Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
G |
T |
4: 129,901,645 (GRCm39) |
C423F |
probably damaging |
Het |
Akap11 |
A |
T |
14: 78,750,220 (GRCm39) |
Y722* |
probably null |
Het |
Albfm1 |
A |
G |
5: 90,727,570 (GRCm39) |
H396R |
possibly damaging |
Het |
Anxa3 |
A |
T |
5: 96,968,288 (GRCm39) |
I114F |
probably damaging |
Het |
Arfgef3 |
T |
A |
10: 18,467,934 (GRCm39) |
R1755S |
probably damaging |
Het |
Atf7ip |
A |
T |
6: 136,537,039 (GRCm39) |
T91S |
possibly damaging |
Het |
Bltp1 |
T |
A |
3: 37,041,314 (GRCm39) |
I2564K |
probably damaging |
Het |
Bmerb1 |
A |
G |
16: 13,804,683 (GRCm39) |
H10R |
possibly damaging |
Het |
Bmp10 |
C |
T |
6: 87,410,557 (GRCm39) |
P117S |
probably benign |
Het |
Bmpr2 |
A |
G |
1: 59,906,583 (GRCm39) |
T559A |
probably benign |
Het |
Cd200r1 |
A |
T |
16: 44,610,039 (GRCm39) |
Y86F |
probably damaging |
Het |
Cemip |
T |
A |
7: 83,596,308 (GRCm39) |
|
probably benign |
Het |
Cfap251 |
T |
C |
5: 123,394,116 (GRCm39) |
V335A |
probably benign |
Het |
Cfap52 |
A |
G |
11: 67,822,548 (GRCm39) |
|
probably null |
Het |
Chml |
T |
C |
1: 175,514,712 (GRCm39) |
H60R |
possibly damaging |
Het |
Cic |
TCCCCC |
TCCCCCCCC |
7: 24,991,095 (GRCm39) |
|
probably benign |
Het |
Clec12a |
A |
G |
6: 129,336,441 (GRCm39) |
Y201C |
probably damaging |
Het |
Col15a1 |
T |
C |
4: 47,258,719 (GRCm39) |
V370A |
probably benign |
Het |
Cpsf3 |
T |
C |
12: 21,351,538 (GRCm39) |
I353T |
probably damaging |
Het |
Csf2rb |
T |
A |
15: 78,230,667 (GRCm39) |
V470E |
probably benign |
Het |
Cyp4a10 |
C |
A |
4: 115,378,291 (GRCm39) |
Q126K |
probably benign |
Het |
Dennd1b |
T |
C |
1: 139,013,652 (GRCm39) |
S249P |
probably damaging |
Het |
Dnase2a |
A |
G |
8: 85,635,625 (GRCm39) |
|
probably null |
Het |
Dpp10 |
T |
C |
1: 123,305,882 (GRCm39) |
N490S |
probably benign |
Het |
Drgx |
A |
T |
14: 32,330,363 (GRCm39) |
N160I |
probably damaging |
Het |
Enc1 |
C |
T |
13: 97,382,243 (GRCm39) |
A251V |
probably benign |
Het |
Fancd2 |
T |
C |
6: 113,562,434 (GRCm39) |
V1258A |
probably benign |
Het |
Fancm |
G |
A |
12: 65,153,666 (GRCm39) |
|
probably null |
Het |
Fbxo16 |
C |
T |
14: 65,536,657 (GRCm39) |
T177I |
probably benign |
Het |
Gm1965 |
T |
C |
6: 89,123,525 (GRCm39) |
|
noncoding transcript |
Het |
Hal |
A |
T |
10: 93,339,401 (GRCm39) |
M497L |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,497,378 (GRCm39) |
L3936S |
possibly damaging |
Het |
Hs3st4 |
G |
T |
7: 123,996,410 (GRCm39) |
G359W |
probably damaging |
Het |
Il6st |
C |
T |
13: 112,639,399 (GRCm39) |
P608L |
probably damaging |
Het |
Kctd18 |
A |
C |
1: 58,004,707 (GRCm39) |
|
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,940,309 (GRCm39) |
S1636T |
probably damaging |
Het |
Lrrn1 |
A |
T |
6: 107,545,311 (GRCm39) |
S370C |
probably damaging |
Het |
Mtcl1 |
A |
C |
17: 66,655,474 (GRCm39) |
C968G |
probably benign |
Het |
Mylip |
G |
A |
13: 45,562,238 (GRCm39) |
A347T |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,291,468 (GRCm39) |
S1157G |
probably benign |
Het |
Ncoa4-ps |
A |
G |
12: 119,226,252 (GRCm39) |
|
noncoding transcript |
Het |
Neu4 |
T |
A |
1: 93,950,200 (GRCm39) |
V53E |
probably damaging |
Het |
Nxpe3 |
T |
C |
16: 55,680,687 (GRCm39) |
I302V |
probably benign |
Het |
Or11i1 |
A |
T |
3: 106,729,576 (GRCm39) |
C100S |
probably damaging |
Het |
Or4c15b |
A |
T |
2: 89,112,811 (GRCm39) |
L243Q |
possibly damaging |
Het |
Otos |
T |
C |
1: 92,572,090 (GRCm39) |
T79A |
probably damaging |
Het |
Pde4a |
T |
C |
9: 21,122,009 (GRCm39) |
I578T |
probably damaging |
Het |
Pramel17 |
T |
A |
4: 101,692,729 (GRCm39) |
M424L |
probably benign |
Het |
Prex2 |
C |
T |
1: 11,240,164 (GRCm39) |
P927S |
probably damaging |
Het |
Prune2 |
A |
T |
19: 17,100,116 (GRCm39) |
K1873N |
probably benign |
Het |
Ptk7 |
C |
A |
17: 46,887,417 (GRCm39) |
|
probably null |
Het |
Reln |
T |
A |
5: 22,200,585 (GRCm39) |
|
probably null |
Het |
Rgl2 |
A |
G |
17: 34,151,749 (GRCm39) |
|
probably benign |
Het |
Rnf145 |
T |
A |
11: 44,448,063 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,724,849 (GRCm39) |
E2488G |
probably damaging |
Het |
Sgo2b |
A |
T |
8: 64,379,664 (GRCm39) |
M1056K |
possibly damaging |
Het |
Snapc4 |
A |
G |
2: 26,259,245 (GRCm39) |
V635A |
probably benign |
Het |
Snx19 |
T |
A |
9: 30,348,763 (GRCm39) |
Y101N |
probably benign |
Het |
Sorl1 |
C |
A |
9: 41,925,746 (GRCm39) |
|
probably null |
Het |
Sp110 |
C |
G |
1: 85,516,839 (GRCm39) |
E219D |
probably damaging |
Het |
Speer4a2 |
A |
T |
5: 26,289,791 (GRCm39) |
I212N |
probably damaging |
Het |
Tmem30b |
G |
A |
12: 73,592,488 (GRCm39) |
P209L |
probably damaging |
Het |
Trbv12-2 |
G |
T |
6: 41,096,081 (GRCm39) |
C52F |
probably damaging |
Het |
Tsc2 |
T |
A |
17: 24,819,343 (GRCm39) |
D1304V |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,214,183 (GRCm39) |
Y487C |
probably damaging |
Het |
Vmn1r10 |
T |
A |
6: 57,090,811 (GRCm39) |
N134K |
probably damaging |
Het |
Wdr27 |
C |
A |
17: 15,141,016 (GRCm39) |
|
probably null |
Het |
Wdr75 |
T |
C |
1: 45,855,638 (GRCm39) |
F430L |
probably damaging |
Het |
Zfp629 |
A |
G |
7: 127,211,299 (GRCm39) |
I170T |
probably damaging |
Het |
|
Other mutations in Bcl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00570:Bcl2
|
APN |
1 |
106,640,088 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03076:Bcl2
|
APN |
1 |
106,471,037 (GRCm39) |
missense |
probably benign |
0.24 |
Croce
|
UTSW |
1 |
106,471,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R0002:Bcl2
|
UTSW |
1 |
106,640,241 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0002:Bcl2
|
UTSW |
1 |
106,640,241 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0083:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0086:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0107:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0183:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0217:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0219:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0346:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0347:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0348:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0361:Bcl2
|
UTSW |
1 |
106,640,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R0470:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0471:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0601:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0609:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R0965:Bcl2
|
UTSW |
1 |
106,640,021 (GRCm39) |
missense |
probably benign |
0.13 |
R1756:Bcl2
|
UTSW |
1 |
106,640,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R2764:Bcl2
|
UTSW |
1 |
106,640,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Bcl2
|
UTSW |
1 |
106,640,338 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6864:Bcl2
|
UTSW |
1 |
106,471,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R7576:Bcl2
|
UTSW |
1 |
106,640,153 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7837:Bcl2
|
UTSW |
1 |
106,471,086 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8176:Bcl2
|
UTSW |
1 |
106,640,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Bcl2
|
UTSW |
1 |
106,471,109 (GRCm39) |
missense |
probably benign |
0.40 |
R9548:Bcl2
|
UTSW |
1 |
106,640,508 (GRCm39) |
missense |
probably benign |
0.00 |
|