Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
A |
G |
16: 20,223,398 (GRCm39) |
V170A |
possibly damaging |
Het |
Adamts2 |
A |
G |
11: 50,666,957 (GRCm39) |
E418G |
probably damaging |
Het |
Adra2b |
T |
C |
2: 127,206,056 (GRCm39) |
L191P |
probably damaging |
Het |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Bag2 |
T |
C |
1: 33,787,358 (GRCm39) |
I55V |
probably benign |
Het |
Bltp2 |
T |
C |
11: 78,156,064 (GRCm39) |
L192P |
possibly damaging |
Het |
Bmpr1b |
T |
C |
3: 141,563,343 (GRCm39) |
I200M |
possibly damaging |
Het |
Cacna1i |
C |
A |
15: 80,243,095 (GRCm39) |
Y417* |
probably null |
Het |
Cdc7 |
T |
A |
5: 107,120,864 (GRCm39) |
I162N |
probably damaging |
Het |
Chchd1 |
T |
C |
14: 20,754,211 (GRCm39) |
I89T |
probably benign |
Het |
Cxcl16 |
T |
C |
11: 70,346,510 (GRCm39) |
N224S |
probably benign |
Het |
Dync1i1 |
T |
G |
6: 5,913,330 (GRCm39) |
L188V |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,051,452 (GRCm39) |
V3161A |
probably benign |
Het |
E2f3 |
T |
A |
13: 30,097,453 (GRCm39) |
K303N |
probably damaging |
Het |
Fermt1 |
T |
C |
2: 132,748,635 (GRCm39) |
T663A |
probably benign |
Het |
Fhod3 |
A |
G |
18: 25,189,390 (GRCm39) |
R611G |
probably damaging |
Het |
Frem3 |
A |
T |
8: 81,339,224 (GRCm39) |
S506C |
probably damaging |
Het |
Gm10318 |
T |
A |
10: 77,688,712 (GRCm39) |
M6K |
unknown |
Het |
Gm6563 |
T |
A |
19: 23,653,480 (GRCm39) |
V90E |
probably damaging |
Het |
Gpc6 |
T |
C |
14: 117,163,384 (GRCm39) |
S13P |
probably benign |
Het |
Gpr107 |
C |
A |
2: 31,066,939 (GRCm39) |
H196Q |
probably benign |
Het |
Heatr1 |
T |
G |
13: 12,425,415 (GRCm39) |
D618E |
probably benign |
Het |
Lrrc27 |
T |
C |
7: 138,808,690 (GRCm39) |
V391A |
probably benign |
Het |
Mindy3 |
T |
G |
2: 12,360,154 (GRCm39) |
K349N |
probably damaging |
Het |
Mllt10 |
T |
C |
2: 18,151,670 (GRCm39) |
V261A |
probably damaging |
Het |
Mrpl48 |
G |
A |
7: 100,232,269 (GRCm39) |
|
probably benign |
Het |
Msantd5f5 |
T |
A |
4: 73,542,641 (GRCm39) |
L47Q |
probably damaging |
Het |
Muc16 |
T |
C |
9: 18,430,927 (GRCm39) |
I8062V |
probably benign |
Het |
Myo7a |
T |
C |
7: 97,740,270 (GRCm39) |
N575D |
possibly damaging |
Het |
Nfrkb |
T |
C |
9: 31,311,261 (GRCm39) |
L370P |
probably damaging |
Het |
Or51t4 |
T |
C |
7: 102,597,804 (GRCm39) |
V44A |
probably damaging |
Het |
Or5b12 |
G |
A |
19: 12,896,959 (GRCm39) |
T238I |
probably damaging |
Het |
Or6y1 |
T |
A |
1: 174,276,742 (GRCm39) |
C184* |
probably null |
Het |
Pdia2 |
A |
T |
17: 26,417,144 (GRCm39) |
L100* |
probably null |
Het |
Prpf31 |
A |
T |
7: 3,635,742 (GRCm39) |
N105I |
probably damaging |
Het |
Rbm20 |
A |
G |
19: 53,839,923 (GRCm39) |
N971D |
probably benign |
Het |
Rnf213 |
T |
A |
11: 119,353,043 (GRCm39) |
M3980K |
|
Het |
Skint6 |
A |
G |
4: 113,095,465 (GRCm39) |
F65L |
possibly damaging |
Het |
Smpd4 |
T |
A |
16: 17,458,884 (GRCm39) |
C536S |
possibly damaging |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Tfpt |
A |
G |
7: 3,632,065 (GRCm39) |
F15S |
possibly damaging |
Het |
Tnp2 |
A |
G |
16: 10,606,372 (GRCm39) |
C32R |
possibly damaging |
Het |
Tns3 |
A |
T |
11: 8,442,971 (GRCm39) |
V464E |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 44,019,545 (GRCm39) |
L824H |
probably damaging |
Het |
Trav15-1-dv6-1 |
A |
G |
14: 53,797,666 (GRCm39) |
D105G |
probably benign |
Het |
Ttc3 |
T |
C |
16: 94,258,238 (GRCm39) |
S1679P |
probably benign |
Het |
Xpo7 |
A |
G |
14: 70,944,837 (GRCm39) |
Y19H |
probably damaging |
Het |
Zswim4 |
G |
A |
8: 84,938,586 (GRCm39) |
R1099W |
probably damaging |
Het |
|
Other mutations in Numbl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00976:Numbl
|
APN |
7 |
26,968,235 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01389:Numbl
|
APN |
7 |
26,980,472 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02671:Numbl
|
APN |
7 |
26,964,327 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Numbl
|
UTSW |
7 |
26,979,027 (GRCm39) |
missense |
probably benign |
|
R0212:Numbl
|
UTSW |
7 |
26,980,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R0709:Numbl
|
UTSW |
7 |
26,973,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Numbl
|
UTSW |
7 |
26,980,379 (GRCm39) |
missense |
probably benign |
|
R2181:Numbl
|
UTSW |
7 |
26,968,346 (GRCm39) |
critical splice donor site |
probably null |
|
R5071:Numbl
|
UTSW |
7 |
26,980,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Numbl
|
UTSW |
7 |
26,980,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Numbl
|
UTSW |
7 |
26,980,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R6134:Numbl
|
UTSW |
7 |
26,980,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R6387:Numbl
|
UTSW |
7 |
26,976,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R6989:Numbl
|
UTSW |
7 |
26,980,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Numbl
|
UTSW |
7 |
26,971,412 (GRCm39) |
splice site |
probably null |
|
R8093:Numbl
|
UTSW |
7 |
26,980,461 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9449:Numbl
|
UTSW |
7 |
26,976,327 (GRCm39) |
missense |
|
|
V7580:Numbl
|
UTSW |
7 |
26,979,027 (GRCm39) |
missense |
probably benign |
|
V7583:Numbl
|
UTSW |
7 |
26,979,027 (GRCm39) |
missense |
probably benign |
|
|