Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afm |
T |
A |
5: 90,679,374 (GRCm39) |
C289* |
probably null |
Het |
Agpat3 |
A |
G |
10: 78,118,989 (GRCm39) |
Y202H |
probably benign |
Het |
Atg4b |
T |
A |
1: 93,715,479 (GRCm39) |
*394R |
probably null |
Het |
Atxn2l |
A |
T |
7: 126,091,377 (GRCm39) |
H1037Q |
probably damaging |
Het |
Baz1a |
T |
C |
12: 54,941,238 (GRCm39) |
Y1504C |
probably damaging |
Het |
Bfsp2 |
T |
C |
9: 103,327,152 (GRCm39) |
N195S |
probably benign |
Het |
Bmpr1b |
T |
G |
3: 141,586,203 (GRCm39) |
S20R |
possibly damaging |
Het |
Bmpr2 |
C |
T |
1: 59,906,860 (GRCm39) |
P651L |
possibly damaging |
Het |
Cfh |
G |
T |
1: 140,026,705 (GRCm39) |
D549E |
probably damaging |
Het |
Cndp2 |
A |
G |
18: 84,693,130 (GRCm39) |
L210P |
probably damaging |
Het |
Col12a1 |
C |
A |
9: 79,581,970 (GRCm39) |
R1427L |
probably benign |
Het |
Col6a5 |
C |
T |
9: 105,822,833 (GRCm39) |
E175K |
unknown |
Het |
Dhx32 |
A |
T |
7: 133,344,470 (GRCm39) |
Y46* |
probably null |
Het |
Dnah9 |
A |
G |
11: 66,059,226 (GRCm39) |
L23P |
possibly damaging |
Het |
Eef2 |
T |
A |
10: 81,014,518 (GRCm39) |
V135E |
probably damaging |
Het |
Eef2k |
A |
T |
7: 120,491,211 (GRCm39) |
I2F |
probably damaging |
Het |
Gzmg |
C |
T |
14: 56,396,926 (GRCm39) |
|
probably null |
Het |
Hr |
T |
C |
14: 70,795,328 (GRCm39) |
I320T |
probably benign |
Het |
Hs3st2 |
A |
G |
7: 121,100,017 (GRCm39) |
I288V |
probably benign |
Het |
Ighv1-31 |
T |
C |
12: 114,793,036 (GRCm39) |
I67V |
probably benign |
Het |
Ksr2 |
T |
C |
5: 117,823,560 (GRCm39) |
C446R |
possibly damaging |
Het |
Lct |
A |
T |
1: 128,221,929 (GRCm39) |
W1537R |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,425,405 (GRCm39) |
|
probably benign |
Het |
Map3k13 |
A |
G |
16: 21,723,882 (GRCm39) |
H288R |
probably benign |
Het |
Mettl25 |
A |
G |
10: 105,668,714 (GRCm39) |
V136A |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,432,221 (GRCm39) |
|
probably null |
Het |
Ndufv3 |
A |
G |
17: 31,746,742 (GRCm39) |
K211E |
possibly damaging |
Het |
Nkiras2 |
A |
T |
11: 100,510,158 (GRCm39) |
|
probably benign |
Het |
Nudcd1 |
T |
C |
15: 44,251,971 (GRCm39) |
E396G |
probably benign |
Het |
Or4g16 |
T |
A |
2: 111,137,379 (GRCm39) |
F276L |
probably damaging |
Het |
Or52a33 |
A |
T |
7: 103,288,702 (GRCm39) |
I215K |
probably damaging |
Het |
Or5b104 |
A |
T |
19: 13,072,490 (GRCm39) |
M1K |
probably null |
Het |
Phaf1 |
T |
A |
8: 105,976,075 (GRCm39) |
I344K |
probably benign |
Het |
Sgk3 |
A |
G |
1: 9,938,699 (GRCm39) |
|
probably benign |
Het |
Sgsm3 |
A |
G |
15: 80,894,612 (GRCm39) |
Y544C |
probably damaging |
Het |
Sirt1 |
T |
C |
10: 63,161,964 (GRCm39) |
E307G |
probably damaging |
Het |
Skint6 |
T |
A |
4: 112,931,296 (GRCm39) |
Q498H |
probably benign |
Het |
Smpdl3b |
T |
C |
4: 132,473,814 (GRCm39) |
K84E |
probably benign |
Het |
Spata31h1 |
A |
G |
10: 82,123,753 (GRCm39) |
F3086L |
probably benign |
Het |
Spcs2 |
A |
G |
7: 99,493,923 (GRCm39) |
S186P |
probably benign |
Het |
Speer4e2 |
C |
T |
5: 15,026,212 (GRCm39) |
|
probably null |
Het |
Steap1 |
A |
T |
5: 5,789,940 (GRCm39) |
D24E |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,054,604 (GRCm39) |
E3328G |
possibly damaging |
Het |
Syt17 |
A |
G |
7: 118,033,054 (GRCm39) |
|
probably null |
Het |
Tdpoz3 |
T |
C |
3: 93,734,399 (GRCm39) |
V358A |
probably benign |
Het |
Tecrl |
C |
T |
5: 83,461,154 (GRCm39) |
R101Q |
probably benign |
Het |
Tmem184a |
C |
A |
5: 139,791,311 (GRCm39) |
A426S |
probably benign |
Het |
Tnc |
T |
C |
4: 63,927,087 (GRCm39) |
D813G |
probably damaging |
Het |
Top1 |
A |
G |
2: 160,547,182 (GRCm39) |
T419A |
possibly damaging |
Het |
Ttll4 |
T |
C |
1: 74,720,975 (GRCm39) |
I547T |
probably damaging |
Het |
Vmn1r193 |
T |
C |
13: 22,403,920 (GRCm39) |
D24G |
possibly damaging |
Het |
Wfs1 |
C |
T |
5: 37,124,287 (GRCm39) |
R792H |
probably damaging |
Het |
Zfp607a |
A |
G |
7: 27,577,944 (GRCm39) |
D338G |
possibly damaging |
Het |
Zfp949 |
C |
T |
9: 88,450,771 (GRCm39) |
R114C |
possibly damaging |
Het |
|
Other mutations in Krtap6-2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03375:Krtap6-2
|
APN |
16 |
89,216,644 (GRCm39) |
missense |
unknown |
|
R1566:Krtap6-2
|
UTSW |
16 |
89,216,626 (GRCm39) |
missense |
unknown |
|
R4896:Krtap6-2
|
UTSW |
16 |
89,216,806 (GRCm39) |
missense |
unknown |
|
R5857:Krtap6-2
|
UTSW |
16 |
89,216,530 (GRCm39) |
missense |
unknown |
|
R6390:Krtap6-2
|
UTSW |
16 |
89,216,834 (GRCm39) |
nonsense |
probably null |
|
R6958:Krtap6-2
|
UTSW |
16 |
89,216,698 (GRCm39) |
missense |
unknown |
|
R7432:Krtap6-2
|
UTSW |
16 |
89,216,761 (GRCm39) |
missense |
unknown |
|
R7454:Krtap6-2
|
UTSW |
16 |
89,216,800 (GRCm39) |
missense |
unknown |
|
R7780:Krtap6-2
|
UTSW |
16 |
89,216,510 (GRCm39) |
nonsense |
probably null |
|
R7981:Krtap6-2
|
UTSW |
16 |
89,216,562 (GRCm39) |
missense |
unknown |
|
R9113:Krtap6-2
|
UTSW |
16 |
89,216,613 (GRCm39) |
small deletion |
probably benign |
|
R9562:Krtap6-2
|
UTSW |
16 |
89,216,722 (GRCm39) |
missense |
unknown |
|
R9565:Krtap6-2
|
UTSW |
16 |
89,216,722 (GRCm39) |
missense |
unknown |
|
R9747:Krtap6-2
|
UTSW |
16 |
89,216,776 (GRCm39) |
missense |
unknown |
|
R9757:Krtap6-2
|
UTSW |
16 |
89,216,958 (GRCm39) |
missense |
unknown |
|
R9762:Krtap6-2
|
UTSW |
16 |
89,216,763 (GRCm39) |
missense |
unknown |
|
|