Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
G |
A |
9: 56,007,303 |
P52S |
unknown |
Het |
Adarb2 |
A |
G |
13: 8,570,384 |
E302G |
probably damaging |
Het |
Adgrf5 |
T |
A |
17: 43,451,179 |
L1255H |
probably damaging |
Het |
Adra1a |
T |
A |
14: 66,638,284 |
I236N |
probably benign |
Het |
As3mt |
T |
C |
19: 46,720,452 |
F295S |
probably damaging |
Het |
Bmp5 |
G |
A |
9: 75,873,360 |
R313Q |
probably damaging |
Het |
Ccnj |
T |
A |
19: 40,844,950 |
S191T |
probably benign |
Het |
Clk2 |
T |
A |
3: 89,173,545 |
|
probably null |
Het |
Cpz |
T |
C |
5: 35,517,656 |
E83G |
probably damaging |
Het |
Cts3 |
A |
G |
13: 61,567,620 |
I133T |
probably benign |
Het |
Dars2 |
C |
T |
1: 161,046,772 |
|
probably null |
Het |
Dsel |
A |
T |
1: 111,861,068 |
V579D |
probably damaging |
Het |
Dync1h1 |
C |
A |
12: 110,635,642 |
A2038E |
probably damaging |
Het |
Eaf1 |
A |
G |
14: 31,494,820 |
|
probably benign |
Het |
Fsip2 |
A |
C |
2: 82,998,180 |
I6774L |
probably benign |
Het |
Glis2 |
T |
C |
16: 4,613,568 |
F320L |
possibly damaging |
Het |
Hcar1 |
A |
G |
5: 123,879,630 |
|
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,750,321 |
H2211Q |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,683,745 |
I2385T |
probably damaging |
Het |
Il16 |
C |
T |
7: 83,644,041 |
E1273K |
probably damaging |
Het |
Inpp5j |
G |
A |
11: 3,501,065 |
T528I |
probably damaging |
Het |
Kbtbd6 |
C |
T |
14: 79,453,187 |
P441S |
probably damaging |
Het |
Kcnt1 |
C |
T |
2: 25,863,843 |
|
probably benign |
Het |
Kif26b |
T |
C |
1: 178,530,741 |
L139P |
probably damaging |
Het |
Klb |
C |
T |
5: 65,348,631 |
Q74* |
probably null |
Het |
L3mbtl1 |
G |
A |
2: 162,967,006 |
V600I |
probably benign |
Het |
Lcp1 |
C |
T |
14: 75,210,506 |
A317V |
possibly damaging |
Het |
Lipc |
C |
T |
9: 70,812,747 |
G326D |
probably damaging |
Het |
Mbnl2 |
T |
A |
14: 120,379,282 |
F103I |
probably benign |
Het |
Mdm1 |
G |
T |
10: 118,164,288 |
E609* |
probably null |
Het |
Med16 |
A |
G |
10: 79,908,816 |
|
probably null |
Het |
Mga |
T |
C |
2: 119,935,527 |
V1424A |
possibly damaging |
Het |
Mocs2 |
G |
T |
13: 114,828,174 |
|
probably null |
Het |
Morc1 |
C |
T |
16: 48,630,900 |
|
probably null |
Het |
Mpc2 |
T |
A |
1: 165,479,511 |
W94R |
probably damaging |
Het |
Mrm3 |
G |
A |
11: 76,250,176 |
V337I |
possibly damaging |
Het |
N4bp3 |
T |
C |
11: 51,645,606 |
H133R |
probably benign |
Het |
Ncam2 |
G |
T |
16: 81,623,368 |
G810V |
probably damaging |
Het |
Nipbl |
T |
C |
15: 8,343,606 |
E1052G |
possibly damaging |
Het |
Nlrp12 |
C |
T |
7: 3,249,257 |
V95M |
probably damaging |
Het |
Nrip1 |
T |
C |
16: 76,293,356 |
N438D |
possibly damaging |
Het |
Nsun4 |
C |
A |
4: 116,051,838 |
M508I |
probably benign |
Het |
Pla2g2c |
T |
C |
4: 138,734,339 |
S40P |
probably damaging |
Het |
Plec |
A |
G |
15: 76,197,978 |
|
probably null |
Het |
Ppfia2 |
G |
T |
10: 106,857,495 |
M620I |
possibly damaging |
Het |
Ppp6c |
A |
G |
2: 39,226,217 |
Y9H |
probably damaging |
Het |
Prkd1 |
A |
T |
12: 50,648,834 |
I47N |
possibly damaging |
Het |
Prr14l |
T |
C |
5: 32,830,684 |
D489G |
probably benign |
Het |
Ptch2 |
T |
A |
4: 117,114,652 |
Y1124N |
probably benign |
Het |
Ptpra |
T |
G |
2: 130,553,400 |
Y808D |
probably damaging |
Het |
Rint1 |
T |
A |
5: 23,815,653 |
F558Y |
possibly damaging |
Het |
Rnf215 |
T |
A |
11: 4,139,792 |
C268* |
probably null |
Het |
Slc25a13 |
T |
C |
6: 6,181,100 |
E28G |
possibly damaging |
Het |
Slc38a8 |
G |
T |
8: 119,499,815 |
Y78* |
probably null |
Het |
Slc4a7 |
T |
C |
14: 14,775,000 |
M810T |
probably damaging |
Het |
Slitrk1 |
A |
G |
14: 108,913,159 |
V40A |
possibly damaging |
Het |
Sobp |
A |
T |
10: 43,022,835 |
S251R |
probably damaging |
Het |
Spata31d1a |
G |
A |
13: 59,703,201 |
S371L |
probably benign |
Het |
Tada2b |
T |
C |
5: 36,476,836 |
T133A |
possibly damaging |
Het |
Tbc1d20 |
A |
G |
2: 152,304,961 |
D90G |
probably benign |
Het |
Tek |
T |
A |
4: 94,827,296 |
I408K |
probably benign |
Het |
Tgfb2 |
A |
G |
1: 186,649,880 |
F150S |
probably benign |
Het |
Tmem63b |
T |
C |
17: 45,666,591 |
T370A |
probably benign |
Het |
Tmem94 |
G |
T |
11: 115,786,256 |
R118L |
possibly damaging |
Het |
Tspan17 |
C |
G |
13: 54,792,621 |
L34V |
probably benign |
Het |
Vmn1r238 |
A |
T |
18: 3,123,151 |
Y88N |
probably damaging |
Het |
Vmn1r85 |
A |
G |
7: 13,085,037 |
I60T |
probably damaging |
Het |
Vmn2r96 |
T |
C |
17: 18,582,767 |
M313T |
probably benign |
Het |
Zp3r |
G |
A |
1: 130,583,480 |
S387F |
probably benign |
Het |
|