Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
A |
17: 48,347,580 (GRCm39) |
K241N |
possibly damaging |
Het |
Adam5 |
A |
T |
8: 25,296,510 (GRCm39) |
S312R |
probably damaging |
Het |
Atg9a |
C |
T |
1: 75,163,086 (GRCm39) |
C338Y |
possibly damaging |
Het |
Cage1 |
T |
C |
13: 38,196,447 (GRCm39) |
E749G |
possibly damaging |
Het |
Catspere2 |
C |
A |
1: 177,931,275 (GRCm39) |
T398K |
unknown |
Het |
Ccdc88b |
T |
C |
19: 6,833,213 (GRCm39) |
E278G |
probably damaging |
Het |
Ccndbp1 |
T |
C |
2: 120,839,013 (GRCm39) |
V8A |
probably benign |
Het |
Cenpt |
T |
C |
8: 106,575,418 (GRCm39) |
D228G |
probably benign |
Het |
Cfap57 |
A |
G |
4: 118,463,731 (GRCm39) |
|
probably null |
Het |
Cyp4a32 |
T |
A |
4: 115,468,422 (GRCm39) |
N301K |
probably benign |
Het |
Epha6 |
T |
C |
16: 60,025,850 (GRCm39) |
T531A |
probably benign |
Het |
Gmeb1 |
A |
T |
4: 131,962,156 (GRCm39) |
C168S |
probably damaging |
Het |
H2-DMa |
G |
A |
17: 34,357,132 (GRCm39) |
R210H |
possibly damaging |
Het |
Ighv1-7 |
T |
G |
12: 114,502,198 (GRCm39) |
T90P |
probably damaging |
Het |
Kalrn |
A |
C |
16: 33,916,249 (GRCm39) |
M1R |
probably null |
Het |
Kcnrg |
CACAACAA |
CACAA |
14: 61,845,009 (GRCm39) |
|
probably benign |
Het |
Krtap14 |
T |
C |
16: 88,622,865 (GRCm39) |
D38G |
possibly damaging |
Het |
Lrrc8e |
A |
G |
8: 4,283,964 (GRCm39) |
N63S |
probably benign |
Het |
Map4k2 |
T |
A |
19: 6,392,814 (GRCm39) |
L152Q |
probably damaging |
Het |
Mcf2l |
A |
G |
8: 13,023,048 (GRCm39) |
D78G |
possibly damaging |
Het |
Ms4a6c |
T |
C |
19: 11,449,851 (GRCm39) |
V81A |
probably benign |
Het |
Mtnr1b |
T |
C |
9: 15,785,660 (GRCm39) |
T33A |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,566,624 (GRCm39) |
Q1965L |
unknown |
Het |
Nfatc2 |
A |
C |
2: 168,328,898 (GRCm39) |
|
probably benign |
Het |
Nlrp9b |
C |
T |
7: 19,779,707 (GRCm39) |
T790I |
possibly damaging |
Het |
Nol4 |
A |
T |
18: 22,902,899 (GRCm39) |
C371S |
probably damaging |
Het |
Ntn1 |
A |
C |
11: 68,148,485 (GRCm39) |
|
probably benign |
Het |
Or14j3 |
A |
G |
17: 37,900,633 (GRCm39) |
S204P |
possibly damaging |
Het |
Orc1 |
T |
C |
4: 108,469,357 (GRCm39) |
V727A |
probably benign |
Het |
Phf20l1 |
C |
T |
15: 66,484,888 (GRCm39) |
Q318* |
probably null |
Het |
Psg18 |
A |
T |
7: 18,083,185 (GRCm39) |
Y323* |
probably null |
Het |
Ptk2b |
T |
C |
14: 66,409,189 (GRCm39) |
Y529C |
probably damaging |
Het |
Rrm1 |
A |
G |
7: 102,108,598 (GRCm39) |
Y374C |
probably damaging |
Het |
Selp |
T |
A |
1: 163,964,765 (GRCm39) |
F476I |
probably damaging |
Het |
Sema3b |
A |
G |
9: 107,478,957 (GRCm39) |
|
probably null |
Het |
Setdb2 |
T |
G |
14: 59,639,849 (GRCm39) |
T665P |
probably damaging |
Het |
Sorbs3 |
T |
C |
14: 70,424,387 (GRCm39) |
Y515C |
probably damaging |
Het |
St13 |
G |
A |
15: 81,272,575 (GRCm39) |
P90S |
possibly damaging |
Het |
Stag1 |
T |
A |
9: 100,836,306 (GRCm39) |
I1197N |
probably damaging |
Het |
Svs3a |
A |
G |
2: 164,132,179 (GRCm39) |
Y250C |
probably damaging |
Het |
Ticam1 |
T |
C |
17: 56,577,428 (GRCm39) |
I556V |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,342,235 (GRCm39) |
L1492* |
probably null |
Het |
Zfp438 |
A |
G |
18: 5,214,379 (GRCm39) |
V193A |
probably benign |
Het |
Zfp729b |
A |
G |
13: 67,739,337 (GRCm39) |
V976A |
probably benign |
Het |
|
Other mutations in Vmn1r180 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00487:Vmn1r180
|
APN |
7 |
23,651,948 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01309:Vmn1r180
|
APN |
7 |
23,652,424 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01793:Vmn1r180
|
APN |
7 |
23,652,668 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02653:Vmn1r180
|
APN |
7 |
23,652,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Vmn1r180
|
APN |
7 |
23,652,710 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03352:Vmn1r180
|
APN |
7 |
23,652,077 (GRCm39) |
nonsense |
probably null |
|
R1298:Vmn1r180
|
UTSW |
7 |
23,652,572 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1701:Vmn1r180
|
UTSW |
7 |
23,652,395 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1702:Vmn1r180
|
UTSW |
7 |
23,652,394 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2122:Vmn1r180
|
UTSW |
7 |
23,652,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4241:Vmn1r180
|
UTSW |
7 |
23,652,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5683:Vmn1r180
|
UTSW |
7 |
23,652,635 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7241:Vmn1r180
|
UTSW |
7 |
23,651,891 (GRCm39) |
missense |
probably damaging |
0.96 |
R7522:Vmn1r180
|
UTSW |
7 |
23,652,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R8749:Vmn1r180
|
UTSW |
7 |
23,652,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R8991:Vmn1r180
|
UTSW |
7 |
23,652,076 (GRCm39) |
missense |
probably benign |
0.06 |
|