Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
C |
11: 120,018,780 (GRCm38) |
V110G |
probably damaging |
Het |
Adcy6 |
A |
C |
15: 98,597,725 (GRCm38) |
|
probably null |
Het |
Adm |
A |
G |
7: 110,629,121 (GRCm38) |
T170A |
probably benign |
Het |
Afap1l2 |
G |
T |
19: 56,930,209 (GRCm38) |
N171K |
probably benign |
Het |
Aph1b |
G |
T |
9: 66,790,618 (GRCm38) |
S112* |
probably null |
Het |
Arhgap23 |
A |
G |
11: 97,452,163 (GRCm38) |
S424G |
probably damaging |
Het |
Asah2 |
T |
A |
19: 32,054,631 (GRCm38) |
N46I |
probably benign |
Het |
Braf |
G |
A |
6: 39,640,549 (GRCm38) |
|
probably benign |
Het |
Brd2 |
C |
T |
17: 34,114,360 (GRCm38) |
R47Q |
probably damaging |
Het |
C2cd5 |
A |
G |
6: 143,012,093 (GRCm38) |
V972A |
probably benign |
Het |
Car9 |
T |
A |
4: 43,511,881 (GRCm38) |
L300H |
probably damaging |
Het |
Chmp3 |
T |
C |
6: 71,552,411 (GRCm38) |
S20P |
probably damaging |
Het |
Chp1 |
A |
G |
2: 119,571,782 (GRCm38) |
N79S |
possibly damaging |
Het |
Cnot2 |
A |
T |
10: 116,498,355 (GRCm38) |
I335N |
probably damaging |
Het |
Cntnap4 |
T |
C |
8: 112,570,151 (GRCm38) |
V6A |
probably benign |
Het |
Ctcf |
T |
A |
8: 105,675,040 (GRCm38) |
|
probably benign |
Het |
Dennd1b |
A |
G |
1: 139,039,986 (GRCm38) |
|
probably benign |
Het |
Dnmbp |
A |
G |
19: 43,856,640 (GRCm38) |
|
probably benign |
Het |
Eef2 |
T |
C |
10: 81,181,586 (GRCm38) |
F782L |
probably benign |
Het |
Eogt |
T |
A |
6: 97,135,233 (GRCm38) |
Y153F |
probably benign |
Het |
Fam81a |
G |
T |
9: 70,096,119 (GRCm38) |
Q237K |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,283,402 (GRCm38) |
T2162S |
probably benign |
Het |
Fcgbpl1 |
T |
A |
7: 28,147,465 (GRCm38) |
C1158S |
probably damaging |
Het |
Gas6 |
T |
C |
8: 13,470,387 (GRCm38) |
I434V |
possibly damaging |
Het |
Gm42417 |
A |
T |
1: 36,532,167 (GRCm38) |
L77Q |
probably damaging |
Het |
Grik3 |
A |
T |
4: 125,623,510 (GRCm38) |
N49Y |
possibly damaging |
Het |
Gucy2e |
A |
T |
11: 69,224,159 (GRCm38) |
V974E |
probably damaging |
Het |
Helz2 |
A |
G |
2: 181,229,656 (GRCm38) |
V2721A |
probably damaging |
Het |
Klhl6 |
GT |
G |
16: 19,956,966 (GRCm38) |
279 |
probably null |
Het |
L3mbtl3 |
T |
C |
10: 26,282,874 (GRCm38) |
|
probably benign |
Het |
Lrrc15 |
A |
T |
16: 30,272,892 (GRCm38) |
V543E |
probably damaging |
Het |
Med13 |
G |
A |
11: 86,276,983 (GRCm38) |
|
probably benign |
Het |
Med25 |
T |
C |
7: 44,892,100 (GRCm38) |
D60G |
probably damaging |
Het |
Mgam |
T |
A |
6: 40,664,892 (GRCm38) |
Y560N |
probably damaging |
Het |
Mlkl |
A |
G |
8: 111,327,873 (GRCm38) |
Y211H |
probably damaging |
Het |
Msl2 |
A |
G |
9: 101,101,294 (GRCm38) |
N289S |
probably benign |
Het |
Nwd2 |
G |
T |
5: 63,806,343 (GRCm38) |
W1090L |
probably damaging |
Het |
Omt2b |
T |
C |
9: 78,328,231 (GRCm38) |
|
probably benign |
Het |
Or4k37 |
A |
G |
2: 111,328,830 (GRCm38) |
D137G |
probably benign |
Het |
Pald1 |
A |
G |
10: 61,341,315 (GRCm38) |
L652P |
probably damaging |
Het |
Pard3b |
T |
A |
1: 62,440,008 (GRCm38) |
|
probably null |
Het |
Prdm15 |
G |
A |
16: 97,794,334 (GRCm38) |
T1098I |
possibly damaging |
Het |
Rock2 |
A |
G |
12: 16,954,953 (GRCm38) |
T436A |
probably benign |
Het |
Sema4c |
A |
T |
1: 36,549,608 (GRCm38) |
D812E |
probably benign |
Het |
Sla |
A |
T |
15: 66,792,249 (GRCm38) |
I91K |
probably benign |
Het |
Slc22a16 |
T |
G |
10: 40,584,967 (GRCm38) |
M255R |
probably damaging |
Het |
Slc49a4 |
A |
T |
16: 35,735,604 (GRCm38) |
V162D |
probably benign |
Het |
Smg8 |
C |
T |
11: 87,086,084 (GRCm38) |
D224N |
possibly damaging |
Het |
Spdef |
A |
T |
17: 27,718,058 (GRCm38) |
D190E |
probably benign |
Het |
Taok1 |
A |
G |
11: 77,573,804 (GRCm38) |
I152T |
probably damaging |
Het |
Tmem220 |
A |
G |
11: 67,025,922 (GRCm38) |
D36G |
probably damaging |
Het |
Tmem235 |
A |
C |
11: 117,864,351 (GRCm38) |
I210L |
probably benign |
Het |
Tmem266 |
C |
T |
9: 55,380,884 (GRCm38) |
|
probably null |
Het |
Tmprss12 |
A |
G |
15: 100,281,039 (GRCm38) |
|
probably benign |
Het |
Trim32 |
G |
A |
4: 65,613,254 (GRCm38) |
R16Q |
probably damaging |
Het |
Usp38 |
T |
A |
8: 80,984,424 (GRCm38) |
|
probably benign |
Het |
Usp44 |
C |
T |
10: 93,846,806 (GRCm38) |
P373S |
possibly damaging |
Het |
Vmn1r209 |
G |
T |
13: 22,805,948 (GRCm38) |
Q191K |
probably damaging |
Het |
Vmn1r70 |
T |
C |
7: 10,634,026 (GRCm38) |
I147T |
probably benign |
Het |
Vmn2r107 |
T |
A |
17: 20,375,132 (GRCm38) |
I649N |
probably damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,091,889 (GRCm38) |
Y269* |
probably null |
Het |
Zan |
C |
T |
5: 137,412,676 (GRCm38) |
|
probably benign |
Het |
Zfp616 |
G |
T |
11: 74,083,480 (GRCm38) |
V192L |
probably benign |
Het |
Zfp644 |
A |
T |
5: 106,638,333 (GRCm38) |
V116D |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,584,650 (GRCm38) |
|
probably benign |
Het |
Zhx3 |
A |
T |
2: 160,779,994 (GRCm38) |
L751* |
probably null |
Het |
Znfx1 |
T |
A |
2: 167,055,411 (GRCm38) |
Q531L |
probably benign |
Het |
|
Other mutations in Krt73 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01082:Krt73
|
APN |
15 |
101,798,937 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL01768:Krt73
|
APN |
15 |
101,798,856 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01836:Krt73
|
APN |
15 |
101,795,896 (GRCm38) |
missense |
probably benign |
0.38 |
IGL02058:Krt73
|
APN |
15 |
101,802,021 (GRCm38) |
missense |
probably benign |
|
IGL02063:Krt73
|
APN |
15 |
101,795,769 (GRCm38) |
splice site |
probably benign |
|
IGL02076:Krt73
|
APN |
15 |
101,799,935 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02878:Krt73
|
APN |
15 |
101,798,826 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03127:Krt73
|
APN |
15 |
101,795,840 (GRCm38) |
missense |
probably benign |
|
R0032:Krt73
|
UTSW |
15 |
101,794,052 (GRCm38) |
missense |
probably benign |
0.30 |
R0109:Krt73
|
UTSW |
15 |
101,796,395 (GRCm38) |
nonsense |
probably null |
|
R0143:Krt73
|
UTSW |
15 |
101,800,773 (GRCm38) |
missense |
probably damaging |
1.00 |
R0233:Krt73
|
UTSW |
15 |
101,802,016 (GRCm38) |
missense |
probably benign |
0.12 |
R0233:Krt73
|
UTSW |
15 |
101,802,016 (GRCm38) |
missense |
probably benign |
0.12 |
R0254:Krt73
|
UTSW |
15 |
101,799,889 (GRCm38) |
splice site |
probably benign |
|
R0256:Krt73
|
UTSW |
15 |
101,801,936 (GRCm38) |
missense |
probably damaging |
1.00 |
R1592:Krt73
|
UTSW |
15 |
101,802,239 (GRCm38) |
nonsense |
probably null |
|
R1681:Krt73
|
UTSW |
15 |
101,802,047 (GRCm38) |
missense |
possibly damaging |
0.70 |
R1696:Krt73
|
UTSW |
15 |
101,799,909 (GRCm38) |
missense |
probably damaging |
1.00 |
R1766:Krt73
|
UTSW |
15 |
101,793,928 (GRCm38) |
missense |
probably damaging |
1.00 |
R2031:Krt73
|
UTSW |
15 |
101,798,764 (GRCm38) |
splice site |
probably benign |
|
R2171:Krt73
|
UTSW |
15 |
101,800,910 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4674:Krt73
|
UTSW |
15 |
101,802,075 (GRCm38) |
missense |
probably benign |
0.22 |
R4777:Krt73
|
UTSW |
15 |
101,794,001 (GRCm38) |
missense |
probably benign |
|
R4869:Krt73
|
UTSW |
15 |
101,796,398 (GRCm38) |
missense |
probably damaging |
1.00 |
R4892:Krt73
|
UTSW |
15 |
101,795,809 (GRCm38) |
missense |
probably damaging |
0.99 |
R5794:Krt73
|
UTSW |
15 |
101,794,829 (GRCm38) |
missense |
probably benign |
0.00 |
R6807:Krt73
|
UTSW |
15 |
101,796,407 (GRCm38) |
missense |
probably damaging |
1.00 |
R6885:Krt73
|
UTSW |
15 |
101,796,398 (GRCm38) |
missense |
probably damaging |
1.00 |
R7489:Krt73
|
UTSW |
15 |
101,793,859 (GRCm38) |
missense |
probably benign |
0.00 |
R7682:Krt73
|
UTSW |
15 |
101,802,045 (GRCm38) |
missense |
probably benign |
0.08 |
R9167:Krt73
|
UTSW |
15 |
101,793,970 (GRCm38) |
missense |
probably benign |
0.00 |
R9795:Krt73
|
UTSW |
15 |
101,802,290 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Krt73
|
UTSW |
15 |
101,793,811 (GRCm38) |
missense |
probably damaging |
1.00 |
|