Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
A |
T |
19: 57,119,434 (GRCm39) |
|
probably null |
Het |
Adpgk |
T |
C |
9: 59,222,300 (GRCm39) |
V409A |
probably benign |
Het |
Agfg2 |
A |
T |
5: 137,665,966 (GRCm39) |
F98I |
probably damaging |
Het |
Arhgap17 |
A |
T |
7: 122,885,791 (GRCm39) |
|
probably benign |
Het |
Asb8 |
T |
C |
15: 98,040,614 (GRCm39) |
Y16C |
probably damaging |
Het |
Atp6v0a2 |
C |
T |
5: 124,779,485 (GRCm39) |
T200I |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Ccnt1 |
A |
T |
15: 98,441,797 (GRCm39) |
D490E |
probably benign |
Het |
Cenpf |
G |
T |
1: 189,389,445 (GRCm39) |
D1462E |
probably damaging |
Het |
Clcn6 |
C |
T |
4: 148,095,202 (GRCm39) |
R736H |
probably damaging |
Het |
Col4a2 |
A |
T |
8: 11,479,358 (GRCm39) |
D747V |
probably benign |
Het |
Cplane1 |
A |
G |
15: 8,299,190 (GRCm39) |
E3126G |
unknown |
Het |
Crybg3 |
T |
C |
16: 59,377,907 (GRCm39) |
T1116A |
probably damaging |
Het |
Csf1r |
T |
A |
18: 61,243,368 (GRCm39) |
L128Q |
probably damaging |
Het |
Ddx17 |
A |
T |
15: 79,422,789 (GRCm39) |
D316E |
probably damaging |
Het |
Ect2l |
T |
A |
10: 18,017,712 (GRCm39) |
D681V |
possibly damaging |
Het |
Ell2 |
A |
T |
13: 75,912,105 (GRCm39) |
K464* |
probably null |
Het |
Eme1 |
G |
T |
11: 94,541,645 (GRCm39) |
P59Q |
probably damaging |
Het |
Etl4 |
T |
C |
2: 20,294,821 (GRCm39) |
S2P |
possibly damaging |
Het |
Fndc9 |
T |
C |
11: 46,128,576 (GRCm39) |
Y32H |
probably damaging |
Het |
Frem1 |
G |
T |
4: 82,877,614 (GRCm39) |
T1321K |
probably benign |
Het |
Gabrg2 |
A |
G |
11: 41,867,418 (GRCm39) |
V67A |
probably benign |
Het |
Gm4553 |
ACAGCAGCTGGACTGACAGCAGCAGGGCTTGCAACAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAG |
ACAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAG |
7: 141,718,602 (GRCm39) |
|
probably benign |
Het |
Gm5145 |
A |
C |
17: 20,790,900 (GRCm39) |
I93L |
possibly damaging |
Het |
Gpld1 |
T |
A |
13: 25,146,758 (GRCm39) |
V240E |
probably damaging |
Het |
Gsc |
T |
A |
12: 104,439,131 (GRCm39) |
S82C |
possibly damaging |
Het |
H2-T10 |
C |
T |
17: 36,431,143 (GRCm39) |
E173K |
probably benign |
Het |
Ifi213 |
A |
T |
1: 173,394,784 (GRCm39) |
S584T |
probably benign |
Het |
Klk1b1 |
T |
C |
7: 43,620,669 (GRCm39) |
I253T |
probably damaging |
Het |
Klra4 |
A |
G |
6: 130,040,113 (GRCm39) |
L53P |
probably damaging |
Het |
Lct |
A |
G |
1: 128,216,722 (GRCm39) |
Y1697H |
probably benign |
Het |
Mrs2 |
T |
A |
13: 25,202,549 (GRCm39) |
D64V |
possibly damaging |
Het |
Muc13 |
A |
G |
16: 33,636,211 (GRCm39) |
Q565R |
probably damaging |
Het |
Nlrp6 |
T |
C |
7: 140,507,353 (GRCm39) |
V873A |
possibly damaging |
Het |
Nup155 |
C |
T |
15: 8,145,926 (GRCm39) |
P159L |
possibly damaging |
Het |
Or10v1 |
A |
T |
19: 11,873,898 (GRCm39) |
H171L |
probably benign |
Het |
Or4m1 |
A |
T |
14: 50,557,573 (GRCm39) |
S240T |
probably damaging |
Het |
Or51a6 |
T |
C |
7: 102,604,887 (GRCm39) |
|
probably null |
Het |
Phip |
T |
G |
9: 82,772,203 (GRCm39) |
M1115L |
probably benign |
Het |
Ppip5k1 |
T |
C |
2: 121,142,390 (GRCm39) |
Q1353R |
probably damaging |
Het |
Ptprb |
C |
G |
10: 116,205,333 (GRCm39) |
P1896A |
probably benign |
Het |
Rgl2 |
T |
C |
17: 34,154,799 (GRCm39) |
L601P |
possibly damaging |
Het |
Sash1 |
C |
T |
10: 8,656,328 (GRCm39) |
W221* |
probably null |
Het |
Skint1 |
A |
C |
4: 111,876,399 (GRCm39) |
T107P |
probably damaging |
Het |
Slc45a4 |
G |
A |
15: 73,477,621 (GRCm39) |
|
probably benign |
Het |
Snx13 |
T |
A |
12: 35,150,624 (GRCm39) |
D309E |
probably benign |
Het |
Spcs1 |
A |
G |
14: 30,722,628 (GRCm39) |
Y64H |
probably benign |
Het |
Tep1 |
A |
T |
14: 51,064,308 (GRCm39) |
Y2434N |
possibly damaging |
Het |
Tnpo3 |
T |
C |
6: 29,568,990 (GRCm39) |
E454G |
possibly damaging |
Het |
Tsg101 |
G |
T |
7: 46,563,183 (GRCm39) |
Q24K |
probably benign |
Het |
Ttc6 |
C |
T |
12: 57,735,353 (GRCm39) |
R1132W |
probably damaging |
Het |
Uts2r |
G |
A |
11: 121,052,234 (GRCm39) |
S366N |
probably benign |
Het |
Wbp4 |
A |
T |
14: 79,709,845 (GRCm39) |
V130E |
probably damaging |
Het |
Zfp592 |
T |
G |
7: 80,674,469 (GRCm39) |
S478A |
probably benign |
Het |
Zfp664 |
A |
T |
5: 124,962,839 (GRCm39) |
K78* |
probably null |
Het |
Zfp738 |
A |
T |
13: 67,821,110 (GRCm39) |
L79* |
probably null |
Het |
Zfyve28 |
C |
T |
5: 34,382,326 (GRCm39) |
R258Q |
probably damaging |
Het |
|
Other mutations in Unkl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01655:Unkl
|
APN |
17 |
25,429,822 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02011:Unkl
|
APN |
17 |
25,437,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02141:Unkl
|
APN |
17 |
25,448,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Unkl
|
UTSW |
17 |
25,449,685 (GRCm39) |
missense |
probably damaging |
0.96 |
R0394:Unkl
|
UTSW |
17 |
25,449,751 (GRCm39) |
critical splice donor site |
probably null |
|
R0638:Unkl
|
UTSW |
17 |
25,427,057 (GRCm39) |
splice site |
probably benign |
|
R1364:Unkl
|
UTSW |
17 |
25,408,597 (GRCm39) |
missense |
probably benign |
|
R1596:Unkl
|
UTSW |
17 |
25,424,707 (GRCm39) |
missense |
probably null |
1.00 |
R1899:Unkl
|
UTSW |
17 |
25,448,434 (GRCm39) |
splice site |
probably null |
|
R1960:Unkl
|
UTSW |
17 |
25,428,619 (GRCm39) |
splice site |
probably benign |
|
R3774:Unkl
|
UTSW |
17 |
25,407,381 (GRCm39) |
splice site |
probably null |
|
R3927:Unkl
|
UTSW |
17 |
25,448,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R5164:Unkl
|
UTSW |
17 |
25,432,083 (GRCm39) |
splice site |
probably null |
|
R5481:Unkl
|
UTSW |
17 |
25,420,146 (GRCm39) |
nonsense |
probably null |
|
R5520:Unkl
|
UTSW |
17 |
25,424,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R5559:Unkl
|
UTSW |
17 |
25,424,687 (GRCm39) |
missense |
probably benign |
0.00 |
R6267:Unkl
|
UTSW |
17 |
25,450,839 (GRCm39) |
makesense |
probably null |
|
R6296:Unkl
|
UTSW |
17 |
25,450,839 (GRCm39) |
makesense |
probably null |
|
R6883:Unkl
|
UTSW |
17 |
25,449,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R6979:Unkl
|
UTSW |
17 |
25,418,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7752:Unkl
|
UTSW |
17 |
25,437,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R8712:Unkl
|
UTSW |
17 |
25,450,689 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9170:Unkl
|
UTSW |
17 |
25,448,350 (GRCm39) |
missense |
probably benign |
0.00 |
R9331:Unkl
|
UTSW |
17 |
25,450,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Unkl
|
UTSW |
17 |
25,448,392 (GRCm39) |
missense |
probably damaging |
0.99 |
|