Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
A |
G |
7: 119,179,856 (GRCm39) |
H358R |
probably benign |
Het |
Arid3c |
A |
G |
4: 41,730,138 (GRCm39) |
L19S |
possibly damaging |
Het |
Arpp21 |
T |
A |
9: 111,986,765 (GRCm39) |
D262V |
probably damaging |
Het |
Atp4a |
A |
C |
7: 30,415,207 (GRCm39) |
I276L |
probably benign |
Het |
Axl |
C |
G |
7: 25,460,982 (GRCm39) |
E676Q |
probably damaging |
Het |
Ces1g |
T |
C |
8: 94,055,118 (GRCm39) |
D193G |
probably damaging |
Het |
Crym |
A |
G |
7: 119,789,005 (GRCm39) |
V274A |
probably damaging |
Het |
Efcab5 |
T |
A |
11: 77,004,546 (GRCm39) |
H924L |
possibly damaging |
Het |
Eif1ad7 |
T |
A |
12: 88,238,709 (GRCm39) |
N17I |
unknown |
Het |
Eif3l |
T |
A |
15: 78,978,423 (GRCm39) |
M560K |
probably benign |
Het |
Fam234b |
C |
A |
6: 135,202,793 (GRCm39) |
Y382* |
probably null |
Het |
Fbxw19 |
T |
C |
9: 109,313,440 (GRCm39) |
K253E |
possibly damaging |
Het |
Fhip1a |
T |
C |
3: 85,638,053 (GRCm39) |
D82G |
probably benign |
Het |
Flt3 |
A |
G |
5: 147,313,790 (GRCm39) |
S87P |
probably benign |
Het |
Garin3 |
A |
T |
11: 46,295,810 (GRCm39) |
I61F |
|
Het |
Ggnbp2 |
A |
G |
11: 84,725,174 (GRCm39) |
L627S |
probably damaging |
Het |
Gm26661 |
T |
G |
14: 7,791,765 (GRCm38) |
V60G |
unknown |
Het |
Golt1a |
T |
C |
1: 133,247,094 (GRCm39) |
L34P |
probably damaging |
Het |
Gp5 |
T |
C |
16: 30,127,808 (GRCm39) |
M289V |
possibly damaging |
Het |
Gpr63 |
C |
G |
4: 25,008,432 (GRCm39) |
H385Q |
possibly damaging |
Het |
Hcn1 |
G |
A |
13: 118,111,901 (GRCm39) |
V622I |
unknown |
Het |
Hipk4 |
A |
G |
7: 27,228,834 (GRCm39) |
D428G |
probably damaging |
Het |
Hs3st1 |
T |
C |
5: 39,772,145 (GRCm39) |
Y166C |
probably damaging |
Het |
Hsd17b3 |
A |
G |
13: 64,206,459 (GRCm39) |
F281S |
possibly damaging |
Het |
Ifih1 |
T |
C |
2: 62,475,950 (GRCm39) |
T109A |
probably benign |
Het |
Ighv1-64 |
T |
A |
12: 115,471,645 (GRCm39) |
|
probably benign |
Het |
Ina |
T |
C |
19: 47,003,816 (GRCm39) |
L208P |
|
Het |
Iqcn |
C |
T |
8: 71,161,794 (GRCm39) |
T329I |
possibly damaging |
Het |
Irak2 |
T |
C |
6: 113,615,604 (GRCm39) |
|
probably null |
Het |
Klhl10 |
G |
A |
11: 100,338,481 (GRCm39) |
E407K |
probably benign |
Het |
Krt81 |
A |
G |
15: 101,361,335 (GRCm39) |
S82P |
probably damaging |
Het |
Ktn1 |
C |
A |
14: 47,948,353 (GRCm39) |
Q963K |
probably benign |
Het |
Lgalsl2 |
G |
A |
7: 5,362,527 (GRCm39) |
V53I |
possibly damaging |
Het |
Lrrc42 |
A |
T |
4: 107,104,913 (GRCm39) |
Y17* |
probably null |
Het |
Lrrc9 |
A |
C |
12: 72,496,171 (GRCm39) |
E15D |
probably damaging |
Het |
Mak |
G |
A |
13: 41,202,839 (GRCm39) |
T203I |
probably benign |
Het |
Masp2 |
T |
C |
4: 148,692,485 (GRCm39) |
V326A |
possibly damaging |
Het |
Mdc1 |
T |
C |
17: 36,164,258 (GRCm39) |
S1269P |
probably benign |
Het |
Mink1 |
G |
A |
11: 70,502,477 (GRCm39) |
V1027M |
probably damaging |
Het |
Mrps10 |
C |
A |
17: 47,686,903 (GRCm39) |
S123* |
probably null |
Het |
Myl10 |
C |
T |
5: 136,729,787 (GRCm39) |
H142Y |
probably damaging |
Het |
Ncan |
T |
C |
8: 70,560,648 (GRCm39) |
Q773R |
possibly damaging |
Het |
Nlrp3 |
T |
A |
11: 59,434,141 (GRCm39) |
M68K |
probably damaging |
Het |
Ntrk1 |
C |
T |
3: 87,698,745 (GRCm39) |
V99M |
possibly damaging |
Het |
Odad3 |
T |
C |
9: 21,903,207 (GRCm39) |
E402G |
probably damaging |
Het |
Or4p22 |
C |
T |
2: 88,317,787 (GRCm39) |
T237I |
probably damaging |
Het |
Or5an1 |
A |
G |
19: 12,260,939 (GRCm39) |
R176G |
probably benign |
Het |
Or8c8 |
A |
G |
9: 38,164,962 (GRCm39) |
K80R |
probably benign |
Het |
Phldb2 |
A |
G |
16: 45,595,437 (GRCm39) |
V830A |
probably damaging |
Het |
Phospho2 |
T |
C |
2: 69,625,913 (GRCm39) |
V23A |
probably damaging |
Het |
Plxnc1 |
G |
A |
10: 94,780,685 (GRCm39) |
|
probably benign |
Het |
Ppcdc |
T |
C |
9: 57,342,280 (GRCm39) |
E14G |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,302,645 (GRCm39) |
Y106C |
probably damaging |
Het |
Rgs22 |
T |
C |
15: 36,087,544 (GRCm39) |
Q582R |
probably benign |
Het |
Rngtt |
T |
A |
4: 33,320,613 (GRCm39) |
Y53* |
probably null |
Het |
Slc12a3 |
T |
G |
8: 95,083,028 (GRCm39) |
|
probably null |
Het |
Slc26a11 |
A |
G |
11: 119,267,730 (GRCm39) |
T456A |
probably benign |
Het |
Slc26a5 |
G |
T |
5: 22,018,334 (GRCm39) |
A677E |
possibly damaging |
Het |
Smurf1 |
T |
C |
5: 144,817,463 (GRCm39) |
T690A |
probably benign |
Het |
Spata24 |
A |
T |
18: 35,790,064 (GRCm39) |
N142K |
probably damaging |
Het |
Ubqlnl |
A |
T |
7: 103,798,962 (GRCm39) |
N178K |
possibly damaging |
Het |
Uggt2 |
A |
G |
14: 119,312,741 (GRCm39) |
|
probably null |
Het |
Vmn1r2 |
C |
A |
4: 3,172,678 (GRCm39) |
A199D |
probably damaging |
Het |
Vmn2r61 |
G |
T |
7: 41,916,619 (GRCm39) |
V411F |
probably benign |
Het |
Vmn2r-ps117 |
T |
A |
17: 19,042,911 (GRCm39) |
F106L |
probably benign |
Het |
Zfp503 |
A |
T |
14: 22,035,353 (GRCm39) |
I521N |
possibly damaging |
Het |
Zfp831 |
T |
C |
2: 174,547,113 (GRCm39) |
V1432A |
probably benign |
Het |
Zfp981 |
T |
A |
4: 146,619,884 (GRCm39) |
L13I |
possibly damaging |
Het |
|
Other mutations in Vmn2r39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02059:Vmn2r39
|
APN |
7 |
9,026,643 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03017:Vmn2r39
|
APN |
7 |
9,017,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R1314:Vmn2r39
|
UTSW |
7 |
9,017,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:Vmn2r39
|
UTSW |
7 |
9,026,687 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1480:Vmn2r39
|
UTSW |
7 |
9,017,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Vmn2r39
|
UTSW |
7 |
9,026,673 (GRCm39) |
missense |
probably benign |
0.01 |
R4120:Vmn2r39
|
UTSW |
7 |
9,026,673 (GRCm39) |
missense |
probably benign |
0.01 |
R4720:Vmn2r39
|
UTSW |
7 |
9,026,469 (GRCm39) |
critical splice donor site |
probably null |
|
R4990:Vmn2r39
|
UTSW |
7 |
9,026,675 (GRCm39) |
missense |
probably benign |
|
R5079:Vmn2r39
|
UTSW |
7 |
9,026,489 (GRCm39) |
missense |
probably benign |
0.05 |
R5695:Vmn2r39
|
UTSW |
7 |
9,028,150 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6131:Vmn2r39
|
UTSW |
7 |
9,017,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R6561:Vmn2r39
|
UTSW |
7 |
9,018,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R7108:Vmn2r39
|
UTSW |
7 |
9,026,667 (GRCm39) |
missense |
probably damaging |
0.96 |
R7122:Vmn2r39
|
UTSW |
7 |
9,017,761 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8793:Vmn2r39
|
UTSW |
7 |
9,028,149 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r39
|
UTSW |
7 |
9,018,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|