Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
C |
A |
12: 118,838,422 (GRCm39) |
V1047L |
probably damaging |
Het |
Akap6 |
G |
A |
12: 53,188,318 (GRCm39) |
A1911T |
probably benign |
Het |
Ank2 |
T |
A |
3: 126,726,838 (GRCm39) |
K819* |
probably null |
Het |
Apc2 |
A |
G |
10: 80,147,183 (GRCm39) |
R746G |
possibly damaging |
Het |
Baz1a |
A |
G |
12: 54,988,345 (GRCm39) |
I268T |
probably benign |
Het |
Bysl |
A |
G |
17: 47,914,865 (GRCm39) |
I206T |
probably benign |
Het |
Ccdc70 |
A |
C |
8: 22,463,357 (GRCm39) |
E49A |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,955,976 (GRCm39) |
H525L |
probably damaging |
Het |
Col4a4 |
T |
C |
1: 82,496,670 (GRCm39) |
E442G |
unknown |
Het |
Cpd |
G |
A |
11: 76,693,133 (GRCm39) |
P718S |
probably benign |
Het |
Dip2b |
T |
A |
15: 100,107,461 (GRCm39) |
I1391N |
probably damaging |
Het |
Dpp9 |
T |
C |
17: 56,501,946 (GRCm39) |
T541A |
probably damaging |
Het |
Dst |
C |
T |
1: 34,218,947 (GRCm39) |
Q1796* |
probably null |
Het |
Gm10267 |
T |
C |
18: 44,291,397 (GRCm39) |
I25V |
probably benign |
Het |
Gm32742 |
C |
T |
9: 51,061,441 (GRCm39) |
R744Q |
probably benign |
Het |
Gm37240 |
T |
C |
3: 84,422,952 (GRCm39) |
Y139C |
probably damaging |
Het |
Gm39115 |
A |
G |
7: 141,689,255 (GRCm39) |
C173R |
unknown |
Het |
Grm6 |
T |
G |
11: 50,750,877 (GRCm39) |
V680G |
probably damaging |
Het |
Grxcr2 |
C |
T |
18: 42,131,956 (GRCm39) |
D38N |
probably damaging |
Het |
Iah1 |
G |
A |
12: 21,366,587 (GRCm39) |
R52H |
probably damaging |
Het |
Ift43 |
A |
G |
12: 86,131,920 (GRCm39) |
Y36C |
possibly damaging |
Het |
Igf2r |
T |
C |
17: 12,945,588 (GRCm39) |
I334V |
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,897,692 (GRCm39) |
Q958L |
possibly damaging |
Het |
Il4i1 |
G |
A |
7: 44,489,263 (GRCm39) |
A343T |
possibly damaging |
Het |
Ints1 |
T |
C |
5: 139,748,217 (GRCm39) |
I1128V |
probably benign |
Het |
Irx1 |
C |
A |
13: 72,111,588 (GRCm39) |
G7V |
probably damaging |
Het |
Krr1 |
A |
G |
10: 111,818,896 (GRCm39) |
R312G |
possibly damaging |
Het |
Lmna |
CAGCACGGTGCGTGAGC |
CAGC |
3: 88,389,857 (GRCm39) |
|
probably null |
Het |
Lpin2 |
A |
T |
17: 71,529,065 (GRCm39) |
N108Y |
probably damaging |
Het |
Man2a1 |
A |
T |
17: 64,943,557 (GRCm39) |
E204V |
possibly damaging |
Het |
Megf8 |
A |
G |
7: 25,030,166 (GRCm39) |
T434A |
possibly damaging |
Het |
Minar1 |
A |
T |
9: 89,484,072 (GRCm39) |
S442T |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,567,285 (GRCm39) |
T1745A |
unknown |
Het |
Mycbp2 |
G |
T |
14: 103,371,474 (GRCm39) |
P4135T |
probably damaging |
Het |
Nuggc |
T |
C |
14: 65,857,045 (GRCm39) |
V398A |
possibly damaging |
Het |
Or1e29 |
A |
T |
11: 73,667,976 (GRCm39) |
M59K |
probably damaging |
Het |
Or5w11 |
C |
T |
2: 87,459,152 (GRCm39) |
A115V |
possibly damaging |
Het |
Or6a2 |
A |
T |
7: 106,600,099 (GRCm39) |
S323T |
probably benign |
Het |
Or6e1 |
G |
T |
14: 54,520,342 (GRCm39) |
N3K |
probably damaging |
Het |
Or6f1 |
A |
G |
7: 85,970,444 (GRCm39) |
S239P |
probably damaging |
Het |
Parg |
A |
G |
14: 31,964,294 (GRCm39) |
N653S |
probably damaging |
Het |
Plek |
A |
G |
11: 16,945,346 (GRCm39) |
F18L |
probably benign |
Het |
Pnoc |
A |
G |
14: 65,639,247 (GRCm39) |
I206T |
possibly damaging |
Het |
Ppp4r3a |
T |
C |
12: 101,049,129 (GRCm39) |
M1V |
probably null |
Het |
Pramel21 |
A |
G |
4: 143,341,699 (GRCm39) |
T43A |
probably benign |
Het |
Psg22 |
T |
C |
7: 18,458,248 (GRCm39) |
V313A |
probably benign |
Het |
Ptk2b |
G |
T |
14: 66,409,546 (GRCm39) |
P497T |
probably damaging |
Het |
Rer1 |
A |
G |
4: 155,160,044 (GRCm39) |
|
probably null |
Het |
Rnf130 |
A |
G |
11: 49,986,618 (GRCm39) |
T321A |
probably benign |
Het |
Rnf207 |
A |
T |
4: 152,397,717 (GRCm39) |
F346I |
probably damaging |
Het |
Rraga |
T |
A |
4: 86,494,574 (GRCm39) |
I140N |
possibly damaging |
Het |
Rusc2 |
A |
T |
4: 43,416,262 (GRCm39) |
M523L |
probably benign |
Het |
Sh3bp1 |
T |
A |
15: 78,792,622 (GRCm39) |
V495D |
probably benign |
Het |
Slc44a5 |
T |
C |
3: 153,945,926 (GRCm39) |
L153P |
probably benign |
Het |
Spag16 |
T |
C |
1: 70,764,072 (GRCm39) |
S631P |
probably damaging |
Het |
Syne1 |
A |
C |
10: 4,984,937 (GRCm39) |
L747R |
probably damaging |
Het |
Tac1 |
A |
G |
6: 7,555,675 (GRCm39) |
E21G |
probably benign |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tln1 |
T |
C |
4: 43,542,957 (GRCm39) |
D1344G |
probably damaging |
Het |
Tnc |
C |
T |
4: 63,926,045 (GRCm39) |
E912K |
probably damaging |
Het |
Trav16d-dv11 |
A |
G |
14: 53,285,037 (GRCm39) |
T38A |
probably benign |
Het |
Trbv15 |
T |
A |
6: 41,118,364 (GRCm39) |
L40Q |
probably damaging |
Het |
Trpa1 |
T |
C |
1: 14,973,455 (GRCm39) |
I288V |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,604,941 (GRCm39) |
I18331N |
probably damaging |
Het |
Tubgcp2 |
A |
T |
7: 139,587,836 (GRCm39) |
I263N |
probably damaging |
Het |
Ugt8a |
T |
C |
3: 125,708,957 (GRCm39) |
H51R |
probably benign |
Het |
Vmn2r2 |
T |
C |
3: 64,023,870 (GRCm39) |
T904A |
probably benign |
Het |
Zfp575 |
G |
A |
7: 24,285,323 (GRCm39) |
T106M |
probably damaging |
Het |
Zfp617 |
A |
G |
8: 72,686,539 (GRCm39) |
T290A |
probably benign |
Het |
Zfp809 |
T |
C |
9: 22,149,863 (GRCm39) |
V120A |
probably benign |
Het |
|
Other mutations in Or1e22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Or1e22
|
APN |
11 |
73,377,398 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02867:Or1e22
|
APN |
11 |
73,376,817 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03202:Or1e22
|
APN |
11 |
73,377,351 (GRCm39) |
nonsense |
probably null |
|
R0207:Or1e22
|
UTSW |
11 |
73,377,401 (GRCm39) |
missense |
probably benign |
0.00 |
R0539:Or1e22
|
UTSW |
11 |
73,376,889 (GRCm39) |
missense |
probably benign |
0.22 |
R1469:Or1e22
|
UTSW |
11 |
73,377,149 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1469:Or1e22
|
UTSW |
11 |
73,377,149 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1835:Or1e22
|
UTSW |
11 |
73,377,200 (GRCm39) |
missense |
probably benign |
0.08 |
R2095:Or1e22
|
UTSW |
11 |
73,377,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3612:Or1e22
|
UTSW |
11 |
73,376,766 (GRCm39) |
missense |
probably benign |
0.23 |
R3983:Or1e22
|
UTSW |
11 |
73,376,961 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4959:Or1e22
|
UTSW |
11 |
73,376,893 (GRCm39) |
nonsense |
probably null |
|
R4983:Or1e22
|
UTSW |
11 |
73,377,623 (GRCm39) |
missense |
probably benign |
0.04 |
R5297:Or1e22
|
UTSW |
11 |
73,377,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R5447:Or1e22
|
UTSW |
11 |
73,377,002 (GRCm39) |
missense |
probably benign |
0.01 |
R5569:Or1e22
|
UTSW |
11 |
73,377,518 (GRCm39) |
missense |
probably damaging |
0.97 |
R5580:Or1e22
|
UTSW |
11 |
73,377,036 (GRCm39) |
missense |
probably benign |
|
R5711:Or1e22
|
UTSW |
11 |
73,377,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Or1e22
|
UTSW |
11 |
73,376,921 (GRCm39) |
nonsense |
probably null |
|
R6974:Or1e22
|
UTSW |
11 |
73,377,299 (GRCm39) |
missense |
probably benign |
0.00 |
R7383:Or1e22
|
UTSW |
11 |
73,376,715 (GRCm39) |
makesense |
probably null |
|
R7661:Or1e22
|
UTSW |
11 |
73,377,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Or1e22
|
UTSW |
11 |
73,376,994 (GRCm39) |
missense |
probably benign |
0.03 |
R7913:Or1e22
|
UTSW |
11 |
73,377,224 (GRCm39) |
missense |
probably benign |
0.01 |
R9400:Or1e22
|
UTSW |
11 |
73,376,807 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Or1e22
|
UTSW |
11 |
73,376,979 (GRCm39) |
missense |
probably benign |
0.36 |
|