Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
T |
C |
6: 83,162,586 (GRCm38) |
S498P |
probably damaging |
Het |
3100002H09Rik |
A |
G |
4: 124,610,694 (GRCm38) |
W22R |
probably damaging |
Het |
AA986860 |
A |
G |
1: 130,743,094 (GRCm38) |
E351G |
probably damaging |
Het |
Acsl5 |
T |
C |
19: 55,280,492 (GRCm38) |
V195A |
probably benign |
Het |
Actmap |
A |
G |
7: 27,202,680 (GRCm38) |
H244R |
probably damaging |
Het |
Adamts10 |
A |
G |
17: 33,537,319 (GRCm38) |
D312G |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,580,617 (GRCm38) |
M211V |
probably damaging |
Het |
Ankfy1 |
C |
T |
11: 72,755,867 (GRCm38) |
R859* |
probably null |
Het |
Atp8b1 |
T |
A |
18: 64,550,432 (GRCm38) |
I742L |
probably benign |
Het |
B3galnt2 |
T |
A |
13: 13,970,769 (GRCm38) |
V89E |
probably damaging |
Het |
Brinp3 |
A |
C |
1: 146,901,890 (GRCm38) |
T692P |
probably damaging |
Het |
C9 |
T |
A |
15: 6,486,762 (GRCm38) |
F349I |
probably damaging |
Het |
Cacna1a |
T |
A |
8: 84,633,433 (GRCm38) |
M1976K |
probably benign |
Het |
Castor2 |
T |
G |
5: 134,125,887 (GRCm38) |
S43R |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,927,975 (GRCm38) |
V1170A |
possibly damaging |
Het |
Celsr1 |
A |
G |
15: 85,931,276 (GRCm38) |
V1846A |
probably benign |
Het |
Ces1f |
A |
T |
8: 93,271,889 (GRCm38) |
Y160N |
possibly damaging |
Het |
Cfap45 |
A |
G |
1: 172,540,572 (GRCm38) |
E377G |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,755,171 (GRCm38) |
M240L |
probably benign |
Het |
Clnk |
G |
A |
5: 38,794,966 (GRCm38) |
T10M |
probably damaging |
Het |
Cntrl |
T |
A |
2: 35,155,279 (GRCm38) |
I781K |
possibly damaging |
Het |
Col11a2 |
G |
A |
17: 34,055,254 (GRCm38) |
G375S |
probably damaging |
Het |
Col6a5 |
T |
A |
9: 105,939,994 (GRCm38) |
I373F |
unknown |
Het |
Dmxl1 |
C |
T |
18: 49,852,367 (GRCm38) |
A227V |
probably benign |
Het |
Dok5 |
A |
G |
2: 170,732,132 (GRCm38) |
N4D |
probably benign |
Het |
Dpysl3 |
A |
T |
18: 43,363,557 (GRCm38) |
V138D |
probably damaging |
Het |
Efs |
A |
T |
14: 54,919,715 (GRCm38) |
Y380N |
probably damaging |
Het |
Eme2 |
G |
A |
17: 24,892,918 (GRCm38) |
S263F |
probably damaging |
Het |
Farp2 |
A |
G |
1: 93,618,553 (GRCm38) |
Q855R |
possibly damaging |
Het |
Fcrl2 |
A |
C |
3: 87,256,707 (GRCm38) |
S372A |
possibly damaging |
Het |
Gadl1 |
C |
T |
9: 115,944,229 (GRCm38) |
A113V |
probably damaging |
Het |
Gda |
T |
A |
19: 21,412,539 (GRCm38) |
E219D |
probably benign |
Het |
Gli1 |
A |
T |
10: 127,332,577 (GRCm38) |
M469K |
probably damaging |
Het |
Gm4847 |
A |
T |
1: 166,641,650 (GRCm38) |
S148R |
probably damaging |
Het |
Golga2 |
T |
C |
2: 32,302,204 (GRCm38) |
V325A |
probably benign |
Het |
Hpf1 |
A |
G |
8: 60,896,749 (GRCm38) |
D137G |
probably damaging |
Het |
Htr2a |
C |
G |
14: 74,705,853 (GRCm38) |
S291* |
probably null |
Het |
Itga5 |
G |
A |
15: 103,356,782 (GRCm38) |
Q233* |
probably null |
Het |
Jazf1 |
C |
A |
6: 52,812,183 (GRCm38) |
R102L |
probably damaging |
Het |
Kif6 |
T |
G |
17: 49,714,113 (GRCm38) |
L322R |
probably damaging |
Het |
Ktn1 |
A |
C |
14: 47,667,416 (GRCm38) |
K217T |
probably damaging |
Het |
Lig4 |
A |
T |
8: 9,973,012 (GRCm38) |
V256E |
possibly damaging |
Het |
Lrp1 |
A |
T |
10: 127,575,286 (GRCm38) |
D1399E |
probably benign |
Het |
Lrp1 |
G |
T |
10: 127,567,364 (GRCm38) |
D2113E |
probably damaging |
Het |
Mmel1 |
A |
G |
4: 154,894,986 (GRCm38) |
E717G |
probably damaging |
Het |
Mndal |
G |
T |
1: 173,871,466 (GRCm38) |
P155H |
possibly damaging |
Het |
Mycbpap |
A |
G |
11: 94,511,623 (GRCm38) |
|
probably null |
Het |
Nedd1 |
T |
C |
10: 92,719,614 (GRCm38) |
E3G |
probably damaging |
Het |
Nlgn1 |
A |
T |
3: 25,435,909 (GRCm38) |
N551K |
probably damaging |
Het |
Nup210 |
G |
A |
6: 91,069,166 (GRCm38) |
P595L |
possibly damaging |
Het |
Or2ag15 |
A |
G |
7: 106,741,005 (GRCm38) |
C310R |
probably benign |
Het |
Or2g25 |
A |
T |
17: 37,659,770 (GRCm38) |
C188S |
probably damaging |
Het |
Or4k52 |
A |
T |
2: 111,780,348 (GRCm38) |
|
probably null |
Het |
Or5ac17 |
T |
G |
16: 59,215,984 (GRCm38) |
T210P |
probably damaging |
Het |
Or5p56 |
A |
G |
7: 107,990,533 (GRCm38) |
H56R |
probably benign |
Het |
Pank3 |
G |
A |
11: 35,781,681 (GRCm38) |
V304M |
probably benign |
Het |
Phf3 |
G |
A |
1: 30,805,648 (GRCm38) |
T1410I |
probably benign |
Het |
Ppm1k |
A |
G |
6: 57,525,157 (GRCm38) |
I7T |
possibly damaging |
Het |
Ppp1r12c |
T |
C |
7: 4,497,425 (GRCm38) |
D73G |
probably damaging |
Het |
Prelid2 |
T |
G |
18: 41,881,267 (GRCm38) |
M165L |
probably benign |
Het |
Prkd3 |
A |
C |
17: 78,952,696 (GRCm38) |
L826R |
probably damaging |
Het |
Ptchd4 |
A |
T |
17: 42,503,542 (GRCm38) |
N778I |
probably damaging |
Het |
Ptprm |
T |
C |
17: 66,693,871 (GRCm38) |
D1063G |
possibly damaging |
Het |
Rab27a |
C |
A |
9: 73,075,482 (GRCm38) |
T23N |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 91,896,086 (GRCm38) |
F949L |
probably benign |
Het |
Rbm33 |
A |
G |
5: 28,337,004 (GRCm38) |
N68D |
probably damaging |
Het |
Rnf20 |
A |
G |
4: 49,638,197 (GRCm38) |
N103S |
possibly damaging |
Het |
Sbno1 |
G |
A |
5: 124,392,612 (GRCm38) |
L875F |
probably damaging |
Het |
Scube1 |
T |
A |
15: 83,628,076 (GRCm38) |
|
probably null |
Het |
Selenbp1 |
G |
A |
3: 94,937,358 (GRCm38) |
V109M |
probably damaging |
Het |
Serpina3c |
T |
A |
12: 104,151,546 (GRCm38) |
I178F |
probably damaging |
Het |
Shisa8 |
C |
T |
15: 82,208,501 (GRCm38) |
G63D |
probably damaging |
Het |
Snx14 |
T |
C |
9: 88,402,224 (GRCm38) |
R464G |
possibly damaging |
Het |
Snx25 |
A |
T |
8: 46,124,082 (GRCm38) |
M1K |
probably null |
Het |
Sorcs3 |
C |
A |
19: 48,706,009 (GRCm38) |
T574K |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,103,783 (GRCm38) |
E6528G |
probably damaging |
Het |
Syt5 |
T |
C |
7: 4,540,246 (GRCm38) |
E338G |
probably damaging |
Het |
Tbk1 |
T |
C |
10: 121,551,318 (GRCm38) |
K691E |
probably benign |
Het |
Tenm3 |
G |
A |
8: 48,395,576 (GRCm38) |
T11I |
probably damaging |
Het |
Thrb |
A |
G |
14: 18,002,597 (GRCm38) |
H87R |
probably damaging |
Het |
Tlr4 |
T |
A |
4: 66,839,696 (GRCm38) |
M242K |
possibly damaging |
Het |
Tm4sf19 |
T |
C |
16: 32,406,002 (GRCm38) |
M56T |
possibly damaging |
Het |
Tmem212 |
T |
A |
3: 27,886,471 (GRCm38) |
R66* |
probably null |
Het |
Tmem39b |
G |
T |
4: 129,684,482 (GRCm38) |
D315E |
probably benign |
Het |
Tnxb |
T |
C |
17: 34,718,638 (GRCm38) |
F3834L |
probably damaging |
Het |
Trim36 |
A |
T |
18: 46,186,183 (GRCm38) |
L225* |
probably null |
Het |
Trim42 |
A |
T |
9: 97,365,679 (GRCm38) |
H321Q |
probably damaging |
Het |
Trio |
G |
T |
15: 27,732,640 (GRCm38) |
Q3052K |
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,978,334 (GRCm38) |
I1091T |
probably benign |
Het |
Tst |
T |
C |
15: 78,399,943 (GRCm38) |
E228G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,871,716 (GRCm38) |
|
probably benign |
Het |
Uap1 |
A |
C |
1: 170,150,941 (GRCm38) |
|
probably null |
Het |
Ush2a |
T |
C |
1: 188,797,814 (GRCm38) |
S3267P |
possibly damaging |
Het |
Usp5 |
T |
C |
6: 124,825,166 (GRCm38) |
T38A |
probably benign |
Het |
Uvssa |
A |
T |
5: 33,387,808 (GRCm38) |
Q84L |
probably damaging |
Het |
Vmn1r159 |
T |
G |
7: 22,843,268 (GRCm38) |
H113P |
probably damaging |
Het |
Vps13d |
A |
T |
4: 145,098,172 (GRCm38) |
|
probably null |
Het |
Zfp182 |
T |
A |
X: 21,031,560 (GRCm38) |
I166L |
probably benign |
Het |
Zfp811 |
A |
T |
17: 32,797,648 (GRCm38) |
Y472N |
probably damaging |
Het |
|
Other mutations in Rgl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Rgl1
|
APN |
1 |
152,571,617 (GRCm38) |
missense |
probably benign |
0.02 |
IGL01065:Rgl1
|
APN |
1 |
152,519,142 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01390:Rgl1
|
APN |
1 |
152,571,588 (GRCm38) |
splice site |
probably benign |
|
IGL01726:Rgl1
|
APN |
1 |
152,519,153 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01837:Rgl1
|
APN |
1 |
152,549,150 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02019:Rgl1
|
APN |
1 |
152,528,469 (GRCm38) |
splice site |
probably benign |
|
IGL02369:Rgl1
|
APN |
1 |
152,533,606 (GRCm38) |
missense |
probably damaging |
1.00 |
R0240:Rgl1
|
UTSW |
1 |
152,554,424 (GRCm38) |
unclassified |
probably benign |
|
R0255:Rgl1
|
UTSW |
1 |
152,552,596 (GRCm38) |
missense |
probably damaging |
1.00 |
R0562:Rgl1
|
UTSW |
1 |
152,539,945 (GRCm38) |
missense |
probably damaging |
1.00 |
R0648:Rgl1
|
UTSW |
1 |
152,536,265 (GRCm38) |
critical splice donor site |
probably null |
|
R0734:Rgl1
|
UTSW |
1 |
152,554,300 (GRCm38) |
missense |
probably damaging |
0.98 |
R1187:Rgl1
|
UTSW |
1 |
152,544,433 (GRCm38) |
missense |
probably benign |
0.14 |
R1595:Rgl1
|
UTSW |
1 |
152,675,023 (GRCm38) |
splice site |
probably benign |
|
R1634:Rgl1
|
UTSW |
1 |
152,524,772 (GRCm38) |
missense |
probably damaging |
1.00 |
R1661:Rgl1
|
UTSW |
1 |
152,533,575 (GRCm38) |
missense |
probably damaging |
0.99 |
R1665:Rgl1
|
UTSW |
1 |
152,533,575 (GRCm38) |
missense |
probably damaging |
0.99 |
R1964:Rgl1
|
UTSW |
1 |
152,549,104 (GRCm38) |
missense |
probably damaging |
1.00 |
R2291:Rgl1
|
UTSW |
1 |
152,536,281 (GRCm38) |
missense |
probably damaging |
1.00 |
R4272:Rgl1
|
UTSW |
1 |
152,536,289 (GRCm38) |
missense |
probably benign |
0.13 |
R4668:Rgl1
|
UTSW |
1 |
152,521,371 (GRCm38) |
missense |
probably damaging |
1.00 |
R4669:Rgl1
|
UTSW |
1 |
152,521,371 (GRCm38) |
missense |
probably damaging |
1.00 |
R4747:Rgl1
|
UTSW |
1 |
152,524,699 (GRCm38) |
nonsense |
probably null |
|
R4830:Rgl1
|
UTSW |
1 |
152,554,330 (GRCm38) |
missense |
probably benign |
0.11 |
R4853:Rgl1
|
UTSW |
1 |
152,557,574 (GRCm38) |
missense |
probably benign |
0.07 |
R4969:Rgl1
|
UTSW |
1 |
152,549,062 (GRCm38) |
splice site |
probably null |
|
R5778:Rgl1
|
UTSW |
1 |
152,552,421 (GRCm38) |
missense |
probably benign |
0.05 |
R5979:Rgl1
|
UTSW |
1 |
152,557,493 (GRCm38) |
missense |
probably damaging |
1.00 |
R6180:Rgl1
|
UTSW |
1 |
152,519,172 (GRCm38) |
missense |
probably damaging |
1.00 |
R6183:Rgl1
|
UTSW |
1 |
152,586,570 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6322:Rgl1
|
UTSW |
1 |
152,552,435 (GRCm38) |
missense |
probably damaging |
0.98 |
R6678:Rgl1
|
UTSW |
1 |
152,524,724 (GRCm38) |
missense |
probably damaging |
1.00 |
R6759:Rgl1
|
UTSW |
1 |
152,533,530 (GRCm38) |
missense |
probably damaging |
0.99 |
R6892:Rgl1
|
UTSW |
1 |
152,539,940 (GRCm38) |
missense |
probably benign |
0.00 |
R7290:Rgl1
|
UTSW |
1 |
152,544,395 (GRCm38) |
missense |
possibly damaging |
0.78 |
R7363:Rgl1
|
UTSW |
1 |
152,519,163 (GRCm38) |
missense |
probably damaging |
1.00 |
R7610:Rgl1
|
UTSW |
1 |
152,552,620 (GRCm38) |
missense |
probably damaging |
1.00 |
R7774:Rgl1
|
UTSW |
1 |
152,554,350 (GRCm38) |
missense |
probably benign |
|
R8140:Rgl1
|
UTSW |
1 |
152,557,501 (GRCm38) |
missense |
probably damaging |
1.00 |
R9188:Rgl1
|
UTSW |
1 |
152,519,171 (GRCm38) |
missense |
probably damaging |
1.00 |
R9190:Rgl1
|
UTSW |
1 |
152,552,611 (GRCm38) |
missense |
probably damaging |
0.96 |
R9297:Rgl1
|
UTSW |
1 |
152,524,703 (GRCm38) |
missense |
possibly damaging |
0.89 |
R9318:Rgl1
|
UTSW |
1 |
152,524,703 (GRCm38) |
missense |
possibly damaging |
0.89 |
R9491:Rgl1
|
UTSW |
1 |
152,549,118 (GRCm38) |
missense |
probably damaging |
1.00 |
R9570:Rgl1
|
UTSW |
1 |
152,554,331 (GRCm38) |
missense |
possibly damaging |
0.47 |
R9610:Rgl1
|
UTSW |
1 |
152,521,364 (GRCm38) |
missense |
probably benign |
0.13 |
R9640:Rgl1
|
UTSW |
1 |
152,521,391 (GRCm38) |
missense |
probably damaging |
1.00 |
RF005:Rgl1
|
UTSW |
1 |
152,521,363 (GRCm38) |
missense |
probably benign |
|
Z1088:Rgl1
|
UTSW |
1 |
152,675,020 (GRCm38) |
start gained |
probably benign |
|
|