Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl3 |
A |
T |
6: 34,780,435 (GRCm39) |
K469N |
probably damaging |
Het |
Aldh2 |
A |
G |
5: 121,718,787 (GRCm39) |
|
probably benign |
Het |
Ankfy1 |
T |
C |
11: 72,619,580 (GRCm39) |
|
probably benign |
Het |
Ankhd1 |
C |
T |
18: 36,711,827 (GRCm39) |
T209I |
probably benign |
Het |
Aox3 |
G |
A |
1: 58,205,046 (GRCm39) |
V754I |
probably benign |
Het |
Arfgef3 |
C |
T |
10: 18,476,292 (GRCm39) |
R1509H |
probably damaging |
Het |
Ccdc157 |
A |
G |
11: 4,101,832 (GRCm39) |
S30P |
probably damaging |
Het |
Cept1 |
T |
A |
3: 106,411,866 (GRCm39) |
E369D |
probably damaging |
Het |
Clcnka |
T |
C |
4: 141,121,798 (GRCm39) |
Y236C |
probably damaging |
Het |
Ddx42 |
A |
T |
11: 106,138,353 (GRCm39) |
L717F |
probably benign |
Het |
Dnah11 |
A |
T |
12: 117,994,026 (GRCm39) |
I2340N |
probably damaging |
Het |
Dsel |
T |
C |
1: 111,787,868 (GRCm39) |
E889G |
probably damaging |
Het |
Fasn |
T |
C |
11: 120,703,552 (GRCm39) |
Y1560C |
probably damaging |
Het |
Gm21970 |
T |
A |
16: 91,190,726 (GRCm39) |
S110T |
possibly damaging |
Het |
Gm826 |
T |
A |
2: 160,169,035 (GRCm39) |
R91S |
unknown |
Het |
Lrrn3 |
A |
G |
12: 41,504,020 (GRCm39) |
L99S |
probably damaging |
Het |
Megf8 |
T |
A |
7: 25,046,773 (GRCm39) |
M1552K |
possibly damaging |
Het |
Mgll |
G |
T |
6: 88,800,173 (GRCm39) |
V191F |
probably damaging |
Het |
Nkapd1 |
T |
C |
9: 50,523,698 (GRCm39) |
N50S |
possibly damaging |
Het |
Nol8 |
C |
A |
13: 49,817,557 (GRCm39) |
H778N |
probably damaging |
Het |
Or1e26 |
T |
A |
11: 73,480,268 (GRCm39) |
T99S |
probably benign |
Het |
Or5b116 |
A |
C |
19: 13,422,807 (GRCm39) |
T144P |
possibly damaging |
Het |
Or8g30 |
A |
T |
9: 39,230,277 (GRCm39) |
M211K |
probably benign |
Het |
Or8k40 |
A |
T |
2: 86,584,366 (GRCm39) |
S239T |
probably damaging |
Het |
Pfkfb3 |
A |
T |
2: 11,506,474 (GRCm39) |
I13N |
probably damaging |
Het |
Pim1 |
T |
A |
17: 29,710,740 (GRCm39) |
D114E |
possibly damaging |
Het |
Pkd1 |
T |
C |
17: 24,792,792 (GRCm39) |
L1493P |
probably damaging |
Het |
Plb1 |
A |
T |
5: 32,502,259 (GRCm39) |
|
probably benign |
Het |
Plch1 |
A |
T |
3: 63,610,015 (GRCm39) |
Y872* |
probably null |
Het |
Rictor |
A |
G |
15: 6,819,079 (GRCm39) |
D1434G |
probably benign |
Het |
Rptor |
G |
A |
11: 119,615,971 (GRCm39) |
G162R |
probably damaging |
Het |
Serping1 |
T |
C |
2: 84,596,162 (GRCm39) |
D424G |
probably damaging |
Het |
Slit2 |
A |
G |
5: 48,377,395 (GRCm39) |
I475V |
possibly damaging |
Het |
Snx31 |
G |
T |
15: 36,525,833 (GRCm39) |
Q289K |
probably benign |
Het |
Tbc1d13 |
G |
A |
2: 30,037,379 (GRCm39) |
A254T |
probably damaging |
Het |
Tek |
T |
C |
4: 94,740,002 (GRCm39) |
I750T |
probably damaging |
Het |
Tet2 |
A |
T |
3: 133,177,159 (GRCm39) |
L1296* |
probably null |
Het |
Tmem145 |
T |
A |
7: 25,014,304 (GRCm39) |
F459I |
probably damaging |
Het |
Uba5 |
A |
T |
9: 103,931,328 (GRCm39) |
V247D |
possibly damaging |
Het |
Vmn1r83 |
T |
C |
7: 12,055,617 (GRCm39) |
M147V |
probably benign |
Het |
Vwde |
T |
C |
6: 13,187,138 (GRCm39) |
D783G |
probably damaging |
Het |
Zfp609 |
A |
G |
9: 65,608,287 (GRCm39) |
S1198P |
probably benign |
Het |
|
Other mutations in Fermt2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01301:Fermt2
|
APN |
14 |
45,702,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01859:Fermt2
|
APN |
14 |
45,697,413 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02719:Fermt2
|
APN |
14 |
45,742,113 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU18:Fermt2
|
UTSW |
14 |
45,702,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Fermt2
|
UTSW |
14 |
45,702,279 (GRCm39) |
missense |
probably damaging |
0.98 |
R0671:Fermt2
|
UTSW |
14 |
45,706,776 (GRCm39) |
missense |
probably benign |
0.09 |
R1172:Fermt2
|
UTSW |
14 |
45,697,425 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1227:Fermt2
|
UTSW |
14 |
45,697,447 (GRCm39) |
missense |
probably benign |
0.19 |
R1480:Fermt2
|
UTSW |
14 |
45,699,244 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2219:Fermt2
|
UTSW |
14 |
45,713,354 (GRCm39) |
missense |
probably benign |
|
R2937:Fermt2
|
UTSW |
14 |
45,741,948 (GRCm39) |
splice site |
probably null |
|
R4765:Fermt2
|
UTSW |
14 |
45,699,693 (GRCm39) |
missense |
probably benign |
0.01 |
R5921:Fermt2
|
UTSW |
14 |
45,702,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Fermt2
|
UTSW |
14 |
45,697,338 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6216:Fermt2
|
UTSW |
14 |
45,697,338 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6254:Fermt2
|
UTSW |
14 |
45,713,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6964:Fermt2
|
UTSW |
14 |
45,702,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R7574:Fermt2
|
UTSW |
14 |
45,706,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7917:Fermt2
|
UTSW |
14 |
45,699,318 (GRCm39) |
missense |
probably damaging |
0.98 |
R8692:Fermt2
|
UTSW |
14 |
45,742,099 (GRCm39) |
nonsense |
probably null |
|
R8861:Fermt2
|
UTSW |
14 |
45,697,466 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8910:Fermt2
|
UTSW |
14 |
45,702,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R8986:Fermt2
|
UTSW |
14 |
45,742,023 (GRCm39) |
missense |
probably benign |
|
|