Other mutations in this stock |
Total: 128 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700069L16Rik |
T |
C |
5: 113,830,813 (GRCm39) |
K59R |
unknown |
Het |
Abcb4 |
T |
C |
5: 8,977,931 (GRCm39) |
V503A |
probably benign |
Het |
Actn4 |
A |
G |
7: 28,596,398 (GRCm39) |
V699A |
probably benign |
Het |
Adam26a |
T |
A |
8: 44,022,358 (GRCm39) |
K377N |
probably benign |
Het |
Ahi1 |
A |
G |
10: 20,839,683 (GRCm39) |
Y198C |
probably damaging |
Het |
Ankrd44 |
G |
A |
1: 54,700,349 (GRCm39) |
Q720* |
probably null |
Het |
Arhgap26 |
A |
T |
18: 39,490,652 (GRCm39) |
M297L |
|
Het |
Arhgef11 |
C |
T |
3: 87,637,788 (GRCm39) |
T1093I |
probably damaging |
Het |
Arhgef25 |
C |
A |
10: 127,018,735 (GRCm39) |
R609S |
probably damaging |
Het |
Arhgef28 |
G |
T |
13: 98,190,472 (GRCm39) |
H162Q |
possibly damaging |
Het |
Atg4b |
A |
G |
1: 93,706,081 (GRCm39) |
E178G |
possibly damaging |
Het |
Atxn1l |
T |
C |
8: 110,459,117 (GRCm39) |
T382A |
probably benign |
Het |
Bdp1 |
A |
G |
13: 100,204,021 (GRCm39) |
V667A |
probably benign |
Het |
C6 |
T |
C |
15: 4,844,344 (GRCm39) |
I922T |
|
Het |
Ccdc191 |
A |
G |
16: 43,751,710 (GRCm39) |
T347A |
probably benign |
Het |
Cd22 |
G |
T |
7: 30,577,172 (GRCm39) |
P45H |
probably damaging |
Het |
Cdc45 |
A |
G |
16: 18,630,300 (GRCm39) |
F6L |
probably benign |
Het |
Cenpj |
T |
C |
14: 56,764,383 (GRCm39) |
E1343G |
possibly damaging |
Het |
Chtf8 |
T |
A |
8: 107,612,735 (GRCm39) |
N68I |
probably benign |
Het |
Cldn8 |
C |
T |
16: 88,359,733 (GRCm39) |
C64Y |
probably damaging |
Het |
Cntnap2 |
G |
T |
6: 46,460,983 (GRCm39) |
S673I |
probably benign |
Het |
Cyp3a13 |
C |
T |
5: 137,909,849 (GRCm39) |
R158K |
probably benign |
Het |
Cyp3a57 |
A |
T |
5: 145,311,039 (GRCm39) |
|
probably null |
Het |
Cyp3a57 |
G |
T |
5: 145,311,040 (GRCm39) |
|
probably null |
Het |
D630045J12Rik |
A |
G |
6: 38,173,898 (GRCm39) |
I90T |
probably benign |
Het |
Dapk2 |
A |
G |
9: 66,157,602 (GRCm39) |
|
probably benign |
Het |
Dmxl1 |
A |
G |
18: 50,026,919 (GRCm39) |
D2009G |
|
Het |
Dnah1 |
C |
T |
14: 31,033,704 (GRCm39) |
V290I |
possibly damaging |
Het |
Doc2g |
A |
T |
19: 4,054,511 (GRCm39) |
|
probably null |
Het |
Dpysl2 |
C |
T |
14: 67,045,402 (GRCm39) |
G457D |
probably damaging |
Het |
Drc1 |
A |
T |
5: 30,521,439 (GRCm39) |
Y700F |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 22,003,531 (GRCm39) |
Y1073H |
probably damaging |
Het |
Epm2aip1 |
T |
A |
9: 111,101,036 (GRCm39) |
M3K |
probably benign |
Het |
Erich3 |
G |
A |
3: 154,415,340 (GRCm39) |
R152Q |
|
Het |
Exoc5 |
C |
T |
14: 49,252,986 (GRCm39) |
R609H |
probably damaging |
Het |
Fam135b |
T |
A |
15: 71,334,189 (GRCm39) |
T1002S |
probably benign |
Het |
Fanca |
C |
T |
8: 124,024,538 (GRCm39) |
E528K |
probably damaging |
Het |
Fsd2 |
C |
A |
7: 81,209,766 (GRCm39) |
M25I |
probably benign |
Het |
Fyco1 |
T |
C |
9: 123,658,139 (GRCm39) |
E679G |
possibly damaging |
Het |
Gas6 |
T |
A |
8: 13,520,294 (GRCm39) |
M465L |
probably damaging |
Het |
Gfra3 |
A |
G |
18: 34,823,879 (GRCm39) |
V365A |
probably benign |
Het |
Gm10269 |
T |
G |
18: 20,815,981 (GRCm39) |
K14Q |
possibly damaging |
Het |
Gm21798 |
G |
A |
15: 64,689,756 (GRCm39) |
|
probably null |
Het |
Gm5916 |
T |
A |
9: 36,032,286 (GRCm39) |
R49S |
probably benign |
Het |
Gpam |
G |
T |
19: 55,072,227 (GRCm39) |
T266N |
possibly damaging |
Het |
Gtse1 |
A |
G |
15: 85,753,109 (GRCm39) |
E408G |
probably benign |
Het |
Hmgcll1 |
A |
T |
9: 76,037,592 (GRCm39) |
|
probably null |
Het |
Hspa12a |
T |
A |
19: 58,787,903 (GRCm39) |
R640* |
probably null |
Het |
Hspa9 |
T |
C |
18: 35,080,982 (GRCm39) |
D233G |
probably damaging |
Het |
Htt |
T |
G |
5: 34,977,368 (GRCm39) |
I751M |
probably benign |
Het |
Hydin |
T |
A |
8: 111,239,766 (GRCm39) |
Y2015* |
probably null |
Het |
Ift43 |
A |
C |
12: 86,208,275 (GRCm39) |
M138L |
probably benign |
Het |
Il11 |
C |
T |
7: 4,779,029 (GRCm39) |
V93M |
probably damaging |
Het |
Iws1 |
T |
A |
18: 32,226,645 (GRCm39) |
F741L |
possibly damaging |
Het |
Jmy |
A |
T |
13: 93,589,397 (GRCm39) |
I620N |
probably damaging |
Het |
Kap |
T |
A |
6: 133,830,689 (GRCm39) |
|
probably benign |
Het |
Kcnk15 |
A |
G |
2: 163,700,217 (GRCm39) |
N152S |
probably damaging |
Het |
Kif16b |
C |
T |
2: 142,691,783 (GRCm39) |
|
probably null |
Het |
Kif16b |
T |
C |
2: 142,743,278 (GRCm39) |
K5R |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,992,400 (GRCm39) |
R555H |
probably damaging |
Het |
Krt36 |
A |
G |
11: 99,994,372 (GRCm39) |
V235A |
possibly damaging |
Het |
Lca5 |
A |
G |
9: 83,283,796 (GRCm39) |
S246P |
probably damaging |
Het |
Maml1 |
T |
C |
11: 50,157,575 (GRCm39) |
D200G |
probably damaging |
Het |
Maml3 |
T |
C |
3: 51,597,868 (GRCm39) |
R939G |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,706,570 (GRCm39) |
T74S |
probably damaging |
Het |
Mib2 |
G |
T |
4: 155,745,351 (GRCm39) |
D125E |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,462,981 (GRCm39) |
L7407* |
probably null |
Het |
Mycbp2 |
A |
T |
14: 103,446,232 (GRCm39) |
N1865K |
probably damaging |
Het |
Naip1 |
A |
G |
13: 100,563,434 (GRCm39) |
L577S |
probably damaging |
Het |
Nell1 |
A |
T |
7: 50,498,399 (GRCm39) |
D652V |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nxph1 |
G |
A |
6: 8,950,312 (GRCm39) |
|
probably benign |
Het |
Oas1h |
T |
A |
5: 121,005,152 (GRCm39) |
I200N |
probably damaging |
Het |
Or2h2b-ps1 |
A |
G |
17: 37,480,867 (GRCm39) |
L122P |
probably damaging |
Het |
Or2h2b-ps1 |
A |
T |
17: 37,480,990 (GRCm39) |
I81N |
probably damaging |
Het |
Or8g53 |
A |
T |
9: 39,683,688 (GRCm39) |
M136K |
probably benign |
Het |
Otog |
A |
T |
7: 45,936,878 (GRCm39) |
Q1529L |
probably benign |
Het |
Otop1 |
A |
T |
5: 38,457,071 (GRCm39) |
I277F |
probably damaging |
Het |
Pax5 |
G |
A |
4: 44,645,661 (GRCm39) |
Q223* |
probably null |
Het |
Pcdha9 |
T |
A |
18: 37,132,998 (GRCm39) |
I689N |
probably benign |
Het |
Pcsk6 |
A |
T |
7: 65,576,975 (GRCm39) |
R138* |
probably null |
Het |
Pitpnm3 |
A |
T |
11: 72,003,132 (GRCm39) |
N59K |
probably damaging |
Het |
Pla2g4d |
G |
A |
2: 120,100,442 (GRCm39) |
T630I |
probably damaging |
Het |
Plekhg5 |
T |
A |
4: 152,188,372 (GRCm39) |
|
probably benign |
Het |
Plxnb1 |
T |
A |
9: 108,937,178 (GRCm39) |
|
probably benign |
Het |
Prss28 |
T |
A |
17: 25,528,395 (GRCm39) |
L6H |
probably damaging |
Het |
Pyroxd1 |
T |
A |
6: 142,302,251 (GRCm39) |
V228E |
|
Het |
Ripk2 |
G |
A |
4: 16,123,699 (GRCm39) |
T492M |
possibly damaging |
Het |
Satb1 |
A |
T |
17: 52,112,381 (GRCm39) |
C78S |
probably damaging |
Het |
Scaf11 |
A |
T |
15: 96,316,557 (GRCm39) |
C1002* |
probably null |
Het |
Scarf2 |
A |
C |
16: 17,622,768 (GRCm39) |
Q499P |
probably damaging |
Het |
Selenbp1 |
T |
A |
3: 94,847,425 (GRCm39) |
M244K |
probably benign |
Het |
Sik2 |
T |
C |
9: 50,806,647 (GRCm39) |
N921S |
probably benign |
Het |
Slc25a1 |
A |
T |
16: 17,743,744 (GRCm39) |
V290E |
probably damaging |
Het |
Slc28a3 |
C |
T |
13: 58,719,254 (GRCm39) |
|
probably benign |
Het |
Slc35b4 |
A |
T |
6: 34,137,442 (GRCm39) |
D213E |
probably benign |
Het |
Slc40a1 |
A |
C |
1: 45,950,495 (GRCm39) |
M319R |
probably damaging |
Het |
Slc8a1 |
A |
T |
17: 81,955,282 (GRCm39) |
F585L |
possibly damaging |
Het |
Slco3a1 |
T |
A |
7: 73,970,324 (GRCm39) |
N428Y |
possibly damaging |
Het |
Slfn2 |
G |
A |
11: 82,960,363 (GRCm39) |
C114Y |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,267,714 (GRCm39) |
|
probably null |
Het |
Spata13 |
T |
A |
14: 60,993,896 (GRCm39) |
L1116Q |
possibly damaging |
Het |
Spmap1 |
C |
T |
11: 97,666,510 (GRCm39) |
V59M |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,177,579 (GRCm39) |
V4965A |
possibly damaging |
Het |
Tacc3 |
G |
T |
5: 33,826,169 (GRCm39) |
V472F |
possibly damaging |
Het |
Tacr3 |
T |
A |
3: 134,560,573 (GRCm39) |
Y171N |
probably damaging |
Het |
Tacr3 |
T |
G |
3: 134,560,718 (GRCm39) |
L219R |
probably damaging |
Het |
Tbx3 |
C |
A |
5: 119,818,886 (GRCm39) |
A507E |
possibly damaging |
Het |
Telo2 |
A |
T |
17: 25,324,402 (GRCm39) |
D494E |
probably damaging |
Het |
Tfip11 |
T |
C |
5: 112,484,921 (GRCm39) |
F744S |
possibly damaging |
Het |
Tgm3 |
A |
C |
2: 129,880,403 (GRCm39) |
N403T |
probably benign |
Het |
Thoc3 |
A |
T |
13: 54,615,708 (GRCm39) |
S119T |
possibly damaging |
Het |
Tmem176b |
A |
T |
6: 48,812,530 (GRCm39) |
I145N |
probably damaging |
Het |
Trio |
T |
A |
15: 27,732,773 (GRCm39) |
Q3036L |
probably benign |
Het |
Trpc4 |
T |
C |
3: 54,102,132 (GRCm39) |
V10A |
probably benign |
Het |
Trpm3 |
A |
G |
19: 22,896,124 (GRCm39) |
Y987C |
probably damaging |
Het |
Tspoap1 |
A |
G |
11: 87,654,394 (GRCm39) |
K225E |
probably damaging |
Het |
Txnrd3 |
A |
T |
6: 89,638,477 (GRCm39) |
Q222L |
possibly damaging |
Het |
Usp34 |
A |
T |
11: 23,414,267 (GRCm39) |
M2756L |
|
Het |
Vmn2r81 |
C |
T |
10: 79,129,704 (GRCm39) |
T865I |
probably damaging |
Het |
Vnn1 |
A |
G |
10: 23,776,714 (GRCm39) |
Y355C |
probably damaging |
Het |
Wipf2 |
A |
T |
11: 98,783,092 (GRCm39) |
S173C |
probably damaging |
Het |
Wnt1 |
A |
T |
15: 98,689,624 (GRCm39) |
H137L |
probably damaging |
Het |
Xylt2 |
A |
T |
11: 94,561,278 (GRCm39) |
C162S |
probably damaging |
Het |
Zfp426 |
T |
C |
9: 20,387,744 (GRCm39) |
E33G |
probably damaging |
Het |
Zfp811 |
A |
C |
17: 33,017,801 (GRCm39) |
C80G |
possibly damaging |
Het |
Zfp931 |
T |
C |
2: 177,709,591 (GRCm39) |
H265R |
probably damaging |
Het |
Zfp931 |
G |
A |
2: 177,709,592 (GRCm39) |
H265Y |
probably damaging |
Het |
|
Other mutations in Adam6b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Adam6b
|
APN |
12 |
113,455,013 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00800:Adam6b
|
APN |
12 |
113,454,062 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01456:Adam6b
|
APN |
12 |
113,455,083 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02232:Adam6b
|
APN |
12 |
113,454,764 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03039:Adam6b
|
APN |
12 |
113,454,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03399:Adam6b
|
APN |
12 |
113,454,728 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03412:Adam6b
|
APN |
12 |
113,455,390 (GRCm39) |
nonsense |
probably null |
|
R0234:Adam6b
|
UTSW |
12 |
113,454,230 (GRCm39) |
missense |
probably damaging |
0.98 |
R0234:Adam6b
|
UTSW |
12 |
113,454,230 (GRCm39) |
missense |
probably damaging |
0.98 |
R0373:Adam6b
|
UTSW |
12 |
113,454,275 (GRCm39) |
missense |
probably benign |
0.15 |
R0402:Adam6b
|
UTSW |
12 |
113,453,615 (GRCm39) |
missense |
probably damaging |
0.96 |
R0420:Adam6b
|
UTSW |
12 |
113,453,614 (GRCm39) |
missense |
probably benign |
0.02 |
R0573:Adam6b
|
UTSW |
12 |
113,455,278 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0884:Adam6b
|
UTSW |
12 |
113,454,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Adam6b
|
UTSW |
12 |
113,455,071 (GRCm39) |
missense |
probably benign |
0.15 |
R1542:Adam6b
|
UTSW |
12 |
113,454,559 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1591:Adam6b
|
UTSW |
12 |
113,453,452 (GRCm39) |
missense |
probably benign |
0.07 |
R1596:Adam6b
|
UTSW |
12 |
113,454,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1675:Adam6b
|
UTSW |
12 |
113,454,664 (GRCm39) |
missense |
probably benign |
0.00 |
R1699:Adam6b
|
UTSW |
12 |
113,454,205 (GRCm39) |
missense |
probably benign |
0.02 |
R1818:Adam6b
|
UTSW |
12 |
113,454,876 (GRCm39) |
missense |
probably benign |
0.15 |
R1829:Adam6b
|
UTSW |
12 |
113,453,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Adam6b
|
UTSW |
12 |
113,455,442 (GRCm39) |
missense |
probably benign |
0.44 |
R1955:Adam6b
|
UTSW |
12 |
113,455,436 (GRCm39) |
missense |
probably benign |
0.16 |
R2040:Adam6b
|
UTSW |
12 |
113,454,364 (GRCm39) |
missense |
probably benign |
0.34 |
R3820:Adam6b
|
UTSW |
12 |
113,453,984 (GRCm39) |
missense |
probably benign |
0.38 |
R4112:Adam6b
|
UTSW |
12 |
113,453,256 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4434:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4435:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4438:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4509:Adam6b
|
UTSW |
12 |
113,453,972 (GRCm39) |
missense |
probably benign |
0.02 |
R5034:Adam6b
|
UTSW |
12 |
113,454,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R5316:Adam6b
|
UTSW |
12 |
113,455,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Adam6b
|
UTSW |
12 |
113,454,200 (GRCm39) |
missense |
possibly damaging |
0.45 |
R5331:Adam6b
|
UTSW |
12 |
113,454,200 (GRCm39) |
missense |
possibly damaging |
0.45 |
R5604:Adam6b
|
UTSW |
12 |
113,454,420 (GRCm39) |
nonsense |
probably null |
|
R5698:Adam6b
|
UTSW |
12 |
113,455,083 (GRCm39) |
missense |
probably benign |
0.30 |
R5877:Adam6b
|
UTSW |
12 |
113,453,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Adam6b
|
UTSW |
12 |
113,455,330 (GRCm39) |
missense |
probably benign |
|
R6254:Adam6b
|
UTSW |
12 |
113,453,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R6371:Adam6b
|
UTSW |
12 |
113,453,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R6617:Adam6b
|
UTSW |
12 |
113,454,152 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6768:Adam6b
|
UTSW |
12 |
113,453,863 (GRCm39) |
missense |
probably benign |
0.01 |
R7002:Adam6b
|
UTSW |
12 |
113,453,327 (GRCm39) |
nonsense |
probably null |
|
R7003:Adam6b
|
UTSW |
12 |
113,453,662 (GRCm39) |
nonsense |
probably null |
|
R7049:Adam6b
|
UTSW |
12 |
113,454,122 (GRCm39) |
missense |
probably damaging |
0.99 |
R7313:Adam6b
|
UTSW |
12 |
113,454,754 (GRCm39) |
missense |
probably benign |
0.00 |
R7372:Adam6b
|
UTSW |
12 |
113,453,784 (GRCm39) |
missense |
probably benign |
0.24 |
R7684:Adam6b
|
UTSW |
12 |
113,455,196 (GRCm39) |
nonsense |
probably null |
|
R7777:Adam6b
|
UTSW |
12 |
113,453,758 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7781:Adam6b
|
UTSW |
12 |
113,454,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R7857:Adam6b
|
UTSW |
12 |
113,454,104 (GRCm39) |
missense |
probably benign |
0.09 |
R8196:Adam6b
|
UTSW |
12 |
113,454,087 (GRCm39) |
missense |
probably benign |
0.19 |
R8423:Adam6b
|
UTSW |
12 |
113,454,530 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8680:Adam6b
|
UTSW |
12 |
113,454,371 (GRCm39) |
missense |
probably benign |
0.05 |
R8762:Adam6b
|
UTSW |
12 |
113,453,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R8792:Adam6b
|
UTSW |
12 |
113,455,310 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8806:Adam6b
|
UTSW |
12 |
113,455,418 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8880:Adam6b
|
UTSW |
12 |
113,454,764 (GRCm39) |
missense |
probably benign |
|
R8977:Adam6b
|
UTSW |
12 |
113,453,996 (GRCm39) |
missense |
probably benign |
0.02 |
R9101:Adam6b
|
UTSW |
12 |
113,455,376 (GRCm39) |
missense |
probably benign |
0.22 |
R9103:Adam6b
|
UTSW |
12 |
113,454,558 (GRCm39) |
nonsense |
probably null |
|
R9334:Adam6b
|
UTSW |
12 |
113,454,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Adam6b
|
UTSW |
12 |
113,454,176 (GRCm39) |
missense |
probably benign |
|
R9683:Adam6b
|
UTSW |
12 |
113,454,176 (GRCm39) |
missense |
probably benign |
|
R9796:Adam6b
|
UTSW |
12 |
113,454,272 (GRCm39) |
missense |
probably damaging |
1.00 |
RF012:Adam6b
|
UTSW |
12 |
113,453,552 (GRCm39) |
missense |
probably damaging |
1.00 |
RF022:Adam6b
|
UTSW |
12 |
113,455,289 (GRCm39) |
missense |
possibly damaging |
0.90 |
T0722:Adam6b
|
UTSW |
12 |
113,454,888 (GRCm39) |
missense |
probably benign |
0.11 |
T0722:Adam6b
|
UTSW |
12 |
113,453,197 (GRCm39) |
missense |
possibly damaging |
0.91 |
|