Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921528I07Rik |
A |
T |
9: 114,133,779 (GRCm39) |
|
noncoding transcript |
Het |
6430548M08Rik |
T |
C |
8: 120,887,153 (GRCm39) |
|
probably null |
Het |
Abca4 |
G |
A |
3: 121,948,948 (GRCm39) |
G531E |
possibly damaging |
Het |
Acad8 |
A |
G |
9: 26,901,923 (GRCm39) |
L147P |
probably damaging |
Het |
Acot10 |
T |
C |
15: 20,666,028 (GRCm39) |
S238G |
probably benign |
Het |
Adamtsl2 |
A |
T |
2: 26,985,487 (GRCm39) |
H457L |
probably benign |
Het |
Ankrd35 |
A |
T |
3: 96,586,524 (GRCm39) |
T67S |
probably damaging |
Het |
Aox1 |
T |
G |
1: 58,373,853 (GRCm39) |
I838S |
possibly damaging |
Het |
Arnt2 |
T |
C |
7: 83,924,594 (GRCm39) |
N411S |
probably damaging |
Het |
Bmpr2 |
T |
C |
1: 59,906,875 (GRCm39) |
L656S |
probably damaging |
Het |
Carns1 |
A |
T |
19: 4,215,475 (GRCm39) |
Y902* |
probably null |
Het |
Cavin1 |
T |
C |
11: 100,849,622 (GRCm39) |
E336G |
probably damaging |
Het |
Cbl |
A |
T |
9: 44,065,145 (GRCm39) |
C728S |
probably benign |
Het |
Ccdc136 |
C |
A |
6: 29,411,280 (GRCm39) |
Q218K |
probably damaging |
Het |
Cdk19 |
C |
A |
10: 40,342,706 (GRCm39) |
T196K |
probably damaging |
Het |
Ceacam20 |
T |
C |
7: 19,719,952 (GRCm39) |
Y495H |
probably damaging |
Het |
Celf2 |
T |
C |
2: 6,726,339 (GRCm39) |
I47V |
probably benign |
Het |
Ces3a |
A |
C |
8: 105,780,055 (GRCm39) |
K299T |
probably damaging |
Het |
Cfap61 |
A |
T |
2: 145,985,056 (GRCm39) |
I967F |
probably damaging |
Het |
Cnksr1 |
C |
T |
4: 133,960,282 (GRCm39) |
|
probably benign |
Het |
Cped1 |
T |
C |
6: 22,237,652 (GRCm39) |
Y923H |
probably benign |
Het |
Crip3 |
T |
C |
17: 46,740,290 (GRCm39) |
L30P |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 16,073,905 (GRCm39) |
I2030T |
possibly damaging |
Het |
Ctse |
C |
A |
1: 131,590,487 (GRCm39) |
P70T |
probably damaging |
Het |
Cyp2b23 |
A |
G |
7: 26,372,159 (GRCm39) |
F429L |
probably damaging |
Het |
Cyp2c66 |
T |
A |
19: 39,165,100 (GRCm39) |
D360E |
probably damaging |
Het |
D8Ertd738e |
A |
T |
8: 84,976,110 (GRCm39) |
L46* |
probably null |
Het |
Dcp2 |
T |
A |
18: 44,548,429 (GRCm39) |
|
probably null |
Het |
Ddx10 |
C |
A |
9: 53,010,513 (GRCm39) |
D834Y |
possibly damaging |
Het |
Ddx19a |
A |
T |
8: 111,705,716 (GRCm39) |
V245E |
probably damaging |
Het |
Dpf2 |
A |
C |
19: 5,954,515 (GRCm39) |
D130E |
probably benign |
Het |
Emc8 |
A |
T |
8: 121,394,518 (GRCm39) |
M67K |
probably damaging |
Het |
Ephb6 |
T |
C |
6: 41,591,536 (GRCm39) |
L231P |
possibly damaging |
Het |
Erp27 |
T |
C |
6: 136,885,150 (GRCm39) |
E216G |
possibly damaging |
Het |
Esco1 |
A |
T |
18: 10,594,734 (GRCm39) |
I184N |
possibly damaging |
Het |
Fdxacb1 |
T |
A |
9: 50,681,560 (GRCm39) |
D11E |
possibly damaging |
Het |
Fhod3 |
C |
T |
18: 25,199,395 (GRCm39) |
P689S |
probably benign |
Het |
Fnip1 |
T |
A |
11: 54,394,385 (GRCm39) |
S940R |
probably damaging |
Het |
Ganc |
G |
T |
2: 120,261,548 (GRCm39) |
V343F |
probably benign |
Het |
Gldn |
T |
A |
9: 54,239,302 (GRCm39) |
L228* |
probably null |
Het |
Gm1123 |
C |
T |
9: 98,891,426 (GRCm39) |
R341H |
probably damaging |
Het |
Gtf2f2 |
T |
C |
14: 76,155,078 (GRCm39) |
Y161C |
probably benign |
Het |
Gtf3c1 |
T |
C |
7: 125,266,510 (GRCm39) |
T979A |
probably damaging |
Het |
H4c1 |
A |
G |
13: 23,944,959 (GRCm39) |
V61A |
probably benign |
Het |
Hmcn2 |
G |
T |
2: 31,325,804 (GRCm39) |
R4277L |
probably benign |
Het |
Hsd17b6 |
T |
A |
10: 127,830,295 (GRCm39) |
|
probably null |
Het |
Igkv12-46 |
T |
C |
6: 69,741,781 (GRCm39) |
T25A |
probably damaging |
Het |
Inpp5e |
G |
A |
2: 26,291,006 (GRCm39) |
R354C |
probably damaging |
Het |
Jcad |
T |
A |
18: 4,680,221 (GRCm39) |
|
probably null |
Het |
Kcna10 |
G |
T |
3: 107,102,010 (GRCm39) |
A214S |
possibly damaging |
Het |
Kit |
T |
C |
5: 75,801,880 (GRCm39) |
|
probably null |
Het |
Kmt2a |
G |
A |
9: 44,735,869 (GRCm39) |
|
probably benign |
Het |
Lama1 |
T |
C |
17: 68,059,429 (GRCm39) |
V604A |
probably benign |
Het |
Mesd |
T |
C |
7: 83,544,964 (GRCm39) |
V138A |
probably damaging |
Het |
Mmp13 |
T |
C |
9: 7,272,580 (GRCm39) |
F9S |
possibly damaging |
Het |
Mocos |
T |
C |
18: 24,799,491 (GRCm39) |
Y242H |
probably benign |
Het |
Mrc1 |
A |
C |
2: 14,298,297 (GRCm39) |
T718P |
probably damaging |
Het |
Msh6 |
T |
C |
17: 88,292,234 (GRCm39) |
S330P |
possibly damaging |
Het |
Myh10 |
A |
G |
11: 68,695,468 (GRCm39) |
K1532E |
probably damaging |
Het |
Nat9 |
T |
C |
11: 115,075,368 (GRCm39) |
N91S |
probably damaging |
Het |
Neto2 |
A |
T |
8: 86,367,691 (GRCm39) |
I351N |
probably damaging |
Het |
Nfx1 |
A |
G |
4: 40,976,367 (GRCm39) |
N14D |
possibly damaging |
Het |
Nlrp4b |
A |
G |
7: 10,448,660 (GRCm39) |
T288A |
possibly damaging |
Het |
Nutm2 |
C |
A |
13: 50,627,033 (GRCm39) |
T396K |
probably benign |
Het |
Ogdhl |
A |
G |
14: 32,054,493 (GRCm39) |
T196A |
probably benign |
Het |
Omg |
T |
A |
11: 79,393,249 (GRCm39) |
N203I |
probably damaging |
Het |
Or52b4i |
A |
G |
7: 102,191,811 (GRCm39) |
I223V |
possibly damaging |
Het |
Or52r1b |
A |
T |
7: 102,691,058 (GRCm39) |
D119V |
probably benign |
Het |
Or5b101 |
A |
T |
19: 13,005,445 (GRCm39) |
F83I |
probably benign |
Het |
Pdgfrb |
A |
G |
18: 61,197,185 (GRCm39) |
Y207C |
probably damaging |
Het |
Pdzd7 |
T |
A |
19: 45,034,126 (GRCm39) |
|
probably benign |
Het |
Pgs1 |
C |
A |
11: 117,894,333 (GRCm39) |
H157N |
probably damaging |
Het |
Pik3c2a |
A |
G |
7: 115,957,923 (GRCm39) |
V1121A |
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,289,432 (GRCm39) |
C1235S |
probably damaging |
Het |
Pms1 |
G |
A |
1: 53,228,633 (GRCm39) |
Q872* |
probably null |
Het |
Ptgs2 |
A |
G |
1: 149,976,835 (GRCm39) |
T23A |
probably benign |
Het |
Rgl1 |
T |
G |
1: 152,397,122 (GRCm39) |
R716S |
probably damaging |
Het |
Rif1 |
A |
G |
2: 52,001,964 (GRCm39) |
E1806G |
probably benign |
Het |
Ripor1 |
T |
C |
8: 106,341,284 (GRCm39) |
V39A |
probably benign |
Het |
Ryr2 |
G |
T |
13: 11,608,003 (GRCm39) |
T868N |
probably benign |
Het |
Sec22b |
A |
T |
3: 97,828,438 (GRCm39) |
D167V |
probably damaging |
Het |
Sec24d |
T |
C |
3: 123,149,423 (GRCm39) |
V810A |
probably damaging |
Het |
Shh |
T |
C |
5: 28,662,853 (GRCm39) |
*438W |
probably null |
Het |
Slc25a12 |
G |
A |
2: 71,145,406 (GRCm39) |
S178L |
probably benign |
Het |
Sorl1 |
A |
T |
9: 41,895,804 (GRCm39) |
W1784R |
probably damaging |
Het |
Sp3 |
A |
T |
2: 72,801,325 (GRCm39) |
S229R |
probably damaging |
Het |
Spata31f3 |
A |
G |
4: 42,871,608 (GRCm39) |
F256L |
probably benign |
Het |
Spdye4c |
G |
A |
2: 128,434,273 (GRCm39) |
V5I |
possibly damaging |
Het |
Spint2 |
A |
T |
7: 28,959,804 (GRCm39) |
V53D |
probably damaging |
Het |
Stard3nl |
T |
A |
13: 19,560,689 (GRCm39) |
N29Y |
probably damaging |
Het |
Stk25 |
A |
G |
1: 93,553,205 (GRCm39) |
S299P |
probably damaging |
Het |
Sult2a3 |
A |
G |
7: 13,856,786 (GRCm39) |
S45P |
probably damaging |
Het |
Thsd7a |
A |
T |
6: 12,408,967 (GRCm39) |
V685E |
probably damaging |
Het |
Tm9sf4 |
T |
A |
2: 153,029,228 (GRCm39) |
V92D |
probably damaging |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Topors |
G |
A |
4: 40,262,669 (GRCm39) |
T205I |
probably damaging |
Het |
Tpo |
T |
A |
12: 30,153,289 (GRCm39) |
Y355F |
probably benign |
Het |
Uba1y |
T |
A |
Y: 826,032 (GRCm39) |
M396K |
possibly damaging |
Het |
Vmn1r50 |
A |
T |
6: 90,084,513 (GRCm39) |
Q86L |
probably benign |
Het |
Vmn2r114 |
A |
C |
17: 23,529,447 (GRCm39) |
N218K |
possibly damaging |
Het |
Vmn2r66 |
T |
A |
7: 84,643,905 (GRCm39) |
N835I |
probably damaging |
Het |
Vps54 |
T |
G |
11: 21,249,989 (GRCm39) |
N458K |
probably benign |
Het |
Zcchc7 |
G |
T |
4: 44,895,964 (GRCm39) |
C304F |
probably damaging |
Het |
Zfp335 |
A |
T |
2: 164,742,206 (GRCm39) |
C593S |
probably damaging |
Het |
Zmynd15 |
C |
G |
11: 70,353,414 (GRCm39) |
P214R |
probably damaging |
Het |
|
Other mutations in Vmn1r77 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Vmn1r77
|
APN |
7 |
11,775,223 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00990:Vmn1r77
|
APN |
7 |
11,775,695 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00990:Vmn1r77
|
APN |
7 |
11,775,403 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01304:Vmn1r77
|
APN |
7 |
11,775,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01360:Vmn1r77
|
APN |
7 |
11,775,315 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01714:Vmn1r77
|
APN |
7 |
11,775,277 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01829:Vmn1r77
|
APN |
7 |
11,775,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02336:Vmn1r77
|
APN |
7 |
11,775,223 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0456:Vmn1r77
|
UTSW |
7 |
11,775,665 (GRCm39) |
nonsense |
probably null |
|
R0622:Vmn1r77
|
UTSW |
7 |
11,775,315 (GRCm39) |
missense |
probably benign |
0.06 |
R1244:Vmn1r77
|
UTSW |
7 |
11,775,847 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1696:Vmn1r77
|
UTSW |
7 |
11,775,547 (GRCm39) |
nonsense |
probably null |
|
R1836:Vmn1r77
|
UTSW |
7 |
11,775,338 (GRCm39) |
missense |
probably benign |
0.00 |
R1898:Vmn1r77
|
UTSW |
7 |
11,775,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R4533:Vmn1r77
|
UTSW |
7 |
11,775,756 (GRCm39) |
missense |
probably benign |
0.02 |
R5381:Vmn1r77
|
UTSW |
7 |
11,775,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R6290:Vmn1r77
|
UTSW |
7 |
11,775,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R6675:Vmn1r77
|
UTSW |
7 |
11,775,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R7032:Vmn1r77
|
UTSW |
7 |
11,776,017 (GRCm39) |
nonsense |
probably null |
|
R7044:Vmn1r77
|
UTSW |
7 |
11,775,761 (GRCm39) |
missense |
probably benign |
0.06 |
R7302:Vmn1r77
|
UTSW |
7 |
11,775,983 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7417:Vmn1r77
|
UTSW |
7 |
11,775,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7436:Vmn1r77
|
UTSW |
7 |
11,775,694 (GRCm39) |
missense |
probably benign |
0.01 |
R8487:Vmn1r77
|
UTSW |
7 |
11,775,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8862:Vmn1r77
|
UTSW |
7 |
11,776,060 (GRCm39) |
missense |
probably benign |
0.19 |
R9614:Vmn1r77
|
UTSW |
7 |
11,775,766 (GRCm39) |
missense |
probably benign |
0.43 |
R9753:Vmn1r77
|
UTSW |
7 |
11,775,659 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn1r77
|
UTSW |
7 |
11,775,695 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Vmn1r77
|
UTSW |
7 |
11,775,674 (GRCm39) |
missense |
|
|
Z1176:Vmn1r77
|
UTSW |
7 |
11,775,524 (GRCm39) |
missense |
probably benign |
0.36 |
Z1176:Vmn1r77
|
UTSW |
7 |
11,775,508 (GRCm39) |
missense |
|
|
Z1177:Vmn1r77
|
UTSW |
7 |
11,775,695 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Vmn1r77
|
UTSW |
7 |
11,775,674 (GRCm39) |
missense |
|
|
Z1177:Vmn1r77
|
UTSW |
7 |
11,775,524 (GRCm39) |
missense |
probably benign |
0.36 |
|