Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam19 |
T |
C |
11: 46,004,445 (GRCm39) |
|
probably benign |
Het |
Add1 |
C |
G |
5: 34,758,740 (GRCm39) |
A18G |
possibly damaging |
Het |
Alk |
T |
C |
17: 72,910,113 (GRCm39) |
K198E |
possibly damaging |
Het |
Angptl1 |
T |
A |
1: 156,684,740 (GRCm39) |
L303Q |
possibly damaging |
Het |
Aox1 |
A |
T |
1: 58,348,186 (GRCm39) |
I635L |
probably benign |
Het |
Atp5mk |
T |
A |
19: 47,074,634 (GRCm39) |
Q9L |
possibly damaging |
Het |
Atp8a2 |
G |
T |
14: 60,097,655 (GRCm39) |
T791K |
probably benign |
Het |
Auts2 |
T |
C |
5: 131,469,325 (GRCm39) |
K664R |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,967,685 (GRCm39) |
|
probably benign |
Het |
Cacna1i |
C |
A |
15: 80,277,869 (GRCm39) |
|
probably null |
Het |
Cacna2d1 |
T |
C |
5: 16,575,625 (GRCm39) |
F1077L |
probably damaging |
Het |
Camkk1 |
C |
T |
11: 72,918,307 (GRCm39) |
R52C |
probably damaging |
Het |
Camkmt |
T |
A |
17: 85,403,958 (GRCm39) |
V60E |
probably damaging |
Het |
Car9 |
G |
T |
4: 43,512,439 (GRCm39) |
|
probably null |
Het |
Cbr2 |
A |
T |
11: 120,622,791 (GRCm39) |
L3Q |
possibly damaging |
Het |
Ccar1 |
A |
T |
10: 62,586,434 (GRCm39) |
D920E |
unknown |
Het |
Cdc20b |
A |
G |
13: 113,192,478 (GRCm39) |
N57S |
probably benign |
Het |
Cep83 |
G |
A |
10: 94,624,525 (GRCm39) |
E601K |
probably damaging |
Het |
Cldn10 |
A |
T |
14: 119,111,080 (GRCm39) |
I176L |
probably benign |
Het |
Cpeb2 |
T |
C |
5: 43,441,273 (GRCm39) |
|
probably benign |
Het |
Crb1 |
A |
G |
1: 139,265,344 (GRCm39) |
S25P |
probably damaging |
Het |
Cyp3a59 |
A |
T |
5: 146,039,684 (GRCm39) |
Y319F |
probably damaging |
Het |
Dst |
C |
T |
1: 34,240,312 (GRCm39) |
S1561F |
probably damaging |
Het |
Dxo |
C |
T |
17: 35,057,270 (GRCm39) |
R221C |
probably damaging |
Het |
Dynlt4 |
A |
T |
4: 116,985,191 (GRCm39) |
T5S |
probably benign |
Het |
Epc2 |
A |
G |
2: 49,439,984 (GRCm39) |
T801A |
possibly damaging |
Het |
Fndc3a |
C |
A |
14: 72,806,384 (GRCm39) |
C373F |
probably damaging |
Het |
Frmpd1 |
T |
C |
4: 45,283,932 (GRCm39) |
S918P |
probably benign |
Het |
Fuca2 |
A |
G |
10: 13,381,587 (GRCm39) |
T84A |
possibly damaging |
Het |
Garin4 |
G |
A |
1: 190,896,682 (GRCm39) |
|
probably benign |
Het |
Gmeb1 |
A |
T |
4: 131,979,051 (GRCm39) |
N21K |
probably benign |
Het |
Htt |
T |
C |
5: 35,021,718 (GRCm39) |
|
probably benign |
Het |
Igsf1 |
T |
C |
X: 48,880,863 (GRCm39) |
R251G |
possibly damaging |
Het |
Itih4 |
A |
T |
14: 30,619,504 (GRCm39) |
H720L |
probably benign |
Het |
Kank4 |
A |
T |
4: 98,663,073 (GRCm39) |
L705* |
probably null |
Het |
Krt34 |
A |
T |
11: 99,931,854 (GRCm39) |
S122T |
probably benign |
Het |
L1td1 |
A |
G |
4: 98,625,517 (GRCm39) |
T571A |
probably benign |
Het |
Lag3 |
T |
C |
6: 124,886,210 (GRCm39) |
T248A |
possibly damaging |
Het |
Lgi1 |
T |
A |
19: 38,272,629 (GRCm39) |
H133Q |
probably benign |
Het |
Map1a |
A |
T |
2: 121,134,607 (GRCm39) |
T1808S |
probably benign |
Het |
Mcm9 |
T |
C |
10: 53,424,752 (GRCm39) |
T613A |
probably damaging |
Het |
Meaf6 |
A |
G |
4: 124,983,931 (GRCm39) |
I111V |
probably benign |
Het |
Mki67 |
G |
A |
7: 135,296,845 (GRCm39) |
P2730S |
possibly damaging |
Het |
Mlc1 |
A |
C |
15: 88,842,350 (GRCm39) |
C337G |
probably damaging |
Het |
Mrc2 |
T |
A |
11: 105,227,482 (GRCm39) |
Y572N |
probably damaging |
Het |
Mterf3 |
T |
C |
13: 67,070,967 (GRCm39) |
N172S |
possibly damaging |
Het |
Or3a1c |
T |
A |
11: 74,046,196 (GRCm39) |
M72K |
probably benign |
Het |
Or4b1 |
A |
T |
2: 89,979,068 (GRCm39) |
|
probably benign |
Het |
Or4c115 |
T |
A |
2: 88,928,064 (GRCm39) |
D69V |
probably damaging |
Het |
Or5ak4 |
A |
T |
2: 85,161,687 (GRCm39) |
L185H |
probably damaging |
Het |
Or6c6c |
T |
C |
10: 129,541,487 (GRCm39) |
S247P |
probably damaging |
Het |
Padi4 |
T |
G |
4: 140,484,881 (GRCm39) |
T327P |
possibly damaging |
Het |
Pkdrej |
G |
T |
15: 85,702,275 (GRCm39) |
D1220E |
probably benign |
Het |
Prokr2 |
T |
A |
2: 132,215,684 (GRCm39) |
Q259L |
probably damaging |
Het |
Ptbp2 |
C |
A |
3: 119,546,754 (GRCm39) |
D43Y |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ralgps2 |
C |
T |
1: 156,660,500 (GRCm39) |
R237Q |
possibly damaging |
Het |
Rap1gds1 |
C |
A |
3: 138,671,624 (GRCm39) |
|
probably null |
Het |
Saa2 |
T |
A |
7: 46,401,716 (GRCm39) |
M1K |
probably null |
Het |
Samd9l |
T |
C |
6: 3,375,426 (GRCm39) |
I612V |
probably damaging |
Het |
Scn10a |
C |
T |
9: 119,442,692 (GRCm39) |
V1518I |
probably benign |
Het |
Serpina6 |
T |
C |
12: 103,618,012 (GRCm39) |
D267G |
probably damaging |
Het |
Sh2d4b |
A |
G |
14: 40,564,329 (GRCm39) |
|
probably null |
Het |
Sh3bp2 |
T |
C |
5: 34,718,034 (GRCm39) |
V505A |
probably benign |
Het |
Smad2 |
A |
G |
18: 76,395,657 (GRCm39) |
E32G |
possibly damaging |
Het |
Smn1 |
T |
G |
13: 100,263,118 (GRCm39) |
D32E |
probably damaging |
Het |
Spata31d1c |
T |
C |
13: 65,182,883 (GRCm39) |
S142P |
possibly damaging |
Het |
Stk39 |
A |
T |
2: 68,221,293 (GRCm39) |
I210N |
probably damaging |
Het |
Tcte2 |
A |
G |
17: 13,937,899 (GRCm39) |
|
probably benign |
Het |
Tctn3 |
C |
A |
19: 40,597,361 (GRCm39) |
E230* |
probably null |
Het |
Tenm2 |
A |
T |
11: 35,937,896 (GRCm39) |
H1592Q |
probably damaging |
Het |
Tescl |
A |
G |
7: 24,032,668 (GRCm39) |
V219A |
probably damaging |
Het |
Tgm6 |
C |
T |
2: 129,993,660 (GRCm39) |
S633L |
probably benign |
Het |
Tmcc1 |
C |
T |
6: 116,110,924 (GRCm39) |
S123N |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ulk2 |
G |
A |
11: 61,670,581 (GRCm39) |
R992C |
probably damaging |
Het |
Vwa5b1 |
G |
A |
4: 138,332,184 (GRCm39) |
H278Y |
probably damaging |
Het |
Wwp2 |
C |
T |
8: 108,275,121 (GRCm39) |
R373W |
probably damaging |
Het |
Zfp24 |
A |
T |
18: 24,150,399 (GRCm39) |
D170E |
possibly damaging |
Het |
Zfp808 |
T |
C |
13: 62,319,311 (GRCm39) |
I180T |
possibly damaging |
Het |
Zfp820 |
T |
A |
17: 22,037,737 (GRCm39) |
Q530H |
probably benign |
Het |
Zfp975 |
A |
T |
7: 42,311,507 (GRCm39) |
Y369N |
probably benign |
Het |
|
Other mutations in Pga5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01660:Pga5
|
APN |
19 |
10,652,456 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Pga5
|
APN |
19 |
10,654,065 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02069:Pga5
|
APN |
19 |
10,646,763 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02197:Pga5
|
APN |
19 |
10,649,277 (GRCm39) |
splice site |
probably benign |
|
IGL02871:Pga5
|
APN |
19 |
10,649,144 (GRCm39) |
splice site |
probably benign |
|
R0238:Pga5
|
UTSW |
19 |
10,646,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Pga5
|
UTSW |
19 |
10,646,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Pga5
|
UTSW |
19 |
10,646,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Pga5
|
UTSW |
19 |
10,646,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R1941:Pga5
|
UTSW |
19 |
10,646,820 (GRCm39) |
splice site |
probably null |
|
R4354:Pga5
|
UTSW |
19 |
10,652,190 (GRCm39) |
critical splice donor site |
probably null |
|
R4568:Pga5
|
UTSW |
19 |
10,649,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5119:Pga5
|
UTSW |
19 |
10,654,053 (GRCm39) |
missense |
probably benign |
0.00 |
R5738:Pga5
|
UTSW |
19 |
10,647,024 (GRCm39) |
missense |
probably benign |
0.05 |
R5864:Pga5
|
UTSW |
19 |
10,652,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R6176:Pga5
|
UTSW |
19 |
10,649,149 (GRCm39) |
splice site |
probably null |
|
R6270:Pga5
|
UTSW |
19 |
10,652,225 (GRCm39) |
missense |
probably benign |
|
R6990:Pga5
|
UTSW |
19 |
10,646,779 (GRCm39) |
missense |
probably benign |
0.03 |
R8056:Pga5
|
UTSW |
19 |
10,654,161 (GRCm39) |
splice site |
probably benign |
|
R8348:Pga5
|
UTSW |
19 |
10,649,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Pga5
|
UTSW |
19 |
10,649,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Pga5
|
UTSW |
19 |
10,655,308 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9352:Pga5
|
UTSW |
19 |
10,646,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Pga5
|
UTSW |
19 |
10,646,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R9383:Pga5
|
UTSW |
19 |
10,646,897 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Pga5
|
UTSW |
19 |
10,646,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|