Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
A |
G |
4: 148,031,075 (GRCm39) |
*635W |
probably null |
Het |
Arhgef26 |
T |
C |
3: 62,340,002 (GRCm39) |
S675P |
probably damaging |
Het |
Bltp1 |
T |
A |
3: 37,012,834 (GRCm39) |
|
probably null |
Het |
Camk2d |
A |
G |
3: 126,628,277 (GRCm39) |
N53S |
probably damaging |
Het |
Carns1 |
A |
T |
19: 4,215,782 (GRCm39) |
M800K |
possibly damaging |
Het |
Ces1f |
A |
T |
8: 93,996,767 (GRCm39) |
|
probably null |
Het |
Chrne |
T |
A |
11: 70,506,086 (GRCm39) |
D426V |
possibly damaging |
Het |
Cntfr |
T |
C |
4: 41,671,035 (GRCm39) |
T43A |
probably damaging |
Het |
Cntn5 |
A |
T |
9: 10,048,758 (GRCm39) |
C63* |
probably null |
Het |
Col12a1 |
G |
A |
9: 79,599,501 (GRCm39) |
T884I |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,307,537 (GRCm39) |
|
probably null |
Het |
Dnajc2 |
A |
T |
5: 21,965,389 (GRCm39) |
S537R |
probably benign |
Het |
Dnajc25 |
T |
C |
4: 59,020,234 (GRCm39) |
I100T |
probably damaging |
Het |
Ephx1 |
C |
A |
1: 180,823,661 (GRCm39) |
G149C |
probably damaging |
Het |
Fam163b |
G |
T |
2: 27,002,698 (GRCm39) |
P100T |
probably damaging |
Het |
Fbxl9 |
A |
G |
8: 106,039,675 (GRCm39) |
|
probably null |
Het |
Fgd5 |
A |
T |
6: 92,039,850 (GRCm39) |
R1017* |
probably null |
Het |
Fibin |
A |
T |
2: 110,192,848 (GRCm39) |
L98Q |
probably damaging |
Het |
Fndc3b |
A |
T |
3: 27,505,481 (GRCm39) |
L929H |
probably damaging |
Het |
Frem1 |
T |
A |
4: 82,918,410 (GRCm39) |
S512C |
probably damaging |
Het |
Gm4922 |
T |
A |
10: 18,659,829 (GRCm39) |
M298L |
probably benign |
Het |
Gstm2 |
G |
A |
3: 107,891,369 (GRCm39) |
|
probably benign |
Het |
Gtf3c2 |
A |
G |
5: 31,317,042 (GRCm39) |
|
probably null |
Het |
Ibtk |
A |
C |
9: 85,590,178 (GRCm39) |
L1026V |
probably benign |
Het |
Il9 |
T |
A |
13: 56,629,684 (GRCm39) |
|
probably benign |
Het |
Inpp4a |
T |
C |
1: 37,432,037 (GRCm39) |
S146P |
probably damaging |
Het |
Kcnab1 |
G |
T |
3: 65,264,435 (GRCm39) |
|
probably benign |
Het |
Mgat4c |
T |
C |
10: 102,224,436 (GRCm39) |
S217P |
probably damaging |
Het |
Mr1 |
T |
C |
1: 155,008,277 (GRCm39) |
M233V |
probably benign |
Het |
Ncoa2 |
G |
A |
1: 13,218,584 (GRCm39) |
T1415I |
probably damaging |
Het |
Oasl2 |
G |
A |
5: 115,049,357 (GRCm39) |
D486N |
probably benign |
Het |
Or1j14 |
A |
T |
2: 36,418,258 (GRCm39) |
Y278F |
probably damaging |
Het |
Or9a7 |
G |
A |
6: 40,521,856 (GRCm39) |
T19I |
probably benign |
Het |
Or9s27 |
T |
C |
1: 92,516,688 (GRCm39) |
I212T |
possibly damaging |
Het |
Pcnx4 |
T |
C |
12: 72,588,587 (GRCm39) |
F132L |
probably damaging |
Het |
Pde5a |
T |
A |
3: 122,636,702 (GRCm39) |
L717Q |
probably damaging |
Het |
Peli2 |
A |
T |
14: 48,465,389 (GRCm39) |
|
probably benign |
Het |
Phf14 |
A |
G |
6: 11,962,657 (GRCm39) |
S435G |
probably damaging |
Het |
Plekhg1 |
T |
A |
10: 3,913,564 (GRCm39) |
H1095Q |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,893,907 (GRCm39) |
|
probably null |
Het |
Plekho1 |
T |
G |
3: 95,899,497 (GRCm39) |
N99H |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,742,395 (GRCm39) |
K457N |
probably benign |
Het |
Ppp1r3a |
T |
C |
6: 14,718,322 (GRCm39) |
E864G |
probably benign |
Het |
Prkab2 |
T |
A |
3: 97,574,715 (GRCm39) |
L237Q |
probably damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ptger3 |
T |
A |
3: 157,273,207 (GRCm39) |
C185S |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,230,709 (GRCm39) |
Y267H |
probably damaging |
Het |
Pum2 |
A |
G |
12: 8,794,654 (GRCm39) |
I715V |
probably benign |
Het |
R3hdm1 |
T |
C |
1: 128,114,573 (GRCm39) |
V518A |
probably damaging |
Het |
Rab3d |
T |
C |
9: 21,827,147 (GRCm39) |
I28V |
probably damaging |
Het |
Rad54b |
T |
C |
4: 11,606,272 (GRCm39) |
L560P |
probably damaging |
Het |
Rgs20 |
A |
G |
1: 5,140,370 (GRCm39) |
|
probably null |
Het |
Sesn1 |
T |
A |
10: 41,781,315 (GRCm39) |
L460H |
probably damaging |
Het |
Slc39a14 |
A |
G |
14: 70,553,885 (GRCm39) |
|
probably null |
Het |
Slco6c1 |
T |
A |
1: 96,990,201 (GRCm39) |
H663L |
probably benign |
Het |
Snx13 |
T |
A |
12: 35,132,926 (GRCm39) |
C63S |
probably benign |
Het |
Spmip4 |
T |
A |
6: 50,560,959 (GRCm39) |
D212V |
probably damaging |
Het |
Strip2 |
T |
C |
6: 29,941,940 (GRCm39) |
|
probably null |
Het |
Syncrip |
A |
G |
9: 88,361,620 (GRCm39) |
|
probably benign |
Het |
Taf15 |
A |
G |
11: 83,395,579 (GRCm39) |
|
probably benign |
Het |
Tbc1d8 |
T |
C |
1: 39,444,368 (GRCm39) |
|
probably null |
Het |
Tgm4 |
T |
A |
9: 122,877,614 (GRCm39) |
C205* |
probably null |
Het |
Tmem212 |
A |
T |
3: 27,940,628 (GRCm39) |
L63Q |
possibly damaging |
Het |
Tmem63a |
G |
A |
1: 180,790,054 (GRCm39) |
|
probably null |
Het |
Trpm5 |
C |
A |
7: 142,636,298 (GRCm39) |
V525L |
probably benign |
Het |
Ttn |
A |
G |
2: 76,537,171 (GRCm39) |
L34919P |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,694,619 (GRCm39) |
|
probably benign |
Het |
Tuba4a |
T |
C |
1: 75,194,069 (GRCm39) |
I4V |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,200,853 (GRCm39) |
D4679G |
possibly damaging |
Het |
Usp2 |
T |
G |
9: 44,003,445 (GRCm39) |
V448G |
probably damaging |
Het |
Usp3 |
A |
G |
9: 66,453,024 (GRCm39) |
|
probably null |
Het |
Zfp341 |
T |
A |
2: 154,470,721 (GRCm39) |
V246E |
probably damaging |
Het |
|
Other mutations in Anxa2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01375:Anxa2
|
APN |
9 |
69,390,301 (GRCm39) |
nonsense |
probably null |
|
IGL02550:Anxa2
|
APN |
9 |
69,374,588 (GRCm39) |
missense |
probably benign |
0.00 |
FR4342:Anxa2
|
UTSW |
9 |
69,387,492 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Anxa2
|
UTSW |
9 |
69,387,487 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Anxa2
|
UTSW |
9 |
69,387,485 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Anxa2
|
UTSW |
9 |
69,387,492 (GRCm39) |
small insertion |
probably benign |
|
R1480:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1482:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1519:Anxa2
|
UTSW |
9 |
69,392,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1610:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1624:Anxa2
|
UTSW |
9 |
69,386,990 (GRCm39) |
missense |
probably benign |
0.10 |
R1672:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1696:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1760:Anxa2
|
UTSW |
9 |
69,397,049 (GRCm39) |
missense |
probably benign |
0.00 |
R1775:Anxa2
|
UTSW |
9 |
69,395,363 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1828:Anxa2
|
UTSW |
9 |
69,390,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1991:Anxa2
|
UTSW |
9 |
69,391,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Anxa2
|
UTSW |
9 |
69,391,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R2029:Anxa2
|
UTSW |
9 |
69,371,762 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2103:Anxa2
|
UTSW |
9 |
69,391,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Anxa2
|
UTSW |
9 |
69,383,410 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2146:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2148:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2149:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2150:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R3848:Anxa2
|
UTSW |
9 |
69,374,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4036:Anxa2
|
UTSW |
9 |
69,395,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R4565:Anxa2
|
UTSW |
9 |
69,397,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Anxa2
|
UTSW |
9 |
69,393,812 (GRCm39) |
missense |
probably benign |
0.41 |
R5172:Anxa2
|
UTSW |
9 |
69,392,533 (GRCm39) |
missense |
probably damaging |
0.99 |
R5181:Anxa2
|
UTSW |
9 |
69,383,347 (GRCm39) |
missense |
probably benign |
0.00 |
R6427:Anxa2
|
UTSW |
9 |
69,383,431 (GRCm39) |
critical splice donor site |
probably null |
|
R6759:Anxa2
|
UTSW |
9 |
69,391,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Anxa2
|
UTSW |
9 |
69,387,410 (GRCm39) |
missense |
unknown |
|
R7734:Anxa2
|
UTSW |
9 |
69,398,764 (GRCm39) |
missense |
probably benign |
0.41 |
R8532:Anxa2
|
UTSW |
9 |
69,374,594 (GRCm39) |
missense |
probably benign |
0.02 |
|