Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
C |
7: 119,936,478 (GRCm39) |
L181P |
probably damaging |
Het |
Aldh3a1 |
A |
T |
11: 61,105,445 (GRCm39) |
I184F |
probably damaging |
Het |
Arl6ip4 |
A |
G |
5: 124,254,596 (GRCm39) |
S30G |
probably benign |
Het |
Atp9b |
T |
C |
18: 80,797,171 (GRCm39) |
E891G |
possibly damaging |
Het |
Brsk1 |
T |
C |
7: 4,710,425 (GRCm39) |
L478P |
possibly damaging |
Het |
Btaf1 |
G |
A |
19: 36,946,537 (GRCm39) |
V448I |
probably damaging |
Het |
Cab39 |
T |
C |
1: 85,746,236 (GRCm39) |
|
probably null |
Het |
Cacna2d4 |
G |
T |
6: 119,258,679 (GRCm39) |
|
probably benign |
Het |
Capzb |
C |
T |
4: 139,018,340 (GRCm39) |
S253L |
probably benign |
Het |
Ccdc174 |
A |
G |
6: 91,867,873 (GRCm39) |
|
probably benign |
Het |
Ccdc180 |
C |
T |
4: 45,927,969 (GRCm39) |
A1168V |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,820,900 (GRCm39) |
|
probably benign |
Het |
Cdh8 |
T |
C |
8: 100,127,546 (GRCm39) |
T22A |
probably benign |
Het |
Cdk10 |
T |
C |
8: 123,957,419 (GRCm39) |
V181A |
probably benign |
Het |
Ceacam15 |
A |
C |
7: 16,407,445 (GRCm39) |
L24* |
probably null |
Het |
Cftr |
A |
C |
6: 18,198,125 (GRCm39) |
T20P |
probably benign |
Het |
Cip2a |
C |
T |
16: 48,819,402 (GRCm39) |
A112V |
probably benign |
Het |
Clstn3 |
T |
C |
6: 124,426,459 (GRCm39) |
T576A |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,516,003 (GRCm39) |
V165I |
unknown |
Het |
Copg2 |
A |
T |
6: 30,838,404 (GRCm39) |
|
probably null |
Het |
Cps1 |
A |
G |
1: 67,178,929 (GRCm39) |
H47R |
probably benign |
Het |
Cytip |
T |
C |
2: 58,024,202 (GRCm39) |
D206G |
possibly damaging |
Het |
Dcaf8l |
G |
A |
X: 88,448,972 (GRCm39) |
R386* |
probably null |
Het |
Dnmt1 |
C |
T |
9: 20,829,489 (GRCm39) |
E824K |
probably damaging |
Het |
Dock7 |
A |
C |
4: 98,877,470 (GRCm39) |
V442G |
probably benign |
Het |
Dsc1 |
T |
G |
18: 20,247,573 (GRCm39) |
K14T |
probably damaging |
Het |
Dync1h1 |
C |
T |
12: 110,582,930 (GRCm39) |
P371L |
probably damaging |
Het |
Enah |
A |
G |
1: 181,734,013 (GRCm39) |
|
probably benign |
Het |
Entrep2 |
C |
T |
7: 64,411,549 (GRCm39) |
V395M |
probably benign |
Het |
Fastkd1 |
T |
C |
2: 69,542,727 (GRCm39) |
T27A |
probably benign |
Het |
Fcho1 |
A |
G |
8: 72,168,168 (GRCm39) |
L248P |
probably damaging |
Het |
Fezf1 |
A |
T |
6: 23,247,028 (GRCm39) |
V268D |
probably damaging |
Het |
Fgd2 |
T |
A |
17: 29,597,321 (GRCm39) |
V547E |
probably benign |
Het |
Flnb |
T |
A |
14: 7,887,682 (GRCm38) |
|
probably benign |
Het |
Gabrg3 |
A |
G |
7: 56,379,454 (GRCm39) |
M316T |
probably damaging |
Het |
Gigyf2 |
T |
C |
1: 87,376,802 (GRCm39) |
F1265L |
probably damaging |
Het |
Git2 |
A |
G |
5: 114,890,342 (GRCm39) |
S271P |
probably damaging |
Het |
Gorab |
T |
C |
1: 163,224,738 (GRCm39) |
D21G |
possibly damaging |
Het |
Gpr179 |
T |
A |
11: 97,229,264 (GRCm39) |
T964S |
possibly damaging |
Het |
Hdac5 |
A |
G |
11: 102,087,078 (GRCm39) |
V1042A |
possibly damaging |
Het |
Hoxa2 |
T |
A |
6: 52,140,540 (GRCm39) |
T149S |
probably damaging |
Het |
Igsf8 |
G |
T |
1: 172,146,974 (GRCm39) |
*108L |
probably null |
Het |
Il1rap |
C |
T |
16: 26,519,855 (GRCm39) |
T307M |
possibly damaging |
Het |
Itih2 |
T |
C |
2: 10,122,205 (GRCm39) |
D232G |
probably benign |
Het |
Jak3 |
A |
G |
8: 72,136,021 (GRCm39) |
Y607C |
probably damaging |
Het |
Kcnh1 |
C |
T |
1: 191,959,361 (GRCm39) |
P305L |
probably damaging |
Het |
Lrrc7 |
T |
A |
3: 157,869,990 (GRCm39) |
I644F |
probably damaging |
Het |
Lrrn2 |
T |
C |
1: 132,865,466 (GRCm39) |
L177P |
probably damaging |
Het |
Lypd8l |
A |
G |
11: 58,502,799 (GRCm39) |
|
probably null |
Het |
Map4k3 |
C |
A |
17: 80,909,622 (GRCm39) |
K712N |
probably damaging |
Het |
Med11 |
A |
G |
11: 70,342,910 (GRCm39) |
T36A |
probably benign |
Het |
Mmp14 |
A |
G |
14: 54,677,891 (GRCm39) |
D504G |
probably damaging |
Het |
Mob1a |
A |
G |
6: 83,311,140 (GRCm39) |
T120A |
probably benign |
Het |
Mr1 |
T |
A |
1: 155,013,436 (GRCm39) |
D47V |
probably damaging |
Het |
Nacad |
G |
T |
11: 6,551,382 (GRCm39) |
A603E |
possibly damaging |
Het |
Nwd1 |
T |
A |
8: 73,394,308 (GRCm39) |
W524R |
probably damaging |
Het |
Or11g26 |
A |
T |
14: 50,752,939 (GRCm39) |
T93S |
probably benign |
Het |
Or13a19 |
T |
A |
7: 139,903,101 (GRCm39) |
M163K |
possibly damaging |
Het |
Or4e1 |
T |
C |
14: 52,701,008 (GRCm39) |
T153A |
probably benign |
Het |
Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
Pde6c |
T |
A |
19: 38,121,694 (GRCm39) |
C101S |
probably benign |
Het |
Pdlim4 |
G |
A |
11: 53,959,713 (GRCm39) |
R16C |
probably damaging |
Het |
Pfkp |
A |
G |
13: 6,655,670 (GRCm39) |
|
probably null |
Het |
Plcg2 |
T |
A |
8: 118,300,104 (GRCm39) |
S225T |
probably benign |
Het |
Pramel1 |
T |
C |
4: 143,124,101 (GRCm39) |
S259P |
probably damaging |
Het |
Pramel27 |
G |
T |
4: 143,578,658 (GRCm39) |
|
probably benign |
Het |
Rc3h2 |
T |
C |
2: 37,301,227 (GRCm39) |
N92D |
possibly damaging |
Het |
Ric8b |
C |
A |
10: 84,837,745 (GRCm39) |
N517K |
probably damaging |
Het |
Rnf34 |
G |
A |
5: 123,002,237 (GRCm39) |
R65H |
probably damaging |
Het |
Rraga |
C |
T |
4: 86,494,564 (GRCm39) |
R137C |
probably damaging |
Het |
Scube2 |
C |
T |
7: 109,403,971 (GRCm39) |
|
probably benign |
Het |
Slc28a2b |
T |
C |
2: 122,352,179 (GRCm39) |
M339T |
probably damaging |
Het |
Spata31d1d |
T |
C |
13: 59,875,787 (GRCm39) |
I583V |
probably benign |
Het |
Suox |
T |
C |
10: 128,506,525 (GRCm39) |
E501G |
probably benign |
Het |
Susd1 |
A |
G |
4: 59,390,561 (GRCm39) |
|
probably benign |
Het |
Tac1 |
T |
C |
6: 7,555,653 (GRCm39) |
S14P |
probably damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,411,596 (GRCm39) |
E1080G |
possibly damaging |
Het |
Tll1 |
A |
C |
8: 64,524,344 (GRCm39) |
S447R |
possibly damaging |
Het |
Tmem132e |
G |
A |
11: 82,334,198 (GRCm39) |
V662M |
probably damaging |
Het |
Upf2 |
G |
T |
2: 6,038,909 (GRCm39) |
|
probably benign |
Het |
Uspl1 |
A |
G |
5: 149,151,767 (GRCm39) |
E989G |
probably damaging |
Het |
Vmn1r58 |
T |
C |
7: 5,413,618 (GRCm39) |
H204R |
probably damaging |
Het |
Vmn2r25 |
A |
T |
6: 123,816,481 (GRCm39) |
C367S |
probably damaging |
Het |
Vps13b |
A |
T |
15: 35,623,803 (GRCm39) |
Q1240L |
probably benign |
Het |
Xrcc1 |
C |
T |
7: 24,269,744 (GRCm39) |
|
probably benign |
Het |
Yeats2 |
T |
G |
16: 20,005,175 (GRCm39) |
V385G |
probably benign |
Het |
|
Other mutations in Pdia3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Pdia3
|
APN |
2 |
121,244,659 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00777:Pdia3
|
APN |
2 |
121,260,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02020:Pdia3
|
APN |
2 |
121,266,900 (GRCm39) |
splice site |
probably null |
|
IGL02437:Pdia3
|
APN |
2 |
121,264,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02988:Pdia3
|
UTSW |
2 |
121,260,037 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4812001:Pdia3
|
UTSW |
2 |
121,264,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Pdia3
|
UTSW |
2 |
121,244,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Pdia3
|
UTSW |
2 |
121,244,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0724:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0880:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0882:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R1157:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R1160:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R1238:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Pdia3
|
UTSW |
2 |
121,262,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Pdia3
|
UTSW |
2 |
121,262,144 (GRCm39) |
missense |
probably benign |
0.20 |
R1854:Pdia3
|
UTSW |
2 |
121,262,144 (GRCm39) |
missense |
probably benign |
0.20 |
R2014:Pdia3
|
UTSW |
2 |
121,265,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Pdia3
|
UTSW |
2 |
121,264,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R4160:Pdia3
|
UTSW |
2 |
121,244,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R4628:Pdia3
|
UTSW |
2 |
121,244,620 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5032:Pdia3
|
UTSW |
2 |
121,244,620 (GRCm39) |
missense |
probably benign |
0.28 |
R5279:Pdia3
|
UTSW |
2 |
121,244,484 (GRCm39) |
unclassified |
probably benign |
|
R5598:Pdia3
|
UTSW |
2 |
121,244,611 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5815:Pdia3
|
UTSW |
2 |
121,266,892 (GRCm39) |
nonsense |
probably null |
|
R7162:Pdia3
|
UTSW |
2 |
121,260,002 (GRCm39) |
missense |
probably benign |
0.00 |
R7729:Pdia3
|
UTSW |
2 |
121,262,838 (GRCm39) |
missense |
possibly damaging |
0.77 |
X0012:Pdia3
|
UTSW |
2 |
121,266,426 (GRCm39) |
missense |
possibly damaging |
0.92 |
|