Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
C |
T |
8: 73,199,043 (GRCm39) |
T150I |
probably benign |
Het |
Adam2 |
T |
C |
14: 66,291,280 (GRCm39) |
N333D |
probably benign |
Het |
Aifm3 |
G |
A |
16: 17,324,174 (GRCm39) |
R578Q |
probably benign |
Het |
Arid2 |
C |
A |
15: 96,268,643 (GRCm39) |
Q919K |
probably benign |
Het |
Atp6v1a |
T |
C |
16: 43,931,451 (GRCm39) |
|
probably benign |
Het |
Bicd1 |
A |
T |
6: 149,415,083 (GRCm39) |
T599S |
probably benign |
Het |
Bltp1 |
T |
C |
3: 36,960,832 (GRCm39) |
|
probably benign |
Het |
Catsperg2 |
T |
A |
7: 29,409,299 (GRCm39) |
R601W |
probably damaging |
Het |
Clca3a2 |
A |
C |
3: 144,792,153 (GRCm39) |
S369R |
possibly damaging |
Het |
Cyfip1 |
T |
G |
7: 55,557,182 (GRCm39) |
V795G |
possibly damaging |
Het |
Ddb1 |
A |
G |
19: 10,599,225 (GRCm39) |
T544A |
probably benign |
Het |
Defb43 |
T |
C |
14: 63,255,329 (GRCm39) |
I54T |
probably damaging |
Het |
Dera |
A |
G |
6: 137,756,643 (GRCm39) |
M89V |
probably benign |
Het |
Fam227b |
T |
A |
2: 125,830,923 (GRCm39) |
K427I |
probably damaging |
Het |
Frk |
A |
G |
10: 34,483,838 (GRCm39) |
I400V |
probably benign |
Het |
Gk5 |
T |
A |
9: 96,011,106 (GRCm39) |
L72H |
probably damaging |
Het |
Gprc6a |
T |
A |
10: 51,504,445 (GRCm39) |
Y133F |
possibly damaging |
Het |
Hecw1 |
A |
G |
13: 14,455,069 (GRCm39) |
L662P |
probably damaging |
Het |
Hecw1 |
G |
T |
13: 14,455,070 (GRCm39) |
L662M |
probably benign |
Het |
Il12b |
T |
A |
11: 44,298,757 (GRCm39) |
S71T |
probably benign |
Het |
Kdm2a |
A |
T |
19: 4,395,538 (GRCm39) |
|
probably benign |
Het |
Lhfpl6 |
A |
G |
3: 52,950,974 (GRCm39) |
R83G |
possibly damaging |
Het |
Magel2 |
C |
A |
7: 62,030,162 (GRCm39) |
T1022K |
unknown |
Het |
Mycbp2 |
C |
A |
14: 103,426,025 (GRCm39) |
V2367F |
possibly damaging |
Het |
Nap1l3 |
C |
T |
X: 121,305,905 (GRCm39) |
G271D |
probably benign |
Het |
Nars2 |
T |
A |
7: 96,689,117 (GRCm39) |
D346E |
possibly damaging |
Het |
Nek11 |
T |
A |
9: 105,121,613 (GRCm39) |
E435D |
probably damaging |
Het |
Nfam1 |
C |
T |
15: 82,894,611 (GRCm39) |
G205R |
probably benign |
Het |
Or10aa1 |
T |
C |
1: 173,869,774 (GRCm39) |
L86P |
probably damaging |
Het |
Or5b118 |
T |
A |
19: 13,448,631 (GRCm39) |
M99K |
probably damaging |
Het |
Otud3 |
G |
A |
4: 138,636,928 (GRCm39) |
R78W |
probably damaging |
Het |
Oxct2a |
C |
T |
4: 123,216,758 (GRCm39) |
A208T |
probably damaging |
Het |
Pcdh11x |
A |
T |
X: 119,310,607 (GRCm39) |
E683D |
probably benign |
Het |
Phtf2 |
C |
A |
5: 21,008,250 (GRCm39) |
V144L |
probably damaging |
Het |
Pkn2 |
T |
C |
3: 142,509,311 (GRCm39) |
|
probably null |
Het |
Puf60 |
T |
A |
15: 75,942,445 (GRCm39) |
D459V |
possibly damaging |
Het |
Ralgapa2 |
A |
G |
2: 146,302,632 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
A |
C |
11: 54,548,255 (GRCm39) |
Q813P |
probably damaging |
Het |
Rsf1 |
A |
T |
7: 97,328,211 (GRCm39) |
D1071V |
possibly damaging |
Het |
Sctr |
T |
C |
1: 119,959,289 (GRCm39) |
|
probably benign |
Het |
Serpini1 |
A |
G |
3: 75,526,481 (GRCm39) |
I244M |
probably benign |
Het |
Tada2a |
C |
A |
11: 83,978,018 (GRCm39) |
|
probably benign |
Het |
Tada3 |
A |
T |
6: 113,352,092 (GRCm39) |
H112Q |
possibly damaging |
Het |
Tnxb |
T |
A |
17: 34,907,694 (GRCm39) |
L1246Q |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,389,353 (GRCm39) |
N449S |
probably damaging |
Het |
Usp34 |
T |
A |
11: 23,370,090 (GRCm39) |
Y1771* |
probably null |
Het |
Vav2 |
A |
T |
2: 27,161,912 (GRCm39) |
|
probably null |
Het |
Virma |
T |
C |
4: 11,542,207 (GRCm39) |
|
probably benign |
Het |
Vmn1r78 |
T |
A |
7: 11,886,725 (GRCm39) |
I112N |
probably damaging |
Het |
Vnn3 |
A |
T |
10: 23,727,698 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or1e35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01288:Or1e35
|
APN |
11 |
73,798,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01618:Or1e35
|
APN |
11 |
73,798,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01995:Or1e35
|
APN |
11 |
73,798,261 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02494:Or1e35
|
APN |
11 |
73,797,550 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02995:Or1e35
|
APN |
11 |
73,798,045 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0018:Or1e35
|
UTSW |
11 |
73,797,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Or1e35
|
UTSW |
11 |
73,797,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Or1e35
|
UTSW |
11 |
73,798,138 (GRCm39) |
missense |
probably damaging |
0.99 |
R1222:Or1e35
|
UTSW |
11 |
73,798,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1737:Or1e35
|
UTSW |
11 |
73,797,911 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1819:Or1e35
|
UTSW |
11 |
73,797,505 (GRCm39) |
missense |
probably benign |
0.02 |
R2994:Or1e35
|
UTSW |
11 |
73,797,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R3195:Or1e35
|
UTSW |
11 |
73,797,484 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4622:Or1e35
|
UTSW |
11 |
73,797,737 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4753:Or1e35
|
UTSW |
11 |
73,797,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5137:Or1e35
|
UTSW |
11 |
73,797,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R5448:Or1e35
|
UTSW |
11 |
73,797,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5604:Or1e35
|
UTSW |
11 |
73,797,853 (GRCm39) |
missense |
probably benign |
0.02 |
R5748:Or1e35
|
UTSW |
11 |
73,797,721 (GRCm39) |
missense |
probably damaging |
0.98 |
R5899:Or1e35
|
UTSW |
11 |
73,797,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Or1e35
|
UTSW |
11 |
73,797,447 (GRCm39) |
nonsense |
probably null |
|
R6388:Or1e35
|
UTSW |
11 |
73,798,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6572:Or1e35
|
UTSW |
11 |
73,797,629 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7241:Or1e35
|
UTSW |
11 |
73,798,058 (GRCm39) |
missense |
probably benign |
0.05 |
R8870:Or1e35
|
UTSW |
11 |
73,797,725 (GRCm39) |
missense |
probably benign |
0.03 |
R9358:Or1e35
|
UTSW |
11 |
73,797,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R9544:Or1e35
|
UTSW |
11 |
73,797,637 (GRCm39) |
missense |
probably benign |
0.14 |
R9645:Or1e35
|
UTSW |
11 |
73,797,713 (GRCm39) |
missense |
probably benign |
|
R9667:Or1e35
|
UTSW |
11 |
73,798,097 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9707:Or1e35
|
UTSW |
11 |
73,798,090 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1177:Or1e35
|
UTSW |
11 |
73,797,439 (GRCm39) |
missense |
probably damaging |
1.00 |
|