Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,298,218 (GRCm38) |
I2655T |
probably damaging |
Het |
Abca13 |
G |
A |
11: 9,293,925 (GRCm38) |
M1929I |
probably benign |
Het |
Acad10 |
A |
G |
5: 121,626,205 (GRCm38) |
V887A |
possibly damaging |
Het |
Acot10 |
T |
C |
15: 20,666,172 (GRCm38) |
E161G |
possibly damaging |
Het |
Astn1 |
C |
T |
1: 158,657,100 (GRCm38) |
P919L |
probably benign |
Het |
Atp1a4 |
T |
A |
1: 172,234,494 (GRCm38) |
D688V |
probably damaging |
Het |
C4bp |
C |
A |
1: 130,636,747 (GRCm38) |
C400F |
probably damaging |
Het |
Col6a6 |
A |
C |
9: 105,774,796 (GRCm38) |
D1005E |
probably damaging |
Het |
Csnk1g3 |
C |
T |
18: 53,953,288 (GRCm38) |
R422C |
probably benign |
Het |
Cutc |
T |
C |
19: 43,753,205 (GRCm38) |
S15P |
probably benign |
Het |
Dgkb |
T |
C |
12: 38,602,838 (GRCm38) |
|
probably null |
Het |
Disc1 |
T |
C |
8: 125,232,993 (GRCm38) |
V748A |
probably benign |
Het |
Dmbt1 |
C |
G |
7: 131,082,587 (GRCm38) |
D778E |
unknown |
Het |
Dmxl2 |
T |
C |
9: 54,383,753 (GRCm38) |
Y2471C |
probably benign |
Het |
Fam185a |
T |
A |
5: 21,438,816 (GRCm38) |
N243K |
probably benign |
Het |
Fchsd2 |
A |
T |
7: 101,253,573 (GRCm38) |
Q386L |
possibly damaging |
Het |
Gm904 |
C |
A |
13: 50,643,417 (GRCm38) |
P49Q |
probably damaging |
Het |
H2-Q10 |
C |
T |
17: 35,470,477 (GRCm38) |
R59C |
probably damaging |
Het |
Ier5l |
A |
G |
2: 30,473,093 (GRCm38) |
Y307H |
possibly damaging |
Het |
Kmt2e |
C |
A |
5: 23,497,092 (GRCm38) |
T906K |
probably benign |
Het |
Kndc1 |
C |
T |
7: 139,913,518 (GRCm38) |
R467W |
probably damaging |
Het |
Muc5ac |
C |
A |
7: 141,810,476 (GRCm38) |
T2508K |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,565,006 (GRCm38) |
M784L |
probably benign |
Het |
Nlrp9b |
T |
A |
7: 20,024,012 (GRCm38) |
C391* |
probably null |
Het |
Nubp2 |
A |
C |
17: 24,884,465 (GRCm38) |
M146R |
probably damaging |
Het |
Or10q3 |
T |
A |
19: 11,871,214 (GRCm38) |
M1L |
probably damaging |
Het |
Or1a1b |
C |
T |
11: 74,206,395 (GRCm38) |
V274M |
possibly damaging |
Het |
Or2ag1b |
T |
A |
7: 106,689,669 (GRCm38) |
S21C |
probably benign |
Het |
Or2b2 |
G |
A |
13: 21,703,915 (GRCm38) |
V305M |
probably benign |
Het |
Or4k45 |
A |
T |
2: 111,565,402 (GRCm38) |
L14H |
probably damaging |
Het |
Or7e166 |
A |
T |
9: 19,713,093 (GRCm38) |
N89Y |
probably benign |
Het |
Otud1 |
T |
C |
2: 19,658,378 (GRCm38) |
V106A |
possibly damaging |
Het |
Pcdhac1 |
T |
A |
18: 37,092,400 (GRCm38) |
Y755* |
probably null |
Het |
Pkd1l3 |
C |
T |
8: 109,623,888 (GRCm38) |
P455L |
possibly damaging |
Het |
Ptprb |
GAGACCCTCGGGAGCACTGCAGAGACCCTCAGGAACACTGCAAAGACCCTCGGGAGCACTGCAGAGACCCTCAGGAACACTGCAAAGACCCTCGGGAGCACTGCAGAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACT |
GAGACCCTCGGGAGCACTGCAGAGACCCTCAGGAACACTGCAAAGACCCTCGGGAGCACTGCAGAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACT |
10: 116,283,572 (GRCm38) |
|
probably benign |
Het |
Samhd1 |
T |
C |
2: 157,099,433 (GRCm38) |
E648G |
probably benign |
Het |
Smarca5 |
T |
C |
8: 80,709,127 (GRCm38) |
T794A |
probably benign |
Het |
Spc24 |
A |
T |
9: 21,757,730 (GRCm38) |
L87H |
probably damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,866,069 (GRCm38) |
|
probably null |
Het |
Stra6l |
G |
A |
4: 45,864,905 (GRCm38) |
R77Q |
probably damaging |
Het |
Tdrd1 |
G |
A |
19: 56,848,649 (GRCm38) |
V472M |
probably benign |
Het |
Tsc2 |
A |
T |
17: 24,604,987 (GRCm38) |
I948K |
possibly damaging |
Het |
Ttc39d |
T |
C |
17: 80,216,005 (GRCm38) |
V31A |
probably benign |
Het |
Vmn1r158 |
A |
T |
7: 22,789,880 (GRCm38) |
C301* |
probably null |
Het |
Vmn2r22 |
A |
T |
6: 123,637,527 (GRCm38) |
L368* |
probably null |
Het |
Vwa1 |
T |
C |
4: 155,772,768 (GRCm38) |
H191R |
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,304,976 (GRCm38) |
V838E |
possibly damaging |
Het |
|
Other mutations in Vmn2r79 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01401:Vmn2r79
|
APN |
7 |
87,037,273 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01675:Vmn2r79
|
APN |
7 |
86,996,648 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01760:Vmn2r79
|
APN |
7 |
87,002,158 (GRCm38) |
missense |
probably benign |
|
IGL01834:Vmn2r79
|
APN |
7 |
87,037,146 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01843:Vmn2r79
|
APN |
7 |
87,037,277 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01914:Vmn2r79
|
APN |
7 |
87,037,363 (GRCm38) |
missense |
probably benign |
0.14 |
IGL01980:Vmn2r79
|
APN |
7 |
87,037,082 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL02438:Vmn2r79
|
APN |
7 |
87,002,536 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02740:Vmn2r79
|
APN |
7 |
87,004,158 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03052:Vmn2r79
|
UTSW |
7 |
87,003,591 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4445001:Vmn2r79
|
UTSW |
7 |
87,002,200 (GRCm38) |
missense |
possibly damaging |
0.46 |
R0096:Vmn2r79
|
UTSW |
7 |
87,037,319 (GRCm38) |
missense |
probably damaging |
1.00 |
R0096:Vmn2r79
|
UTSW |
7 |
87,037,319 (GRCm38) |
missense |
probably damaging |
1.00 |
R0270:Vmn2r79
|
UTSW |
7 |
87,003,386 (GRCm38) |
missense |
probably benign |
0.00 |
R0336:Vmn2r79
|
UTSW |
7 |
87,002,079 (GRCm38) |
missense |
probably benign |
0.15 |
R0418:Vmn2r79
|
UTSW |
7 |
87,002,403 (GRCm38) |
missense |
probably benign |
0.18 |
R1070:Vmn2r79
|
UTSW |
7 |
87,003,473 (GRCm38) |
missense |
probably damaging |
1.00 |
R1234:Vmn2r79
|
UTSW |
7 |
87,004,099 (GRCm38) |
missense |
possibly damaging |
0.71 |
R1459:Vmn2r79
|
UTSW |
7 |
87,037,794 (GRCm38) |
missense |
probably benign |
0.01 |
R1513:Vmn2r79
|
UTSW |
7 |
87,037,444 (GRCm38) |
missense |
probably benign |
0.01 |
R1624:Vmn2r79
|
UTSW |
7 |
87,004,039 (GRCm38) |
critical splice acceptor site |
probably null |
|
R1633:Vmn2r79
|
UTSW |
7 |
87,037,834 (GRCm38) |
missense |
possibly damaging |
0.52 |
R1676:Vmn2r79
|
UTSW |
7 |
87,002,631 (GRCm38) |
missense |
probably benign |
|
R1781:Vmn2r79
|
UTSW |
7 |
87,002,347 (GRCm38) |
missense |
probably benign |
0.00 |
R1794:Vmn2r79
|
UTSW |
7 |
87,001,413 (GRCm38) |
missense |
probably benign |
0.37 |
R1823:Vmn2r79
|
UTSW |
7 |
87,037,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R2013:Vmn2r79
|
UTSW |
7 |
87,004,081 (GRCm38) |
missense |
possibly damaging |
0.50 |
R2018:Vmn2r79
|
UTSW |
7 |
87,002,426 (GRCm38) |
missense |
probably benign |
0.07 |
R2019:Vmn2r79
|
UTSW |
7 |
87,002,426 (GRCm38) |
missense |
probably benign |
0.07 |
R2177:Vmn2r79
|
UTSW |
7 |
86,996,631 (GRCm38) |
missense |
possibly damaging |
0.94 |
R2984:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R3719:Vmn2r79
|
UTSW |
7 |
87,002,037 (GRCm38) |
missense |
probably benign |
0.05 |
R3798:Vmn2r79
|
UTSW |
7 |
87,002,194 (GRCm38) |
missense |
possibly damaging |
0.88 |
R3969:Vmn2r79
|
UTSW |
7 |
87,003,593 (GRCm38) |
missense |
probably damaging |
1.00 |
R4182:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4183:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4245:Vmn2r79
|
UTSW |
7 |
87,002,416 (GRCm38) |
missense |
possibly damaging |
0.73 |
R4301:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4391:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4393:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4394:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4396:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4397:Vmn2r79
|
UTSW |
7 |
87,001,891 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4592:Vmn2r79
|
UTSW |
7 |
87,004,111 (GRCm38) |
missense |
possibly damaging |
0.86 |
R4697:Vmn2r79
|
UTSW |
7 |
87,037,960 (GRCm38) |
missense |
probably damaging |
0.98 |
R4897:Vmn2r79
|
UTSW |
7 |
87,001,467 (GRCm38) |
missense |
probably benign |
|
R5016:Vmn2r79
|
UTSW |
7 |
87,037,340 (GRCm38) |
missense |
probably benign |
0.00 |
R5058:Vmn2r79
|
UTSW |
7 |
87,002,215 (GRCm38) |
missense |
probably damaging |
0.98 |
R5177:Vmn2r79
|
UTSW |
7 |
87,001,969 (GRCm38) |
missense |
probably damaging |
0.97 |
R6078:Vmn2r79
|
UTSW |
7 |
87,004,111 (GRCm38) |
missense |
possibly damaging |
0.86 |
R6079:Vmn2r79
|
UTSW |
7 |
87,004,111 (GRCm38) |
missense |
possibly damaging |
0.86 |
R6138:Vmn2r79
|
UTSW |
7 |
87,004,111 (GRCm38) |
missense |
possibly damaging |
0.86 |
R6257:Vmn2r79
|
UTSW |
7 |
87,002,570 (GRCm38) |
missense |
probably benign |
0.27 |
R6260:Vmn2r79
|
UTSW |
7 |
87,037,157 (GRCm38) |
missense |
probably benign |
0.00 |
R6307:Vmn2r79
|
UTSW |
7 |
87,037,768 (GRCm38) |
missense |
probably damaging |
1.00 |
R6323:Vmn2r79
|
UTSW |
7 |
87,001,314 (GRCm38) |
missense |
probably benign |
0.05 |
R6374:Vmn2r79
|
UTSW |
7 |
87,002,290 (GRCm38) |
missense |
probably benign |
0.02 |
R6530:Vmn2r79
|
UTSW |
7 |
87,002,044 (GRCm38) |
missense |
possibly damaging |
0.91 |
R6546:Vmn2r79
|
UTSW |
7 |
87,003,533 (GRCm38) |
missense |
probably benign |
0.01 |
R6682:Vmn2r79
|
UTSW |
7 |
87,004,162 (GRCm38) |
missense |
possibly damaging |
0.69 |
R6858:Vmn2r79
|
UTSW |
7 |
87,037,372 (GRCm38) |
missense |
probably benign |
|
R6965:Vmn2r79
|
UTSW |
7 |
87,001,892 (GRCm38) |
missense |
probably benign |
0.10 |
R7130:Vmn2r79
|
UTSW |
7 |
87,002,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R7156:Vmn2r79
|
UTSW |
7 |
87,037,643 (GRCm38) |
missense |
probably damaging |
0.98 |
R7604:Vmn2r79
|
UTSW |
7 |
87,003,384 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7691:Vmn2r79
|
UTSW |
7 |
87,037,903 (GRCm38) |
missense |
probably damaging |
0.96 |
R8055:Vmn2r79
|
UTSW |
7 |
87,037,333 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8070:Vmn2r79
|
UTSW |
7 |
87,002,128 (GRCm38) |
missense |
probably benign |
|
R8073:Vmn2r79
|
UTSW |
7 |
87,002,254 (GRCm38) |
missense |
probably benign |
0.00 |
R8145:Vmn2r79
|
UTSW |
7 |
87,037,654 (GRCm38) |
missense |
probably benign |
0.02 |
R8263:Vmn2r79
|
UTSW |
7 |
87,037,518 (GRCm38) |
missense |
possibly damaging |
0.89 |
R8350:Vmn2r79
|
UTSW |
7 |
87,037,533 (GRCm38) |
nonsense |
probably null |
|
R8814:Vmn2r79
|
UTSW |
7 |
87,002,506 (GRCm38) |
missense |
probably benign |
0.00 |
R8862:Vmn2r79
|
UTSW |
7 |
86,996,504 (GRCm38) |
missense |
probably benign |
0.23 |
R9146:Vmn2r79
|
UTSW |
7 |
87,001,473 (GRCm38) |
nonsense |
probably null |
|
R9276:Vmn2r79
|
UTSW |
7 |
87,037,837 (GRCm38) |
missense |
probably damaging |
1.00 |
R9361:Vmn2r79
|
UTSW |
7 |
87,003,614 (GRCm38) |
critical splice donor site |
probably null |
|
R9676:Vmn2r79
|
UTSW |
7 |
87,037,244 (GRCm38) |
missense |
probably damaging |
1.00 |
U15987:Vmn2r79
|
UTSW |
7 |
87,004,111 (GRCm38) |
missense |
possibly damaging |
0.86 |
X0054:Vmn2r79
|
UTSW |
7 |
87,004,062 (GRCm38) |
missense |
probably benign |
0.01 |
Z1088:Vmn2r79
|
UTSW |
7 |
87,002,341 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r79
|
UTSW |
7 |
87,037,169 (GRCm38) |
missense |
probably benign |
|
Z1176:Vmn2r79
|
UTSW |
7 |
87,002,318 (GRCm38) |
missense |
probably benign |
0.00 |
|