Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh3a2 |
T |
C |
11: 61,153,094 (GRCm39) |
K211E |
probably damaging |
Het |
Apba2 |
G |
T |
7: 64,393,020 (GRCm39) |
A514S |
probably damaging |
Het |
Aspm |
C |
T |
1: 139,389,182 (GRCm39) |
T615I |
probably benign |
Het |
Atrnl1 |
T |
A |
19: 57,766,359 (GRCm39) |
F1232Y |
probably benign |
Het |
B4galt3 |
A |
G |
1: 171,101,617 (GRCm39) |
D197G |
probably damaging |
Het |
Calcrl |
T |
G |
2: 84,200,400 (GRCm39) |
N127H |
possibly damaging |
Het |
Camkv |
T |
G |
9: 107,825,262 (GRCm39) |
I421S |
possibly damaging |
Het |
Cdc123 |
T |
C |
2: 5,808,765 (GRCm39) |
D237G |
possibly damaging |
Het |
Cilp |
A |
G |
9: 65,187,333 (GRCm39) |
T1143A |
probably benign |
Het |
Col5a1 |
G |
A |
2: 27,854,123 (GRCm39) |
R569K |
unknown |
Het |
Cpn1 |
T |
C |
19: 43,958,599 (GRCm39) |
I201V |
probably damaging |
Het |
Cr1l |
T |
C |
1: 194,806,027 (GRCm39) |
D152G |
probably benign |
Het |
Csf2rb |
A |
T |
15: 78,232,746 (GRCm39) |
E684D |
probably benign |
Het |
Csmd2 |
A |
T |
4: 128,294,163 (GRCm39) |
N1164I |
|
Het |
Ddx42 |
A |
G |
11: 106,132,435 (GRCm39) |
N486S |
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,060,040 (GRCm39) |
I2848T |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,674,505 (GRCm39) |
D424G |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,732,081 (GRCm39) |
H4275R |
probably benign |
Het |
Epha6 |
G |
A |
16: 59,476,117 (GRCm39) |
T1083M |
probably damaging |
Het |
Fzd1 |
A |
G |
5: 4,807,216 (GRCm39) |
I122T |
probably damaging |
Het |
Gm28042 |
T |
C |
2: 119,871,705 (GRCm39) |
F914S |
probably damaging |
Het |
Gpatch11 |
A |
G |
17: 79,146,547 (GRCm39) |
D64G |
probably benign |
Het |
Hinfp |
A |
G |
9: 44,209,083 (GRCm39) |
V345A |
possibly damaging |
Het |
Hoxd8 |
C |
T |
2: 74,536,115 (GRCm39) |
S75L |
probably benign |
Het |
Igsf1 |
A |
G |
X: 48,884,191 (GRCm39) |
M2T |
possibly damaging |
Het |
Mcm3 |
C |
A |
1: 20,879,905 (GRCm39) |
D531Y |
probably damaging |
Het |
Msantd1 |
C |
T |
5: 35,080,861 (GRCm39) |
R264* |
probably null |
Het |
Nadk2 |
A |
G |
15: 9,071,774 (GRCm39) |
T65A |
probably damaging |
Het |
Nbea |
AC |
A |
3: 55,998,393 (GRCm39) |
|
probably null |
Het |
Neb |
T |
C |
2: 52,089,456 (GRCm39) |
D5172G |
probably null |
Het |
Nlrp9a |
G |
T |
7: 26,258,038 (GRCm39) |
R552I |
possibly damaging |
Het |
Nr3c2 |
A |
G |
8: 77,636,236 (GRCm39) |
T446A |
probably benign |
Het |
Or4x11 |
T |
C |
2: 89,867,842 (GRCm39) |
I193T |
probably benign |
Het |
Or51g2 |
C |
T |
7: 102,623,112 (GRCm39) |
W29* |
probably null |
Het |
Or52s6 |
C |
A |
7: 103,092,165 (GRCm39) |
R55L |
possibly damaging |
Het |
Or7g21 |
T |
A |
9: 19,032,984 (GRCm39) |
C241* |
probably null |
Het |
Pcdhb10 |
A |
G |
18: 37,546,553 (GRCm39) |
Q543R |
possibly damaging |
Het |
Pcdhga6 |
A |
G |
18: 37,841,102 (GRCm39) |
H274R |
possibly damaging |
Het |
Pknox1 |
A |
G |
17: 31,809,672 (GRCm39) |
D92G |
probably damaging |
Het |
Pnpla6 |
C |
T |
8: 3,573,294 (GRCm39) |
P386L |
probably benign |
Het |
Rlf |
G |
C |
4: 121,007,487 (GRCm39) |
P608A |
possibly damaging |
Het |
Sardh |
A |
T |
2: 27,105,065 (GRCm39) |
I686N |
probably damaging |
Het |
Sstr3 |
G |
T |
15: 78,423,792 (GRCm39) |
N318K |
probably damaging |
Het |
St6gal1 |
A |
G |
16: 23,140,168 (GRCm39) |
Y113C |
probably damaging |
Het |
Syndig1 |
T |
C |
2: 149,845,160 (GRCm39) |
F228L |
probably damaging |
Het |
Ttll5 |
T |
A |
12: 85,937,795 (GRCm39) |
C375* |
probably null |
Het |
Zscan4c |
T |
A |
7: 10,740,824 (GRCm39) |
S114R |
probably benign |
Het |
|
Other mutations in Krt42 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01411:Krt42
|
APN |
11 |
100,154,167 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4377001:Krt42
|
UTSW |
11 |
100,153,931 (GRCm39) |
missense |
probably damaging |
0.97 |
R0135:Krt42
|
UTSW |
11 |
100,153,985 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0535:Krt42
|
UTSW |
11 |
100,155,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R1169:Krt42
|
UTSW |
11 |
100,154,171 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1456:Krt42
|
UTSW |
11 |
100,160,436 (GRCm39) |
missense |
probably benign |
0.04 |
R1456:Krt42
|
UTSW |
11 |
100,160,435 (GRCm39) |
missense |
probably benign |
0.00 |
R1913:Krt42
|
UTSW |
11 |
100,158,075 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4655:Krt42
|
UTSW |
11 |
100,160,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R5527:Krt42
|
UTSW |
11 |
100,154,121 (GRCm39) |
unclassified |
probably benign |
|
R6049:Krt42
|
UTSW |
11 |
100,157,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Krt42
|
UTSW |
11 |
100,160,542 (GRCm39) |
missense |
probably benign |
0.00 |
R7748:Krt42
|
UTSW |
11 |
100,157,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R7979:Krt42
|
UTSW |
11 |
100,155,865 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8030:Krt42
|
UTSW |
11 |
100,155,865 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8031:Krt42
|
UTSW |
11 |
100,155,865 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8063:Krt42
|
UTSW |
11 |
100,155,865 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8108:Krt42
|
UTSW |
11 |
100,157,783 (GRCm39) |
missense |
probably benign |
0.01 |
R9040:Krt42
|
UTSW |
11 |
100,157,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Krt42
|
UTSW |
11 |
100,155,867 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1177:Krt42
|
UTSW |
11 |
100,157,894 (GRCm39) |
missense |
probably damaging |
0.98 |
|