Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
A |
T |
10: 87,000,970 (GRCm39) |
D54V |
probably damaging |
Het |
Adamts18 |
C |
A |
8: 114,440,976 (GRCm39) |
|
probably benign |
Het |
Angptl3 |
T |
A |
4: 98,919,399 (GRCm39) |
L53Q |
probably damaging |
Het |
Apc |
A |
G |
18: 34,447,588 (GRCm39) |
T1461A |
probably damaging |
Het |
Arl11 |
T |
A |
14: 61,548,535 (GRCm39) |
V115D |
probably damaging |
Het |
Cabp4 |
C |
A |
19: 4,188,560 (GRCm39) |
V173L |
possibly damaging |
Het |
Casq1 |
T |
A |
1: 172,042,672 (GRCm39) |
D230V |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,936,824 (GRCm39) |
I821V |
possibly damaging |
Het |
Cfap65 |
T |
C |
1: 74,944,239 (GRCm39) |
Y1494C |
probably benign |
Het |
Chd1 |
T |
A |
17: 15,951,069 (GRCm39) |
S215T |
probably damaging |
Het |
Csf2rb2 |
T |
C |
15: 78,169,049 (GRCm39) |
E593G |
possibly damaging |
Het |
Cstf1 |
A |
G |
2: 172,217,795 (GRCm39) |
D136G |
probably damaging |
Het |
Ddx19b |
T |
C |
8: 111,737,910 (GRCm39) |
|
probably benign |
Het |
Dido1 |
A |
T |
2: 180,303,716 (GRCm39) |
L1396Q |
probably benign |
Het |
F12 |
T |
A |
13: 55,568,880 (GRCm39) |
Q294L |
possibly damaging |
Het |
Far2 |
A |
T |
6: 148,058,889 (GRCm39) |
I192F |
probably damaging |
Het |
Fshb |
T |
A |
2: 106,889,218 (GRCm39) |
I29F |
probably damaging |
Het |
Gcgr |
T |
A |
11: 120,427,811 (GRCm39) |
Y251N |
probably benign |
Het |
Gpr158 |
A |
G |
2: 21,831,890 (GRCm39) |
I997V |
possibly damaging |
Het |
Gprc5d |
A |
G |
6: 135,093,613 (GRCm39) |
V98A |
probably damaging |
Het |
H2-T23 |
T |
C |
17: 36,342,580 (GRCm39) |
E186G |
probably damaging |
Het |
Khdrbs3 |
C |
T |
15: 68,896,685 (GRCm39) |
T115I |
probably benign |
Het |
Kifap3 |
C |
T |
1: 163,689,597 (GRCm39) |
T527M |
probably damaging |
Het |
Mfsd2a |
C |
T |
4: 122,842,332 (GRCm39) |
A512T |
probably benign |
Het |
Mmp9 |
A |
G |
2: 164,791,235 (GRCm39) |
D135G |
probably benign |
Het |
Mylk |
T |
C |
16: 34,784,016 (GRCm39) |
V1394A |
probably benign |
Het |
Nek9 |
A |
C |
12: 85,358,110 (GRCm39) |
|
probably null |
Het |
Or51q1c |
T |
C |
7: 103,652,866 (GRCm39) |
I128T |
probably damaging |
Het |
Or8k16 |
T |
C |
2: 85,520,402 (GRCm39) |
S210P |
probably damaging |
Het |
P2rx2 |
T |
A |
5: 110,490,276 (GRCm39) |
|
probably benign |
Het |
P4htm |
A |
G |
9: 108,456,977 (GRCm39) |
L410P |
probably damaging |
Het |
Pik3c2a |
A |
T |
7: 115,963,748 (GRCm39) |
W921R |
probably benign |
Het |
Pnisr |
T |
C |
4: 21,862,175 (GRCm39) |
F288L |
probably benign |
Het |
Ppp4r3a |
C |
T |
12: 101,024,582 (GRCm39) |
|
probably null |
Het |
Prss34 |
T |
C |
17: 25,518,251 (GRCm39) |
S144P |
probably damaging |
Het |
Qrsl1 |
T |
C |
10: 43,758,110 (GRCm39) |
T328A |
probably benign |
Het |
Rab33b |
A |
T |
3: 51,391,945 (GRCm39) |
T65S |
probably damaging |
Het |
Rdh8 |
A |
G |
9: 20,736,637 (GRCm39) |
S235G |
possibly damaging |
Het |
Rrp12 |
T |
C |
19: 41,884,500 (GRCm39) |
K6R |
probably benign |
Het |
Sec24a |
T |
C |
11: 51,587,560 (GRCm39) |
D1025G |
probably benign |
Het |
Sgo2a |
T |
G |
1: 58,055,509 (GRCm39) |
N564K |
probably damaging |
Het |
Slc43a3 |
A |
T |
2: 84,774,612 (GRCm39) |
M130L |
probably benign |
Het |
Soat1 |
T |
C |
1: 156,274,145 (GRCm39) |
I89V |
probably benign |
Het |
St3gal5 |
A |
G |
6: 72,126,157 (GRCm39) |
D307G |
probably null |
Het |
Stxbp3-ps |
C |
T |
19: 9,535,193 (GRCm39) |
|
noncoding transcript |
Het |
Tacr2 |
A |
G |
10: 62,097,469 (GRCm39) |
|
probably benign |
Het |
Tg |
C |
T |
15: 66,606,435 (GRCm39) |
T193I |
probably benign |
Het |
Tnik |
A |
G |
3: 28,596,179 (GRCm39) |
T191A |
probably damaging |
Het |
Trim27 |
T |
C |
13: 21,374,256 (GRCm39) |
|
probably benign |
Het |
Usf2 |
A |
T |
7: 30,646,417 (GRCm39) |
C134* |
probably null |
Het |
Usp14 |
A |
G |
18: 10,001,769 (GRCm39) |
|
probably null |
Het |
Usp47 |
T |
C |
7: 111,692,270 (GRCm39) |
S911P |
possibly damaging |
Het |
Vmn1r73 |
T |
A |
7: 11,490,574 (GRCm39) |
S131T |
possibly damaging |
Het |
Vmn2r80 |
T |
C |
10: 79,030,145 (GRCm39) |
I657T |
probably damaging |
Het |
Zfp935 |
A |
T |
13: 62,602,701 (GRCm39) |
C166* |
probably null |
Het |
|
Other mutations in Ermn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01138:Ermn
|
APN |
2 |
57,942,707 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01620:Ermn
|
APN |
2 |
57,942,502 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03354:Ermn
|
APN |
2 |
57,942,634 (GRCm39) |
missense |
probably benign |
0.26 |
FR4304:Ermn
|
UTSW |
2 |
57,938,098 (GRCm39) |
unclassified |
probably benign |
|
FR4304:Ermn
|
UTSW |
2 |
57,938,090 (GRCm39) |
unclassified |
probably benign |
|
FR4449:Ermn
|
UTSW |
2 |
57,938,086 (GRCm39) |
unclassified |
probably benign |
|
FR4548:Ermn
|
UTSW |
2 |
57,938,100 (GRCm39) |
unclassified |
probably benign |
|
FR4548:Ermn
|
UTSW |
2 |
57,938,087 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Ermn
|
UTSW |
2 |
57,938,081 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Ermn
|
UTSW |
2 |
57,938,100 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Ermn
|
UTSW |
2 |
57,938,092 (GRCm39) |
unclassified |
probably benign |
|
R0827:Ermn
|
UTSW |
2 |
57,938,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1655:Ermn
|
UTSW |
2 |
57,942,596 (GRCm39) |
missense |
probably benign |
0.01 |
R1799:Ermn
|
UTSW |
2 |
57,938,249 (GRCm39) |
missense |
probably benign |
0.06 |
R5691:Ermn
|
UTSW |
2 |
57,937,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6311:Ermn
|
UTSW |
2 |
57,941,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6704:Ermn
|
UTSW |
2 |
57,938,046 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7444:Ermn
|
UTSW |
2 |
57,938,079 (GRCm39) |
unclassified |
probably benign |
|
R9217:Ermn
|
UTSW |
2 |
57,938,010 (GRCm39) |
missense |
probably damaging |
1.00 |
RF028:Ermn
|
UTSW |
2 |
57,938,078 (GRCm39) |
unclassified |
probably benign |
|
RF031:Ermn
|
UTSW |
2 |
57,938,078 (GRCm39) |
unclassified |
probably benign |
|
|