Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
A |
T |
7: 40,642,480 (GRCm39) |
T141S |
probably benign |
Het |
4930578I06Rik |
G |
A |
14: 64,223,714 (GRCm39) |
R21* |
probably null |
Het |
Abca15 |
A |
G |
7: 119,965,009 (GRCm39) |
E757G |
possibly damaging |
Het |
Abca5 |
T |
C |
11: 110,192,353 (GRCm39) |
T720A |
probably benign |
Het |
Actr5 |
T |
A |
2: 158,474,376 (GRCm39) |
|
probably null |
Het |
Adgrl3 |
T |
C |
5: 81,841,563 (GRCm39) |
|
probably benign |
Het |
Adra1a |
A |
G |
14: 66,875,241 (GRCm39) |
D72G |
probably damaging |
Het |
Ahcyl |
T |
C |
16: 45,974,264 (GRCm39) |
E371G |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,985,242 (GRCm39) |
L2175F |
probably benign |
Het |
AK157302 |
A |
G |
13: 21,679,833 (GRCm39) |
T120A |
possibly damaging |
Het |
Asic1 |
C |
A |
15: 99,596,780 (GRCm39) |
H525Q |
probably benign |
Het |
Atxn7l2 |
T |
C |
3: 108,112,090 (GRCm39) |
D335G |
possibly damaging |
Het |
Bpgm |
G |
T |
6: 34,481,284 (GRCm39) |
R227L |
possibly damaging |
Het |
Calm4 |
T |
A |
13: 3,888,320 (GRCm39) |
V142E |
possibly damaging |
Het |
Catsperg1 |
A |
T |
7: 28,890,044 (GRCm39) |
L721Q |
probably damaging |
Het |
Cdh26 |
A |
G |
2: 178,091,691 (GRCm39) |
I83M |
probably damaging |
Het |
Cep295 |
A |
C |
9: 15,234,050 (GRCm39) |
S2249A |
possibly damaging |
Het |
Cfhr4 |
G |
A |
1: 139,629,584 (GRCm39) |
T799I |
probably benign |
Het |
Cln3 |
A |
G |
7: 126,179,361 (GRCm39) |
F139L |
probably damaging |
Het |
Cmpk2 |
T |
A |
12: 26,528,055 (GRCm39) |
L424Q |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,615,130 (GRCm39) |
V53E |
probably benign |
Het |
Csmd1 |
G |
A |
8: 15,968,208 (GRCm39) |
R3140C |
possibly damaging |
Het |
Dagla |
A |
G |
19: 10,248,922 (GRCm39) |
W11R |
probably damaging |
Het |
Dbx2 |
C |
T |
15: 95,522,778 (GRCm39) |
V310M |
probably benign |
Het |
Disp2 |
T |
A |
2: 118,622,717 (GRCm39) |
C1150S |
probably benign |
Het |
Dock3 |
T |
C |
9: 106,900,987 (GRCm39) |
D326G |
probably damaging |
Het |
Dph1 |
G |
T |
11: 75,076,783 (GRCm39) |
|
probably benign |
Het |
Dyrk1b |
C |
A |
7: 27,886,059 (GRCm39) |
T594K |
probably damaging |
Het |
Evx2 |
C |
A |
2: 74,486,331 (GRCm39) |
A353S |
probably benign |
Het |
Garin1b |
T |
A |
6: 29,326,576 (GRCm39) |
V231E |
probably benign |
Het |
Greb1 |
A |
C |
12: 16,746,443 (GRCm39) |
S1276A |
probably benign |
Het |
Hhipl1 |
T |
A |
12: 108,285,661 (GRCm39) |
C490* |
probably null |
Het |
Hmmr |
G |
T |
11: 40,606,729 (GRCm39) |
T231K |
probably damaging |
Het |
Hspa4l |
A |
C |
3: 40,733,832 (GRCm39) |
E526D |
probably benign |
Het |
Ibsp |
A |
G |
5: 104,458,000 (GRCm39) |
E179G |
probably benign |
Het |
Ift140 |
C |
T |
17: 25,254,777 (GRCm39) |
A150V |
probably benign |
Het |
Igf2bp2 |
A |
G |
16: 21,889,059 (GRCm39) |
S416P |
probably benign |
Het |
Ighe |
T |
C |
12: 113,235,363 (GRCm39) |
K294E |
unknown |
Het |
Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
Kng2 |
T |
A |
16: 22,819,344 (GRCm39) |
N231Y |
possibly damaging |
Het |
Lca5 |
A |
T |
9: 83,281,792 (GRCm39) |
C331S |
probably benign |
Het |
Lrrc1 |
A |
G |
9: 77,379,488 (GRCm39) |
I101T |
possibly damaging |
Het |
Lrrk2 |
A |
T |
15: 91,699,619 (GRCm39) |
I2489L |
probably benign |
Het |
Lyz3 |
A |
G |
10: 117,073,635 (GRCm39) |
F66S |
probably benign |
Het |
Mapk9 |
A |
C |
11: 49,754,400 (GRCm39) |
N51T |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Nek2 |
T |
A |
1: 191,554,627 (GRCm39) |
V113D |
probably damaging |
Het |
Nr4a3 |
C |
A |
4: 48,051,903 (GRCm39) |
A248E |
probably benign |
Het |
Nrp1 |
T |
C |
8: 129,229,099 (GRCm39) |
I859T |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 103,803,652 (GRCm39) |
Y195* |
probably null |
Het |
Or13j1 |
T |
A |
4: 43,706,400 (GRCm39) |
H56L |
possibly damaging |
Het |
Or1n2 |
T |
A |
2: 36,797,671 (GRCm39) |
W238R |
probably damaging |
Het |
Or8g35 |
A |
G |
9: 39,381,119 (GRCm39) |
L301P |
probably damaging |
Het |
Oxtr |
C |
T |
6: 112,454,138 (GRCm39) |
R42Q |
probably benign |
Het |
Pcnx2 |
A |
G |
8: 126,566,426 (GRCm39) |
W1006R |
probably damaging |
Het |
Pdpk1 |
T |
C |
17: 24,317,145 (GRCm39) |
|
probably null |
Het |
Ryr2 |
T |
A |
13: 11,637,838 (GRCm39) |
H3731L |
probably damaging |
Het |
Sdr16c5 |
T |
G |
4: 4,016,116 (GRCm39) |
E103D |
possibly damaging |
Het |
Setdb2 |
A |
C |
14: 59,654,919 (GRCm39) |
S324A |
possibly damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc17a8 |
A |
T |
10: 89,412,488 (GRCm39) |
I499K |
probably damaging |
Het |
Slc2a9 |
T |
A |
5: 38,537,285 (GRCm39) |
I389F |
probably damaging |
Het |
Slc30a1 |
T |
C |
1: 191,641,536 (GRCm39) |
V394A |
probably damaging |
Het |
Slc41a2 |
A |
G |
10: 83,119,592 (GRCm39) |
I390T |
possibly damaging |
Het |
Slco1a1 |
A |
G |
6: 141,864,187 (GRCm39) |
|
probably null |
Het |
Slit2 |
A |
G |
5: 48,433,016 (GRCm39) |
K1053E |
possibly damaging |
Het |
Smarca2 |
T |
A |
19: 26,668,791 (GRCm39) |
L930Q |
probably damaging |
Het |
Snx6 |
T |
C |
12: 54,798,574 (GRCm39) |
H387R |
probably damaging |
Het |
Sox5 |
A |
T |
6: 143,779,165 (GRCm39) |
M622K |
possibly damaging |
Het |
Ston1 |
C |
A |
17: 88,942,709 (GRCm39) |
N38K |
possibly damaging |
Het |
Strbp |
C |
T |
2: 37,474,089 (GRCm39) |
V658I |
probably damaging |
Het |
Strn3 |
T |
C |
12: 51,657,231 (GRCm39) |
|
probably null |
Het |
Suco |
T |
G |
1: 161,687,072 (GRCm39) |
D96A |
probably benign |
Het |
Suco |
A |
G |
1: 161,691,601 (GRCm39) |
|
probably benign |
Het |
Sytl2 |
A |
T |
7: 90,030,061 (GRCm39) |
|
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,580,290 (GRCm39) |
M25L |
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,580,292 (GRCm39) |
D91V |
probably damaging |
Het |
Tmem50b |
C |
T |
16: 91,380,174 (GRCm39) |
A68T |
probably damaging |
Het |
Tmprss11e |
G |
A |
5: 86,855,206 (GRCm39) |
Q400* |
probably null |
Het |
Tnfsf13b |
G |
A |
8: 10,081,661 (GRCm39) |
|
probably null |
Het |
Trappc8 |
A |
G |
18: 20,970,245 (GRCm39) |
V916A |
probably damaging |
Het |
Trdn |
G |
T |
10: 33,350,449 (GRCm39) |
V673F |
probably damaging |
Het |
Trim28 |
G |
T |
7: 12,759,711 (GRCm39) |
|
probably benign |
Het |
Txnrd2 |
T |
C |
16: 18,291,632 (GRCm39) |
V427A |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,204,587 (GRCm39) |
|
probably benign |
Het |
Vmn1r36 |
A |
G |
6: 66,693,404 (GRCm39) |
L51P |
probably damaging |
Het |
Vmn1r63 |
T |
A |
7: 5,806,063 (GRCm39) |
M190L |
possibly damaging |
Het |
Vmn2r116 |
T |
A |
17: 23,606,286 (GRCm39) |
N399K |
probably damaging |
Het |
Vmn2r117 |
T |
C |
17: 23,694,488 (GRCm39) |
N453S |
probably benign |
Het |
Wbp1l |
T |
A |
19: 46,643,109 (GRCm39) |
I370N |
probably damaging |
Het |
Zfp445 |
T |
C |
9: 122,682,046 (GRCm39) |
K632E |
probably benign |
Het |
Zfp850 |
C |
T |
7: 27,688,819 (GRCm39) |
R463H |
probably damaging |
Het |
Zyg11a |
A |
G |
4: 108,062,054 (GRCm39) |
L249P |
probably damaging |
Het |
|