Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
T |
C |
5: 109,884,917 (GRCm39) |
R314G |
unknown |
Het |
Abca13 |
G |
A |
11: 9,244,559 (GRCm39) |
V2141M |
probably benign |
Het |
Abcc10 |
G |
A |
17: 46,634,710 (GRCm39) |
A431V |
possibly damaging |
Het |
Acod1 |
A |
G |
14: 103,292,414 (GRCm39) |
R313G |
probably damaging |
Het |
Adam3 |
G |
T |
8: 25,193,928 (GRCm39) |
S361R |
probably damaging |
Het |
Ahcyl2 |
C |
T |
6: 29,768,874 (GRCm39) |
T113M |
possibly damaging |
Het |
Ano8 |
C |
A |
8: 71,933,561 (GRCm39) |
R577L |
unknown |
Het |
Arhgef7 |
T |
A |
8: 11,869,646 (GRCm39) |
S653R |
probably damaging |
Het |
Atp10a |
G |
A |
7: 58,469,418 (GRCm39) |
V1090I |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,966,216 (GRCm39) |
M4048V |
probably benign |
Het |
C3 |
G |
A |
17: 57,530,950 (GRCm39) |
P384S |
probably damaging |
Het |
Camkk1 |
A |
T |
11: 72,928,757 (GRCm39) |
E432V |
probably damaging |
Het |
Celsr3 |
T |
A |
9: 108,726,032 (GRCm39) |
V3087D |
probably benign |
Het |
Ckap4 |
A |
G |
10: 84,363,543 (GRCm39) |
S507P |
probably damaging |
Het |
Coq6 |
G |
A |
12: 84,420,464 (GRCm39) |
M471I |
probably benign |
Het |
Csmd2 |
C |
A |
4: 128,171,004 (GRCm39) |
H332Q |
|
Het |
Cxcr1 |
T |
A |
1: 74,231,231 (GRCm39) |
N264Y |
probably damaging |
Het |
Dchs2 |
C |
A |
3: 83,036,032 (GRCm39) |
R260S |
possibly damaging |
Het |
Elmod2 |
C |
A |
8: 84,057,761 (GRCm39) |
A41S |
possibly damaging |
Het |
Emilin2 |
G |
A |
17: 71,581,781 (GRCm39) |
T315I |
probably benign |
Het |
Eml1 |
A |
G |
12: 108,482,842 (GRCm39) |
N487S |
probably benign |
Het |
Epn1 |
G |
T |
7: 5,096,369 (GRCm39) |
R221L |
probably benign |
Het |
Faah |
A |
G |
4: 115,874,772 (GRCm39) |
V28A |
probably benign |
Het |
Fbl |
G |
A |
7: 27,876,689 (GRCm39) |
R230H |
probably benign |
Het |
Fsip2 |
C |
T |
2: 82,805,907 (GRCm39) |
S742F |
probably damaging |
Het |
Gm5460 |
A |
G |
14: 33,767,769 (GRCm39) |
D184G |
possibly damaging |
Het |
Gpatch2l |
T |
C |
12: 86,307,408 (GRCm39) |
V262A |
probably damaging |
Het |
Grin2c |
A |
T |
11: 115,142,052 (GRCm39) |
L789* |
probably null |
Het |
H1f0 |
C |
T |
15: 78,912,947 (GRCm39) |
P9L |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,460,864 (GRCm39) |
T948A |
probably benign |
Het |
Herc2 |
G |
A |
7: 55,780,932 (GRCm39) |
G1199D |
probably damaging |
Het |
Hoxb7 |
G |
T |
11: 96,177,617 (GRCm39) |
A22S |
possibly damaging |
Het |
Ifih1 |
T |
A |
2: 62,439,618 (GRCm39) |
I519F |
probably damaging |
Het |
Ifit1bl1 |
T |
A |
19: 34,571,498 (GRCm39) |
I320F |
possibly damaging |
Het |
Iqgap2 |
T |
C |
13: 95,774,261 (GRCm39) |
T1320A |
probably benign |
Het |
Kat2a |
A |
G |
11: 100,602,178 (GRCm39) |
V192A |
probably damaging |
Het |
Kat6b |
A |
C |
14: 21,672,077 (GRCm39) |
H329P |
probably damaging |
Het |
Klhl29 |
A |
G |
12: 5,260,056 (GRCm39) |
L54P |
probably benign |
Het |
Kntc1 |
A |
T |
5: 123,925,112 (GRCm39) |
I1142F |
possibly damaging |
Het |
Lipo3 |
A |
G |
19: 33,533,864 (GRCm39) |
Y323H |
probably damaging |
Het |
Lmtk3 |
G |
A |
7: 45,441,994 (GRCm39) |
V351I |
probably damaging |
Het |
Lrrc8b |
T |
C |
5: 105,633,888 (GRCm39) |
S787P |
probably benign |
Het |
Magi1 |
A |
G |
6: 93,660,058 (GRCm39) |
I1179T |
probably damaging |
Het |
Mapk11 |
T |
C |
15: 89,028,631 (GRCm39) |
D269G |
probably benign |
Het |
Mfsd13a |
T |
G |
19: 46,354,868 (GRCm39) |
I15R |
probably benign |
Het |
Myo1h |
G |
A |
5: 114,499,366 (GRCm39) |
V143I |
possibly damaging |
Het |
Naaladl1 |
T |
C |
19: 6,156,917 (GRCm39) |
I187T |
possibly damaging |
Het |
Nos1 |
G |
A |
5: 118,034,871 (GRCm39) |
V416M |
probably damaging |
Het |
Or14a256 |
G |
A |
7: 86,265,065 (GRCm39) |
R263C |
possibly damaging |
Het |
Or14j8 |
A |
G |
17: 38,263,559 (GRCm39) |
S119P |
probably damaging |
Het |
Or8k30 |
T |
G |
2: 86,338,914 (GRCm39) |
I37S |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,460,170 (GRCm39) |
T1373A |
probably damaging |
Het |
Pcdh18 |
T |
G |
3: 49,699,667 (GRCm39) |
M932L |
probably damaging |
Het |
Pcdhb15 |
T |
A |
18: 37,608,683 (GRCm39) |
H638Q |
probably benign |
Het |
Pcdhb19 |
A |
G |
18: 37,630,628 (GRCm39) |
E141G |
possibly damaging |
Het |
Pds5b |
T |
G |
5: 150,693,256 (GRCm39) |
L656R |
probably damaging |
Het |
Plcl1 |
T |
C |
1: 55,445,587 (GRCm39) |
L14P |
probably benign |
Het |
Pzp |
A |
T |
6: 128,499,128 (GRCm39) |
I173N |
|
Het |
Rnf123 |
C |
T |
9: 107,937,008 (GRCm39) |
R849H |
probably damaging |
Het |
Sfrp5 |
T |
C |
19: 42,188,225 (GRCm39) |
D198G |
probably damaging |
Het |
Sftpb |
G |
C |
6: 72,283,843 (GRCm39) |
A147P |
probably benign |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Slc5a3 |
T |
A |
16: 91,874,615 (GRCm39) |
V224D |
probably benign |
Het |
Smad5 |
T |
A |
13: 56,875,417 (GRCm39) |
Y202N |
probably benign |
Het |
Smok2b |
A |
G |
17: 13,453,881 (GRCm39) |
I14V |
probably damaging |
Het |
Tas2r108 |
T |
A |
6: 40,471,121 (GRCm39) |
I199K |
probably damaging |
Het |
Tcea2 |
A |
G |
2: 181,322,227 (GRCm39) |
I10V |
probably damaging |
Het |
Tfg |
G |
A |
16: 56,524,868 (GRCm39) |
R113* |
probably null |
Het |
Tubb4a |
A |
T |
17: 57,388,034 (GRCm39) |
L331I |
probably benign |
Het |
Ugt2b37 |
A |
G |
5: 87,402,046 (GRCm39) |
V195A |
probably damaging |
Het |
Umad1 |
A |
G |
6: 8,401,096 (GRCm39) |
H55R |
unknown |
Het |
Vmn1r176 |
A |
T |
7: 23,534,743 (GRCm39) |
Y137N |
probably damaging |
Het |
Vmn1r44 |
T |
A |
6: 89,870,473 (GRCm39) |
M73K |
possibly damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,821,233 (GRCm39) |
T69A |
|
Het |
Vmn2r59 |
A |
T |
7: 41,696,254 (GRCm39) |
Y163N |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,830,137 (GRCm39) |
D1514E |
probably benign |
Het |
Vsir |
A |
G |
10: 60,193,732 (GRCm39) |
D65G |
possibly damaging |
Het |
Ypel3 |
A |
T |
7: 126,379,262 (GRCm39) |
M112L |
probably benign |
Het |
Zfp26 |
T |
A |
9: 20,347,830 (GRCm39) |
K911N |
probably damaging |
Het |
Zfp362 |
C |
T |
4: 128,670,980 (GRCm39) |
R346Q |
probably damaging |
Het |
Zfp595 |
A |
T |
13: 67,465,407 (GRCm39) |
Y288* |
probably null |
Het |
Zfyve28 |
G |
T |
5: 34,400,633 (GRCm39) |
Q22K |
possibly damaging |
Het |
Zswim4 |
T |
G |
8: 84,963,539 (GRCm39) |
D32A |
probably damaging |
Het |
|
Other mutations in Slc30a6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01336:Slc30a6
|
APN |
17 |
74,715,834 (GRCm39) |
splice site |
probably benign |
|
IGL01592:Slc30a6
|
APN |
17 |
74,726,523 (GRCm39) |
splice site |
probably benign |
|
IGL02556:Slc30a6
|
APN |
17 |
74,711,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03033:Slc30a6
|
APN |
17 |
74,716,373 (GRCm39) |
nonsense |
probably null |
|
IGL03149:Slc30a6
|
APN |
17 |
74,730,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0355:Slc30a6
|
UTSW |
17 |
74,730,198 (GRCm39) |
missense |
probably benign |
|
R0791:Slc30a6
|
UTSW |
17 |
74,722,640 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0792:Slc30a6
|
UTSW |
17 |
74,722,640 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1507:Slc30a6
|
UTSW |
17 |
74,715,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R1517:Slc30a6
|
UTSW |
17 |
74,715,842 (GRCm39) |
missense |
probably benign |
0.25 |
R1585:Slc30a6
|
UTSW |
17 |
74,725,610 (GRCm39) |
splice site |
probably benign |
|
R1944:Slc30a6
|
UTSW |
17 |
74,715,858 (GRCm39) |
missense |
probably damaging |
0.99 |
R2925:Slc30a6
|
UTSW |
17 |
74,708,999 (GRCm39) |
splice site |
probably benign |
|
R3891:Slc30a6
|
UTSW |
17 |
74,726,541 (GRCm39) |
missense |
probably benign |
0.19 |
R4840:Slc30a6
|
UTSW |
17 |
74,712,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Slc30a6
|
UTSW |
17 |
74,719,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5330:Slc30a6
|
UTSW |
17 |
74,730,190 (GRCm39) |
missense |
probably benign |
0.24 |
R5331:Slc30a6
|
UTSW |
17 |
74,730,190 (GRCm39) |
missense |
probably benign |
0.24 |
R5562:Slc30a6
|
UTSW |
17 |
74,719,700 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6458:Slc30a6
|
UTSW |
17 |
74,730,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R6681:Slc30a6
|
UTSW |
17 |
74,711,027 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7419:Slc30a6
|
UTSW |
17 |
74,730,424 (GRCm39) |
missense |
probably benign |
|
R7457:Slc30a6
|
UTSW |
17 |
74,714,233 (GRCm39) |
missense |
probably benign |
0.05 |
R7596:Slc30a6
|
UTSW |
17 |
74,722,664 (GRCm39) |
missense |
probably benign |
0.00 |
R7844:Slc30a6
|
UTSW |
17 |
74,711,088 (GRCm39) |
splice site |
probably null |
|
R8043:Slc30a6
|
UTSW |
17 |
74,730,018 (GRCm39) |
missense |
probably damaging |
0.99 |
R8097:Slc30a6
|
UTSW |
17 |
74,719,693 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8465:Slc30a6
|
UTSW |
17 |
74,722,661 (GRCm39) |
missense |
probably benign |
0.04 |
R8557:Slc30a6
|
UTSW |
17 |
74,712,685 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8878:Slc30a6
|
UTSW |
17 |
74,730,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R9035:Slc30a6
|
UTSW |
17 |
74,726,586 (GRCm39) |
missense |
probably benign |
0.23 |
R9632:Slc30a6
|
UTSW |
17 |
74,730,059 (GRCm39) |
missense |
probably benign |
0.01 |
T0722:Slc30a6
|
UTSW |
17 |
74,719,319 (GRCm39) |
critical splice donor site |
probably null |
|
X0003:Slc30a6
|
UTSW |
17 |
74,719,319 (GRCm39) |
critical splice donor site |
probably null |
|
|