Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810037I17Rik |
G |
A |
3: 122,718,274 (GRCm39) |
A56T |
probably benign |
Het |
4930438A08Rik |
A |
T |
11: 58,178,296 (GRCm39) |
I119F |
|
Het |
Abca12 |
A |
T |
1: 71,332,599 (GRCm39) |
I1254N |
probably damaging |
Het |
Abcb11 |
G |
T |
2: 69,138,809 (GRCm39) |
Y157* |
probably null |
Het |
Adcy7 |
G |
A |
8: 89,044,675 (GRCm39) |
|
probably null |
Het |
Adnp |
A |
G |
2: 168,026,798 (GRCm39) |
Y166H |
probably damaging |
Het |
Adprhl1 |
A |
G |
8: 13,275,279 (GRCm39) |
V493A |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,611,685 (GRCm39) |
T562A |
probably benign |
Het |
Amotl1 |
T |
A |
9: 14,504,320 (GRCm39) |
N296I |
possibly damaging |
Het |
Ankar |
A |
G |
1: 72,713,210 (GRCm39) |
V693A |
probably benign |
Het |
Ankrd16 |
T |
C |
2: 11,786,318 (GRCm39) |
V189A |
probably benign |
Het |
Bmp1 |
A |
G |
14: 70,757,338 (GRCm39) |
L47P |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,248,476 (GRCm39) |
D429G |
probably benign |
Het |
Cadps2 |
T |
A |
6: 23,688,927 (GRCm39) |
E127D |
probably benign |
Het |
Cd109 |
A |
T |
9: 78,577,042 (GRCm39) |
I580F |
possibly damaging |
Het |
Cdrt4 |
T |
A |
11: 62,842,124 (GRCm39) |
I2N |
unknown |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Chuk |
A |
T |
19: 44,095,789 (GRCm39) |
W15R |
probably damaging |
Het |
Cpvl |
C |
T |
6: 53,951,779 (GRCm39) |
M1I |
probably null |
Het |
Cyfip1 |
A |
G |
7: 55,549,758 (GRCm39) |
M642V |
probably damaging |
Het |
Dhh |
T |
A |
15: 98,795,757 (GRCm39) |
R133* |
probably null |
Het |
Dnmt3b |
G |
A |
2: 153,507,980 (GRCm39) |
V212M |
probably benign |
Het |
Dync2li1 |
A |
G |
17: 84,957,137 (GRCm39) |
S301G |
probably benign |
Het |
Epas1 |
A |
C |
17: 87,133,990 (GRCm39) |
I500L |
possibly damaging |
Het |
Ephb4 |
A |
T |
5: 137,352,824 (GRCm39) |
I136F |
possibly damaging |
Het |
Foxg1 |
T |
C |
12: 49,431,320 (GRCm39) |
F18L |
unknown |
Het |
Frem1 |
T |
C |
4: 82,920,057 (GRCm39) |
E432G |
probably damaging |
Het |
Gpld1 |
A |
T |
13: 25,136,900 (GRCm39) |
S73C |
probably damaging |
Het |
Hddc3 |
A |
G |
7: 79,993,328 (GRCm39) |
I52V |
probably benign |
Het |
Hmgcll1 |
A |
T |
9: 75,991,732 (GRCm39) |
T252S |
probably damaging |
Het |
Igsf10 |
G |
A |
3: 59,243,843 (GRCm39) |
R164W |
probably damaging |
Het |
Jph2 |
A |
G |
2: 163,180,606 (GRCm39) |
V675A |
probably benign |
Het |
Kifap3 |
T |
C |
1: 163,689,666 (GRCm39) |
F550S |
probably benign |
Het |
Klk15 |
C |
T |
7: 43,587,790 (GRCm39) |
H73Y |
possibly damaging |
Het |
Kplce |
C |
T |
3: 92,775,951 (GRCm39) |
G244D |
probably benign |
Het |
L1td1 |
T |
C |
4: 98,625,932 (GRCm39) |
V643A |
possibly damaging |
Het |
L3mbtl3 |
C |
T |
10: 26,212,155 (GRCm39) |
M255I |
unknown |
Het |
Layn |
T |
A |
9: 50,968,837 (GRCm39) |
D302V |
probably damaging |
Het |
Lpcat4 |
A |
G |
2: 112,072,418 (GRCm39) |
I136V |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,382,807 (GRCm39) |
D3658V |
probably damaging |
Het |
Metap1d |
T |
C |
2: 71,352,900 (GRCm39) |
L243S |
possibly damaging |
Het |
Midn |
T |
A |
10: 79,990,275 (GRCm39) |
H315Q |
probably damaging |
Het |
Mtrex |
A |
T |
13: 113,050,888 (GRCm39) |
|
probably null |
Het |
Myb |
C |
T |
10: 21,030,612 (GRCm39) |
D62N |
probably benign |
Het |
Myh2 |
T |
C |
11: 67,077,522 (GRCm39) |
S886P |
probably benign |
Het |
Nemf |
T |
C |
12: 69,388,093 (GRCm39) |
I396V |
probably damaging |
Het |
Nemp1 |
T |
G |
10: 127,525,227 (GRCm39) |
V127G |
possibly damaging |
Het |
Nkx3-1 |
C |
T |
14: 69,428,227 (GRCm39) |
T25M |
possibly damaging |
Het |
Nmral1 |
A |
C |
16: 4,531,631 (GRCm39) |
L208R |
probably damaging |
Het |
Nol6 |
A |
T |
4: 41,116,422 (GRCm39) |
I989N |
probably benign |
Het |
Or12e7 |
T |
A |
2: 87,287,907 (GRCm39) |
C133S |
possibly damaging |
Het |
Palld |
A |
T |
8: 62,173,571 (GRCm39) |
S363T |
probably damaging |
Het |
Pcdha11 |
A |
G |
18: 37,144,512 (GRCm39) |
D201G |
probably damaging |
Het |
Per2 |
A |
G |
1: 91,366,081 (GRCm39) |
C339R |
probably damaging |
Het |
Phactr4 |
T |
C |
4: 132,097,874 (GRCm39) |
T455A |
possibly damaging |
Het |
Phc2 |
T |
C |
4: 128,617,062 (GRCm39) |
I445T |
probably damaging |
Het |
Pmepa1 |
T |
C |
2: 173,117,962 (GRCm39) |
T6A |
probably benign |
Het |
Polr1a |
T |
C |
6: 71,931,755 (GRCm39) |
F945L |
probably damaging |
Het |
Ppp2r5e |
T |
A |
12: 75,640,063 (GRCm39) |
K13* |
probably null |
Het |
Ptafr |
T |
C |
4: 132,306,613 (GRCm39) |
M1T |
probably null |
Het |
Rbms1 |
G |
A |
2: 60,610,087 (GRCm39) |
P208S |
probably benign |
Het |
Scg3 |
T |
A |
9: 75,558,955 (GRCm39) |
I419F |
probably damaging |
Het |
Scn1a |
T |
C |
2: 66,130,099 (GRCm39) |
T219A |
probably benign |
Het |
Sec14l4 |
A |
G |
11: 3,989,977 (GRCm39) |
D92G |
probably damaging |
Het |
Senp3 |
G |
T |
11: 69,569,085 (GRCm39) |
Q359K |
probably damaging |
Het |
Sirt1 |
T |
C |
10: 63,172,857 (GRCm39) |
D142G |
probably damaging |
Het |
Skint2 |
T |
C |
4: 112,483,039 (GRCm39) |
M148T |
possibly damaging |
Het |
Slc30a10 |
T |
A |
1: 185,187,391 (GRCm39) |
M44K |
probably damaging |
Het |
Snai2 |
T |
A |
16: 14,524,792 (GRCm39) |
D99E |
probably damaging |
Het |
Spg7 |
A |
G |
8: 123,807,408 (GRCm39) |
K395E |
possibly damaging |
Het |
Sphk2 |
G |
A |
7: 45,360,337 (GRCm39) |
H556Y |
possibly damaging |
Het |
Supt6 |
A |
C |
11: 78,116,612 (GRCm39) |
F637L |
probably benign |
Het |
Tcam1 |
A |
G |
11: 106,177,292 (GRCm39) |
N428S |
probably damaging |
Het |
Tctn3 |
C |
T |
19: 40,596,692 (GRCm39) |
R276K |
probably benign |
Het |
Timm29 |
G |
A |
9: 21,504,656 (GRCm39) |
R108H |
probably damaging |
Het |
Tlr9 |
A |
T |
9: 106,102,752 (GRCm39) |
E681V |
possibly damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tns3 |
T |
C |
11: 8,400,094 (GRCm39) |
K1169E |
probably damaging |
Het |
Trim72 |
A |
C |
7: 127,608,315 (GRCm39) |
D271A |
possibly damaging |
Het |
Trpv4 |
A |
T |
5: 114,772,622 (GRCm39) |
D369E |
probably benign |
Het |
Ttn |
A |
G |
2: 76,583,192 (GRCm39) |
L22567P |
probably damaging |
Het |
Uimc1 |
G |
A |
13: 55,223,652 (GRCm39) |
P207S |
probably damaging |
Het |
Unc5d |
A |
T |
8: 29,165,448 (GRCm39) |
V781E |
probably damaging |
Het |
Upk3bl |
C |
T |
5: 136,086,076 (GRCm39) |
P4L |
unknown |
Het |
Vmn1r201 |
A |
G |
13: 22,659,670 (GRCm39) |
N295D |
probably benign |
Het |
Zfyve28 |
T |
C |
5: 34,374,788 (GRCm39) |
T409A |
probably benign |
Het |
|
Other mutations in Vmn2r69 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01019:Vmn2r69
|
APN |
7 |
85,055,739 (GRCm39) |
missense |
probably benign |
|
IGL01457:Vmn2r69
|
APN |
7 |
85,055,836 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01760:Vmn2r69
|
APN |
7 |
85,056,072 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01834:Vmn2r69
|
APN |
7 |
85,061,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02001:Vmn2r69
|
APN |
7 |
85,056,434 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02057:Vmn2r69
|
APN |
7 |
85,060,990 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02289:Vmn2r69
|
APN |
7 |
85,056,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02472:Vmn2r69
|
APN |
7 |
85,058,960 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02478:Vmn2r69
|
APN |
7 |
85,055,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02554:Vmn2r69
|
APN |
7 |
85,059,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02723:Vmn2r69
|
APN |
7 |
85,059,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Vmn2r69
|
UTSW |
7 |
85,060,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R0560:Vmn2r69
|
UTSW |
7 |
85,058,922 (GRCm39) |
critical splice donor site |
probably null |
|
R0909:Vmn2r69
|
UTSW |
7 |
85,055,873 (GRCm39) |
missense |
probably benign |
0.00 |
R0976:Vmn2r69
|
UTSW |
7 |
85,056,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1158:Vmn2r69
|
UTSW |
7 |
85,059,058 (GRCm39) |
splice site |
probably benign |
|
R1459:Vmn2r69
|
UTSW |
7 |
85,055,908 (GRCm39) |
nonsense |
probably null |
|
R1482:Vmn2r69
|
UTSW |
7 |
85,056,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Vmn2r69
|
UTSW |
7 |
85,060,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R2016:Vmn2r69
|
UTSW |
7 |
85,056,493 (GRCm39) |
missense |
probably damaging |
0.98 |
R2108:Vmn2r69
|
UTSW |
7 |
85,059,404 (GRCm39) |
missense |
probably benign |
|
R2571:Vmn2r69
|
UTSW |
7 |
85,064,764 (GRCm39) |
missense |
probably benign |
|
R2910:Vmn2r69
|
UTSW |
7 |
85,055,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2920:Vmn2r69
|
UTSW |
7 |
85,060,973 (GRCm39) |
missense |
probably benign |
0.08 |
R3708:Vmn2r69
|
UTSW |
7 |
85,061,029 (GRCm39) |
missense |
probably damaging |
0.98 |
R3710:Vmn2r69
|
UTSW |
7 |
85,055,601 (GRCm39) |
missense |
probably benign |
|
R4757:Vmn2r69
|
UTSW |
7 |
85,061,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R4823:Vmn2r69
|
UTSW |
7 |
85,060,508 (GRCm39) |
missense |
probably benign |
0.21 |
R4870:Vmn2r69
|
UTSW |
7 |
85,060,793 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4918:Vmn2r69
|
UTSW |
7 |
85,055,967 (GRCm39) |
missense |
probably benign |
0.06 |
R5022:Vmn2r69
|
UTSW |
7 |
85,060,367 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5174:Vmn2r69
|
UTSW |
7 |
85,064,739 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5200:Vmn2r69
|
UTSW |
7 |
85,055,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R5278:Vmn2r69
|
UTSW |
7 |
85,060,991 (GRCm39) |
missense |
probably benign |
0.02 |
R5643:Vmn2r69
|
UTSW |
7 |
85,056,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R5996:Vmn2r69
|
UTSW |
7 |
85,061,117 (GRCm39) |
splice site |
probably null |
|
R6083:Vmn2r69
|
UTSW |
7 |
85,055,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R6140:Vmn2r69
|
UTSW |
7 |
85,060,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R6306:Vmn2r69
|
UTSW |
7 |
85,064,799 (GRCm39) |
missense |
probably benign |
0.04 |
R6330:Vmn2r69
|
UTSW |
7 |
85,060,835 (GRCm39) |
missense |
probably benign |
|
R6380:Vmn2r69
|
UTSW |
7 |
85,061,067 (GRCm39) |
missense |
probably benign |
|
R6466:Vmn2r69
|
UTSW |
7 |
85,056,378 (GRCm39) |
missense |
probably benign |
0.01 |
R6542:Vmn2r69
|
UTSW |
7 |
85,060,413 (GRCm39) |
nonsense |
probably null |
|
R6583:Vmn2r69
|
UTSW |
7 |
85,059,017 (GRCm39) |
missense |
probably benign |
|
R6623:Vmn2r69
|
UTSW |
7 |
85,056,309 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6709:Vmn2r69
|
UTSW |
7 |
85,061,069 (GRCm39) |
missense |
probably benign |
0.03 |
R6732:Vmn2r69
|
UTSW |
7 |
85,060,351 (GRCm39) |
missense |
probably benign |
0.00 |
R6741:Vmn2r69
|
UTSW |
7 |
85,061,724 (GRCm39) |
missense |
probably benign |
0.01 |
R7070:Vmn2r69
|
UTSW |
7 |
85,060,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R7234:Vmn2r69
|
UTSW |
7 |
85,056,315 (GRCm39) |
missense |
probably benign |
0.22 |
R7323:Vmn2r69
|
UTSW |
7 |
85,060,972 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7427:Vmn2r69
|
UTSW |
7 |
85,060,467 (GRCm39) |
missense |
probably benign |
0.28 |
R7428:Vmn2r69
|
UTSW |
7 |
85,060,467 (GRCm39) |
missense |
probably benign |
0.28 |
R7453:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
frame shift |
probably null |
|
R7532:Vmn2r69
|
UTSW |
7 |
85,059,622 (GRCm39) |
missense |
probably benign |
0.36 |
R7556:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
frame shift |
probably null |
|
R7562:Vmn2r69
|
UTSW |
7 |
85,056,420 (GRCm39) |
missense |
probably benign |
|
R7592:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
frame shift |
probably null |
|
R7708:Vmn2r69
|
UTSW |
7 |
85,061,755 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7803:Vmn2r69
|
UTSW |
7 |
85,056,324 (GRCm39) |
missense |
probably benign |
0.00 |
R7960:Vmn2r69
|
UTSW |
7 |
85,055,973 (GRCm39) |
missense |
probably benign |
|
R7966:Vmn2r69
|
UTSW |
7 |
85,060,762 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8071:Vmn2r69
|
UTSW |
7 |
85,055,713 (GRCm39) |
nonsense |
probably null |
|
R8237:Vmn2r69
|
UTSW |
7 |
85,060,340 (GRCm39) |
missense |
probably benign |
0.02 |
R8347:Vmn2r69
|
UTSW |
7 |
85,064,838 (GRCm39) |
missense |
probably benign |
0.00 |
R8737:Vmn2r69
|
UTSW |
7 |
85,055,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Vmn2r69
|
UTSW |
7 |
85,064,883 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R8831:Vmn2r69
|
UTSW |
7 |
85,059,018 (GRCm39) |
nonsense |
probably null |
|
R8856:Vmn2r69
|
UTSW |
7 |
85,061,663 (GRCm39) |
missense |
probably benign |
0.00 |
R8998:Vmn2r69
|
UTSW |
7 |
85,060,307 (GRCm39) |
missense |
probably benign |
0.33 |
R8999:Vmn2r69
|
UTSW |
7 |
85,060,307 (GRCm39) |
missense |
probably benign |
0.33 |
R9161:Vmn2r69
|
UTSW |
7 |
85,056,177 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9494:Vmn2r69
|
UTSW |
7 |
85,060,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R9494:Vmn2r69
|
UTSW |
7 |
85,056,084 (GRCm39) |
missense |
probably benign |
0.08 |
R9541:Vmn2r69
|
UTSW |
7 |
85,056,209 (GRCm39) |
missense |
probably benign |
|
R9620:Vmn2r69
|
UTSW |
7 |
85,061,504 (GRCm39) |
missense |
probably benign |
0.10 |
Z1176:Vmn2r69
|
UTSW |
7 |
85,055,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|