Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
T |
16: 4,669,368 (GRCm39) |
T745S |
possibly damaging |
Het |
Abca12 |
T |
C |
1: 71,319,552 (GRCm39) |
I1777V |
probably benign |
Het |
Abhd6 |
T |
C |
14: 8,028,353 (GRCm38) |
L28P |
probably damaging |
Het |
Arfgef2 |
A |
G |
2: 166,736,577 (GRCm39) |
M1750V |
probably benign |
Het |
Atrn |
T |
C |
2: 130,817,908 (GRCm39) |
F821L |
probably benign |
Het |
Cbx3 |
A |
G |
6: 51,458,748 (GRCm39) |
E71G |
possibly damaging |
Het |
Ccdc14 |
G |
A |
16: 34,530,022 (GRCm39) |
A482T |
probably damaging |
Het |
Cdh15 |
G |
T |
8: 123,593,574 (GRCm39) |
A723S |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,736,054 (GRCm39) |
S488G |
probably damaging |
Het |
Ddx55 |
C |
A |
5: 124,694,883 (GRCm39) |
H104N |
possibly damaging |
Het |
Det1 |
G |
T |
7: 78,493,257 (GRCm39) |
T249N |
possibly damaging |
Het |
Disp3 |
A |
G |
4: 148,354,973 (GRCm39) |
S348P |
possibly damaging |
Het |
Dnah6 |
T |
G |
6: 73,137,896 (GRCm39) |
N936T |
probably damaging |
Het |
Dnajc11 |
A |
T |
4: 152,054,357 (GRCm39) |
N188Y |
probably damaging |
Het |
Etaa1 |
G |
A |
11: 17,897,559 (GRCm39) |
T186I |
possibly damaging |
Het |
Fhip1a |
T |
C |
3: 85,580,111 (GRCm39) |
D698G |
probably benign |
Het |
Ftl1-ps1 |
T |
A |
13: 74,555,138 (GRCm39) |
V139E |
probably benign |
Het |
Fzd10 |
A |
G |
5: 128,679,303 (GRCm39) |
K341R |
probably benign |
Het |
Galnt7 |
A |
G |
8: 57,985,739 (GRCm39) |
Y544H |
probably benign |
Het |
Gm21190 |
T |
A |
5: 15,730,814 (GRCm39) |
I181F |
possibly damaging |
Het |
Gm3604 |
T |
C |
13: 62,517,363 (GRCm39) |
N332D |
probably damaging |
Het |
Gm47996 |
G |
T |
1: 151,086,055 (GRCm39) |
E45D |
possibly damaging |
Het |
Gm5475 |
T |
A |
15: 100,321,893 (GRCm39) |
L14Q |
unknown |
Het |
Gmcl1 |
G |
T |
6: 86,698,408 (GRCm39) |
A163E |
probably damaging |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Gpr182 |
T |
C |
10: 127,586,783 (GRCm39) |
Y56C |
probably damaging |
Het |
Gxylt2 |
T |
A |
6: 100,710,188 (GRCm39) |
W110R |
probably damaging |
Het |
Hivep3 |
G |
T |
4: 119,952,632 (GRCm39) |
R316L |
possibly damaging |
Het |
Hnf1a |
T |
C |
5: 115,093,336 (GRCm39) |
T310A |
probably benign |
Het |
Igkv6-32 |
A |
G |
6: 70,051,547 (GRCm39) |
F8L |
probably benign |
Het |
Kcnq1 |
A |
G |
7: 142,916,389 (GRCm39) |
N550D |
probably damaging |
Het |
Lrrc40 |
T |
G |
3: 157,757,419 (GRCm39) |
Y249* |
probably null |
Het |
Lrrc43 |
T |
A |
5: 123,639,192 (GRCm39) |
M407K |
probably benign |
Het |
Map2k6 |
A |
C |
11: 110,373,411 (GRCm39) |
E21D |
probably benign |
Het |
Mcoln1 |
T |
A |
8: 3,558,740 (GRCm39) |
I246N |
possibly damaging |
Het |
Msantd5f6 |
A |
T |
4: 73,321,759 (GRCm39) |
V92E |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,079,536 (GRCm39) |
K998E |
probably damaging |
Het |
Myo1b |
C |
T |
1: 51,797,034 (GRCm39) |
|
probably null |
Het |
Numbl |
T |
A |
7: 26,980,461 (GRCm39) |
M481K |
possibly damaging |
Het |
Nxpe4 |
G |
T |
9: 48,307,852 (GRCm39) |
V319F |
probably benign |
Het |
Pam |
C |
A |
1: 97,813,357 (GRCm39) |
D358Y |
probably damaging |
Het |
Papola |
A |
G |
12: 105,775,836 (GRCm39) |
M251V |
probably damaging |
Het |
Pcnx1 |
C |
T |
12: 81,965,593 (GRCm39) |
R59* |
probably null |
Het |
Prelid2 |
A |
G |
18: 42,065,700 (GRCm39) |
S112P |
probably damaging |
Het |
Ptgfrn |
T |
C |
3: 100,963,753 (GRCm39) |
T620A |
probably benign |
Het |
Ptgfrn |
C |
T |
3: 100,980,257 (GRCm39) |
R361Q |
probably benign |
Het |
Pygm |
T |
A |
19: 6,436,072 (GRCm39) |
M148K |
probably damaging |
Het |
Ren1 |
T |
A |
1: 133,287,812 (GRCm39) |
I382N |
probably damaging |
Het |
Rev1 |
T |
C |
1: 38,114,097 (GRCm39) |
|
probably benign |
Het |
Sdsl |
T |
C |
5: 120,598,017 (GRCm39) |
K159E |
probably benign |
Het |
Serinc4 |
T |
C |
2: 121,285,434 (GRCm39) |
N203S |
possibly damaging |
Het |
Slc12a2 |
A |
G |
18: 58,012,423 (GRCm39) |
H182R |
probably benign |
Het |
Sned1 |
C |
A |
1: 93,202,387 (GRCm39) |
T677K |
possibly damaging |
Het |
Ston2 |
G |
A |
12: 91,710,460 (GRCm39) |
T3I |
probably damaging |
Het |
Tnf |
T |
C |
17: 35,420,072 (GRCm39) |
T77A |
probably benign |
Het |
Trav6-2 |
G |
A |
14: 52,905,126 (GRCm39) |
G49E |
probably benign |
Het |
Trav7-4 |
A |
T |
14: 53,699,140 (GRCm39) |
I96F |
probably damaging |
Het |
Trmu |
T |
A |
15: 85,766,921 (GRCm39) |
D43E |
probably benign |
Het |
Uggt1 |
T |
A |
1: 36,266,566 (GRCm39) |
Q136L |
probably damaging |
Het |
Ugt1a5 |
T |
A |
1: 88,094,304 (GRCm39) |
Y177* |
probably null |
Het |
Vmn1r126 |
T |
C |
7: 21,034,516 (GRCm39) |
R293G |
probably damaging |
Het |
Vmn2r89 |
A |
G |
14: 51,693,699 (GRCm39) |
I350V |
probably benign |
Het |
Vps11 |
A |
T |
9: 44,267,529 (GRCm39) |
L361Q |
probably damaging |
Het |
Zfp467 |
A |
G |
6: 48,420,366 (GRCm39) |
L5P |
possibly damaging |
Het |
Zfp652 |
A |
G |
11: 95,640,288 (GRCm39) |
H71R |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,820,082 (GRCm39) |
K994E |
probably benign |
Het |
|
Other mutations in Angpt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Angpt1
|
APN |
15 |
42,339,863 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02671:Angpt1
|
APN |
15 |
42,539,790 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02876:Angpt1
|
APN |
15 |
42,290,373 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03077:Angpt1
|
APN |
15 |
42,339,818 (GRCm39) |
nonsense |
probably null |
|
IGL03334:Angpt1
|
APN |
15 |
42,359,808 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0226:Angpt1
|
UTSW |
15 |
42,331,631 (GRCm39) |
missense |
probably benign |
0.01 |
R1774:Angpt1
|
UTSW |
15 |
42,387,012 (GRCm39) |
missense |
probably damaging |
0.99 |
R1800:Angpt1
|
UTSW |
15 |
42,375,800 (GRCm39) |
missense |
probably damaging |
0.96 |
R1967:Angpt1
|
UTSW |
15 |
42,301,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4093:Angpt1
|
UTSW |
15 |
42,386,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4477:Angpt1
|
UTSW |
15 |
42,331,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4629:Angpt1
|
UTSW |
15 |
42,301,796 (GRCm39) |
missense |
probably benign |
0.01 |
R4647:Angpt1
|
UTSW |
15 |
42,539,580 (GRCm39) |
missense |
probably benign |
0.02 |
R4648:Angpt1
|
UTSW |
15 |
42,539,580 (GRCm39) |
missense |
probably benign |
0.02 |
R4750:Angpt1
|
UTSW |
15 |
42,539,797 (GRCm39) |
missense |
probably benign |
0.00 |
R5222:Angpt1
|
UTSW |
15 |
42,539,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Angpt1
|
UTSW |
15 |
42,301,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5457:Angpt1
|
UTSW |
15 |
42,386,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5526:Angpt1
|
UTSW |
15 |
42,375,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R6154:Angpt1
|
UTSW |
15 |
42,387,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R6904:Angpt1
|
UTSW |
15 |
42,323,136 (GRCm39) |
missense |
probably benign |
0.00 |
R7009:Angpt1
|
UTSW |
15 |
42,386,991 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7101:Angpt1
|
UTSW |
15 |
42,386,965 (GRCm39) |
missense |
probably benign |
0.18 |
R7139:Angpt1
|
UTSW |
15 |
42,539,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7234:Angpt1
|
UTSW |
15 |
42,323,121 (GRCm39) |
missense |
probably benign |
0.25 |
R7830:Angpt1
|
UTSW |
15 |
42,539,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Angpt1
|
UTSW |
15 |
42,359,752 (GRCm39) |
missense |
probably benign |
0.00 |
R8073:Angpt1
|
UTSW |
15 |
42,301,699 (GRCm39) |
missense |
probably benign |
0.00 |
R8331:Angpt1
|
UTSW |
15 |
42,539,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R8391:Angpt1
|
UTSW |
15 |
42,375,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Angpt1
|
UTSW |
15 |
42,290,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8508:Angpt1
|
UTSW |
15 |
42,375,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R8787:Angpt1
|
UTSW |
15 |
42,375,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R9297:Angpt1
|
UTSW |
15 |
42,301,751 (GRCm39) |
missense |
probably benign |
|
R9318:Angpt1
|
UTSW |
15 |
42,301,751 (GRCm39) |
missense |
probably benign |
|
R9746:Angpt1
|
UTSW |
15 |
42,539,837 (GRCm39) |
missense |
probably benign |
|
|