Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
C |
6: 128,535,655 (GRCm39) |
|
probably null |
Het |
Birc6 |
C |
A |
17: 74,969,774 (GRCm39) |
H383Q |
probably damaging |
Het |
C2 |
C |
A |
17: 35,083,079 (GRCm39) |
A431S |
probably benign |
Het |
C3ar1 |
C |
T |
6: 122,827,105 (GRCm39) |
V371M |
probably damaging |
Het |
Chd1l |
G |
A |
3: 97,494,483 (GRCm39) |
A399V |
probably damaging |
Het |
Ckap2l |
A |
G |
2: 129,127,414 (GRCm39) |
S255P |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,436,558 (GRCm39) |
I842F |
probably benign |
Het |
Cmc2 |
G |
T |
8: 117,620,896 (GRCm39) |
H28Q |
probably damaging |
Het |
Col11a2 |
C |
T |
17: 34,262,291 (GRCm39) |
P176L |
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,744,783 (GRCm39) |
D1404G |
probably damaging |
Het |
Dld |
G |
A |
12: 31,382,190 (GRCm39) |
P506S |
probably benign |
Het |
Dsg3 |
T |
C |
18: 20,672,927 (GRCm39) |
M866T |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,375 (GRCm39) |
I451T |
possibly damaging |
Het |
Fosb |
T |
C |
7: 19,041,152 (GRCm39) |
T114A |
probably benign |
Het |
Foxd4 |
T |
A |
19: 24,878,198 (GRCm39) |
M1L |
possibly damaging |
Het |
Fstl5 |
T |
A |
3: 76,615,108 (GRCm39) |
I723N |
probably benign |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Hdlbp |
A |
G |
1: 93,357,186 (GRCm39) |
S299P |
possibly damaging |
Het |
Mast4 |
G |
A |
13: 102,897,890 (GRCm39) |
R650C |
probably damaging |
Het |
Micu3 |
A |
G |
8: 40,819,238 (GRCm39) |
T306A |
probably benign |
Het |
Mylk2 |
A |
G |
2: 152,755,613 (GRCm39) |
Q259R |
possibly damaging |
Het |
Nfkbiz |
T |
C |
16: 55,642,325 (GRCm39) |
N31S |
probably damaging |
Het |
Nisch |
A |
T |
14: 30,893,444 (GRCm39) |
|
probably benign |
Het |
Nudt17 |
T |
C |
3: 96,615,080 (GRCm39) |
|
probably benign |
Het |
Oprm1 |
A |
C |
10: 6,780,063 (GRCm39) |
I242L |
probably damaging |
Het |
Or13a26 |
T |
C |
7: 140,284,616 (GRCm39) |
W151R |
probably damaging |
Het |
Or14c39 |
T |
C |
7: 86,343,760 (GRCm39) |
V32A |
probably benign |
Het |
Or2y1d |
A |
C |
11: 49,321,828 (GRCm39) |
H175P |
probably damaging |
Het |
Otud6b |
A |
G |
4: 14,826,496 (GRCm39) |
|
probably benign |
Het |
Pamr1 |
A |
T |
2: 102,472,519 (GRCm39) |
D606V |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,308,817 (GRCm39) |
|
probably benign |
Het |
Pom121l2 |
T |
C |
13: 22,166,502 (GRCm39) |
S258P |
probably damaging |
Het |
Rcsd1 |
T |
A |
1: 165,483,403 (GRCm39) |
D196V |
possibly damaging |
Het |
Sbf2 |
C |
T |
7: 110,040,759 (GRCm39) |
R356Q |
probably damaging |
Het |
Serpinf1 |
A |
G |
11: 75,304,731 (GRCm39) |
|
probably null |
Het |
Slc22a30 |
T |
G |
19: 8,313,086 (GRCm39) |
|
probably benign |
Het |
Strn4 |
G |
T |
7: 16,550,384 (GRCm39) |
S36I |
probably benign |
Het |
Taar6 |
A |
G |
10: 23,861,177 (GRCm39) |
L123P |
probably damaging |
Het |
Thbs1 |
G |
T |
2: 117,943,137 (GRCm39) |
R5L |
unknown |
Het |
Timp3 |
T |
C |
10: 86,181,650 (GRCm39) |
Y174H |
probably benign |
Het |
Trpm2 |
C |
T |
10: 77,768,061 (GRCm39) |
V813M |
probably damaging |
Het |
Uox |
C |
T |
3: 146,330,332 (GRCm39) |
R163* |
probably null |
Het |
Vcan |
A |
T |
13: 89,852,951 (GRCm39) |
S670T |
probably damaging |
Het |
|
Other mutations in Vmn1r65 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01636:Vmn1r65
|
APN |
7 |
6,011,720 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02821:Vmn1r65
|
APN |
7 |
6,011,893 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0991:Vmn1r65
|
UTSW |
7 |
6,012,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R1457:Vmn1r65
|
UTSW |
7 |
6,012,156 (GRCm39) |
missense |
probably benign |
0.10 |
R1507:Vmn1r65
|
UTSW |
7 |
6,012,108 (GRCm39) |
missense |
probably benign |
0.13 |
R1856:Vmn1r65
|
UTSW |
7 |
6,011,265 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2914:Vmn1r65
|
UTSW |
7 |
6,012,040 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5147:Vmn1r65
|
UTSW |
7 |
6,011,818 (GRCm39) |
missense |
probably benign |
0.01 |
R5279:Vmn1r65
|
UTSW |
7 |
6,011,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Vmn1r65
|
UTSW |
7 |
6,011,809 (GRCm39) |
nonsense |
probably null |
|
R5409:Vmn1r65
|
UTSW |
7 |
6,012,012 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5646:Vmn1r65
|
UTSW |
7 |
6,012,223 (GRCm39) |
missense |
probably benign |
0.01 |
R5963:Vmn1r65
|
UTSW |
7 |
6,011,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Vmn1r65
|
UTSW |
7 |
6,011,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Vmn1r65
|
UTSW |
7 |
6,011,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R7958:Vmn1r65
|
UTSW |
7 |
6,011,254 (GRCm39) |
missense |
probably benign |
0.01 |
R8121:Vmn1r65
|
UTSW |
7 |
6,011,464 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8345:Vmn1r65
|
UTSW |
7 |
6,011,256 (GRCm39) |
missense |
probably benign |
|
R8725:Vmn1r65
|
UTSW |
7 |
6,011,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Vmn1r65
|
UTSW |
7 |
6,011,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Vmn1r65
|
UTSW |
7 |
6,011,769 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9279:Vmn1r65
|
UTSW |
7 |
6,011,988 (GRCm39) |
missense |
probably benign |
0.06 |
R9778:Vmn1r65
|
UTSW |
7 |
6,011,387 (GRCm39) |
nonsense |
probably null |
|
|