Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
C |
A |
1: 71,302,647 (GRCm39) |
V2191L |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,565,764 (GRCm39) |
Y4796C |
probably damaging |
Het |
Actn2 |
A |
T |
13: 12,315,835 (GRCm39) |
M228K |
probably damaging |
Het |
Agbl1 |
T |
G |
7: 76,064,465 (GRCm39) |
|
probably null |
Het |
Ahi1 |
T |
G |
10: 20,846,875 (GRCm39) |
V435G |
possibly damaging |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Arhgap6 |
A |
G |
X: 167,579,496 (GRCm39) |
T94A |
probably benign |
Het |
Atg4c |
C |
A |
4: 99,109,463 (GRCm39) |
N143K |
possibly damaging |
Het |
Bcor |
G |
A |
X: 11,923,862 (GRCm39) |
A578V |
possibly damaging |
Het |
Bop1 |
A |
G |
15: 76,339,487 (GRCm39) |
V286A |
probably damaging |
Het |
C1qtnf12 |
A |
G |
4: 156,050,922 (GRCm39) |
N297S |
probably benign |
Het |
Cacna1a |
A |
T |
8: 85,356,304 (GRCm39) |
Q1887L |
possibly damaging |
Het |
Cadps2 |
G |
T |
6: 23,838,998 (GRCm39) |
|
probably benign |
Het |
Chl1 |
T |
C |
6: 103,692,362 (GRCm39) |
|
probably null |
Het |
Cnot2 |
A |
G |
10: 116,342,185 (GRCm39) |
I173T |
probably benign |
Het |
Cntnap5b |
T |
A |
1: 100,311,199 (GRCm39) |
I564N |
probably benign |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Cyp2j11 |
G |
A |
4: 96,204,595 (GRCm39) |
T317I |
probably damaging |
Het |
Dcaf8l |
T |
C |
X: 88,449,883 (GRCm39) |
D82G |
possibly damaging |
Het |
Dennd3 |
A |
T |
15: 73,426,909 (GRCm39) |
H762L |
probably benign |
Het |
Dgkd |
T |
G |
1: 87,809,643 (GRCm39) |
N110K |
probably damaging |
Het |
Dhx8 |
A |
T |
11: 101,629,203 (GRCm39) |
R198* |
probably null |
Het |
Dnah8 |
A |
T |
17: 30,956,232 (GRCm39) |
I2071F |
probably damaging |
Het |
Dsc3 |
C |
T |
18: 20,098,695 (GRCm39) |
R828Q |
probably damaging |
Het |
Fbxl4 |
T |
C |
4: 22,427,333 (GRCm39) |
F525L |
possibly damaging |
Het |
Glb1 |
T |
C |
9: 114,279,716 (GRCm39) |
Y375H |
probably damaging |
Het |
Gpatch1 |
A |
G |
7: 34,998,701 (GRCm39) |
V343A |
probably benign |
Het |
Gpr139 |
A |
G |
7: 118,744,192 (GRCm39) |
V131A |
probably benign |
Het |
Hamp |
T |
C |
7: 30,642,137 (GRCm39) |
T34A |
possibly damaging |
Het |
Homer2 |
T |
G |
7: 81,274,043 (GRCm39) |
D51A |
possibly damaging |
Het |
Hspa1l |
C |
T |
17: 35,196,366 (GRCm39) |
A135V |
probably damaging |
Het |
Igsf10 |
A |
G |
3: 59,243,998 (GRCm39) |
M112T |
possibly damaging |
Het |
Ikbkb |
A |
T |
8: 23,172,761 (GRCm39) |
L153Q |
probably damaging |
Het |
Kif19a |
A |
T |
11: 114,671,594 (GRCm39) |
I158F |
probably damaging |
Het |
L1cam |
A |
T |
X: 72,904,747 (GRCm39) |
F536Y |
probably damaging |
Het |
Lamb3 |
T |
C |
1: 193,010,212 (GRCm39) |
V275A |
probably benign |
Het |
Lhx1 |
A |
T |
11: 84,410,647 (GRCm39) |
S226T |
probably benign |
Het |
Llcfc1 |
G |
A |
6: 41,662,155 (GRCm39) |
G53D |
possibly damaging |
Het |
Loxl4 |
A |
G |
19: 42,592,631 (GRCm39) |
|
probably null |
Het |
Magee1 |
A |
T |
X: 104,166,564 (GRCm39) |
D783V |
probably damaging |
Het |
Mak |
T |
C |
13: 41,195,513 (GRCm39) |
K400R |
probably benign |
Het |
Mgat4c |
T |
C |
10: 102,224,790 (GRCm39) |
F335L |
probably benign |
Het |
Mgat4f |
T |
A |
1: 134,318,251 (GRCm39) |
M341K |
probably damaging |
Het |
Mospd2 |
A |
G |
X: 163,739,473 (GRCm39) |
|
probably null |
Het |
Mtor |
T |
C |
4: 148,540,469 (GRCm39) |
F245L |
possibly damaging |
Het |
Mycbp2 |
G |
A |
14: 103,393,358 (GRCm39) |
H3068Y |
probably damaging |
Het |
Myo5a |
T |
A |
9: 75,087,429 (GRCm39) |
L1095H |
probably damaging |
Het |
Nlrp1a |
T |
A |
11: 71,013,733 (GRCm39) |
K506* |
probably null |
Het |
Or5d18 |
C |
A |
2: 87,864,943 (GRCm39) |
C180F |
probably damaging |
Het |
Parvb |
A |
G |
15: 84,116,369 (GRCm39) |
K33E |
possibly damaging |
Het |
Phkb |
A |
G |
8: 86,744,115 (GRCm39) |
D588G |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,783,064 (GRCm39) |
I752N |
probably damaging |
Het |
Pkhd1 |
C |
A |
1: 20,484,444 (GRCm39) |
|
probably null |
Het |
Plod3 |
C |
T |
5: 137,016,627 (GRCm39) |
R30* |
probably null |
Het |
Ppfia4 |
T |
C |
1: 134,240,372 (GRCm39) |
I591V |
probably benign |
Het |
Prickle2 |
A |
G |
6: 92,402,652 (GRCm39) |
L112P |
probably damaging |
Het |
Ptgs2 |
G |
T |
1: 149,981,465 (GRCm39) |
A583S |
probably benign |
Het |
Pycr2 |
T |
C |
1: 180,734,413 (GRCm39) |
V231A |
probably damaging |
Het |
Ralgapa2 |
T |
C |
2: 146,273,807 (GRCm39) |
D540G |
probably benign |
Het |
Rasal1 |
T |
A |
5: 120,800,096 (GRCm39) |
I150N |
probably damaging |
Het |
Rimkla |
T |
A |
4: 119,331,779 (GRCm39) |
M140L |
possibly damaging |
Het |
Sacs |
T |
C |
14: 61,410,827 (GRCm39) |
L34P |
probably damaging |
Het |
Sema3d |
A |
G |
5: 12,534,926 (GRCm39) |
Y106C |
probably damaging |
Het |
Serpinb8 |
T |
A |
1: 107,533,657 (GRCm39) |
D237E |
probably benign |
Het |
Slc19a2 |
T |
C |
1: 164,089,657 (GRCm39) |
W158R |
probably damaging |
Het |
Sorbs1 |
A |
T |
19: 40,365,268 (GRCm39) |
F172I |
possibly damaging |
Het |
Spaca7 |
A |
T |
8: 12,636,447 (GRCm39) |
D91V |
probably damaging |
Het |
Tead3 |
A |
G |
17: 28,552,638 (GRCm39) |
F187L |
probably damaging |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Tmem131 |
C |
A |
1: 36,851,690 (GRCm39) |
V938L |
probably benign |
Het |
Tmem132c |
T |
A |
5: 127,540,026 (GRCm39) |
W351R |
probably damaging |
Het |
Tmem178b |
A |
T |
6: 40,184,435 (GRCm39) |
Q111L |
probably damaging |
Het |
Trap1 |
T |
C |
16: 3,878,624 (GRCm39) |
D236G |
probably damaging |
Het |
Trim45 |
T |
A |
3: 100,839,360 (GRCm39) |
L754* |
probably null |
Het |
Tubgcp5 |
A |
G |
7: 55,449,259 (GRCm39) |
E152G |
probably damaging |
Het |
Uaca |
A |
T |
9: 60,776,961 (GRCm39) |
L447F |
probably damaging |
Het |
Vps51 |
A |
G |
19: 6,118,164 (GRCm39) |
V777A |
probably benign |
Het |
Wdr11 |
A |
G |
7: 129,230,807 (GRCm39) |
|
probably null |
Het |
Zfp462 |
T |
A |
4: 55,013,670 (GRCm39) |
S1879T |
probably benign |
Het |
Zfr2 |
T |
G |
10: 81,077,950 (GRCm39) |
V259G |
probably benign |
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 |
|
R2149:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2150:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2437:Anxa2
|
UTSW |
9 |
69,397,046 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|