Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
CGGG |
CGGGGGG |
15: 76,833,863 (GRCm39) |
|
probably benign |
Het |
Acad8 |
T |
C |
9: 26,890,481 (GRCm39) |
I276V |
probably benign |
Het |
Adgrg7 |
A |
T |
16: 56,550,661 (GRCm39) |
Y684N |
probably damaging |
Het |
Akap9 |
C |
T |
5: 4,042,077 (GRCm39) |
T1370I |
possibly damaging |
Het |
Akna |
C |
G |
4: 63,292,627 (GRCm39) |
G1094A |
probably benign |
Het |
Catsperb |
C |
A |
12: 101,568,942 (GRCm39) |
Y871* |
probably null |
Het |
Clcn4 |
T |
G |
7: 7,293,427 (GRCm39) |
Y443S |
probably damaging |
Het |
Clcn6 |
T |
A |
4: 148,098,740 (GRCm39) |
T463S |
possibly damaging |
Het |
Colec10 |
A |
G |
15: 54,325,947 (GRCm39) |
D259G |
probably damaging |
Het |
Ctnna2 |
A |
T |
6: 77,613,827 (GRCm39) |
D254E |
possibly damaging |
Het |
Depdc1a |
G |
A |
3: 159,221,786 (GRCm39) |
|
probably null |
Het |
Fezf2 |
A |
T |
14: 12,343,986 (GRCm38) |
C302S |
probably damaging |
Het |
Flnc |
T |
C |
6: 29,451,634 (GRCm39) |
I1591T |
possibly damaging |
Het |
Kidins220 |
A |
G |
12: 25,107,143 (GRCm39) |
|
probably null |
Het |
Mctp2 |
C |
A |
7: 71,739,987 (GRCm39) |
C801F |
possibly damaging |
Het |
Myo1e |
A |
G |
9: 70,232,157 (GRCm39) |
I229V |
probably benign |
Het |
Or5t17 |
A |
T |
2: 86,833,266 (GRCm39) |
K318* |
probably null |
Het |
Or8c17 |
G |
A |
9: 38,180,757 (GRCm39) |
C308Y |
possibly damaging |
Het |
Ppp3r1 |
T |
C |
11: 17,144,786 (GRCm39) |
V133A |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,011,099 (GRCm39) |
Y2389N |
probably benign |
Het |
Sidt1 |
A |
G |
16: 44,102,249 (GRCm39) |
S304P |
possibly damaging |
Het |
Siglecf |
T |
A |
7: 43,004,995 (GRCm39) |
S408R |
possibly damaging |
Het |
Stat5a |
T |
A |
11: 100,765,752 (GRCm39) |
C279* |
probably null |
Het |
Tas2r105 |
A |
G |
6: 131,663,789 (GRCm39) |
V213A |
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,634,554 (GRCm39) |
D751G |
probably damaging |
Het |
Tektl1 |
T |
C |
10: 78,588,727 (GRCm39) |
T28A |
probably benign |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Usp46 |
A |
G |
5: 74,193,136 (GRCm39) |
Y47H |
probably damaging |
Het |
Vmn1r34 |
T |
A |
6: 66,614,688 (GRCm39) |
M17L |
probably benign |
Het |
Vmn2r120 |
T |
A |
17: 57,843,718 (GRCm39) |
D42V |
possibly damaging |
Het |
Wdr20 |
A |
G |
12: 110,759,950 (GRCm39) |
T279A |
probably benign |
Het |
Zfyve1 |
A |
G |
12: 83,641,296 (GRCm39) |
V120A |
probably benign |
Het |
|
Other mutations in Dlec1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01106:Dlec1
|
APN |
9 |
118,931,853 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01137:Dlec1
|
APN |
9 |
118,966,379 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01338:Dlec1
|
APN |
9 |
118,949,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01652:Dlec1
|
APN |
9 |
118,972,975 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01923:Dlec1
|
APN |
9 |
118,957,182 (GRCm39) |
splice site |
probably null |
|
IGL02186:Dlec1
|
APN |
9 |
118,972,695 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02597:Dlec1
|
APN |
9 |
118,963,604 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02667:Dlec1
|
APN |
9 |
118,956,534 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02718:Dlec1
|
APN |
9 |
118,966,354 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02731:Dlec1
|
APN |
9 |
118,976,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02831:Dlec1
|
APN |
9 |
118,972,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03390:Dlec1
|
APN |
9 |
118,952,288 (GRCm39) |
missense |
probably benign |
0.00 |
I2288:Dlec1
|
UTSW |
9 |
118,972,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Dlec1
|
UTSW |
9 |
118,934,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:Dlec1
|
UTSW |
9 |
118,971,934 (GRCm39) |
missense |
probably benign |
|
R0554:Dlec1
|
UTSW |
9 |
118,944,070 (GRCm39) |
missense |
probably benign |
0.44 |
R0611:Dlec1
|
UTSW |
9 |
118,941,167 (GRCm39) |
missense |
probably benign |
0.01 |
R1344:Dlec1
|
UTSW |
9 |
118,959,085 (GRCm39) |
missense |
probably benign |
0.09 |
R1467:Dlec1
|
UTSW |
9 |
118,971,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Dlec1
|
UTSW |
9 |
118,971,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Dlec1
|
UTSW |
9 |
118,957,071 (GRCm39) |
splice site |
probably benign |
|
R1539:Dlec1
|
UTSW |
9 |
118,956,518 (GRCm39) |
missense |
probably benign |
0.00 |
R1768:Dlec1
|
UTSW |
9 |
118,975,075 (GRCm39) |
splice site |
probably null |
|
R1809:Dlec1
|
UTSW |
9 |
118,965,767 (GRCm39) |
missense |
probably benign |
0.00 |
R1830:Dlec1
|
UTSW |
9 |
118,967,858 (GRCm39) |
missense |
probably benign |
0.00 |
R1901:Dlec1
|
UTSW |
9 |
118,931,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R2060:Dlec1
|
UTSW |
9 |
118,941,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R2092:Dlec1
|
UTSW |
9 |
118,950,912 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2237:Dlec1
|
UTSW |
9 |
118,967,259 (GRCm39) |
critical splice donor site |
probably null |
|
R2983:Dlec1
|
UTSW |
9 |
118,975,241 (GRCm39) |
missense |
probably benign |
0.00 |
R3117:Dlec1
|
UTSW |
9 |
118,972,971 (GRCm39) |
splice site |
probably null |
|
R3816:Dlec1
|
UTSW |
9 |
118,953,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Dlec1
|
UTSW |
9 |
118,972,129 (GRCm39) |
splice site |
probably benign |
|
R3965:Dlec1
|
UTSW |
9 |
118,957,649 (GRCm39) |
missense |
probably benign |
0.01 |
R4024:Dlec1
|
UTSW |
9 |
118,966,408 (GRCm39) |
missense |
probably damaging |
0.98 |
R4026:Dlec1
|
UTSW |
9 |
118,966,408 (GRCm39) |
missense |
probably damaging |
0.98 |
R4272:Dlec1
|
UTSW |
9 |
118,972,231 (GRCm39) |
missense |
probably damaging |
0.98 |
R4545:Dlec1
|
UTSW |
9 |
118,957,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R4546:Dlec1
|
UTSW |
9 |
118,957,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R4601:Dlec1
|
UTSW |
9 |
118,976,202 (GRCm39) |
critical splice donor site |
probably null |
|
R4695:Dlec1
|
UTSW |
9 |
118,972,221 (GRCm39) |
missense |
probably benign |
0.00 |
R4996:Dlec1
|
UTSW |
9 |
118,975,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R5321:Dlec1
|
UTSW |
9 |
118,941,669 (GRCm39) |
missense |
probably benign |
0.02 |
R5521:Dlec1
|
UTSW |
9 |
118,972,469 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5650:Dlec1
|
UTSW |
9 |
118,972,662 (GRCm39) |
nonsense |
probably null |
|
R5825:Dlec1
|
UTSW |
9 |
118,972,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R5941:Dlec1
|
UTSW |
9 |
118,955,380 (GRCm39) |
missense |
probably damaging |
0.98 |
R6056:Dlec1
|
UTSW |
9 |
118,950,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R6111:Dlec1
|
UTSW |
9 |
118,931,692 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6156:Dlec1
|
UTSW |
9 |
118,939,281 (GRCm39) |
critical splice donor site |
probably null |
|
R6160:Dlec1
|
UTSW |
9 |
118,972,387 (GRCm39) |
missense |
probably benign |
0.02 |
R6195:Dlec1
|
UTSW |
9 |
118,966,321 (GRCm39) |
missense |
probably benign |
0.00 |
R6364:Dlec1
|
UTSW |
9 |
118,950,939 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6480:Dlec1
|
UTSW |
9 |
118,976,758 (GRCm39) |
missense |
probably benign |
0.34 |
R6808:Dlec1
|
UTSW |
9 |
118,955,242 (GRCm39) |
missense |
probably benign |
0.01 |
R6813:Dlec1
|
UTSW |
9 |
118,941,170 (GRCm39) |
missense |
probably benign |
0.02 |
R7019:Dlec1
|
UTSW |
9 |
118,941,490 (GRCm39) |
missense |
probably benign |
0.01 |
R7048:Dlec1
|
UTSW |
9 |
118,972,472 (GRCm39) |
splice site |
probably null |
|
R7187:Dlec1
|
UTSW |
9 |
118,941,214 (GRCm39) |
missense |
probably benign |
0.14 |
R7230:Dlec1
|
UTSW |
9 |
118,953,606 (GRCm39) |
splice site |
probably null |
|
R7585:Dlec1
|
UTSW |
9 |
118,971,819 (GRCm39) |
missense |
probably benign |
0.06 |
R8342:Dlec1
|
UTSW |
9 |
118,968,457 (GRCm39) |
missense |
probably benign |
0.01 |
R8480:Dlec1
|
UTSW |
9 |
118,972,335 (GRCm39) |
splice site |
probably null |
|
R8481:Dlec1
|
UTSW |
9 |
118,972,335 (GRCm39) |
splice site |
probably null |
|
R8485:Dlec1
|
UTSW |
9 |
118,957,659 (GRCm39) |
missense |
probably benign |
0.33 |
R8520:Dlec1
|
UTSW |
9 |
118,941,277 (GRCm39) |
missense |
probably benign |
0.00 |
R8556:Dlec1
|
UTSW |
9 |
118,955,289 (GRCm39) |
missense |
probably benign |
0.13 |
R8755:Dlec1
|
UTSW |
9 |
118,967,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R8805:Dlec1
|
UTSW |
9 |
118,941,650 (GRCm39) |
missense |
probably benign |
|
R8813:Dlec1
|
UTSW |
9 |
118,956,498 (GRCm39) |
missense |
probably benign |
0.16 |
R8983:Dlec1
|
UTSW |
9 |
118,957,419 (GRCm39) |
missense |
probably benign |
0.00 |
R9040:Dlec1
|
UTSW |
9 |
118,950,985 (GRCm39) |
missense |
probably benign |
0.04 |
R9085:Dlec1
|
UTSW |
9 |
118,953,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Dlec1
|
UTSW |
9 |
118,941,541 (GRCm39) |
missense |
probably benign |
0.05 |
R9467:Dlec1
|
UTSW |
9 |
118,971,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Dlec1
|
UTSW |
9 |
118,956,533 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Dlec1
|
UTSW |
9 |
118,967,854 (GRCm39) |
missense |
probably benign |
0.13 |
Z1177:Dlec1
|
UTSW |
9 |
118,976,477 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Dlec1
|
UTSW |
9 |
118,963,541 (GRCm39) |
missense |
probably benign |
0.34 |
|