Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afmid |
T |
A |
11: 117,725,599 (GRCm39) |
D95E |
possibly damaging |
Het |
Ak7 |
A |
G |
12: 105,708,535 (GRCm39) |
E330G |
probably damaging |
Het |
B3gat2 |
A |
C |
1: 23,802,272 (GRCm39) |
D186A |
probably damaging |
Het |
Baz1a |
G |
A |
12: 55,022,093 (GRCm39) |
T63M |
probably damaging |
Het |
Bhmt2 |
A |
T |
13: 93,799,779 (GRCm39) |
M219K |
probably benign |
Het |
Cd200r1 |
A |
G |
16: 44,609,975 (GRCm39) |
T65A |
probably benign |
Het |
Cdc14a |
T |
C |
3: 116,087,676 (GRCm39) |
E494G |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,385,686 (GRCm39) |
L2198P |
probably damaging |
Het |
Col4a2 |
T |
A |
8: 11,449,739 (GRCm39) |
D117E |
probably damaging |
Het |
Ddr2 |
C |
A |
1: 169,814,623 (GRCm39) |
V607L |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,729,687 (GRCm39) |
Y763C |
probably damaging |
Het |
Ecscr |
T |
A |
18: 35,849,857 (GRCm39) |
T93S |
probably benign |
Het |
Eogt |
C |
T |
6: 97,097,139 (GRCm39) |
R321H |
probably damaging |
Het |
Fam174c |
G |
A |
10: 80,008,963 (GRCm39) |
G55E |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,784,635 (GRCm39) |
S873P |
probably damaging |
Het |
Gm29735 |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
7: 141,710,266 (GRCm39) |
|
probably benign |
Het |
Gm8247 |
A |
G |
14: 44,823,859 (GRCm39) |
I182V |
|
Het |
Gpatch2 |
T |
C |
1: 186,958,394 (GRCm39) |
S250P |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,244,859 (GRCm39) |
D183G |
probably benign |
Het |
Hspa5 |
T |
C |
2: 34,665,138 (GRCm39) |
V433A |
probably damaging |
Het |
Igkv8-30 |
C |
A |
6: 70,094,590 (GRCm39) |
Q4H |
probably benign |
Het |
Igkv8-30 |
T |
G |
6: 70,094,591 (GRCm39) |
Q4P |
probably damaging |
Het |
Kcnj5 |
T |
G |
9: 32,233,472 (GRCm39) |
N281T |
probably damaging |
Het |
L1td1 |
A |
G |
4: 98,624,855 (GRCm39) |
E350G |
possibly damaging |
Het |
Layn |
T |
C |
9: 50,985,173 (GRCm39) |
T128A |
possibly damaging |
Het |
Liph |
T |
C |
16: 21,814,089 (GRCm39) |
M11V |
probably benign |
Het |
Lrp1b |
C |
T |
2: 40,691,524 (GRCm39) |
|
probably null |
Het |
Mcrip1 |
A |
C |
11: 120,435,505 (GRCm39) |
|
probably null |
Het |
Myh1 |
G |
A |
11: 67,098,285 (GRCm39) |
E486K |
probably damaging |
Het |
Nav1 |
T |
C |
1: 135,398,746 (GRCm39) |
K612R |
possibly damaging |
Het |
Nek10 |
A |
G |
14: 14,846,621 (GRCm38) |
K245E |
probably benign |
Het |
Nipal1 |
T |
A |
5: 72,824,198 (GRCm39) |
S181T |
probably damaging |
Het |
Nme8 |
A |
C |
13: 19,862,053 (GRCm39) |
L192R |
probably damaging |
Het |
Nol7 |
G |
A |
13: 43,560,307 (GRCm39) |
|
probably null |
Het |
Oas1b |
G |
A |
5: 120,955,837 (GRCm39) |
R205H |
not run |
Het |
Or13j1 |
A |
G |
4: 43,706,082 (GRCm39) |
I162T |
possibly damaging |
Het |
Or4f56 |
T |
G |
2: 111,704,167 (GRCm39) |
E11A |
possibly damaging |
Het |
Or5w15 |
A |
G |
2: 87,568,489 (GRCm39) |
Y60H |
probably damaging |
Het |
Pcdhgb6 |
T |
C |
18: 37,876,701 (GRCm39) |
S470P |
probably benign |
Het |
Pdzk1ip1 |
A |
T |
4: 114,946,305 (GRCm39) |
H55L |
possibly damaging |
Het |
Pibf1 |
T |
A |
14: 99,344,752 (GRCm39) |
M124K |
possibly damaging |
Het |
Prr36 |
C |
T |
8: 4,266,458 (GRCm39) |
G31R |
probably damaging |
Het |
Ptchd4 |
C |
A |
17: 42,814,079 (GRCm39) |
A660D |
probably damaging |
Het |
Qsox2 |
A |
G |
2: 26,110,718 (GRCm39) |
V166A |
possibly damaging |
Het |
Rb1cc1 |
A |
T |
1: 6,308,607 (GRCm39) |
Y164F |
probably damaging |
Het |
Rest |
C |
A |
5: 77,430,331 (GRCm39) |
H917N |
probably benign |
Het |
Rlig1 |
T |
C |
10: 100,425,073 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,315,024 (GRCm39) |
C955R |
|
Het |
Scn7a |
T |
A |
2: 66,518,139 (GRCm39) |
N1024I |
possibly damaging |
Het |
Sec11c |
T |
A |
18: 65,947,963 (GRCm39) |
D134E |
probably damaging |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Spo11 |
T |
A |
2: 172,823,985 (GRCm39) |
|
probably null |
Het |
Srd5a3 |
T |
C |
5: 76,301,419 (GRCm39) |
I216T |
probably benign |
Het |
Tcaf3 |
T |
C |
6: 42,570,864 (GRCm39) |
N296S |
probably benign |
Het |
Tepsin |
T |
C |
11: 119,984,643 (GRCm39) |
D259G |
probably damaging |
Het |
Themis |
G |
A |
10: 28,657,873 (GRCm39) |
S300N |
probably benign |
Het |
Trhr2 |
T |
A |
8: 123,087,396 (GRCm39) |
T15S |
probably benign |
Het |
Uts2r |
T |
C |
11: 121,051,706 (GRCm39) |
V190A |
probably benign |
Het |
Vmn2r77 |
A |
C |
7: 86,451,035 (GRCm39) |
D307A |
probably benign |
Het |
Xpa |
G |
T |
4: 46,183,078 (GRCm39) |
T237K |
probably benign |
Het |
Zfp1006 |
A |
T |
8: 129,946,502 (GRCm39) |
C108S |
probably benign |
Het |
Zfp335 |
A |
G |
2: 164,735,164 (GRCm39) |
|
probably null |
Het |
Zfp451 |
A |
T |
1: 33,808,974 (GRCm39) |
D962E |
probably damaging |
Het |
Zfp60 |
A |
G |
7: 27,437,830 (GRCm39) |
T46A |
probably damaging |
Het |
|
Other mutations in Zfy1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0149:Zfy1
|
UTSW |
Y |
726,121 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0361:Zfy1
|
UTSW |
Y |
726,121 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0529:Zfy1
|
UTSW |
Y |
726,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0837:Zfy1
|
UTSW |
Y |
725,850 (GRCm39) |
nonsense |
probably null |
|
R0945:Zfy1
|
UTSW |
Y |
725,983 (GRCm39) |
missense |
probably damaging |
0.98 |
R1163:Zfy1
|
UTSW |
Y |
725,611 (GRCm39) |
missense |
probably damaging |
0.98 |
R1394:Zfy1
|
UTSW |
Y |
725,957 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1806:Zfy1
|
UTSW |
Y |
725,620 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1928:Zfy1
|
UTSW |
Y |
729,733 (GRCm39) |
missense |
unknown |
|
R2374:Zfy1
|
UTSW |
Y |
726,392 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2374:Zfy1
|
UTSW |
Y |
726,391 (GRCm39) |
missense |
probably damaging |
0.99 |
R2889:Zfy1
|
UTSW |
Y |
726,307 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2980:Zfy1
|
UTSW |
Y |
739,054 (GRCm39) |
missense |
unknown |
|
R3437:Zfy1
|
UTSW |
Y |
726,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4454:Zfy1
|
UTSW |
Y |
725,518 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4529:Zfy1
|
UTSW |
Y |
726,511 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4656:Zfy1
|
UTSW |
Y |
729,626 (GRCm39) |
missense |
unknown |
|
R5049:Zfy1
|
UTSW |
Y |
726,004 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5087:Zfy1
|
UTSW |
Y |
732,964 (GRCm39) |
missense |
unknown |
|
R5347:Zfy1
|
UTSW |
Y |
725,950 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5428:Zfy1
|
UTSW |
Y |
726,205 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5825:Zfy1
|
UTSW |
Y |
726,531 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6256:Zfy1
|
UTSW |
Y |
738,765 (GRCm39) |
missense |
unknown |
|
R7065:Zfy1
|
UTSW |
Y |
725,428 (GRCm39) |
missense |
probably benign |
0.33 |
R7134:Zfy1
|
UTSW |
Y |
725,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R7358:Zfy1
|
UTSW |
Y |
735,141 (GRCm39) |
missense |
unknown |
|
R7513:Zfy1
|
UTSW |
Y |
759,852 (GRCm39) |
missense |
unknown |
|
R7747:Zfy1
|
UTSW |
Y |
725,496 (GRCm39) |
nonsense |
probably null |
|
R7900:Zfy1
|
UTSW |
Y |
725,519 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8052:Zfy1
|
UTSW |
Y |
726,004 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8377:Zfy1
|
UTSW |
Y |
725,723 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8795:Zfy1
|
UTSW |
Y |
738,945 (GRCm39) |
missense |
unknown |
|
R8854:Zfy1
|
UTSW |
Y |
726,501 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8936:Zfy1
|
UTSW |
Y |
738,726 (GRCm39) |
missense |
unknown |
|
R9098:Zfy1
|
UTSW |
Y |
725,987 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9146:Zfy1
|
UTSW |
Y |
726,033 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9209:Zfy1
|
UTSW |
Y |
732,990 (GRCm39) |
missense |
unknown |
|
R9310:Zfy1
|
UTSW |
Y |
727,634 (GRCm39) |
missense |
unknown |
|
R9726:Zfy1
|
UTSW |
Y |
725,476 (GRCm39) |
missense |
possibly damaging |
0.53 |
|