Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
G |
T |
5: 124,078,812 (GRCm38) |
Y447* |
probably null |
Het |
Abl2 |
T |
C |
1: 156,559,071 (GRCm38) |
V8A |
probably benign |
Het |
Adam33 |
C |
T |
2: 131,058,337 (GRCm38) |
R103K |
unknown |
Het |
Adamts13 |
G |
T |
2: 26,990,585 (GRCm38) |
A727S |
not run |
Het |
Alpk2 |
A |
T |
18: 65,306,254 (GRCm38) |
C689* |
probably null |
Het |
Amt |
C |
T |
9: 108,297,215 (GRCm38) |
Q60* |
probably null |
Het |
Ankrd12 |
A |
G |
17: 66,027,250 (GRCm38) |
|
probably null |
Het |
Ankrd28 |
A |
T |
14: 31,706,813 (GRCm38) |
N920K |
probably damaging |
Het |
Ankrd36 |
T |
C |
11: 5,635,359 (GRCm38) |
L390P |
probably damaging |
Het |
Arvcf |
T |
G |
16: 18,389,198 (GRCm38) |
H7Q |
probably benign |
Het |
Asns |
A |
G |
6: 7,677,978 (GRCm38) |
S367P |
probably damaging |
Het |
BC005537 |
C |
T |
13: 24,803,399 (GRCm38) |
R7W |
possibly damaging |
Het |
C7 |
T |
A |
15: 5,007,710 (GRCm38) |
H562L |
probably benign |
Het |
Ccdc77 |
T |
C |
6: 120,350,373 (GRCm38) |
D37G |
probably damaging |
Het |
Cdc14a |
C |
T |
3: 116,404,587 (GRCm38) |
A58T |
probably damaging |
Het |
Cdc42bpb |
C |
T |
12: 111,336,025 (GRCm38) |
|
probably null |
Het |
Corin |
A |
T |
5: 72,301,624 (GRCm38) |
F1068L |
probably benign |
Het |
Epb42 |
T |
G |
2: 121,034,435 (GRCm38) |
K58N |
probably benign |
Het |
Ercc3 |
T |
A |
18: 32,248,243 (GRCm38) |
S371T |
probably damaging |
Het |
Fam193a |
A |
C |
5: 34,431,180 (GRCm38) |
K358Q |
probably damaging |
Het |
Fem1a |
G |
A |
17: 56,257,522 (GRCm38) |
C205Y |
probably benign |
Het |
Fh1 |
G |
A |
1: 175,612,178 (GRCm38) |
T233M |
probably damaging |
Het |
Ftsj3 |
CCTTCTTCTTCTTCTTCT |
CCTTCTTCTTCTTCT |
11: 106,252,551 (GRCm38) |
|
probably benign |
Het |
Gabra6 |
T |
C |
11: 42,316,462 (GRCm38) |
N265S |
probably damaging |
Het |
Gm10801 |
C |
CGTG |
2: 98,663,807 (GRCm38) |
|
probably null |
Het |
Gm996 |
A |
T |
2: 25,577,808 (GRCm38) |
L697Q |
probably damaging |
Het |
Grm6 |
T |
A |
11: 50,863,082 (GRCm38) |
C738S |
probably damaging |
Het |
Gtsf1 |
C |
T |
15: 103,428,569 (GRCm38) |
|
probably benign |
Het |
Hcrtr2 |
T |
A |
9: 76,232,914 (GRCm38) |
Y364F |
probably damaging |
Het |
Ick |
G |
T |
9: 78,135,645 (GRCm38) |
V51F |
probably damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,593,936 (GRCm38) |
I374V |
probably benign |
Het |
Il31ra |
A |
T |
13: 112,541,251 (GRCm38) |
F250L |
probably benign |
Het |
Iqgap1 |
A |
G |
7: 80,809,059 (GRCm38) |
V37A |
probably benign |
Het |
Izumo3 |
A |
T |
4: 92,145,023 (GRCm38) |
I182K |
probably damaging |
Het |
Kidins220 |
G |
A |
12: 24,988,556 (GRCm38) |
A36T |
probably damaging |
Het |
Lrrtm1 |
G |
T |
6: 77,244,253 (GRCm38) |
R231L |
probably damaging |
Het |
Micalcl |
A |
T |
7: 112,412,976 (GRCm38) |
S678C |
probably damaging |
Het |
Mme |
T |
G |
3: 63,364,867 (GRCm38) |
F629C |
probably damaging |
Het |
Muc5b |
T |
A |
7: 141,857,341 (GRCm38) |
H1341Q |
unknown |
Het |
Olfr1339 |
T |
A |
4: 118,734,902 (GRCm38) |
D124E |
probably damaging |
Het |
Olfr1391 |
A |
G |
11: 49,328,202 (GRCm38) |
S264G |
probably benign |
Het |
Olfr495 |
A |
G |
7: 108,396,089 (GRCm38) |
H323R |
probably benign |
Het |
Olfr513 |
A |
T |
7: 108,755,569 (GRCm38) |
T238S |
probably damaging |
Het |
Olfr61 |
A |
G |
7: 140,637,724 (GRCm38) |
T8A |
possibly damaging |
Het |
Parm1 |
A |
T |
5: 91,593,865 (GRCm38) |
M31L |
probably benign |
Het |
Pcdhb18 |
G |
A |
18: 37,489,821 (GRCm38) |
C68Y |
probably benign |
Het |
Pkn3 |
A |
T |
2: 30,079,622 (GRCm38) |
E35V |
probably damaging |
Het |
Pla2g4a |
A |
T |
1: 149,872,744 (GRCm38) |
Y238N |
probably damaging |
Het |
Pld6 |
T |
C |
11: 59,787,271 (GRCm38) |
D122G |
probably damaging |
Het |
Prag1 |
G |
T |
8: 36,103,255 (GRCm38) |
A331S |
possibly damaging |
Het |
Rbm44 |
A |
G |
1: 91,168,829 (GRCm38) |
D970G |
probably benign |
Het |
Rps6kc1 |
A |
G |
1: 190,773,654 (GRCm38) |
V1037A |
probably benign |
Het |
Slc12a7 |
T |
C |
13: 73,805,469 (GRCm38) |
V766A |
probably benign |
Het |
Spata18 |
A |
G |
5: 73,668,610 (GRCm38) |
T87A |
|
Het |
St3gal3 |
T |
C |
4: 117,940,123 (GRCm38) |
M308V |
probably benign |
Het |
Stx19 |
T |
C |
16: 62,822,286 (GRCm38) |
L155S |
probably benign |
Het |
Tespa1 |
A |
T |
10: 130,356,883 (GRCm38) |
T145S |
probably damaging |
Het |
Timm21 |
A |
C |
18: 84,947,721 (GRCm38) |
F221V |
possibly damaging |
Het |
Tlr1 |
A |
T |
5: 64,924,921 (GRCm38) |
F771Y |
probably damaging |
Het |
Tmem150a |
C |
A |
6: 72,358,623 (GRCm38) |
L125I |
unknown |
Het |
Txlna |
C |
T |
4: 129,632,157 (GRCm38) |
R299H |
probably damaging |
Het |
Txndc16 |
A |
T |
14: 45,144,960 (GRCm38) |
N609K |
probably benign |
Het |
Upf1 |
T |
C |
8: 70,352,858 (GRCm38) |
T46A |
probably benign |
Het |
Zfp266 |
T |
C |
9: 20,500,330 (GRCm38) |
N184D |
probably benign |
Het |
Zfp407 |
A |
G |
18: 84,209,922 (GRCm38) |
V1854A |
possibly damaging |
Het |
Zfp626 |
T |
A |
7: 27,818,370 (GRCm38) |
C259S |
possibly damaging |
Het |
|
Other mutations in Try4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01773:Try4
|
APN |
6 |
41,305,026 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02216:Try4
|
APN |
6 |
41,305,031 (GRCm38) |
missense |
probably benign |
|
R0537:Try4
|
UTSW |
6 |
41,304,362 (GRCm38) |
missense |
probably benign |
|
R0731:Try4
|
UTSW |
6 |
41,304,367 (GRCm38) |
missense |
probably benign |
0.01 |
R1113:Try4
|
UTSW |
6 |
41,305,374 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1833:Try4
|
UTSW |
6 |
41,303,431 (GRCm38) |
missense |
probably damaging |
0.98 |
R2246:Try4
|
UTSW |
6 |
41,305,472 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4131:Try4
|
UTSW |
6 |
41,305,401 (GRCm38) |
nonsense |
probably null |
|
R4414:Try4
|
UTSW |
6 |
41,304,971 (GRCm38) |
missense |
possibly damaging |
0.84 |
R5457:Try4
|
UTSW |
6 |
41,303,421 (GRCm38) |
missense |
probably damaging |
1.00 |
R5707:Try4
|
UTSW |
6 |
41,305,043 (GRCm38) |
missense |
possibly damaging |
0.65 |
R6023:Try4
|
UTSW |
6 |
41,303,421 (GRCm38) |
missense |
probably damaging |
1.00 |
R7131:Try4
|
UTSW |
6 |
41,304,403 (GRCm38) |
missense |
probably benign |
0.03 |
R8051:Try4
|
UTSW |
6 |
41,305,062 (GRCm38) |
missense |
probably damaging |
0.99 |
R9320:Try4
|
UTSW |
6 |
41,305,074 (GRCm38) |
critical splice donor site |
probably null |
|
R9730:Try4
|
UTSW |
6 |
41,305,062 (GRCm38) |
missense |
probably damaging |
1.00 |
RF007:Try4
|
UTSW |
6 |
41,305,363 (GRCm38) |
missense |
probably damaging |
1.00 |
|