Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
A |
G |
5: 8,773,187 (GRCm39) |
N805S |
probably damaging |
Het |
Acat2 |
A |
G |
17: 13,178,893 (GRCm39) |
V60A |
probably benign |
Het |
Adam6b |
A |
G |
12: 113,454,754 (GRCm39) |
I524V |
probably benign |
Het |
Adamts16 |
C |
T |
13: 70,921,074 (GRCm39) |
W590* |
probably null |
Het |
Adamts9 |
C |
T |
6: 92,835,102 (GRCm39) |
G1257D |
probably damaging |
Het |
Adgrf5 |
C |
T |
17: 43,755,974 (GRCm39) |
T644I |
probably benign |
Het |
Adgrf5 |
T |
G |
17: 43,763,368 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,668,634 (GRCm39) |
T2641A |
possibly damaging |
Het |
Agap3 |
T |
C |
5: 24,657,382 (GRCm39) |
F60L |
probably benign |
Het |
Akap9 |
C |
A |
5: 4,054,933 (GRCm39) |
T1626K |
probably damaging |
Het |
Ampd3 |
C |
A |
7: 110,405,261 (GRCm39) |
D603E |
probably damaging |
Het |
Angpt4 |
T |
A |
2: 151,767,326 (GRCm39) |
V119E |
probably benign |
Het |
Atp6v1a |
T |
C |
16: 43,934,980 (GRCm39) |
T70A |
probably benign |
Het |
Borcs5 |
C |
T |
6: 134,687,143 (GRCm39) |
T167M |
probably damaging |
Het |
Btbd19 |
T |
A |
4: 116,978,616 (GRCm39) |
S156C |
probably damaging |
Het |
Camkk2 |
C |
T |
5: 122,875,574 (GRCm39) |
R492Q |
possibly damaging |
Het |
Casr |
T |
C |
16: 36,330,033 (GRCm39) |
I434V |
probably damaging |
Het |
Cd4 |
G |
T |
6: 124,844,066 (GRCm39) |
T394K |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,237,517 (GRCm39) |
L1006P |
probably damaging |
Het |
Crx |
G |
A |
7: 15,601,857 (GRCm39) |
P274S |
probably damaging |
Het |
Crybg1 |
T |
A |
10: 43,865,107 (GRCm39) |
I1457F |
probably damaging |
Het |
Cul4a |
C |
A |
8: 13,171,676 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
T |
A |
2: 104,085,910 (GRCm39) |
T196S |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,580,567 (GRCm39) |
E1995G |
probably benign |
Het |
Dnm1 |
T |
A |
2: 32,226,021 (GRCm39) |
T353S |
probably damaging |
Het |
Ect2l |
T |
A |
10: 18,044,149 (GRCm39) |
T329S |
probably damaging |
Het |
Elp2 |
T |
A |
18: 24,742,716 (GRCm39) |
S83T |
probably benign |
Het |
Exosc7 |
A |
G |
9: 122,948,013 (GRCm39) |
T39A |
probably benign |
Het |
Fam135a |
C |
A |
1: 24,096,473 (GRCm39) |
V91F |
probably damaging |
Het |
Gab2 |
G |
T |
7: 96,731,005 (GRCm39) |
|
probably benign |
Het |
Gbf1 |
A |
T |
19: 46,268,793 (GRCm39) |
I1408F |
possibly damaging |
Het |
Glis3 |
C |
T |
19: 28,508,419 (GRCm39) |
E522K |
probably damaging |
Het |
Gm10375 |
A |
T |
14: 43,842,314 (GRCm39) |
C139S |
possibly damaging |
Het |
Gm26558 |
T |
C |
2: 70,492,211 (GRCm39) |
E81G |
unknown |
Het |
Gm35315 |
C |
T |
5: 110,227,091 (GRCm39) |
C116Y |
probably benign |
Het |
Gm3676 |
T |
A |
14: 41,366,064 (GRCm39) |
I84F |
probably damaging |
Het |
Gm7145 |
T |
A |
1: 117,913,932 (GRCm39) |
H271Q |
probably damaging |
Het |
Gpat2 |
T |
A |
2: 127,270,215 (GRCm39) |
I76N |
probably damaging |
Het |
Hipk1 |
A |
T |
3: 103,685,574 (GRCm39) |
S14T |
unknown |
Het |
Hlcs |
C |
A |
16: 94,068,362 (GRCm39) |
S286I |
probably damaging |
Het |
Ighg1 |
A |
T |
12: 113,293,078 (GRCm39) |
F204Y |
|
Het |
Igsf10 |
T |
C |
3: 59,236,837 (GRCm39) |
I1115V |
probably benign |
Het |
Klk7 |
A |
T |
7: 43,462,299 (GRCm39) |
H97L |
probably damaging |
Het |
Kmt2d |
A |
T |
15: 98,754,504 (GRCm39) |
D1605E |
unknown |
Het |
Leng8 |
T |
A |
7: 4,142,525 (GRCm39) |
I49N |
possibly damaging |
Het |
Lingo4 |
A |
T |
3: 94,310,451 (GRCm39) |
D463V |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,389,337 (GRCm39) |
N3193I |
probably damaging |
Het |
Lrrc7 |
T |
A |
3: 157,866,111 (GRCm39) |
Y1210F |
probably damaging |
Het |
Mki67 |
G |
C |
7: 135,296,400 (GRCm39) |
A2878G |
probably benign |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mtcl3 |
T |
A |
10: 29,072,875 (GRCm39) |
Y722* |
probably null |
Het |
Mucl2 |
C |
T |
15: 103,929,445 (GRCm39) |
|
probably null |
Het |
Myh6 |
A |
T |
14: 55,197,727 (GRCm39) |
D470E |
probably benign |
Het |
Myo1e |
T |
C |
9: 70,266,667 (GRCm39) |
|
probably null |
Het |
Myo7a |
G |
A |
7: 97,713,402 (GRCm39) |
R1647W |
probably damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nmral1 |
C |
T |
16: 4,531,660 (GRCm39) |
M198I |
probably benign |
Het |
Nrap |
C |
A |
19: 56,330,700 (GRCm39) |
L1120F |
probably damaging |
Het |
Nup155 |
T |
A |
15: 8,184,406 (GRCm39) |
I1267N |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,898,414 (GRCm39) |
P6616S |
unknown |
Het |
Ocstamp |
T |
G |
2: 165,239,229 (GRCm39) |
D319A |
probably damaging |
Het |
Ooep |
T |
C |
9: 78,285,433 (GRCm39) |
D61G |
probably damaging |
Het |
Or10p1 |
A |
G |
10: 129,443,949 (GRCm39) |
S134P |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,493,810 (GRCm39) |
I135F |
probably damaging |
Het |
Or52ad1 |
A |
G |
7: 102,995,538 (GRCm39) |
V199A |
probably benign |
Het |
Or6c5c |
T |
C |
10: 129,298,856 (GRCm39) |
S104P |
probably damaging |
Het |
Or7g35 |
A |
G |
9: 19,495,938 (GRCm39) |
Y35C |
probably damaging |
Het |
Otoa |
A |
G |
7: 120,701,765 (GRCm39) |
E148G |
probably benign |
Het |
Ovgp1 |
A |
T |
3: 105,894,387 (GRCm39) |
D720V |
unknown |
Het |
Padi2 |
T |
A |
4: 140,660,079 (GRCm39) |
F294I |
probably damaging |
Het |
Pcdha7 |
T |
A |
18: 37,107,471 (GRCm39) |
N165K |
probably damaging |
Het |
Pcdhb6 |
C |
A |
18: 37,468,261 (GRCm39) |
P394H |
probably damaging |
Het |
Pcdhga6 |
T |
C |
18: 37,841,072 (GRCm39) |
V264A |
possibly damaging |
Het |
Pik3ap1 |
G |
T |
19: 41,284,815 (GRCm39) |
D623E |
possibly damaging |
Het |
Prdm10 |
A |
T |
9: 31,268,456 (GRCm39) |
K802* |
probably null |
Het |
Ptgfrn |
G |
A |
3: 100,980,363 (GRCm39) |
L326F |
possibly damaging |
Het |
Rgsl1 |
T |
G |
1: 153,683,622 (GRCm39) |
|
probably null |
Het |
Rock1 |
T |
G |
18: 10,129,317 (GRCm39) |
T347P |
possibly damaging |
Het |
Rprd2 |
G |
A |
3: 95,684,022 (GRCm39) |
P338S |
probably damaging |
Het |
Sdk1 |
A |
T |
5: 141,923,377 (GRCm39) |
N333Y |
probably damaging |
Het |
Setd4 |
T |
A |
16: 93,388,132 (GRCm39) |
H118L |
probably benign |
Het |
Sirt3 |
G |
A |
7: 140,458,039 (GRCm39) |
P37S |
|
Het |
Slc16a9 |
G |
T |
10: 70,119,000 (GRCm39) |
G440W |
probably damaging |
Het |
Slc22a23 |
T |
A |
13: 34,367,161 (GRCm39) |
I616F |
probably damaging |
Het |
Slc30a8 |
A |
C |
15: 52,180,707 (GRCm39) |
D102A |
probably damaging |
Het |
Slc6a4 |
T |
A |
11: 76,901,527 (GRCm39) |
D87E |
possibly damaging |
Het |
Slc9a4 |
A |
C |
1: 40,668,663 (GRCm39) |
T769P |
probably benign |
Het |
Sspo |
A |
T |
6: 48,431,762 (GRCm39) |
Y685F |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,450,390 (GRCm39) |
Q2560K |
probably benign |
Het |
Stpg1 |
T |
A |
4: 135,256,827 (GRCm39) |
L206Q |
probably damaging |
Het |
Stt3b |
A |
T |
9: 115,095,183 (GRCm39) |
Y283N |
probably damaging |
Het |
Sult4a1 |
T |
C |
15: 83,970,814 (GRCm39) |
E197G |
probably damaging |
Het |
Syne1 |
T |
G |
10: 4,997,635 (GRCm39) |
D444A |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,064,845 (GRCm39) |
V1425E |
possibly damaging |
Het |
Tgm4 |
A |
G |
9: 122,891,556 (GRCm39) |
D557G |
probably benign |
Het |
Tmcc3 |
A |
G |
10: 94,266,434 (GRCm39) |
|
probably benign |
Het |
Tnfrsf8 |
T |
A |
4: 145,000,952 (GRCm39) |
N385Y |
probably benign |
Het |
Ttc4 |
T |
C |
4: 106,536,017 (GRCm39) |
D15G |
possibly damaging |
Het |
Tut1 |
A |
G |
19: 8,941,413 (GRCm39) |
N400S |
probably benign |
Het |
Usp39 |
T |
C |
6: 72,313,413 (GRCm39) |
K259R |
probably benign |
Het |
Vmn1r215 |
C |
T |
13: 23,260,484 (GRCm39) |
H175Y |
probably benign |
Het |
Vmn1r36 |
A |
T |
6: 66,693,107 (GRCm39) |
M256K |
probably benign |
Het |
Zfp128 |
T |
A |
7: 12,624,461 (GRCm39) |
H276Q |
possibly damaging |
Het |
Zfp276 |
T |
C |
8: 123,994,562 (GRCm39) |
M543T |
probably damaging |
Het |
Zfp354c |
A |
T |
11: 50,705,483 (GRCm39) |
Y531N |
probably damaging |
Het |
Zfp532 |
T |
A |
18: 65,756,076 (GRCm39) |
M3K |
probably damaging |
Het |
Zfp64 |
T |
G |
2: 168,741,810 (GRCm39) |
K373Q |
probably damaging |
Het |
Zfp764l1 |
C |
T |
7: 126,990,856 (GRCm39) |
S377N |
probably benign |
Het |
Zfp983 |
T |
G |
17: 21,880,413 (GRCm39) |
S114A |
probably damaging |
Het |
Zranb1 |
G |
A |
7: 132,584,481 (GRCm39) |
R583K |
probably damaging |
Het |
|
Other mutations in B4galt3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02019:B4galt3
|
APN |
1 |
171,099,362 (GRCm39) |
missense |
probably damaging |
1.00 |
BB004:B4galt3
|
UTSW |
1 |
171,099,342 (GRCm39) |
nonsense |
probably null |
|
BB014:B4galt3
|
UTSW |
1 |
171,099,342 (GRCm39) |
nonsense |
probably null |
|
R0026:B4galt3
|
UTSW |
1 |
171,101,831 (GRCm39) |
unclassified |
probably benign |
|
R0126:B4galt3
|
UTSW |
1 |
171,103,738 (GRCm39) |
missense |
probably damaging |
0.97 |
R0537:B4galt3
|
UTSW |
1 |
171,101,821 (GRCm39) |
unclassified |
probably benign |
|
R1478:B4galt3
|
UTSW |
1 |
171,103,938 (GRCm39) |
missense |
probably benign |
0.11 |
R2012:B4galt3
|
UTSW |
1 |
171,100,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2207:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2353:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2354:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2438:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2439:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3039:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3051:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3709:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3710:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3741:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3742:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3813:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4058:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4059:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4323:B4galt3
|
UTSW |
1 |
171,103,515 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4367:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4368:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4370:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4371:B4galt3
|
UTSW |
1 |
171,101,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4486:B4galt3
|
UTSW |
1 |
171,099,343 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4538:B4galt3
|
UTSW |
1 |
171,100,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R5557:B4galt3
|
UTSW |
1 |
171,100,089 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7927:B4galt3
|
UTSW |
1 |
171,099,342 (GRCm39) |
nonsense |
probably null |
|
R8222:B4galt3
|
UTSW |
1 |
171,100,253 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8552:B4galt3
|
UTSW |
1 |
171,101,917 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8804:B4galt3
|
UTSW |
1 |
171,103,947 (GRCm39) |
missense |
probably benign |
0.33 |
R8859:B4galt3
|
UTSW |
1 |
171,099,241 (GRCm39) |
missense |
unknown |
|
R9150:B4galt3
|
UTSW |
1 |
171,103,899 (GRCm39) |
missense |
probably benign |
|
R9265:B4galt3
|
UTSW |
1 |
171,101,617 (GRCm39) |
missense |
probably damaging |
1.00 |
|