Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam30 |
T |
A |
3: 98,068,679 (GRCm39) |
C43S |
probably damaging |
Het |
Adamts6 |
A |
T |
13: 104,449,412 (GRCm39) |
Y274F |
probably damaging |
Het |
Ap2b1 |
A |
G |
11: 83,256,471 (GRCm39) |
|
probably null |
Het |
Atm |
A |
C |
9: 53,361,921 (GRCm39) |
L2732R |
probably damaging |
Het |
Bbox1 |
A |
G |
2: 110,100,525 (GRCm39) |
V224A |
probably benign |
Het |
Bmpr1a |
T |
C |
14: 34,156,690 (GRCm39) |
D112G |
probably benign |
Het |
Cdk19 |
A |
G |
10: 40,270,391 (GRCm39) |
I67V |
probably benign |
Het |
Cds2 |
A |
G |
2: 132,139,191 (GRCm39) |
T145A |
probably benign |
Het |
Chd9 |
A |
G |
8: 91,777,912 (GRCm39) |
D2641G |
probably damaging |
Het |
Chn2 |
G |
T |
6: 54,249,963 (GRCm39) |
R24M |
probably damaging |
Het |
Chuk |
T |
C |
19: 44,088,613 (GRCm39) |
I121V |
probably null |
Het |
Ctsr |
A |
T |
13: 61,309,659 (GRCm39) |
D183E |
probably benign |
Het |
Elp3 |
T |
C |
14: 65,797,630 (GRCm39) |
E347G |
possibly damaging |
Het |
Fhip1a |
A |
G |
3: 85,572,690 (GRCm39) |
S988P |
possibly damaging |
Het |
Gnas |
A |
G |
2: 174,141,958 (GRCm39) |
N709S |
possibly damaging |
Het |
Gramd2b |
T |
C |
18: 56,618,296 (GRCm39) |
S199P |
probably damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,246,622 (GRCm39) |
C1562* |
probably null |
Het |
Ifit1bl1 |
T |
A |
19: 34,572,188 (GRCm39) |
I90F |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,921,141 (GRCm39) |
H1313Q |
possibly damaging |
Het |
Ighj4 |
T |
C |
12: 113,392,176 (GRCm39) |
|
probably benign |
Het |
Kansl2 |
G |
T |
15: 98,429,636 (GRCm39) |
P132Q |
possibly damaging |
Het |
Lman1 |
T |
C |
18: 66,120,932 (GRCm39) |
H430R |
possibly damaging |
Het |
Lrrk2 |
T |
C |
15: 91,699,686 (GRCm39) |
I2511T |
probably benign |
Het |
Lvrn |
C |
A |
18: 47,010,036 (GRCm39) |
P395T |
possibly damaging |
Het |
Myrip |
C |
A |
9: 120,293,764 (GRCm39) |
S753* |
probably null |
Het |
Nectin4 |
A |
G |
1: 171,213,301 (GRCm39) |
S408G |
probably benign |
Het |
Or14j8 |
A |
G |
17: 38,263,681 (GRCm39) |
I78T |
probably benign |
Het |
Or52ae9 |
T |
C |
7: 103,390,207 (GRCm39) |
K80R |
probably benign |
Het |
Pcdhb13 |
T |
C |
18: 37,576,873 (GRCm39) |
I417T |
probably damaging |
Het |
Per2 |
T |
C |
1: 91,357,172 (GRCm39) |
T664A |
possibly damaging |
Het |
Plec |
A |
T |
15: 76,056,962 (GRCm39) |
L4347Q |
probably damaging |
Het |
Poln |
A |
G |
5: 34,261,295 (GRCm39) |
S561P |
probably benign |
Het |
Polr1a |
T |
C |
6: 71,942,690 (GRCm39) |
F1177L |
probably benign |
Het |
Ptprb |
A |
T |
10: 116,189,754 (GRCm39) |
R1804S |
probably benign |
Het |
Rhof |
C |
T |
5: 123,257,588 (GRCm39) |
V181M |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Slc22a12 |
T |
C |
19: 6,588,818 (GRCm39) |
E281G |
probably damaging |
Het |
Slco6b1 |
T |
A |
1: 96,915,622 (GRCm39) |
|
noncoding transcript |
Het |
Stac |
C |
A |
9: 111,433,126 (GRCm39) |
|
probably null |
Het |
Tcof1 |
C |
A |
18: 60,952,673 (GRCm39) |
A898S |
unknown |
Het |
Tep1 |
C |
T |
14: 51,081,191 (GRCm39) |
R1349Q |
possibly damaging |
Het |
Thoc6 |
A |
T |
17: 23,888,319 (GRCm39) |
|
probably benign |
Het |
Tmem179 |
A |
T |
12: 112,477,461 (GRCm39) |
F8I |
possibly damaging |
Het |
Tnpo3 |
A |
G |
6: 29,560,091 (GRCm39) |
L684P |
probably damaging |
Het |
Ubash3a |
T |
C |
17: 31,456,249 (GRCm39) |
Y506H |
probably damaging |
Het |
Umps |
G |
A |
16: 33,777,288 (GRCm39) |
Q431* |
probably null |
Het |
Unc13c |
A |
G |
9: 73,481,289 (GRCm39) |
|
probably null |
Het |
Vmn1r210 |
A |
T |
13: 23,011,779 (GRCm39) |
M169K |
probably benign |
Het |
Zfp946 |
C |
T |
17: 22,673,548 (GRCm39) |
Q101* |
probably null |
Het |
|
Other mutations in Pramel24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00976:Pramel24
|
APN |
4 |
143,453,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01122:Pramel24
|
APN |
4 |
143,454,971 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02314:Pramel24
|
APN |
4 |
143,455,012 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03089:Pramel24
|
APN |
4 |
143,452,703 (GRCm39) |
missense |
probably benign |
0.43 |
IGL03338:Pramel24
|
APN |
4 |
143,453,312 (GRCm39) |
missense |
probably benign |
0.01 |
R0233:Pramel24
|
UTSW |
4 |
143,452,633 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0233:Pramel24
|
UTSW |
4 |
143,452,633 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0349:Pramel24
|
UTSW |
4 |
143,453,629 (GRCm39) |
missense |
probably benign |
0.00 |
R0681:Pramel24
|
UTSW |
4 |
143,454,622 (GRCm39) |
missense |
probably benign |
|
R0963:Pramel24
|
UTSW |
4 |
143,453,678 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1114:Pramel24
|
UTSW |
4 |
143,453,425 (GRCm39) |
missense |
probably benign |
0.01 |
R2070:Pramel24
|
UTSW |
4 |
143,453,472 (GRCm39) |
nonsense |
probably null |
|
R2475:Pramel24
|
UTSW |
4 |
143,453,395 (GRCm39) |
missense |
probably benign |
0.14 |
R3824:Pramel24
|
UTSW |
4 |
143,453,255 (GRCm39) |
missense |
probably benign |
0.00 |
R4050:Pramel24
|
UTSW |
4 |
143,453,692 (GRCm39) |
missense |
probably benign |
0.01 |
R4273:Pramel24
|
UTSW |
4 |
143,453,416 (GRCm39) |
nonsense |
probably null |
|
R4280:Pramel24
|
UTSW |
4 |
143,452,592 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4921:Pramel24
|
UTSW |
4 |
143,454,896 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5223:Pramel24
|
UTSW |
4 |
143,454,591 (GRCm39) |
missense |
probably benign |
0.00 |
R7256:Pramel24
|
UTSW |
4 |
143,452,849 (GRCm39) |
missense |
probably benign |
0.23 |
R7640:Pramel24
|
UTSW |
4 |
143,453,276 (GRCm39) |
missense |
probably benign |
0.00 |
R7666:Pramel24
|
UTSW |
4 |
143,455,085 (GRCm39) |
missense |
probably benign |
0.00 |
R7683:Pramel24
|
UTSW |
4 |
143,453,284 (GRCm39) |
nonsense |
probably null |
|
R7981:Pramel24
|
UTSW |
4 |
143,453,452 (GRCm39) |
missense |
probably benign |
0.01 |
R8856:Pramel24
|
UTSW |
4 |
143,453,303 (GRCm39) |
missense |
probably benign |
0.33 |
R9050:Pramel24
|
UTSW |
4 |
143,453,329 (GRCm39) |
missense |
probably benign |
0.03 |
R9739:Pramel24
|
UTSW |
4 |
143,454,997 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9757:Pramel24
|
UTSW |
4 |
143,454,992 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Pramel24
|
UTSW |
4 |
143,453,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|