Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Acaca |
G |
T |
11: 84,136,120 (GRCm39) |
E492* |
probably null |
Het |
Acp7 |
T |
A |
7: 28,315,968 (GRCm39) |
K206M |
probably benign |
Het |
Agbl1 |
T |
A |
7: 76,239,251 (GRCm39) |
F584I |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,930,946 (GRCm39) |
I929V |
possibly damaging |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Arhgef40 |
A |
G |
14: 52,238,357 (GRCm39) |
I1279V |
possibly damaging |
Het |
Arl14 |
A |
C |
3: 69,130,371 (GRCm39) |
T173P |
probably damaging |
Het |
Asap1 |
A |
G |
15: 64,184,302 (GRCm39) |
S44P |
probably damaging |
Het |
Btbd7 |
C |
A |
12: 102,751,456 (GRCm39) |
A1103S |
probably benign |
Het |
Capn10 |
T |
A |
1: 92,865,653 (GRCm39) |
|
probably null |
Het |
Capn7 |
T |
C |
14: 31,091,759 (GRCm39) |
F719L |
probably benign |
Het |
Casp7 |
G |
A |
19: 56,429,414 (GRCm39) |
D267N |
probably benign |
Het |
Ccdc13 |
C |
A |
9: 121,643,356 (GRCm39) |
K348N |
probably damaging |
Het |
Chchd1 |
T |
C |
14: 20,753,178 (GRCm39) |
F13L |
probably benign |
Het |
Clcn6 |
T |
A |
4: 148,099,018 (GRCm39) |
M442L |
possibly damaging |
Het |
Col6a3 |
T |
C |
1: 90,755,602 (GRCm39) |
E229G |
probably benign |
Het |
Cyb5r3 |
A |
G |
15: 83,038,755 (GRCm39) |
F278S |
probably damaging |
Het |
Dhx16 |
C |
T |
17: 36,201,978 (GRCm39) |
Q1002* |
probably null |
Het |
Dppa4 |
T |
C |
16: 48,111,378 (GRCm39) |
L121P |
probably benign |
Het |
Dpyd |
A |
G |
3: 118,710,741 (GRCm39) |
E383G |
probably damaging |
Het |
Eif4g3 |
A |
G |
4: 137,853,900 (GRCm39) |
T489A |
probably benign |
Het |
Elovl1 |
G |
T |
4: 118,288,832 (GRCm39) |
V174L |
probably damaging |
Het |
Elp3 |
T |
C |
14: 65,788,851 (GRCm39) |
K392E |
possibly damaging |
Het |
Fancd2os |
C |
A |
6: 113,574,985 (GRCm39) |
W7L |
probably damaging |
Het |
Fchsd2 |
A |
G |
7: 100,759,991 (GRCm39) |
T23A |
possibly damaging |
Het |
Gabrp |
C |
G |
11: 33,504,308 (GRCm39) |
A336P |
possibly damaging |
Het |
Gcm2 |
T |
A |
13: 41,263,387 (GRCm39) |
Y15F |
possibly damaging |
Het |
Gpr132 |
G |
A |
12: 112,816,416 (GRCm39) |
R137C |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,372,717 (GRCm39) |
E3091G |
probably damaging |
Het |
Homer1 |
A |
T |
13: 93,492,610 (GRCm39) |
M184L |
probably benign |
Het |
Izumo1r |
T |
C |
9: 14,812,145 (GRCm39) |
E117G |
probably damaging |
Het |
Kcnt1 |
C |
T |
2: 25,791,921 (GRCm39) |
Q590* |
probably null |
Het |
Lama1 |
G |
T |
17: 68,077,982 (GRCm39) |
C1139F |
probably damaging |
Het |
Med29 |
C |
T |
7: 28,086,239 (GRCm39) |
A190T |
probably benign |
Het |
Muc4 |
T |
C |
16: 32,569,600 (GRCm39) |
V220A |
probably benign |
Het |
Mxra8 |
G |
T |
4: 155,927,378 (GRCm39) |
V388L |
probably benign |
Het |
Myo5a |
T |
C |
9: 75,051,463 (GRCm39) |
|
probably null |
Het |
Myrip |
A |
G |
9: 120,290,499 (GRCm39) |
Y706C |
probably damaging |
Het |
Nphp4 |
T |
C |
4: 152,590,942 (GRCm39) |
V313A |
probably benign |
Het |
Oga |
A |
C |
19: 45,765,436 (GRCm39) |
S124A |
probably benign |
Het |
Olfm2 |
T |
G |
9: 20,579,840 (GRCm39) |
|
probably null |
Het |
Or10ag52 |
T |
A |
2: 87,044,072 (GRCm39) |
S279T |
probably benign |
Het |
Pcdh15 |
C |
T |
10: 74,462,620 (GRCm39) |
P1398L |
probably damaging |
Het |
Pdpr |
A |
G |
8: 111,841,443 (GRCm39) |
E225G |
possibly damaging |
Het |
Pigs |
C |
A |
11: 78,219,595 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
T |
A |
1: 20,658,755 (GRCm39) |
T159S |
probably damaging |
Het |
Plk4 |
A |
G |
3: 40,768,021 (GRCm39) |
T87A |
possibly damaging |
Het |
Plxna4 |
T |
C |
6: 32,192,657 (GRCm39) |
Y768C |
probably damaging |
Het |
Prl3d3 |
T |
A |
13: 27,343,064 (GRCm39) |
|
probably null |
Het |
Pygb |
T |
C |
2: 150,662,808 (GRCm39) |
|
probably null |
Het |
Rnf114 |
T |
C |
2: 167,352,854 (GRCm39) |
I118T |
possibly damaging |
Het |
Sbno2 |
A |
G |
10: 79,894,287 (GRCm39) |
L1099P |
probably benign |
Het |
Scaper |
T |
C |
9: 55,714,916 (GRCm39) |
K791E |
probably damaging |
Het |
Serping1 |
T |
C |
2: 84,601,889 (GRCm39) |
T194A |
probably damaging |
Het |
Slc12a9 |
A |
G |
5: 137,319,665 (GRCm39) |
S617P |
possibly damaging |
Het |
Slk |
G |
A |
19: 47,624,896 (GRCm39) |
R1039H |
probably damaging |
Het |
Sntb1 |
T |
A |
15: 55,655,535 (GRCm39) |
E227V |
probably benign |
Het |
Sostdc1 |
C |
A |
12: 36,364,407 (GRCm39) |
P39T |
probably benign |
Het |
Spred1 |
C |
T |
2: 116,983,486 (GRCm39) |
R16* |
probably null |
Het |
Srpk2 |
A |
G |
5: 23,723,475 (GRCm39) |
I547T |
probably damaging |
Het |
Stt3a |
A |
G |
9: 36,670,610 (GRCm39) |
Y54H |
probably damaging |
Het |
Stt3b |
A |
T |
9: 115,095,215 (GRCm39) |
L272H |
probably damaging |
Het |
Syne2 |
T |
A |
12: 76,154,991 (GRCm39) |
|
probably null |
Het |
Uso1 |
A |
T |
5: 92,346,196 (GRCm39) |
E793V |
possibly damaging |
Het |
Usp15 |
A |
T |
10: 122,966,892 (GRCm39) |
L476* |
probably null |
Het |
Vmn1r189 |
T |
C |
13: 22,286,336 (GRCm39) |
Y167C |
probably damaging |
Het |
Vmn2r24 |
A |
G |
6: 123,763,938 (GRCm39) |
T272A |
possibly damaging |
Het |
Vps13a |
A |
T |
19: 16,646,054 (GRCm39) |
H1994Q |
probably damaging |
Het |
Zbtb10 |
T |
C |
3: 9,330,252 (GRCm39) |
S537P |
probably damaging |
Het |
Zbtb12 |
T |
C |
17: 35,114,859 (GRCm39) |
S215P |
possibly damaging |
Het |
Zfp346 |
T |
C |
13: 55,260,915 (GRCm39) |
M81T |
probably benign |
Het |
Zfp800 |
T |
C |
6: 28,244,512 (GRCm39) |
D151G |
probably null |
Het |
|
Other mutations in Or10x4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01649:Or10x4
|
APN |
1 |
174,218,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Or10x4
|
UTSW |
1 |
174,218,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Or10x4
|
UTSW |
1 |
174,219,486 (GRCm39) |
missense |
probably benign |
0.00 |
R1906:Or10x4
|
UTSW |
1 |
174,218,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R1996:Or10x4
|
UTSW |
1 |
174,218,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R2009:Or10x4
|
UTSW |
1 |
174,218,995 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4745:Or10x4
|
UTSW |
1 |
174,219,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5294:Or10x4
|
UTSW |
1 |
174,218,791 (GRCm39) |
missense |
probably benign |
|
R5297:Or10x4
|
UTSW |
1 |
174,218,766 (GRCm39) |
missense |
probably benign |
0.21 |
R5784:Or10x4
|
UTSW |
1 |
174,218,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R5857:Or10x4
|
UTSW |
1 |
174,218,674 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6943:Or10x4
|
UTSW |
1 |
174,219,407 (GRCm39) |
nonsense |
probably null |
|
R6975:Or10x4
|
UTSW |
1 |
174,219,243 (GRCm39) |
missense |
probably benign |
0.10 |
R7114:Or10x4
|
UTSW |
1 |
174,218,805 (GRCm39) |
missense |
probably damaging |
0.96 |
R7614:Or10x4
|
UTSW |
1 |
174,219,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R8036:Or10x4
|
UTSW |
1 |
174,219,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8674:Or10x4
|
UTSW |
1 |
174,219,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Or10x4
|
UTSW |
1 |
174,218,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777-TAIL:Or10x4
|
UTSW |
1 |
174,218,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Or10x4
|
UTSW |
1 |
174,218,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R9178:Or10x4
|
UTSW |
1 |
174,219,229 (GRCm39) |
missense |
probably benign |
0.36 |
R9256:Or10x4
|
UTSW |
1 |
174,219,109 (GRCm39) |
missense |
probably benign |
0.11 |
R9449:Or10x4
|
UTSW |
1 |
174,218,742 (GRCm39) |
missense |
probably benign |
|
R9668:Or10x4
|
UTSW |
1 |
174,218,898 (GRCm39) |
missense |
probably benign |
0.04 |
|