Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
A |
G |
12: 55,126,786 (GRCm39) |
L26P |
probably benign |
Het |
Aff1 |
A |
T |
5: 103,931,670 (GRCm39) |
H104L |
possibly damaging |
Het |
Apon |
T |
C |
10: 128,090,847 (GRCm39) |
I175T |
probably benign |
Het |
C2cd6 |
A |
C |
1: 59,115,830 (GRCm39) |
F168V |
probably benign |
Het |
Cgn |
C |
T |
3: 94,685,405 (GRCm39) |
|
probably benign |
Het |
Cramp1 |
G |
A |
17: 25,192,516 (GRCm39) |
P956L |
probably damaging |
Het |
Cyp2e1 |
G |
A |
7: 140,344,767 (GRCm39) |
V78M |
probably damaging |
Het |
Cyp4b1 |
G |
A |
4: 115,499,076 (GRCm39) |
P97S |
probably damaging |
Het |
Fads2 |
G |
T |
19: 10,069,136 (GRCm39) |
P96Q |
possibly damaging |
Het |
Fcer2a |
T |
C |
8: 3,738,310 (GRCm39) |
D120G |
possibly damaging |
Het |
Fhip1b |
A |
G |
7: 105,038,517 (GRCm39) |
S241P |
probably damaging |
Het |
Gm21972 |
G |
T |
1: 86,061,450 (GRCm39) |
A887S |
probably damaging |
Het |
Grk6 |
A |
G |
13: 55,601,003 (GRCm39) |
D295G |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,740,668 (GRCm39) |
V270D |
possibly damaging |
Het |
Kcnk2 |
T |
A |
1: 189,027,878 (GRCm39) |
I126F |
possibly damaging |
Het |
Kifap3 |
T |
G |
1: 163,656,718 (GRCm39) |
V346G |
possibly damaging |
Het |
Kpna1 |
T |
A |
16: 35,820,616 (GRCm39) |
N20K |
probably damaging |
Het |
Krt33b |
A |
G |
11: 99,916,298 (GRCm39) |
|
probably benign |
Het |
Krtap9-5 |
T |
C |
11: 99,839,427 (GRCm39) |
C43R |
possibly damaging |
Het |
Lars1 |
G |
A |
18: 42,361,715 (GRCm39) |
|
probably benign |
Het |
Lifr |
T |
C |
15: 7,207,417 (GRCm39) |
W540R |
probably benign |
Het |
Lrp1b |
A |
G |
2: 41,358,981 (GRCm39) |
S631P |
probably damaging |
Het |
Mbd1 |
G |
T |
18: 74,407,553 (GRCm39) |
R111L |
probably benign |
Het |
Meltf |
C |
T |
16: 31,711,602 (GRCm39) |
T576M |
probably damaging |
Het |
Mmp20 |
G |
A |
9: 7,643,995 (GRCm39) |
G228S |
probably damaging |
Het |
Mob4 |
A |
G |
1: 55,175,867 (GRCm39) |
D37G |
possibly damaging |
Het |
Msr1 |
T |
C |
8: 40,073,048 (GRCm39) |
K234E |
possibly damaging |
Het |
Myof |
A |
G |
19: 37,899,607 (GRCm39) |
V1764A |
probably damaging |
Het |
Naaladl1 |
A |
G |
19: 6,156,229 (GRCm39) |
Y105C |
possibly damaging |
Het |
Nisch |
A |
G |
14: 30,895,101 (GRCm39) |
V1065A |
probably damaging |
Het |
Npas4 |
A |
T |
19: 5,035,094 (GRCm39) |
|
probably benign |
Het |
Or4c124 |
T |
C |
2: 89,156,039 (GRCm39) |
T162A |
possibly damaging |
Het |
Pdss2 |
A |
G |
10: 43,269,997 (GRCm39) |
D280G |
probably benign |
Het |
Plk3 |
A |
G |
4: 116,990,125 (GRCm39) |
I182T |
probably damaging |
Het |
Ppm1k |
A |
G |
6: 57,487,711 (GRCm39) |
W371R |
probably damaging |
Het |
Samm50 |
T |
C |
15: 84,082,864 (GRCm39) |
|
probably null |
Het |
Scaper |
G |
T |
9: 55,510,116 (GRCm39) |
T640K |
possibly damaging |
Het |
Sun3 |
A |
C |
11: 8,973,285 (GRCm39) |
|
probably benign |
Het |
Svep1 |
T |
A |
4: 58,111,451 (GRCm39) |
K1056M |
possibly damaging |
Het |
Tgs1 |
C |
A |
4: 3,604,813 (GRCm39) |
P745Q |
probably benign |
Het |
Tomm20l |
A |
T |
12: 71,164,388 (GRCm39) |
|
probably benign |
Het |
Usp38 |
A |
C |
8: 81,738,905 (GRCm39) |
L237V |
probably damaging |
Het |
Zan |
G |
A |
5: 137,426,136 (GRCm39) |
P2547S |
unknown |
Het |
|
Other mutations in Vmn1r210 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00938:Vmn1r210
|
APN |
13 |
23,011,538 (GRCm39) |
nonsense |
probably null |
|
IGL01541:Vmn1r210
|
APN |
13 |
23,011,778 (GRCm39) |
missense |
probably benign |
|
IGL01610:Vmn1r210
|
APN |
13 |
23,011,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01632:Vmn1r210
|
APN |
13 |
23,011,366 (GRCm39) |
makesense |
probably null |
|
IGL03268:Vmn1r210
|
APN |
13 |
23,011,405 (GRCm39) |
missense |
probably benign |
0.40 |
R0227:Vmn1r210
|
UTSW |
13 |
23,011,561 (GRCm39) |
missense |
probably benign |
0.02 |
R0629:Vmn1r210
|
UTSW |
13 |
23,012,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Vmn1r210
|
UTSW |
13 |
23,011,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R4125:Vmn1r210
|
UTSW |
13 |
23,011,779 (GRCm39) |
missense |
probably benign |
0.00 |
R4132:Vmn1r210
|
UTSW |
13 |
23,011,819 (GRCm39) |
missense |
probably benign |
0.00 |
R4773:Vmn1r210
|
UTSW |
13 |
23,011,374 (GRCm39) |
missense |
probably benign |
0.00 |
R5653:Vmn1r210
|
UTSW |
13 |
23,011,378 (GRCm39) |
nonsense |
probably null |
|
R6128:Vmn1r210
|
UTSW |
13 |
23,012,277 (GRCm39) |
nonsense |
probably null |
|
R6452:Vmn1r210
|
UTSW |
13 |
23,011,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R6501:Vmn1r210
|
UTSW |
13 |
23,011,705 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6864:Vmn1r210
|
UTSW |
13 |
23,011,713 (GRCm39) |
missense |
probably benign |
0.06 |
R7623:Vmn1r210
|
UTSW |
13 |
23,011,405 (GRCm39) |
missense |
probably benign |
0.40 |
R7991:Vmn1r210
|
UTSW |
13 |
23,011,684 (GRCm39) |
missense |
probably benign |
0.01 |
R9244:Vmn1r210
|
UTSW |
13 |
23,012,089 (GRCm39) |
missense |
probably benign |
0.02 |
R9439:Vmn1r210
|
UTSW |
13 |
23,011,397 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9538:Vmn1r210
|
UTSW |
13 |
23,011,837 (GRCm39) |
nonsense |
probably null |
|
R9732:Vmn1r210
|
UTSW |
13 |
23,011,379 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9794:Vmn1r210
|
UTSW |
13 |
23,011,432 (GRCm39) |
missense |
probably damaging |
0.97 |
|