Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,217 (GRCm39) |
V217M |
probably benign |
Het |
Abca4 |
A |
G |
3: 121,973,394 (GRCm39) |
Q1074R |
probably benign |
Het |
Ablim1 |
T |
C |
19: 57,170,718 (GRCm39) |
|
probably benign |
Het |
Acox2 |
A |
T |
14: 8,256,081 (GRCm38) |
D79E |
probably benign |
Het |
Bpifb9b |
A |
G |
2: 154,158,197 (GRCm39) |
I440V |
probably benign |
Het |
Ccdc7a |
T |
A |
8: 129,516,601 (GRCm39) |
T118S |
possibly damaging |
Het |
Cntln |
T |
C |
4: 84,875,286 (GRCm39) |
I240T |
probably damaging |
Het |
Col15a1 |
T |
C |
4: 47,208,536 (GRCm39) |
|
probably null |
Het |
Cox18 |
A |
G |
5: 90,362,877 (GRCm39) |
F326S |
probably damaging |
Het |
Dnm1l |
C |
A |
16: 16,176,639 (GRCm39) |
V31L |
probably benign |
Het |
Dst |
C |
A |
1: 34,236,327 (GRCm39) |
L3578M |
possibly damaging |
Het |
Fbxw24 |
G |
A |
9: 109,452,599 (GRCm39) |
T132I |
probably damaging |
Het |
Fchsd1 |
A |
G |
18: 38,100,823 (GRCm39) |
V120A |
probably benign |
Het |
Fibcd1 |
T |
C |
2: 31,706,643 (GRCm39) |
E396G |
probably damaging |
Het |
Fryl |
G |
T |
5: 73,257,696 (GRCm39) |
T702K |
probably damaging |
Het |
Gatb |
A |
T |
3: 85,511,868 (GRCm39) |
I208F |
probably damaging |
Het |
Gzmd |
T |
C |
14: 56,367,158 (GRCm39) |
I245V |
probably damaging |
Het |
Lats2 |
G |
A |
14: 57,940,495 (GRCm39) |
A119V |
probably damaging |
Het |
Lztfl1 |
A |
T |
9: 123,540,119 (GRCm39) |
F129L |
probably benign |
Het |
Meak7 |
T |
C |
8: 120,490,787 (GRCm39) |
N320S |
probably benign |
Het |
Mmp2 |
A |
T |
8: 93,557,253 (GRCm39) |
Y53F |
probably damaging |
Het |
Mttp |
G |
A |
3: 137,810,704 (GRCm39) |
R637C |
probably damaging |
Het |
Ndufa8 |
A |
C |
2: 35,939,312 (GRCm39) |
|
probably benign |
Het |
Nek11 |
A |
T |
9: 105,175,538 (GRCm39) |
M302K |
probably benign |
Het |
Nek6 |
A |
G |
2: 38,404,797 (GRCm39) |
|
probably null |
Het |
Numa1 |
C |
T |
7: 101,650,787 (GRCm39) |
A1506V |
probably damaging |
Het |
Plxdc1 |
A |
T |
11: 97,869,522 (GRCm39) |
|
probably null |
Het |
Poteg |
C |
A |
8: 27,938,048 (GRCm39) |
T6K |
probably benign |
Het |
Rbm26 |
A |
T |
14: 105,380,274 (GRCm39) |
N514K |
possibly damaging |
Het |
Rnf145 |
T |
C |
11: 44,450,942 (GRCm39) |
L422P |
probably damaging |
Het |
Scn5a |
G |
T |
9: 119,368,811 (GRCm39) |
T238K |
probably damaging |
Het |
Shd |
G |
A |
17: 56,283,315 (GRCm39) |
A315T |
probably damaging |
Het |
Sirpd |
A |
G |
3: 15,361,614 (GRCm39) |
*179R |
probably null |
Het |
Slco5a1 |
T |
G |
1: 12,951,525 (GRCm39) |
T593P |
possibly damaging |
Het |
Stard9 |
G |
A |
2: 120,545,140 (GRCm39) |
R4560H |
possibly damaging |
Het |
Traf3ip3 |
C |
T |
1: 192,876,823 (GRCm39) |
|
probably null |
Het |
Trpm1 |
G |
C |
7: 63,897,155 (GRCm39) |
K252N |
probably damaging |
Het |
Ttc7b |
A |
T |
12: 100,339,803 (GRCm39) |
I584K |
possibly damaging |
Het |
Wdfy3 |
G |
T |
5: 102,033,064 (GRCm39) |
H2215Q |
probably benign |
Het |
Wls |
G |
A |
3: 159,578,748 (GRCm39) |
M103I |
probably damaging |
Het |
Zmat4 |
T |
C |
8: 24,238,523 (GRCm39) |
|
probably null |
Het |
Zmynd15 |
G |
T |
11: 70,353,387 (GRCm39) |
C334F |
probably damaging |
Het |
|
Other mutations in Vmn1r218 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02014:Vmn1r218
|
APN |
13 |
23,321,001 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02670:Vmn1r218
|
APN |
13 |
23,321,174 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03085:Vmn1r218
|
APN |
13 |
23,321,481 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03334:Vmn1r218
|
APN |
13 |
23,320,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Vmn1r218
|
UTSW |
13 |
23,321,225 (GRCm39) |
nonsense |
probably null |
|
R0049:Vmn1r218
|
UTSW |
13 |
23,321,225 (GRCm39) |
nonsense |
probably null |
|
R1387:Vmn1r218
|
UTSW |
13 |
23,321,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Vmn1r218
|
UTSW |
13 |
23,320,683 (GRCm39) |
missense |
probably damaging |
0.96 |
R3713:Vmn1r218
|
UTSW |
13 |
23,321,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Vmn1r218
|
UTSW |
13 |
23,321,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4038:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4039:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4432:Vmn1r218
|
UTSW |
13 |
23,321,412 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5255:Vmn1r218
|
UTSW |
13 |
23,320,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5521:Vmn1r218
|
UTSW |
13 |
23,320,743 (GRCm39) |
missense |
probably benign |
0.01 |
R7384:Vmn1r218
|
UTSW |
13 |
23,320,895 (GRCm39) |
missense |
probably benign |
0.00 |
R7565:Vmn1r218
|
UTSW |
13 |
23,320,830 (GRCm39) |
missense |
probably benign |
0.05 |
R8178:Vmn1r218
|
UTSW |
13 |
23,321,472 (GRCm39) |
missense |
probably benign |
0.08 |
R9225:Vmn1r218
|
UTSW |
13 |
23,320,824 (GRCm39) |
missense |
probably benign |
0.04 |
R9609:Vmn1r218
|
UTSW |
13 |
23,320,839 (GRCm39) |
missense |
probably benign |
0.01 |
R9734:Vmn1r218
|
UTSW |
13 |
23,321,034 (GRCm39) |
missense |
probably damaging |
1.00 |
|