Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
G |
T |
5: 124,216,875 (GRCm39) |
Y447* |
probably null |
Het |
Abl2 |
T |
C |
1: 156,386,641 (GRCm39) |
V8A |
probably benign |
Het |
Adam33 |
C |
T |
2: 130,900,257 (GRCm39) |
R103K |
unknown |
Het |
Adamts13 |
G |
T |
2: 26,880,597 (GRCm39) |
A727S |
not run |
Het |
Ajm1 |
A |
T |
2: 25,467,820 (GRCm39) |
L697Q |
probably damaging |
Het |
Alpk2 |
A |
T |
18: 65,439,325 (GRCm39) |
C689* |
probably null |
Het |
Amt |
C |
T |
9: 108,174,414 (GRCm39) |
Q60* |
probably null |
Het |
Ankrd12 |
A |
G |
17: 66,334,245 (GRCm39) |
|
probably null |
Het |
Ankrd28 |
A |
T |
14: 31,428,770 (GRCm39) |
N920K |
probably damaging |
Het |
Ankrd36 |
T |
C |
11: 5,585,359 (GRCm39) |
L390P |
probably damaging |
Het |
Arvcf |
T |
G |
16: 18,207,063 (GRCm39) |
H7Q |
probably benign |
Het |
Asns |
A |
G |
6: 7,677,978 (GRCm39) |
S367P |
probably damaging |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
C7 |
T |
A |
15: 5,037,192 (GRCm39) |
H562L |
probably benign |
Het |
Ccdc77 |
T |
C |
6: 120,327,334 (GRCm39) |
D37G |
probably damaging |
Het |
Cdc14a |
C |
T |
3: 116,198,236 (GRCm39) |
A58T |
probably damaging |
Het |
Cdc42bpb |
C |
T |
12: 111,302,459 (GRCm39) |
|
probably null |
Het |
Cilk1 |
G |
T |
9: 78,042,927 (GRCm39) |
V51F |
probably damaging |
Het |
Corin |
A |
T |
5: 72,458,967 (GRCm39) |
F1068L |
probably benign |
Het |
Epb42 |
T |
G |
2: 120,864,916 (GRCm39) |
K58N |
probably benign |
Het |
Ercc3 |
T |
A |
18: 32,381,296 (GRCm39) |
S371T |
probably damaging |
Het |
Fam193a |
A |
C |
5: 34,588,524 (GRCm39) |
K358Q |
probably damaging |
Het |
Fem1a |
G |
A |
17: 56,564,522 (GRCm39) |
C205Y |
probably benign |
Het |
Fh1 |
G |
A |
1: 175,439,744 (GRCm39) |
T233M |
probably damaging |
Het |
Ftsj3 |
CCTTCTTCTTCTTCTTCT |
CCTTCTTCTTCTTCT |
11: 106,143,377 (GRCm39) |
|
probably benign |
Het |
Gabra6 |
T |
C |
11: 42,207,289 (GRCm39) |
N265S |
probably damaging |
Het |
Gm10801 |
C |
CGTG |
2: 98,494,152 (GRCm39) |
|
probably null |
Het |
Grm6 |
T |
A |
11: 50,753,909 (GRCm39) |
C738S |
probably damaging |
Het |
Gtsf1 |
C |
T |
15: 103,336,996 (GRCm39) |
|
probably benign |
Het |
Hcrtr2 |
T |
A |
9: 76,140,196 (GRCm39) |
Y364F |
probably damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,336 (GRCm39) |
I374V |
probably benign |
Het |
Il31ra |
A |
T |
13: 112,677,785 (GRCm39) |
F250L |
probably benign |
Het |
Iqgap1 |
A |
G |
7: 80,458,807 (GRCm39) |
V37A |
probably benign |
Het |
Izumo3 |
A |
T |
4: 92,033,260 (GRCm39) |
I182K |
probably damaging |
Het |
Kidins220 |
G |
A |
12: 25,038,555 (GRCm39) |
A36T |
probably damaging |
Het |
Lrrtm1 |
G |
T |
6: 77,221,236 (GRCm39) |
R231L |
probably damaging |
Het |
Mical2 |
A |
T |
7: 112,012,183 (GRCm39) |
S678C |
probably damaging |
Het |
Mme |
T |
G |
3: 63,272,288 (GRCm39) |
F629C |
probably damaging |
Het |
Muc5b |
T |
A |
7: 141,411,078 (GRCm39) |
H1341Q |
unknown |
Het |
Or13a28 |
A |
G |
7: 140,217,637 (GRCm39) |
T8A |
possibly damaging |
Het |
Or13p5 |
T |
A |
4: 118,592,099 (GRCm39) |
D124E |
probably damaging |
Het |
Or2y1e |
A |
G |
11: 49,219,029 (GRCm39) |
S264G |
probably benign |
Het |
Or5e1 |
A |
T |
7: 108,354,776 (GRCm39) |
T238S |
probably damaging |
Het |
Or5p70 |
A |
G |
7: 107,995,296 (GRCm39) |
H323R |
probably benign |
Het |
Parm1 |
A |
T |
5: 91,741,724 (GRCm39) |
M31L |
probably benign |
Het |
Pcdhb18 |
G |
A |
18: 37,622,874 (GRCm39) |
C68Y |
probably benign |
Het |
Pkn3 |
A |
T |
2: 29,969,634 (GRCm39) |
E35V |
probably damaging |
Het |
Pla2g4a |
A |
T |
1: 149,748,495 (GRCm39) |
Y238N |
probably damaging |
Het |
Pld6 |
T |
C |
11: 59,678,097 (GRCm39) |
D122G |
probably damaging |
Het |
Prag1 |
G |
T |
8: 36,570,409 (GRCm39) |
A331S |
possibly damaging |
Het |
Rbm44 |
A |
G |
1: 91,096,551 (GRCm39) |
D970G |
probably benign |
Het |
Rps6kc1 |
A |
G |
1: 190,505,851 (GRCm39) |
V1037A |
probably benign |
Het |
Slc12a7 |
T |
C |
13: 73,953,588 (GRCm39) |
V766A |
probably benign |
Het |
St3gal3 |
T |
C |
4: 117,797,320 (GRCm39) |
M308V |
probably benign |
Het |
Stx19 |
T |
C |
16: 62,642,649 (GRCm39) |
L155S |
probably benign |
Het |
Tespa1 |
A |
T |
10: 130,192,752 (GRCm39) |
T145S |
probably damaging |
Het |
Timm21 |
A |
C |
18: 84,965,846 (GRCm39) |
F221V |
possibly damaging |
Het |
Tlr1 |
A |
T |
5: 65,082,264 (GRCm39) |
F771Y |
probably damaging |
Het |
Tmem150a |
C |
A |
6: 72,335,606 (GRCm39) |
L125I |
unknown |
Het |
Try4 |
T |
C |
6: 41,279,229 (GRCm39) |
L4P |
possibly damaging |
Het |
Txlna |
C |
T |
4: 129,525,950 (GRCm39) |
R299H |
probably damaging |
Het |
Txndc16 |
A |
T |
14: 45,382,417 (GRCm39) |
N609K |
probably benign |
Het |
Upf1 |
T |
C |
8: 70,805,508 (GRCm39) |
T46A |
probably benign |
Het |
Zfp266 |
T |
C |
9: 20,411,626 (GRCm39) |
N184D |
probably benign |
Het |
Zfp407 |
A |
G |
18: 84,228,047 (GRCm39) |
V1854A |
possibly damaging |
Het |
Zfp626 |
T |
A |
7: 27,517,795 (GRCm39) |
C259S |
possibly damaging |
Het |
|
Other mutations in Spata18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00228:Spata18
|
APN |
5 |
73,815,097 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01331:Spata18
|
APN |
5 |
73,827,024 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01394:Spata18
|
APN |
5 |
73,836,688 (GRCm39) |
splice site |
probably null |
|
IGL01994:Spata18
|
APN |
5 |
73,814,944 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02192:Spata18
|
APN |
5 |
73,829,861 (GRCm39) |
splice site |
probably null |
|
IGL02253:Spata18
|
APN |
5 |
73,825,939 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03195:Spata18
|
APN |
5 |
73,828,591 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03204:Spata18
|
APN |
5 |
73,828,449 (GRCm39) |
splice site |
probably benign |
|
ANU74:Spata18
|
UTSW |
5 |
73,828,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Spata18
|
UTSW |
5 |
73,824,224 (GRCm39) |
missense |
probably benign |
0.00 |
R0557:Spata18
|
UTSW |
5 |
73,809,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Spata18
|
UTSW |
5 |
73,826,888 (GRCm39) |
missense |
probably damaging |
0.98 |
R1901:Spata18
|
UTSW |
5 |
73,828,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Spata18
|
UTSW |
5 |
73,834,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Spata18
|
UTSW |
5 |
73,824,244 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2229:Spata18
|
UTSW |
5 |
73,824,244 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2896:Spata18
|
UTSW |
5 |
73,815,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Spata18
|
UTSW |
5 |
73,836,423 (GRCm39) |
intron |
probably benign |
|
R3716:Spata18
|
UTSW |
5 |
73,824,193 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3717:Spata18
|
UTSW |
5 |
73,824,193 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4061:Spata18
|
UTSW |
5 |
73,828,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R4299:Spata18
|
UTSW |
5 |
73,824,245 (GRCm39) |
missense |
probably benign |
0.36 |
R4963:Spata18
|
UTSW |
5 |
73,836,336 (GRCm39) |
missense |
probably damaging |
0.96 |
R5603:Spata18
|
UTSW |
5 |
73,828,575 (GRCm39) |
missense |
probably benign |
0.12 |
R6381:Spata18
|
UTSW |
5 |
73,832,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R6581:Spata18
|
UTSW |
5 |
73,826,859 (GRCm39) |
missense |
probably benign |
0.14 |
R7062:Spata18
|
UTSW |
5 |
73,816,636 (GRCm39) |
missense |
probably benign |
0.08 |
R7591:Spata18
|
UTSW |
5 |
73,829,759 (GRCm39) |
missense |
|
|
R7682:Spata18
|
UTSW |
5 |
73,826,008 (GRCm39) |
missense |
|
|
R7688:Spata18
|
UTSW |
5 |
73,809,005 (GRCm39) |
missense |
probably benign |
0.14 |
R8051:Spata18
|
UTSW |
5 |
73,827,063 (GRCm39) |
missense |
|
|
R8765:Spata18
|
UTSW |
5 |
73,825,992 (GRCm39) |
missense |
|
|
R8951:Spata18
|
UTSW |
5 |
73,828,572 (GRCm39) |
missense |
probably damaging |
0.99 |
R9505:Spata18
|
UTSW |
5 |
73,809,017 (GRCm39) |
critical splice donor site |
probably null |
|
R9514:Spata18
|
UTSW |
5 |
73,829,840 (GRCm39) |
missense |
|
|
R9515:Spata18
|
UTSW |
5 |
73,829,840 (GRCm39) |
missense |
|
|
X0061:Spata18
|
UTSW |
5 |
73,824,202 (GRCm39) |
missense |
possibly damaging |
0.68 |
|