Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
T |
2: 69,113,014 (GRCm39) |
|
probably null |
Het |
Abcc8 |
T |
G |
7: 45,806,543 (GRCm39) |
R388S |
probably benign |
Het |
Abhd18 |
C |
T |
3: 40,889,361 (GRCm39) |
R414* |
probably null |
Het |
Acap1 |
C |
T |
11: 69,780,324 (GRCm39) |
V40I |
probably benign |
Het |
Actn1 |
C |
A |
12: 80,251,745 (GRCm39) |
G111* |
probably null |
Het |
Adamts19 |
T |
C |
18: 59,105,903 (GRCm39) |
|
probably null |
Het |
Agtpbp1 |
T |
G |
13: 59,678,872 (GRCm39) |
K145N |
probably damaging |
Het |
AI661453 |
A |
G |
17: 47,777,959 (GRCm39) |
|
probably benign |
Het |
Ap4e1 |
T |
C |
2: 126,903,467 (GRCm39) |
S790P |
probably benign |
Het |
Asmt |
A |
G |
X: 169,109,524 (GRCm39) |
E168G |
possibly damaging |
Het |
Atp2a3 |
T |
A |
11: 72,866,240 (GRCm39) |
S287T |
probably damaging |
Het |
AY358078 |
T |
A |
14: 52,063,519 (GRCm39) |
D388E |
probably damaging |
Het |
Bicd1 |
A |
T |
6: 149,415,050 (GRCm39) |
T588S |
probably benign |
Het |
Birc6 |
T |
G |
17: 74,905,057 (GRCm39) |
N1283K |
probably benign |
Het |
Cacna1e |
T |
A |
1: 154,353,563 (GRCm39) |
Q423L |
probably damaging |
Het |
Capn3 |
T |
A |
2: 120,326,418 (GRCm39) |
Y537N |
probably damaging |
Het |
Ccn3 |
T |
A |
15: 54,612,750 (GRCm39) |
V253E |
probably benign |
Het |
Cep295 |
C |
T |
9: 15,252,179 (GRCm39) |
E397K |
probably damaging |
Het |
Chgb |
T |
C |
2: 132,628,418 (GRCm39) |
S48P |
possibly damaging |
Het |
Cidec |
T |
A |
6: 113,405,193 (GRCm39) |
Y159F |
probably damaging |
Het |
Clec18a |
T |
C |
8: 111,808,234 (GRCm39) |
S66G |
possibly damaging |
Het |
Cpsf1 |
G |
A |
15: 76,487,360 (GRCm39) |
T138M |
probably benign |
Het |
Dclre1c |
C |
T |
2: 3,439,022 (GRCm39) |
R61W |
probably damaging |
Het |
Eef1akmt1 |
A |
C |
14: 57,787,911 (GRCm39) |
V149G |
probably benign |
Het |
Fam131b |
T |
C |
6: 42,297,818 (GRCm39) |
T112A |
possibly damaging |
Het |
Fbln2 |
A |
G |
6: 91,211,283 (GRCm39) |
E409G |
probably damaging |
Het |
Fkbp15 |
G |
A |
4: 62,222,618 (GRCm39) |
P1094S |
probably benign |
Het |
Fpr1 |
A |
G |
17: 18,097,879 (GRCm39) |
S37P |
probably benign |
Het |
Fryl |
G |
T |
5: 73,265,836 (GRCm39) |
T495K |
probably damaging |
Het |
Gja6 |
A |
T |
X: 159,686,374 (GRCm39) |
I186N |
possibly damaging |
Het |
Gm4922 |
T |
C |
10: 18,659,388 (GRCm39) |
T445A |
probably benign |
Het |
Gria2 |
G |
A |
3: 80,709,664 (GRCm39) |
L10F |
probably benign |
Het |
Gspt2 |
A |
G |
X: 93,681,025 (GRCm39) |
D388G |
possibly damaging |
Het |
Hdc |
T |
A |
2: 126,458,107 (GRCm39) |
I72F |
probably damaging |
Het |
Ift70b |
A |
G |
2: 75,768,402 (GRCm39) |
L117P |
probably damaging |
Het |
Igf2r |
T |
C |
17: 12,911,625 (GRCm39) |
K1905E |
probably benign |
Het |
Il33 |
A |
G |
19: 29,934,304 (GRCm39) |
D155G |
possibly damaging |
Het |
Klk1b9 |
C |
T |
7: 43,628,979 (GRCm39) |
T161I |
probably benign |
Het |
Mfsd12 |
C |
A |
10: 81,193,515 (GRCm39) |
H28Q |
probably damaging |
Het |
Mgat5 |
A |
T |
1: 127,387,696 (GRCm39) |
I551F |
possibly damaging |
Het |
Miga2 |
A |
T |
2: 30,272,000 (GRCm39) |
D25V |
probably damaging |
Het |
Mlc1 |
T |
C |
15: 88,858,782 (GRCm39) |
N122S |
possibly damaging |
Het |
Mmp20 |
T |
A |
9: 7,645,293 (GRCm39) |
M281K |
probably benign |
Het |
Muc5ac |
C |
A |
7: 141,366,889 (GRCm39) |
P2232T |
possibly damaging |
Het |
N4bp2l2 |
A |
G |
5: 150,584,748 (GRCm39) |
S411P |
possibly damaging |
Het |
Ngef |
G |
A |
1: 87,415,626 (GRCm39) |
S346L |
probably damaging |
Het |
Or10j27 |
C |
T |
1: 172,958,418 (GRCm39) |
R122H |
possibly damaging |
Het |
Or2t6 |
A |
G |
14: 14,175,854 (GRCm38) |
I76T |
probably benign |
Het |
Or4c112 |
T |
A |
2: 88,853,487 (GRCm39) |
T287S |
probably damaging |
Het |
Or4f15 |
T |
A |
2: 111,814,429 (GRCm39) |
M5L |
probably benign |
Het |
Or51aa2 |
T |
C |
7: 103,187,566 (GRCm39) |
I292V |
possibly damaging |
Het |
Or52m2 |
C |
T |
7: 102,263,747 (GRCm39) |
V150M |
probably damaging |
Het |
Or56b2 |
T |
C |
7: 104,337,690 (GRCm39) |
I156T |
probably benign |
Het |
Or6c215 |
T |
C |
10: 129,637,530 (GRCm39) |
Y288C |
probably damaging |
Het |
Or6c6 |
T |
A |
10: 129,186,561 (GRCm39) |
I43N |
probably damaging |
Het |
Pecam1 |
G |
T |
11: 106,586,763 (GRCm39) |
H150N |
possibly damaging |
Het |
Polr3c |
A |
T |
3: 96,621,689 (GRCm39) |
|
probably null |
Het |
Pop1 |
A |
C |
15: 34,530,617 (GRCm39) |
Q1005P |
probably damaging |
Het |
Prss22 |
G |
A |
17: 24,215,288 (GRCm39) |
P163S |
probably damaging |
Het |
Prss33 |
G |
A |
17: 24,053,172 (GRCm39) |
A223V |
probably damaging |
Het |
Prss53 |
C |
T |
7: 127,486,565 (GRCm39) |
V354I |
probably benign |
Het |
Rab3gap2 |
C |
T |
1: 184,968,221 (GRCm39) |
T191I |
probably damaging |
Het |
Rictor |
T |
C |
15: 6,805,637 (GRCm39) |
F608L |
probably benign |
Het |
Ryr3 |
T |
A |
2: 112,484,837 (GRCm39) |
E3884V |
probably null |
Het |
Scaf11 |
G |
A |
15: 96,316,721 (GRCm39) |
R948* |
probably null |
Het |
Sec61g |
A |
T |
11: 16,456,444 (GRCm39) |
V40E |
probably damaging |
Het |
Serpinb3d |
A |
T |
1: 107,008,518 (GRCm39) |
F116I |
possibly damaging |
Het |
Sipa1l3 |
T |
C |
7: 29,099,036 (GRCm39) |
D411G |
probably benign |
Het |
Slc13a3 |
T |
C |
2: 165,275,984 (GRCm39) |
N254S |
possibly damaging |
Het |
Slc35a2 |
T |
A |
X: 7,759,064 (GRCm39) |
L110Q |
probably damaging |
Het |
Spata31d1b |
G |
C |
13: 59,864,194 (GRCm39) |
L447F |
probably benign |
Het |
Spsb2 |
T |
C |
6: 124,786,329 (GRCm39) |
|
probably null |
Het |
Tent4b |
C |
T |
8: 88,973,112 (GRCm39) |
T277M |
probably damaging |
Het |
Tmcc3 |
T |
C |
10: 94,414,468 (GRCm39) |
S57P |
possibly damaging |
Het |
Traf7 |
A |
G |
17: 24,729,476 (GRCm39) |
V445A |
probably damaging |
Het |
Trib1 |
A |
G |
15: 59,521,192 (GRCm39) |
S61G |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,726,893 (GRCm39) |
F36I |
probably damaging |
Het |
Tshz3 |
T |
C |
7: 36,469,247 (GRCm39) |
I412T |
probably damaging |
Het |
Tsku |
T |
C |
7: 98,001,353 (GRCm39) |
Y326C |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,712,038 (GRCm39) |
|
probably benign |
Het |
Ugt1a6a |
G |
A |
1: 88,066,470 (GRCm39) |
R92H |
probably benign |
Het |
Vmn1r63 |
A |
G |
7: 5,806,254 (GRCm39) |
V126A |
probably benign |
Het |
Vmn2r84 |
T |
A |
10: 130,221,878 (GRCm39) |
S781C |
probably damaging |
Het |
Wdr91 |
T |
A |
6: 34,869,297 (GRCm39) |
H409L |
probably damaging |
Het |
Wnt7a |
T |
A |
6: 91,342,938 (GRCm39) |
T315S |
possibly damaging |
Het |
Zdhhc25 |
A |
G |
15: 88,485,027 (GRCm39) |
T121A |
probably benign |
Het |
Zfp109 |
T |
C |
7: 23,928,743 (GRCm39) |
H222R |
probably benign |
Het |
Zfp286 |
A |
G |
11: 62,670,646 (GRCm39) |
S476P |
probably damaging |
Het |
Zfp605 |
T |
C |
5: 110,275,418 (GRCm39) |
Y179H |
probably damaging |
Het |
Zfp955a |
T |
C |
17: 33,460,620 (GRCm39) |
H504R |
probably damaging |
Het |
Zswim2 |
T |
A |
2: 83,746,007 (GRCm39) |
N477I |
possibly damaging |
Het |
|
Other mutations in Adam26b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00703:Adam26b
|
APN |
8 |
43,973,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00806:Adam26b
|
APN |
8 |
43,974,379 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00984:Adam26b
|
APN |
8 |
43,973,410 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01081:Adam26b
|
APN |
8 |
43,972,975 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01783:Adam26b
|
APN |
8 |
43,974,798 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02021:Adam26b
|
APN |
8 |
43,972,909 (GRCm39) |
missense |
probably benign |
|
IGL02707:Adam26b
|
APN |
8 |
43,972,895 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03112:Adam26b
|
APN |
8 |
43,974,549 (GRCm39) |
missense |
probably benign |
|
R0195:Adam26b
|
UTSW |
8 |
43,973,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R0453:Adam26b
|
UTSW |
8 |
43,973,387 (GRCm39) |
missense |
probably benign |
0.00 |
R0562:Adam26b
|
UTSW |
8 |
43,973,408 (GRCm39) |
missense |
probably benign |
0.36 |
R0645:Adam26b
|
UTSW |
8 |
43,973,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Adam26b
|
UTSW |
8 |
43,973,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R1697:Adam26b
|
UTSW |
8 |
43,974,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R1739:Adam26b
|
UTSW |
8 |
43,974,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Adam26b
|
UTSW |
8 |
43,972,948 (GRCm39) |
missense |
probably benign |
0.00 |
R1767:Adam26b
|
UTSW |
8 |
43,972,948 (GRCm39) |
missense |
probably benign |
0.00 |
R3747:Adam26b
|
UTSW |
8 |
43,974,234 (GRCm39) |
missense |
probably benign |
0.07 |
R3748:Adam26b
|
UTSW |
8 |
43,974,234 (GRCm39) |
missense |
probably benign |
0.07 |
R3750:Adam26b
|
UTSW |
8 |
43,974,234 (GRCm39) |
missense |
probably benign |
0.07 |
R3771:Adam26b
|
UTSW |
8 |
43,973,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Adam26b
|
UTSW |
8 |
43,973,409 (GRCm39) |
missense |
probably benign |
0.09 |
R4652:Adam26b
|
UTSW |
8 |
43,974,375 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4790:Adam26b
|
UTSW |
8 |
43,973,764 (GRCm39) |
missense |
probably benign |
0.19 |
R4859:Adam26b
|
UTSW |
8 |
43,973,296 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5059:Adam26b
|
UTSW |
8 |
43,973,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5191:Adam26b
|
UTSW |
8 |
43,973,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R5540:Adam26b
|
UTSW |
8 |
43,974,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Adam26b
|
UTSW |
8 |
43,973,529 (GRCm39) |
missense |
probably benign |
0.00 |
R5886:Adam26b
|
UTSW |
8 |
43,973,310 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5935:Adam26b
|
UTSW |
8 |
43,974,335 (GRCm39) |
missense |
probably benign |
0.00 |
R5983:Adam26b
|
UTSW |
8 |
43,974,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R6544:Adam26b
|
UTSW |
8 |
43,974,818 (GRCm39) |
missense |
probably damaging |
0.98 |
R6610:Adam26b
|
UTSW |
8 |
43,974,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R6668:Adam26b
|
UTSW |
8 |
43,973,727 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6966:Adam26b
|
UTSW |
8 |
43,974,472 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7545:Adam26b
|
UTSW |
8 |
43,974,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R7596:Adam26b
|
UTSW |
8 |
43,973,237 (GRCm39) |
missense |
probably benign |
|
R7634:Adam26b
|
UTSW |
8 |
43,974,034 (GRCm39) |
missense |
probably benign |
|
R7657:Adam26b
|
UTSW |
8 |
43,974,579 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7692:Adam26b
|
UTSW |
8 |
43,973,832 (GRCm39) |
missense |
probably benign |
0.00 |
R7769:Adam26b
|
UTSW |
8 |
43,974,732 (GRCm39) |
missense |
probably benign |
0.00 |
R7912:Adam26b
|
UTSW |
8 |
43,973,245 (GRCm39) |
missense |
probably benign |
0.13 |
R7918:Adam26b
|
UTSW |
8 |
43,974,138 (GRCm39) |
missense |
probably benign |
0.14 |
R8286:Adam26b
|
UTSW |
8 |
43,972,998 (GRCm39) |
missense |
probably benign |
0.05 |
R8897:Adam26b
|
UTSW |
8 |
43,974,009 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8922:Adam26b
|
UTSW |
8 |
43,973,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R9075:Adam26b
|
UTSW |
8 |
43,973,405 (GRCm39) |
missense |
probably benign |
0.07 |
R9225:Adam26b
|
UTSW |
8 |
43,973,453 (GRCm39) |
nonsense |
probably null |
|
X0066:Adam26b
|
UTSW |
8 |
43,973,041 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1088:Adam26b
|
UTSW |
8 |
43,973,634 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Adam26b
|
UTSW |
8 |
43,974,459 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Adam26b
|
UTSW |
8 |
43,973,735 (GRCm39) |
missense |
probably benign |
0.24 |
|