Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,074,689 (GRCm39) |
N577S |
probably benign |
Het |
Ang4 |
A |
G |
14: 52,001,529 (GRCm39) |
S140P |
probably damaging |
Het |
Ankdd1b |
T |
C |
13: 96,556,306 (GRCm39) |
|
probably null |
Het |
Anln |
G |
T |
9: 22,274,019 (GRCm39) |
A606D |
probably benign |
Het |
Ano5 |
T |
G |
7: 51,237,480 (GRCm39) |
V768G |
possibly damaging |
Het |
Ccdc180 |
A |
T |
4: 45,900,461 (GRCm39) |
Y275F |
possibly damaging |
Het |
Chpf |
T |
C |
1: 75,453,271 (GRCm39) |
Y334C |
probably damaging |
Het |
Cibar2 |
T |
C |
8: 120,893,372 (GRCm39) |
D273G |
probably benign |
Het |
Cox20 |
A |
T |
1: 178,150,126 (GRCm39) |
Y100F |
probably benign |
Het |
Dbn1 |
T |
C |
13: 55,623,322 (GRCm39) |
D433G |
possibly damaging |
Het |
Dclre1a |
A |
T |
19: 56,519,684 (GRCm39) |
I983N |
probably damaging |
Het |
Dok6 |
A |
T |
18: 89,578,182 (GRCm39) |
H78Q |
probably benign |
Het |
Efcab3 |
G |
A |
11: 104,624,539 (GRCm39) |
D878N |
probably benign |
Het |
Fpr1 |
A |
T |
17: 18,097,634 (GRCm39) |
F118L |
probably benign |
Het |
Fscn3 |
A |
G |
6: 28,430,175 (GRCm39) |
Y115C |
probably damaging |
Het |
Gabra4 |
A |
C |
5: 71,798,256 (GRCm39) |
|
probably null |
Het |
Gm45861 |
T |
C |
8: 28,072,751 (GRCm39) |
V1290A |
unknown |
Het |
Hivep1 |
T |
C |
13: 42,308,828 (GRCm39) |
V356A |
probably benign |
Het |
Ikbip |
T |
C |
10: 90,937,617 (GRCm39) |
Y97H |
possibly damaging |
Het |
Il10 |
A |
G |
1: 130,947,805 (GRCm39) |
T53A |
probably benign |
Het |
Inpp5f |
T |
C |
7: 128,296,526 (GRCm39) |
V959A |
probably benign |
Het |
Insr |
T |
C |
8: 3,308,415 (GRCm39) |
E207G |
probably benign |
Het |
Kndc1 |
T |
A |
7: 139,503,731 (GRCm39) |
S1012T |
probably damaging |
Het |
Krtap5-1 |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
7: 141,850,333 (GRCm39) |
|
probably benign |
Het |
Ksr2 |
T |
C |
5: 117,693,329 (GRCm39) |
V259A |
probably benign |
Het |
Lox |
A |
T |
18: 52,658,194 (GRCm39) |
Y326* |
probably null |
Het |
Lpin2 |
C |
A |
17: 71,537,269 (GRCm39) |
T272N |
probably benign |
Het |
Lrp2 |
C |
T |
2: 69,295,128 (GRCm39) |
E3397K |
probably damaging |
Het |
Megf11 |
G |
A |
9: 64,602,709 (GRCm39) |
C850Y |
possibly damaging |
Het |
Morc1 |
T |
C |
16: 48,319,147 (GRCm39) |
F284L |
probably benign |
Het |
Moxd2 |
T |
A |
6: 40,862,378 (GRCm39) |
D147V |
possibly damaging |
Het |
Mrpl21 |
T |
C |
19: 3,337,752 (GRCm39) |
L153P |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,280,917 (GRCm39) |
T1432A |
probably benign |
Het |
Naip6 |
T |
A |
13: 100,451,979 (GRCm39) |
D211V |
probably damaging |
Het |
Ncoa5 |
T |
C |
2: 164,854,816 (GRCm39) |
H102R |
possibly damaging |
Het |
Ndel1 |
A |
T |
11: 68,720,806 (GRCm39) |
C293* |
probably null |
Het |
Ninl |
A |
T |
2: 150,808,016 (GRCm39) |
M82K |
probably benign |
Het |
Nrcam |
G |
A |
12: 44,587,858 (GRCm39) |
|
probably null |
Het |
Nup210l |
A |
T |
3: 90,030,036 (GRCm39) |
I250L |
probably benign |
Het |
Obscn |
T |
C |
11: 58,968,776 (GRCm39) |
E2532G |
possibly damaging |
Het |
Or1e1 |
C |
A |
11: 73,244,585 (GRCm39) |
A2E |
probably benign |
Het |
Or5v1 |
G |
T |
17: 37,809,868 (GRCm39) |
G109C |
probably damaging |
Het |
Or8j3c |
A |
G |
2: 86,253,583 (GRCm39) |
F146L |
probably benign |
Het |
Osgin1 |
G |
A |
8: 120,171,773 (GRCm39) |
S189N |
possibly damaging |
Het |
Otud7b |
A |
G |
3: 96,062,690 (GRCm39) |
E643G |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,571,727 (GRCm39) |
T1222S |
probably damaging |
Het |
Pwp1 |
C |
T |
10: 85,723,914 (GRCm39) |
R472W |
probably damaging |
Het |
Rad21 |
T |
C |
15: 51,836,538 (GRCm39) |
Y211C |
probably damaging |
Het |
Rexo1 |
A |
G |
10: 80,386,572 (GRCm39) |
V162A |
probably benign |
Het |
Rtl1 |
C |
T |
12: 109,560,589 (GRCm39) |
V417I |
probably benign |
Het |
Setbp1 |
G |
A |
18: 78,826,639 (GRCm39) |
P1325S |
probably benign |
Het |
Shld1 |
A |
G |
2: 132,592,510 (GRCm39) |
T186A |
probably damaging |
Het |
Shld2 |
A |
G |
14: 33,959,523 (GRCm39) |
Y820H |
probably damaging |
Het |
Skint7 |
G |
T |
4: 111,839,423 (GRCm39) |
C239F |
probably benign |
Het |
Slc25a1 |
A |
G |
16: 17,744,138 (GRCm39) |
L221P |
probably benign |
Het |
Snrnp70 |
T |
A |
7: 45,026,214 (GRCm39) |
D385V |
unknown |
Het |
Sp7 |
A |
C |
15: 102,267,533 (GRCm39) |
V109G |
probably benign |
Het |
Syne1 |
A |
T |
10: 5,082,078 (GRCm39) |
Y849N |
probably damaging |
Het |
Tas2r108 |
T |
C |
6: 40,470,790 (GRCm39) |
F89L |
possibly damaging |
Het |
Tcf3 |
C |
T |
10: 80,246,301 (GRCm39) |
A581T |
possibly damaging |
Het |
Tcta |
A |
G |
9: 108,182,986 (GRCm39) |
L53P |
probably damaging |
Het |
Traf3ip2 |
C |
G |
10: 39,502,451 (GRCm39) |
Q200E |
probably damaging |
Het |
Trgc1 |
A |
T |
13: 19,400,691 (GRCm39) |
Y140F |
|
Het |
Tyk2 |
A |
T |
9: 21,036,263 (GRCm39) |
C75S |
probably damaging |
Het |
Ugt3a1 |
G |
A |
15: 9,311,903 (GRCm39) |
G382R |
probably damaging |
Het |
Upp2 |
G |
T |
2: 58,664,127 (GRCm39) |
|
probably null |
Het |
Vmn1r212 |
A |
T |
13: 23,067,323 (GRCm39) |
F337I |
unknown |
Het |
Vmn1r58 |
T |
C |
7: 5,414,242 (GRCm39) |
|
probably benign |
Het |
Vps13d |
A |
T |
4: 144,830,246 (GRCm39) |
V2856D |
|
Het |
Wdr37 |
A |
C |
13: 8,886,911 (GRCm39) |
L292R |
probably damaging |
Het |
Yipf3 |
T |
C |
17: 46,561,790 (GRCm39) |
I199T |
probably benign |
Het |
Zdhhc23 |
A |
G |
16: 43,791,907 (GRCm39) |
S289P |
possibly damaging |
Het |
Zfp229 |
A |
T |
17: 21,965,131 (GRCm39) |
K454* |
probably null |
Het |
|
Other mutations in Chrdl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00850:Chrdl2
|
APN |
7 |
99,683,848 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00965:Chrdl2
|
APN |
7 |
99,655,860 (GRCm39) |
splice site |
probably null |
|
IGL01320:Chrdl2
|
APN |
7 |
99,666,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01322:Chrdl2
|
APN |
7 |
99,666,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01977:Chrdl2
|
APN |
7 |
99,671,263 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02170:Chrdl2
|
APN |
7 |
99,683,821 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02478:Chrdl2
|
APN |
7 |
99,670,190 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02745:Chrdl2
|
APN |
7 |
99,670,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03117:Chrdl2
|
APN |
7 |
99,676,787 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03377:Chrdl2
|
APN |
7 |
99,671,259 (GRCm39) |
missense |
probably benign |
0.03 |
Measley
|
UTSW |
7 |
99,659,328 (GRCm39) |
critical splice donor site |
probably null |
|
R1453:Chrdl2
|
UTSW |
7 |
99,666,197 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1900:Chrdl2
|
UTSW |
7 |
99,682,871 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2092:Chrdl2
|
UTSW |
7 |
99,670,184 (GRCm39) |
nonsense |
probably null |
|
R3421:Chrdl2
|
UTSW |
7 |
99,673,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R3949:Chrdl2
|
UTSW |
7 |
99,678,412 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4305:Chrdl2
|
UTSW |
7 |
99,671,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R4306:Chrdl2
|
UTSW |
7 |
99,671,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Chrdl2
|
UTSW |
7 |
99,655,748 (GRCm39) |
unclassified |
probably benign |
|
R5208:Chrdl2
|
UTSW |
7 |
99,673,129 (GRCm39) |
missense |
probably damaging |
0.96 |
R5327:Chrdl2
|
UTSW |
7 |
99,677,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R5859:Chrdl2
|
UTSW |
7 |
99,670,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5928:Chrdl2
|
UTSW |
7 |
99,659,200 (GRCm39) |
start gained |
probably benign |
|
R6706:Chrdl2
|
UTSW |
7 |
99,659,328 (GRCm39) |
critical splice donor site |
probably null |
|
R7027:Chrdl2
|
UTSW |
7 |
99,671,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Chrdl2
|
UTSW |
7 |
99,677,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R7357:Chrdl2
|
UTSW |
7 |
99,678,414 (GRCm39) |
missense |
probably benign |
0.00 |
R7468:Chrdl2
|
UTSW |
7 |
99,659,332 (GRCm39) |
splice site |
probably null |
|
R7870:Chrdl2
|
UTSW |
7 |
99,659,249 (GRCm39) |
missense |
unknown |
|
R7887:Chrdl2
|
UTSW |
7 |
99,678,457 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8394:Chrdl2
|
UTSW |
7 |
99,666,292 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8436:Chrdl2
|
UTSW |
7 |
99,676,940 (GRCm39) |
critical splice donor site |
probably null |
|
R8958:Chrdl2
|
UTSW |
7 |
99,670,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R9242:Chrdl2
|
UTSW |
7 |
99,655,743 (GRCm39) |
unclassified |
probably benign |
|
|