Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730596B20Rik |
A |
G |
6: 52,156,500 (GRCm39) |
|
probably benign |
Het |
Acan |
A |
G |
7: 78,749,530 (GRCm39) |
S11G |
probably null |
Het |
Ankrd13d |
A |
C |
19: 4,332,256 (GRCm39) |
V56G |
probably damaging |
Het |
Arl15 |
A |
G |
13: 114,104,151 (GRCm39) |
Y76C |
probably damaging |
Het |
Aspg |
G |
A |
12: 112,087,432 (GRCm39) |
C296Y |
probably damaging |
Het |
Astl |
T |
A |
2: 127,187,889 (GRCm39) |
D101E |
probably benign |
Het |
Bmpr2 |
A |
G |
1: 59,881,977 (GRCm39) |
N202S |
probably benign |
Het |
Borcs7 |
T |
C |
19: 46,690,003 (GRCm39) |
*106Q |
probably null |
Het |
Brip1 |
A |
G |
11: 85,955,865 (GRCm39) |
S883P |
possibly damaging |
Het |
Cacng2 |
A |
T |
15: 78,002,991 (GRCm39) |
L34Q |
probably damaging |
Het |
Catip |
A |
C |
1: 74,402,077 (GRCm39) |
D84A |
probably damaging |
Het |
Ccdc162 |
A |
G |
10: 41,510,037 (GRCm39) |
L856S |
possibly damaging |
Het |
Ccdc38 |
A |
G |
10: 93,417,608 (GRCm39) |
K500E |
probably damaging |
Het |
Ccser2 |
T |
C |
14: 36,663,122 (GRCm39) |
K21E |
probably damaging |
Het |
Cd93 |
A |
T |
2: 148,283,439 (GRCm39) |
Y636N |
probably damaging |
Het |
Cep128 |
A |
T |
12: 91,262,998 (GRCm39) |
N300K |
possibly damaging |
Het |
Cfap44 |
A |
G |
16: 44,269,460 (GRCm39) |
T1155A |
probably benign |
Het |
Clec16a |
T |
C |
16: 10,447,951 (GRCm39) |
L550P |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,618,787 (GRCm39) |
Y1867C |
probably damaging |
Het |
Cul3 |
A |
T |
1: 80,249,249 (GRCm39) |
I674N |
probably damaging |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Cyp2d34 |
T |
C |
15: 82,500,552 (GRCm39) |
H429R |
probably benign |
Het |
Dab2ip |
T |
A |
2: 35,582,267 (GRCm39) |
C4* |
probably null |
Het |
Dcaf1 |
A |
G |
9: 106,731,446 (GRCm39) |
E641G |
probably damaging |
Het |
Dda1 |
T |
A |
8: 71,927,276 (GRCm39) |
|
probably benign |
Het |
Dmgdh |
C |
T |
13: 93,888,960 (GRCm39) |
T866I |
probably benign |
Het |
Ect2l |
T |
C |
10: 18,037,250 (GRCm39) |
T383A |
probably benign |
Het |
Ets2 |
A |
G |
16: 95,515,416 (GRCm39) |
N181D |
probably benign |
Het |
Ezh2 |
A |
G |
6: 47,529,357 (GRCm39) |
F222L |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,342,216 (GRCm39) |
L1503P |
probably damaging |
Het |
Fsip2 |
C |
A |
2: 82,809,777 (GRCm39) |
A2032E |
probably damaging |
Het |
Gm1818 |
C |
T |
12: 48,602,346 (GRCm39) |
|
noncoding transcript |
Het |
Gm9493 |
A |
G |
19: 23,597,106 (GRCm39) |
S1G |
probably damaging |
Het |
Grin2b |
A |
G |
6: 135,710,942 (GRCm39) |
I868T |
possibly damaging |
Het |
Ift22 |
A |
T |
5: 136,939,987 (GRCm39) |
T17S |
possibly damaging |
Het |
Il4ra |
T |
C |
7: 125,170,735 (GRCm39) |
W216R |
probably damaging |
Het |
Kcnj6 |
A |
T |
16: 94,633,236 (GRCm39) |
W274R |
probably damaging |
Het |
Kctd19 |
G |
A |
8: 106,123,082 (GRCm39) |
H111Y |
probably damaging |
Het |
Kremen2 |
A |
G |
17: 23,961,679 (GRCm39) |
V276A |
probably benign |
Het |
Lig1 |
C |
A |
7: 13,022,598 (GRCm39) |
Q143K |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,403,359 (GRCm39) |
D2071E |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,404,536 (GRCm39) |
M475I |
probably damaging |
Het |
Mbtd1 |
G |
A |
11: 93,820,485 (GRCm39) |
A427T |
probably damaging |
Het |
Myof |
A |
G |
19: 37,915,429 (GRCm39) |
|
probably null |
Het |
Nbeal2 |
T |
C |
9: 110,470,945 (GRCm39) |
D308G |
possibly damaging |
Het |
Ncdn |
T |
C |
4: 126,638,824 (GRCm39) |
Q665R |
probably benign |
Het |
Nkd1 |
T |
C |
8: 89,316,442 (GRCm39) |
|
probably null |
Het |
Nktr |
G |
A |
9: 121,577,455 (GRCm39) |
|
probably benign |
Het |
Npc1l1 |
A |
T |
11: 6,167,806 (GRCm39) |
M995K |
possibly damaging |
Het |
Or10ag59 |
C |
A |
2: 87,406,363 (GRCm39) |
R312S |
probably benign |
Het |
Or11g7 |
A |
T |
14: 50,691,201 (GRCm39) |
R231* |
probably null |
Het |
Or14n1-ps1 |
T |
A |
7: 86,092,397 (GRCm39) |
C69* |
probably null |
Het |
Padi4 |
T |
C |
4: 140,487,351 (GRCm39) |
T184A |
probably damaging |
Het |
Pgm2l1 |
C |
T |
7: 99,915,881 (GRCm39) |
P409S |
probably benign |
Het |
Pgpep1 |
G |
A |
8: 71,105,101 (GRCm39) |
T53M |
probably damaging |
Het |
Pgr |
T |
C |
9: 8,902,006 (GRCm39) |
L513P |
probably damaging |
Het |
Pikfyve |
T |
A |
1: 65,311,730 (GRCm39) |
I1989N |
probably damaging |
Het |
Prrc2a |
T |
C |
17: 35,371,716 (GRCm39) |
T1806A |
probably benign |
Het |
Psd |
T |
C |
19: 46,311,753 (GRCm39) |
E309G |
possibly damaging |
Het |
Qtrt1 |
C |
T |
9: 21,323,299 (GRCm39) |
T50I |
probably damaging |
Het |
Rims2 |
A |
C |
15: 39,538,416 (GRCm39) |
T1320P |
probably damaging |
Het |
Scn11a |
T |
G |
9: 119,594,514 (GRCm39) |
N1293T |
probably damaging |
Het |
Scn8a |
T |
C |
15: 100,872,548 (GRCm39) |
F529S |
possibly damaging |
Het |
Sec14l4 |
A |
T |
11: 3,985,142 (GRCm39) |
D25V |
possibly damaging |
Het |
Sema3a |
C |
T |
5: 13,615,832 (GRCm39) |
R419C |
probably damaging |
Het |
Slc12a1 |
T |
C |
2: 125,032,133 (GRCm39) |
Y595H |
probably damaging |
Het |
Slc25a28 |
A |
T |
19: 43,655,364 (GRCm39) |
H170Q |
possibly damaging |
Het |
Slc26a1 |
T |
A |
5: 108,821,631 (GRCm39) |
Q86L |
probably damaging |
Het |
Slc48a1 |
T |
A |
15: 97,687,798 (GRCm39) |
W51R |
probably damaging |
Het |
Sptlc3 |
T |
A |
2: 139,423,533 (GRCm39) |
V309D |
probably damaging |
Het |
Srcap |
G |
A |
7: 127,140,528 (GRCm39) |
S1375N |
probably damaging |
Het |
Tanc1 |
C |
A |
2: 59,647,837 (GRCm39) |
H986Q |
possibly damaging |
Het |
Tbc1d4 |
A |
G |
14: 101,727,353 (GRCm39) |
V486A |
probably damaging |
Het |
Tceanc2 |
T |
C |
4: 107,004,776 (GRCm39) |
D124G |
probably damaging |
Het |
Tdrd9 |
A |
G |
12: 111,979,720 (GRCm39) |
M402V |
possibly damaging |
Het |
Tmem132d |
T |
C |
5: 127,861,934 (GRCm39) |
D729G |
probably damaging |
Het |
Tmem62 |
T |
A |
2: 120,807,943 (GRCm39) |
I55N |
probably damaging |
Het |
Tnfrsf21 |
A |
T |
17: 43,350,606 (GRCm39) |
N257Y |
possibly damaging |
Het |
Trappc3 |
T |
C |
4: 126,167,834 (GRCm39) |
L131P |
probably damaging |
Het |
Vmn2r25 |
A |
T |
6: 123,799,900 (GRCm39) |
M814K |
possibly damaging |
Het |
Vwa8 |
A |
T |
14: 79,320,313 (GRCm39) |
D1108V |
probably benign |
Het |
Xrcc4 |
C |
G |
13: 90,139,198 (GRCm39) |
A241P |
possibly damaging |
Het |
Xylt1 |
T |
A |
7: 117,191,135 (GRCm39) |
D310E |
probably benign |
Het |
Zfp27 |
T |
G |
7: 29,594,444 (GRCm39) |
H507P |
possibly damaging |
Het |
Zfp341 |
C |
T |
2: 154,466,954 (GRCm39) |
P108S |
probably benign |
Het |
Zfp641 |
T |
C |
15: 98,190,816 (GRCm39) |
N76S |
probably benign |
Het |
Zfp936 |
T |
C |
7: 42,839,787 (GRCm39) |
V418A |
probably benign |
Het |
|
Other mutations in Vmn2r87 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01090:Vmn2r87
|
APN |
10 |
130,333,247 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
IGL01295:Vmn2r87
|
APN |
10 |
130,307,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01411:Vmn2r87
|
APN |
10 |
130,308,429 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01680:Vmn2r87
|
APN |
10 |
130,315,586 (GRCm39) |
nonsense |
probably null |
|
IGL01822:Vmn2r87
|
APN |
10 |
130,307,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01835:Vmn2r87
|
APN |
10 |
130,314,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01965:Vmn2r87
|
APN |
10 |
130,314,924 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02562:Vmn2r87
|
APN |
10 |
130,314,513 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02665:Vmn2r87
|
APN |
10 |
130,333,049 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03202:Vmn2r87
|
APN |
10 |
130,333,091 (GRCm39) |
missense |
probably benign |
|
FR4304:Vmn2r87
|
UTSW |
10 |
130,314,583 (GRCm39) |
missense |
probably benign |
0.01 |
FR4340:Vmn2r87
|
UTSW |
10 |
130,314,583 (GRCm39) |
missense |
probably benign |
0.01 |
FR4342:Vmn2r87
|
UTSW |
10 |
130,314,583 (GRCm39) |
missense |
probably benign |
0.01 |
FR4589:Vmn2r87
|
UTSW |
10 |
130,314,583 (GRCm39) |
missense |
probably benign |
0.01 |
LCD18:Vmn2r87
|
UTSW |
10 |
130,314,583 (GRCm39) |
missense |
probably benign |
0.01 |
R0344:Vmn2r87
|
UTSW |
10 |
130,315,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Vmn2r87
|
UTSW |
10 |
130,307,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R0384:Vmn2r87
|
UTSW |
10 |
130,307,712 (GRCm39) |
missense |
probably benign |
|
R1144:Vmn2r87
|
UTSW |
10 |
130,312,098 (GRCm39) |
splice site |
probably benign |
|
R1172:Vmn2r87
|
UTSW |
10 |
130,313,453 (GRCm39) |
missense |
probably benign |
0.03 |
R1860:Vmn2r87
|
UTSW |
10 |
130,315,755 (GRCm39) |
missense |
probably benign |
0.00 |
R1866:Vmn2r87
|
UTSW |
10 |
130,308,441 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1897:Vmn2r87
|
UTSW |
10 |
130,307,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2360:Vmn2r87
|
UTSW |
10 |
130,315,631 (GRCm39) |
missense |
probably damaging |
0.99 |
R2909:Vmn2r87
|
UTSW |
10 |
130,314,865 (GRCm39) |
missense |
probably damaging |
0.99 |
R3874:Vmn2r87
|
UTSW |
10 |
130,315,856 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4113:Vmn2r87
|
UTSW |
10 |
130,315,691 (GRCm39) |
missense |
probably benign |
|
R4190:Vmn2r87
|
UTSW |
10 |
130,308,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R4197:Vmn2r87
|
UTSW |
10 |
130,315,779 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4201:Vmn2r87
|
UTSW |
10 |
130,308,448 (GRCm39) |
missense |
probably benign |
0.03 |
R4202:Vmn2r87
|
UTSW |
10 |
130,308,448 (GRCm39) |
missense |
probably benign |
0.03 |
R4368:Vmn2r87
|
UTSW |
10 |
130,315,676 (GRCm39) |
missense |
probably benign |
0.44 |
R4485:Vmn2r87
|
UTSW |
10 |
130,315,678 (GRCm39) |
nonsense |
probably null |
|
R4537:Vmn2r87
|
UTSW |
10 |
130,308,054 (GRCm39) |
missense |
probably benign |
0.12 |
R4590:Vmn2r87
|
UTSW |
10 |
130,315,014 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4752:Vmn2r87
|
UTSW |
10 |
130,314,336 (GRCm39) |
nonsense |
probably null |
|
R4873:Vmn2r87
|
UTSW |
10 |
130,308,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Vmn2r87
|
UTSW |
10 |
130,308,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R4923:Vmn2r87
|
UTSW |
10 |
130,314,435 (GRCm39) |
missense |
probably damaging |
0.99 |
R4970:Vmn2r87
|
UTSW |
10 |
130,314,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Vmn2r87
|
UTSW |
10 |
130,308,298 (GRCm39) |
missense |
probably damaging |
0.96 |
R5112:Vmn2r87
|
UTSW |
10 |
130,314,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R5187:Vmn2r87
|
UTSW |
10 |
130,333,208 (GRCm39) |
missense |
probably null |
0.99 |
R5618:Vmn2r87
|
UTSW |
10 |
130,315,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Vmn2r87
|
UTSW |
10 |
130,315,807 (GRCm39) |
missense |
probably benign |
0.01 |
R6287:Vmn2r87
|
UTSW |
10 |
130,314,291 (GRCm39) |
critical splice donor site |
probably null |
|
R6383:Vmn2r87
|
UTSW |
10 |
130,314,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R6576:Vmn2r87
|
UTSW |
10 |
130,314,654 (GRCm39) |
missense |
probably benign |
0.05 |
R6742:Vmn2r87
|
UTSW |
10 |
130,308,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R7086:Vmn2r87
|
UTSW |
10 |
130,333,178 (GRCm39) |
missense |
probably benign |
0.00 |
R7162:Vmn2r87
|
UTSW |
10 |
130,313,416 (GRCm39) |
missense |
probably benign |
0.08 |
R7419:Vmn2r87
|
UTSW |
10 |
130,307,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R7425:Vmn2r87
|
UTSW |
10 |
130,314,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R7443:Vmn2r87
|
UTSW |
10 |
130,308,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R7571:Vmn2r87
|
UTSW |
10 |
130,314,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R7663:Vmn2r87
|
UTSW |
10 |
130,308,054 (GRCm39) |
missense |
probably damaging |
0.97 |
R7716:Vmn2r87
|
UTSW |
10 |
130,308,018 (GRCm39) |
missense |
probably benign |
0.09 |
R7793:Vmn2r87
|
UTSW |
10 |
130,313,413 (GRCm39) |
missense |
probably benign |
0.05 |
R7806:Vmn2r87
|
UTSW |
10 |
130,315,679 (GRCm39) |
missense |
probably benign |
|
R7841:Vmn2r87
|
UTSW |
10 |
130,333,095 (GRCm39) |
missense |
probably benign |
0.31 |
R8326:Vmn2r87
|
UTSW |
10 |
130,308,180 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8411:Vmn2r87
|
UTSW |
10 |
130,308,126 (GRCm39) |
missense |
probably damaging |
0.99 |
R8445:Vmn2r87
|
UTSW |
10 |
130,313,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R8540:Vmn2r87
|
UTSW |
10 |
130,314,762 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8892:Vmn2r87
|
UTSW |
10 |
130,308,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R9093:Vmn2r87
|
UTSW |
10 |
130,308,165 (GRCm39) |
missense |
probably benign |
0.08 |
R9623:Vmn2r87
|
UTSW |
10 |
130,315,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R9667:Vmn2r87
|
UTSW |
10 |
130,314,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R9797:Vmn2r87
|
UTSW |
10 |
130,312,064 (GRCm39) |
missense |
probably benign |
0.44 |
R9797:Vmn2r87
|
UTSW |
10 |
130,308,138 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Vmn2r87
|
UTSW |
10 |
130,308,183 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Vmn2r87
|
UTSW |
10 |
130,307,713 (GRCm39) |
missense |
probably benign |
0.04 |
|