Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadsb |
C |
T |
7: 131,027,518 (GRCm39) |
Q63* |
probably null |
Het |
Adam26b |
A |
T |
8: 43,973,408 (GRCm39) |
N531K |
probably benign |
Het |
Agt |
A |
G |
8: 125,286,014 (GRCm39) |
I356T |
probably benign |
Het |
Ankmy1 |
A |
T |
1: 92,827,413 (GRCm39) |
|
probably benign |
Het |
Anxa3 |
C |
T |
5: 96,960,743 (GRCm39) |
S49L |
possibly damaging |
Het |
Arap3 |
C |
A |
18: 38,108,593 (GRCm39) |
R1279L |
probably damaging |
Het |
Azin1 |
A |
G |
15: 38,493,825 (GRCm39) |
I266T |
probably benign |
Het |
Btnl7-ps |
T |
C |
17: 34,752,498 (GRCm39) |
|
noncoding transcript |
Het |
Car5a |
T |
A |
8: 122,671,469 (GRCm39) |
T22S |
probably benign |
Het |
Card6 |
A |
G |
15: 5,134,648 (GRCm39) |
I185T |
probably damaging |
Het |
Ccdc81 |
T |
C |
7: 89,552,437 (GRCm39) |
D11G |
probably benign |
Het |
Cep170b |
T |
C |
12: 112,705,623 (GRCm39) |
V1127A |
probably benign |
Het |
Ces1h |
T |
C |
8: 94,083,771 (GRCm39) |
I390M |
unknown |
Het |
Col9a1 |
T |
A |
1: 24,218,360 (GRCm39) |
|
probably null |
Het |
Cwc27 |
C |
A |
13: 104,797,865 (GRCm39) |
E365* |
probably null |
Het |
Cyb561a3 |
T |
C |
19: 10,564,074 (GRCm39) |
V138A |
probably benign |
Het |
Dcaf1 |
T |
C |
9: 106,721,321 (GRCm39) |
|
probably benign |
Het |
Dnah17 |
A |
G |
11: 117,963,726 (GRCm39) |
Y2516H |
probably damaging |
Het |
Dsc2 |
T |
A |
18: 20,174,594 (GRCm39) |
N521Y |
probably damaging |
Het |
Dst |
G |
A |
1: 34,267,062 (GRCm39) |
E4835K |
probably damaging |
Het |
Duox2 |
T |
C |
2: 122,120,080 (GRCm39) |
E810G |
probably damaging |
Het |
Dusp15 |
T |
C |
2: 152,793,268 (GRCm39) |
N3S |
possibly damaging |
Het |
Eif1ad9 |
A |
G |
12: 88,296,436 (GRCm39) |
D138G |
unknown |
Het |
Epha4 |
T |
C |
1: 77,365,124 (GRCm39) |
K625R |
probably benign |
Het |
Fcgbpl1 |
G |
A |
7: 27,862,115 (GRCm39) |
V2394I |
probably benign |
Het |
Gata5 |
C |
T |
2: 179,969,552 (GRCm39) |
|
probably null |
Het |
Grm5 |
A |
G |
7: 87,252,227 (GRCm39) |
N159S |
probably damaging |
Het |
Hivep3 |
T |
A |
4: 119,953,751 (GRCm39) |
M689K |
probably benign |
Het |
Ift56 |
T |
A |
6: 38,378,064 (GRCm39) |
V292E |
probably damaging |
Het |
Ilvbl |
G |
T |
10: 78,419,321 (GRCm39) |
G499C |
probably damaging |
Het |
Inpp4b |
T |
C |
8: 82,494,780 (GRCm39) |
I65T |
possibly damaging |
Het |
Jarid2 |
T |
C |
13: 45,055,835 (GRCm39) |
V208A |
probably damaging |
Het |
Kcnh4 |
T |
C |
11: 100,641,070 (GRCm39) |
M460V |
possibly damaging |
Het |
Klhl22 |
A |
G |
16: 17,610,488 (GRCm39) |
N580D |
probably benign |
Het |
Klk15 |
T |
A |
7: 43,588,269 (GRCm39) |
C192* |
probably null |
Het |
Klk1b9 |
A |
G |
7: 43,445,090 (GRCm39) |
E194G |
probably damaging |
Het |
Lama1 |
G |
T |
17: 68,122,954 (GRCm39) |
G2779V |
probably damaging |
Het |
Lmln |
C |
T |
16: 32,937,455 (GRCm39) |
R607* |
probably null |
Het |
Maea |
T |
C |
5: 33,529,645 (GRCm39) |
V377A |
probably benign |
Het |
Matk |
A |
T |
10: 81,095,525 (GRCm39) |
Y115F |
probably benign |
Het |
Mettl18 |
A |
G |
1: 163,824,062 (GRCm39) |
K128E |
probably benign |
Het |
Mrps22 |
T |
C |
9: 98,474,746 (GRCm39) |
H246R |
probably benign |
Het |
Msln |
A |
T |
17: 25,971,980 (GRCm39) |
M79K |
probably benign |
Het |
Myf6 |
G |
A |
10: 107,330,420 (GRCm39) |
P49L |
probably benign |
Het |
Nat1 |
C |
T |
8: 67,943,963 (GRCm39) |
T113I |
possibly damaging |
Het |
Ncor2 |
C |
T |
5: 125,162,093 (GRCm39) |
V394M |
unknown |
Het |
Oas1c |
T |
C |
5: 120,943,669 (GRCm39) |
|
probably benign |
Het |
Or8k21 |
T |
A |
2: 86,144,869 (GRCm39) |
T254S |
probably benign |
Het |
Otp |
A |
T |
13: 95,013,917 (GRCm39) |
T112S |
probably damaging |
Het |
Pcdh7 |
A |
G |
5: 57,877,405 (GRCm39) |
N320S |
probably damaging |
Het |
Pdzd2 |
G |
T |
15: 12,592,364 (GRCm39) |
F93L |
probably damaging |
Het |
Phf20l1 |
A |
G |
15: 66,481,453 (GRCm39) |
E283G |
probably damaging |
Het |
Polr1e |
T |
C |
4: 45,029,421 (GRCm39) |
F342S |
probably damaging |
Het |
Pp2d1 |
T |
A |
17: 53,846,196 (GRCm39) |
|
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,664,291 (GRCm39) |
|
probably null |
Het |
Reg3g |
A |
T |
6: 78,444,471 (GRCm39) |
H107Q |
possibly damaging |
Het |
Samd4 |
T |
C |
14: 47,314,966 (GRCm39) |
C309R |
probably damaging |
Het |
Sestd1 |
C |
A |
2: 77,061,066 (GRCm39) |
W104L |
probably benign |
Het |
Sfmbt1 |
T |
A |
14: 30,533,330 (GRCm39) |
|
probably null |
Het |
Slc22a21 |
T |
A |
11: 53,870,446 (GRCm39) |
K80* |
probably null |
Het |
Snx20 |
T |
A |
8: 89,356,630 (GRCm39) |
Q62L |
probably benign |
Het |
Spef1l |
T |
C |
7: 139,557,026 (GRCm39) |
M120V |
probably benign |
Het |
Stk40 |
C |
A |
4: 126,032,594 (GRCm39) |
|
probably benign |
Het |
Taf2 |
A |
T |
15: 54,885,584 (GRCm39) |
|
probably benign |
Het |
Tcf23 |
C |
T |
5: 31,127,654 (GRCm39) |
P152L |
probably damaging |
Het |
Tex29 |
T |
C |
8: 11,894,138 (GRCm39) |
|
probably benign |
Het |
Tjp3 |
A |
G |
10: 81,116,389 (GRCm39) |
V235A |
probably damaging |
Het |
Tns3 |
A |
T |
11: 8,443,262 (GRCm39) |
I367N |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,543,255 (GRCm39) |
M33244L |
probably benign |
Het |
Ush2a |
A |
T |
1: 188,089,044 (GRCm39) |
N333I |
probably damaging |
Het |
Usp34 |
T |
C |
11: 23,382,406 (GRCm39) |
|
probably benign |
Het |
Vmn1r204 |
A |
C |
13: 22,740,848 (GRCm39) |
S160R |
probably benign |
Het |
Vmn2r75 |
C |
T |
7: 85,797,449 (GRCm39) |
W788* |
probably null |
Het |
Vwa5b1 |
T |
C |
4: 138,363,022 (GRCm39) |
|
probably benign |
Het |
Zbtb7a |
A |
G |
10: 80,984,163 (GRCm39) |
E535G |
probably benign |
Het |
Zfp1004 |
T |
A |
2: 150,034,494 (GRCm39) |
C303S |
probably damaging |
Het |
Zranb3 |
T |
C |
1: 127,964,295 (GRCm39) |
D144G |
probably benign |
Het |
|
Other mutations in Rgl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Rgl1
|
APN |
1 |
152,447,368 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01065:Rgl1
|
APN |
1 |
152,394,893 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01390:Rgl1
|
APN |
1 |
152,447,339 (GRCm39) |
splice site |
probably benign |
|
IGL01726:Rgl1
|
APN |
1 |
152,394,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01837:Rgl1
|
APN |
1 |
152,424,901 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02019:Rgl1
|
APN |
1 |
152,404,220 (GRCm39) |
splice site |
probably benign |
|
IGL02369:Rgl1
|
APN |
1 |
152,409,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Rgl1
|
UTSW |
1 |
152,430,175 (GRCm39) |
unclassified |
probably benign |
|
R0255:Rgl1
|
UTSW |
1 |
152,428,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Rgl1
|
UTSW |
1 |
152,412,016 (GRCm39) |
critical splice donor site |
probably null |
|
R0734:Rgl1
|
UTSW |
1 |
152,430,051 (GRCm39) |
missense |
probably damaging |
0.98 |
R1187:Rgl1
|
UTSW |
1 |
152,420,184 (GRCm39) |
missense |
probably benign |
0.14 |
R1522:Rgl1
|
UTSW |
1 |
152,462,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Rgl1
|
UTSW |
1 |
152,550,774 (GRCm39) |
splice site |
probably benign |
|
R1634:Rgl1
|
UTSW |
1 |
152,400,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R1661:Rgl1
|
UTSW |
1 |
152,409,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R1665:Rgl1
|
UTSW |
1 |
152,409,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R1964:Rgl1
|
UTSW |
1 |
152,424,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Rgl1
|
UTSW |
1 |
152,412,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R4272:Rgl1
|
UTSW |
1 |
152,412,040 (GRCm39) |
missense |
probably benign |
0.13 |
R4668:Rgl1
|
UTSW |
1 |
152,397,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Rgl1
|
UTSW |
1 |
152,397,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Rgl1
|
UTSW |
1 |
152,400,450 (GRCm39) |
nonsense |
probably null |
|
R4830:Rgl1
|
UTSW |
1 |
152,430,081 (GRCm39) |
missense |
probably benign |
0.11 |
R4853:Rgl1
|
UTSW |
1 |
152,433,325 (GRCm39) |
missense |
probably benign |
0.07 |
R4969:Rgl1
|
UTSW |
1 |
152,424,813 (GRCm39) |
splice site |
probably null |
|
R5778:Rgl1
|
UTSW |
1 |
152,428,172 (GRCm39) |
missense |
probably benign |
0.05 |
R5979:Rgl1
|
UTSW |
1 |
152,433,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R6180:Rgl1
|
UTSW |
1 |
152,394,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R6183:Rgl1
|
UTSW |
1 |
152,462,321 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6322:Rgl1
|
UTSW |
1 |
152,428,186 (GRCm39) |
missense |
probably damaging |
0.98 |
R6678:Rgl1
|
UTSW |
1 |
152,400,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6759:Rgl1
|
UTSW |
1 |
152,409,281 (GRCm39) |
missense |
probably damaging |
0.99 |
R6892:Rgl1
|
UTSW |
1 |
152,415,691 (GRCm39) |
missense |
probably benign |
0.00 |
R7290:Rgl1
|
UTSW |
1 |
152,420,146 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7363:Rgl1
|
UTSW |
1 |
152,394,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R7610:Rgl1
|
UTSW |
1 |
152,428,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R7774:Rgl1
|
UTSW |
1 |
152,430,101 (GRCm39) |
missense |
probably benign |
|
R8140:Rgl1
|
UTSW |
1 |
152,433,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R9188:Rgl1
|
UTSW |
1 |
152,394,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Rgl1
|
UTSW |
1 |
152,428,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R9297:Rgl1
|
UTSW |
1 |
152,400,454 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9318:Rgl1
|
UTSW |
1 |
152,400,454 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9491:Rgl1
|
UTSW |
1 |
152,424,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Rgl1
|
UTSW |
1 |
152,430,082 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9610:Rgl1
|
UTSW |
1 |
152,397,115 (GRCm39) |
missense |
probably benign |
0.13 |
R9640:Rgl1
|
UTSW |
1 |
152,397,142 (GRCm39) |
missense |
probably damaging |
1.00 |
RF005:Rgl1
|
UTSW |
1 |
152,397,114 (GRCm39) |
missense |
probably benign |
|
Z1088:Rgl1
|
UTSW |
1 |
152,550,771 (GRCm39) |
start gained |
probably benign |
|
|