Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 8,988,189 (GRCm39) |
K3158E |
possibly damaging |
Het |
Ak7 |
G |
A |
12: 105,679,834 (GRCm39) |
V123M |
probably benign |
Het |
Ankmy1 |
A |
T |
1: 92,816,372 (GRCm39) |
N247K |
probably benign |
Het |
Atp1a1 |
A |
G |
3: 101,494,259 (GRCm39) |
V447A |
probably benign |
Het |
Atp1a4 |
A |
C |
1: 172,067,332 (GRCm39) |
M600R |
probably damaging |
Het |
Baat |
A |
G |
4: 49,502,727 (GRCm39) |
Y132H |
probably damaging |
Het |
Ceacam15 |
A |
G |
7: 16,405,906 (GRCm39) |
V215A |
probably damaging |
Het |
Celf2 |
G |
T |
2: 6,590,831 (GRCm39) |
N279K |
possibly damaging |
Het |
Cfap96 |
A |
T |
8: 46,423,505 (GRCm39) |
I69N |
probably damaging |
Het |
Clec14a |
C |
T |
12: 58,314,767 (GRCm39) |
R285H |
probably benign |
Het |
Ctnna1 |
T |
G |
18: 35,312,880 (GRCm39) |
I244R |
possibly damaging |
Het |
Dcxr |
T |
A |
11: 120,617,130 (GRCm39) |
N105Y |
possibly damaging |
Het |
Dnajc6 |
T |
C |
4: 101,468,461 (GRCm39) |
F166L |
probably damaging |
Het |
Ercc3 |
G |
A |
18: 32,378,624 (GRCm39) |
A202T |
probably benign |
Het |
Faf1 |
A |
G |
4: 109,584,625 (GRCm39) |
D67G |
probably benign |
Het |
Fancm |
G |
A |
12: 65,171,718 (GRCm39) |
R1786H |
probably benign |
Het |
Fnbp1 |
A |
G |
2: 30,926,552 (GRCm39) |
|
probably null |
Het |
Frem2 |
A |
G |
3: 53,455,228 (GRCm39) |
L2116S |
possibly damaging |
Het |
Gbp5 |
A |
G |
3: 142,209,546 (GRCm39) |
E164G |
probably benign |
Het |
Gm4922 |
A |
T |
10: 18,660,007 (GRCm39) |
Y238* |
probably null |
Het |
Gm8257 |
A |
G |
14: 44,893,774 (GRCm39) |
Y62H |
probably damaging |
Het |
Grin2b |
A |
G |
6: 135,755,739 (GRCm39) |
F525S |
probably damaging |
Het |
Hjv |
T |
G |
3: 96,434,869 (GRCm39) |
S203A |
probably benign |
Het |
Hsd17b3 |
C |
A |
13: 64,210,984 (GRCm39) |
|
probably null |
Het |
Ighv1-23 |
T |
A |
12: 114,728,179 (GRCm39) |
Q81L |
probably benign |
Het |
Inpp4b |
T |
C |
8: 82,696,164 (GRCm39) |
V366A |
probably damaging |
Het |
Jak1 |
G |
T |
4: 101,036,791 (GRCm39) |
A283D |
possibly damaging |
Het |
Kmt2d |
G |
T |
15: 98,748,140 (GRCm39) |
|
probably benign |
Het |
Mbtps1 |
A |
T |
8: 120,262,086 (GRCm39) |
D354E |
probably damaging |
Het |
Mettl17 |
T |
C |
14: 52,126,246 (GRCm39) |
V218A |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Nfat5 |
C |
T |
8: 108,093,855 (GRCm39) |
Q699* |
probably null |
Het |
Or4s2b |
G |
A |
2: 88,508,240 (GRCm39) |
V14I |
probably benign |
Het |
Or4s2b |
T |
G |
2: 88,508,523 (GRCm39) |
V101G |
probably benign |
Het |
Or7e174 |
C |
A |
9: 20,012,540 (GRCm39) |
H162N |
probably benign |
Het |
Osbpl7 |
C |
A |
11: 96,947,095 (GRCm39) |
S265R |
possibly damaging |
Het |
Pcdh15 |
A |
G |
10: 74,430,046 (GRCm39) |
T1258A |
probably damaging |
Het |
Pcdh20 |
A |
T |
14: 88,705,866 (GRCm39) |
L478Q |
probably damaging |
Het |
Pde11a |
A |
G |
2: 75,988,677 (GRCm39) |
V488A |
probably benign |
Het |
Phactr1 |
A |
T |
13: 43,248,441 (GRCm39) |
E463D |
probably benign |
Het |
Phaf1 |
C |
A |
8: 105,973,520 (GRCm39) |
N282K |
possibly damaging |
Het |
Samd9l |
A |
T |
6: 3,373,935 (GRCm39) |
Y1109N |
probably damaging |
Het |
Samd9l |
GAA |
GAAA |
6: 3,373,937 (GRCm39) |
|
probably null |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Serpinb12 |
T |
A |
1: 106,876,883 (GRCm39) |
D66E |
probably benign |
Het |
Slco1a6 |
C |
A |
6: 142,047,378 (GRCm39) |
C404F |
probably benign |
Het |
Spaca6 |
C |
T |
17: 18,051,387 (GRCm39) |
A21V |
probably damaging |
Het |
Sphkap |
G |
T |
1: 83,256,782 (GRCm39) |
Y322* |
probably null |
Het |
Sptlc3 |
G |
A |
2: 139,478,600 (GRCm39) |
V520I |
probably benign |
Het |
Stox2 |
A |
G |
8: 47,645,970 (GRCm39) |
S497P |
probably damaging |
Het |
Syt9 |
A |
T |
7: 107,035,594 (GRCm39) |
K204* |
probably null |
Het |
Taf3 |
A |
G |
2: 9,957,468 (GRCm39) |
V233A |
probably damaging |
Het |
Tbccd1 |
T |
C |
16: 22,637,285 (GRCm39) |
|
probably null |
Het |
Tdrd5 |
T |
A |
1: 156,111,944 (GRCm39) |
T479S |
probably benign |
Het |
Tex10 |
T |
C |
4: 48,452,946 (GRCm39) |
D671G |
probably benign |
Het |
Tgtp2 |
T |
C |
11: 48,949,811 (GRCm39) |
T254A |
probably damaging |
Het |
Tmtc2 |
T |
C |
10: 105,249,391 (GRCm39) |
Y114C |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Ubac1 |
A |
T |
2: 25,888,989 (GRCm39) |
I402N |
probably damaging |
Het |
Zmat1 |
A |
T |
X: 133,873,694 (GRCm39) |
S566T |
probably damaging |
Homo |
|
Other mutations in Sgk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03048:Sgk2
|
UTSW |
2 |
162,837,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R0319:Sgk2
|
UTSW |
2 |
162,837,592 (GRCm39) |
splice site |
probably benign |
|
R0563:Sgk2
|
UTSW |
2 |
162,846,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R0947:Sgk2
|
UTSW |
2 |
162,848,758 (GRCm39) |
missense |
probably benign |
0.35 |
R1624:Sgk2
|
UTSW |
2 |
162,839,779 (GRCm39) |
missense |
probably benign |
0.20 |
R1975:Sgk2
|
UTSW |
2 |
162,846,080 (GRCm39) |
missense |
probably benign |
|
R1977:Sgk2
|
UTSW |
2 |
162,846,080 (GRCm39) |
missense |
probably benign |
|
R2085:Sgk2
|
UTSW |
2 |
162,854,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Sgk2
|
UTSW |
2 |
162,841,099 (GRCm39) |
splice site |
probably null |
|
R2873:Sgk2
|
UTSW |
2 |
162,836,449 (GRCm39) |
splice site |
probably benign |
|
R2874:Sgk2
|
UTSW |
2 |
162,836,449 (GRCm39) |
splice site |
probably benign |
|
R2919:Sgk2
|
UTSW |
2 |
162,841,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Sgk2
|
UTSW |
2 |
162,841,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R4660:Sgk2
|
UTSW |
2 |
162,839,763 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5517:Sgk2
|
UTSW |
2 |
162,839,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5531:Sgk2
|
UTSW |
2 |
162,836,624 (GRCm39) |
missense |
probably benign |
0.00 |
R6143:Sgk2
|
UTSW |
2 |
162,841,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7355:Sgk2
|
UTSW |
2 |
162,854,987 (GRCm39) |
missense |
probably benign |
0.02 |
R7825:Sgk2
|
UTSW |
2 |
162,848,801 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7837:Sgk2
|
UTSW |
2 |
162,845,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Sgk2
|
UTSW |
2 |
162,848,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R8843:Sgk2
|
UTSW |
2 |
162,854,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Sgk2
|
UTSW |
2 |
162,854,975 (GRCm39) |
missense |
probably benign |
0.06 |
|