Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
T |
5: 8,980,796 (GRCm39) |
N593Y |
probably damaging |
Het |
Adamts16 |
C |
T |
13: 70,940,005 (GRCm39) |
S406N |
possibly damaging |
Het |
Adgrg1 |
G |
A |
8: 95,733,928 (GRCm39) |
V350I |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,659,030 (GRCm39) |
D2051E |
probably damaging |
Het |
Adrb2 |
C |
A |
18: 62,312,484 (GRCm39) |
V114L |
probably damaging |
Het |
Ago3 |
A |
G |
4: 126,247,520 (GRCm39) |
V599A |
probably damaging |
Het |
AI837181 |
T |
C |
19: 5,476,257 (GRCm39) |
V140A |
probably damaging |
Het |
Ankrd16 |
T |
A |
2: 11,788,443 (GRCm39) |
|
probably null |
Het |
Arnt2 |
A |
G |
7: 83,992,959 (GRCm39) |
S194P |
probably benign |
Het |
Art2b |
T |
C |
7: 101,229,153 (GRCm39) |
N249D |
probably benign |
Het |
Atat1 |
A |
G |
17: 36,220,232 (GRCm39) |
L60P |
probably damaging |
Het |
Atp2b1 |
A |
T |
10: 98,858,793 (GRCm39) |
I1159F |
probably damaging |
Het |
Atrip |
T |
A |
9: 108,900,935 (GRCm39) |
I135F |
probably damaging |
Het |
Bbs4 |
T |
G |
9: 59,237,698 (GRCm39) |
|
probably null |
Het |
Bdp1 |
A |
T |
13: 100,210,889 (GRCm39) |
|
probably null |
Het |
Best2 |
A |
G |
8: 85,737,390 (GRCm39) |
|
probably null |
Het |
Cacna1c |
A |
G |
6: 118,583,227 (GRCm39) |
I1516T |
probably damaging |
Het |
Cadps2 |
T |
C |
6: 23,599,479 (GRCm39) |
I276V |
probably damaging |
Het |
Carmil3 |
T |
C |
14: 55,736,087 (GRCm39) |
S610P |
probably damaging |
Het |
Caskin1 |
A |
G |
17: 24,719,745 (GRCm39) |
I375V |
probably damaging |
Het |
Ccdc168 |
G |
A |
1: 44,101,009 (GRCm39) |
P30S |
probably damaging |
Het |
Ccdc92b |
A |
G |
11: 74,520,835 (GRCm39) |
I46V |
probably benign |
Het |
Clec11a |
G |
T |
7: 43,954,098 (GRCm39) |
T285K |
probably benign |
Het |
Clk3 |
G |
T |
9: 57,672,469 (GRCm39) |
T111K |
probably benign |
Het |
Col6a6 |
G |
A |
9: 105,586,583 (GRCm39) |
R1813C |
probably damaging |
Het |
Col7a1 |
G |
A |
9: 108,789,078 (GRCm39) |
V798I |
unknown |
Het |
Ctrb1 |
C |
A |
8: 112,416,151 (GRCm39) |
W45L |
probably damaging |
Het |
Cubn |
T |
A |
2: 13,283,349 (GRCm39) |
S3530C |
probably benign |
Het |
Dio1 |
A |
G |
4: 107,163,977 (GRCm39) |
|
probably null |
Het |
Dock5 |
A |
T |
14: 67,994,584 (GRCm39) |
Y1825* |
probably null |
Het |
Duox1 |
A |
T |
2: 122,177,001 (GRCm39) |
Q1476L |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 7,001,377 (GRCm39) |
H3877Q |
probably damaging |
Het |
Enkd1 |
A |
G |
8: 106,434,208 (GRCm39) |
S85P |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,794,758 (GRCm39) |
D139G |
probably benign |
Het |
Ern1 |
A |
G |
11: 106,312,776 (GRCm39) |
S202P |
probably damaging |
Het |
F11r |
T |
C |
1: 171,289,459 (GRCm39) |
Y261H |
probably damaging |
Het |
Glp2r |
A |
T |
11: 67,637,618 (GRCm39) |
S138T |
probably benign |
Het |
Gpt2 |
A |
G |
8: 86,244,625 (GRCm39) |
Y306C |
probably damaging |
Het |
Grid2 |
G |
C |
6: 63,886,045 (GRCm39) |
R147P |
probably damaging |
Het |
Gtdc1 |
A |
G |
2: 44,642,198 (GRCm39) |
F128L |
possibly damaging |
Het |
H2-T15 |
A |
G |
17: 36,368,897 (GRCm39) |
F61S |
probably damaging |
Het |
Hacd4 |
T |
C |
4: 88,341,303 (GRCm39) |
T154A |
possibly damaging |
Het |
Heatr6 |
G |
T |
11: 83,660,046 (GRCm39) |
L530F |
probably damaging |
Het |
Hoxd8 |
A |
T |
2: 74,537,056 (GRCm39) |
D256V |
probably damaging |
Het |
Ints6 |
T |
C |
14: 62,931,089 (GRCm39) |
N865D |
probably benign |
Het |
Itpkc |
G |
T |
7: 26,927,084 (GRCm39) |
P277T |
possibly damaging |
Het |
Klc4 |
T |
C |
17: 46,947,553 (GRCm39) |
N383S |
probably damaging |
Het |
Klra6 |
T |
C |
6: 129,995,908 (GRCm39) |
Y150C |
possibly damaging |
Het |
Krt32 |
T |
A |
11: 99,975,670 (GRCm39) |
|
probably null |
Het |
Krt33a |
T |
C |
11: 99,903,535 (GRCm39) |
N199S |
probably benign |
Het |
Krt39 |
A |
C |
11: 99,410,649 (GRCm39) |
D174E |
probably damaging |
Het |
Krt82 |
G |
A |
15: 101,456,970 (GRCm39) |
R137W |
probably damaging |
Het |
Lgmn |
A |
T |
12: 102,368,183 (GRCm39) |
S193T |
probably damaging |
Het |
Limch1 |
G |
A |
5: 67,156,442 (GRCm39) |
R300H |
probably damaging |
Het |
Lrpap1 |
T |
A |
5: 35,254,974 (GRCm39) |
I221F |
probably benign |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,264,459 (GRCm39) |
D4883G |
probably damaging |
Het |
Man2b2 |
A |
G |
5: 36,973,524 (GRCm39) |
V485A |
probably benign |
Het |
Map3k19 |
T |
C |
1: 127,750,859 (GRCm39) |
T831A |
probably benign |
Het |
Mdfic2 |
A |
G |
6: 98,225,151 (GRCm39) |
I44T |
probably benign |
Het |
Megf6 |
C |
G |
4: 154,340,523 (GRCm39) |
D471E |
possibly damaging |
Het |
Mettl8 |
A |
T |
2: 70,803,623 (GRCm39) |
F268L |
probably damaging |
Het |
Miip |
T |
C |
4: 147,950,422 (GRCm39) |
E58G |
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,466,840 (GRCm39) |
S1308C |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,392,909 (GRCm39) |
F2194L |
probably damaging |
Het |
Nav3 |
T |
C |
10: 109,552,391 (GRCm39) |
N1817S |
probably damaging |
Het |
Ndel1 |
A |
T |
11: 68,720,746 (GRCm39) |
H313Q |
probably benign |
Het |
Neb |
A |
T |
2: 52,118,862 (GRCm39) |
H3931Q |
probably benign |
Het |
Nfkb2 |
T |
A |
19: 46,296,491 (GRCm39) |
V253E |
probably damaging |
Het |
Niban1 |
T |
C |
1: 151,571,979 (GRCm39) |
I308T |
probably damaging |
Het |
Nono |
T |
C |
X: 100,485,429 (GRCm39) |
|
probably null |
Het |
Npc1l1 |
T |
A |
11: 6,164,588 (GRCm39) |
I1154F |
possibly damaging |
Het |
Nr2e1 |
T |
C |
10: 42,448,774 (GRCm39) |
T155A |
probably benign |
Het |
Oosp2 |
C |
T |
19: 11,626,959 (GRCm39) |
|
probably null |
Het |
Or2b2 |
A |
T |
13: 21,887,287 (GRCm39) |
I39F |
possibly damaging |
Het |
Pdap1 |
G |
A |
5: 145,069,726 (GRCm39) |
T93I |
probably benign |
Het |
Pde6c |
T |
A |
19: 38,145,967 (GRCm39) |
D418E |
probably damaging |
Het |
Pdha1 |
T |
A |
X: 158,910,354 (GRCm39) |
D255V |
probably damaging |
Het |
Polr2h |
T |
A |
16: 20,537,796 (GRCm39) |
D64E |
probably benign |
Het |
Psmb3 |
T |
C |
11: 97,601,981 (GRCm39) |
F117S |
probably benign |
Het |
Ptprq |
A |
T |
10: 107,418,249 (GRCm39) |
M1709K |
probably benign |
Het |
Rbm15 |
C |
T |
3: 107,238,868 (GRCm39) |
R510H |
probably damaging |
Het |
Rgs7 |
A |
T |
1: 174,980,769 (GRCm39) |
M85K |
possibly damaging |
Het |
Rpl27-ps3 |
T |
A |
18: 6,332,669 (GRCm39) |
V13D |
probably damaging |
Het |
Rtp2 |
T |
A |
16: 23,746,316 (GRCm39) |
D105V |
possibly damaging |
Het |
Scd3 |
T |
C |
19: 44,224,219 (GRCm39) |
Y151H |
probably benign |
Het |
Slco1a4 |
T |
C |
6: 141,785,276 (GRCm39) |
I105V |
probably benign |
Het |
Sun3 |
T |
C |
11: 8,988,296 (GRCm39) |
I9V |
probably benign |
Het |
Syne2 |
T |
C |
12: 76,121,318 (GRCm39) |
V5928A |
probably damaging |
Het |
Tbr1 |
T |
A |
2: 61,642,600 (GRCm39) |
S622T |
probably damaging |
Het |
Tgm3 |
A |
G |
2: 129,871,889 (GRCm39) |
N306D |
probably damaging |
Het |
Tmem132d |
A |
G |
5: 127,860,828 (GRCm39) |
*1098Q |
probably null |
Het |
Tmem140 |
T |
C |
6: 34,849,747 (GRCm39) |
Y88H |
probably damaging |
Het |
Trim60 |
A |
T |
8: 65,453,964 (GRCm39) |
V95E |
possibly damaging |
Het |
Vamp3 |
A |
G |
4: 151,140,617 (GRCm39) |
|
probably null |
Het |
Vmn1r235 |
A |
C |
17: 21,481,785 (GRCm39) |
T37P |
probably damaging |
Het |
Vmn2r81 |
T |
G |
10: 79,129,571 (GRCm39) |
L821V |
probably damaging |
Het |
Vmn2r97 |
A |
G |
17: 19,160,500 (GRCm39) |
D545G |
probably benign |
Het |
Vps13c |
A |
T |
9: 67,793,558 (GRCm39) |
D437V |
probably damaging |
Het |
Wtip |
A |
T |
7: 33,818,363 (GRCm39) |
M268K |
probably benign |
Het |
Zfhx2 |
G |
T |
14: 55,312,189 (GRCm39) |
F168L |
probably benign |
Het |
Zscan22 |
G |
A |
7: 12,637,767 (GRCm39) |
R53K |
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 |
|
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 |
R9432:Slc30a6
|
UTSW |
17 |
74,719,699 (GRCm39) |
missense |
possibly damaging |
0.66 |
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 |
|
|