Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
T |
7: 120,139,934 (GRCm39) |
K1533M |
probably damaging |
Het |
Aldh1l2 |
C |
T |
10: 83,356,202 (GRCm39) |
V63I |
probably benign |
Het |
Atr |
A |
G |
9: 95,747,372 (GRCm39) |
H218R |
probably benign |
Het |
Atxn7l1 |
T |
A |
12: 33,408,662 (GRCm39) |
S275T |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 119,034,263 (GRCm39) |
K88R |
probably damaging |
Het |
Ccl7 |
T |
C |
11: 81,937,412 (GRCm39) |
Y49H |
probably damaging |
Het |
Cers5 |
A |
G |
15: 99,636,544 (GRCm39) |
|
probably null |
Het |
Chuk |
T |
C |
19: 44,071,076 (GRCm39) |
E543G |
probably damaging |
Het |
Dip2c |
T |
C |
13: 9,697,043 (GRCm39) |
V1318A |
probably damaging |
Het |
Ercc5 |
A |
G |
1: 44,206,512 (GRCm39) |
H475R |
probably benign |
Het |
Fat3 |
A |
G |
9: 16,288,818 (GRCm39) |
L235P |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,211,721 (GRCm39) |
C892* |
probably null |
Het |
Fbxw8 |
T |
C |
5: 118,230,740 (GRCm39) |
T354A |
possibly damaging |
Het |
Fsip2 |
A |
C |
2: 82,817,601 (GRCm39) |
T4445P |
possibly damaging |
Het |
Gpld1 |
A |
T |
13: 25,155,397 (GRCm39) |
Q344L |
probably benign |
Het |
Hao1 |
A |
T |
2: 134,347,545 (GRCm39) |
D253E |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,246,266 (GRCm39) |
D745G |
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,793,397 (GRCm39) |
T658A |
probably benign |
Het |
Klhl35 |
A |
G |
7: 99,122,544 (GRCm39) |
|
probably benign |
Het |
Lnx2 |
C |
T |
5: 146,978,836 (GRCm39) |
|
probably null |
Het |
Map3k5 |
T |
C |
10: 19,876,321 (GRCm39) |
V160A |
probably damaging |
Het |
Masp2 |
A |
T |
4: 148,698,469 (GRCm39) |
I517F |
possibly damaging |
Het |
Mc4r |
A |
T |
18: 66,992,251 (GRCm39) |
Y287* |
probably null |
Het |
Mthfr |
A |
G |
4: 148,126,211 (GRCm39) |
D94G |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,559,114 (GRCm39) |
I2393T |
unknown |
Het |
Mybbp1a |
G |
T |
11: 72,336,838 (GRCm39) |
V557L |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,536,183 (GRCm39) |
W256R |
probably damaging |
Het |
Nacad |
G |
A |
11: 6,550,902 (GRCm39) |
S763L |
probably benign |
Het |
Nebl |
A |
G |
2: 17,735,641 (GRCm39) |
V11A |
probably benign |
Het |
Notch1 |
A |
T |
2: 26,358,743 (GRCm39) |
C1363S |
probably damaging |
Het |
Nphp3 |
A |
G |
9: 103,909,105 (GRCm39) |
N772D |
probably benign |
Het |
Nqo2 |
G |
A |
13: 34,163,634 (GRCm39) |
V98M |
probably damaging |
Het |
Pak4 |
A |
G |
7: 28,264,692 (GRCm39) |
I70T |
possibly damaging |
Het |
Pbx2 |
A |
G |
17: 34,812,574 (GRCm39) |
K2E |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,255,202 (GRCm39) |
T352A |
probably benign |
Het |
Polr1g |
G |
A |
7: 19,091,558 (GRCm39) |
T183I |
possibly damaging |
Het |
Pop1 |
T |
C |
15: 34,526,456 (GRCm39) |
Y684H |
probably damaging |
Het |
Rpa1 |
A |
G |
11: 75,205,721 (GRCm39) |
V212A |
probably damaging |
Het |
Rpap2 |
A |
G |
5: 107,768,536 (GRCm39) |
E458G |
probably damaging |
Het |
Sin3a |
T |
C |
9: 57,002,708 (GRCm39) |
V200A |
possibly damaging |
Het |
Sla |
T |
C |
15: 66,654,447 (GRCm39) |
T280A |
probably null |
Het |
Slc22a26 |
A |
T |
19: 7,763,812 (GRCm39) |
I406K |
possibly damaging |
Het |
Slc24a1 |
T |
C |
9: 64,844,545 (GRCm39) |
N606S |
unknown |
Het |
Slc39a10 |
G |
A |
1: 46,866,567 (GRCm39) |
T443M |
probably damaging |
Het |
Smg1 |
A |
T |
7: 117,762,553 (GRCm39) |
|
probably benign |
Het |
Sra1 |
G |
A |
18: 36,803,336 (GRCm39) |
A9V |
probably damaging |
Het |
Stard4 |
A |
G |
18: 33,342,109 (GRCm39) |
V47A |
probably damaging |
Het |
Stat4 |
A |
T |
1: 52,113,836 (GRCm39) |
D182V |
possibly damaging |
Het |
Syt1 |
A |
G |
10: 108,467,668 (GRCm39) |
F210L |
probably damaging |
Het |
Ube2q1 |
T |
A |
3: 89,688,667 (GRCm39) |
|
probably null |
Het |
Wnt8a |
T |
C |
18: 34,678,599 (GRCm39) |
F138L |
possibly damaging |
Het |
Zfp623 |
T |
A |
15: 75,820,470 (GRCm39) |
D475E |
probably benign |
Het |
Zfp646 |
C |
T |
7: 127,477,897 (GRCm39) |
R25W |
probably damaging |
Het |
|
Other mutations in Vmn1r159 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
ANU23:Vmn1r159
|
UTSW |
7 |
22,542,588 (GRCm39) |
missense |
probably damaging |
0.99 |
R1183:Vmn1r159
|
UTSW |
7 |
22,543,019 (GRCm39) |
missense |
probably null |
0.80 |
R1522:Vmn1r159
|
UTSW |
7 |
22,542,693 (GRCm39) |
missense |
probably damaging |
0.98 |
R1700:Vmn1r159
|
UTSW |
7 |
22,542,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R2570:Vmn1r159
|
UTSW |
7 |
22,542,307 (GRCm39) |
missense |
probably benign |
0.07 |
R3620:Vmn1r159
|
UTSW |
7 |
22,542,258 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4939:Vmn1r159
|
UTSW |
7 |
22,542,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Vmn1r159
|
UTSW |
7 |
22,542,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6365:Vmn1r159
|
UTSW |
7 |
22,542,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Vmn1r159
|
UTSW |
7 |
22,542,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R7633:Vmn1r159
|
UTSW |
7 |
22,542,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Vmn1r159
|
UTSW |
7 |
22,542,487 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7846:Vmn1r159
|
UTSW |
7 |
22,542,696 (GRCm39) |
missense |
probably benign |
0.01 |
R8008:Vmn1r159
|
UTSW |
7 |
22,542,665 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8019:Vmn1r159
|
UTSW |
7 |
22,542,248 (GRCm39) |
missense |
probably benign |
0.01 |
R8222:Vmn1r159
|
UTSW |
7 |
22,542,608 (GRCm39) |
nonsense |
probably null |
|
R8291:Vmn1r159
|
UTSW |
7 |
22,542,255 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8817:Vmn1r159
|
UTSW |
7 |
22,542,559 (GRCm39) |
missense |
probably benign |
0.04 |
R9170:Vmn1r159
|
UTSW |
7 |
22,542,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R9242:Vmn1r159
|
UTSW |
7 |
22,542,912 (GRCm39) |
missense |
probably benign |
0.00 |
R9467:Vmn1r159
|
UTSW |
7 |
22,542,141 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9525:Vmn1r159
|
UTSW |
7 |
22,542,417 (GRCm39) |
missense |
probably damaging |
0.96 |
R9601:Vmn1r159
|
UTSW |
7 |
22,542,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R9699:Vmn1r159
|
UTSW |
7 |
22,542,675 (GRCm39) |
missense |
probably damaging |
0.98 |
|