Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
T |
A |
2: 152,282,808 (GRCm39) |
I221K |
possibly damaging |
Het |
Abhd16a |
T |
A |
17: 35,321,318 (GRCm39) |
S498T |
probably benign |
Het |
Adamts18 |
G |
A |
8: 114,463,357 (GRCm39) |
R830* |
probably null |
Het |
Ankrd27 |
A |
G |
7: 35,332,417 (GRCm39) |
D848G |
probably benign |
Het |
Art3 |
A |
G |
5: 92,551,478 (GRCm39) |
Y279C |
probably damaging |
Het |
Atp2c2 |
A |
G |
8: 120,481,002 (GRCm39) |
T797A |
probably benign |
Het |
Ccdc121rt1 |
A |
T |
1: 181,338,829 (GRCm39) |
V41E |
possibly damaging |
Het |
Ccdc122 |
A |
T |
14: 77,305,381 (GRCm39) |
I12F |
possibly damaging |
Het |
Ccdc154 |
T |
C |
17: 25,389,888 (GRCm39) |
L508P |
probably damaging |
Het |
Cdk5r2 |
A |
G |
1: 74,894,831 (GRCm39) |
D192G |
probably damaging |
Het |
Cgn |
C |
T |
3: 94,685,564 (GRCm39) |
A320T |
probably benign |
Het |
Cklf |
A |
G |
8: 104,988,184 (GRCm39) |
K106E |
probably benign |
Het |
Clec12a |
C |
A |
6: 129,330,628 (GRCm39) |
T70K |
probably benign |
Het |
Clock |
A |
G |
5: 76,402,258 (GRCm39) |
V134A |
possibly damaging |
Het |
CN725425 |
G |
A |
15: 91,129,904 (GRCm39) |
A256T |
possibly damaging |
Het |
Csf1r |
A |
T |
18: 61,262,119 (GRCm39) |
I792F |
probably damaging |
Het |
Csn1s1 |
T |
G |
5: 87,821,120 (GRCm39) |
S33A |
probably benign |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
D5Ertd579e |
A |
G |
5: 36,830,249 (GRCm39) |
V25A |
probably benign |
Het |
D630045J12Rik |
C |
T |
6: 38,125,302 (GRCm39) |
V1571M |
possibly damaging |
Het |
Ddx5 |
C |
A |
11: 106,675,833 (GRCm39) |
V286L |
possibly damaging |
Het |
Deup1 |
G |
A |
9: 15,523,310 (GRCm39) |
Q58* |
probably null |
Het |
Dnhd1 |
T |
G |
7: 105,362,840 (GRCm39) |
L3801V |
probably benign |
Het |
Dph2 |
T |
A |
4: 117,748,527 (GRCm39) |
D82V |
probably damaging |
Het |
Ercc6 |
A |
G |
14: 32,296,859 (GRCm39) |
D1283G |
probably damaging |
Het |
Evi5l |
G |
T |
8: 4,255,406 (GRCm39) |
V477L |
probably benign |
Het |
Fam91a1 |
A |
G |
15: 58,303,059 (GRCm39) |
T323A |
probably benign |
Het |
Fanca |
G |
A |
8: 124,035,261 (GRCm39) |
T228M |
probably damaging |
Het |
Fat4 |
T |
G |
3: 39,037,195 (GRCm39) |
S3616A |
probably benign |
Het |
Fbxo16 |
G |
T |
14: 65,558,746 (GRCm39) |
A302S |
probably benign |
Het |
Fkbp5 |
T |
C |
17: 28,647,343 (GRCm39) |
E164G |
probably damaging |
Het |
Fpr-rs3 |
T |
C |
17: 20,844,211 (GRCm39) |
Y310C |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,815,169 (GRCm39) |
I3634T |
probably benign |
Het |
Gm6327 |
T |
C |
16: 12,578,845 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
A |
T |
14: 30,735,462 (GRCm39) |
N411K |
possibly damaging |
Het |
Golga1 |
A |
T |
2: 38,929,118 (GRCm39) |
D308E |
probably damaging |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gsap |
A |
T |
5: 21,459,037 (GRCm39) |
T501S |
probably benign |
Het |
Helq |
A |
G |
5: 100,940,737 (GRCm39) |
|
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,234,108 (GRCm39) |
H291R |
probably benign |
Het |
Htt |
A |
T |
5: 34,970,367 (GRCm39) |
D505V |
probably damaging |
Het |
Ildr1 |
C |
T |
16: 36,528,660 (GRCm39) |
T35I |
probably benign |
Het |
Iqgap2 |
A |
G |
13: 95,794,305 (GRCm39) |
|
probably null |
Het |
Kansl1 |
C |
T |
11: 104,315,147 (GRCm39) |
R297H |
probably damaging |
Het |
Kat2b-ps |
T |
C |
5: 93,539,644 (GRCm39) |
|
noncoding transcript |
Het |
Kbtbd2 |
A |
G |
6: 56,758,943 (GRCm39) |
F60S |
probably benign |
Het |
Kcnt2 |
A |
T |
1: 140,537,388 (GRCm39) |
S1116C |
probably damaging |
Het |
Krt9 |
C |
T |
11: 100,079,538 (GRCm39) |
G618E |
unknown |
Het |
Lsm5 |
A |
T |
6: 56,680,309 (GRCm39) |
D44E |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,734,418 (GRCm39) |
D3275G |
probably benign |
Het |
Mindy2 |
A |
T |
9: 70,512,453 (GRCm39) |
V599E |
possibly damaging |
Het |
Nelfa |
A |
G |
5: 34,059,162 (GRCm39) |
V231A |
probably benign |
Het |
Nepro |
T |
C |
16: 44,555,156 (GRCm39) |
Y411H |
probably benign |
Het |
Nes |
T |
A |
3: 87,882,983 (GRCm39) |
L414Q |
probably damaging |
Het |
Neurl2 |
T |
A |
2: 164,675,122 (GRCm39) |
|
probably null |
Het |
Nkx1-1 |
G |
T |
5: 33,588,410 (GRCm39) |
Q293K |
possibly damaging |
Het |
Nphp3 |
C |
T |
9: 103,909,198 (GRCm39) |
H803Y |
probably benign |
Het |
Obscn |
A |
G |
11: 59,023,292 (GRCm39) |
V695A |
probably damaging |
Het |
Or10v5 |
A |
G |
19: 11,806,300 (GRCm39) |
L30P |
probably benign |
Het |
Or12d15 |
G |
A |
17: 37,693,910 (GRCm39) |
A151T |
probably damaging |
Het |
Or2f1 |
T |
C |
6: 42,721,621 (GRCm39) |
S217P |
probably damaging |
Het |
Or2t48 |
T |
C |
11: 58,419,903 (GRCm39) |
E303G |
probably benign |
Het |
Or4c106 |
T |
C |
2: 88,682,516 (GRCm39) |
V74A |
possibly damaging |
Het |
Or4f17-ps1 |
T |
A |
2: 111,357,969 (GRCm39) |
F103L |
probably damaging |
Het |
Or4p7 |
T |
A |
2: 88,221,674 (GRCm39) |
L28I |
probably benign |
Het |
Or7g35 |
A |
G |
9: 19,496,504 (GRCm39) |
T224A |
probably benign |
Het |
Or8d2b |
A |
G |
9: 38,789,400 (GRCm39) |
*309W |
probably null |
Het |
Orai3 |
T |
A |
7: 127,373,348 (GRCm39) |
L283Q |
probably damaging |
Het |
Pcdhb13 |
A |
T |
18: 37,576,237 (GRCm39) |
D205V |
probably benign |
Het |
Pdlim5 |
G |
A |
3: 142,017,740 (GRCm39) |
|
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,375,734 (GRCm39) |
V1467A |
probably damaging |
Het |
Pgm3 |
A |
G |
9: 86,444,732 (GRCm39) |
S268P |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,207,751 (GRCm39) |
I1420N |
probably damaging |
Het |
Pigp |
C |
A |
16: 94,160,006 (GRCm39) |
G134V |
probably benign |
Het |
Pik3c2g |
T |
C |
6: 139,789,657 (GRCm39) |
Y385H |
possibly damaging |
Het |
Pnliprp2 |
G |
A |
19: 58,754,750 (GRCm39) |
E265K |
probably benign |
Het |
Psmd13 |
T |
A |
7: 140,466,766 (GRCm39) |
Y117* |
probably null |
Het |
Ptprq |
C |
T |
10: 107,522,416 (GRCm39) |
V546I |
probably damaging |
Het |
Pum1 |
T |
G |
4: 130,396,448 (GRCm39) |
S68A |
probably benign |
Het |
Rnf167 |
T |
A |
11: 70,540,701 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,318,983 (GRCm39) |
V1148A |
possibly damaging |
Het |
Rnf216 |
T |
C |
5: 143,076,071 (GRCm39) |
E271G |
probably benign |
Het |
Ros1 |
A |
T |
10: 52,031,087 (GRCm39) |
I506N |
probably damaging |
Het |
Rpl37 |
G |
A |
15: 5,147,128 (GRCm39) |
R56Q |
possibly damaging |
Het |
Rpl41 |
A |
C |
10: 128,384,576 (GRCm39) |
|
probably benign |
Het |
Rttn |
A |
T |
18: 89,060,292 (GRCm39) |
H998L |
probably damaging |
Het |
Sacs |
G |
T |
14: 61,450,571 (GRCm39) |
A4206S |
probably damaging |
Het |
Slc22a14 |
CTTTCCTGAA |
C |
9: 119,003,101 (GRCm39) |
|
probably benign |
Het |
Slc39a3 |
A |
T |
10: 80,866,796 (GRCm39) |
W317R |
probably damaging |
Het |
Snd1 |
C |
A |
6: 28,884,250 (GRCm39) |
Y766* |
probably null |
Het |
Snrpd1 |
T |
C |
18: 10,626,835 (GRCm39) |
V34A |
probably benign |
Het |
Spire2 |
T |
A |
8: 124,083,583 (GRCm39) |
I189N |
probably damaging |
Het |
Stard6 |
A |
C |
18: 70,631,631 (GRCm39) |
D74A |
possibly damaging |
Het |
Sufu |
C |
T |
19: 46,463,991 (GRCm39) |
T401I |
possibly damaging |
Het |
Taar7b |
T |
A |
10: 23,876,243 (GRCm39) |
F136Y |
probably benign |
Het |
Taf6 |
G |
A |
5: 138,181,465 (GRCm39) |
Q156* |
probably null |
Het |
Tcp11l2 |
A |
G |
10: 84,427,027 (GRCm39) |
I164V |
probably damaging |
Het |
Tead4 |
T |
C |
6: 128,247,950 (GRCm39) |
D29G |
probably damaging |
Het |
Tns4 |
G |
T |
11: 98,966,039 (GRCm39) |
P448Q |
probably damaging |
Het |
Trappc9 |
G |
T |
15: 72,808,905 (GRCm39) |
N540K |
probably damaging |
Het |
Trbv28 |
C |
T |
6: 41,248,788 (GRCm39) |
S106F |
probably damaging |
Het |
Usp16 |
T |
A |
16: 87,277,802 (GRCm39) |
M684K |
probably damaging |
Het |
Usp45 |
A |
T |
4: 21,815,372 (GRCm39) |
T362S |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,836,961 (GRCm39) |
M2861K |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,278,536 (GRCm39) |
S267P |
probably damaging |
Het |
Wdfy3 |
C |
T |
5: 102,090,985 (GRCm39) |
D532N |
probably benign |
Het |
Zbtb34 |
T |
A |
2: 33,301,626 (GRCm39) |
Q305L |
probably benign |
Het |
Zfp267 |
C |
T |
3: 36,218,285 (GRCm39) |
R102C |
possibly damaging |
Het |
Zfp352 |
T |
A |
4: 90,112,376 (GRCm39) |
V172E |
probably benign |
Het |
Zfp454 |
T |
C |
11: 50,764,950 (GRCm39) |
N161D |
probably benign |
Het |
Zfp804b |
A |
T |
5: 6,821,198 (GRCm39) |
S622T |
probably damaging |
Het |
Zswim4 |
G |
T |
8: 84,938,852 (GRCm39) |
A1010D |
probably benign |
Het |
|
Other mutations in Slc36a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03104:Slc36a3
|
APN |
11 |
55,015,946 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03241:Slc36a3
|
APN |
11 |
55,015,934 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0632:Slc36a3
|
UTSW |
11 |
55,015,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R1117:Slc36a3
|
UTSW |
11 |
55,037,006 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1549:Slc36a3
|
UTSW |
11 |
55,033,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R3423:Slc36a3
|
UTSW |
11 |
55,033,607 (GRCm39) |
missense |
probably benign |
0.00 |
R3425:Slc36a3
|
UTSW |
11 |
55,033,607 (GRCm39) |
missense |
probably benign |
0.00 |
R3791:Slc36a3
|
UTSW |
11 |
55,015,982 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3980:Slc36a3
|
UTSW |
11 |
55,026,209 (GRCm39) |
missense |
probably benign |
|
R4970:Slc36a3
|
UTSW |
11 |
55,039,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R4986:Slc36a3
|
UTSW |
11 |
55,037,592 (GRCm39) |
makesense |
probably null |
|
R5112:Slc36a3
|
UTSW |
11 |
55,039,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Slc36a3
|
UTSW |
11 |
55,037,006 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5534:Slc36a3
|
UTSW |
11 |
55,033,595 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5580:Slc36a3
|
UTSW |
11 |
55,026,279 (GRCm39) |
missense |
probably benign |
0.14 |
R5682:Slc36a3
|
UTSW |
11 |
55,016,489 (GRCm39) |
missense |
probably benign |
0.00 |
R5779:Slc36a3
|
UTSW |
11 |
55,026,094 (GRCm39) |
nonsense |
probably null |
|
R5841:Slc36a3
|
UTSW |
11 |
55,016,547 (GRCm39) |
nonsense |
probably null |
|
R6228:Slc36a3
|
UTSW |
11 |
55,015,777 (GRCm39) |
missense |
probably benign |
0.01 |
R6483:Slc36a3
|
UTSW |
11 |
55,026,089 (GRCm39) |
missense |
probably benign |
0.01 |
R6908:Slc36a3
|
UTSW |
11 |
55,040,712 (GRCm39) |
intron |
probably benign |
|
R6927:Slc36a3
|
UTSW |
11 |
55,020,519 (GRCm39) |
missense |
probably damaging |
0.98 |
R7828:Slc36a3
|
UTSW |
11 |
55,042,024 (GRCm39) |
missense |
probably benign |
0.00 |
R7995:Slc36a3
|
UTSW |
11 |
55,020,495 (GRCm39) |
missense |
probably benign |
0.04 |
R8212:Slc36a3
|
UTSW |
11 |
55,015,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R8238:Slc36a3
|
UTSW |
11 |
55,022,433 (GRCm39) |
missense |
probably benign |
0.05 |
R8239:Slc36a3
|
UTSW |
11 |
55,022,433 (GRCm39) |
missense |
probably benign |
0.05 |
R8329:Slc36a3
|
UTSW |
11 |
55,039,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R8929:Slc36a3
|
UTSW |
11 |
55,028,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R9034:Slc36a3
|
UTSW |
11 |
55,016,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R9489:Slc36a3
|
UTSW |
11 |
55,040,726 (GRCm39) |
missense |
unknown |
|
R9506:Slc36a3
|
UTSW |
11 |
55,039,457 (GRCm39) |
missense |
probably benign |
0.14 |
R9661:Slc36a3
|
UTSW |
11 |
55,015,984 (GRCm39) |
missense |
probably benign |
0.00 |
R9696:Slc36a3
|
UTSW |
11 |
55,026,161 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9735:Slc36a3
|
UTSW |
11 |
55,026,104 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Slc36a3
|
UTSW |
11 |
55,026,278 (GRCm39) |
missense |
probably damaging |
0.97 |
|