Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
A |
7: 120,139,378 (GRCm39) |
L1470Q |
probably damaging |
Het |
Abraxas2 |
G |
A |
7: 132,476,584 (GRCm39) |
R105Q |
probably damaging |
Het |
Arhgap23 |
G |
T |
11: 97,335,154 (GRCm39) |
V70L |
probably benign |
Het |
Bicd1 |
T |
C |
6: 149,414,448 (GRCm39) |
I387T |
probably benign |
Het |
Cd59b |
G |
A |
2: 103,909,286 (GRCm39) |
|
probably null |
Het |
Chn2 |
T |
C |
6: 54,267,436 (GRCm39) |
|
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,924,748 (GRCm39) |
S14G |
possibly damaging |
Het |
Col5a2 |
A |
G |
1: 45,446,195 (GRCm39) |
I461T |
probably benign |
Het |
Dele1 |
G |
A |
18: 38,394,317 (GRCm39) |
V505I |
probably benign |
Het |
Dnlz |
T |
C |
2: 26,241,380 (GRCm39) |
N116S |
probably damaging |
Het |
Esyt2 |
A |
G |
12: 116,331,330 (GRCm39) |
N736S |
probably damaging |
Het |
F11 |
T |
C |
8: 45,702,114 (GRCm39) |
T267A |
probably benign |
Het |
Fam234b |
T |
G |
6: 135,194,072 (GRCm39) |
S242A |
possibly damaging |
Het |
Gadd45b |
A |
G |
10: 80,766,181 (GRCm39) |
N11S |
probably benign |
Het |
Garnl3 |
T |
C |
2: 32,896,816 (GRCm39) |
T608A |
possibly damaging |
Het |
Gata3 |
T |
C |
2: 9,879,620 (GRCm39) |
T119A |
probably benign |
Het |
Gm10647 |
A |
G |
9: 66,705,777 (GRCm39) |
|
probably benign |
Het |
Gm10936 |
G |
A |
10: 117,084,035 (GRCm39) |
|
noncoding transcript |
Het |
Gzmd |
A |
G |
14: 56,367,161 (GRCm39) |
W244R |
probably damaging |
Het |
Hdac2 |
T |
A |
10: 36,865,180 (GRCm39) |
D131E |
probably benign |
Het |
Hira |
T |
A |
16: 18,774,921 (GRCm39) |
F949I |
probably benign |
Het |
Ighv15-2 |
T |
G |
12: 114,528,657 (GRCm39) |
|
probably benign |
Het |
Il3 |
A |
G |
11: 54,156,506 (GRCm39) |
|
probably null |
Het |
Itgae |
A |
C |
11: 73,002,168 (GRCm39) |
M91L |
probably benign |
Het |
Jkampl |
A |
G |
6: 73,446,402 (GRCm39) |
L49P |
possibly damaging |
Het |
Kat2b |
A |
G |
17: 53,948,238 (GRCm39) |
E336G |
probably damaging |
Het |
Kctd21 |
T |
A |
7: 96,997,298 (GRCm39) |
I257N |
probably benign |
Het |
Kif23 |
C |
G |
9: 61,832,976 (GRCm39) |
|
probably benign |
Het |
Lgi3 |
A |
T |
14: 70,770,261 (GRCm39) |
I109L |
probably benign |
Het |
Lhx9 |
A |
T |
1: 138,766,417 (GRCm39) |
C124S |
probably damaging |
Het |
Lipo4 |
A |
G |
19: 33,479,006 (GRCm39) |
V278A |
probably benign |
Het |
Lrch3 |
T |
A |
16: 32,782,124 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
T |
C |
2: 40,486,995 (GRCm39) |
E142G |
probably damaging |
Het |
Map9 |
G |
A |
3: 82,267,290 (GRCm39) |
|
probably benign |
Het |
Miox |
C |
T |
15: 89,218,657 (GRCm39) |
|
probably benign |
Het |
Mndal |
A |
T |
1: 173,685,079 (GRCm39) |
|
probably benign |
Het |
Mug2 |
G |
T |
6: 122,051,673 (GRCm39) |
V952L |
possibly damaging |
Het |
Nepn |
A |
T |
10: 52,276,533 (GRCm39) |
T29S |
probably damaging |
Het |
Or4k5 |
T |
G |
14: 50,386,092 (GRCm39) |
K80Q |
probably damaging |
Het |
Or8d1b |
A |
G |
9: 38,887,574 (GRCm39) |
I201V |
probably benign |
Het |
Or8k53 |
T |
C |
2: 86,178,072 (GRCm39) |
I13V |
possibly damaging |
Het |
Phf3 |
A |
T |
1: 30,844,146 (GRCm39) |
D1604E |
probably benign |
Het |
Plekhn1 |
T |
C |
4: 156,312,700 (GRCm39) |
R53G |
probably benign |
Het |
Prickle1 |
A |
G |
15: 93,408,658 (GRCm39) |
L47P |
possibly damaging |
Het |
Ptar1 |
T |
A |
19: 23,695,459 (GRCm39) |
C309S |
probably benign |
Het |
Rapgef2 |
A |
T |
3: 79,011,412 (GRCm39) |
S224R |
probably damaging |
Het |
Rimoc1 |
T |
C |
15: 4,015,776 (GRCm39) |
K263E |
probably damaging |
Het |
Siglecg |
G |
A |
7: 43,060,595 (GRCm39) |
G325D |
probably damaging |
Het |
Skor2 |
A |
T |
18: 76,946,793 (GRCm39) |
I172F |
unknown |
Het |
Slc9a1 |
A |
G |
4: 133,147,916 (GRCm39) |
K645E |
probably benign |
Het |
St14 |
T |
A |
9: 31,019,580 (GRCm39) |
|
probably null |
Het |
Tas2r120 |
T |
A |
6: 132,634,552 (GRCm39) |
Y211* |
probably null |
Het |
Tbxa2r |
C |
A |
10: 81,168,734 (GRCm39) |
T141K |
possibly damaging |
Het |
Tpd52l1 |
A |
G |
10: 31,255,252 (GRCm39) |
S32P |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,540,468 (GRCm39) |
R34173W |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,623,474 (GRCm39) |
V15368L |
possibly damaging |
Het |
Tyms |
A |
G |
5: 30,268,256 (GRCm39) |
I148T |
probably damaging |
Het |
Vmn1r45 |
A |
T |
6: 89,910,492 (GRCm39) |
Y159* |
probably null |
Het |
Vmn1r58 |
A |
C |
7: 5,413,865 (GRCm39) |
S122A |
probably benign |
Het |
Vmn2r13 |
C |
A |
5: 109,322,915 (GRCm39) |
V125L |
probably benign |
Het |
Vmn2r92 |
C |
T |
17: 18,388,219 (GRCm39) |
A408V |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,887,407 (GRCm39) |
I3272T |
probably benign |
Het |
Wfdc8 |
A |
G |
2: 164,439,105 (GRCm39) |
Y426H |
probably benign |
Het |
Zfp948 |
A |
T |
17: 21,807,556 (GRCm39) |
K249N |
probably damaging |
Het |
Zfyve1 |
A |
G |
12: 83,601,847 (GRCm39) |
|
probably benign |
Het |
Zyg11a |
G |
A |
4: 108,061,838 (GRCm39) |
T321I |
probably damaging |
Het |
|
Other mutations in Or14a260 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Or14a260
|
APN |
7 |
85,985,269 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02419:Or14a260
|
APN |
7 |
85,984,870 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02519:Or14a260
|
APN |
7 |
85,984,789 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02750:Or14a260
|
APN |
7 |
85,984,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Or14a260
|
UTSW |
7 |
85,984,803 (GRCm39) |
missense |
probably benign |
0.02 |
R0134:Or14a260
|
UTSW |
7 |
85,984,803 (GRCm39) |
missense |
probably benign |
0.02 |
R1025:Or14a260
|
UTSW |
7 |
85,985,113 (GRCm39) |
missense |
probably benign |
0.09 |
R1511:Or14a260
|
UTSW |
7 |
85,985,553 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1674:Or14a260
|
UTSW |
7 |
85,984,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Or14a260
|
UTSW |
7 |
85,984,955 (GRCm39) |
nonsense |
probably null |
|
R4588:Or14a260
|
UTSW |
7 |
85,984,852 (GRCm39) |
missense |
probably benign |
0.00 |
R5637:Or14a260
|
UTSW |
7 |
85,984,812 (GRCm39) |
missense |
probably benign |
0.00 |
R6163:Or14a260
|
UTSW |
7 |
85,985,592 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6407:Or14a260
|
UTSW |
7 |
85,985,277 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7342:Or14a260
|
UTSW |
7 |
85,985,295 (GRCm39) |
missense |
probably benign |
0.00 |
R8066:Or14a260
|
UTSW |
7 |
85,985,014 (GRCm39) |
missense |
probably benign |
0.00 |
R8155:Or14a260
|
UTSW |
7 |
85,985,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R8158:Or14a260
|
UTSW |
7 |
85,984,885 (GRCm39) |
missense |
probably benign |
0.01 |
|