Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck5 |
A |
G |
15: 76,478,535 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
A |
G |
14: 33,091,467 (GRCm39) |
M681V |
probably damaging |
Het |
Armh4 |
T |
A |
14: 50,007,893 (GRCm39) |
T527S |
probably damaging |
Het |
Atp10d |
T |
C |
5: 72,454,318 (GRCm39) |
L189P |
probably damaging |
Het |
BC034090 |
A |
G |
1: 155,108,196 (GRCm39) |
C384R |
probably benign |
Het |
Ccdc180 |
T |
A |
4: 45,941,877 (GRCm39) |
L1380Q |
probably damaging |
Het |
Cd209c |
T |
C |
8: 4,004,635 (GRCm39) |
|
noncoding transcript |
Het |
Csf1 |
T |
A |
3: 107,664,055 (GRCm39) |
T38S |
probably damaging |
Het |
Csn1s2a |
T |
C |
5: 87,923,680 (GRCm39) |
V12A |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,867,498 (GRCm39) |
D235G |
probably benign |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Frmd3 |
T |
A |
4: 74,046,535 (GRCm39) |
|
probably null |
Het |
Gart |
G |
A |
16: 91,430,982 (GRCm39) |
A360V |
probably benign |
Het |
Gm7251 |
T |
A |
13: 49,958,676 (GRCm39) |
|
noncoding transcript |
Het |
Gon4l |
C |
A |
3: 88,814,694 (GRCm39) |
P1888T |
probably benign |
Het |
Hk1 |
C |
A |
10: 62,151,319 (GRCm39) |
K10N |
probably damaging |
Het |
Itgal |
A |
G |
7: 126,927,453 (GRCm39) |
Y981C |
probably benign |
Het |
Kcp |
C |
T |
6: 29,493,202 (GRCm39) |
C107Y |
probably damaging |
Het |
Kdm2a |
C |
T |
19: 4,379,082 (GRCm39) |
V138M |
probably benign |
Het |
Kit |
T |
C |
5: 75,801,159 (GRCm39) |
I515T |
probably benign |
Het |
Kmt2c |
C |
T |
5: 25,520,324 (GRCm39) |
V1929I |
probably benign |
Het |
Krt33a |
T |
C |
11: 99,903,253 (GRCm39) |
E263G |
possibly damaging |
Het |
Mark2 |
T |
C |
19: 7,268,054 (GRCm39) |
I50V |
possibly damaging |
Het |
Mug2 |
G |
T |
6: 122,047,966 (GRCm39) |
|
probably null |
Het |
Mvk |
A |
G |
5: 114,591,022 (GRCm39) |
|
probably benign |
Het |
Myh6 |
T |
A |
14: 55,199,565 (GRCm39) |
I249F |
probably damaging |
Het |
Naa15 |
T |
C |
3: 51,355,786 (GRCm39) |
I229T |
possibly damaging |
Het |
Napb |
A |
C |
2: 148,574,184 (GRCm39) |
|
probably null |
Het |
Ncoa3 |
T |
G |
2: 165,896,417 (GRCm39) |
L440R |
possibly damaging |
Het |
Or52ae7 |
T |
C |
7: 103,119,278 (GRCm39) |
S11P |
probably damaging |
Het |
Or8g52 |
T |
A |
9: 39,631,103 (GRCm39) |
F193L |
probably benign |
Het |
Osbpl8 |
T |
A |
10: 111,105,280 (GRCm39) |
I245N |
possibly damaging |
Het |
Pdia4 |
G |
A |
6: 47,775,326 (GRCm39) |
R495W |
probably damaging |
Het |
Pfn4 |
T |
A |
12: 4,820,182 (GRCm39) |
D10E |
probably damaging |
Het |
Plekha5 |
T |
C |
6: 140,525,191 (GRCm39) |
Y376H |
probably damaging |
Het |
Pole |
T |
A |
5: 110,485,071 (GRCm39) |
I395K |
possibly damaging |
Het |
Prcc |
A |
G |
3: 87,774,714 (GRCm39) |
Y363H |
probably damaging |
Het |
Ptprc |
A |
T |
1: 137,995,663 (GRCm39) |
M982K |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,357,264 (GRCm39) |
F252I |
probably benign |
Het |
Pusl1 |
A |
G |
4: 155,975,037 (GRCm39) |
V188A |
probably benign |
Het |
Rad54l2 |
A |
G |
9: 106,570,421 (GRCm39) |
S1300P |
probably benign |
Het |
Rpl11 |
G |
A |
4: 135,778,454 (GRCm39) |
|
probably benign |
Het |
Rtel1 |
T |
A |
2: 180,997,589 (GRCm39) |
H1104Q |
probably damaging |
Het |
Setbp1 |
T |
C |
18: 78,903,137 (GRCm39) |
R177G |
probably damaging |
Het |
Skint6 |
T |
C |
4: 113,093,715 (GRCm39) |
T143A |
possibly damaging |
Het |
Steep1 |
C |
A |
X: 36,087,812 (GRCm39) |
C206F |
probably benign |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Ttc23l |
CT |
CTTGGATT |
15: 10,537,648 (GRCm39) |
|
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,537,652 (GRCm39) |
S206L |
probably benign |
Het |
Zfp583 |
A |
G |
7: 6,320,680 (GRCm39) |
S111P |
possibly damaging |
Het |
Zmiz1 |
T |
C |
14: 25,636,434 (GRCm39) |
S140P |
probably damaging |
Het |
|
Other mutations in Cenpp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00419:Cenpp
|
APN |
13 |
49,801,132 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01323:Cenpp
|
APN |
13 |
49,801,118 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01397:Cenpp
|
APN |
13 |
49,794,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01553:Cenpp
|
APN |
13 |
49,618,252 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02489:Cenpp
|
APN |
13 |
49,803,594 (GRCm39) |
splice site |
probably null |
|
IGL03024:Cenpp
|
APN |
13 |
49,617,730 (GRCm39) |
missense |
probably benign |
0.16 |
R0218:Cenpp
|
UTSW |
13 |
49,801,108 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0660:Cenpp
|
UTSW |
13 |
49,618,173 (GRCm39) |
missense |
probably benign |
0.00 |
R1868:Cenpp
|
UTSW |
13 |
49,794,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4097:Cenpp
|
UTSW |
13 |
49,647,265 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4595:Cenpp
|
UTSW |
13 |
49,794,710 (GRCm39) |
missense |
probably benign |
0.09 |
R5173:Cenpp
|
UTSW |
13 |
49,618,258 (GRCm39) |
frame shift |
probably null |
|
R5174:Cenpp
|
UTSW |
13 |
49,618,258 (GRCm39) |
frame shift |
probably null |
|
R5953:Cenpp
|
UTSW |
13 |
49,806,161 (GRCm39) |
missense |
probably damaging |
0.99 |
R7054:Cenpp
|
UTSW |
13 |
49,619,233 (GRCm39) |
missense |
probably damaging |
0.97 |
R8452:Cenpp
|
UTSW |
13 |
49,683,887 (GRCm39) |
splice site |
probably null |
|
R9602:Cenpp
|
UTSW |
13 |
49,801,049 (GRCm39) |
missense |
probably damaging |
1.00 |
RF023:Cenpp
|
UTSW |
13 |
49,803,620 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Cenpp
|
UTSW |
13 |
49,801,134 (GRCm39) |
splice site |
probably null |
|
|