Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 78,902,448 (GRCm39) |
K623E |
probably damaging |
Het |
Adam30 |
A |
T |
3: 98,070,266 (GRCm39) |
I700F |
probably damaging |
Het |
Adam5 |
A |
T |
8: 25,276,167 (GRCm39) |
M500K |
probably benign |
Het |
Adgb |
A |
T |
10: 10,274,687 (GRCm39) |
S755T |
possibly damaging |
Het |
Adgrv1 |
C |
T |
13: 81,534,124 (GRCm39) |
G5819D |
probably damaging |
Het |
Ank3 |
T |
A |
10: 69,763,557 (GRCm39) |
Y17N |
probably damaging |
Het |
Ano2 |
A |
T |
6: 125,969,918 (GRCm39) |
M745L |
probably benign |
Het |
Arap2 |
A |
G |
5: 62,872,074 (GRCm39) |
|
probably null |
Het |
Atg2a |
A |
T |
19: 6,291,759 (GRCm39) |
|
probably benign |
Het |
AU021092 |
G |
T |
16: 5,038,312 (GRCm39) |
|
probably null |
Het |
Bbs1 |
A |
T |
19: 4,940,749 (GRCm39) |
L578Q |
probably damaging |
Het |
Brd9 |
A |
T |
13: 74,108,433 (GRCm39) |
E589D |
probably damaging |
Het |
Calr4 |
A |
G |
4: 109,101,442 (GRCm39) |
D108G |
probably benign |
Het |
Ccdc82 |
A |
G |
9: 13,272,798 (GRCm39) |
D429G |
probably damaging |
Het |
Cdh22 |
G |
T |
2: 164,988,550 (GRCm39) |
N268K |
probably damaging |
Het |
Ceacam12 |
G |
A |
7: 17,801,312 (GRCm39) |
G97D |
probably damaging |
Het |
Clcn1 |
A |
G |
6: 42,291,096 (GRCm39) |
D990G |
probably damaging |
Het |
Cyp2c40 |
T |
C |
19: 39,801,004 (GRCm39) |
T84A |
probably benign |
Het |
Dnah7a |
G |
A |
1: 53,472,181 (GRCm39) |
P3529S |
probably damaging |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Efna3 |
GAGCAGCAGCAGCAGCAGCAGC |
GAGCAGCAGCAGCAGCAGC |
3: 89,230,105 (GRCm39) |
|
probably benign |
Het |
Ehd2 |
G |
A |
7: 15,697,389 (GRCm39) |
Q4* |
probably null |
Het |
Eml5 |
A |
G |
12: 98,760,715 (GRCm39) |
V1726A |
possibly damaging |
Het |
Esam |
A |
G |
9: 37,439,544 (GRCm39) |
T10A |
probably benign |
Het |
Fbxl6 |
A |
G |
15: 76,422,633 (GRCm39) |
L95P |
probably benign |
Het |
Fbxw18 |
T |
A |
9: 109,505,947 (GRCm39) |
L441F |
probably damaging |
Het |
Fbxw4 |
A |
G |
19: 45,624,766 (GRCm39) |
S73P |
probably benign |
Het |
Fndc1 |
T |
A |
17: 7,991,479 (GRCm39) |
H739L |
unknown |
Het |
Foxp1 |
G |
A |
6: 98,943,037 (GRCm39) |
T237I |
probably damaging |
Het |
Greb1 |
A |
T |
12: 16,724,771 (GRCm39) |
I1801N |
probably damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hoxa13 |
G |
T |
6: 52,236,908 (GRCm39) |
N281K |
probably damaging |
Het |
Hspg2 |
A |
G |
4: 137,296,829 (GRCm39) |
T4328A |
probably damaging |
Het |
Htr2a |
C |
G |
14: 74,882,474 (GRCm39) |
Y153* |
probably null |
Het |
Iglv1 |
C |
A |
16: 18,903,844 (GRCm39) |
A92S |
probably damaging |
Het |
Itih1 |
A |
G |
14: 30,653,152 (GRCm39) |
S759P |
probably damaging |
Het |
Kctd1 |
G |
T |
18: 15,102,688 (GRCm39) |
S831* |
probably null |
Het |
Kif20a |
T |
A |
18: 34,761,199 (GRCm39) |
S265T |
probably damaging |
Het |
Kif22 |
T |
A |
7: 126,630,228 (GRCm39) |
E436V |
possibly damaging |
Het |
Kif27 |
A |
G |
13: 58,459,051 (GRCm39) |
W927R |
probably damaging |
Het |
Lcorl |
G |
A |
5: 45,933,832 (GRCm39) |
P66L |
probably damaging |
Het |
Lct |
A |
G |
1: 128,255,451 (GRCm39) |
L197P |
probably damaging |
Het |
Lefty1 |
T |
C |
1: 180,762,714 (GRCm39) |
S14P |
unknown |
Het |
Lnp1 |
A |
G |
16: 56,737,855 (GRCm39) |
S78P |
possibly damaging |
Het |
Map3k19 |
A |
T |
1: 127,750,569 (GRCm39) |
H927Q |
probably benign |
Het |
Meiosin |
C |
A |
7: 18,834,814 (GRCm39) |
|
probably benign |
Het |
Mta3 |
A |
G |
17: 84,099,222 (GRCm39) |
T430A |
probably benign |
Het |
Muc2 |
G |
T |
7: 141,282,875 (GRCm39) |
C627F |
probably damaging |
Het |
Myh13 |
A |
G |
11: 67,245,588 (GRCm39) |
D1076G |
probably benign |
Het |
Nck2 |
T |
A |
1: 43,572,729 (GRCm39) |
M1K |
probably null |
Het |
Nipal1 |
A |
G |
5: 72,820,898 (GRCm39) |
N131S |
probably damaging |
Het |
Nlrp9c |
T |
C |
7: 26,077,426 (GRCm39) |
|
probably null |
Het |
Nr2f2 |
A |
G |
7: 70,007,946 (GRCm39) |
S179P |
probably damaging |
Het |
Or1j16 |
A |
G |
2: 36,530,063 (GRCm39) |
D4G |
probably benign |
Het |
Or1j21 |
A |
T |
2: 36,683,980 (GRCm39) |
H244L |
probably damaging |
Het |
Or9g19 |
A |
T |
2: 85,600,652 (GRCm39) |
N169I |
probably benign |
Het |
Oxt |
G |
T |
2: 130,418,163 (GRCm39) |
|
probably benign |
Het |
Pank2 |
T |
A |
2: 131,122,181 (GRCm39) |
Y235* |
probably null |
Het |
Pear1 |
A |
G |
3: 87,659,440 (GRCm39) |
L798P |
possibly damaging |
Het |
Pex14 |
T |
C |
4: 149,046,156 (GRCm39) |
H258R |
probably benign |
Het |
Pmpcb |
A |
G |
5: 21,962,031 (GRCm39) |
I487V |
probably benign |
Het |
Ppie |
T |
C |
4: 123,031,362 (GRCm39) |
E44G |
probably benign |
Het |
Ppp1r9a |
A |
T |
6: 4,905,639 (GRCm39) |
R65* |
probably null |
Het |
Ralgapb |
T |
C |
2: 158,288,075 (GRCm39) |
S371P |
probably damaging |
Het |
Ros1 |
T |
C |
10: 51,977,881 (GRCm39) |
H1455R |
probably benign |
Het |
Sacs |
C |
A |
14: 61,450,275 (GRCm39) |
T4107K |
possibly damaging |
Het |
Sec24a |
G |
A |
11: 51,622,718 (GRCm39) |
T386M |
probably damaging |
Het |
Slc10a4 |
A |
T |
5: 73,169,593 (GRCm39) |
Y207F |
possibly damaging |
Het |
Slc30a10 |
T |
C |
1: 185,187,508 (GRCm39) |
L83P |
probably damaging |
Het |
Slc38a9 |
T |
A |
13: 112,840,093 (GRCm39) |
L324* |
probably null |
Het |
Slc7a9 |
A |
T |
7: 35,165,277 (GRCm39) |
Q474L |
probably damaging |
Het |
Smc5 |
C |
A |
19: 23,191,534 (GRCm39) |
V875L |
possibly damaging |
Het |
Snap91 |
T |
C |
9: 86,707,053 (GRCm39) |
R246G |
probably damaging |
Het |
Sned1 |
A |
G |
1: 93,203,196 (GRCm39) |
|
probably null |
Het |
Spink14 |
G |
A |
18: 44,164,938 (GRCm39) |
G85E |
probably benign |
Het |
Srsf11 |
C |
T |
3: 157,728,981 (GRCm39) |
|
probably benign |
Het |
St13 |
A |
G |
15: 81,283,506 (GRCm39) |
|
probably null |
Het |
Stk10 |
A |
G |
11: 32,553,761 (GRCm39) |
M593V |
possibly damaging |
Het |
Tafa1 |
A |
G |
6: 96,092,721 (GRCm39) |
H35R |
probably benign |
Het |
Tex21 |
C |
A |
12: 76,245,707 (GRCm39) |
A530S |
probably benign |
Het |
Tln2 |
T |
A |
9: 67,131,363 (GRCm39) |
K1394N |
probably damaging |
Het |
Trhr2 |
C |
A |
8: 123,084,118 (GRCm39) |
R294L |
probably damaging |
Het |
Unc79 |
A |
T |
12: 103,149,708 (GRCm39) |
I2408F |
probably damaging |
Het |
Wdr24 |
T |
C |
17: 26,045,552 (GRCm39) |
L429P |
probably damaging |
Het |
Wwp2 |
T |
A |
8: 108,210,039 (GRCm39) |
I139N |
possibly damaging |
Het |
Zfp111 |
G |
A |
7: 23,897,554 (GRCm39) |
R686C |
unknown |
Het |
Zfp268 |
A |
T |
4: 145,350,811 (GRCm39) |
|
probably benign |
Het |
Zyg11a |
A |
G |
4: 108,046,878 (GRCm39) |
V532A |
probably benign |
Het |
|
Other mutations in A530064D06Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01377:A530064D06Rik
|
APN |
17 |
48,460,108 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01761:A530064D06Rik
|
APN |
17 |
48,460,127 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02001:A530064D06Rik
|
APN |
17 |
48,473,842 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02995:A530064D06Rik
|
APN |
17 |
48,470,456 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03109:A530064D06Rik
|
APN |
17 |
48,473,628 (GRCm39) |
missense |
probably benign |
0.13 |
FR4340:A530064D06Rik
|
UTSW |
17 |
48,470,549 (GRCm39) |
small deletion |
probably benign |
|
FR4589:A530064D06Rik
|
UTSW |
17 |
48,470,549 (GRCm39) |
small deletion |
probably benign |
|
IGL02984:A530064D06Rik
|
UTSW |
17 |
48,470,448 (GRCm39) |
missense |
probably benign |
0.06 |
R0206:A530064D06Rik
|
UTSW |
17 |
48,470,486 (GRCm39) |
missense |
probably benign |
0.00 |
R0206:A530064D06Rik
|
UTSW |
17 |
48,470,486 (GRCm39) |
missense |
probably benign |
0.00 |
R0660:A530064D06Rik
|
UTSW |
17 |
48,473,759 (GRCm39) |
missense |
probably benign |
0.18 |
R0664:A530064D06Rik
|
UTSW |
17 |
48,473,759 (GRCm39) |
missense |
probably benign |
0.18 |
R0671:A530064D06Rik
|
UTSW |
17 |
48,473,824 (GRCm39) |
missense |
probably benign |
0.05 |
R1587:A530064D06Rik
|
UTSW |
17 |
48,473,585 (GRCm39) |
missense |
probably benign |
0.20 |
R4087:A530064D06Rik
|
UTSW |
17 |
48,473,678 (GRCm39) |
missense |
probably damaging |
0.96 |
R4089:A530064D06Rik
|
UTSW |
17 |
48,473,678 (GRCm39) |
missense |
probably damaging |
0.96 |
R4963:A530064D06Rik
|
UTSW |
17 |
48,470,582 (GRCm39) |
missense |
probably benign |
0.34 |
R5060:A530064D06Rik
|
UTSW |
17 |
48,474,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R5083:A530064D06Rik
|
UTSW |
17 |
48,473,558 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5219:A530064D06Rik
|
UTSW |
17 |
48,470,518 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6189:A530064D06Rik
|
UTSW |
17 |
48,474,222 (GRCm39) |
start gained |
probably benign |
|
R6420:A530064D06Rik
|
UTSW |
17 |
48,473,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R6439:A530064D06Rik
|
UTSW |
17 |
48,473,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:A530064D06Rik
|
UTSW |
17 |
48,460,057 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:A530064D06Rik
|
UTSW |
17 |
48,473,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|