Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,241,836 (GRCm39) |
D1233G |
probably benign |
Het |
Abcc8 |
G |
A |
7: 45,772,284 (GRCm39) |
R832W |
probably damaging |
Het |
Atp10b |
A |
G |
11: 43,092,981 (GRCm39) |
T439A |
probably damaging |
Het |
Brd10 |
C |
A |
19: 29,693,796 (GRCm39) |
S1966I |
probably damaging |
Het |
C130073F10Rik |
T |
A |
4: 101,747,953 (GRCm39) |
N74Y |
possibly damaging |
Het |
Cct8 |
G |
A |
16: 87,288,200 (GRCm39) |
S124L |
probably damaging |
Het |
Cdh9 |
T |
A |
15: 16,848,568 (GRCm39) |
|
probably benign |
Het |
Cep290 |
C |
T |
10: 100,330,828 (GRCm39) |
|
probably benign |
Het |
Chrng |
T |
A |
1: 87,133,575 (GRCm39) |
L10H |
probably damaging |
Het |
Cnn3 |
T |
C |
3: 121,250,786 (GRCm39) |
L189S |
probably benign |
Het |
Cog4 |
A |
G |
8: 111,585,157 (GRCm39) |
|
probably benign |
Het |
Cxcl12 |
A |
G |
6: 117,153,111 (GRCm39) |
|
probably benign |
Het |
Eif2b2 |
G |
A |
12: 85,270,230 (GRCm39) |
A257T |
probably damaging |
Het |
Entrep2 |
A |
T |
7: 64,469,625 (GRCm39) |
V41E |
probably damaging |
Het |
Fanca |
G |
A |
8: 124,031,020 (GRCm39) |
|
probably benign |
Het |
Fcgbpl1 |
A |
G |
7: 27,858,903 (GRCm39) |
Q2341R |
possibly damaging |
Het |
Fktn |
G |
A |
4: 53,734,880 (GRCm39) |
G173R |
probably damaging |
Het |
Gabbr2 |
T |
C |
4: 46,674,464 (GRCm39) |
N841S |
probably benign |
Het |
Gm5622 |
T |
A |
14: 51,899,647 (GRCm39) |
V167E |
possibly damaging |
Het |
Gnaq |
T |
C |
19: 16,355,651 (GRCm39) |
V289A |
probably benign |
Het |
Gpatch2l |
T |
G |
12: 86,307,439 (GRCm39) |
D272E |
possibly damaging |
Het |
Gzmg |
G |
A |
14: 56,395,263 (GRCm39) |
T74I |
probably benign |
Het |
Ikzf2 |
G |
A |
1: 69,578,474 (GRCm39) |
A271V |
possibly damaging |
Het |
Lig4 |
T |
C |
8: 10,021,176 (GRCm39) |
D868G |
possibly damaging |
Het |
Mfsd6 |
T |
C |
1: 52,747,764 (GRCm39) |
E367G |
possibly damaging |
Het |
Mpz |
T |
C |
1: 170,987,533 (GRCm39) |
L223P |
probably damaging |
Het |
Muc17 |
T |
C |
5: 137,175,674 (GRCm39) |
|
probably benign |
Het |
Or2f1b |
C |
A |
6: 42,739,613 (GRCm39) |
T209K |
possibly damaging |
Het |
Pdcd2 |
G |
T |
17: 15,746,846 (GRCm39) |
N104K |
probably damaging |
Het |
Pigg |
G |
T |
5: 108,465,154 (GRCm39) |
G129V |
probably damaging |
Het |
Ppp3cc |
T |
C |
14: 70,483,311 (GRCm39) |
Y254C |
probably damaging |
Het |
Prl3b1 |
G |
A |
13: 27,427,848 (GRCm39) |
A53T |
probably benign |
Het |
Psg23 |
A |
G |
7: 18,348,645 (GRCm39) |
V54A |
probably benign |
Het |
Psmd3 |
A |
G |
11: 98,573,746 (GRCm39) |
D64G |
probably damaging |
Het |
Psmg2 |
CTTCAGTT |
CTTCAGTTCAGTT |
18: 67,779,095 (GRCm39) |
|
probably null |
Het |
Ptgdr |
T |
A |
14: 45,090,799 (GRCm39) |
I320F |
probably damaging |
Het |
Rad50 |
T |
A |
11: 53,574,072 (GRCm39) |
K722* |
probably null |
Het |
Rasl10b |
G |
A |
11: 83,308,665 (GRCm39) |
|
probably null |
Het |
Rgs9 |
G |
A |
11: 109,138,977 (GRCm39) |
S255L |
probably benign |
Het |
Ror1 |
C |
T |
4: 100,298,334 (GRCm39) |
P569L |
possibly damaging |
Het |
Scn8a |
A |
G |
15: 100,933,422 (GRCm39) |
D1501G |
probably damaging |
Het |
Sema3c |
A |
G |
5: 17,883,330 (GRCm39) |
T313A |
possibly damaging |
Het |
Serpinc1 |
T |
A |
1: 160,821,094 (GRCm39) |
F59L |
probably damaging |
Het |
Sike1 |
A |
G |
3: 102,903,500 (GRCm39) |
D63G |
possibly damaging |
Het |
Slc25a11 |
T |
A |
11: 70,536,352 (GRCm39) |
|
probably null |
Het |
Slc32a1 |
A |
G |
2: 158,453,240 (GRCm39) |
M27V |
probably benign |
Het |
Smc5 |
A |
G |
19: 23,187,807 (GRCm39) |
V1003A |
probably damaging |
Het |
Tll2 |
G |
A |
19: 41,108,667 (GRCm39) |
R328C |
probably damaging |
Het |
Topaz1 |
A |
G |
9: 122,577,315 (GRCm39) |
E75G |
possibly damaging |
Het |
Tspan3 |
A |
T |
9: 56,054,783 (GRCm39) |
V48E |
probably benign |
Het |
Ugt1a6b |
T |
C |
1: 88,035,358 (GRCm39) |
I232T |
probably benign |
Het |
Unc79 |
A |
G |
12: 103,122,772 (GRCm39) |
K2290E |
probably damaging |
Het |
Vmn1r19 |
T |
C |
6: 57,381,656 (GRCm39) |
F70L |
probably benign |
Het |
|
Other mutations in Rsad2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01431:Rsad2
|
APN |
12 |
26,498,666 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02237:Rsad2
|
APN |
12 |
26,506,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R0077:Rsad2
|
UTSW |
12 |
26,506,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R0472:Rsad2
|
UTSW |
12 |
26,504,167 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1392:Rsad2
|
UTSW |
12 |
26,495,439 (GRCm39) |
missense |
probably benign |
0.00 |
R1392:Rsad2
|
UTSW |
12 |
26,495,439 (GRCm39) |
missense |
probably benign |
0.00 |
R1393:Rsad2
|
UTSW |
12 |
26,506,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R1860:Rsad2
|
UTSW |
12 |
26,500,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R2286:Rsad2
|
UTSW |
12 |
26,500,675 (GRCm39) |
missense |
probably benign |
0.20 |
R3430:Rsad2
|
UTSW |
12 |
26,506,418 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R5304:Rsad2
|
UTSW |
12 |
26,500,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Rsad2
|
UTSW |
12 |
26,497,150 (GRCm39) |
critical splice donor site |
probably null |
|
R6052:Rsad2
|
UTSW |
12 |
26,500,577 (GRCm39) |
missense |
probably benign |
0.02 |
R6084:Rsad2
|
UTSW |
12 |
26,504,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Rsad2
|
UTSW |
12 |
26,506,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Rsad2
|
UTSW |
12 |
26,506,418 (GRCm39) |
start codon destroyed |
possibly damaging |
0.89 |
R7158:Rsad2
|
UTSW |
12 |
26,500,779 (GRCm39) |
splice site |
probably null |
|
R7229:Rsad2
|
UTSW |
12 |
26,504,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8330:Rsad2
|
UTSW |
12 |
26,506,405 (GRCm39) |
missense |
probably benign |
|
R9557:Rsad2
|
UTSW |
12 |
26,495,521 (GRCm39) |
missense |
probably damaging |
0.98 |
R9788:Rsad2
|
UTSW |
12 |
26,500,577 (GRCm39) |
missense |
probably benign |
0.02 |
|