Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts3 |
T |
C |
5: 90,009,256 (GRCm39) |
S136G |
probably benign |
Het |
Apba3 |
T |
A |
10: 81,108,180 (GRCm39) |
N445K |
probably damaging |
Het |
Aqp6 |
A |
G |
15: 99,501,652 (GRCm39) |
K237E |
possibly damaging |
Het |
Arhgap23 |
A |
G |
11: 97,391,169 (GRCm39) |
T1229A |
probably benign |
Het |
Bpifb1 |
T |
C |
2: 154,056,071 (GRCm39) |
I379T |
probably damaging |
Het |
Bpnt2 |
G |
A |
4: 4,778,207 (GRCm39) |
T177I |
probably damaging |
Het |
Ccdc169 |
A |
G |
3: 55,047,530 (GRCm39) |
D7G |
probably damaging |
Het |
Daam2 |
T |
A |
17: 49,787,755 (GRCm39) |
K453* |
probably null |
Het |
Dennd4c |
T |
C |
4: 86,729,849 (GRCm39) |
L817P |
probably damaging |
Het |
Efcab6 |
T |
A |
15: 83,755,189 (GRCm39) |
R1376W |
probably damaging |
Het |
Esrra |
G |
T |
19: 6,891,214 (GRCm39) |
A182E |
possibly damaging |
Het |
Fam234b |
T |
A |
6: 135,203,874 (GRCm39) |
V392E |
probably damaging |
Het |
Fanca |
A |
G |
8: 123,997,999 (GRCm39) |
V1229A |
probably benign |
Het |
Fdps |
G |
T |
3: 89,006,693 (GRCm39) |
Q66K |
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,499,438 (GRCm39) |
D1269E |
probably benign |
Het |
Foxred1 |
G |
A |
9: 35,116,932 (GRCm39) |
R353W |
probably damaging |
Het |
Gabrg2 |
C |
T |
11: 41,858,451 (GRCm39) |
V226I |
possibly damaging |
Het |
Gcnt2 |
C |
A |
13: 41,014,343 (GRCm39) |
C171* |
probably null |
Het |
Glyat |
C |
A |
19: 12,617,172 (GRCm39) |
A8E |
probably damaging |
Het |
Golgb1 |
C |
A |
16: 36,695,758 (GRCm39) |
R86S |
unknown |
Het |
Hc |
T |
A |
2: 34,940,431 (GRCm39) |
T136S |
probably damaging |
Het |
Hdac1 |
G |
T |
4: 129,411,259 (GRCm39) |
S421* |
probably null |
Het |
Hmcn2 |
G |
T |
2: 31,246,298 (GRCm39) |
A756S |
possibly damaging |
Het |
Igkv8-26 |
A |
G |
6: 70,170,571 (GRCm39) |
N54S |
probably benign |
Het |
Itgae |
T |
A |
11: 73,012,786 (GRCm39) |
V706E |
possibly damaging |
Het |
Itgax |
G |
A |
7: 127,747,262 (GRCm39) |
V992M |
probably damaging |
Het |
Klk10 |
A |
G |
7: 43,433,851 (GRCm39) |
D221G |
probably benign |
Het |
Klkb1 |
T |
C |
8: 45,731,150 (GRCm39) |
I205V |
probably benign |
Het |
Kpna2 |
T |
C |
11: 106,889,583 (GRCm39) |
N8S |
probably null |
Het |
L3mbtl1 |
A |
C |
2: 162,806,434 (GRCm39) |
T442P |
possibly damaging |
Het |
Lrp1b |
C |
T |
2: 40,551,561 (GRCm39) |
C4181Y |
|
Het |
Mcat |
T |
C |
15: 83,431,872 (GRCm39) |
Y332C |
probably damaging |
Het |
Mecom |
T |
C |
3: 30,010,534 (GRCm39) |
D648G |
probably damaging |
Het |
Mesp2 |
A |
T |
7: 79,460,717 (GRCm39) |
D14V |
probably damaging |
Het |
Mlh3 |
A |
T |
12: 85,314,973 (GRCm39) |
Y404* |
probably null |
Het |
Mterf3 |
A |
T |
13: 67,065,212 (GRCm39) |
F230I |
probably damaging |
Het |
Nrxn3 |
T |
C |
12: 89,478,832 (GRCm39) |
V602A |
probably benign |
Het |
Or4a74 |
T |
A |
2: 89,439,571 (GRCm39) |
I292F |
possibly damaging |
Het |
Plekhg6 |
A |
G |
6: 125,351,623 (GRCm39) |
F209L |
probably damaging |
Het |
Pmp22 |
C |
A |
11: 63,049,174 (GRCm39) |
A139D |
probably damaging |
Het |
Polr2e |
T |
C |
10: 79,874,404 (GRCm39) |
D34G |
possibly damaging |
Het |
Ppard |
T |
A |
17: 28,516,091 (GRCm39) |
L105H |
probably damaging |
Het |
Ptpn14 |
T |
A |
1: 189,582,942 (GRCm39) |
D596E |
probably benign |
Het |
Ptprz1 |
C |
T |
6: 23,002,518 (GRCm39) |
A1536V |
not run |
Het |
Qng1 |
T |
A |
13: 58,529,649 (GRCm39) |
H321L |
probably damaging |
Het |
Rabgap1 |
TGGGG |
TGGG |
2: 37,392,908 (GRCm39) |
|
probably null |
Het |
Retreg1 |
T |
A |
15: 25,971,727 (GRCm39) |
D222E |
probably benign |
Het |
Rmnd1 |
T |
C |
10: 4,363,404 (GRCm39) |
K282R |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Sall3 |
C |
T |
18: 81,015,267 (GRCm39) |
R887H |
possibly damaging |
Het |
Samd3 |
A |
G |
10: 26,139,711 (GRCm39) |
D281G |
probably benign |
Het |
Scube1 |
T |
A |
15: 83,497,653 (GRCm39) |
D766V |
probably damaging |
Het |
Sec24b |
TGC |
TGCAGC |
3: 129,834,460 (GRCm39) |
|
probably benign |
Het |
Slc2a2 |
A |
G |
3: 28,752,166 (GRCm39) |
M1V |
probably null |
Het |
Slc39a2 |
A |
T |
14: 52,132,488 (GRCm39) |
T144S |
probably benign |
Het |
Slc5a9 |
T |
C |
4: 111,734,937 (GRCm39) |
H619R |
probably benign |
Het |
Slco4a1 |
T |
C |
2: 180,113,048 (GRCm39) |
F427L |
probably benign |
Het |
Snapc3 |
C |
A |
4: 83,336,073 (GRCm39) |
Y28* |
probably null |
Het |
St3gal6 |
C |
T |
16: 58,293,800 (GRCm39) |
R243H |
probably benign |
Het |
Stat2 |
T |
A |
10: 128,113,066 (GRCm39) |
N119K |
possibly damaging |
Het |
Syne2 |
G |
C |
12: 76,013,145 (GRCm39) |
V2779L |
probably benign |
Het |
Tacc1 |
T |
A |
8: 25,691,301 (GRCm39) |
M1L |
probably damaging |
Het |
Tbc1d32 |
A |
T |
10: 56,027,929 (GRCm39) |
F724L |
possibly damaging |
Het |
Ttc23l |
A |
G |
15: 10,533,766 (GRCm39) |
I259T |
possibly damaging |
Het |
Ucn2 |
T |
C |
9: 108,815,292 (GRCm39) |
I18T |
probably benign |
Het |
Wdr35 |
G |
C |
12: 9,074,886 (GRCm39) |
A1000P |
probably benign |
Het |
Wnk1 |
C |
A |
6: 119,906,789 (GRCm39) |
C244F |
possibly damaging |
Het |
Zeb2 |
T |
G |
2: 44,884,625 (GRCm39) |
D1022A |
probably damaging |
Het |
Zfp26 |
A |
T |
9: 20,349,129 (GRCm39) |
H478Q |
probably damaging |
Het |
Zfp410 |
A |
G |
12: 84,378,630 (GRCm39) |
K265R |
probably benign |
Het |
Zfp575 |
T |
C |
7: 24,286,093 (GRCm39) |
D21G |
probably benign |
Het |
|
Other mutations in Cyp2f2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00911:Cyp2f2
|
APN |
7 |
26,821,354 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00953:Cyp2f2
|
APN |
7 |
26,829,242 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL01781:Cyp2f2
|
APN |
7 |
26,829,846 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02817:Cyp2f2
|
APN |
7 |
26,828,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Cyp2f2
|
APN |
7 |
26,831,996 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0464:Cyp2f2
|
UTSW |
7 |
26,831,962 (GRCm39) |
missense |
probably benign |
0.00 |
R1481:Cyp2f2
|
UTSW |
7 |
26,821,302 (GRCm39) |
missense |
probably benign |
0.00 |
R1635:Cyp2f2
|
UTSW |
7 |
26,829,149 (GRCm39) |
missense |
probably benign |
0.11 |
R1826:Cyp2f2
|
UTSW |
7 |
26,831,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R1989:Cyp2f2
|
UTSW |
7 |
26,828,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R5098:Cyp2f2
|
UTSW |
7 |
26,829,304 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6305:Cyp2f2
|
UTSW |
7 |
26,828,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R6472:Cyp2f2
|
UTSW |
7 |
26,828,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Cyp2f2
|
UTSW |
7 |
26,831,993 (GRCm39) |
missense |
probably benign |
0.00 |
R7814:Cyp2f2
|
UTSW |
7 |
26,828,678 (GRCm39) |
missense |
probably benign |
0.00 |
R7823:Cyp2f2
|
UTSW |
7 |
26,828,678 (GRCm39) |
missense |
probably benign |
0.00 |
R7824:Cyp2f2
|
UTSW |
7 |
26,828,678 (GRCm39) |
missense |
probably benign |
0.00 |
R7825:Cyp2f2
|
UTSW |
7 |
26,828,678 (GRCm39) |
missense |
probably benign |
0.00 |
R8141:Cyp2f2
|
UTSW |
7 |
26,828,678 (GRCm39) |
missense |
probably benign |
0.00 |
R8142:Cyp2f2
|
UTSW |
7 |
26,828,678 (GRCm39) |
missense |
probably benign |
0.00 |
R8143:Cyp2f2
|
UTSW |
7 |
26,828,678 (GRCm39) |
missense |
probably benign |
0.00 |
R8351:Cyp2f2
|
UTSW |
7 |
26,821,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R8809:Cyp2f2
|
UTSW |
7 |
26,831,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R9095:Cyp2f2
|
UTSW |
7 |
26,830,667 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9548:Cyp2f2
|
UTSW |
7 |
26,829,170 (GRCm39) |
missense |
probably benign |
0.45 |
R9726:Cyp2f2
|
UTSW |
7 |
26,821,411 (GRCm39) |
missense |
probably damaging |
0.99 |
X0064:Cyp2f2
|
UTSW |
7 |
26,832,709 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cyp2f2
|
UTSW |
7 |
26,821,332 (GRCm39) |
missense |
possibly damaging |
0.52 |
|