Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,328,397 (GRCm39) |
Y3490F |
|
Het |
Abcc1 |
T |
C |
16: 14,214,225 (GRCm39) |
V167A |
probably benign |
Het |
Abcd2 |
G |
A |
15: 91,073,149 (GRCm39) |
R337C |
probably damaging |
Het |
Adcy1 |
A |
G |
11: 7,111,877 (GRCm39) |
D914G |
probably benign |
Het |
Ahnak |
G |
T |
19: 8,984,567 (GRCm39) |
L1950F |
probably damaging |
Het |
Alox5ap |
T |
C |
5: 149,201,994 (GRCm39) |
|
probably null |
Het |
Ank |
C |
T |
15: 27,562,834 (GRCm39) |
H181Y |
possibly damaging |
Het |
Ankrd44 |
T |
A |
1: 54,706,680 (GRCm39) |
D592V |
possibly damaging |
Het |
Ap4m1 |
T |
A |
5: 138,174,185 (GRCm39) |
N185K |
possibly damaging |
Het |
Arhgef28 |
T |
A |
13: 98,082,210 (GRCm39) |
D1199V |
probably damaging |
Het |
Arnt |
T |
C |
3: 95,397,691 (GRCm39) |
|
probably null |
Het |
Atcay |
C |
T |
10: 81,060,298 (GRCm39) |
V13M |
probably benign |
Het |
B4galt3 |
T |
C |
1: 171,099,241 (GRCm39) |
S2P |
unknown |
Het |
Bicra |
A |
T |
7: 15,721,737 (GRCm39) |
S593R |
possibly damaging |
Het |
Brsk2 |
A |
C |
7: 141,552,415 (GRCm39) |
Q633P |
probably damaging |
Het |
Cacna1c |
T |
A |
6: 118,653,280 (GRCm39) |
S909C |
|
Het |
Ccdc7a |
G |
A |
8: 129,788,113 (GRCm39) |
T72M |
probably benign |
Het |
Cct2 |
A |
T |
10: 116,896,739 (GRCm39) |
F155I |
possibly damaging |
Het |
Cdv3 |
G |
T |
9: 103,233,594 (GRCm39) |
P194T |
probably damaging |
Het |
Cenpc1 |
A |
T |
5: 86,160,153 (GRCm39) |
V895E |
probably benign |
Het |
Cep170b |
T |
C |
12: 112,702,881 (GRCm39) |
V448A |
probably benign |
Het |
Chil3 |
G |
A |
3: 106,071,440 (GRCm39) |
R75C |
possibly damaging |
Het |
Cnfn |
A |
T |
7: 25,067,869 (GRCm39) |
C24S |
probably benign |
Het |
Cnga3 |
A |
G |
1: 37,299,852 (GRCm39) |
K191E |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,587,681 (GRCm39) |
Y1153* |
probably null |
Het |
Coq4 |
C |
A |
2: 29,685,491 (GRCm39) |
H168Q |
probably damaging |
Het |
Dennd2b |
T |
A |
7: 109,123,863 (GRCm39) |
K1132M |
probably damaging |
Het |
Dnajc14 |
G |
A |
10: 128,642,488 (GRCm39) |
V137I |
probably benign |
Het |
Efr3a |
T |
C |
15: 65,726,614 (GRCm39) |
L569P |
probably damaging |
Het |
Epb41l3 |
A |
T |
17: 69,591,575 (GRCm39) |
E677D |
probably benign |
Het |
Esp8 |
G |
A |
17: 40,841,013 (GRCm39) |
M91I |
unknown |
Het |
Fubp1 |
A |
T |
3: 151,937,669 (GRCm39) |
|
probably benign |
Het |
Gldc |
G |
T |
19: 30,116,779 (GRCm39) |
A391D |
probably damaging |
Het |
Gm17728 |
A |
G |
17: 9,641,027 (GRCm39) |
T46A |
probably benign |
Het |
Gm5798 |
A |
G |
14: 41,072,603 (GRCm39) |
K112E |
probably damaging |
Het |
Gpnmb |
A |
G |
6: 49,028,964 (GRCm39) |
|
probably benign |
Het |
Grwd1 |
T |
C |
7: 45,475,298 (GRCm39) |
T415A |
probably benign |
Het |
Gsdma3 |
C |
G |
11: 98,522,086 (GRCm39) |
A172G |
possibly damaging |
Het |
Hltf |
C |
T |
3: 20,119,566 (GRCm39) |
Q204* |
probably null |
Het |
Igf1r |
T |
G |
7: 67,833,211 (GRCm39) |
V457G |
possibly damaging |
Het |
Inhbc |
A |
T |
10: 127,192,984 (GRCm39) |
M344K |
probably damaging |
Het |
Jak3 |
C |
T |
8: 72,131,160 (GRCm39) |
A60V |
probably benign |
Het |
Kif13b |
A |
G |
14: 64,979,882 (GRCm39) |
T511A |
probably benign |
Het |
Lama2 |
T |
A |
10: 27,335,384 (GRCm39) |
N97I |
possibly damaging |
Het |
Limd2 |
T |
A |
11: 106,049,576 (GRCm39) |
D104V |
probably damaging |
Het |
Loxl3 |
T |
A |
6: 83,014,526 (GRCm39) |
C145S |
probably damaging |
Het |
Lrrc37 |
A |
C |
11: 103,506,370 (GRCm39) |
I1866S |
unknown |
Het |
Lrrc73 |
A |
G |
17: 46,565,455 (GRCm39) |
N62S |
probably benign |
Het |
Lrrtm4 |
A |
G |
6: 79,998,870 (GRCm39) |
D94G |
probably damaging |
Het |
Lsm3 |
C |
A |
6: 91,499,252 (GRCm39) |
F86L |
probably damaging |
Het |
Map10 |
T |
C |
8: 126,397,291 (GRCm39) |
V228A |
probably benign |
Het |
Mcidas |
A |
C |
13: 113,130,664 (GRCm39) |
S54R |
possibly damaging |
Het |
Me3 |
T |
C |
7: 89,455,876 (GRCm39) |
Y243H |
probably damaging |
Het |
Mgat4b |
A |
G |
11: 50,121,674 (GRCm39) |
T89A |
possibly damaging |
Het |
Mmp16 |
T |
A |
4: 18,054,355 (GRCm39) |
|
probably benign |
Het |
Mtmr9 |
G |
A |
14: 63,781,226 (GRCm39) |
|
probably benign |
Het |
Myo1b |
G |
T |
1: 51,836,198 (GRCm39) |
A331E |
probably damaging |
Het |
Ncoa6 |
C |
T |
2: 155,248,388 (GRCm39) |
V1639M |
possibly damaging |
Het |
Nek9 |
C |
T |
12: 85,353,120 (GRCm39) |
G752R |
probably damaging |
Het |
Nufip2 |
A |
G |
11: 77,584,069 (GRCm39) |
Y661C |
probably benign |
Het |
Or10w1 |
T |
A |
19: 13,632,246 (GRCm39) |
V151E |
probably damaging |
Het |
Or1n2 |
C |
T |
2: 36,797,516 (GRCm39) |
A186V |
possibly damaging |
Het |
Or51t4 |
A |
T |
7: 102,598,373 (GRCm39) |
I234F |
probably damaging |
Het |
Or7g16 |
T |
C |
9: 18,726,992 (GRCm39) |
I199M |
possibly damaging |
Het |
Or8g55 |
G |
A |
9: 39,784,894 (GRCm39) |
G108S |
probably benign |
Het |
Oxct2a |
A |
G |
4: 123,216,322 (GRCm39) |
L353S |
probably benign |
Het |
Parvg |
A |
G |
15: 84,222,001 (GRCm39) |
I243V |
probably benign |
Het |
Pcdhgb7 |
C |
A |
18: 37,886,349 (GRCm39) |
N506K |
possibly damaging |
Het |
Peg10 |
T |
TCCA |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pgghg |
G |
A |
7: 140,525,367 (GRCm39) |
|
probably null |
Het |
Phrf1 |
G |
T |
7: 140,836,516 (GRCm39) |
G263W |
unknown |
Het |
Ppfia1 |
A |
C |
7: 144,032,762 (GRCm39) |
|
probably null |
Het |
Prss37 |
T |
A |
6: 40,491,897 (GRCm39) |
I228F |
probably damaging |
Het |
Ptpro |
A |
T |
6: 137,403,782 (GRCm39) |
K921* |
probably null |
Het |
Rictor |
T |
G |
15: 6,813,067 (GRCm39) |
L940R |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,420,183 (GRCm39) |
S310P |
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,483,564 (GRCm39) |
V4091A |
probably damaging |
Het |
Saxo4 |
T |
A |
19: 10,459,599 (GRCm39) |
Y36F |
probably damaging |
Het |
Sirt5 |
T |
A |
13: 43,524,327 (GRCm39) |
M33K |
possibly damaging |
Het |
Slc25a30 |
T |
A |
14: 76,008,917 (GRCm39) |
Y90F |
probably benign |
Het |
Stimate |
T |
A |
14: 30,588,629 (GRCm39) |
Y119N |
probably damaging |
Het |
Stk11 |
G |
A |
10: 79,964,269 (GRCm39) |
D388N |
probably benign |
Het |
Tgm1 |
C |
A |
14: 55,949,686 (GRCm39) |
R126L |
probably benign |
Het |
Tmem129 |
G |
T |
5: 33,811,837 (GRCm39) |
T321N |
probably benign |
Het |
Tnfrsf11a |
A |
T |
1: 105,772,244 (GRCm39) |
|
probably null |
Het |
Tor1aip1 |
A |
G |
1: 155,907,190 (GRCm39) |
C195R |
probably benign |
Het |
Tpr |
A |
G |
1: 150,284,597 (GRCm39) |
E428G |
possibly damaging |
Het |
Trps1 |
T |
A |
15: 50,685,769 (GRCm39) |
D802V |
possibly damaging |
Het |
Usp17lc |
T |
A |
7: 103,064,316 (GRCm39) |
S6T |
probably benign |
Het |
Vangl1 |
C |
A |
3: 102,065,758 (GRCm39) |
R459L |
|
Het |
Vmn1r43 |
T |
C |
6: 89,846,937 (GRCm39) |
Y183C |
probably damaging |
Het |
Vmn2r110 |
C |
T |
17: 20,794,560 (GRCm39) |
C703Y |
probably damaging |
Het |
Vmn2r54 |
T |
C |
7: 12,363,702 (GRCm39) |
Q397R |
possibly damaging |
Het |
Vmn2r88 |
T |
C |
14: 51,656,263 (GRCm39) |
V824A |
probably damaging |
Het |
Vmn2r89 |
A |
T |
14: 51,693,170 (GRCm39) |
Y79F |
probably benign |
Het |
Vnn1 |
T |
C |
10: 23,780,484 (GRCm39) |
S491P |
probably benign |
Het |
Zbbx |
A |
G |
3: 74,968,741 (GRCm39) |
F572L |
unknown |
Het |
Zc3h4 |
A |
T |
7: 16,168,939 (GRCm39) |
Q1091L |
unknown |
Het |
Zfp503 |
C |
T |
14: 22,037,286 (GRCm39) |
V106I |
possibly damaging |
Het |
Zfp874a |
T |
C |
13: 67,590,647 (GRCm39) |
T346A |
probably benign |
Het |
|
Other mutations in Ccn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00801:Ccn1
|
APN |
3 |
145,354,365 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02500:Ccn1
|
APN |
3 |
145,354,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02963:Ccn1
|
APN |
3 |
145,353,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03170:Ccn1
|
APN |
3 |
145,355,514 (GRCm39) |
missense |
probably benign |
0.01 |
R0018:Ccn1
|
UTSW |
3 |
145,355,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R0846:Ccn1
|
UTSW |
3 |
145,353,525 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0964:Ccn1
|
UTSW |
3 |
145,353,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1234:Ccn1
|
UTSW |
3 |
145,355,594 (GRCm39) |
start gained |
probably benign |
|
R1968:Ccn1
|
UTSW |
3 |
145,353,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R1989:Ccn1
|
UTSW |
3 |
145,353,498 (GRCm39) |
missense |
probably benign |
0.31 |
R2071:Ccn1
|
UTSW |
3 |
145,354,428 (GRCm39) |
nonsense |
probably null |
|
R5622:Ccn1
|
UTSW |
3 |
145,355,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R5639:Ccn1
|
UTSW |
3 |
145,354,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R5734:Ccn1
|
UTSW |
3 |
145,354,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R5792:Ccn1
|
UTSW |
3 |
145,354,413 (GRCm39) |
missense |
probably benign |
|
R6129:Ccn1
|
UTSW |
3 |
145,354,986 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6689:Ccn1
|
UTSW |
3 |
145,353,543 (GRCm39) |
missense |
probably benign |
|
R7131:Ccn1
|
UTSW |
3 |
145,354,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R7289:Ccn1
|
UTSW |
3 |
145,354,428 (GRCm39) |
nonsense |
probably null |
|
R7699:Ccn1
|
UTSW |
3 |
145,354,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Ccn1
|
UTSW |
3 |
145,354,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Ccn1
|
UTSW |
3 |
145,354,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R9651:Ccn1
|
UTSW |
3 |
145,354,583 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ccn1
|
UTSW |
3 |
145,354,410 (GRCm39) |
missense |
probably benign |
0.00 |
|