Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
G |
A |
11: 58,767,619 (GRCm39) |
E39K |
probably damaging |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Aktip |
T |
A |
8: 91,856,388 (GRCm39) |
S30C |
probably damaging |
Het |
Anxa10 |
G |
T |
8: 62,530,977 (GRCm39) |
H78N |
probably damaging |
Het |
Aoah |
C |
T |
13: 21,095,293 (GRCm39) |
R196W |
probably damaging |
Het |
Arl4c |
A |
T |
1: 88,629,152 (GRCm39) |
W79R |
probably damaging |
Het |
Brd2 |
A |
T |
17: 34,332,669 (GRCm39) |
D178E |
probably benign |
Het |
Cacna1e |
G |
A |
1: 154,577,037 (GRCm39) |
P120L |
probably damaging |
Het |
Cdh16 |
A |
T |
8: 105,342,697 (GRCm39) |
M17K |
probably benign |
Het |
Cdhr17 |
A |
T |
5: 17,029,683 (GRCm39) |
D473V |
probably damaging |
Het |
Chit1 |
A |
G |
1: 134,071,798 (GRCm39) |
T103A |
possibly damaging |
Het |
Clcn3 |
T |
C |
8: 61,387,607 (GRCm39) |
Y214C |
probably damaging |
Het |
Coch |
T |
A |
12: 51,649,536 (GRCm39) |
D282E |
probably damaging |
Het |
Col1a2 |
C |
A |
6: 4,538,035 (GRCm39) |
S1181R |
unknown |
Het |
Col6a2 |
T |
C |
10: 76,442,978 (GRCm39) |
D506G |
probably damaging |
Het |
Crx |
A |
T |
7: 15,602,032 (GRCm39) |
Y215* |
probably null |
Het |
Fasn |
A |
T |
11: 120,713,012 (GRCm39) |
S58T |
probably benign |
Het |
Fhip1a |
T |
C |
3: 85,580,651 (GRCm39) |
E518G |
possibly damaging |
Het |
Garem1 |
A |
T |
18: 21,262,881 (GRCm39) |
D644E |
probably benign |
Het |
H2-Q2 |
A |
C |
17: 35,562,217 (GRCm39) |
T155P |
probably damaging |
Het |
Insr |
A |
T |
8: 3,242,572 (GRCm39) |
I49N |
probably damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Lnpep |
A |
G |
17: 17,773,454 (GRCm39) |
M639T |
probably benign |
Het |
Lypd11 |
G |
A |
7: 24,425,481 (GRCm39) |
A3V |
probably damaging |
Het |
Map3k20 |
C |
T |
2: 72,240,503 (GRCm39) |
S333F |
probably damaging |
Het |
Miga2 |
A |
G |
2: 30,261,229 (GRCm39) |
S175G |
probably benign |
Het |
Muc3a |
A |
T |
5: 137,244,579 (GRCm39) |
I191N |
probably damaging |
Het |
Ncoa2 |
A |
G |
1: 13,244,595 (GRCm39) |
V701A |
probably damaging |
Het |
Nid2 |
T |
C |
14: 19,828,851 (GRCm39) |
V565A |
probably damaging |
Het |
Nova2 |
G |
A |
7: 18,691,794 (GRCm39) |
A244T |
unknown |
Het |
Numbl |
G |
C |
7: 26,980,739 (GRCm39) |
A574P |
probably damaging |
Het |
Oas3 |
A |
G |
5: 120,907,113 (GRCm39) |
V508A |
unknown |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Otx1 |
A |
T |
11: 21,949,406 (GRCm39) |
L24H |
probably damaging |
Het |
Pcdhb21 |
T |
A |
18: 37,647,461 (GRCm39) |
S197T |
probably benign |
Het |
Pck2 |
T |
A |
14: 55,781,419 (GRCm39) |
M180K |
probably damaging |
Het |
Pgr |
T |
C |
9: 8,900,740 (GRCm39) |
V91A |
possibly damaging |
Het |
Phtf1 |
A |
T |
3: 103,911,721 (GRCm39) |
M643L |
probably damaging |
Het |
Prokr1 |
T |
C |
6: 87,565,837 (GRCm39) |
T3A |
possibly damaging |
Het |
Ptgs1 |
T |
C |
2: 36,141,190 (GRCm39) |
Y546H |
probably damaging |
Het |
Rasa1 |
A |
G |
13: 85,374,745 (GRCm39) |
L742P |
probably benign |
Het |
Rbbp6 |
T |
C |
7: 122,596,534 (GRCm39) |
|
probably null |
Het |
Rgs22 |
A |
G |
15: 36,107,194 (GRCm39) |
L64P |
probably damaging |
Het |
Rnf213 |
A |
T |
11: 119,302,296 (GRCm39) |
I407F |
probably damaging |
Het |
Rp1l1 |
C |
T |
14: 64,267,545 (GRCm39) |
P1044S |
probably damaging |
Het |
Scin |
G |
A |
12: 40,110,578 (GRCm39) |
P690L |
probably damaging |
Het |
Septin9 |
T |
C |
11: 117,242,987 (GRCm39) |
L58P |
probably damaging |
Het |
Slc1a7 |
A |
G |
4: 107,869,633 (GRCm39) |
E566G |
probably damaging |
Het |
Speer4f1 |
G |
A |
5: 17,681,140 (GRCm39) |
R6Q |
probably benign |
Het |
Tnxb |
A |
T |
17: 34,890,986 (GRCm39) |
Y443F |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,135,143 (GRCm39) |
I79V |
probably benign |
Het |
Ttll6 |
C |
T |
11: 96,030,568 (GRCm39) |
T245I |
possibly damaging |
Het |
Vmn2r26 |
T |
C |
6: 124,038,444 (GRCm39) |
I673T |
probably damaging |
Het |
|
Other mutations in Zfp60 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03353:Zfp60
|
APN |
7 |
27,447,759 (GRCm39) |
nonsense |
probably null |
|
PIT4494001:Zfp60
|
UTSW |
7 |
27,448,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1281:Zfp60
|
UTSW |
7 |
27,437,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1643:Zfp60
|
UTSW |
7 |
27,436,400 (GRCm39) |
missense |
probably damaging |
0.98 |
R1883:Zfp60
|
UTSW |
7 |
27,449,435 (GRCm39) |
missense |
probably benign |
0.00 |
R1930:Zfp60
|
UTSW |
7 |
27,436,382 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R3623:Zfp60
|
UTSW |
7 |
27,448,753 (GRCm39) |
missense |
probably benign |
0.01 |
R3624:Zfp60
|
UTSW |
7 |
27,448,753 (GRCm39) |
missense |
probably benign |
0.01 |
R3875:Zfp60
|
UTSW |
7 |
27,449,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R5296:Zfp60
|
UTSW |
7 |
27,437,955 (GRCm39) |
intron |
probably benign |
|
R5491:Zfp60
|
UTSW |
7 |
27,447,940 (GRCm39) |
splice site |
probably null |
|
R5724:Zfp60
|
UTSW |
7 |
27,447,758 (GRCm39) |
missense |
probably benign |
|
R6312:Zfp60
|
UTSW |
7 |
27,448,201 (GRCm39) |
missense |
probably damaging |
0.99 |
R6477:Zfp60
|
UTSW |
7 |
27,449,228 (GRCm39) |
missense |
probably benign |
0.00 |
R6649:Zfp60
|
UTSW |
7 |
27,448,151 (GRCm39) |
missense |
probably benign |
0.00 |
R6653:Zfp60
|
UTSW |
7 |
27,448,151 (GRCm39) |
missense |
probably benign |
0.00 |
R7041:Zfp60
|
UTSW |
7 |
27,448,451 (GRCm39) |
missense |
probably benign |
0.05 |
R7166:Zfp60
|
UTSW |
7 |
27,448,937 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7185:Zfp60
|
UTSW |
7 |
27,437,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R7334:Zfp60
|
UTSW |
7 |
27,448,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Zfp60
|
UTSW |
7 |
27,448,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Zfp60
|
UTSW |
7 |
27,448,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R7561:Zfp60
|
UTSW |
7 |
27,447,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Zfp60
|
UTSW |
7 |
27,447,740 (GRCm39) |
missense |
probably benign |
0.00 |
R7961:Zfp60
|
UTSW |
7 |
27,447,881 (GRCm39) |
missense |
probably benign |
0.01 |
|