Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankdd1a |
C |
T |
9: 65,420,001 (GRCm39) |
G92S |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,414,568 (GRCm39) |
M1221K |
unknown |
Het |
Arl10 |
G |
A |
13: 54,726,662 (GRCm39) |
V147M |
probably damaging |
Het |
Bbs4 |
T |
C |
9: 59,243,651 (GRCm39) |
N152S |
probably benign |
Het |
Cacna2d2 |
T |
G |
9: 107,404,515 (GRCm39) |
|
probably benign |
Het |
Capn9 |
A |
G |
8: 125,340,582 (GRCm39) |
E582G |
probably benign |
Het |
Cct2 |
A |
T |
10: 116,898,004 (GRCm39) |
L61Q |
probably damaging |
Het |
Clip4 |
A |
G |
17: 72,106,071 (GRCm39) |
I85V |
probably damaging |
Het |
Daam2 |
A |
T |
17: 49,797,332 (GRCm39) |
L151Q |
possibly damaging |
Het |
Dlst |
T |
A |
12: 85,177,807 (GRCm39) |
I400N |
possibly damaging |
Het |
Dock7 |
A |
T |
4: 98,968,089 (GRCm39) |
|
probably benign |
Het |
Dynlrb2 |
A |
G |
8: 117,242,449 (GRCm39) |
N93S |
probably benign |
Het |
Efl1 |
A |
G |
7: 82,335,899 (GRCm39) |
T407A |
probably benign |
Het |
Emilin1 |
A |
G |
5: 31,077,517 (GRCm39) |
D891G |
possibly damaging |
Het |
Enpp4 |
A |
C |
17: 44,413,049 (GRCm39) |
S162A |
probably benign |
Het |
Epas1 |
A |
G |
17: 87,112,717 (GRCm39) |
D105G |
probably damaging |
Het |
Fcgbpl1 |
T |
A |
7: 27,846,204 (GRCm39) |
Y965* |
probably null |
Het |
Gcn1 |
T |
A |
5: 115,747,927 (GRCm39) |
I1778N |
probably damaging |
Het |
Gm14496 |
A |
C |
2: 181,633,140 (GRCm39) |
D41A |
probably damaging |
Het |
Gm7008 |
T |
A |
12: 40,273,257 (GRCm39) |
|
probably benign |
Het |
Hcfc2 |
G |
A |
10: 82,545,852 (GRCm39) |
S246N |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,815,974 (GRCm39) |
N1366S |
probably damaging |
Het |
Lgmn |
T |
C |
12: 102,361,986 (GRCm39) |
R372G |
possibly damaging |
Het |
Map2k7 |
A |
G |
8: 4,293,818 (GRCm39) |
M153V |
possibly damaging |
Het |
Megf8 |
T |
A |
7: 25,045,842 (GRCm39) |
|
probably null |
Het |
Mgat4c |
A |
C |
10: 102,224,983 (GRCm39) |
E399A |
probably benign |
Het |
Myorg |
A |
G |
4: 41,499,183 (GRCm39) |
V149A |
possibly damaging |
Het |
Nfat5 |
C |
T |
8: 108,094,584 (GRCm39) |
Q942* |
probably null |
Het |
Notch4 |
A |
G |
17: 34,803,587 (GRCm39) |
E1502G |
probably damaging |
Het |
Optn |
A |
C |
2: 5,037,963 (GRCm39) |
I410M |
probably damaging |
Het |
Or6b9 |
G |
T |
7: 106,555,763 (GRCm39) |
P127T |
probably damaging |
Het |
Or8c17 |
A |
T |
9: 38,180,564 (GRCm39) |
I252L |
possibly damaging |
Het |
Ppp1ca |
G |
A |
19: 4,244,698 (GRCm39) |
|
probably benign |
Het |
Pramel5 |
C |
A |
4: 143,999,771 (GRCm39) |
L105F |
possibly damaging |
Het |
Rad54b |
T |
A |
4: 11,610,502 (GRCm39) |
N706K |
probably damaging |
Het |
Rgs11 |
A |
T |
17: 26,421,968 (GRCm39) |
T6S |
probably benign |
Het |
Sbf1 |
T |
C |
15: 89,179,683 (GRCm39) |
H1308R |
probably benign |
Het |
Scart2 |
G |
A |
7: 139,877,772 (GRCm39) |
G918D |
possibly damaging |
Het |
Sec31a |
T |
C |
5: 100,533,984 (GRCm39) |
|
probably benign |
Het |
Sh2d5 |
G |
A |
4: 137,985,553 (GRCm39) |
D334N |
probably benign |
Het |
Skint5 |
T |
A |
4: 113,742,988 (GRCm39) |
I360F |
unknown |
Het |
Slc12a1 |
G |
A |
2: 125,026,735 (GRCm39) |
D457N |
probably damaging |
Het |
Slco2a1 |
C |
T |
9: 102,962,017 (GRCm39) |
A563V |
probably damaging |
Het |
Snrnp35 |
G |
A |
5: 124,628,471 (GRCm39) |
A95T |
probably damaging |
Het |
Snx25 |
C |
A |
8: 46,569,318 (GRCm39) |
R193L |
possibly damaging |
Het |
Stxbp5 |
T |
G |
10: 9,638,565 (GRCm39) |
Q1078P |
probably damaging |
Het |
Tmc2 |
A |
T |
2: 130,082,073 (GRCm39) |
I419F |
probably damaging |
Het |
Tmem87a |
A |
T |
2: 120,190,557 (GRCm39) |
W525R |
probably damaging |
Het |
Trhde |
A |
T |
10: 114,428,013 (GRCm39) |
S428T |
probably damaging |
Het |
Trp73 |
G |
A |
4: 154,165,943 (GRCm39) |
A42V |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,679,316 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,598,846 (GRCm39) |
V19356M |
probably damaging |
Het |
Vwa5b2 |
A |
T |
16: 20,423,576 (GRCm39) |
Q1163L |
probably benign |
Het |
Washc2 |
T |
A |
6: 116,208,593 (GRCm39) |
|
probably benign |
Het |
Wdr70 |
T |
G |
15: 8,112,030 (GRCm39) |
K71T |
possibly damaging |
Het |
Zbtb41 |
T |
C |
1: 139,368,186 (GRCm39) |
S625P |
possibly damaging |
Het |
Zfp518b |
A |
G |
5: 38,830,686 (GRCm39) |
S440P |
probably damaging |
Het |
Zfp518b |
A |
G |
5: 38,831,132 (GRCm39) |
V291A |
probably damaging |
Het |
Zmym2 |
G |
A |
14: 57,148,526 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn1r170 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02005:Vmn1r170
|
APN |
7 |
23,306,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02216:Vmn1r170
|
APN |
7 |
23,305,915 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02749:Vmn1r170
|
APN |
7 |
23,305,716 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02807:Vmn1r170
|
APN |
7 |
23,305,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02828:Vmn1r170
|
APN |
7 |
23,305,943 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02971:Vmn1r170
|
APN |
7 |
23,305,759 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03073:Vmn1r170
|
APN |
7 |
23,306,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03151:Vmn1r170
|
APN |
7 |
23,306,002 (GRCm39) |
missense |
probably benign |
0.35 |
R0079:Vmn1r170
|
UTSW |
7 |
23,305,735 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0266:Vmn1r170
|
UTSW |
7 |
23,305,906 (GRCm39) |
missense |
probably benign |
0.00 |
R0980:Vmn1r170
|
UTSW |
7 |
23,305,759 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1345:Vmn1r170
|
UTSW |
7 |
23,305,787 (GRCm39) |
missense |
probably benign |
0.00 |
R1620:Vmn1r170
|
UTSW |
7 |
23,305,754 (GRCm39) |
missense |
probably benign |
0.30 |
R1713:Vmn1r170
|
UTSW |
7 |
23,306,288 (GRCm39) |
missense |
probably benign |
0.30 |
R1745:Vmn1r170
|
UTSW |
7 |
23,305,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R1974:Vmn1r170
|
UTSW |
7 |
23,305,906 (GRCm39) |
missense |
probably benign |
0.00 |
R2163:Vmn1r170
|
UTSW |
7 |
23,306,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R3812:Vmn1r170
|
UTSW |
7 |
23,305,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Vmn1r170
|
UTSW |
7 |
23,306,087 (GRCm39) |
missense |
probably benign |
0.25 |
R5309:Vmn1r170
|
UTSW |
7 |
23,305,880 (GRCm39) |
missense |
probably damaging |
0.97 |
R5378:Vmn1r170
|
UTSW |
7 |
23,305,963 (GRCm39) |
missense |
probably benign |
0.00 |
R5379:Vmn1r170
|
UTSW |
7 |
23,306,054 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5661:Vmn1r170
|
UTSW |
7 |
23,306,231 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5673:Vmn1r170
|
UTSW |
7 |
23,305,630 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6181:Vmn1r170
|
UTSW |
7 |
23,305,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R6192:Vmn1r170
|
UTSW |
7 |
23,305,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Vmn1r170
|
UTSW |
7 |
23,306,320 (GRCm39) |
missense |
not run |
|
R7667:Vmn1r170
|
UTSW |
7 |
23,306,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Vmn1r170
|
UTSW |
7 |
23,306,321 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8699:Vmn1r170
|
UTSW |
7 |
23,306,080 (GRCm39) |
nonsense |
probably null |
|
R8927:Vmn1r170
|
UTSW |
7 |
23,305,814 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8928:Vmn1r170
|
UTSW |
7 |
23,305,814 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9269:Vmn1r170
|
UTSW |
7 |
23,306,263 (GRCm39) |
missense |
probably benign |
0.02 |
R9569:Vmn1r170
|
UTSW |
7 |
23,306,294 (GRCm39) |
missense |
probably benign |
0.19 |
X0060:Vmn1r170
|
UTSW |
7 |
23,306,368 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Vmn1r170
|
UTSW |
7 |
23,305,835 (GRCm39) |
missense |
possibly damaging |
0.89 |
|