Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,629,359 (GRCm39) |
V1323I |
probably damaging |
Het |
Adam20 |
G |
A |
8: 41,248,490 (GRCm39) |
R200H |
probably benign |
Het |
Ahnak |
GATCTCTAT |
GAT |
19: 8,984,393 (GRCm39) |
|
probably benign |
Het |
Cbr3 |
A |
G |
16: 93,481,941 (GRCm39) |
D99G |
probably benign |
Het |
Ccdc17 |
T |
A |
4: 116,455,090 (GRCm39) |
L215Q |
probably damaging |
Het |
Cep350 |
A |
G |
1: 155,751,107 (GRCm39) |
Y2022H |
probably benign |
Het |
Cimip2c |
G |
C |
5: 30,641,261 (GRCm39) |
D170H |
possibly damaging |
Het |
Cnbd2 |
T |
C |
2: 156,183,547 (GRCm39) |
S338P |
probably benign |
Het |
D5Ertd579e |
A |
T |
5: 36,787,029 (GRCm39) |
V113D |
possibly damaging |
Het |
Dhx30 |
A |
G |
9: 109,916,718 (GRCm39) |
F570S |
probably damaging |
Het |
Ephb1 |
T |
C |
9: 101,848,384 (GRCm39) |
N679S |
probably damaging |
Het |
Faxc |
T |
C |
4: 21,993,307 (GRCm39) |
I317T |
probably damaging |
Het |
Fgd5 |
T |
C |
6: 91,965,290 (GRCm39) |
Y508H |
possibly damaging |
Het |
Foxd2 |
G |
T |
4: 114,765,195 (GRCm39) |
A275E |
unknown |
Het |
Fut9 |
C |
A |
4: 25,620,679 (GRCm39) |
S45I |
probably benign |
Het |
Gm5148 |
T |
C |
3: 37,768,801 (GRCm39) |
N140D |
unknown |
Het |
Gpr37l1 |
C |
T |
1: 135,089,391 (GRCm39) |
G225S |
probably damaging |
Het |
Gramd1c |
G |
A |
16: 43,825,840 (GRCm39) |
S107L |
possibly damaging |
Het |
Gtpbp2 |
A |
G |
17: 46,478,301 (GRCm39) |
D483G |
|
Het |
Ik |
G |
A |
18: 36,886,566 (GRCm39) |
R346H |
probably benign |
Het |
Ino80e |
A |
T |
7: 126,461,098 (GRCm39) |
Y50N |
unknown |
Het |
Irag1 |
A |
T |
7: 110,470,640 (GRCm39) |
S898T |
possibly damaging |
Het |
Kbtbd2 |
A |
G |
6: 56,756,566 (GRCm39) |
V390A |
probably benign |
Het |
Limch1 |
A |
C |
5: 67,156,360 (GRCm39) |
N276H |
probably damaging |
Het |
Negr1 |
T |
G |
3: 156,774,936 (GRCm39) |
|
probably null |
Het |
Ngef |
G |
A |
1: 87,431,010 (GRCm39) |
P269L |
probably damaging |
Het |
Nlrp14 |
G |
A |
7: 106,781,626 (GRCm39) |
M274I |
probably benign |
Het |
Nr1d1 |
T |
C |
11: 98,662,943 (GRCm39) |
I17V |
probably benign |
Het |
Or10ad1b |
T |
A |
15: 98,124,902 (GRCm39) |
D210V |
probably damaging |
Het |
Or5p64 |
A |
G |
7: 107,855,198 (GRCm39) |
I49T |
probably benign |
Het |
Ppip5k2 |
A |
G |
1: 97,677,312 (GRCm39) |
V334A |
|
Het |
Ppp1r9a |
G |
A |
6: 5,045,936 (GRCm39) |
V467I |
probably damaging |
Het |
Ppp2r2c |
A |
G |
5: 37,097,488 (GRCm39) |
I225V |
possibly damaging |
Het |
Ptpro |
A |
T |
6: 137,345,108 (GRCm39) |
N38I |
probably damaging |
Het |
Scn2a |
C |
A |
2: 65,579,149 (GRCm39) |
Q1495K |
possibly damaging |
Het |
Scn7a |
A |
T |
2: 66,519,902 (GRCm39) |
Y1001N |
possibly damaging |
Het |
Sfi1 |
ACA |
ACATCTTCCCAAAGCCAGTCA |
11: 3,103,382 (GRCm39) |
|
probably benign |
Het |
Sh3bgrl2 |
T |
A |
9: 83,430,513 (GRCm39) |
M1K |
probably null |
Het |
Slc25a12 |
C |
T |
2: 71,109,899 (GRCm39) |
V516M |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,091,000 (GRCm39) |
L1402P |
probably damaging |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Svop |
A |
G |
5: 114,198,169 (GRCm39) |
S135P |
probably benign |
Het |
Sycp2 |
G |
T |
2: 178,035,957 (GRCm39) |
D243E |
probably damaging |
Het |
Tcerg1 |
T |
C |
18: 42,706,413 (GRCm39) |
F1030S |
probably damaging |
Het |
Tecta |
T |
A |
9: 42,286,596 (GRCm39) |
N687Y |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,081,759 (GRCm39) |
H1230Q |
|
Het |
Tfap2b |
T |
C |
1: 19,284,373 (GRCm39) |
S94P |
probably damaging |
Het |
Tll2 |
C |
A |
19: 41,092,238 (GRCm39) |
G533V |
probably damaging |
Het |
Vmn2r55 |
A |
G |
7: 12,402,061 (GRCm39) |
V409A |
probably damaging |
Het |
Wdr41 |
A |
G |
13: 95,145,373 (GRCm39) |
E194G |
probably damaging |
Het |
Zan |
G |
T |
5: 137,398,817 (GRCm39) |
S4182R |
unknown |
Het |
Zfpl1 |
T |
C |
19: 6,134,074 (GRCm39) |
Y40C |
probably damaging |
Het |
Znrf3 |
C |
A |
11: 5,232,454 (GRCm39) |
R257L |
possibly damaging |
Het |
|
Other mutations in Or4k35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01552:Or4k35
|
APN |
2 |
111,100,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02550:Or4k35
|
APN |
2 |
111,100,349 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02661:Or4k35
|
APN |
2 |
111,099,811 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02940:Or4k35
|
APN |
2 |
111,100,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R0121:Or4k35
|
UTSW |
2 |
111,100,659 (GRCm39) |
missense |
probably benign |
0.01 |
R0402:Or4k35
|
UTSW |
2 |
111,100,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R0903:Or4k35
|
UTSW |
2 |
111,100,701 (GRCm39) |
missense |
probably benign |
|
R1804:Or4k35
|
UTSW |
2 |
111,100,275 (GRCm39) |
missense |
probably benign |
|
R1806:Or4k35
|
UTSW |
2 |
111,100,622 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1965:Or4k35
|
UTSW |
2 |
111,099,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R3718:Or4k35
|
UTSW |
2 |
111,100,571 (GRCm39) |
missense |
probably benign |
|
R4044:Or4k35
|
UTSW |
2 |
111,099,927 (GRCm39) |
missense |
probably benign |
0.01 |
R4401:Or4k35
|
UTSW |
2 |
111,100,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R4518:Or4k35
|
UTSW |
2 |
111,100,263 (GRCm39) |
missense |
probably benign |
|
R5309:Or4k35
|
UTSW |
2 |
111,100,655 (GRCm39) |
missense |
probably benign |
0.00 |
R5312:Or4k35
|
UTSW |
2 |
111,100,655 (GRCm39) |
missense |
probably benign |
0.00 |
R5367:Or4k35
|
UTSW |
2 |
111,100,235 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5727:Or4k35
|
UTSW |
2 |
111,100,197 (GRCm39) |
nonsense |
probably null |
|
R5772:Or4k35
|
UTSW |
2 |
111,100,057 (GRCm39) |
nonsense |
probably null |
|
R5827:Or4k35
|
UTSW |
2 |
111,100,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R5882:Or4k35
|
UTSW |
2 |
111,100,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R6036:Or4k35
|
UTSW |
2 |
111,099,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Or4k35
|
UTSW |
2 |
111,099,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R6728:Or4k35
|
UTSW |
2 |
111,100,018 (GRCm39) |
missense |
probably benign |
0.00 |
R7629:Or4k35
|
UTSW |
2 |
111,100,221 (GRCm39) |
missense |
probably benign |
0.00 |
R8377:Or4k35
|
UTSW |
2 |
111,099,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R8870:Or4k35
|
UTSW |
2 |
111,100,464 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9100:Or4k35
|
UTSW |
2 |
111,100,094 (GRCm39) |
missense |
probably benign |
0.35 |
R9668:Or4k35
|
UTSW |
2 |
111,100,287 (GRCm39) |
missense |
probably benign |
0.03 |
R9690:Or4k35
|
UTSW |
2 |
111,099,822 (GRCm39) |
missense |
probably damaging |
0.98 |
|