16,196,982 (GRCm39) |
I56N |
probably damaging |
Het |
Gpr139 |
T |
C |
7: 118,744,306 (GRCm39) |
D93G |
probably benign |
Het |
Hars1 |
C |
T |
18: 36,904,234 (GRCm39) |
R215H |
probably benign |
Het |
Helz2 |
C |
A |
2: 180,873,882 (GRCm39) |
W2204L |
probably damaging |
Het |
Ift70b |
A |
G |
2: 75,767,055 (GRCm39) |
V566A |
probably damaging |
Het |
Itgb6 |
A |
T |
2: 60,435,480 (GRCm39) |
C757S |
possibly damaging |
Het |
Kpnb1 |
G |
A |
11: 97,078,398 (GRCm39) |
T5I |
probably benign |
Het |
Krt82 |
T |
C |
15: 101,454,035 (GRCm39) |
|
probably benign |
Het |
Lgals9 |
T |
A |
11: 78,860,546 (GRCm39) |
K175N |
possibly damaging |
Het |
Lrp2 |
A |
G |
2: 69,258,998 (GRCm39) |
I4564T |
probably benign |
Het |
Mblac1 |
A |
G |
5: 138,192,798 (GRCm39) |
T47A |
possibly damaging |
Het |
Med12l |
G |
A |
3: 58,949,822 (GRCm39) |
D182N |
probably damaging |
Het |
Megf9 |
A |
G |
4: 70,353,585 (GRCm39) |
I407T |
probably benign |
Het |
Mtmr6 |
A |
T |
14: 60,529,578 (GRCm39) |
|
probably null |
Het |
Mtor |
A |
G |
4: 148,624,907 (GRCm39) |
T2173A |
probably benign |
Het |
Mzt1 |
A |
T |
14: 99,277,938 (GRCm39) |
|
probably benign |
Het |
Narf |
T |
C |
11: 121,143,690 (GRCm39) |
L444P |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,408,271 (GRCm39) |
Q1305L |
possibly damaging |
Het |
Ntsr1 |
A |
G |
2: 180,184,374 (GRCm39) |
Y359C |
probably damaging |
Het |
Olfm1 |
A |
G |
2: 28,104,640 (GRCm39) |
D159G |
possibly damaging |
Het |
Pcdh1 |
C |
T |
18: 38,322,975 (GRCm39) |
V953I |
probably damaging |
Het |
Pcdhb11 |
A |
T |
18: 37,556,887 (GRCm39) |
D739V |
probably damaging |
Het |
Pdgfd |
A |
G |
9: 6,359,769 (GRCm39) |
N280S |
probably damaging |
Het |
Per2 |
A |
T |
1: 91,366,054 (GRCm39) |
|
probably null |
Het |
Pfkp |
G |
T |
13: 6,672,028 (GRCm39) |
C122* |
probably null |
Het |
Plxna4 |
G |
A |
6: 32,169,232 (GRCm39) |
R1322W |
probably damaging |
Het |
Ppox |
A |
G |
1: 171,106,818 (GRCm39) |
L202P |
probably damaging |
Het |
Ppp1r3e |
G |
A |
14: 55,114,588 (GRCm39) |
P58L |
probably benign |
Het |
Prr23a2 |
A |
C |
9: 98,739,086 (GRCm39) |
N148T |
probably benign |
Het |
Psd |
T |
C |
19: 46,302,649 (GRCm39) |
T842A |
probably damaging |
Het |
Ranbp2 |
C |
T |
10: 58,314,236 (GRCm39) |
A1652V |
probably benign |
Het |
Rragd |
G |
A |
4: 33,007,103 (GRCm39) |
V144M |
probably damaging |
Het |
Sema6a |
T |
G |
18: 47,381,643 (GRCm39) |
D968A |
probably damaging |
Het |
Slc30a5 |
A |
T |
13: 100,945,793 (GRCm39) |
|
probably null |
Het |
Snx17 |
G |
T |
5: 31,353,895 (GRCm39) |
|
probably null |
Het |
Styxl2 |
A |
T |
1: 165,928,853 (GRCm39) |
M253K |
possibly damaging |
Het |
Syt14 |
G |
T |
1: 192,613,111 (GRCm39) |
T563K |
probably damaging |
Het |
Tada3 |
T |
C |
6: 113,352,175 (GRCm39) |
K85E |
probably damaging |
Het |
Tspear |
T |
C |
10: 77,716,921 (GRCm39) |
V532A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,723,453 (GRCm39) |
C6426S |
possibly damaging |
Het |
Unc79 |
T |
C |
12: 103,060,437 (GRCm39) |
|
probably benign |
Het |
Usp19 |
A |
G |
9: 108,371,584 (GRCm39) |
|
probably null |
Het |
Vav3 |
G |
A |
3: 109,434,746 (GRCm39) |
D426N |
probably damaging |
Het |
Vezt |
T |
C |
10: 93,842,958 (GRCm39) |
|
probably null |
Het |
Vldlr |
G |
T |
19: 27,213,655 (GRCm39) |
R114L |
probably benign |
Het |
Wwc2 |
C |
T |
8: 48,321,414 (GRCm39) |
V567I |
unknown |
Het |
Zfp423 |
T |
C |
8: 88,507,237 (GRCm39) |
T911A |
probably damaging |
Het |
Zfp719 |
A |
G |
7: 43,238,677 (GRCm39) |
|
probably null |
Het |
Zkscan16 |
A |
T |
4: 58,956,597 (GRCm39) |
H293L |
possibly damaging |
Het |
Zkscan6 |
A |
C |
11: 65,719,525 (GRCm39) |
N515T |
possibly damaging |
Het |
Znfx1 |
A |
G |
2: 166,897,575 (GRCm39) |
S450P |
probably damaging |
Het |
|
Other mutations in Or2l13b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01635:Or2l13b
|
APN |
16 |
19,348,845 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02139:Or2l13b
|
APN |
16 |
19,349,640 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02347:Or2l13b
|
APN |
16 |
19,349,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03402:Or2l13b
|
APN |
16 |
19,349,667 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R1496:Or2l13b
|
UTSW |
16 |
19,349,133 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1707:Or2l13b
|
UTSW |
16 |
19,348,927 (GRCm39) |
missense |
probably benign |
0.18 |
R2006:Or2l13b
|
UTSW |
16 |
19,349,455 (GRCm39) |
missense |
probably benign |
0.02 |
R2220:Or2l13b
|
UTSW |
16 |
19,348,895 (GRCm39) |
nonsense |
probably null |
|
R3734:Or2l13b
|
UTSW |
16 |
19,349,398 (GRCm39) |
missense |
probably damaging |
0.99 |
R4134:Or2l13b
|
UTSW |
16 |
19,349,452 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4135:Or2l13b
|
UTSW |
16 |
19,349,452 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4538:Or2l13b
|
UTSW |
16 |
19,349,381 (GRCm39) |
nonsense |
probably null |
|
R4631:Or2l13b
|
UTSW |
16 |
19,348,891 (GRCm39) |
nonsense |
probably null |
|
R4633:Or2l13b
|
UTSW |
16 |
19,349,034 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4872:Or2l13b
|
UTSW |
16 |
19,349,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R4910:Or2l13b
|
UTSW |
16 |
19,348,768 (GRCm39) |
missense |
probably benign |
0.03 |
R4945:Or2l13b
|
UTSW |
16 |
19,349,307 (GRCm39) |
missense |
probably benign |
0.03 |
R5345:Or2l13b
|
UTSW |
16 |
19,349,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Or2l13b
|
UTSW |
16 |
19,349,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R5899:Or2l13b
|
UTSW |
16 |
19,349,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R7074:Or2l13b
|
UTSW |
16 |
19,348,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7439:Or2l13b
|
UTSW |
16 |
19,349,650 (GRCm39) |
missense |
probably benign |
0.03 |
R7723:Or2l13b
|
UTSW |
16 |
19,349,358 (GRCm39) |
nonsense |
probably null |
|
R7860:Or2l13b
|
UTSW |
16 |
19,349,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Or2l13b
|
UTSW |
16 |
19,349,536 (GRCm39) |
missense |
|
|
R9515:Or2l13b
|
UTSW |
16 |
19,349,026 (GRCm39) |
missense |
probably benign |
0.00 |
|