Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
C |
2: 68,741,456 |
S559P |
probably benign |
Het |
A430005L14Rik |
T |
A |
4: 153,959,857 |
C42S |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,273,967 |
T449S |
probably benign |
Het |
Acvr1c |
T |
A |
2: 58,315,975 |
Q41L |
probably benign |
Het |
Adamts13 |
C |
T |
2: 26,973,990 |
P60L |
probably benign |
Het |
Adamts20 |
T |
C |
15: 94,347,718 |
T568A |
possibly damaging |
Het |
Ago1 |
T |
C |
4: 126,454,394 |
I44V |
probably null |
Het |
Agtpbp1 |
TGAAGATGCATCTTGAGAAGA |
TGAAGA |
13: 59,475,803 |
|
probably null |
Het |
Ankrd28 |
A |
T |
14: 31,745,336 |
V39E |
possibly damaging |
Het |
Apaf1 |
A |
G |
10: 91,061,814 |
V269A |
possibly damaging |
Het |
Asna1 |
T |
C |
8: 85,025,160 |
S36G |
probably damaging |
Het |
Astn1 |
A |
G |
1: 158,520,521 |
N506D |
probably damaging |
Het |
BC051019 |
G |
A |
7: 109,720,551 |
Q102* |
probably null |
Het |
Bpifb5 |
A |
G |
2: 154,233,279 |
T376A |
possibly damaging |
Het |
Ccdc121 |
G |
T |
1: 181,510,986 |
Q134K |
probably benign |
Het |
Ccl20 |
ATT |
ATTT |
1: 83,117,855 |
|
probably null |
Het |
Ccl6 |
G |
T |
11: 83,589,337 |
P68T |
possibly damaging |
Het |
Cd300ld |
A |
T |
11: 114,987,330 |
F119I |
probably benign |
Het |
Cdk2ap2 |
A |
G |
19: 4,097,903 |
M57V |
possibly damaging |
Het |
Chkb |
C |
T |
15: 89,428,766 |
G36E |
probably damaging |
Het |
Col11a1 |
A |
G |
3: 114,165,293 |
|
probably null |
Het |
Ctla2b |
T |
C |
13: 60,896,067 |
Y120C |
probably damaging |
Het |
Ctnnd1 |
T |
C |
2: 84,620,360 |
N172S |
probably benign |
Het |
Cyp2a22 |
G |
A |
7: 26,934,772 |
P319L |
probably damaging |
Het |
Dcaf12 |
A |
C |
4: 41,302,804 |
V117G |
probably damaging |
Het |
Ddx6 |
A |
G |
9: 44,607,534 |
T48A |
probably benign |
Het |
Dgki |
T |
C |
6: 36,865,801 |
D923G |
possibly damaging |
Het |
Dhx37 |
G |
T |
5: 125,427,464 |
T345K |
probably damaging |
Het |
Dhx9 |
A |
T |
1: 153,456,111 |
Y1370* |
probably null |
Het |
Dnah7b |
T |
C |
1: 46,142,087 |
S1045P |
possibly damaging |
Het |
Dnmbp |
G |
C |
19: 43,850,173 |
T1071S |
possibly damaging |
Het |
Dspp |
T |
A |
5: 104,178,559 |
S929R |
unknown |
Het |
Dst |
A |
T |
1: 34,184,063 |
E1625D |
probably damaging |
Het |
Egflam |
T |
A |
15: 7,242,567 |
H630L |
probably benign |
Het |
Elane |
T |
C |
10: 79,887,759 |
V186A |
possibly damaging |
Het |
Fam209 |
C |
A |
2: 172,472,769 |
N59K |
probably benign |
Het |
Gbe1 |
A |
G |
16: 70,528,926 |
E617G |
probably damaging |
Het |
Gfra1 |
A |
G |
19: 58,300,275 |
L246P |
probably damaging |
Het |
Gm14139 |
T |
A |
2: 150,192,947 |
M396K |
probably benign |
Het |
Gria2 |
T |
C |
3: 80,710,805 |
T308A |
probably benign |
Het |
Grip2 |
A |
T |
6: 91,779,850 |
V540D |
probably benign |
Het |
Hhipl1 |
A |
T |
12: 108,321,859 |
I575F |
possibly damaging |
Het |
Itga2b |
C |
A |
11: 102,467,339 |
A187S |
probably benign |
Het |
Kalrn |
C |
A |
16: 34,028,045 |
R469M |
probably damaging |
Het |
Kif23 |
A |
T |
9: 61,927,384 |
C426* |
probably null |
Het |
Lck |
T |
C |
4: 129,548,937 |
N475S |
probably benign |
Het |
Leng8 |
A |
G |
7: 4,145,074 |
N642S |
probably damaging |
Het |
Lingo4 |
T |
A |
3: 94,403,075 |
I440N |
probably damaging |
Het |
Lrrc4 |
A |
G |
6: 28,830,905 |
F237S |
probably damaging |
Het |
Magel2 |
G |
A |
7: 62,379,096 |
V583I |
unknown |
Het |
Naip2 |
A |
T |
13: 100,144,588 |
I1316N |
probably damaging |
Het |
Naip6 |
C |
T |
13: 100,300,729 |
G429S |
probably benign |
Het |
Noct |
C |
T |
3: 51,248,044 |
R78C |
probably damaging |
Het |
Npbwr1 |
A |
G |
1: 5,917,175 |
V40A |
possibly damaging |
Het |
Nsd2 |
A |
G |
5: 33,843,402 |
N88D |
probably damaging |
Het |
Olfr1020 |
T |
A |
2: 85,850,400 |
V316E |
probably benign |
Het |
Olfr1066 |
T |
C |
2: 86,455,473 |
H266R |
probably benign |
Het |
Olfr389 |
T |
A |
11: 73,776,713 |
I205F |
probably benign |
Het |
Olfr800 |
T |
A |
10: 129,660,421 |
I205N |
probably benign |
Het |
Pak7 |
T |
A |
2: 136,116,637 |
H177L |
probably benign |
Het |
Pard3 |
C |
T |
8: 127,064,347 |
|
probably null |
Het |
Pde4c |
A |
G |
8: 70,747,358 |
|
probably null |
Het |
Pde6h |
T |
A |
6: 136,963,205 |
I63N |
probably damaging |
Het |
Phldb2 |
T |
C |
16: 45,774,195 |
K916E |
possibly damaging |
Het |
Ppig |
T |
C |
2: 69,741,644 |
S236P |
unknown |
Het |
Ptprd |
T |
C |
4: 75,954,122 |
Y1370C |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,516,120 |
T352A |
probably benign |
Het |
Rab3gap1 |
A |
G |
1: 127,903,719 |
Y177C |
possibly damaging |
Het |
Rasgef1a |
G |
A |
6: 118,089,196 |
V457M |
probably benign |
Het |
Scel |
A |
T |
14: 103,610,790 |
T616S |
possibly damaging |
Het |
Sel1l |
A |
T |
12: 91,826,550 |
Y228* |
probably null |
Het |
Sgms1 |
A |
G |
19: 32,159,683 |
V161A |
possibly damaging |
Het |
Slfnl1 |
T |
C |
4: 120,533,227 |
L25P |
probably benign |
Het |
Smad5 |
A |
G |
13: 56,737,374 |
T432A |
probably damaging |
Het |
Sohlh2 |
T |
C |
3: 55,192,341 |
|
probably null |
Het |
Sphkap |
A |
T |
1: 83,276,662 |
M835K |
probably damaging |
Het |
Sqor |
A |
C |
2: 122,798,098 |
T174P |
probably damaging |
Het |
Stkld1 |
T |
C |
2: 26,952,747 |
V577A |
probably damaging |
Het |
Sulf2 |
T |
A |
2: 166,080,853 |
E652D |
probably benign |
Het |
Sycp2 |
T |
A |
2: 178,378,055 |
Q556L |
probably benign |
Het |
Syk |
A |
G |
13: 52,611,238 |
T134A |
probably benign |
Het |
Tas2r122 |
T |
A |
6: 132,711,622 |
I103F |
possibly damaging |
Het |
Tex10 |
A |
G |
4: 48,451,940 |
W729R |
probably damaging |
Het |
Tex261 |
G |
T |
6: 83,773,731 |
P95T |
probably damaging |
Het |
Tm2d2 |
T |
C |
8: 25,017,507 |
S47P |
probably benign |
Het |
Tmem2 |
A |
G |
19: 21,801,987 |
D387G |
probably benign |
Het |
Tmem95 |
A |
G |
11: 69,876,991 |
S128P |
probably damaging |
Het |
Tnxb |
G |
A |
17: 34,692,579 |
A1619T |
possibly damaging |
Het |
Trappc9 |
A |
G |
15: 73,058,036 |
I157T |
probably damaging |
Het |
Unc13c |
T |
A |
9: 73,483,615 |
|
probably null |
Het |
Upb1 |
A |
T |
10: 75,429,969 |
Y210F |
probably damaging |
Het |
Urb1 |
T |
C |
16: 90,762,344 |
M1684V |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,078,682 |
P727S |
possibly damaging |
Het |
Zfp551 |
A |
T |
7: 12,416,349 |
S378T |
probably damaging |
Het |
Zfp598 |
T |
C |
17: 24,669,924 |
V56A |
possibly damaging |
Het |
Zfp945 |
C |
T |
17: 22,857,249 |
|
probably null |
Het |
|