Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Add2 |
A |
G |
6: 86,083,234 (GRCm39) |
N444S |
possibly damaging |
Het |
Atp2b2 |
A |
T |
6: 113,739,813 (GRCm39) |
Y823* |
probably null |
Het |
Atp2c1 |
A |
C |
9: 105,290,242 (GRCm39) |
|
probably benign |
Het |
Capns1 |
A |
T |
7: 29,891,644 (GRCm39) |
D133E |
probably benign |
Het |
Cast |
A |
G |
13: 74,884,871 (GRCm39) |
V361A |
probably damaging |
Het |
Cd69 |
G |
A |
6: 129,245,223 (GRCm39) |
|
probably benign |
Het |
Celsr2 |
T |
A |
3: 108,321,378 (GRCm39) |
D478V |
probably damaging |
Het |
Cenpf |
T |
C |
1: 189,391,849 (GRCm39) |
E661G |
probably damaging |
Het |
Chrna1 |
A |
G |
2: 73,404,985 (GRCm39) |
|
probably benign |
Het |
Clec5a |
C |
A |
6: 40,554,983 (GRCm39) |
V138F |
probably damaging |
Het |
Ctsj |
T |
A |
13: 61,151,634 (GRCm39) |
I95F |
probably benign |
Het |
Dcaf1 |
T |
A |
9: 106,735,139 (GRCm39) |
S696T |
probably benign |
Het |
Dcp1a |
T |
C |
14: 30,241,636 (GRCm39) |
|
probably null |
Het |
Dnajc14 |
C |
T |
10: 128,642,725 (GRCm39) |
P216S |
possibly damaging |
Het |
Dst |
T |
C |
1: 34,218,930 (GRCm39) |
I1790T |
possibly damaging |
Het |
Ehmt1 |
A |
T |
2: 24,705,818 (GRCm39) |
H789Q |
probably damaging |
Het |
Exoc7 |
A |
T |
11: 116,192,007 (GRCm39) |
L188Q |
probably damaging |
Het |
Faap100 |
A |
G |
11: 120,261,561 (GRCm39) |
L823P |
probably damaging |
Het |
Fdxacb1 |
T |
A |
9: 50,683,896 (GRCm39) |
S620T |
probably benign |
Het |
Fhl2 |
C |
T |
1: 43,167,562 (GRCm39) |
R177Q |
probably benign |
Het |
Gars1 |
C |
A |
6: 55,040,084 (GRCm39) |
T337K |
probably damaging |
Het |
Ggta1 |
A |
T |
2: 35,312,211 (GRCm39) |
F56I |
probably damaging |
Het |
Gm10715 |
A |
C |
9: 3,038,062 (GRCm39) |
|
probably benign |
Het |
Gpr108 |
T |
A |
17: 57,544,482 (GRCm39) |
I343F |
probably damaging |
Het |
Gpr12 |
T |
A |
5: 146,520,629 (GRCm39) |
I98F |
possibly damaging |
Het |
Hk2 |
A |
G |
6: 82,737,219 (GRCm39) |
L3P |
probably damaging |
Het |
Imp4 |
C |
A |
1: 34,479,258 (GRCm39) |
|
probably benign |
Het |
Insrr |
G |
A |
3: 87,720,888 (GRCm39) |
V1049M |
probably damaging |
Het |
Klhl24 |
T |
C |
16: 19,933,331 (GRCm39) |
V314A |
probably damaging |
Het |
Krt32 |
A |
T |
11: 99,978,733 (GRCm39) |
V107D |
possibly damaging |
Het |
Krtap5-1 |
G |
A |
7: 141,850,242 (GRCm39) |
Q189* |
probably null |
Het |
Lrrc9 |
A |
G |
12: 72,553,178 (GRCm39) |
E1360G |
probably damaging |
Het |
Mdc1 |
G |
T |
17: 36,157,083 (GRCm39) |
L163F |
possibly damaging |
Het |
Mroh1 |
T |
G |
15: 76,276,661 (GRCm39) |
|
probably null |
Het |
Myh8 |
A |
G |
11: 67,192,418 (GRCm39) |
|
probably benign |
Het |
Ndufab1 |
A |
T |
7: 121,692,949 (GRCm39) |
|
probably benign |
Het |
Nek3 |
A |
G |
8: 22,648,735 (GRCm39) |
|
probably benign |
Het |
Ngly1 |
A |
T |
14: 16,260,636 (GRCm38) |
I107L |
probably benign |
Het |
Nkain4 |
A |
T |
2: 180,577,728 (GRCm39) |
|
probably null |
Het |
Nsd2 |
T |
A |
5: 34,022,132 (GRCm39) |
|
probably benign |
Het |
Or4n4 |
A |
G |
14: 50,518,801 (GRCm39) |
I303T |
probably benign |
Het |
Or5t9 |
A |
T |
2: 86,659,300 (GRCm39) |
H68L |
probably damaging |
Het |
Or7e166 |
T |
A |
9: 19,624,314 (GRCm39) |
Y64N |
probably damaging |
Het |
Or8b12 |
T |
A |
9: 37,657,805 (GRCm39) |
I125N |
probably damaging |
Het |
Pcnt |
G |
A |
10: 76,248,417 (GRCm39) |
Q901* |
probably null |
Het |
Pctp |
C |
A |
11: 89,881,913 (GRCm39) |
W81C |
probably damaging |
Het |
Pik3r5 |
A |
T |
11: 68,386,773 (GRCm39) |
I801F |
probably damaging |
Het |
Ptprj |
A |
T |
2: 90,299,942 (GRCm39) |
N193K |
probably benign |
Het |
Rab11fip1 |
A |
T |
8: 27,642,788 (GRCm39) |
D670E |
probably benign |
Het |
Racgap1 |
T |
C |
15: 99,530,628 (GRCm39) |
K201E |
probably benign |
Het |
Ranbp2 |
T |
C |
10: 58,316,086 (GRCm39) |
F2269L |
probably damaging |
Het |
Rint1 |
C |
A |
5: 24,024,478 (GRCm39) |
A760D |
possibly damaging |
Het |
Ryr2 |
G |
A |
13: 11,680,848 (GRCm39) |
P3166S |
probably damaging |
Het |
Snap29 |
A |
G |
16: 17,240,367 (GRCm39) |
N158D |
probably benign |
Het |
Speer4c1 |
A |
C |
5: 15,919,214 (GRCm39) |
|
probably benign |
Het |
St6galnac1 |
G |
T |
11: 116,657,473 (GRCm39) |
|
probably benign |
Het |
Strc |
G |
A |
2: 121,209,717 (GRCm39) |
T202I |
probably damaging |
Het |
Stxbp4 |
A |
G |
11: 90,385,426 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
T |
10: 5,309,059 (GRCm39) |
M650K |
probably damaging |
Het |
Tbc1d2b |
C |
T |
9: 90,105,487 (GRCm39) |
|
probably benign |
Het |
Tcfl5 |
A |
T |
2: 180,280,419 (GRCm39) |
I328N |
possibly damaging |
Het |
Tenm2 |
A |
G |
11: 36,164,235 (GRCm39) |
Y337H |
probably damaging |
Het |
Tgfbr2 |
T |
C |
9: 115,939,204 (GRCm39) |
K233E |
possibly damaging |
Het |
Tnk2 |
T |
C |
16: 32,484,699 (GRCm39) |
|
probably benign |
Het |
Trbv13-2 |
A |
G |
6: 41,098,471 (GRCm39) |
|
probably benign |
Het |
Tut4 |
T |
C |
4: 108,370,725 (GRCm39) |
Y875H |
probably benign |
Het |
Usp6nl |
T |
A |
2: 6,432,360 (GRCm39) |
|
probably benign |
Het |
Vmn2r62 |
A |
G |
7: 42,437,396 (GRCm39) |
S363P |
possibly damaging |
Het |
Vnn3 |
T |
C |
10: 23,727,869 (GRCm39) |
I93T |
possibly damaging |
Het |
Ylpm1 |
A |
G |
12: 85,091,258 (GRCm39) |
D1108G |
probably damaging |
Het |
Zbtb17 |
G |
A |
4: 141,190,691 (GRCm39) |
G170S |
probably benign |
Het |
Zfyve26 |
T |
C |
12: 79,320,084 (GRCm39) |
E1087G |
probably benign |
Het |
|
Other mutations in Or5e1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02491:Or5e1
|
APN |
7 |
108,354,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03086:Or5e1
|
APN |
7 |
108,355,003 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4340:Or5e1
|
UTSW |
7 |
108,354,161 (GRCm39) |
small insertion |
probably benign |
|
R0218:Or5e1
|
UTSW |
7 |
108,354,781 (GRCm39) |
nonsense |
probably null |
|
R1103:Or5e1
|
UTSW |
7 |
108,354,090 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1251:Or5e1
|
UTSW |
7 |
108,354,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R1450:Or5e1
|
UTSW |
7 |
108,354,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1582:Or5e1
|
UTSW |
7 |
108,354,317 (GRCm39) |
missense |
probably benign |
0.04 |
R1608:Or5e1
|
UTSW |
7 |
108,354,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R1726:Or5e1
|
UTSW |
7 |
108,354,215 (GRCm39) |
missense |
probably benign |
0.00 |
R1880:Or5e1
|
UTSW |
7 |
108,354,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Or5e1
|
UTSW |
7 |
108,354,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Or5e1
|
UTSW |
7 |
108,354,430 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2216:Or5e1
|
UTSW |
7 |
108,354,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4006:Or5e1
|
UTSW |
7 |
108,354,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R4603:Or5e1
|
UTSW |
7 |
108,354,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R4881:Or5e1
|
UTSW |
7 |
108,354,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R5132:Or5e1
|
UTSW |
7 |
108,354,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Or5e1
|
UTSW |
7 |
108,354,924 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5679:Or5e1
|
UTSW |
7 |
108,354,203 (GRCm39) |
missense |
probably damaging |
0.97 |
R5848:Or5e1
|
UTSW |
7 |
108,354,781 (GRCm39) |
nonsense |
probably null |
|
R5911:Or5e1
|
UTSW |
7 |
108,354,882 (GRCm39) |
missense |
probably benign |
0.36 |
R6474:Or5e1
|
UTSW |
7 |
108,354,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R7016:Or5e1
|
UTSW |
7 |
108,354,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:Or5e1
|
UTSW |
7 |
108,354,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R8113:Or5e1
|
UTSW |
7 |
108,354,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8385:Or5e1
|
UTSW |
7 |
108,354,511 (GRCm39) |
nonsense |
probably null |
|
R9429:Or5e1
|
UTSW |
7 |
108,354,412 (GRCm39) |
missense |
probably damaging |
0.98 |
R9746:Or5e1
|
UTSW |
7 |
108,354,639 (GRCm39) |
missense |
probably benign |
|
Z1088:Or5e1
|
UTSW |
7 |
108,354,311 (GRCm39) |
missense |
probably benign |
0.13 |
|