Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd24 |
C |
T |
10: 81,482,143 (GRCm39) |
T88I |
probably damaging |
Het |
Atm |
A |
T |
9: 53,364,675 (GRCm39) |
V49D |
probably damaging |
Het |
Bub1b |
G |
T |
2: 118,467,199 (GRCm39) |
E841* |
probably null |
Het |
Cdh20 |
A |
T |
1: 110,027,836 (GRCm39) |
N527I |
probably damaging |
Het |
Cdh22 |
G |
A |
2: 164,958,314 (GRCm39) |
|
probably benign |
Het |
Cog1 |
T |
C |
11: 113,550,127 (GRCm39) |
L262P |
probably damaging |
Het |
Col22a1 |
T |
C |
15: 71,878,797 (GRCm39) |
H120R |
possibly damaging |
Het |
Col4a2 |
T |
C |
8: 11,483,749 (GRCm39) |
S890P |
probably benign |
Het |
Cubn |
T |
C |
2: 13,340,978 (GRCm39) |
I2248V |
probably benign |
Het |
Evpl |
T |
C |
11: 116,112,665 (GRCm39) |
E1675G |
probably damaging |
Het |
Faiml |
G |
A |
9: 99,114,545 (GRCm39) |
P115S |
probably benign |
Het |
Gak |
C |
T |
5: 108,754,743 (GRCm39) |
|
probably null |
Het |
Galntl6 |
C |
T |
8: 58,988,939 (GRCm39) |
|
probably null |
Het |
Glyr1 |
T |
C |
16: 4,836,346 (GRCm39) |
Y501C |
probably benign |
Het |
Gm9847 |
G |
T |
12: 14,545,082 (GRCm39) |
|
noncoding transcript |
Het |
Gria4 |
T |
G |
9: 4,427,026 (GRCm39) |
|
probably benign |
Het |
Il36b |
A |
G |
2: 24,044,672 (GRCm39) |
N24S |
probably benign |
Het |
Il6st |
C |
A |
13: 112,639,392 (GRCm39) |
H606N |
possibly damaging |
Het |
Itprid1 |
A |
G |
6: 55,866,174 (GRCm39) |
Q189R |
probably damaging |
Het |
Kctd10 |
A |
G |
5: 114,505,389 (GRCm39) |
F202L |
probably damaging |
Het |
Kif17 |
T |
A |
4: 137,989,978 (GRCm39) |
D55E |
probably damaging |
Het |
Klf1 |
C |
T |
8: 85,629,775 (GRCm39) |
A200V |
possibly damaging |
Het |
Klhl32 |
A |
T |
4: 24,629,275 (GRCm39) |
Y497* |
probably null |
Het |
Kng2 |
G |
T |
16: 22,816,076 (GRCm39) |
|
probably benign |
Het |
Lats1 |
T |
C |
10: 7,577,611 (GRCm39) |
V245A |
possibly damaging |
Het |
Mbd3l2 |
A |
T |
9: 18,356,254 (GRCm39) |
D193V |
probably damaging |
Het |
Ms4a18 |
A |
T |
19: 10,974,695 (GRCm39) |
V332D |
possibly damaging |
Het |
Mss51 |
T |
C |
14: 20,537,591 (GRCm39) |
I47V |
probably benign |
Het |
Myoz2 |
G |
A |
3: 122,827,861 (GRCm39) |
T19M |
probably benign |
Het |
Nampt |
T |
A |
12: 32,880,309 (GRCm39) |
N67K |
probably benign |
Het |
Ncor2 |
A |
T |
5: 125,107,776 (GRCm39) |
I1607K |
probably damaging |
Het |
Nudt4 |
T |
C |
10: 95,399,600 (GRCm39) |
Q7R |
probably damaging |
Het |
Or5b119 |
A |
G |
19: 13,457,173 (GRCm39) |
Y130H |
probably damaging |
Het |
Or5b121 |
T |
A |
19: 13,507,802 (GRCm39) |
I255N |
probably damaging |
Het |
Or8b12i |
T |
A |
9: 20,082,463 (GRCm39) |
I135F |
probably damaging |
Het |
Pgm2 |
A |
T |
5: 64,273,709 (GRCm39) |
M565L |
probably benign |
Het |
Phactr1 |
T |
G |
13: 43,288,651 (GRCm39) |
F639V |
possibly damaging |
Het |
Plod3 |
C |
A |
5: 137,017,571 (GRCm39) |
R165S |
probably damaging |
Het |
Polr2b |
T |
A |
5: 77,468,193 (GRCm39) |
N164K |
probably benign |
Het |
Rcbtb2 |
G |
A |
14: 73,399,491 (GRCm39) |
G52S |
probably damaging |
Het |
Rfc1 |
A |
G |
5: 65,468,382 (GRCm39) |
|
probably null |
Het |
Rheb |
A |
G |
5: 25,012,601 (GRCm39) |
|
probably null |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
Ripor2 |
G |
A |
13: 24,905,817 (GRCm39) |
|
probably null |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Scg3 |
A |
T |
9: 75,584,092 (GRCm39) |
D136E |
probably damaging |
Het |
Slc10a4 |
C |
T |
5: 73,164,923 (GRCm39) |
L172F |
probably damaging |
Het |
Slc35c2 |
A |
G |
2: 165,123,299 (GRCm39) |
Y113H |
probably damaging |
Het |
Slc47a1 |
T |
A |
11: 61,235,318 (GRCm39) |
D505V |
probably benign |
Het |
Snap29 |
C |
A |
16: 17,246,113 (GRCm39) |
D244E |
possibly damaging |
Het |
Taar1 |
T |
C |
10: 23,797,168 (GRCm39) |
F289L |
probably benign |
Het |
Thbs2 |
T |
A |
17: 14,893,568 (GRCm39) |
N871Y |
probably damaging |
Het |
Tmem108 |
T |
A |
9: 103,377,162 (GRCm39) |
T96S |
possibly damaging |
Het |
Tnk2 |
G |
T |
16: 32,489,620 (GRCm39) |
|
probably null |
Het |
Trak1 |
T |
A |
9: 121,302,028 (GRCm39) |
M928K |
possibly damaging |
Het |
Tuba3b |
A |
G |
6: 145,564,559 (GRCm39) |
I110V |
probably benign |
Het |
Tyk2 |
A |
G |
9: 21,022,281 (GRCm39) |
|
probably benign |
Het |
Ugt1a9 |
T |
A |
1: 87,998,759 (GRCm39) |
C70S |
probably benign |
Het |
Vmn2r10 |
A |
T |
5: 109,151,410 (GRCm39) |
I68K |
possibly damaging |
Het |
Wfs1 |
T |
C |
5: 37,124,845 (GRCm39) |
E682G |
probably damaging |
Het |
Zfp213 |
T |
C |
17: 23,778,481 (GRCm39) |
|
probably null |
Het |
Zfp809 |
T |
C |
9: 22,146,434 (GRCm39) |
V41A |
probably benign |
Het |
Zfp831 |
A |
G |
2: 174,547,539 (GRCm39) |
K1574R |
possibly damaging |
Het |
|
Other mutations in Fgg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01357:Fgg
|
APN |
3 |
82,921,535 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01713:Fgg
|
APN |
3 |
82,915,723 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02288:Fgg
|
APN |
3 |
82,915,460 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02994:Fgg
|
APN |
3 |
82,915,781 (GRCm39) |
missense |
probably benign |
|
PIT4519001:Fgg
|
UTSW |
3 |
82,920,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R1251:Fgg
|
UTSW |
3 |
82,920,287 (GRCm39) |
missense |
probably benign |
0.03 |
R2400:Fgg
|
UTSW |
3 |
82,915,494 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2436:Fgg
|
UTSW |
3 |
82,921,496 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3429:Fgg
|
UTSW |
3 |
82,920,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Fgg
|
UTSW |
3 |
82,920,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Fgg
|
UTSW |
3 |
82,917,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Fgg
|
UTSW |
3 |
82,917,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Fgg
|
UTSW |
3 |
82,915,677 (GRCm39) |
splice site |
probably benign |
|
R4898:Fgg
|
UTSW |
3 |
82,915,847 (GRCm39) |
missense |
probably benign |
0.02 |
R4938:Fgg
|
UTSW |
3 |
82,920,175 (GRCm39) |
missense |
probably benign |
0.00 |
R4967:Fgg
|
UTSW |
3 |
82,920,072 (GRCm39) |
missense |
probably benign |
0.33 |
R5635:Fgg
|
UTSW |
3 |
82,918,730 (GRCm39) |
missense |
probably benign |
0.07 |
R5740:Fgg
|
UTSW |
3 |
82,918,832 (GRCm39) |
missense |
probably benign |
0.01 |
R6307:Fgg
|
UTSW |
3 |
82,920,283 (GRCm39) |
missense |
probably damaging |
0.98 |
R6731:Fgg
|
UTSW |
3 |
82,920,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R6936:Fgg
|
UTSW |
3 |
82,915,727 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7582:Fgg
|
UTSW |
3 |
82,921,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R7769:Fgg
|
UTSW |
3 |
82,920,433 (GRCm39) |
splice site |
probably null |
|
R8258:Fgg
|
UTSW |
3 |
82,917,477 (GRCm39) |
nonsense |
probably null |
|
R8259:Fgg
|
UTSW |
3 |
82,917,477 (GRCm39) |
nonsense |
probably null |
|
R8290:Fgg
|
UTSW |
3 |
82,920,141 (GRCm39) |
missense |
probably benign |
0.00 |
R8810:Fgg
|
UTSW |
3 |
82,920,322 (GRCm39) |
missense |
probably damaging |
0.96 |
R8826:Fgg
|
UTSW |
3 |
82,921,625 (GRCm39) |
missense |
probably benign |
|
|