Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
T |
C |
3: 124,350,365 (GRCm39) |
|
probably benign |
Het |
AA467197 |
A |
G |
2: 122,481,182 (GRCm39) |
T57A |
probably benign |
Het |
Akap11 |
A |
T |
14: 78,733,345 (GRCm39) |
D1852E |
probably damaging |
Het |
Arg2 |
T |
A |
12: 79,178,605 (GRCm39) |
|
probably null |
Het |
Arhgef4 |
A |
G |
1: 34,845,107 (GRCm39) |
D1437G |
probably benign |
Het |
AW551984 |
C |
A |
9: 39,500,418 (GRCm39) |
R780L |
probably benign |
Het |
Baz1a |
T |
A |
12: 54,974,352 (GRCm39) |
K503* |
probably null |
Het |
Bltp3a |
C |
A |
17: 28,112,227 (GRCm39) |
N1167K |
probably benign |
Het |
Cdk2ap1 |
A |
T |
5: 124,484,207 (GRCm39) |
H96Q |
probably damaging |
Het |
Col11a1 |
T |
A |
3: 114,010,859 (GRCm39) |
|
probably null |
Het |
Col12a1 |
A |
T |
9: 79,585,665 (GRCm39) |
|
probably null |
Het |
Col22a1 |
G |
A |
15: 71,679,777 (GRCm39) |
P877S |
unknown |
Het |
Col7a1 |
A |
T |
9: 108,797,441 (GRCm39) |
N1681Y |
probably null |
Het |
Dennd1b |
T |
G |
1: 139,067,130 (GRCm39) |
S398A |
possibly damaging |
Het |
Fgd2 |
C |
T |
17: 29,580,135 (GRCm39) |
|
probably benign |
Het |
Hadh |
T |
C |
3: 131,042,192 (GRCm39) |
S98G |
probably benign |
Het |
Has2 |
C |
T |
15: 56,531,656 (GRCm39) |
R353H |
probably damaging |
Het |
Heg1 |
T |
C |
16: 33,547,783 (GRCm39) |
S857P |
probably benign |
Het |
Hemgn |
T |
A |
4: 46,400,732 (GRCm39) |
R43* |
probably null |
Het |
Htr4 |
A |
T |
18: 62,570,692 (GRCm39) |
H249L |
possibly damaging |
Het |
Hycc2 |
A |
G |
1: 58,569,076 (GRCm39) |
L501P |
probably damaging |
Het |
Iqgap3 |
T |
C |
3: 88,022,281 (GRCm39) |
S495P |
probably benign |
Het |
Kars1 |
T |
C |
8: 112,732,271 (GRCm39) |
D99G |
probably benign |
Het |
Krt40 |
T |
A |
11: 99,428,394 (GRCm39) |
S333C |
probably damaging |
Het |
Lamc2 |
T |
C |
1: 152,999,871 (GRCm39) |
I1163V |
probably damaging |
Het |
Lrrn2 |
A |
T |
1: 132,866,065 (GRCm39) |
I377F |
possibly damaging |
Het |
Mcm5 |
T |
A |
8: 75,842,530 (GRCm39) |
I268N |
probably damaging |
Het |
Mmp21 |
G |
T |
7: 133,276,300 (GRCm39) |
H514Q |
probably damaging |
Het |
Mtcl1 |
G |
A |
17: 66,645,014 (GRCm39) |
P1478S |
probably damaging |
Het |
Mybbp1a |
A |
G |
11: 72,336,492 (GRCm39) |
T495A |
possibly damaging |
Het |
Myo10 |
T |
A |
15: 25,701,688 (GRCm39) |
V21E |
probably damaging |
Het |
Nap1l4 |
A |
G |
7: 143,091,982 (GRCm39) |
S49P |
probably benign |
Het |
Ncoa2 |
G |
A |
1: 13,247,316 (GRCm39) |
S369F |
probably damaging |
Het |
Niban2 |
A |
C |
2: 32,812,109 (GRCm39) |
Y397S |
probably benign |
Het |
Pon2 |
A |
G |
6: 5,265,316 (GRCm39) |
|
probably benign |
Het |
Ppdpf |
T |
C |
2: 180,829,673 (GRCm39) |
S43P |
probably benign |
Het |
Psmd6 |
A |
G |
14: 14,112,393 (GRCm38) |
|
probably benign |
Het |
Ptprk |
G |
T |
10: 28,368,957 (GRCm39) |
R643L |
probably damaging |
Het |
Ptprq |
T |
A |
10: 107,524,368 (GRCm39) |
Y455F |
probably benign |
Het |
Sec23b |
G |
A |
2: 144,408,679 (GRCm39) |
|
probably benign |
Het |
Sh3pxd2a |
A |
G |
19: 47,256,465 (GRCm39) |
L751P |
probably damaging |
Het |
Snx6 |
T |
A |
12: 54,830,228 (GRCm39) |
H77L |
probably damaging |
Het |
Svep1 |
C |
A |
4: 58,048,188 (GRCm39) |
C3472F |
possibly damaging |
Het |
Trpd52l3 |
A |
T |
19: 29,981,396 (GRCm39) |
E50D |
probably damaging |
Het |
Ttc33 |
A |
G |
15: 5,246,809 (GRCm39) |
D205G |
probably damaging |
Het |
Tubgcp3 |
A |
T |
8: 12,699,797 (GRCm39) |
V352E |
probably benign |
Het |
Tulp2 |
T |
G |
7: 45,171,734 (GRCm39) |
F436C |
probably damaging |
Het |
Vmn1r123 |
T |
A |
7: 20,896,282 (GRCm39) |
M58K |
possibly damaging |
Het |
Vmn2r113 |
T |
C |
17: 23,174,931 (GRCm39) |
V514A |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,862,329 (GRCm39) |
V2982A |
probably benign |
Het |
Ywhaq |
T |
C |
12: 21,445,001 (GRCm39) |
T215A |
possibly damaging |
Het |
Zfp677 |
A |
T |
17: 21,617,135 (GRCm39) |
H64L |
probably damaging |
Het |
|
Other mutations in Or5g9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00920:Or5g9
|
APN |
2 |
85,552,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01862:Or5g9
|
APN |
2 |
85,552,472 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02868:Or5g9
|
APN |
2 |
85,551,919 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02904:Or5g9
|
APN |
2 |
85,552,099 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03347:Or5g9
|
APN |
2 |
85,552,151 (GRCm39) |
missense |
probably benign |
0.01 |
R1148:Or5g9
|
UTSW |
2 |
85,552,620 (GRCm39) |
nonsense |
probably null |
|
R1148:Or5g9
|
UTSW |
2 |
85,552,620 (GRCm39) |
nonsense |
probably null |
|
R1446:Or5g9
|
UTSW |
2 |
85,551,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R3782:Or5g9
|
UTSW |
2 |
85,552,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4343:Or5g9
|
UTSW |
2 |
85,552,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4836:Or5g9
|
UTSW |
2 |
85,551,793 (GRCm39) |
missense |
probably benign |
|
R4845:Or5g9
|
UTSW |
2 |
85,551,836 (GRCm39) |
nonsense |
probably null |
|
R5490:Or5g9
|
UTSW |
2 |
85,552,666 (GRCm39) |
missense |
probably benign |
0.01 |
R5534:Or5g9
|
UTSW |
2 |
85,552,331 (GRCm39) |
missense |
probably benign |
0.35 |
R5679:Or5g9
|
UTSW |
2 |
85,552,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Or5g9
|
UTSW |
2 |
85,551,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Or5g9
|
UTSW |
2 |
85,552,675 (GRCm39) |
missense |
probably benign |
0.28 |
R7024:Or5g9
|
UTSW |
2 |
85,551,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Or5g9
|
UTSW |
2 |
85,551,818 (GRCm39) |
missense |
probably damaging |
0.97 |
R7174:Or5g9
|
UTSW |
2 |
85,552,297 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8079:Or5g9
|
UTSW |
2 |
85,552,387 (GRCm39) |
missense |
probably benign |
0.07 |
R8082:Or5g9
|
UTSW |
2 |
85,551,824 (GRCm39) |
missense |
probably benign |
0.01 |
R8213:Or5g9
|
UTSW |
2 |
85,551,845 (GRCm39) |
missense |
probably null |
1.00 |
R9103:Or5g9
|
UTSW |
2 |
85,552,527 (GRCm39) |
nonsense |
probably null |
|
R9387:Or5g9
|
UTSW |
2 |
85,551,806 (GRCm39) |
missense |
probably benign |
0.00 |
R9508:Or5g9
|
UTSW |
2 |
85,552,165 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9679:Or5g9
|
UTSW |
2 |
85,552,482 (GRCm39) |
missense |
probably damaging |
0.99 |
R9776:Or5g9
|
UTSW |
2 |
85,552,145 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Or5g9
|
UTSW |
2 |
85,552,322 (GRCm39) |
missense |
probably damaging |
1.00 |
|