Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
A |
T |
17: 36,270,629 (GRCm39) |
|
probably null |
Het |
Abr |
T |
A |
11: 76,346,509 (GRCm39) |
E434V |
probably damaging |
Het |
Acaca |
T |
A |
11: 84,202,133 (GRCm39) |
L197Q |
probably damaging |
Het |
Acot10 |
A |
G |
15: 20,666,018 (GRCm39) |
I241T |
probably benign |
Het |
Acp6 |
T |
C |
3: 97,075,312 (GRCm39) |
V182A |
probably benign |
Het |
Ahnak2 |
G |
A |
12: 112,739,812 (GRCm39) |
T1420I |
possibly damaging |
Het |
Akr1c6 |
A |
T |
13: 4,497,018 (GRCm39) |
K153N |
probably benign |
Het |
Ank3 |
T |
C |
10: 69,721,030 (GRCm39) |
L600P |
probably damaging |
Het |
Arhgef1 |
G |
A |
7: 24,624,447 (GRCm39) |
A824T |
probably damaging |
Het |
B230307C23Rik |
T |
A |
16: 97,809,891 (GRCm39) |
N22K |
possibly damaging |
Het |
Btn1a1 |
A |
G |
13: 23,648,324 (GRCm39) |
|
probably benign |
Het |
Cenpf |
G |
A |
1: 189,404,824 (GRCm39) |
T352I |
possibly damaging |
Het |
Ces4a |
C |
A |
8: 105,869,121 (GRCm39) |
F185L |
probably benign |
Het |
Cobl |
A |
G |
11: 12,325,825 (GRCm39) |
W217R |
probably damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,086,945 (GRCm39) |
N677S |
probably benign |
Het |
Ddx51 |
C |
A |
5: 110,803,908 (GRCm39) |
T390N |
possibly damaging |
Het |
Drd5 |
T |
G |
5: 38,477,310 (GRCm39) |
V101G |
probably damaging |
Het |
Elmo3 |
C |
T |
8: 106,033,985 (GRCm39) |
P244L |
probably benign |
Het |
Esrrg |
G |
A |
1: 187,878,555 (GRCm39) |
R189H |
probably damaging |
Het |
Fxr2 |
A |
G |
11: 69,534,667 (GRCm39) |
T183A |
probably benign |
Het |
Gjd4 |
T |
C |
18: 9,280,613 (GRCm39) |
H155R |
probably benign |
Het |
Hivep2 |
T |
A |
10: 14,007,011 (GRCm39) |
|
probably null |
Het |
Ints10 |
T |
C |
8: 69,246,624 (GRCm39) |
|
probably benign |
Het |
Kank4 |
T |
C |
4: 98,667,209 (GRCm39) |
T413A |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,847,735 (GRCm39) |
V568A |
probably damaging |
Het |
Mobp |
A |
G |
9: 119,997,419 (GRCm39) |
|
probably benign |
Het |
Mpst |
A |
G |
15: 78,294,708 (GRCm39) |
S147G |
probably benign |
Het |
Myo5b |
A |
T |
18: 74,795,741 (GRCm39) |
Y559F |
possibly damaging |
Het |
Nceh1 |
T |
C |
3: 27,237,288 (GRCm39) |
I21T |
probably damaging |
Het |
Or4f7 |
T |
C |
2: 111,644,523 (GRCm39) |
K183E |
probably benign |
Het |
Phf8-ps |
A |
T |
17: 33,285,739 (GRCm39) |
C354* |
probably null |
Het |
Ralgps1 |
A |
T |
2: 33,166,171 (GRCm39) |
V126E |
probably damaging |
Het |
Rnls |
A |
G |
19: 33,359,823 (GRCm39) |
V115A |
probably damaging |
Het |
Scn1a |
A |
T |
2: 66,108,013 (GRCm39) |
V1554D |
probably damaging |
Het |
Slc16a11 |
T |
A |
11: 70,106,258 (GRCm39) |
D165E |
probably damaging |
Het |
Slc16a5 |
A |
G |
11: 115,353,501 (GRCm39) |
T23A |
probably benign |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc3a1 |
A |
T |
17: 85,335,881 (GRCm39) |
|
probably null |
Het |
Slitrk6 |
A |
T |
14: 110,987,185 (GRCm39) |
*841K |
probably null |
Het |
Syngr1 |
A |
G |
15: 79,975,647 (GRCm39) |
Y18C |
possibly damaging |
Het |
Tarbp1 |
T |
G |
8: 127,155,709 (GRCm39) |
D1343A |
probably benign |
Het |
Vac14 |
T |
A |
8: 111,360,961 (GRCm39) |
I177N |
probably damaging |
Het |
Vmn1r218 |
A |
T |
13: 23,320,881 (GRCm39) |
D76V |
possibly damaging |
Het |
Wdr75 |
T |
A |
1: 45,838,277 (GRCm39) |
I62N |
probably damaging |
Het |
Zfp12 |
A |
T |
5: 143,226,134 (GRCm39) |
I68L |
probably null |
Het |
Zswim8 |
T |
A |
14: 20,771,719 (GRCm39) |
Y1551N |
probably damaging |
Het |
|
Other mutations in Clybl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Clybl
|
APN |
14 |
122,616,610 (GRCm39) |
splice site |
probably benign |
|
IGL01380:Clybl
|
APN |
14 |
122,616,761 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01589:Clybl
|
APN |
14 |
122,608,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02043:Clybl
|
APN |
14 |
122,616,664 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03111:Clybl
|
APN |
14 |
122,639,395 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Clybl
|
APN |
14 |
122,639,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R2104:Clybl
|
UTSW |
14 |
122,548,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:Clybl
|
UTSW |
14 |
122,621,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5067:Clybl
|
UTSW |
14 |
122,616,701 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5138:Clybl
|
UTSW |
14 |
122,608,716 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5620:Clybl
|
UTSW |
14 |
122,548,755 (GRCm39) |
missense |
probably damaging |
0.97 |
R6982:Clybl
|
UTSW |
14 |
122,639,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Clybl
|
UTSW |
14 |
122,608,732 (GRCm39) |
nonsense |
probably null |
|
R8055:Clybl
|
UTSW |
14 |
122,615,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R8837:Clybl
|
UTSW |
14 |
122,419,194 (GRCm39) |
critical splice donor site |
probably null |
|
R9071:Clybl
|
UTSW |
14 |
122,608,697 (GRCm39) |
missense |
probably benign |
0.03 |
R9183:Clybl
|
UTSW |
14 |
122,639,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Clybl
|
UTSW |
14 |
122,621,670 (GRCm39) |
missense |
probably benign |
0.20 |
R9318:Clybl
|
UTSW |
14 |
122,608,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R9596:Clybl
|
UTSW |
14 |
122,548,768 (GRCm39) |
missense |
probably benign |
0.01 |
|