Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,126,989 (GRCm39) |
I1227V |
probably benign |
Het |
Acte1 |
G |
T |
7: 143,434,902 (GRCm39) |
|
probably null |
Het |
Adamts17 |
T |
C |
7: 66,489,645 (GRCm39) |
L21P |
probably damaging |
Het |
Adcy1 |
T |
C |
11: 7,094,766 (GRCm39) |
V564A |
probably damaging |
Het |
Adgre1 |
A |
G |
17: 57,748,275 (GRCm39) |
N492D |
probably benign |
Het |
Aldh1b1 |
G |
A |
4: 45,803,811 (GRCm39) |
V450M |
probably damaging |
Het |
Arv1 |
T |
A |
8: 125,457,685 (GRCm39) |
H196Q |
probably damaging |
Het |
Atp9a |
A |
T |
2: 168,517,163 (GRCm39) |
I390N |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,098,969 (GRCm39) |
I1277V |
|
Het |
Capn10 |
T |
C |
1: 92,871,665 (GRCm39) |
|
probably null |
Het |
Casq2 |
A |
G |
3: 102,052,700 (GRCm39) |
D404G |
unknown |
Het |
Cenpf |
T |
C |
1: 189,392,271 (GRCm39) |
|
probably null |
Het |
Cep295nl |
G |
A |
11: 118,224,766 (GRCm39) |
P26L |
possibly damaging |
Het |
Chmp4c |
T |
G |
3: 10,454,974 (GRCm39) |
S214A |
probably benign |
Het |
Chrna5 |
T |
C |
9: 54,912,156 (GRCm39) |
F319L |
probably benign |
Het |
Csmd1 |
G |
T |
8: 16,011,532 (GRCm39) |
T2507K |
probably benign |
Het |
Ctnnd2 |
T |
C |
15: 30,967,037 (GRCm39) |
M996T |
probably damaging |
Het |
Dbf4 |
T |
C |
5: 8,448,102 (GRCm39) |
T328A |
unknown |
Het |
Ddc |
C |
T |
11: 11,779,132 (GRCm39) |
V331I |
probably benign |
Het |
Fads2b |
A |
T |
2: 85,330,649 (GRCm39) |
C219* |
probably null |
Het |
Fat1 |
T |
A |
8: 45,463,498 (GRCm39) |
W1347R |
probably damaging |
Het |
Fbxw21 |
A |
G |
9: 108,986,727 (GRCm39) |
F51L |
probably benign |
Het |
Gng2 |
G |
T |
14: 19,925,961 (GRCm39) |
H44N |
probably damaging |
Het |
Hps5 |
G |
A |
7: 46,438,619 (GRCm39) |
T38I |
possibly damaging |
Het |
Igf2 |
G |
A |
7: 142,208,153 (GRCm39) |
R64C |
probably damaging |
Het |
Inpp4b |
C |
T |
8: 82,759,758 (GRCm39) |
A601V |
probably damaging |
Het |
Kdm2a |
A |
G |
19: 4,395,606 (GRCm39) |
Y342H |
probably benign |
Het |
Kidins220 |
C |
A |
12: 25,107,110 (GRCm39) |
T1430K |
probably benign |
Het |
Knl1 |
T |
C |
2: 118,898,829 (GRCm39) |
C177R |
possibly damaging |
Het |
Kynu |
T |
A |
2: 43,569,768 (GRCm39) |
F350Y |
probably damaging |
Het |
Lama4 |
T |
C |
10: 38,973,137 (GRCm39) |
L1568P |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,618,574 (GRCm39) |
S281T |
|
Het |
Or2y3 |
A |
T |
17: 38,393,629 (GRCm39) |
V80D |
probably damaging |
Het |
Or5h23 |
A |
G |
16: 58,906,802 (GRCm39) |
S15P |
probably benign |
Het |
Or8c19-ps1 |
C |
T |
9: 38,220,463 (GRCm39) |
T124M |
probably benign |
Het |
Orc3 |
G |
A |
4: 34,607,181 (GRCm39) |
R50* |
probably null |
Het |
Osbpl6 |
T |
A |
2: 76,378,716 (GRCm39) |
D124E |
probably damaging |
Het |
Parp4 |
TG |
T |
14: 56,832,790 (GRCm39) |
|
probably null |
Het |
Parp4 |
T |
C |
14: 56,852,224 (GRCm39) |
|
probably null |
Het |
Pcdhb18 |
A |
C |
18: 37,625,004 (GRCm39) |
H778P |
probably benign |
Het |
Polg |
A |
T |
7: 79,105,860 (GRCm39) |
Y710N |
probably benign |
Het |
Ppp2r2b |
C |
A |
18: 42,779,025 (GRCm39) |
R370L |
possibly damaging |
Het |
Raet1e |
C |
T |
10: 22,057,872 (GRCm39) |
T213I |
possibly damaging |
Het |
Reln |
T |
A |
5: 22,193,705 (GRCm39) |
S1418C |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,285,689 (GRCm39) |
S427G |
probably benign |
Het |
Rhobtb2 |
G |
A |
14: 70,025,376 (GRCm39) |
H633Y |
probably damaging |
Het |
Serpina3i |
T |
C |
12: 104,234,881 (GRCm39) |
V404A |
probably damaging |
Het |
Serpinb8 |
T |
C |
1: 107,526,769 (GRCm39) |
|
probably null |
Het |
Sorl1 |
G |
T |
9: 41,900,739 (GRCm39) |
Q1658K |
probably damaging |
Het |
Tmem26 |
G |
A |
10: 68,559,816 (GRCm39) |
W29* |
probably null |
Het |
Togaram2 |
A |
G |
17: 71,996,408 (GRCm39) |
E137G |
probably damaging |
Het |
Ttc39b |
A |
G |
4: 83,151,023 (GRCm39) |
L524S |
probably damaging |
Het |
Usp43 |
T |
C |
11: 67,767,345 (GRCm39) |
N675S |
probably damaging |
Het |
Vmn2r104 |
A |
G |
17: 20,268,439 (GRCm39) |
L10P |
possibly damaging |
Het |
Zbtb1 |
G |
A |
12: 76,432,773 (GRCm39) |
R253Q |
probably damaging |
Het |
Zfp354b |
T |
A |
11: 50,820,256 (GRCm39) |
R36S |
probably damaging |
Het |
|
Other mutations in Krt32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01089:Krt32
|
APN |
11 |
99,978,605 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01454:Krt32
|
APN |
11 |
99,974,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Krt32
|
APN |
11 |
99,978,967 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02502:Krt32
|
APN |
11 |
99,978,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02967:Krt32
|
APN |
11 |
99,974,876 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02799:Krt32
|
UTSW |
11 |
99,978,733 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0840:Krt32
|
UTSW |
11 |
99,972,068 (GRCm39) |
missense |
probably benign |
0.00 |
R1503:Krt32
|
UTSW |
11 |
99,974,936 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1944:Krt32
|
UTSW |
11 |
99,975,670 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1945:Krt32
|
UTSW |
11 |
99,975,670 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2426:Krt32
|
UTSW |
11 |
99,977,192 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3774:Krt32
|
UTSW |
11 |
99,978,947 (GRCm39) |
missense |
probably benign |
0.00 |
R3775:Krt32
|
UTSW |
11 |
99,978,947 (GRCm39) |
missense |
probably benign |
0.00 |
R3776:Krt32
|
UTSW |
11 |
99,978,947 (GRCm39) |
missense |
probably benign |
0.00 |
R5522:Krt32
|
UTSW |
11 |
99,977,497 (GRCm39) |
critical splice donor site |
probably null |
|
R5794:Krt32
|
UTSW |
11 |
99,975,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R6109:Krt32
|
UTSW |
11 |
99,978,791 (GRCm39) |
missense |
probably benign |
0.01 |
R6994:Krt32
|
UTSW |
11 |
99,977,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Krt32
|
UTSW |
11 |
99,972,050 (GRCm39) |
missense |
probably benign |
0.18 |
R7577:Krt32
|
UTSW |
11 |
99,972,047 (GRCm39) |
missense |
probably benign |
0.00 |
R8249:Krt32
|
UTSW |
11 |
99,977,548 (GRCm39) |
missense |
probably benign |
0.00 |
R9207:Krt32
|
UTSW |
11 |
99,977,580 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9305:Krt32
|
UTSW |
11 |
99,972,029 (GRCm39) |
missense |
probably benign |
0.00 |
R9684:Krt32
|
UTSW |
11 |
99,977,308 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Krt32
|
UTSW |
11 |
99,979,042 (GRCm39) |
missense |
probably benign |
|
Z1177:Krt32
|
UTSW |
11 |
99,974,895 (GRCm39) |
missense |
possibly damaging |
0.95 |
|