Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn2 |
T |
C |
13: 12,311,365 (GRCm39) |
E260G |
probably benign |
Het |
AI429214 |
G |
T |
8: 37,460,920 (GRCm39) |
D23Y |
possibly damaging |
Het |
Alms1 |
A |
G |
6: 85,596,830 (GRCm39) |
Y1021C |
probably damaging |
Het |
Ang5 |
A |
G |
14: 44,200,074 (GRCm39) |
D46G |
probably benign |
Het |
Ano9 |
T |
A |
7: 140,683,003 (GRCm39) |
D635V |
probably benign |
Het |
Apob |
C |
T |
12: 8,061,256 (GRCm39) |
T3246I |
possibly damaging |
Het |
Arhgef25 |
T |
C |
10: 127,025,390 (GRCm39) |
E63G |
probably benign |
Het |
B3gnt4 |
A |
C |
5: 123,649,342 (GRCm39) |
I236L |
probably damaging |
Het |
Bmper |
T |
A |
9: 23,292,759 (GRCm39) |
I356N |
possibly damaging |
Het |
Capn3 |
A |
G |
2: 120,331,732 (GRCm39) |
E614G |
probably benign |
Het |
Ccdc90b |
T |
A |
7: 92,221,776 (GRCm39) |
H118Q |
probably damaging |
Het |
Cdcp3 |
G |
T |
7: 130,824,634 (GRCm39) |
C243F |
probably damaging |
Het |
Cdh2 |
A |
T |
18: 16,776,985 (GRCm39) |
|
probably null |
Het |
Chmp7 |
C |
T |
14: 69,958,405 (GRCm39) |
V255I |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,352,979 (GRCm39) |
S2711T |
probably damaging |
Het |
Gabrg1 |
T |
A |
5: 70,939,707 (GRCm39) |
K137* |
probably null |
Het |
Gdi2 |
T |
A |
13: 3,604,400 (GRCm39) |
|
probably null |
Het |
Glyr1 |
A |
G |
16: 4,836,877 (GRCm39) |
V429A |
probably benign |
Het |
Gm5938 |
T |
A |
X: 77,172,161 (GRCm39) |
|
probably null |
Het |
Golt1b |
T |
C |
6: 142,341,979 (GRCm39) |
L121P |
probably damaging |
Het |
Gpi1 |
T |
C |
7: 33,902,302 (GRCm39) |
N471S |
probably damaging |
Het |
Ifi204 |
G |
A |
1: 173,589,296 (GRCm39) |
T45M |
possibly damaging |
Het |
Il18r1 |
A |
G |
1: 40,530,380 (GRCm39) |
N369S |
possibly damaging |
Het |
Kcnh1 |
G |
T |
1: 192,187,722 (GRCm39) |
|
probably null |
Het |
Kitl |
G |
A |
10: 99,915,993 (GRCm39) |
|
probably null |
Het |
Krt33a |
A |
T |
11: 99,905,004 (GRCm39) |
D167E |
possibly damaging |
Het |
Lax1 |
A |
G |
1: 133,607,971 (GRCm39) |
S257P |
probably damaging |
Het |
Lepr |
T |
C |
4: 101,672,309 (GRCm39) |
I1111T |
probably benign |
Het |
Lrrcc1 |
G |
A |
3: 14,612,315 (GRCm39) |
R356H |
probably damaging |
Het |
Map1a |
A |
G |
2: 121,134,272 (GRCm39) |
D1458G |
possibly damaging |
Het |
Med11 |
T |
C |
11: 70,342,921 (GRCm39) |
|
probably null |
Het |
Mtmr2 |
T |
C |
9: 13,707,353 (GRCm39) |
Y230H |
possibly damaging |
Het |
Nup93 |
T |
C |
8: 94,954,485 (GRCm39) |
|
probably null |
Het |
Ovch2 |
A |
G |
7: 107,389,402 (GRCm39) |
V342A |
probably benign |
Het |
Ovgp1 |
A |
G |
3: 105,894,228 (GRCm39) |
|
probably benign |
Het |
Oxtr |
A |
T |
6: 112,466,067 (GRCm39) |
L231Q |
probably damaging |
Het |
Prap1 |
A |
G |
7: 139,676,075 (GRCm39) |
T30A |
probably damaging |
Het |
Scg2 |
G |
A |
1: 79,414,217 (GRCm39) |
P169S |
probably damaging |
Het |
Scube2 |
A |
G |
7: 109,424,666 (GRCm39) |
V549A |
possibly damaging |
Het |
Slc22a12 |
A |
T |
19: 6,592,571 (GRCm39) |
V57D |
possibly damaging |
Het |
Slc22a28 |
A |
C |
19: 8,041,858 (GRCm39) |
C450G |
probably benign |
Het |
Tas2r120 |
A |
T |
6: 132,634,572 (GRCm39) |
Q218L |
probably benign |
Het |
Tbx15 |
A |
G |
3: 99,259,190 (GRCm39) |
T354A |
possibly damaging |
Het |
Trim24 |
A |
G |
6: 37,935,612 (GRCm39) |
T868A |
probably benign |
Het |
Ttn |
T |
A |
2: 76,598,684 (GRCm39) |
M19410L |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Upb1 |
G |
A |
10: 75,272,051 (GRCm39) |
R288H |
probably damaging |
Het |
Wdr20rt |
T |
A |
12: 65,273,007 (GRCm39) |
W56R |
probably damaging |
Het |
Wdr62 |
T |
G |
7: 29,967,328 (GRCm39) |
I309L |
probably damaging |
Het |
Zer1 |
G |
A |
2: 29,998,286 (GRCm39) |
L342F |
probably damaging |
Het |
Zfp40 |
T |
C |
17: 23,397,344 (GRCm39) |
D51G |
possibly damaging |
Het |
Zfp64 |
G |
A |
2: 168,768,662 (GRCm39) |
H317Y |
probably damaging |
Het |
|
Other mutations in Or51ag1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01924:Or51ag1
|
APN |
7 |
103,156,003 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02179:Or51ag1
|
APN |
7 |
103,155,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Or51ag1
|
APN |
7 |
103,155,295 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02507:Or51ag1
|
APN |
7 |
103,155,925 (GRCm39) |
nonsense |
probably null |
|
IGL02562:Or51ag1
|
APN |
7 |
103,155,423 (GRCm39) |
nonsense |
probably null |
|
IGL02806:Or51ag1
|
APN |
7 |
103,155,210 (GRCm39) |
missense |
probably benign |
0.10 |
R0743:Or51ag1
|
UTSW |
7 |
103,156,069 (GRCm39) |
nonsense |
probably null |
|
R0884:Or51ag1
|
UTSW |
7 |
103,156,069 (GRCm39) |
nonsense |
probably null |
|
R1673:Or51ag1
|
UTSW |
7 |
103,155,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R1752:Or51ag1
|
UTSW |
7 |
103,155,765 (GRCm39) |
missense |
probably benign |
0.02 |
R1800:Or51ag1
|
UTSW |
7 |
103,155,248 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2043:Or51ag1
|
UTSW |
7 |
103,156,150 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R2566:Or51ag1
|
UTSW |
7 |
103,155,367 (GRCm39) |
missense |
probably benign |
0.08 |
R4433:Or51ag1
|
UTSW |
7 |
103,155,346 (GRCm39) |
missense |
probably benign |
0.04 |
R5206:Or51ag1
|
UTSW |
7 |
103,155,309 (GRCm39) |
nonsense |
probably null |
|
R5470:Or51ag1
|
UTSW |
7 |
103,155,716 (GRCm39) |
missense |
probably benign |
0.00 |
R6020:Or51ag1
|
UTSW |
7 |
103,156,006 (GRCm39) |
missense |
probably benign |
|
R6848:Or51ag1
|
UTSW |
7 |
103,155,664 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7222:Or51ag1
|
UTSW |
7 |
103,155,664 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7832:Or51ag1
|
UTSW |
7 |
103,155,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Or51ag1
|
UTSW |
7 |
103,156,052 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7893:Or51ag1
|
UTSW |
7 |
103,155,817 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9293:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9335:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9567:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9615:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9653:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
|