Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
A |
G |
7: 27,260,022 (GRCm39) |
T25A |
possibly damaging |
Het |
Abca17 |
T |
C |
17: 24,486,632 (GRCm39) |
Y1465C |
possibly damaging |
Het |
Adgrb1 |
C |
T |
15: 74,459,956 (GRCm39) |
R530W |
probably damaging |
Het |
Ak9 |
A |
G |
10: 41,203,585 (GRCm39) |
T159A |
possibly damaging |
Het |
Akap13 |
G |
A |
7: 75,259,340 (GRCm39) |
G655S |
possibly damaging |
Het |
Amer2 |
T |
A |
14: 60,617,123 (GRCm39) |
D439E |
possibly damaging |
Het |
Arfgef2 |
T |
A |
2: 166,703,558 (GRCm39) |
M870K |
probably damaging |
Het |
Arhgef33 |
T |
C |
17: 80,656,935 (GRCm39) |
F150S |
probably damaging |
Het |
Arid2 |
A |
T |
15: 96,268,064 (GRCm39) |
T726S |
probably benign |
Het |
Atf7ip2 |
G |
A |
16: 10,052,195 (GRCm39) |
V225I |
probably damaging |
Het |
Atp12a |
A |
T |
14: 56,603,545 (GRCm39) |
E50V |
probably damaging |
Het |
Bdkrb1 |
A |
G |
12: 105,570,761 (GRCm39) |
N109S |
probably benign |
Het |
Cald1 |
A |
G |
6: 34,722,646 (GRCm39) |
E104G |
probably damaging |
Het |
Capn15 |
A |
G |
17: 26,183,878 (GRCm39) |
V267A |
probably benign |
Het |
Ccng2 |
A |
T |
5: 93,421,241 (GRCm39) |
K250N |
possibly damaging |
Het |
Ccr10 |
T |
A |
11: 101,065,210 (GRCm39) |
N107Y |
probably benign |
Het |
Cntn2 |
T |
C |
1: 132,449,017 (GRCm39) |
N664S |
probably damaging |
Het |
Cyp24a1 |
T |
G |
2: 170,327,963 (GRCm39) |
E426D |
probably benign |
Het |
Cyp26a1 |
A |
G |
19: 37,689,626 (GRCm39) |
S441G |
probably benign |
Het |
Cyp4f14 |
T |
A |
17: 33,128,145 (GRCm39) |
K290M |
possibly damaging |
Het |
Dcp2 |
T |
A |
18: 44,533,391 (GRCm39) |
L114Q |
probably damaging |
Het |
Dhrs7 |
A |
G |
12: 72,699,894 (GRCm39) |
F246S |
possibly damaging |
Het |
Dlg1 |
T |
C |
16: 31,600,616 (GRCm39) |
V167A |
probably damaging |
Het |
Dnmt3b |
A |
T |
2: 153,518,630 (GRCm39) |
K598* |
probably null |
Het |
Dph7 |
T |
C |
2: 24,859,692 (GRCm39) |
|
probably null |
Het |
Ehbp1 |
T |
C |
11: 22,003,441 (GRCm39) |
M1103V |
probably damaging |
Het |
Ell2 |
T |
C |
13: 75,917,677 (GRCm39) |
S536P |
probably damaging |
Het |
Ero1a |
A |
T |
14: 45,537,392 (GRCm39) |
V178E |
probably damaging |
Het |
Faf2 |
T |
A |
13: 54,786,067 (GRCm39) |
*50R |
probably null |
Het |
Fbxl14 |
A |
T |
6: 119,457,107 (GRCm39) |
N96I |
probably damaging |
Het |
Fcrl2 |
T |
C |
3: 87,166,825 (GRCm39) |
Y56C |
possibly damaging |
Het |
Foxc1 |
T |
A |
13: 31,992,782 (GRCm39) |
M531K |
unknown |
Het |
Foxp1 |
A |
C |
6: 98,922,663 (GRCm39) |
S391A |
probably benign |
Het |
Frem2 |
A |
T |
3: 53,563,463 (GRCm39) |
L348* |
probably null |
Het |
Fsd1 |
T |
A |
17: 56,295,257 (GRCm39) |
|
probably null |
Het |
Gab2 |
A |
G |
7: 96,872,840 (GRCm39) |
E81G |
probably damaging |
Het |
Gcat |
G |
A |
15: 78,919,995 (GRCm39) |
V196M |
probably damaging |
Het |
Gfy |
T |
C |
7: 44,827,470 (GRCm39) |
T209A |
possibly damaging |
Het |
Ggt7 |
T |
C |
2: 155,336,899 (GRCm39) |
N531S |
possibly damaging |
Het |
Gnai3 |
A |
G |
3: 108,016,775 (GRCm39) |
I343T |
probably damaging |
Het |
H2-DMa |
A |
T |
17: 34,357,387 (GRCm39) |
Q220L |
probably benign |
Het |
Heatr1 |
A |
G |
13: 12,438,602 (GRCm39) |
I1346V |
possibly damaging |
Het |
Igfbp1 |
T |
A |
11: 7,147,978 (GRCm39) |
V7D |
probably benign |
Het |
Igfbp1 |
T |
C |
11: 7,151,922 (GRCm39) |
W242R |
probably damaging |
Het |
Kbtbd2 |
T |
G |
6: 56,756,326 (GRCm39) |
K470T |
probably benign |
Het |
Klb |
G |
C |
5: 65,506,089 (GRCm39) |
R112P |
possibly damaging |
Het |
Klhl25 |
G |
T |
7: 75,516,591 (GRCm39) |
G499V |
probably damaging |
Het |
Krt7 |
A |
T |
15: 101,321,307 (GRCm39) |
T375S |
probably benign |
Het |
Krt73 |
G |
A |
15: 101,708,344 (GRCm39) |
L238F |
probably damaging |
Het |
Lama5 |
G |
T |
2: 179,844,279 (GRCm39) |
H331Q |
probably damaging |
Het |
Leng8 |
T |
G |
7: 4,148,135 (GRCm39) |
F663V |
probably damaging |
Het |
Lrp12 |
G |
T |
15: 39,741,757 (GRCm39) |
H338Q |
probably damaging |
Het |
Lrp6 |
T |
A |
6: 134,445,686 (GRCm39) |
R1042S |
probably damaging |
Het |
Map6 |
T |
A |
7: 98,966,664 (GRCm39) |
|
probably null |
Het |
Mdn1 |
T |
C |
4: 32,700,417 (GRCm39) |
F1459L |
possibly damaging |
Het |
Mmp1b |
T |
C |
9: 7,386,699 (GRCm39) |
T142A |
probably damaging |
Het |
Mmp23 |
T |
A |
4: 155,735,166 (GRCm39) |
*392C |
probably null |
Het |
Nlrp4a |
C |
T |
7: 26,149,959 (GRCm39) |
S522F |
probably damaging |
Het |
Nup93 |
T |
G |
8: 95,023,183 (GRCm39) |
F254V |
probably benign |
Het |
Oas1h |
G |
T |
5: 121,000,885 (GRCm39) |
|
probably null |
Het |
Ocstamp |
A |
G |
2: 165,238,094 (GRCm39) |
L390P |
probably damaging |
Het |
Olfm1 |
C |
A |
2: 28,098,128 (GRCm39) |
Y20* |
probably null |
Het |
Or10ac1 |
C |
T |
6: 42,515,537 (GRCm39) |
V140M |
probably benign |
Het |
Or13a26 |
A |
T |
7: 140,284,409 (GRCm39) |
K82* |
probably null |
Het |
Or52ae7 |
T |
C |
7: 103,119,384 (GRCm39) |
V46A |
probably benign |
Het |
Or5as1 |
A |
G |
2: 86,980,724 (GRCm39) |
F94L |
probably benign |
Het |
Or7g33 |
A |
G |
9: 19,449,190 (GRCm39) |
F12S |
probably damaging |
Het |
Pgghg |
T |
C |
7: 140,525,224 (GRCm39) |
V410A |
possibly damaging |
Het |
Polr2b |
T |
A |
5: 77,490,495 (GRCm39) |
D878E |
probably benign |
Het |
Pspc1 |
T |
C |
14: 57,001,700 (GRCm39) |
T225A |
probably benign |
Het |
Rad21l |
A |
T |
2: 151,510,447 (GRCm39) |
Y3N |
probably damaging |
Het |
Rbl2 |
A |
G |
8: 91,812,352 (GRCm39) |
N280S |
probably benign |
Het |
Rdm1 |
C |
A |
11: 101,521,694 (GRCm39) |
Q150K |
probably benign |
Het |
Ro60 |
T |
A |
1: 143,633,575 (GRCm39) |
I508F |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,862,188 (GRCm39) |
F932I |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,746,543 (GRCm39) |
M2003K |
probably benign |
Het |
Scfd2 |
T |
C |
5: 74,691,539 (GRCm39) |
T248A |
probably benign |
Het |
Slc22a16 |
G |
A |
10: 40,460,923 (GRCm39) |
A242T |
possibly damaging |
Het |
Slit3 |
C |
A |
11: 35,566,750 (GRCm39) |
N1007K |
probably damaging |
Het |
Sntg2 |
C |
A |
12: 30,317,062 (GRCm39) |
G187C |
probably damaging |
Het |
Spag5 |
T |
C |
11: 78,212,152 (GRCm39) |
V1060A |
probably damaging |
Het |
Spg7 |
G |
A |
8: 123,816,964 (GRCm39) |
V552I |
probably benign |
Het |
Spns2 |
T |
A |
11: 72,347,173 (GRCm39) |
T434S |
probably benign |
Het |
Srpk2 |
C |
T |
5: 23,753,492 (GRCm39) |
W87* |
probably null |
Het |
St3gal3 |
T |
C |
4: 117,797,589 (GRCm39) |
I268V |
possibly damaging |
Het |
Stat6 |
T |
C |
10: 127,488,918 (GRCm39) |
C356R |
probably damaging |
Het |
Stx8 |
A |
G |
11: 67,902,248 (GRCm39) |
Q144R |
probably damaging |
Het |
Tcn2 |
C |
A |
11: 3,872,169 (GRCm39) |
L319F |
probably damaging |
Het |
Tex14 |
T |
C |
11: 87,402,371 (GRCm39) |
I486T |
possibly damaging |
Het |
Thtpa |
T |
C |
14: 55,333,242 (GRCm39) |
V109A |
probably benign |
Het |
Tmem127 |
C |
A |
2: 127,090,627 (GRCm39) |
L48I |
probably damaging |
Het |
Tnfaip8 |
A |
T |
18: 50,223,290 (GRCm39) |
K9* |
probably null |
Het |
Tnfrsf1b |
T |
A |
4: 144,954,044 (GRCm39) |
T102S |
probably benign |
Het |
Tor1aip1 |
A |
T |
1: 155,893,262 (GRCm39) |
M110K |
possibly damaging |
Het |
Trim10 |
A |
T |
17: 37,188,073 (GRCm39) |
K430* |
probably null |
Het |
Trpv6 |
A |
G |
6: 41,598,702 (GRCm39) |
V641A |
possibly damaging |
Het |
Ttf1 |
T |
G |
2: 28,960,014 (GRCm39) |
Y541D |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,594,750 (GRCm39) |
V20432A |
probably damaging |
Het |
Vac14 |
A |
T |
8: 111,359,079 (GRCm39) |
|
probably null |
Het |
Vipr2 |
G |
T |
12: 116,102,777 (GRCm39) |
A296S |
probably benign |
Het |
Vmn1r1 |
T |
C |
1: 181,985,624 (GRCm39) |
R14G |
probably benign |
Het |
Vmn1r178 |
T |
A |
7: 23,593,625 (GRCm39) |
N151K |
probably damaging |
Het |
Vmn1r58 |
T |
A |
7: 5,413,727 (GRCm39) |
I168F |
possibly damaging |
Het |
Vmn1r77 |
C |
T |
7: 11,775,547 (GRCm39) |
Q40* |
probably null |
Het |
Vmn2r76 |
T |
C |
7: 85,880,464 (GRCm39) |
N74S |
possibly damaging |
Het |
Zc2hc1c |
T |
A |
12: 85,337,555 (GRCm39) |
M404K |
possibly 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 |
|
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 |
|
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 |
|