Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
A |
G |
10: 85,469,665 (GRCm39) |
Y862C |
probably damaging |
Het |
Anapc1 |
T |
C |
2: 128,465,851 (GRCm39) |
K1648E |
probably benign |
Het |
Arhgef10 |
C |
T |
8: 14,980,198 (GRCm39) |
A146V |
probably benign |
Het |
Atp7a |
A |
T |
X: 105,113,494 (GRCm39) |
N34I |
probably benign |
Het |
Casq2 |
A |
G |
3: 102,033,953 (GRCm39) |
Y232C |
probably damaging |
Het |
Cdan1 |
A |
T |
2: 120,555,720 (GRCm39) |
N738K |
probably benign |
Het |
Cdh24 |
A |
G |
14: 54,870,972 (GRCm39) |
V132A |
possibly damaging |
Het |
Chd5 |
C |
A |
4: 152,456,169 (GRCm39) |
T946K |
probably damaging |
Het |
Clip4 |
T |
C |
17: 72,156,965 (GRCm39) |
|
probably benign |
Het |
Copz2 |
T |
C |
11: 96,748,425 (GRCm39) |
|
probably benign |
Het |
Cyp2c39 |
C |
A |
19: 39,549,331 (GRCm39) |
S283* |
probably null |
Het |
Far1 |
A |
T |
7: 113,150,463 (GRCm39) |
T264S |
probably benign |
Het |
Iqgap1 |
A |
G |
7: 80,373,633 (GRCm39) |
L1452P |
probably damaging |
Het |
Irx5 |
A |
C |
8: 93,087,400 (GRCm39) |
N444T |
possibly damaging |
Het |
Kcnip2 |
A |
G |
19: 45,784,712 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,761,712 (GRCm39) |
M546K |
unknown |
Het |
Lrrc37a |
A |
G |
11: 103,395,113 (GRCm39) |
L104S |
probably benign |
Het |
Med12 |
T |
C |
X: 100,328,538 (GRCm39) |
L1143P |
probably damaging |
Het |
Mtcl1 |
T |
C |
17: 66,645,016 (GRCm39) |
H1477R |
probably benign |
Het |
Nkap |
T |
A |
X: 36,411,437 (GRCm39) |
|
probably benign |
Het |
Ntmt2 |
A |
G |
1: 163,544,656 (GRCm39) |
V109A |
probably benign |
Het |
Or10a2 |
A |
T |
7: 106,673,646 (GRCm39) |
T204S |
possibly damaging |
Het |
Osbpl6 |
C |
T |
2: 76,386,318 (GRCm39) |
Q214* |
probably null |
Het |
Pex1 |
C |
T |
5: 3,685,865 (GRCm39) |
T1202I |
possibly damaging |
Het |
Prrc2b |
A |
T |
2: 32,109,625 (GRCm39) |
N1066I |
probably damaging |
Het |
Psmg1 |
T |
C |
16: 95,788,497 (GRCm39) |
E152G |
probably damaging |
Het |
Scn10a |
A |
G |
9: 119,439,189 (GRCm39) |
I1560T |
probably damaging |
Het |
Shd |
A |
G |
17: 56,280,987 (GRCm39) |
E221G |
possibly damaging |
Het |
Slc39a4 |
T |
C |
15: 76,497,824 (GRCm39) |
T478A |
probably benign |
Het |
Snx2 |
A |
G |
18: 53,343,444 (GRCm39) |
I281V |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Tmem161a |
A |
T |
8: 70,634,693 (GRCm39) |
R297S |
probably damaging |
Het |
Tns1 |
A |
G |
1: 74,025,032 (GRCm39) |
|
probably null |
Het |
Ugt2b36 |
G |
A |
5: 87,228,783 (GRCm39) |
T420M |
probably damaging |
Het |
Wdfy4 |
G |
A |
14: 32,812,818 (GRCm39) |
R1652* |
probably null |
Het |
Zap70 |
T |
A |
1: 36,811,001 (GRCm39) |
Y178* |
probably null |
Het |
Zdhhc3 |
A |
G |
9: 122,929,456 (GRCm39) |
F60L |
probably damaging |
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 |
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 |
R4023:Dlec1
|
UTSW |
9 |
118,966,408 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|