Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
A |
G |
16: 88,555,902 (GRCm39) |
T39A |
probably damaging |
Het |
Abca3 |
G |
A |
17: 24,596,681 (GRCm39) |
G378D |
probably damaging |
Het |
Abtb2 |
T |
C |
2: 103,397,565 (GRCm39) |
V165A |
possibly damaging |
Het |
Ache |
A |
G |
5: 137,288,504 (GRCm39) |
E70G |
probably damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,588,119 (GRCm39) |
T623A |
probably benign |
Het |
Ahdc1 |
G |
A |
4: 132,791,935 (GRCm39) |
V1059I |
probably benign |
Het |
Ajuba |
G |
A |
14: 54,810,915 (GRCm39) |
Q357* |
probably null |
Het |
Ano7 |
A |
T |
1: 93,330,700 (GRCm39) |
D54V |
|
Het |
Apob |
A |
T |
12: 8,055,072 (GRCm39) |
D1357V |
probably damaging |
Het |
Atad2b |
T |
A |
12: 5,067,992 (GRCm39) |
Y997N |
probably damaging |
Het |
Bhlhe22 |
C |
A |
3: 18,110,006 (GRCm39) |
T352K |
probably damaging |
Het |
Bsn |
T |
C |
9: 107,992,533 (GRCm39) |
E1073G |
probably damaging |
Het |
Bzw2 |
G |
A |
12: 36,180,054 (GRCm39) |
R58* |
probably null |
Het |
C7 |
G |
T |
15: 5,023,725 (GRCm39) |
S694R |
probably benign |
Het |
Cbr2 |
T |
A |
11: 120,621,087 (GRCm39) |
H170L |
probably benign |
Het |
Cdcp3 |
G |
A |
7: 130,837,641 (GRCm39) |
W512* |
probably null |
Het |
Cgas |
C |
A |
9: 78,340,315 (GRCm39) |
K472N |
probably benign |
Het |
Ckap2l |
T |
C |
2: 129,126,975 (GRCm39) |
N401S |
probably benign |
Het |
Cldn1 |
A |
G |
16: 26,190,346 (GRCm39) |
F11L |
probably benign |
Het |
Cmtr1 |
A |
G |
17: 29,895,174 (GRCm39) |
T118A |
probably benign |
Het |
Cog6 |
T |
C |
3: 52,890,610 (GRCm39) |
E610G |
probably benign |
Het |
Col3a1 |
G |
T |
1: 45,371,301 (GRCm39) |
A451S |
probably null |
Het |
Cr1l |
T |
A |
1: 194,799,878 (GRCm39) |
R265S |
probably benign |
Het |
Dapk1 |
T |
C |
13: 60,902,024 (GRCm39) |
I951T |
probably benign |
Het |
Dnah9 |
T |
C |
11: 66,009,770 (GRCm39) |
N706D |
probably benign |
Het |
Dpysl5 |
A |
T |
5: 30,940,539 (GRCm39) |
T239S |
probably benign |
Het |
Ect2l |
T |
A |
10: 18,004,894 (GRCm39) |
Y913F |
probably benign |
Het |
Elf5 |
C |
A |
2: 103,269,641 (GRCm39) |
A74D |
possibly damaging |
Het |
Erap1 |
T |
C |
13: 74,814,258 (GRCm39) |
V399A |
probably benign |
Het |
Ercc4 |
A |
G |
16: 12,965,657 (GRCm39) |
D763G |
probably damaging |
Het |
Fam222b |
T |
A |
11: 78,045,683 (GRCm39) |
C415S |
possibly damaging |
Het |
Fat4 |
A |
C |
3: 39,031,511 (GRCm39) |
N2432T |
probably damaging |
Het |
Fbn2 |
G |
T |
18: 58,186,833 (GRCm39) |
C1689* |
probably null |
Het |
Frrs1l |
T |
A |
4: 56,972,282 (GRCm39) |
T140S |
probably damaging |
Het |
Gm5141 |
A |
T |
13: 62,924,877 (GRCm39) |
H10Q |
possibly damaging |
Het |
Inafm1 |
A |
T |
7: 16,007,079 (GRCm39) |
L46Q |
probably damaging |
Het |
Irak2 |
T |
C |
6: 113,650,045 (GRCm39) |
L260P |
probably damaging |
Het |
Kat2b |
T |
C |
17: 53,977,706 (GRCm39) |
L751P |
probably damaging |
Het |
Kcnh1 |
T |
A |
1: 192,019,913 (GRCm39) |
I413N |
probably benign |
Het |
Kirrel1 |
T |
C |
3: 86,990,695 (GRCm39) |
D709G |
probably benign |
Het |
Lama4 |
T |
C |
10: 38,956,536 (GRCm39) |
V1153A |
possibly damaging |
Het |
Lipg |
A |
T |
18: 75,088,655 (GRCm39) |
F98L |
probably benign |
Het |
Lman1 |
T |
C |
18: 66,127,936 (GRCm39) |
E236G |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,409,325 (GRCm39) |
D1598V |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,650,384 (GRCm39) |
N230Y |
probably damaging |
Het |
Maneal |
T |
C |
4: 124,750,983 (GRCm39) |
S258G |
possibly damaging |
Het |
Marchf10 |
T |
A |
11: 105,281,532 (GRCm39) |
E251V |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,215,570 (GRCm39) |
I1484T |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,647,534 (GRCm39) |
N1882I |
probably benign |
Het |
Neb |
G |
A |
2: 52,110,212 (GRCm39) |
A212V |
probably benign |
Het |
Obscn |
G |
A |
11: 58,903,672 (GRCm39) |
S7434L |
probably benign |
Het |
Or14j8 |
A |
C |
17: 38,263,048 (GRCm39) |
I289S |
probably damaging |
Het |
Or1ad8 |
T |
A |
11: 50,898,223 (GRCm39) |
C141* |
probably null |
Het |
Or1j12 |
A |
T |
2: 36,342,872 (GRCm39) |
I92F |
probably damaging |
Het |
Or4k47 |
T |
C |
2: 111,451,538 (GRCm39) |
M294V |
probably benign |
Het |
Or8g2b |
A |
G |
9: 39,750,753 (GRCm39) |
M8V |
probably benign |
Het |
Orc6 |
T |
C |
8: 86,029,590 (GRCm39) |
|
probably null |
Het |
Otogl |
T |
G |
10: 107,710,394 (GRCm39) |
E565A |
possibly damaging |
Het |
Papss1 |
A |
G |
3: 131,290,899 (GRCm39) |
Q214R |
probably benign |
Het |
Pck2 |
G |
A |
14: 55,786,169 (GRCm39) |
V653M |
probably benign |
Het |
Plxna4 |
G |
A |
6: 32,192,113 (GRCm39) |
Q826* |
probably null |
Het |
Pms1 |
T |
A |
1: 53,295,889 (GRCm39) |
T161S |
probably benign |
Het |
Prkar2a |
C |
A |
9: 108,617,669 (GRCm39) |
N242K |
probably damaging |
Het |
Prss1 |
T |
A |
6: 41,439,690 (GRCm39) |
I141N |
probably damaging |
Het |
Puf60 |
A |
G |
15: 75,943,717 (GRCm39) |
V235A |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,437,252 (GRCm39) |
F65Y |
probably benign |
Het |
Rasgef1b |
T |
C |
5: 99,447,898 (GRCm39) |
E104G |
unknown |
Het |
Rcn3 |
T |
C |
7: 44,734,333 (GRCm39) |
Y225C |
probably damaging |
Het |
Rhot1 |
G |
C |
11: 80,137,560 (GRCm39) |
W354S |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,417,513 (GRCm39) |
S1200G |
possibly damaging |
Het |
Scaper |
T |
A |
9: 55,745,460 (GRCm39) |
K603* |
probably null |
Het |
Selenbp1 |
G |
A |
3: 94,851,745 (GRCm39) |
V429I |
possibly damaging |
Het |
Shank1 |
T |
C |
7: 44,002,564 (GRCm39) |
Y1428H |
possibly damaging |
Het |
Slc11a1 |
G |
T |
1: 74,422,830 (GRCm39) |
W361L |
possibly damaging |
Het |
Spta1 |
A |
T |
1: 174,050,837 (GRCm39) |
D1772V |
possibly damaging |
Het |
St8sia6 |
T |
C |
2: 13,661,721 (GRCm39) |
H370R |
probably damaging |
Het |
Stkld1 |
A |
T |
2: 26,842,726 (GRCm39) |
D566V |
probably damaging |
Het |
Tango6 |
T |
C |
8: 107,415,791 (GRCm39) |
V204A |
probably benign |
Het |
Tdrd5 |
G |
A |
1: 156,129,293 (GRCm39) |
A139V |
probably damaging |
Het |
Tenm2 |
A |
T |
11: 36,062,263 (GRCm39) |
V534E |
probably damaging |
Het |
Tfip11 |
A |
T |
5: 112,479,044 (GRCm39) |
Q204L |
probably benign |
Het |
Tlr4 |
A |
T |
4: 66,759,430 (GRCm39) |
Q741L |
probably damaging |
Het |
Tmem18 |
A |
G |
12: 30,638,654 (GRCm39) |
M111V |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,042,292 (GRCm39) |
N1167S |
probably benign |
Het |
Trappc3 |
C |
T |
4: 126,168,945 (GRCm39) |
A145V |
possibly damaging |
Het |
Trbj2-3 |
T |
C |
6: 41,520,176 (GRCm39) |
F7S |
probably damaging |
Het |
Vinac1 |
A |
G |
2: 128,880,238 (GRCm39) |
S563P |
|
Het |
Vmn1r212 |
T |
A |
13: 23,067,731 (GRCm39) |
M201L |
probably benign |
Het |
Xaf1 |
C |
A |
11: 72,194,201 (GRCm39) |
C27* |
probably null |
Het |
Zeb1 |
T |
C |
18: 5,767,703 (GRCm39) |
V738A |
probably benign |
Het |
Zfp524 |
A |
T |
7: 5,020,883 (GRCm39) |
H137L |
probably damaging |
Het |
Zfyve19 |
A |
T |
2: 119,047,118 (GRCm39) |
H367L |
probably damaging |
Het |
Zim1 |
G |
A |
7: 6,680,872 (GRCm39) |
Q264* |
probably null |
Het |
|
Other mutations in Setd5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00816:Setd5
|
APN |
6 |
113,088,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02102:Setd5
|
APN |
6 |
113,127,946 (GRCm39) |
nonsense |
probably null |
|
IGL02105:Setd5
|
APN |
6 |
113,094,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02202:Setd5
|
APN |
6 |
113,127,976 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02221:Setd5
|
APN |
6 |
113,098,131 (GRCm39) |
splice site |
probably benign |
|
IGL02382:Setd5
|
APN |
6 |
113,120,601 (GRCm39) |
missense |
probably benign |
|
IGL02394:Setd5
|
APN |
6 |
113,087,859 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02442:Setd5
|
APN |
6 |
113,087,341 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02480:Setd5
|
APN |
6 |
113,120,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02940:Setd5
|
APN |
6 |
113,091,899 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0320:Setd5
|
UTSW |
6 |
113,088,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R0479:Setd5
|
UTSW |
6 |
113,091,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Setd5
|
UTSW |
6 |
113,096,398 (GRCm39) |
nonsense |
probably null |
|
R1528:Setd5
|
UTSW |
6 |
113,098,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R1530:Setd5
|
UTSW |
6 |
113,086,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2176:Setd5
|
UTSW |
6 |
113,128,114 (GRCm39) |
missense |
probably benign |
0.23 |
R2191:Setd5
|
UTSW |
6 |
113,088,390 (GRCm39) |
nonsense |
probably null |
|
R2286:Setd5
|
UTSW |
6 |
113,096,571 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4163:Setd5
|
UTSW |
6 |
113,096,545 (GRCm39) |
missense |
probably benign |
|
R4294:Setd5
|
UTSW |
6 |
113,088,281 (GRCm39) |
intron |
probably benign |
|
R4300:Setd5
|
UTSW |
6 |
113,127,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Setd5
|
UTSW |
6 |
113,088,281 (GRCm39) |
intron |
probably benign |
|
R4370:Setd5
|
UTSW |
6 |
113,098,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:Setd5
|
UTSW |
6 |
113,128,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Setd5
|
UTSW |
6 |
113,126,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Setd5
|
UTSW |
6 |
113,114,922 (GRCm39) |
missense |
probably damaging |
0.96 |
R5345:Setd5
|
UTSW |
6 |
113,092,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Setd5
|
UTSW |
6 |
113,098,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5556:Setd5
|
UTSW |
6 |
113,124,463 (GRCm39) |
missense |
probably benign |
0.00 |
R5582:Setd5
|
UTSW |
6 |
113,091,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R5838:Setd5
|
UTSW |
6 |
113,096,396 (GRCm39) |
missense |
probably benign |
0.40 |
R5941:Setd5
|
UTSW |
6 |
113,105,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Setd5
|
UTSW |
6 |
113,087,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R6146:Setd5
|
UTSW |
6 |
113,098,773 (GRCm39) |
critical splice donor site |
probably null |
|
R6394:Setd5
|
UTSW |
6 |
113,092,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R6694:Setd5
|
UTSW |
6 |
113,120,669 (GRCm39) |
missense |
probably benign |
|
R7058:Setd5
|
UTSW |
6 |
113,092,532 (GRCm39) |
missense |
probably benign |
0.16 |
R7060:Setd5
|
UTSW |
6 |
113,094,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:Setd5
|
UTSW |
6 |
113,098,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Setd5
|
UTSW |
6 |
113,124,518 (GRCm39) |
missense |
probably benign |
0.21 |
R7438:Setd5
|
UTSW |
6 |
113,092,043 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7515:Setd5
|
UTSW |
6 |
113,087,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7621:Setd5
|
UTSW |
6 |
113,121,010 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7652:Setd5
|
UTSW |
6 |
113,098,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Setd5
|
UTSW |
6 |
113,105,418 (GRCm39) |
missense |
probably benign |
0.00 |
R8083:Setd5
|
UTSW |
6 |
113,091,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8175:Setd5
|
UTSW |
6 |
113,091,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8252:Setd5
|
UTSW |
6 |
113,127,916 (GRCm39) |
missense |
probably benign |
0.01 |
R8268:Setd5
|
UTSW |
6 |
113,126,651 (GRCm39) |
critical splice donor site |
probably null |
|
R8271:Setd5
|
UTSW |
6 |
113,092,031 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8424:Setd5
|
UTSW |
6 |
113,126,644 (GRCm39) |
missense |
probably benign |
0.12 |
R8508:Setd5
|
UTSW |
6 |
113,098,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R8801:Setd5
|
UTSW |
6 |
113,127,853 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8864:Setd5
|
UTSW |
6 |
113,088,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Setd5
|
UTSW |
6 |
113,098,755 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9522:Setd5
|
UTSW |
6 |
113,091,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Setd5
|
UTSW |
6 |
113,121,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Setd5
|
UTSW |
6 |
113,128,366 (GRCm39) |
missense |
probably benign |
0.13 |
R9711:Setd5
|
UTSW |
6 |
113,093,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Setd5
|
UTSW |
6 |
113,128,366 (GRCm39) |
missense |
probably benign |
0.13 |
X0017:Setd5
|
UTSW |
6 |
113,127,129 (GRCm39) |
missense |
probably null |
1.00 |
Z1176:Setd5
|
UTSW |
6 |
113,115,057 (GRCm39) |
missense |
probably benign |
|
Z1191:Setd5
|
UTSW |
6 |
113,091,957 (GRCm39) |
missense |
probably benign |
0.04 |
|