Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
G |
9: 46,215,303 (GRCm39) |
|
probably benign |
Het |
Abcc9 |
A |
G |
6: 142,571,457 (GRCm39) |
|
probably benign |
Het |
Adamts2 |
G |
A |
11: 50,679,494 (GRCm39) |
G825R |
probably damaging |
Het |
Adgre1 |
A |
T |
17: 57,750,990 (GRCm39) |
R555W |
probably benign |
Het |
Apob |
T |
A |
12: 8,038,781 (GRCm39) |
V398D |
probably damaging |
Het |
Arid4b |
A |
G |
13: 14,334,856 (GRCm39) |
N355S |
probably benign |
Het |
Asb3 |
G |
T |
11: 30,979,021 (GRCm39) |
D143Y |
probably damaging |
Het |
Birc6 |
G |
A |
17: 74,925,419 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
A |
G |
8: 85,310,360 (GRCm39) |
M1425V |
probably damaging |
Het |
Capn9 |
A |
G |
8: 125,332,583 (GRCm39) |
E474G |
probably damaging |
Het |
Capza2 |
T |
C |
6: 17,660,764 (GRCm39) |
S155P |
probably damaging |
Het |
Ccdc125 |
A |
G |
13: 100,823,622 (GRCm39) |
N202S |
possibly damaging |
Het |
Ccn1 |
A |
G |
3: 145,354,023 (GRCm39) |
C256R |
probably damaging |
Het |
Chrm5 |
T |
A |
2: 112,310,445 (GRCm39) |
T224S |
probably benign |
Het |
Chtop |
C |
T |
3: 90,409,422 (GRCm39) |
|
probably null |
Het |
Clip1 |
T |
C |
5: 123,753,217 (GRCm39) |
|
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,552,604 (GRCm39) |
T14A |
possibly damaging |
Het |
Dcaf8 |
T |
C |
1: 172,000,478 (GRCm39) |
V212A |
possibly damaging |
Het |
Fam114a1 |
T |
C |
5: 65,166,389 (GRCm39) |
M240T |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,504,246 (GRCm39) |
Y4580H |
probably damaging |
Het |
Glipr1 |
G |
A |
10: 111,821,698 (GRCm39) |
R200* |
probably null |
Het |
Gm6408 |
A |
T |
5: 146,419,192 (GRCm39) |
Y69F |
probably benign |
Het |
Gpt2 |
T |
C |
8: 86,249,885 (GRCm39) |
S456P |
probably benign |
Het |
Kat8 |
T |
C |
7: 127,519,751 (GRCm39) |
F225S |
probably benign |
Het |
Lin28a |
A |
T |
4: 133,735,284 (GRCm39) |
C67* |
probably null |
Het |
Mtarc2 |
T |
C |
1: 184,564,786 (GRCm39) |
E155G |
probably benign |
Het |
Myoz3 |
G |
A |
18: 60,712,543 (GRCm39) |
T104M |
possibly damaging |
Het |
Nek9 |
C |
T |
12: 85,350,289 (GRCm39) |
M928I |
probably benign |
Het |
Nlrp9a |
G |
C |
7: 26,270,065 (GRCm39) |
A831P |
probably damaging |
Het |
Nop53 |
T |
C |
7: 15,679,887 (GRCm39) |
|
probably null |
Het |
Ofcc1 |
T |
A |
13: 40,241,325 (GRCm39) |
T728S |
probably damaging |
Het |
Pabpc4l |
T |
A |
3: 46,401,124 (GRCm39) |
|
probably null |
Het |
Rbm34 |
T |
C |
8: 127,696,880 (GRCm39) |
|
probably null |
Het |
Relch |
T |
C |
1: 105,631,608 (GRCm39) |
|
probably benign |
Het |
Robo2 |
C |
T |
16: 74,149,672 (GRCm39) |
C52Y |
probably damaging |
Het |
Rpgr |
G |
A |
X: 10,032,511 (GRCm39) |
P857L |
probably benign |
Het |
Scn2a |
A |
G |
2: 65,548,066 (GRCm39) |
Y57C |
possibly damaging |
Het |
Selp |
C |
T |
1: 163,971,460 (GRCm39) |
|
probably benign |
Het |
Skp2 |
T |
C |
15: 9,139,566 (GRCm39) |
D43G |
possibly damaging |
Het |
Smad5 |
T |
A |
13: 56,871,617 (GRCm39) |
S71T |
probably damaging |
Het |
Sorcs1 |
G |
T |
19: 50,171,213 (GRCm39) |
H892N |
probably benign |
Het |
Sox6 |
C |
T |
7: 115,140,856 (GRCm39) |
|
probably null |
Het |
St3gal1 |
A |
T |
15: 66,978,522 (GRCm39) |
I333N |
probably damaging |
Het |
Tex15 |
C |
A |
8: 34,036,364 (GRCm39) |
Q97K |
probably benign |
Het |
Tnxb |
A |
T |
17: 34,917,884 (GRCm39) |
T2266S |
possibly damaging |
Het |
Tpbgl |
C |
A |
7: 99,274,949 (GRCm39) |
G303C |
probably damaging |
Het |
Trat1 |
A |
T |
16: 48,555,304 (GRCm39) |
S143T |
possibly damaging |
Het |
Trpm8 |
T |
A |
1: 88,283,002 (GRCm39) |
V763E |
probably benign |
Het |
Ttc21a |
G |
A |
9: 119,795,732 (GRCm39) |
D1189N |
probably benign |
Het |
Usp7 |
T |
C |
16: 8,519,845 (GRCm39) |
N178D |
possibly damaging |
Het |
Zfp217 |
T |
C |
2: 169,961,064 (GRCm39) |
D421G |
possibly damaging |
Het |
Zfp382 |
T |
C |
7: 29,833,855 (GRCm39) |
F502S |
probably damaging |
Het |
|
Other mutations in Lactb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Lactb2
|
APN |
1 |
13,730,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00595:Lactb2
|
APN |
1 |
13,700,350 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00730:Lactb2
|
APN |
1 |
13,717,740 (GRCm39) |
splice site |
probably benign |
|
R0371:Lactb2
|
UTSW |
1 |
13,720,984 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0782:Lactb2
|
UTSW |
1 |
13,717,675 (GRCm39) |
missense |
probably benign |
0.18 |
R1670:Lactb2
|
UTSW |
1 |
13,730,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R2324:Lactb2
|
UTSW |
1 |
13,708,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2418:Lactb2
|
UTSW |
1 |
13,730,563 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3500:Lactb2
|
UTSW |
1 |
13,730,673 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4345:Lactb2
|
UTSW |
1 |
13,730,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Lactb2
|
UTSW |
1 |
13,717,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Lactb2
|
UTSW |
1 |
13,717,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Lactb2
|
UTSW |
1 |
13,708,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Lactb2
|
UTSW |
1 |
13,700,356 (GRCm39) |
missense |
probably benign |
0.22 |
R5658:Lactb2
|
UTSW |
1 |
13,697,642 (GRCm39) |
missense |
probably benign |
0.03 |
R5918:Lactb2
|
UTSW |
1 |
13,720,954 (GRCm39) |
missense |
probably benign |
0.32 |
R6419:Lactb2
|
UTSW |
1 |
13,708,459 (GRCm39) |
nonsense |
probably null |
|
|