Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd10 |
A |
G |
16: 45,552,303 (GRCm39) |
M190T |
probably benign |
Het |
Abhd5 |
A |
G |
9: 122,207,005 (GRCm39) |
Y250C |
probably damaging |
Het |
Ace2 |
A |
G |
X: 162,923,728 (GRCm39) |
N24S |
probably benign |
Het |
Adamtsl2 |
A |
G |
2: 26,985,570 (GRCm39) |
M485V |
probably benign |
Het |
Adamtsl4 |
G |
T |
3: 95,588,357 (GRCm39) |
P577H |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Apc |
T |
C |
18: 34,402,282 (GRCm39) |
Y141H |
probably damaging |
Het |
Arsi |
A |
T |
18: 61,049,443 (GRCm39) |
T109S |
possibly damaging |
Het |
Asb3 |
G |
A |
11: 31,031,355 (GRCm39) |
|
probably null |
Het |
Atm |
T |
C |
9: 53,355,297 (GRCm39) |
D2899G |
probably damaging |
Het |
Bcas3 |
G |
A |
11: 85,348,704 (GRCm39) |
V199I |
probably damaging |
Het |
Bub1 |
T |
C |
2: 127,661,255 (GRCm39) |
K279E |
probably damaging |
Het |
C3 |
A |
T |
17: 57,530,974 (GRCm39) |
|
probably null |
Het |
Cadm2 |
A |
T |
16: 66,528,357 (GRCm39) |
I326N |
probably benign |
Het |
Ccr3 |
T |
C |
9: 123,829,336 (GRCm39) |
S224P |
possibly damaging |
Het |
Cdhr4 |
A |
G |
9: 107,874,843 (GRCm39) |
T638A |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,263,677 (GRCm39) |
I4V |
probably benign |
Het |
Csf2rb2 |
A |
T |
15: 78,176,744 (GRCm39) |
V216E |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,868,257 (GRCm39) |
D754E |
possibly damaging |
Het |
Dnaaf1 |
T |
C |
8: 120,309,471 (GRCm39) |
|
probably null |
Het |
Dnah11 |
A |
C |
12: 117,984,088 (GRCm39) |
Y2466D |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
E2f7 |
T |
C |
10: 110,616,763 (GRCm39) |
Y668H |
probably benign |
Het |
Ehmt1 |
A |
T |
2: 24,727,630 (GRCm39) |
S735T |
probably damaging |
Het |
Eomes |
T |
C |
9: 118,307,920 (GRCm39) |
F65L |
probably benign |
Het |
Ercc6l2 |
T |
C |
13: 64,019,802 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
A |
T |
5: 110,526,300 (GRCm39) |
L439Q |
probably damaging |
Het |
Fyco1 |
C |
T |
9: 123,626,581 (GRCm39) |
|
probably null |
Het |
Gfm2 |
A |
G |
13: 97,291,950 (GRCm39) |
T229A |
probably benign |
Het |
Gm7735 |
G |
A |
16: 88,966,433 (GRCm39) |
G19D |
unknown |
Het |
Gnpda1 |
T |
C |
18: 38,466,243 (GRCm39) |
|
probably null |
Het |
Gpr6 |
T |
A |
10: 40,946,649 (GRCm39) |
Y311F |
possibly damaging |
Het |
Gprc6a |
A |
T |
10: 51,491,304 (GRCm39) |
V744E |
probably damaging |
Het |
Grin3a |
C |
T |
4: 49,665,510 (GRCm39) |
D1042N |
possibly damaging |
Het |
Gstm3 |
A |
G |
3: 107,873,450 (GRCm39) |
C174R |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,471,487 (GRCm39) |
E2670G |
possibly damaging |
Het |
Hsd3b6 |
A |
T |
3: 98,713,503 (GRCm39) |
Y265* |
probably null |
Het |
Hus1 |
T |
A |
11: 8,961,110 (GRCm39) |
M1L |
probably null |
Het |
Idi2l |
G |
A |
13: 8,991,764 (GRCm39) |
P221S |
possibly damaging |
Het |
Ifi213 |
T |
G |
1: 173,396,668 (GRCm39) |
|
probably null |
Het |
Igf2r |
A |
C |
17: 12,917,138 (GRCm39) |
N1587K |
probably benign |
Het |
Ints1 |
A |
T |
5: 139,753,505 (GRCm39) |
V709E |
probably damaging |
Het |
Ints8 |
C |
A |
4: 11,235,552 (GRCm39) |
R359L |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lrp1b |
C |
T |
2: 41,000,769 (GRCm39) |
E2152K |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,336,968 (GRCm39) |
V1268D |
possibly damaging |
Het |
Mpo |
T |
C |
11: 87,686,901 (GRCm39) |
Y177H |
probably damaging |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Mprip |
A |
G |
11: 59,660,717 (GRCm39) |
K2166R |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,382,636 (GRCm39) |
Y1544H |
probably damaging |
Het |
Neu1 |
G |
A |
17: 35,153,374 (GRCm39) |
R299Q |
probably benign |
Het |
Nfxl1 |
C |
A |
5: 72,671,675 (GRCm39) |
|
probably null |
Het |
Nrp2 |
T |
A |
1: 62,783,436 (GRCm39) |
I179N |
probably damaging |
Het |
Nup153 |
A |
G |
13: 46,846,986 (GRCm39) |
|
probably null |
Het |
Or1j4 |
C |
A |
2: 36,740,355 (GRCm39) |
A99E |
possibly damaging |
Het |
Or2g7 |
G |
T |
17: 38,378,746 (GRCm39) |
R228L |
possibly damaging |
Het |
Or5p54 |
A |
T |
7: 107,554,709 (GRCm39) |
H287L |
probably benign |
Het |
Or6c6c |
A |
T |
10: 129,541,490 (GRCm39) |
I248L |
probably benign |
Het |
Or8g27 |
A |
T |
9: 39,129,318 (GRCm39) |
I222F |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,124,774 (GRCm39) |
D300E |
probably damaging |
Het |
Pkhd1 |
C |
A |
1: 20,623,798 (GRCm39) |
G766* |
probably null |
Het |
Plagl1 |
A |
C |
10: 13,004,391 (GRCm39) |
|
probably benign |
Het |
Prkcq |
A |
T |
2: 11,237,380 (GRCm39) |
Y53F |
probably damaging |
Het |
Psg18 |
T |
C |
7: 18,084,799 (GRCm39) |
E99G |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,033,476 (GRCm39) |
H1921Q |
probably damaging |
Het |
Rcc1l |
A |
G |
5: 134,184,629 (GRCm39) |
V391A |
probably benign |
Het |
Sdr42e1 |
C |
T |
8: 118,391,763 (GRCm39) |
V11I |
probably damaging |
Het |
Slc12a3 |
C |
A |
8: 95,067,158 (GRCm39) |
N404K |
probably damaging |
Het |
Slc38a4 |
T |
C |
15: 96,906,878 (GRCm39) |
M287V |
probably benign |
Het |
Slc6a8 |
A |
T |
X: 72,720,492 (GRCm39) |
I96F |
possibly damaging |
Het |
Smyd2 |
A |
G |
1: 189,629,623 (GRCm39) |
S136P |
probably damaging |
Het |
Sox11 |
A |
G |
12: 27,391,702 (GRCm39) |
Y236H |
probably damaging |
Het |
Tbc1d2 |
G |
A |
4: 46,637,652 (GRCm39) |
P198L |
possibly damaging |
Het |
Tcof1 |
G |
T |
18: 60,968,845 (GRCm39) |
A256E |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,555,497 (GRCm39) |
Y2726C |
probably damaging |
Het |
Tnfsf14 |
T |
A |
17: 57,497,867 (GRCm39) |
R122W |
probably damaging |
Het |
Tril |
T |
C |
6: 53,796,068 (GRCm39) |
T385A |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,762,684 (GRCm39) |
T2386A |
probably benign |
Het |
Tspear |
T |
A |
10: 77,706,253 (GRCm39) |
L341H |
possibly damaging |
Het |
Uba7 |
A |
G |
9: 107,856,487 (GRCm39) |
M595V |
probably benign |
Het |
Usp43 |
GC |
G |
11: 67,746,566 (GRCm39) |
|
probably null |
Het |
Utrn |
C |
A |
10: 12,312,108 (GRCm39) |
D616Y |
probably damaging |
Het |
Vmn2r69 |
T |
C |
7: 85,059,404 (GRCm39) |
I502V |
probably benign |
Het |
Vps13d |
C |
A |
4: 144,801,617 (GRCm39) |
G419C |
probably damaging |
Het |
Zbtb25 |
A |
T |
12: 76,396,880 (GRCm39) |
M114K |
probably benign |
Het |
Zcchc4 |
A |
G |
5: 52,953,474 (GRCm39) |
Y161C |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,808,593 (GRCm39) |
F1484I |
possibly damaging |
Het |
Zfp326 |
A |
G |
5: 106,062,646 (GRCm39) |
|
probably benign |
Het |
Zfp395 |
T |
A |
14: 65,630,565 (GRCm39) |
S372T |
probably benign |
Het |
Zfp423 |
T |
A |
8: 88,507,806 (GRCm39) |
E825V |
possibly damaging |
Het |
Zfp445 |
A |
T |
9: 122,681,305 (GRCm39) |
Y879N |
probably benign |
Het |
Zfp451 |
A |
G |
1: 33,818,248 (GRCm39) |
I77T |
possibly damaging |
Het |
Zfp85 |
A |
T |
13: 67,897,003 (GRCm39) |
S356R |
probably benign |
Het |
|
Other mutations in Cabcoco1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Cabcoco1
|
APN |
10 |
68,377,635 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00644:Cabcoco1
|
APN |
10 |
68,369,730 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02253:Cabcoco1
|
APN |
10 |
68,272,107 (GRCm39) |
splice site |
probably null |
|
R0060:Cabcoco1
|
UTSW |
10 |
68,369,692 (GRCm39) |
splice site |
probably null |
|
R0629:Cabcoco1
|
UTSW |
10 |
68,352,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R0968:Cabcoco1
|
UTSW |
10 |
68,272,202 (GRCm39) |
missense |
probably benign |
0.00 |
R2154:Cabcoco1
|
UTSW |
10 |
68,267,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R3076:Cabcoco1
|
UTSW |
10 |
68,361,475 (GRCm39) |
missense |
possibly damaging |
0.62 |
R3077:Cabcoco1
|
UTSW |
10 |
68,361,475 (GRCm39) |
missense |
possibly damaging |
0.62 |
R3872:Cabcoco1
|
UTSW |
10 |
68,352,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Cabcoco1
|
UTSW |
10 |
68,377,599 (GRCm39) |
missense |
probably benign |
|
R6299:Cabcoco1
|
UTSW |
10 |
68,272,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R6460:Cabcoco1
|
UTSW |
10 |
68,352,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R7127:Cabcoco1
|
UTSW |
10 |
68,272,160 (GRCm39) |
missense |
probably benign |
0.26 |
R8509:Cabcoco1
|
UTSW |
10 |
68,267,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R8719:Cabcoco1
|
UTSW |
10 |
68,272,671 (GRCm39) |
critical splice donor site |
probably benign |
|
R8911:Cabcoco1
|
UTSW |
10 |
68,377,584 (GRCm39) |
missense |
probably benign |
|
R9180:Cabcoco1
|
UTSW |
10 |
68,272,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Cabcoco1
|
UTSW |
10 |
68,272,725 (GRCm39) |
missense |
possibly damaging |
0.50 |
|