Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
A |
G |
15: 81,948,152 (GRCm39) |
N683S |
probably benign |
Het |
Ahi1 |
T |
A |
10: 20,931,012 (GRCm39) |
F46I |
possibly damaging |
Het |
Als2 |
C |
T |
1: 59,206,650 (GRCm39) |
V1598I |
probably benign |
Het |
Arid1b |
A |
T |
17: 5,392,428 (GRCm39) |
D1986V |
probably damaging |
Het |
Bhlhe41 |
T |
A |
6: 145,810,989 (GRCm39) |
D2V |
probably damaging |
Het |
Borcs6 |
A |
G |
11: 68,951,072 (GRCm39) |
D150G |
possibly damaging |
Het |
Ccdc88a |
G |
T |
11: 29,398,050 (GRCm39) |
R261L |
probably damaging |
Het |
Ccne2 |
T |
A |
4: 11,198,723 (GRCm39) |
|
probably benign |
Het |
Cenpk |
A |
G |
13: 104,385,903 (GRCm39) |
D266G |
probably damaging |
Het |
Ces2b |
T |
C |
8: 105,561,563 (GRCm39) |
V219A |
probably damaging |
Het |
Cpa1 |
A |
G |
6: 30,645,169 (GRCm39) |
R382G |
probably damaging |
Het |
Cplx4 |
G |
T |
18: 66,089,984 (GRCm39) |
T145N |
probably damaging |
Het |
Cyp19a1 |
T |
C |
9: 54,079,102 (GRCm39) |
I269V |
probably benign |
Het |
Dennd3 |
A |
G |
15: 73,440,545 (GRCm39) |
Y1192C |
probably benign |
Het |
Dpp6 |
T |
C |
5: 27,923,471 (GRCm39) |
Y694H |
probably damaging |
Het |
Eea1 |
C |
A |
10: 95,877,346 (GRCm39) |
N1353K |
probably benign |
Het |
Fam111a |
T |
A |
19: 12,561,488 (GRCm39) |
|
probably null |
Het |
Fat1 |
T |
C |
8: 45,442,204 (GRCm39) |
S1169P |
probably benign |
Het |
Frk |
G |
T |
10: 34,360,067 (GRCm39) |
A23S |
probably benign |
Het |
Fyb2 |
T |
C |
4: 104,861,118 (GRCm39) |
V594A |
probably damaging |
Het |
Gtpbp3 |
C |
A |
8: 71,942,064 (GRCm39) |
|
probably benign |
Het |
Hoxa5 |
G |
T |
6: 52,179,688 (GRCm39) |
A229D |
probably damaging |
Het |
Ift25 |
G |
A |
4: 107,130,866 (GRCm39) |
C52Y |
possibly damaging |
Het |
Igf2r |
A |
T |
17: 12,913,007 (GRCm39) |
F1780L |
possibly damaging |
Het |
Kdm1a |
T |
C |
4: 136,279,846 (GRCm39) |
I719V |
probably benign |
Het |
Lama1 |
G |
A |
17: 68,111,531 (GRCm39) |
G2261R |
probably damaging |
Het |
Lmx1b |
G |
T |
2: 33,457,216 (GRCm39) |
Q206K |
probably benign |
Het |
Lrrtm4 |
G |
A |
6: 79,998,786 (GRCm39) |
G66D |
probably damaging |
Het |
Myg1 |
G |
T |
15: 102,240,594 (GRCm39) |
G90C |
probably damaging |
Het |
Nbea |
C |
T |
3: 55,539,407 (GRCm39) |
V2785I |
probably benign |
Het |
Ncr1 |
C |
A |
7: 4,341,225 (GRCm39) |
P35Q |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,033,855 (GRCm39) |
C326S |
probably damaging |
Het |
Or12j2 |
T |
C |
7: 139,916,072 (GRCm39) |
F99S |
possibly damaging |
Het |
Or3a1 |
G |
T |
11: 74,225,519 (GRCm39) |
H179Q |
possibly damaging |
Het |
Or52r1 |
A |
T |
7: 102,537,243 (GRCm39) |
V39E |
possibly damaging |
Het |
Pde4d |
A |
G |
13: 110,084,795 (GRCm39) |
Y520C |
probably damaging |
Het |
Ppm1d |
A |
G |
11: 85,217,770 (GRCm39) |
M178V |
possibly damaging |
Het |
Samd3 |
G |
A |
10: 26,147,762 (GRCm39) |
R479K |
probably benign |
Het |
Semp2l2b |
T |
A |
10: 21,943,057 (GRCm39) |
I308F |
possibly damaging |
Het |
Serpinb6a |
A |
G |
13: 34,102,782 (GRCm39) |
V226A |
probably benign |
Het |
Slc26a4 |
T |
C |
12: 31,575,475 (GRCm39) |
E737G |
probably benign |
Het |
Slc34a3 |
A |
G |
2: 25,121,069 (GRCm39) |
C340R |
probably damaging |
Het |
Spata31d1b |
C |
A |
13: 59,866,941 (GRCm39) |
|
probably benign |
Het |
Trappc12 |
A |
G |
12: 28,797,013 (GRCm39) |
V173A |
probably benign |
Het |
Vmn2r66 |
A |
T |
7: 84,644,723 (GRCm39) |
D562E |
probably benign |
Het |
Zfp395 |
C |
T |
14: 65,633,344 (GRCm39) |
P451L |
probably benign |
Het |
|
Other mutations in Jade2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01323:Jade2
|
APN |
11 |
51,716,165 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01935:Jade2
|
APN |
11 |
51,719,211 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02987:Jade2
|
APN |
11 |
51,721,308 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02990:Jade2
|
APN |
11 |
51,722,074 (GRCm39) |
splice site |
probably benign |
|
IGL03172:Jade2
|
APN |
11 |
51,716,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Jade2
|
UTSW |
11 |
51,722,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Jade2
|
UTSW |
11 |
51,709,365 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3410:Jade2
|
UTSW |
11 |
51,708,050 (GRCm39) |
missense |
probably benign |
|
R3886:Jade2
|
UTSW |
11 |
51,721,326 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4846:Jade2
|
UTSW |
11 |
51,711,975 (GRCm39) |
missense |
probably benign |
|
R4916:Jade2
|
UTSW |
11 |
51,707,909 (GRCm39) |
missense |
probably benign |
0.01 |
R5420:Jade2
|
UTSW |
11 |
51,709,434 (GRCm39) |
missense |
probably benign |
0.21 |
R5446:Jade2
|
UTSW |
11 |
51,707,786 (GRCm39) |
missense |
probably benign |
|
R5657:Jade2
|
UTSW |
11 |
51,707,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Jade2
|
UTSW |
11 |
51,717,413 (GRCm39) |
nonsense |
probably null |
|
R6031:Jade2
|
UTSW |
11 |
51,717,413 (GRCm39) |
nonsense |
probably null |
|
R6116:Jade2
|
UTSW |
11 |
51,726,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R7039:Jade2
|
UTSW |
11 |
51,719,186 (GRCm39) |
missense |
probably damaging |
0.97 |
R7270:Jade2
|
UTSW |
11 |
51,708,011 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7702:Jade2
|
UTSW |
11 |
51,707,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R7797:Jade2
|
UTSW |
11 |
51,708,126 (GRCm39) |
missense |
probably benign |
0.00 |
R8054:Jade2
|
UTSW |
11 |
51,709,441 (GRCm39) |
missense |
probably benign |
0.00 |
R8243:Jade2
|
UTSW |
11 |
51,708,045 (GRCm39) |
missense |
probably benign |
|
R8371:Jade2
|
UTSW |
11 |
51,715,959 (GRCm39) |
missense |
probably benign |
0.04 |
R8984:Jade2
|
UTSW |
11 |
51,715,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Jade2
|
UTSW |
11 |
51,708,454 (GRCm39) |
missense |
probably benign |
0.00 |
R9135:Jade2
|
UTSW |
11 |
51,715,951 (GRCm39) |
missense |
probably benign |
|
R9143:Jade2
|
UTSW |
11 |
51,715,930 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Jade2
|
UTSW |
11 |
51,739,821 (GRCm39) |
missense |
probably null |
0.20 |
Z1177:Jade2
|
UTSW |
11 |
51,707,817 (GRCm39) |
missense |
probably damaging |
0.96 |
|