Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061I04Rik |
C |
A |
17: 36,203,820 (GRCm39) |
K291N |
probably damaging |
Het |
Adgra1 |
A |
G |
7: 139,456,102 (GRCm39) |
T577A |
probably damaging |
Het |
Akip1 |
T |
A |
7: 109,308,188 (GRCm39) |
I152N |
possibly damaging |
Het |
Armc9 |
A |
G |
1: 86,130,240 (GRCm39) |
Y8C |
probably damaging |
Het |
Atp1a4 |
A |
T |
1: 172,085,223 (GRCm39) |
V66E |
possibly damaging |
Het |
Atp2a3 |
A |
T |
11: 72,872,623 (GRCm39) |
T724S |
probably damaging |
Het |
Bmp1 |
C |
A |
14: 70,730,284 (GRCm39) |
R416L |
probably damaging |
Het |
Bmt2 |
G |
T |
6: 13,663,300 (GRCm39) |
A66E |
probably benign |
Het |
Bscl2 |
A |
T |
19: 8,825,523 (GRCm39) |
D403V |
possibly damaging |
Het |
Cbx2 |
T |
A |
11: 118,919,935 (GRCm39) |
I500N |
probably damaging |
Het |
Cd84 |
A |
T |
1: 171,700,887 (GRCm39) |
H216L |
possibly damaging |
Het |
Cdhr18 |
A |
T |
14: 13,856,724 (GRCm38) |
D462E |
probably benign |
Het |
Ceacam15 |
T |
C |
7: 16,407,410 (GRCm39) |
T36A |
probably benign |
Het |
Cebpd |
A |
G |
16: 15,705,385 (GRCm39) |
D66G |
probably damaging |
Het |
Cntnap4 |
A |
G |
8: 113,512,468 (GRCm39) |
Y610C |
probably damaging |
Het |
Col11a2 |
T |
C |
17: 34,283,267 (GRCm39) |
|
probably null |
Het |
Col17a1 |
T |
C |
19: 47,651,497 (GRCm39) |
|
probably null |
Het |
Cracr2b |
A |
G |
7: 141,043,451 (GRCm39) |
D43G |
probably damaging |
Het |
Dgkz |
T |
A |
2: 91,768,691 (GRCm39) |
K697* |
probably null |
Het |
Dnah7b |
T |
A |
1: 46,256,317 (GRCm39) |
D1873E |
possibly damaging |
Het |
Dst |
G |
A |
1: 34,314,784 (GRCm39) |
E6472K |
possibly damaging |
Het |
Duox2 |
T |
C |
2: 122,111,414 (GRCm39) |
D1428G |
probably damaging |
Het |
Elmod2 |
T |
C |
8: 84,043,537 (GRCm39) |
N210S |
probably damaging |
Het |
Ephx1 |
A |
G |
1: 180,822,256 (GRCm39) |
F220S |
probably damaging |
Het |
F13b |
A |
G |
1: 139,429,542 (GRCm39) |
Y20C |
unknown |
Het |
Fbn2 |
T |
A |
18: 58,173,265 (GRCm39) |
N2051I |
possibly damaging |
Het |
Gabrg2 |
G |
A |
11: 41,859,650 (GRCm39) |
H201Y |
probably damaging |
Het |
Gbgt1 |
T |
C |
2: 28,388,453 (GRCm39) |
F46S |
possibly damaging |
Het |
Gjd4 |
A |
G |
18: 9,280,578 (GRCm39) |
S167P |
probably damaging |
Het |
Heatr5a |
T |
C |
12: 51,924,130 (GRCm39) |
N2028D |
probably benign |
Het |
Heca |
T |
C |
10: 17,791,057 (GRCm39) |
H333R |
probably benign |
Het |
Herc1 |
T |
C |
9: 66,298,740 (GRCm39) |
S625P |
probably damaging |
Het |
Ighv1-55 |
T |
C |
12: 115,172,175 (GRCm39) |
|
probably benign |
Het |
Ighv5-8 |
G |
A |
12: 113,618,777 (GRCm39) |
S64N |
probably benign |
Het |
Itga1 |
G |
T |
13: 115,138,227 (GRCm39) |
|
probably null |
Het |
Kif21a |
C |
A |
15: 90,824,748 (GRCm39) |
R1342L |
possibly damaging |
Het |
Ksr1 |
G |
A |
11: 78,965,186 (GRCm39) |
P118S |
possibly damaging |
Het |
Lat2 |
T |
C |
5: 134,634,911 (GRCm39) |
N100S |
probably damaging |
Het |
Lrit3 |
T |
A |
3: 129,582,121 (GRCm39) |
D501V |
probably damaging |
Het |
Lrrfip1 |
T |
A |
1: 91,031,042 (GRCm39) |
|
probably null |
Het |
Lyst |
G |
A |
13: 13,809,968 (GRCm39) |
R546H |
probably damaging |
Het |
Med21 |
T |
A |
6: 146,551,691 (GRCm39) |
L114H |
probably damaging |
Het |
Mfap4 |
A |
T |
11: 61,376,336 (GRCm39) |
|
probably benign |
Het |
Mpdz |
G |
A |
4: 81,302,049 (GRCm39) |
R233W |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Ncapd3 |
T |
C |
9: 27,006,038 (GRCm39) |
|
probably benign |
Het |
Neto2 |
T |
G |
8: 86,396,333 (GRCm39) |
H104P |
probably damaging |
Het |
Nr1h2 |
T |
C |
7: 44,201,979 (GRCm39) |
T36A |
possibly damaging |
Het |
Nudt16l2 |
T |
C |
9: 105,021,647 (GRCm39) |
D133G |
probably benign |
Het |
Or13a20 |
A |
T |
7: 140,232,074 (GRCm39) |
M61L |
probably damaging |
Het |
Or4a79 |
T |
C |
2: 89,551,838 (GRCm39) |
I206V |
probably benign |
Het |
Or51ab3 |
T |
G |
7: 103,201,183 (GRCm39) |
L64V |
probably damaging |
Het |
Or51g2 |
A |
G |
7: 102,623,013 (GRCm39) |
M62T |
probably damaging |
Het |
Or52p1 |
T |
A |
7: 104,267,631 (GRCm39) |
C248* |
probably null |
Het |
Or5p52 |
A |
G |
7: 107,502,567 (GRCm39) |
I214M |
probably damaging |
Het |
Or5p72 |
T |
C |
7: 108,022,309 (GRCm39) |
V177A |
possibly damaging |
Het |
Or8b4 |
T |
C |
9: 37,830,882 (GRCm39) |
*310R |
probably null |
Het |
Pcbp3 |
A |
G |
10: 76,606,869 (GRCm39) |
L241S |
possibly damaging |
Het |
Pcf11 |
G |
A |
7: 92,308,985 (GRCm39) |
|
probably benign |
Het |
Podxl |
G |
A |
6: 31,503,579 (GRCm39) |
T254M |
possibly damaging |
Het |
Prr27 |
A |
C |
5: 87,991,100 (GRCm39) |
E237D |
possibly damaging |
Het |
Rdh16 |
G |
T |
10: 127,637,316 (GRCm39) |
V84F |
probably damaging |
Het |
Rnf26 |
A |
T |
9: 44,023,428 (GRCm39) |
D273E |
probably benign |
Het |
Rpl13a |
A |
T |
7: 44,776,242 (GRCm39) |
|
probably benign |
Het |
Rpl3l |
A |
G |
17: 24,952,584 (GRCm39) |
K239E |
probably benign |
Het |
Rsf1 |
A |
AGGGCGACGG |
7: 97,229,111 (GRCm39) |
|
probably null |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Ryk |
A |
G |
9: 102,768,415 (GRCm39) |
D352G |
possibly damaging |
Het |
Setd1b |
T |
A |
5: 123,299,061 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
G |
A |
7: 126,070,618 (GRCm39) |
A361V |
possibly damaging |
Het |
Slc35f3 |
A |
T |
8: 127,047,935 (GRCm39) |
K92* |
probably null |
Het |
Slc39a10 |
A |
G |
1: 46,857,144 (GRCm39) |
|
probably benign |
Het |
Slc47a1 |
G |
A |
11: 61,253,857 (GRCm39) |
T194I |
probably benign |
Het |
Slc6a3 |
C |
A |
13: 73,692,936 (GRCm39) |
N185K |
probably damaging |
Het |
Stag1 |
T |
C |
9: 100,730,758 (GRCm39) |
V391A |
probably damaging |
Het |
Syne2 |
A |
C |
12: 75,996,075 (GRCm39) |
N2206T |
probably damaging |
Het |
Tbc1d23 |
C |
A |
16: 57,003,325 (GRCm39) |
R481I |
possibly damaging |
Het |
Tcstv7b |
T |
C |
13: 120,702,362 (GRCm39) |
W53R |
probably damaging |
Het |
Tfam |
A |
G |
10: 71,069,225 (GRCm39) |
S166P |
probably benign |
Het |
Tmem63a |
A |
G |
1: 180,784,056 (GRCm39) |
H212R |
probably benign |
Het |
Txndc11 |
T |
A |
16: 10,902,745 (GRCm39) |
Q634L |
possibly damaging |
Het |
Usp31 |
T |
C |
7: 121,306,548 (GRCm39) |
|
probably benign |
Het |
Vmn2r17 |
A |
T |
5: 109,575,049 (GRCm39) |
T119S |
probably benign |
Het |
Vsig1 |
A |
G |
X: 139,833,861 (GRCm39) |
D227G |
probably damaging |
Het |
Zfhx2 |
G |
A |
14: 55,304,678 (GRCm39) |
P1102L |
probably benign |
Het |
Zfp715 |
T |
C |
7: 42,949,444 (GRCm39) |
Q172R |
probably benign |
Het |
Zfp872 |
A |
G |
9: 22,108,701 (GRCm39) |
D53G |
probably damaging |
Het |
Zswim8 |
G |
A |
14: 20,764,681 (GRCm39) |
D684N |
probably benign |
Het |
|
Other mutations in Vmn1r204 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00819:Vmn1r204
|
APN |
13 |
22,741,117 (GRCm39) |
nonsense |
probably null |
|
IGL01349:Vmn1r204
|
APN |
13 |
22,740,504 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02653:Vmn1r204
|
APN |
13 |
22,740,800 (GRCm39) |
missense |
probably benign |
0.34 |
R0029:Vmn1r204
|
UTSW |
13 |
22,740,588 (GRCm39) |
missense |
probably benign |
0.12 |
R0078:Vmn1r204
|
UTSW |
13 |
22,740,379 (GRCm39) |
missense |
probably benign |
0.01 |
R0562:Vmn1r204
|
UTSW |
13 |
22,740,848 (GRCm39) |
missense |
probably benign |
0.00 |
R1124:Vmn1r204
|
UTSW |
13 |
22,741,209 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1521:Vmn1r204
|
UTSW |
13 |
22,741,248 (GRCm39) |
missense |
probably benign |
0.30 |
R1544:Vmn1r204
|
UTSW |
13 |
22,740,465 (GRCm39) |
missense |
probably benign |
0.13 |
R2238:Vmn1r204
|
UTSW |
13 |
22,740,993 (GRCm39) |
missense |
probably benign |
0.01 |
R2418:Vmn1r204
|
UTSW |
13 |
22,740,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2419:Vmn1r204
|
UTSW |
13 |
22,740,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Vmn1r204
|
UTSW |
13 |
22,741,014 (GRCm39) |
missense |
probably benign |
0.02 |
R4782:Vmn1r204
|
UTSW |
13 |
22,740,867 (GRCm39) |
missense |
probably benign |
0.03 |
R4985:Vmn1r204
|
UTSW |
13 |
22,741,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:Vmn1r204
|
UTSW |
13 |
22,741,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Vmn1r204
|
UTSW |
13 |
22,740,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6652:Vmn1r204
|
UTSW |
13 |
22,740,573 (GRCm39) |
missense |
probably damaging |
0.99 |
R6943:Vmn1r204
|
UTSW |
13 |
22,740,474 (GRCm39) |
missense |
probably benign |
0.00 |
R7264:Vmn1r204
|
UTSW |
13 |
22,741,167 (GRCm39) |
missense |
probably benign |
0.23 |
R7299:Vmn1r204
|
UTSW |
13 |
22,740,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R7301:Vmn1r204
|
UTSW |
13 |
22,740,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Vmn1r204
|
UTSW |
13 |
22,740,754 (GRCm39) |
nonsense |
probably null |
|
R7872:Vmn1r204
|
UTSW |
13 |
22,740,404 (GRCm39) |
missense |
probably benign |
0.00 |
R8495:Vmn1r204
|
UTSW |
13 |
22,740,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R9110:Vmn1r204
|
UTSW |
13 |
22,740,564 (GRCm39) |
missense |
possibly damaging |
0.80 |
|