Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
G |
T |
7: 119,815,524 (GRCm39) |
M257I |
probably benign |
Het |
Adam23 |
T |
C |
1: 63,584,627 (GRCm39) |
V345A |
probably damaging |
Het |
Anxa6 |
T |
G |
11: 54,902,578 (GRCm39) |
N52T |
possibly damaging |
Het |
Arhgef15 |
G |
A |
11: 68,841,938 (GRCm39) |
H496Y |
probably damaging |
Het |
Atp2a3 |
A |
G |
11: 72,872,765 (GRCm39) |
E771G |
probably damaging |
Het |
B3gnt5 |
A |
G |
16: 19,588,347 (GRCm39) |
T189A |
possibly damaging |
Het |
Becn1 |
A |
T |
11: 101,186,230 (GRCm39) |
S125T |
probably damaging |
Het |
Bltp1 |
T |
G |
3: 37,050,697 (GRCm39) |
M3011R |
possibly damaging |
Het |
Ccdc180 |
A |
G |
4: 45,900,484 (GRCm39) |
M283V |
probably benign |
Het |
Cdh17 |
T |
C |
4: 11,771,323 (GRCm39) |
F35S |
probably damaging |
Het |
Clcn1 |
T |
A |
6: 42,282,477 (GRCm39) |
I515N |
probably damaging |
Het |
Cyp4f17 |
A |
G |
17: 32,743,068 (GRCm39) |
Y247C |
probably damaging |
Het |
Dcp1a |
T |
A |
14: 30,240,899 (GRCm39) |
H236Q |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 117,874,764 (GRCm39) |
N4034Y |
probably damaging |
Het |
Dsg1a |
A |
G |
18: 20,473,599 (GRCm39) |
I891V |
possibly damaging |
Het |
Eid3 |
A |
G |
10: 82,703,441 (GRCm39) |
N301D |
probably damaging |
Het |
Fbxw14 |
A |
C |
9: 109,116,071 (GRCm39) |
|
probably benign |
Het |
Fzd8 |
A |
G |
18: 9,214,474 (GRCm39) |
T519A |
probably benign |
Het |
Gldc |
C |
G |
19: 30,078,212 (GRCm39) |
M928I |
probably benign |
Het |
Gpr3 |
C |
A |
4: 132,938,538 (GRCm39) |
V45L |
possibly damaging |
Het |
Gramd1b |
A |
T |
9: 40,215,780 (GRCm39) |
I690K |
probably benign |
Het |
Grhl2 |
T |
A |
15: 37,270,912 (GRCm39) |
D33E |
probably damaging |
Het |
Kcnj4 |
C |
A |
15: 79,369,920 (GRCm39) |
R20L |
probably damaging |
Het |
Klhl5 |
A |
G |
5: 65,305,989 (GRCm39) |
I319V |
probably benign |
Het |
Lars2 |
A |
T |
9: 123,221,892 (GRCm39) |
E135D |
possibly damaging |
Het |
Map9 |
T |
A |
3: 82,291,270 (GRCm39) |
Y602N |
possibly damaging |
Het |
Mphosph9 |
A |
T |
5: 124,463,027 (GRCm39) |
L6* |
probably null |
Het |
Naa35 |
C |
T |
13: 59,748,761 (GRCm39) |
T131M |
probably damaging |
Het |
Nucb2 |
T |
A |
7: 116,121,136 (GRCm39) |
L22Q |
possibly damaging |
Het |
Or8g26 |
A |
G |
9: 39,096,062 (GRCm39) |
Y193C |
probably damaging |
Het |
Or8k28 |
C |
A |
2: 86,286,078 (GRCm39) |
C179F |
probably damaging |
Het |
Pcdhb6 |
C |
T |
18: 37,468,837 (GRCm39) |
T586I |
probably benign |
Het |
Ppcs |
A |
T |
4: 119,279,330 (GRCm39) |
L74Q |
probably damaging |
Het |
Ppp6r3 |
A |
T |
19: 3,517,216 (GRCm39) |
V677D |
probably benign |
Het |
Psg27 |
C |
T |
7: 18,294,337 (GRCm39) |
G357S |
probably damaging |
Het |
Ptgdr2 |
A |
G |
19: 10,918,380 (GRCm39) |
N299S |
probably damaging |
Het |
Relb |
T |
A |
7: 19,353,762 (GRCm39) |
I39F |
probably damaging |
Het |
Ripor2 |
T |
A |
13: 24,901,651 (GRCm39) |
S907R |
possibly damaging |
Het |
Rnf170 |
T |
G |
8: 26,629,043 (GRCm39) |
D172E |
probably benign |
Het |
Rnf31 |
C |
A |
14: 55,832,396 (GRCm39) |
Q273K |
probably benign |
Het |
Rrp36 |
A |
T |
17: 46,983,336 (GRCm39) |
S93T |
probably damaging |
Het |
Rsad1 |
A |
T |
11: 94,439,100 (GRCm39) |
V120D |
probably benign |
Het |
Ryr3 |
C |
T |
2: 112,661,441 (GRCm39) |
A1870T |
probably damaging |
Het |
Serpina10 |
T |
G |
12: 103,595,063 (GRCm39) |
D52A |
probably benign |
Het |
Slc47a1 |
A |
G |
11: 61,261,055 (GRCm39) |
I115T |
probably benign |
Het |
Spag17 |
T |
A |
3: 99,920,543 (GRCm39) |
M426K |
probably benign |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Sptbn4 |
T |
G |
7: 27,063,592 (GRCm39) |
E2283A |
possibly damaging |
Het |
Top3a |
A |
G |
11: 60,633,877 (GRCm39) |
C740R |
probably damaging |
Het |
Tpgs2 |
A |
T |
18: 25,291,365 (GRCm39) |
V33E |
probably damaging |
Het |
Treh |
T |
C |
9: 44,592,823 (GRCm39) |
I116T |
probably damaging |
Het |
Trpm3 |
A |
T |
19: 22,955,952 (GRCm39) |
N1138I |
possibly damaging |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Vamp9 |
A |
T |
5: 100,089,094 (GRCm39) |
N120Y |
probably damaging |
Het |
Zswim9 |
G |
T |
7: 12,994,456 (GRCm39) |
Q567K |
probably benign |
Het |
|
Other mutations in Fbrs |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02476:Fbrs
|
APN |
7 |
127,086,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Fbrs
|
UTSW |
7 |
127,088,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R0096:Fbrs
|
UTSW |
7 |
127,088,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R0133:Fbrs
|
UTSW |
7 |
127,088,782 (GRCm39) |
splice site |
probably benign |
|
R1579:Fbrs
|
UTSW |
7 |
127,084,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R1617:Fbrs
|
UTSW |
7 |
127,086,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Fbrs
|
UTSW |
7 |
127,086,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Fbrs
|
UTSW |
7 |
127,085,163 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2426:Fbrs
|
UTSW |
7 |
127,086,511 (GRCm39) |
splice site |
probably null |
|
R5797:Fbrs
|
UTSW |
7 |
127,086,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R5952:Fbrs
|
UTSW |
7 |
127,086,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R6659:Fbrs
|
UTSW |
7 |
127,087,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6988:Fbrs
|
UTSW |
7 |
127,078,680 (GRCm39) |
unclassified |
probably benign |
|
R7055:Fbrs
|
UTSW |
7 |
127,086,956 (GRCm39) |
critical splice donor site |
probably null |
|
R7319:Fbrs
|
UTSW |
7 |
127,081,985 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7349:Fbrs
|
UTSW |
7 |
127,081,971 (GRCm39) |
missense |
probably damaging |
0.99 |
R7423:Fbrs
|
UTSW |
7 |
127,088,633 (GRCm39) |
nonsense |
probably null |
|
R7760:Fbrs
|
UTSW |
7 |
127,088,572 (GRCm39) |
missense |
probably damaging |
0.96 |
R8199:Fbrs
|
UTSW |
7 |
127,086,956 (GRCm39) |
critical splice donor site |
probably null |
|
R8458:Fbrs
|
UTSW |
7 |
127,082,329 (GRCm39) |
missense |
probably damaging |
0.98 |
R8459:Fbrs
|
UTSW |
7 |
127,082,329 (GRCm39) |
missense |
probably damaging |
0.98 |
R9433:Fbrs
|
UTSW |
7 |
127,084,272 (GRCm39) |
missense |
probably benign |
0.03 |
|