Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actbl2 |
T |
A |
13: 111,391,956 (GRCm39) |
V97E |
possibly damaging |
Het |
Actl7a |
A |
T |
4: 56,744,498 (GRCm39) |
T342S |
probably damaging |
Het |
Alcam |
A |
G |
16: 52,088,749 (GRCm39) |
S554P |
probably damaging |
Het |
Ano3 |
T |
C |
2: 110,780,638 (GRCm39) |
|
probably benign |
Het |
Atad2b |
T |
A |
12: 5,060,390 (GRCm39) |
|
probably null |
Het |
Baz2a |
T |
C |
10: 127,961,139 (GRCm39) |
S1621P |
possibly damaging |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
GGTTCTGTGGTCACT |
GGTTCTGTGGTCACTAGTTCTGTGGTCACT |
3: 95,795,484 (GRCm39) |
|
probably benign |
Het |
BC028528 |
GTCACTGGTTCTGTGGTCACTGGTTCTGTG |
GTCACTGGTTCTGTGATCACTGGTTCTGTGGTCACTGGTTCTGTG |
3: 95,795,463 (GRCm39) |
|
probably benign |
Het |
Best1 |
T |
A |
19: 9,966,639 (GRCm39) |
|
probably null |
Het |
Catip |
G |
T |
1: 74,408,089 (GRCm39) |
E474* |
probably null |
Het |
Comp |
A |
G |
8: 70,826,509 (GRCm39) |
D28G |
probably benign |
Het |
Crebbp |
G |
A |
16: 3,944,353 (GRCm39) |
R600W |
probably benign |
Het |
Cyfip1 |
A |
G |
7: 55,521,997 (GRCm39) |
|
probably null |
Het |
Ddr1 |
A |
G |
17: 35,995,174 (GRCm39) |
S675P |
probably damaging |
Het |
Dhtkd1 |
A |
T |
2: 5,926,898 (GRCm39) |
|
probably null |
Het |
F2rl1 |
G |
A |
13: 95,650,522 (GRCm39) |
A120V |
probably damaging |
Het |
Fam136a |
A |
G |
6: 86,342,784 (GRCm39) |
N24D |
probably benign |
Het |
Fbxw10 |
C |
A |
11: 62,765,994 (GRCm39) |
Q755K |
probably benign |
Het |
Fbxw16 |
C |
A |
9: 109,268,657 (GRCm39) |
Q244H |
possibly damaging |
Het |
Gabrg2 |
T |
C |
11: 41,807,119 (GRCm39) |
K373E |
probably benign |
Het |
Herc3 |
G |
A |
6: 58,820,795 (GRCm39) |
V60I |
probably benign |
Het |
Igkv19-93 |
T |
A |
6: 68,713,477 (GRCm39) |
K51* |
probably null |
Het |
Krt23 |
T |
A |
11: 99,383,626 (GRCm39) |
K89* |
probably null |
Het |
Mavs |
A |
G |
2: 131,087,395 (GRCm39) |
T298A |
probably benign |
Het |
Mlec |
T |
C |
5: 115,288,181 (GRCm39) |
Y198C |
probably damaging |
Het |
Ncam2 |
C |
A |
16: 81,386,689 (GRCm39) |
N689K |
probably benign |
Het |
Nfkbia |
A |
G |
12: 55,538,546 (GRCm39) |
I82T |
probably damaging |
Het |
Or12d14-ps1 |
A |
G |
17: 37,673,496 (GRCm39) |
I163V |
probably benign |
Het |
Or12j2 |
A |
G |
7: 139,915,895 (GRCm39) |
N40S |
probably damaging |
Het |
Or7a35 |
A |
T |
10: 78,853,341 (GRCm39) |
I62F |
probably benign |
Het |
Or8b43 |
A |
G |
9: 38,360,942 (GRCm39) |
Y258C |
probably damaging |
Het |
Pom121l2 |
A |
T |
13: 22,166,796 (GRCm39) |
I356F |
probably benign |
Het |
Ppip5k1 |
A |
T |
2: 121,168,096 (GRCm39) |
L719Q |
probably damaging |
Het |
Satb1 |
A |
T |
17: 52,089,752 (GRCm39) |
V365D |
possibly damaging |
Het |
Scrn2 |
T |
C |
11: 96,921,712 (GRCm39) |
Y61H |
probably damaging |
Het |
Siglec1 |
C |
T |
2: 130,914,602 (GRCm39) |
V1505M |
probably damaging |
Het |
Slc2a10 |
A |
G |
2: 165,356,802 (GRCm39) |
N154S |
probably damaging |
Het |
Slc39a10 |
A |
T |
1: 46,874,290 (GRCm39) |
H337Q |
probably benign |
Het |
Slc39a12 |
T |
A |
2: 14,404,939 (GRCm39) |
|
probably null |
Het |
Slc6a6 |
T |
G |
6: 91,701,832 (GRCm39) |
L80R |
probably damaging |
Het |
Slit1 |
T |
C |
19: 41,590,074 (GRCm39) |
Y1404C |
probably damaging |
Het |
Sowahc |
A |
G |
10: 59,059,121 (GRCm39) |
E419G |
probably damaging |
Het |
Ssh1 |
T |
C |
5: 114,095,441 (GRCm39) |
|
probably null |
Het |
Stab1 |
C |
A |
14: 30,874,552 (GRCm39) |
C952F |
probably damaging |
Het |
Stat5a |
T |
C |
11: 100,765,850 (GRCm39) |
M312T |
possibly damaging |
Het |
Tex2 |
A |
G |
11: 106,439,562 (GRCm39) |
I606T |
unknown |
Het |
Tex55 |
T |
C |
16: 38,648,809 (GRCm39) |
E100G |
possibly damaging |
Het |
Zfp959 |
A |
G |
17: 56,204,886 (GRCm39) |
I308V |
probably benign |
Het |
|
Other mutations in Vmn1r19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00948:Vmn1r19
|
APN |
6 |
57,382,247 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01287:Vmn1r19
|
APN |
6 |
57,382,179 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Vmn1r19
|
APN |
6 |
57,381,857 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01895:Vmn1r19
|
APN |
6 |
57,382,245 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02676:Vmn1r19
|
APN |
6 |
57,382,025 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03040:Vmn1r19
|
APN |
6 |
57,382,347 (GRCm39) |
missense |
unknown |
|
IGL03087:Vmn1r19
|
APN |
6 |
57,381,476 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4802001:Vmn1r19
|
UTSW |
6 |
57,382,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R0319:Vmn1r19
|
UTSW |
6 |
57,381,600 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1368:Vmn1r19
|
UTSW |
6 |
57,381,656 (GRCm39) |
missense |
probably benign |
0.01 |
R1997:Vmn1r19
|
UTSW |
6 |
57,382,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R2920:Vmn1r19
|
UTSW |
6 |
57,381,909 (GRCm39) |
missense |
probably benign |
0.03 |
R3857:Vmn1r19
|
UTSW |
6 |
57,382,098 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4090:Vmn1r19
|
UTSW |
6 |
57,381,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R4547:Vmn1r19
|
UTSW |
6 |
57,381,774 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4823:Vmn1r19
|
UTSW |
6 |
57,382,219 (GRCm39) |
nonsense |
probably null |
|
R4951:Vmn1r19
|
UTSW |
6 |
57,381,927 (GRCm39) |
missense |
probably benign |
0.36 |
R5077:Vmn1r19
|
UTSW |
6 |
57,382,026 (GRCm39) |
missense |
probably benign |
0.00 |
R5459:Vmn1r19
|
UTSW |
6 |
57,381,475 (GRCm39) |
nonsense |
probably null |
|
R5625:Vmn1r19
|
UTSW |
6 |
57,382,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R5690:Vmn1r19
|
UTSW |
6 |
57,381,780 (GRCm39) |
missense |
probably benign |
0.10 |
R5761:Vmn1r19
|
UTSW |
6 |
57,382,338 (GRCm39) |
missense |
unknown |
|
R6124:Vmn1r19
|
UTSW |
6 |
57,381,602 (GRCm39) |
missense |
probably benign |
0.02 |
R6373:Vmn1r19
|
UTSW |
6 |
57,382,317 (GRCm39) |
missense |
unknown |
|
R6476:Vmn1r19
|
UTSW |
6 |
57,381,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R6938:Vmn1r19
|
UTSW |
6 |
57,381,992 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7027:Vmn1r19
|
UTSW |
6 |
57,381,475 (GRCm39) |
nonsense |
probably null |
|
R7359:Vmn1r19
|
UTSW |
6 |
57,382,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R7893:Vmn1r19
|
UTSW |
6 |
57,381,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R8481:Vmn1r19
|
UTSW |
6 |
57,381,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R8487:Vmn1r19
|
UTSW |
6 |
57,382,166 (GRCm39) |
missense |
probably benign |
0.03 |
R8812:Vmn1r19
|
UTSW |
6 |
57,381,436 (GRCm39) |
start gained |
probably benign |
|
R8907:Vmn1r19
|
UTSW |
6 |
57,381,991 (GRCm39) |
missense |
probably benign |
|
R8976:Vmn1r19
|
UTSW |
6 |
57,381,719 (GRCm39) |
missense |
probably benign |
0.01 |
R9277:Vmn1r19
|
UTSW |
6 |
57,382,322 (GRCm39) |
missense |
unknown |
|
|