Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankfy1 |
G |
A |
11: 72,641,005 (GRCm39) |
|
probably null |
Het |
Arid1b |
A |
G |
17: 5,385,262 (GRCm39) |
Y1340C |
probably damaging |
Het |
Bcl2 |
C |
A |
1: 106,640,508 (GRCm39) |
A35S |
probably benign |
Het |
Brf2 |
A |
T |
8: 27,614,623 (GRCm39) |
S188T |
probably benign |
Het |
Carmil1 |
C |
A |
13: 24,460,516 (GRCm39) |
G21V |
probably damaging |
Het |
Cavin4 |
T |
C |
4: 48,663,956 (GRCm39) |
V112A |
probably benign |
Het |
Cd300lf |
T |
C |
11: 115,007,858 (GRCm39) |
E319G |
probably benign |
Het |
Cd44 |
A |
T |
2: 102,661,832 (GRCm39) |
D587E |
possibly damaging |
Het |
Cfap53 |
A |
T |
18: 74,438,040 (GRCm39) |
T239S |
possibly damaging |
Het |
Cma2 |
A |
C |
14: 56,211,256 (GRCm39) |
I239L |
probably damaging |
Het |
Cnot1 |
A |
T |
8: 96,482,854 (GRCm39) |
M733K |
probably benign |
Het |
Cyp4f40 |
G |
A |
17: 32,890,158 (GRCm39) |
R276H |
probably benign |
Het |
Cytip |
A |
T |
2: 58,041,141 (GRCm39) |
F88L |
probably damaging |
Het |
Dnaaf2 |
T |
C |
12: 69,244,776 (GRCm39) |
N95S |
probably damaging |
Het |
Dnah5 |
C |
A |
15: 28,328,025 (GRCm39) |
T2133K |
possibly damaging |
Het |
Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 72,684,217 (GRCm39) |
|
probably benign |
Het |
Elapor2 |
G |
A |
5: 9,490,859 (GRCm39) |
G623D |
probably damaging |
Het |
Epn2 |
A |
T |
11: 61,436,988 (GRCm39) |
S195T |
probably benign |
Het |
Exoc3 |
A |
T |
13: 74,330,285 (GRCm39) |
Y521N |
possibly damaging |
Het |
Fbxo10 |
C |
A |
4: 45,058,970 (GRCm39) |
V256L |
probably damaging |
Het |
Fis1 |
A |
T |
5: 136,991,907 (GRCm39) |
T34S |
probably benign |
Het |
Gm10309 |
A |
T |
17: 86,806,161 (GRCm39) |
C118S |
unknown |
Het |
Grip1 |
G |
A |
10: 119,874,569 (GRCm39) |
E778K |
possibly damaging |
Het |
Hook1 |
T |
A |
4: 95,891,808 (GRCm39) |
V340E |
probably damaging |
Het |
Ifng |
C |
A |
10: 118,277,128 (GRCm39) |
H23Q |
probably benign |
Het |
Lect2 |
C |
T |
13: 56,694,660 (GRCm39) |
E32K |
probably benign |
Het |
Lrp1 |
T |
G |
10: 127,388,733 (GRCm39) |
T3239P |
probably damaging |
Het |
Lrrc14b |
T |
A |
13: 74,511,996 (GRCm39) |
Y28F |
probably benign |
Het |
Maml3 |
A |
T |
3: 51,763,791 (GRCm39) |
V391E |
possibly damaging |
Het |
Map3k8 |
C |
T |
18: 4,349,141 (GRCm39) |
R59H |
probably benign |
Het |
Med1 |
G |
T |
11: 98,070,884 (GRCm39) |
L120I |
possibly damaging |
Het |
Muc5b |
C |
A |
7: 141,421,648 (GRCm39) |
H4349N |
possibly damaging |
Het |
Myo1h |
C |
T |
5: 114,499,154 (GRCm39) |
P110S |
probably benign |
Het |
Nol10 |
T |
G |
12: 17,466,144 (GRCm39) |
I513S |
possibly damaging |
Het |
Nphs1 |
C |
T |
7: 30,180,875 (GRCm39) |
S1093F |
probably benign |
Het |
Or12e10 |
A |
T |
2: 87,641,097 (GRCm39) |
N311I |
probably damaging |
Het |
Or4b1b |
T |
C |
2: 90,111,991 (GRCm39) |
*309W |
probably null |
Het |
Or56b1b |
A |
T |
7: 108,164,334 (GRCm39) |
S223T |
possibly damaging |
Het |
Or5p72 |
A |
T |
7: 108,022,416 (GRCm39) |
T213S |
possibly damaging |
Het |
Or5w8 |
A |
T |
2: 87,688,040 (GRCm39) |
I174F |
probably damaging |
Het |
Pcdh17 |
A |
T |
14: 84,685,402 (GRCm39) |
Y623F |
possibly damaging |
Het |
Pdzd8 |
T |
A |
19: 59,289,826 (GRCm39) |
I525F |
probably benign |
Het |
Peak1 |
G |
T |
9: 56,113,917 (GRCm39) |
Q1675K |
probably benign |
Het |
Perm1 |
T |
C |
4: 156,302,290 (GRCm39) |
V278A |
probably benign |
Het |
Ppp2r5d |
G |
A |
17: 46,998,527 (GRCm39) |
R115C |
probably damaging |
Het |
Rnf169 |
A |
T |
7: 99,574,690 (GRCm39) |
L635Q |
probably damaging |
Het |
Sacs |
A |
G |
14: 61,440,692 (GRCm39) |
T913A |
probably benign |
Het |
Sh3bp1 |
A |
T |
15: 78,788,673 (GRCm39) |
I233F |
possibly damaging |
Het |
Skint9 |
T |
G |
4: 112,276,346 (GRCm39) |
L8F |
probably benign |
Het |
Slc1a4 |
A |
T |
11: 20,258,041 (GRCm39) |
N360K |
probably damaging |
Het |
Slc22a16 |
T |
A |
10: 40,460,865 (GRCm39) |
Y243* |
probably null |
Het |
Slc22a19 |
C |
A |
19: 7,659,219 (GRCm39) |
|
probably null |
Het |
Smarcal1 |
T |
C |
1: 72,671,999 (GRCm39) |
I840T |
possibly damaging |
Het |
Spata13 |
A |
G |
14: 60,991,303 (GRCm39) |
K1019E |
possibly damaging |
Het |
Steap1 |
A |
G |
5: 5,790,700 (GRCm39) |
S83P |
possibly damaging |
Het |
Synj2bp |
T |
C |
12: 81,551,382 (GRCm39) |
H78R |
probably damaging |
Het |
Tcstv7a |
T |
A |
13: 120,289,924 (GRCm39) |
I91F |
probably benign |
Het |
Tjp3 |
T |
C |
10: 81,113,833 (GRCm39) |
E475G |
probably damaging |
Het |
Top3a |
A |
G |
11: 60,644,768 (GRCm39) |
V312A |
probably benign |
Het |
Traip |
C |
A |
9: 107,833,099 (GRCm39) |
T45N |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,573,691 (GRCm39) |
Y25734C |
probably damaging |
Het |
Unc79 |
T |
A |
12: 102,977,495 (GRCm39) |
V166D |
probably damaging |
Het |
Urgcp |
C |
A |
11: 5,667,622 (GRCm39) |
V282F |
possibly damaging |
Het |
Vmn1r184 |
G |
A |
7: 25,966,734 (GRCm39) |
S160N |
probably benign |
Het |
Wdfy3 |
T |
C |
5: 102,033,059 (GRCm39) |
D2231G |
probably damaging |
Het |
Zan |
C |
T |
5: 137,401,323 (GRCm39) |
G4132D |
unknown |
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 |
R7599:Cyp2f2
|
UTSW |
7 |
26,830,784 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|