Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
A |
T |
12: 55,095,772 (GRCm39) |
|
probably null |
Het |
Aatf |
T |
C |
11: 84,402,323 (GRCm39) |
D121G |
probably benign |
Het |
Amer2 |
T |
A |
14: 60,617,176 (GRCm39) |
L331H |
probably damaging |
Het |
Ang4 |
T |
G |
14: 52,001,829 (GRCm39) |
K40Q |
probably benign |
Het |
Aspm |
A |
C |
1: 139,398,498 (GRCm39) |
|
probably null |
Het |
Cacna1c |
A |
T |
6: 118,728,432 (GRCm39) |
D337E |
probably benign |
Het |
Ccdc124 |
T |
C |
8: 71,321,429 (GRCm39) |
E134G |
probably benign |
Het |
Ccdc7a |
G |
T |
8: 129,711,464 (GRCm39) |
A312E |
probably benign |
Het |
Cd209g |
A |
G |
8: 4,186,845 (GRCm39) |
D130G |
probably damaging |
Het |
Cd320 |
T |
C |
17: 34,066,549 (GRCm39) |
S96P |
probably benign |
Het |
Cenatac |
A |
T |
9: 44,329,245 (GRCm39) |
F14Y |
probably damaging |
Het |
Clu |
C |
G |
14: 66,210,815 (GRCm39) |
Q134E |
probably damaging |
Het |
Cnksr3 |
T |
A |
10: 7,110,777 (GRCm39) |
H28L |
probably benign |
Het |
Cntnap1 |
T |
C |
11: 101,067,159 (GRCm39) |
|
probably null |
Het |
Col22a1 |
C |
T |
15: 71,732,915 (GRCm39) |
C546Y |
unknown |
Het |
Col6a3 |
C |
T |
1: 90,706,565 (GRCm39) |
V2183I |
unknown |
Het |
Cop1 |
A |
G |
1: 159,152,638 (GRCm39) |
|
probably benign |
Het |
Cpne8 |
T |
C |
15: 90,563,438 (GRCm39) |
I24V |
probably benign |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Dennd5b |
G |
A |
6: 148,911,270 (GRCm39) |
L978F |
possibly damaging |
Het |
Depdc1a |
G |
T |
3: 159,229,550 (GRCm39) |
M627I |
probably benign |
Het |
Dnah3 |
A |
T |
7: 119,555,424 (GRCm39) |
N2721K |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dsg1b |
A |
G |
18: 20,541,925 (GRCm39) |
T811A |
possibly damaging |
Het |
Emilin1 |
C |
G |
5: 31,076,695 (GRCm39) |
Q847E |
probably benign |
Het |
Epha3 |
A |
T |
16: 63,472,775 (GRCm39) |
V370D |
probably benign |
Het |
Epha5 |
T |
A |
5: 84,298,342 (GRCm39) |
T406S |
probably damaging |
Het |
Ephb1 |
A |
T |
9: 101,918,159 (GRCm39) |
I450N |
probably benign |
Het |
Ephb2 |
A |
G |
4: 136,423,321 (GRCm39) |
M319T |
probably benign |
Het |
Eps15l1 |
A |
G |
8: 73,132,833 (GRCm39) |
|
probably null |
Het |
Fbxo9 |
G |
A |
9: 77,993,168 (GRCm39) |
|
probably benign |
Het |
Fgd5 |
T |
C |
6: 91,966,281 (GRCm39) |
I838T |
probably damaging |
Het |
Fnbp4 |
T |
C |
2: 90,596,174 (GRCm39) |
F582L |
probably damaging |
Het |
Frs3 |
T |
C |
17: 48,000,187 (GRCm39) |
|
probably null |
Het |
Fscb |
C |
T |
12: 64,520,393 (GRCm39) |
V358I |
possibly damaging |
Het |
Fus |
G |
T |
7: 127,566,727 (GRCm39) |
|
probably benign |
Het |
Fyb1 |
CCTCTCTCTCTCTCTCTCTCT |
CCTCTCTCTCTCTCTCTCT |
15: 6,676,092 (GRCm39) |
|
probably benign |
Het |
Glra3 |
A |
T |
8: 56,444,270 (GRCm39) |
I77F |
possibly damaging |
Het |
Gm4454 |
C |
T |
7: 38,269,860 (GRCm39) |
|
noncoding transcript |
Het |
Gng3 |
G |
A |
19: 8,815,625 (GRCm39) |
A37V |
possibly damaging |
Het |
Grin3b |
T |
A |
10: 79,812,191 (GRCm39) |
|
probably benign |
Het |
Herpud1 |
A |
G |
8: 95,118,422 (GRCm39) |
Y41C |
probably damaging |
Het |
Igkv4-92 |
G |
C |
6: 68,732,028 (GRCm39) |
S115R |
possibly damaging |
Het |
Ikbip |
T |
A |
10: 90,931,848 (GRCm39) |
I164N |
probably benign |
Het |
Kank1 |
A |
G |
19: 25,388,759 (GRCm39) |
T783A |
probably benign |
Het |
Kcnq3 |
A |
T |
15: 65,903,254 (GRCm39) |
V152E |
possibly damaging |
Het |
Kif23 |
C |
T |
9: 61,839,153 (GRCm39) |
R314H |
probably damaging |
Het |
Klc4 |
T |
C |
17: 46,955,287 (GRCm39) |
H49R |
probably benign |
Het |
Klhl20 |
A |
T |
1: 160,930,575 (GRCm39) |
I309N |
possibly damaging |
Het |
Lgals4 |
A |
G |
7: 28,540,701 (GRCm39) |
Y268C |
probably damaging |
Het |
Lingo4 |
A |
G |
3: 94,306,761 (GRCm39) |
Q13R |
probably benign |
Het |
Lmtk2 |
C |
A |
5: 144,113,265 (GRCm39) |
F1328L |
probably damaging |
Het |
Mapk14 |
A |
G |
17: 28,960,765 (GRCm39) |
R179G |
probably damaging |
Het |
Mbd3l1 |
A |
T |
9: 18,396,201 (GRCm39) |
T109S |
probably benign |
Het |
Megf6 |
T |
C |
4: 154,351,907 (GRCm39) |
F1169L |
possibly damaging |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Myh1 |
T |
C |
11: 67,115,300 (GRCm39) |
|
probably benign |
Het |
Nav3 |
T |
C |
10: 109,716,553 (GRCm39) |
I172V |
probably benign |
Het |
Nemp1 |
T |
A |
10: 127,529,399 (GRCm39) |
L178Q |
probably damaging |
Het |
Numa1 |
T |
C |
7: 101,641,881 (GRCm39) |
S110P |
probably damaging |
Het |
Or4a75 |
A |
G |
2: 89,447,769 (GRCm39) |
Y256H |
probably damaging |
Het |
Or4c117 |
T |
C |
2: 88,955,845 (GRCm39) |
T77A |
probably benign |
Het |
Or51k1 |
A |
G |
7: 103,661,312 (GRCm39) |
I199T |
probably damaging |
Het |
Or5ak25 |
A |
G |
2: 85,268,813 (GRCm39) |
S230P |
probably damaging |
Het |
Or8k30 |
T |
C |
2: 86,339,171 (GRCm39) |
Y123H |
probably damaging |
Het |
Or9q1 |
A |
T |
19: 13,805,458 (GRCm39) |
F101I |
probably damaging |
Het |
Pard3b |
T |
G |
1: 62,383,219 (GRCm39) |
M771R |
probably damaging |
Het |
Phkg2 |
A |
G |
7: 127,181,551 (GRCm39) |
I245V |
probably damaging |
Het |
Pik3cg |
A |
T |
12: 32,254,103 (GRCm39) |
M628K |
possibly damaging |
Het |
Poln |
A |
G |
5: 34,264,429 (GRCm39) |
|
probably null |
Het |
Ppip5k1 |
A |
T |
2: 121,142,871 (GRCm39) |
S1172T |
probably damaging |
Het |
Prdm5 |
A |
T |
6: 65,847,446 (GRCm39) |
H363L |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,496,173 (GRCm39) |
Y788C |
probably damaging |
Het |
Prrc2c |
T |
A |
1: 162,520,116 (GRCm39) |
R2076S |
probably damaging |
Het |
Sh2d2a |
A |
G |
3: 87,756,728 (GRCm39) |
Y191C |
probably damaging |
Het |
Slc20a1 |
T |
C |
2: 129,041,919 (GRCm39) |
I94T |
probably damaging |
Het |
Sptbn2 |
T |
C |
19: 4,801,686 (GRCm39) |
V2366A |
probably benign |
Het |
Stab2 |
T |
A |
10: 86,796,087 (GRCm39) |
M387L |
probably benign |
Het |
Syne2 |
T |
G |
12: 75,987,993 (GRCm39) |
M1718R |
probably damaging |
Het |
Synm |
G |
T |
7: 67,384,235 (GRCm39) |
F700L |
probably benign |
Het |
Tmco4 |
T |
C |
4: 138,718,012 (GRCm39) |
F51L |
possibly damaging |
Het |
Tmem104 |
C |
A |
11: 115,095,962 (GRCm39) |
P168T |
probably damaging |
Het |
Tril |
G |
T |
6: 53,795,905 (GRCm39) |
T439K |
probably benign |
Het |
Trim2 |
A |
G |
3: 84,085,042 (GRCm39) |
L559P |
probably damaging |
Het |
Trim3 |
A |
G |
7: 105,268,335 (GRCm39) |
V149A |
probably damaging |
Het |
Triml2 |
A |
G |
8: 43,640,717 (GRCm39) |
N191S |
probably benign |
Het |
Usp4 |
A |
G |
9: 108,258,617 (GRCm39) |
D16G |
probably benign |
Het |
Vmn2r58 |
G |
A |
7: 41,486,885 (GRCm39) |
T670I |
probably damaging |
Het |
Vmn2r97 |
G |
T |
17: 19,160,436 (GRCm39) |
G524* |
probably null |
Het |
Xpo5 |
C |
A |
17: 46,531,743 (GRCm39) |
F426L |
probably damaging |
Het |
Zfp800 |
A |
G |
6: 28,247,190 (GRCm39) |
L84S |
probably damaging |
Het |
Zranb2 |
T |
G |
3: 157,252,378 (GRCm39) |
|
probably benign |
Het |
Zswim4 |
C |
T |
8: 84,953,296 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Mrgpra1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00903:Mrgpra1
|
APN |
7 |
46,985,326 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01317:Mrgpra1
|
APN |
7 |
46,985,372 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01718:Mrgpra1
|
APN |
7 |
46,985,675 (GRCm39) |
splice site |
probably null |
|
IGL02252:Mrgpra1
|
APN |
7 |
46,984,912 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03301:Mrgpra1
|
APN |
7 |
46,985,164 (GRCm39) |
missense |
probably benign |
|
R0012:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R1019:Mrgpra1
|
UTSW |
7 |
46,984,833 (GRCm39) |
missense |
probably benign |
0.00 |
R2224:Mrgpra1
|
UTSW |
7 |
46,984,854 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2520:Mrgpra1
|
UTSW |
7 |
46,985,020 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2924:Mrgpra1
|
UTSW |
7 |
46,984,618 (GRCm39) |
splice site |
probably null |
|
R3038:Mrgpra1
|
UTSW |
7 |
46,984,744 (GRCm39) |
nonsense |
probably null |
|
R3900:Mrgpra1
|
UTSW |
7 |
46,985,275 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4692:Mrgpra1
|
UTSW |
7 |
46,985,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R4784:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R4785:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R5031:Mrgpra1
|
UTSW |
7 |
46,984,985 (GRCm39) |
nonsense |
probably null |
|
R6760:Mrgpra1
|
UTSW |
7 |
46,984,789 (GRCm39) |
missense |
probably benign |
0.03 |
R7305:Mrgpra1
|
UTSW |
7 |
46,985,203 (GRCm39) |
missense |
probably benign |
0.38 |
R7348:Mrgpra1
|
UTSW |
7 |
46,985,157 (GRCm39) |
missense |
probably benign |
0.09 |
R7837:Mrgpra1
|
UTSW |
7 |
46,985,076 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8158:Mrgpra1
|
UTSW |
7 |
46,985,204 (GRCm39) |
nonsense |
probably null |
|
R8856:Mrgpra1
|
UTSW |
7 |
46,985,583 (GRCm39) |
missense |
probably benign |
0.30 |
R9100:Mrgpra1
|
UTSW |
7 |
46,984,732 (GRCm39) |
missense |
probably damaging |
0.97 |
R9694:Mrgpra1
|
UTSW |
7 |
46,985,268 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Mrgpra1
|
UTSW |
7 |
46,985,623 (GRCm39) |
missense |
probably benign |
|
|