Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,203,893 (GRCm39) |
I398K |
possibly damaging |
Het |
Acad9 |
A |
G |
3: 36,129,323 (GRCm39) |
|
probably benign |
Het |
Acsm2 |
T |
C |
7: 119,153,704 (GRCm39) |
S5P |
unknown |
Het |
Akp3 |
T |
C |
1: 87,054,667 (GRCm39) |
I334T |
probably damaging |
Het |
Amy1 |
C |
T |
3: 113,357,311 (GRCm39) |
R176H |
probably benign |
Het |
Ank2 |
A |
T |
3: 126,736,337 (GRCm39) |
|
probably benign |
Het |
Cav1 |
C |
A |
6: 17,307,918 (GRCm39) |
N23K |
probably damaging |
Het |
Cep126 |
A |
G |
9: 8,112,120 (GRCm39) |
V151A |
probably benign |
Het |
Cnot1 |
A |
G |
8: 96,481,606 (GRCm39) |
|
probably null |
Het |
Crim1 |
T |
A |
17: 78,623,146 (GRCm39) |
V448E |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 48,655,278 (GRCm39) |
E8G |
possibly damaging |
Het |
Ddx31 |
A |
T |
2: 28,764,185 (GRCm39) |
I464F |
probably damaging |
Het |
Ddx54 |
A |
G |
5: 120,764,432 (GRCm39) |
|
probably benign |
Het |
Dhx16 |
A |
G |
17: 36,193,762 (GRCm39) |
E319G |
probably damaging |
Het |
Efl1 |
A |
G |
7: 82,301,107 (GRCm39) |
D37G |
probably damaging |
Het |
Epha5 |
T |
C |
5: 84,298,228 (GRCm39) |
R444G |
probably damaging |
Het |
Exoc2 |
C |
A |
13: 31,004,606 (GRCm39) |
C859F |
probably benign |
Het |
Gbx2 |
T |
C |
1: 89,860,908 (GRCm39) |
|
probably benign |
Het |
Gm12258 |
G |
A |
11: 58,750,285 (GRCm39) |
A9T |
probably benign |
Het |
Gpr141b |
T |
G |
13: 19,913,300 (GRCm39) |
|
noncoding transcript |
Het |
Grm4 |
A |
G |
17: 27,654,129 (GRCm39) |
V607A |
probably benign |
Het |
Gvin3 |
T |
C |
7: 106,200,677 (GRCm39) |
|
noncoding transcript |
Het |
Ighv1-74 |
C |
A |
12: 115,766,455 (GRCm39) |
W55L |
probably damaging |
Het |
Irx4 |
C |
A |
13: 73,415,626 (GRCm39) |
Y138* |
probably null |
Het |
Itpr1 |
C |
A |
6: 108,482,988 (GRCm39) |
T2352K |
probably benign |
Het |
Kcnk3 |
T |
G |
5: 30,745,854 (GRCm39) |
V65G |
probably damaging |
Het |
Mctp2 |
T |
C |
7: 71,908,923 (GRCm39) |
E130G |
probably benign |
Het |
Mgat5 |
C |
A |
1: 127,310,676 (GRCm39) |
R197S |
probably benign |
Het |
Mpg |
T |
C |
11: 32,177,951 (GRCm39) |
|
probably null |
Het |
Muc5b |
T |
C |
7: 141,417,910 (GRCm39) |
C3619R |
probably damaging |
Het |
Myo15b |
G |
A |
11: 115,764,583 (GRCm39) |
V1321I |
probably benign |
Het |
Myo1b |
T |
C |
1: 51,815,391 (GRCm39) |
T658A |
probably damaging |
Het |
Nomo1 |
T |
C |
7: 45,692,037 (GRCm39) |
S154P |
possibly damaging |
Het |
Nsd1 |
T |
A |
13: 55,411,217 (GRCm39) |
F1423I |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or9g3 |
A |
G |
2: 85,584,183 (GRCm39) |
|
probably benign |
Het |
Osbpl6 |
A |
G |
2: 76,379,856 (GRCm39) |
R149G |
probably damaging |
Het |
Pacc1 |
A |
G |
1: 191,080,568 (GRCm39) |
S263G |
probably damaging |
Het |
Papola |
T |
A |
12: 105,777,300 (GRCm39) |
W281R |
probably damaging |
Het |
Pole |
C |
T |
5: 110,485,153 (GRCm39) |
|
probably benign |
Het |
Rptn |
A |
G |
3: 93,305,334 (GRCm39) |
N889S |
possibly damaging |
Het |
Scn10a |
A |
G |
9: 119,460,626 (GRCm39) |
S1084P |
probably damaging |
Het |
Scnm1 |
T |
C |
3: 95,037,596 (GRCm39) |
I157V |
probably benign |
Het |
Siglece |
T |
C |
7: 43,308,760 (GRCm39) |
T198A |
probably damaging |
Het |
Sptb |
T |
A |
12: 76,650,942 (GRCm39) |
M1678L |
probably benign |
Het |
Taf8 |
A |
T |
17: 47,809,467 (GRCm39) |
M98K |
probably damaging |
Het |
Tead2 |
T |
A |
7: 44,870,138 (GRCm39) |
|
probably benign |
Het |
Trrap |
C |
T |
5: 144,744,201 (GRCm39) |
|
silent |
Het |
Ttn |
G |
T |
2: 76,775,914 (GRCm39) |
N1709K |
probably damaging |
Het |
Ube3a |
T |
C |
7: 58,926,768 (GRCm39) |
|
probably benign |
Het |
Ube3c |
T |
C |
5: 29,804,054 (GRCm39) |
|
probably benign |
Het |
Unc80 |
T |
C |
1: 66,567,123 (GRCm39) |
S910P |
probably damaging |
Het |
Usp30 |
G |
A |
5: 114,257,682 (GRCm39) |
R280Q |
possibly damaging |
Het |
Vsx1 |
T |
C |
2: 150,530,457 (GRCm39) |
S142G |
possibly damaging |
Het |
Wdr95 |
T |
G |
5: 149,517,947 (GRCm39) |
C360G |
probably benign |
Het |
Zbtb4 |
A |
G |
11: 69,669,040 (GRCm39) |
I588V |
probably benign |
Het |
Zdhhc4 |
A |
T |
5: 143,310,604 (GRCm39) |
|
probably benign |
Het |
Zfp568 |
C |
A |
7: 29,697,288 (GRCm39) |
N69K |
probably damaging |
Het |
|
Other mutations in Sertad2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03008:Sertad2
|
APN |
11 |
20,597,798 (GRCm39) |
splice site |
probably benign |
|
wisteria
|
UTSW |
11 |
20,598,664 (GRCm39) |
frame shift |
probably null |
|
PIT4366001:Sertad2
|
UTSW |
11 |
20,598,116 (GRCm39) |
missense |
probably benign |
0.03 |
R1171:Sertad2
|
UTSW |
11 |
20,598,091 (GRCm39) |
missense |
probably benign |
0.01 |
R1306:Sertad2
|
UTSW |
11 |
20,598,388 (GRCm39) |
missense |
probably benign |
|
R3834:Sertad2
|
UTSW |
11 |
20,598,482 (GRCm39) |
missense |
probably benign |
0.15 |
R4087:Sertad2
|
UTSW |
11 |
20,598,664 (GRCm39) |
frame shift |
probably null |
|
R4940:Sertad2
|
UTSW |
11 |
20,597,899 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5232:Sertad2
|
UTSW |
11 |
20,598,344 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5621:Sertad2
|
UTSW |
11 |
20,598,061 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5891:Sertad2
|
UTSW |
11 |
20,597,884 (GRCm39) |
missense |
probably benign |
0.30 |
R6006:Sertad2
|
UTSW |
11 |
20,597,884 (GRCm39) |
missense |
probably benign |
0.30 |
R6007:Sertad2
|
UTSW |
11 |
20,597,884 (GRCm39) |
missense |
probably benign |
0.30 |
R6048:Sertad2
|
UTSW |
11 |
20,598,436 (GRCm39) |
missense |
probably benign |
|
R9135:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9136:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9137:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9138:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9431:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
|