Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
T |
C |
15: 64,655,629 (GRCm39) |
T617A |
probably benign |
Het |
Agl |
A |
T |
3: 116,578,795 (GRCm39) |
I446N |
probably benign |
Het |
Aox1 |
C |
T |
1: 58,107,451 (GRCm39) |
P575L |
probably benign |
Het |
Ap2m1 |
A |
T |
16: 20,358,269 (GRCm39) |
I96F |
probably benign |
Het |
Arhgap15 |
A |
G |
2: 44,006,642 (GRCm39) |
D253G |
probably damaging |
Het |
Arsa |
A |
T |
15: 89,359,152 (GRCm39) |
C171* |
probably null |
Het |
Arsb |
G |
T |
13: 93,908,491 (GRCm39) |
R69L |
probably benign |
Het |
Asb13 |
G |
A |
13: 3,684,180 (GRCm39) |
|
probably null |
Het |
Cebpz |
C |
T |
17: 79,233,342 (GRCm39) |
|
probably null |
Het |
Ces2h |
A |
T |
8: 105,741,127 (GRCm39) |
I40L |
probably benign |
Het |
Cfhr4 |
A |
G |
1: 139,660,039 (GRCm39) |
|
probably null |
Het |
Csmd2 |
T |
C |
4: 128,350,723 (GRCm39) |
|
probably null |
Het |
Cxadr |
T |
A |
16: 78,125,949 (GRCm39) |
N106K |
possibly damaging |
Het |
Ddo |
T |
C |
10: 40,507,770 (GRCm39) |
C56R |
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,046,412 (GRCm39) |
G3192D |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,962,465 (GRCm39) |
V49E |
probably benign |
Het |
Epha10 |
T |
C |
4: 124,807,472 (GRCm39) |
Y578H |
|
Het |
Fbxw16 |
T |
C |
9: 109,270,135 (GRCm39) |
D202G |
probably damaging |
Het |
Gzf1 |
T |
C |
2: 148,530,083 (GRCm39) |
V538A |
possibly damaging |
Het |
Igha |
T |
A |
12: 113,220,019 (GRCm39) |
|
probably benign |
Het |
Iqce |
G |
T |
5: 140,663,839 (GRCm39) |
Q457K |
probably benign |
Het |
Kbtbd3 |
A |
G |
9: 4,330,846 (GRCm39) |
K407E |
possibly damaging |
Het |
Lipt1 |
A |
G |
1: 37,914,703 (GRCm39) |
E253G |
probably damaging |
Het |
Mrnip |
G |
A |
11: 50,087,800 (GRCm39) |
W107* |
probably null |
Het |
Mroh4 |
T |
C |
15: 74,497,357 (GRCm39) |
T224A |
probably damaging |
Het |
Ncoa2 |
A |
T |
1: 13,218,661 (GRCm39) |
S1389R |
probably benign |
Het |
Npffr2 |
A |
G |
5: 89,731,173 (GRCm39) |
I368V |
probably benign |
Het |
Nrdc |
C |
T |
4: 108,895,182 (GRCm39) |
L469F |
probably damaging |
Het |
Nup210l |
A |
T |
3: 90,092,883 (GRCm39) |
Q1279L |
probably damaging |
Het |
Or4k47 |
T |
A |
2: 111,451,819 (GRCm39) |
N200I |
probably damaging |
Het |
Or7e170 |
A |
G |
9: 19,795,410 (GRCm39) |
Y64H |
probably damaging |
Het |
Pcdha4 |
T |
G |
18: 37,085,961 (GRCm39) |
I48S |
probably damaging |
Het |
Pip5kl1 |
A |
G |
2: 32,469,101 (GRCm39) |
Y211C |
possibly damaging |
Het |
Prrt4 |
A |
T |
6: 29,170,035 (GRCm39) |
S806T |
possibly damaging |
Het |
Ptpn20 |
T |
A |
14: 33,352,902 (GRCm39) |
Y214N |
probably damaging |
Het |
Ptprt |
A |
T |
2: 161,417,661 (GRCm39) |
N938K |
probably damaging |
Het |
Scn2a |
G |
T |
2: 65,594,013 (GRCm39) |
V1621L |
probably benign |
Het |
Senp3 |
A |
G |
11: 69,569,087 (GRCm39) |
I358T |
probably damaging |
Het |
Sf3b1 |
A |
T |
1: 55,042,508 (GRCm39) |
S461T |
probably benign |
Het |
Slc22a2 |
C |
T |
17: 12,828,917 (GRCm39) |
T341I |
probably damaging |
Het |
Slc38a7 |
A |
T |
8: 96,568,295 (GRCm39) |
D363E |
probably benign |
Het |
Slc6a5 |
T |
C |
7: 49,598,090 (GRCm39) |
|
probably null |
Het |
Smo |
T |
A |
6: 29,759,851 (GRCm39) |
V650E |
probably damaging |
Het |
Spata17 |
G |
A |
1: 186,872,577 (GRCm39) |
T31I |
unknown |
Het |
Sstr2 |
T |
A |
11: 113,515,423 (GRCm39) |
I114N |
possibly damaging |
Het |
Styxl1 |
T |
C |
5: 135,788,023 (GRCm39) |
Y146C |
probably damaging |
Het |
Synpo2l |
T |
C |
14: 20,711,243 (GRCm39) |
Q688R |
possibly damaging |
Het |
Tmem245 |
C |
T |
4: 56,925,155 (GRCm39) |
R322H |
probably benign |
Het |
Tnxb |
A |
G |
17: 34,890,398 (GRCm39) |
E247G |
unknown |
Het |
Ttc28 |
A |
T |
5: 111,414,544 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,718,416 (GRCm39) |
I7255N |
unknown |
Het |
Ttn |
C |
A |
2: 76,652,768 (GRCm39) |
|
probably null |
Het |
Unc13b |
C |
T |
4: 43,165,791 (GRCm39) |
R204C |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,619,787 (GRCm39) |
|
probably null |
Het |
Vps53 |
A |
T |
11: 75,937,962 (GRCm39) |
F753I |
probably damaging |
Het |
Ypel1 |
G |
T |
16: 16,918,124 (GRCm39) |
S97R |
probably benign |
Het |
Zdbf2 |
A |
G |
1: 63,343,264 (GRCm39) |
T548A |
possibly damaging |
Het |
Zfp747 |
G |
A |
7: 126,973,672 (GRCm39) |
T166M |
probably damaging |
Het |
|
Other mutations in Canx |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00675:Canx
|
APN |
11 |
50,191,823 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03089:Canx
|
APN |
11 |
50,195,309 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1428:Canx
|
UTSW |
11 |
50,199,221 (GRCm39) |
splice site |
probably benign |
|
R1876:Canx
|
UTSW |
11 |
50,195,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Canx
|
UTSW |
11 |
50,195,252 (GRCm39) |
missense |
probably damaging |
0.97 |
R2058:Canx
|
UTSW |
11 |
50,195,252 (GRCm39) |
missense |
probably damaging |
0.97 |
R2088:Canx
|
UTSW |
11 |
50,201,217 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2126:Canx
|
UTSW |
11 |
50,195,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R2217:Canx
|
UTSW |
11 |
50,201,694 (GRCm39) |
missense |
probably benign |
0.24 |
R2218:Canx
|
UTSW |
11 |
50,201,694 (GRCm39) |
missense |
probably benign |
0.24 |
R2386:Canx
|
UTSW |
11 |
50,187,933 (GRCm39) |
missense |
probably benign |
|
R3716:Canx
|
UTSW |
11 |
50,195,301 (GRCm39) |
missense |
probably benign |
0.14 |
R3957:Canx
|
UTSW |
11 |
50,199,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Canx
|
UTSW |
11 |
50,190,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R4402:Canx
|
UTSW |
11 |
50,195,265 (GRCm39) |
missense |
probably benign |
0.13 |
R4825:Canx
|
UTSW |
11 |
50,199,636 (GRCm39) |
missense |
probably benign |
0.42 |
R5252:Canx
|
UTSW |
11 |
50,199,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R5385:Canx
|
UTSW |
11 |
50,192,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Canx
|
UTSW |
11 |
50,191,844 (GRCm39) |
missense |
probably benign |
0.00 |
R5820:Canx
|
UTSW |
11 |
50,199,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R6052:Canx
|
UTSW |
11 |
50,187,946 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7259:Canx
|
UTSW |
11 |
50,192,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R7603:Canx
|
UTSW |
11 |
50,202,455 (GRCm39) |
missense |
probably benign |
|
R7715:Canx
|
UTSW |
11 |
50,201,631 (GRCm39) |
missense |
probably benign |
0.13 |
R8063:Canx
|
UTSW |
11 |
50,199,173 (GRCm39) |
nonsense |
probably null |
|
R8069:Canx
|
UTSW |
11 |
50,202,531 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8494:Canx
|
UTSW |
11 |
50,202,609 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8508:Canx
|
UTSW |
11 |
50,202,474 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8941:Canx
|
UTSW |
11 |
50,195,270 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9153:Canx
|
UTSW |
11 |
50,188,162 (GRCm39) |
missense |
probably benign |
|
R9722:Canx
|
UTSW |
11 |
50,195,301 (GRCm39) |
missense |
probably benign |
0.14 |
|