Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900011O08Rik |
A |
G |
16: 13,986,819 |
H10R |
possibly damaging |
Het |
4932438A13Rik |
T |
A |
3: 36,987,165 |
I2564K |
probably damaging |
Het |
5830473C10Rik |
A |
G |
5: 90,579,711 |
H396R |
possibly damaging |
Het |
Adgrb2 |
G |
T |
4: 130,007,852 |
C423F |
probably damaging |
Het |
Akap11 |
A |
T |
14: 78,512,780 |
Y722* |
probably null |
Het |
Anxa3 |
A |
T |
5: 96,820,429 |
I114F |
probably damaging |
Het |
Arfgef3 |
T |
A |
10: 18,592,186 |
R1755S |
probably damaging |
Het |
Atf7ip |
A |
T |
6: 136,560,041 |
T91S |
possibly damaging |
Het |
B020004J07Rik |
T |
A |
4: 101,835,532 |
M424L |
probably benign |
Het |
Bcl2 |
C |
A |
1: 106,712,646 |
A79S |
probably benign |
Het |
Bmp10 |
C |
T |
6: 87,433,575 |
P117S |
probably benign |
Het |
Bmpr2 |
A |
G |
1: 59,867,424 |
T559A |
probably benign |
Het |
Cd200r1 |
A |
T |
16: 44,789,676 |
Y86F |
probably damaging |
Het |
Cemip |
T |
A |
7: 83,947,100 |
|
probably benign |
Het |
Cfap52 |
A |
G |
11: 67,931,722 |
|
probably null |
Het |
Chml |
T |
C |
1: 175,687,146 |
H60R |
possibly damaging |
Het |
Cic |
TCCCCC |
TCCCCCCCC |
7: 25,291,670 |
|
probably benign |
Het |
Clec12a |
A |
G |
6: 129,359,478 |
Y201C |
probably damaging |
Het |
Col15a1 |
T |
C |
4: 47,258,719 |
V370A |
probably benign |
Het |
Cpsf3 |
T |
C |
12: 21,301,537 |
I353T |
probably damaging |
Het |
Csf2rb |
T |
A |
15: 78,346,467 |
V470E |
probably benign |
Het |
Cyp4a10 |
C |
A |
4: 115,521,094 |
Q126K |
probably benign |
Het |
Dennd1b |
T |
C |
1: 139,085,914 |
S249P |
probably damaging |
Het |
Dnase2a |
A |
G |
8: 84,908,996 |
|
probably null |
Het |
Dpp10 |
T |
C |
1: 123,378,153 |
N490S |
probably benign |
Het |
Enc1 |
C |
T |
13: 97,245,735 |
A251V |
probably benign |
Het |
Fancd2 |
T |
C |
6: 113,585,473 |
V1258A |
probably benign |
Het |
Fancm |
G |
A |
12: 65,106,892 |
|
probably null |
Het |
Fbxo16 |
C |
T |
14: 65,299,208 |
T177I |
probably benign |
Het |
Gm10471 |
A |
T |
5: 26,084,793 |
I212N |
probably damaging |
Het |
Gm1965 |
T |
C |
6: 89,146,543 |
|
noncoding transcript |
Het |
Gm6768 |
A |
G |
12: 119,262,517 |
|
noncoding transcript |
Het |
Hal |
A |
T |
10: 93,503,539 |
M497L |
probably damaging |
Het |
Hs3st4 |
G |
T |
7: 124,397,187 |
G359W |
probably damaging |
Het |
Il6st |
C |
T |
13: 112,502,865 |
P608L |
probably damaging |
Het |
Kctd18 |
A |
C |
1: 57,965,548 |
|
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,802,246 |
S1636T |
probably damaging |
Het |
Lrrn1 |
A |
T |
6: 107,568,350 |
S370C |
probably damaging |
Het |
Mtcl1 |
A |
C |
17: 66,348,479 |
C968G |
probably benign |
Het |
Mylip |
G |
A |
13: 45,408,762 |
A347T |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,154,960 |
S1157G |
probably benign |
Het |
Neu4 |
T |
A |
1: 94,022,478 |
V53E |
probably damaging |
Het |
Nxpe3 |
T |
C |
16: 55,860,324 |
I302V |
probably benign |
Het |
Olfr1229 |
A |
T |
2: 89,282,467 |
L243Q |
possibly damaging |
Het |
Olfr266 |
A |
T |
3: 106,822,260 |
C100S |
probably damaging |
Het |
Otos |
T |
C |
1: 92,644,368 |
T79A |
probably damaging |
Het |
Pde4a |
T |
C |
9: 21,210,713 |
I578T |
probably damaging |
Het |
Prex2 |
C |
T |
1: 11,169,940 |
P927S |
probably damaging |
Het |
Prrxl1 |
A |
T |
14: 32,608,406 |
N160I |
probably damaging |
Het |
Prune2 |
A |
T |
19: 17,122,752 |
K1873N |
probably benign |
Het |
Ptk7 |
C |
A |
17: 46,576,491 |
|
probably null |
Het |
Reln |
T |
A |
5: 21,995,587 |
|
probably null |
Het |
Rgl2 |
A |
G |
17: 33,932,775 |
|
probably benign |
Het |
Rnf145 |
T |
A |
11: 44,557,236 |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,709,963 |
E2488G |
probably damaging |
Het |
Sgo2b |
A |
T |
8: 63,926,630 |
M1056K |
possibly damaging |
Het |
Snapc4 |
A |
G |
2: 26,369,233 |
V635A |
probably benign |
Het |
Snx19 |
T |
A |
9: 30,437,467 |
Y101N |
probably benign |
Het |
Sorl1 |
C |
A |
9: 42,014,450 |
|
probably null |
Het |
Sp110 |
C |
G |
1: 85,589,118 |
E219D |
probably damaging |
Het |
Tmem30b |
G |
A |
12: 73,545,714 |
P209L |
probably damaging |
Het |
Trbv12-2 |
G |
T |
6: 41,119,147 |
C52F |
probably damaging |
Het |
Tsc2 |
T |
A |
17: 24,600,369 |
D1304V |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,066,324 |
Y487C |
probably damaging |
Het |
Vmn1r10 |
T |
A |
6: 57,113,826 |
N134K |
probably damaging |
Het |
Wdr27 |
C |
A |
17: 14,920,754 |
|
probably null |
Het |
Wdr66 |
T |
C |
5: 123,256,053 |
V335A |
probably benign |
Het |
Wdr75 |
T |
C |
1: 45,816,478 |
F430L |
probably damaging |
Het |
Zfp629 |
A |
G |
7: 127,612,127 |
I170T |
probably damaging |
Het |
|