Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
AC |
A |
11: 9,632,032 (GRCm39) |
|
probably null |
Het |
Abca6 |
A |
T |
11: 110,082,546 (GRCm39) |
F1142L |
probably benign |
Het |
Ap1g1 |
T |
A |
8: 110,577,764 (GRCm39) |
|
probably null |
Het |
Apob |
T |
C |
12: 8,058,238 (GRCm39) |
V2207A |
probably benign |
Het |
Chd3 |
A |
G |
11: 69,260,069 (GRCm39) |
|
probably benign |
Het |
Coch |
C |
A |
12: 51,643,290 (GRCm39) |
Y103* |
probably null |
Het |
Cul3 |
A |
T |
1: 80,259,133 (GRCm39) |
D382E |
possibly damaging |
Het |
Cul5 |
T |
C |
9: 53,554,034 (GRCm39) |
T291A |
probably benign |
Het |
Dab1 |
T |
C |
4: 104,545,645 (GRCm39) |
|
probably null |
Het |
Dmtf1 |
A |
G |
5: 9,190,356 (GRCm39) |
|
probably benign |
Het |
Dpp4 |
T |
C |
2: 62,217,474 (GRCm39) |
Y41C |
probably damaging |
Het |
Eif2ak4 |
A |
G |
2: 118,238,841 (GRCm39) |
I45M |
probably damaging |
Het |
Epn3 |
T |
C |
11: 94,386,923 (GRCm39) |
K149R |
probably damaging |
Het |
Flnc |
A |
G |
6: 29,455,537 (GRCm39) |
E2029G |
probably damaging |
Het |
Gm5799 |
A |
G |
14: 43,782,116 (GRCm39) |
N96S |
probably damaging |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Grik5 |
T |
C |
7: 24,762,319 (GRCm39) |
H224R |
possibly damaging |
Het |
Lpar6 |
A |
T |
14: 73,476,537 (GRCm39) |
E166V |
probably benign |
Het |
Mical1 |
T |
C |
10: 41,360,985 (GRCm39) |
L683P |
probably damaging |
Het |
Mis18bp1 |
T |
C |
12: 65,196,149 (GRCm39) |
I538M |
possibly damaging |
Het |
Mobp |
A |
G |
9: 119,997,311 (GRCm39) |
R77G |
possibly damaging |
Het |
Muc21 |
G |
T |
17: 35,931,633 (GRCm39) |
|
probably benign |
Het |
Mylk |
A |
G |
16: 34,797,383 (GRCm39) |
H1614R |
probably benign |
Het |
Or2y16 |
T |
C |
11: 49,334,713 (GRCm39) |
F12L |
probably benign |
Het |
Or4p18 |
G |
A |
2: 88,233,266 (GRCm39) |
T4I |
probably benign |
Het |
Or7c19 |
T |
C |
8: 85,957,205 (GRCm39) |
L27P |
probably damaging |
Het |
Osbpl1a |
C |
T |
18: 12,895,697 (GRCm39) |
V390I |
probably benign |
Het |
Pcdha7 |
C |
A |
18: 37,107,705 (GRCm39) |
D243E |
probably benign |
Het |
Pi4ka |
A |
T |
16: 17,168,770 (GRCm39) |
N653K |
possibly damaging |
Het |
Plin5 |
T |
G |
17: 56,422,548 (GRCm39) |
|
probably null |
Het |
Plod1 |
A |
G |
4: 148,000,758 (GRCm39) |
|
probably benign |
Het |
Psd3 |
T |
C |
8: 68,149,641 (GRCm39) |
K372E |
probably damaging |
Het |
Psmd11 |
C |
T |
11: 80,351,566 (GRCm39) |
T263I |
probably benign |
Het |
Ptprt |
A |
T |
2: 161,769,676 (GRCm39) |
N396K |
probably benign |
Het |
Rab39 |
T |
C |
9: 53,597,800 (GRCm39) |
E155G |
probably damaging |
Het |
Rimbp2 |
T |
C |
5: 128,874,712 (GRCm39) |
D293G |
probably benign |
Het |
Rnf220 |
T |
C |
4: 117,146,471 (GRCm39) |
|
probably benign |
Het |
Rnmt |
C |
T |
18: 68,454,430 (GRCm39) |
|
probably benign |
Het |
Slc10a1 |
T |
A |
12: 81,002,802 (GRCm39) |
I279F |
probably damaging |
Het |
Sp140l1 |
G |
A |
1: 85,078,288 (GRCm39) |
R54* |
probably null |
Het |
Taar6 |
A |
G |
10: 23,861,250 (GRCm39) |
Y99H |
probably damaging |
Het |
Tas2r144 |
T |
A |
6: 42,193,048 (GRCm39) |
F263I |
probably benign |
Het |
Tex15 |
T |
A |
8: 34,061,768 (GRCm39) |
N399K |
possibly damaging |
Het |
Tlr9 |
T |
A |
9: 106,103,151 (GRCm39) |
V814D |
possibly damaging |
Het |
Tmem53 |
T |
A |
4: 117,122,908 (GRCm39) |
|
probably benign |
Het |
Ubap2l |
T |
C |
3: 89,928,337 (GRCm39) |
I511V |
possibly damaging |
Het |
Vmn2r60 |
T |
C |
7: 41,844,935 (GRCm39) |
M766T |
probably damaging |
Het |
Zfp462 |
T |
C |
4: 55,011,115 (GRCm39) |
V1027A |
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 |
R4377:Cenpp
|
UTSW |
13 |
49,647,907 (GRCm39) |
utr 3 prime |
probably benign |
|
R4595:Cenpp
|
UTSW |
13 |
49,794,710 (GRCm39) |
missense |
probably benign |
0.09 |
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 |
|
|