Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,247,203 (GRCm39) |
S2317G |
probably benign |
Het |
Acap2 |
A |
C |
16: 30,926,934 (GRCm39) |
L502R |
probably benign |
Het |
Amotl2 |
A |
G |
9: 102,605,549 (GRCm39) |
E467G |
probably damaging |
Het |
Apbb1ip |
A |
T |
2: 22,743,147 (GRCm39) |
|
probably null |
Het |
Armc9 |
C |
G |
1: 86,090,437 (GRCm39) |
D77E |
probably benign |
Het |
Art1 |
T |
A |
7: 101,755,531 (GRCm39) |
S8T |
possibly damaging |
Het |
Asic5 |
G |
A |
3: 81,916,872 (GRCm39) |
A321T |
possibly damaging |
Het |
Astn2 |
A |
G |
4: 66,103,612 (GRCm39) |
I267T |
unknown |
Het |
Bmp8a |
T |
C |
4: 123,236,182 (GRCm39) |
N107S |
probably benign |
Het |
Card14 |
T |
A |
11: 119,228,573 (GRCm39) |
L633Q |
probably damaging |
Het |
Chpf |
C |
T |
1: 75,455,698 (GRCm39) |
V18M |
possibly damaging |
Het |
Cog7 |
T |
C |
7: 121,536,362 (GRCm39) |
I493V |
probably benign |
Het |
Col3a1 |
A |
T |
1: 45,386,971 (GRCm39) |
N1394I |
unknown |
Het |
Crybg1 |
C |
T |
10: 43,873,254 (GRCm39) |
D1285N |
probably benign |
Het |
Depdc7 |
A |
G |
2: 104,553,463 (GRCm39) |
V395A |
possibly damaging |
Het |
Dido1 |
G |
A |
2: 180,329,286 (GRCm39) |
L379F |
probably damaging |
Het |
Dnajc13 |
G |
T |
9: 104,115,713 (GRCm39) |
T32N |
probably benign |
Het |
Dok2 |
T |
A |
14: 71,013,468 (GRCm39) |
S133R |
probably benign |
Het |
Ehbp1l1 |
C |
T |
19: 5,766,410 (GRCm39) |
R1311H |
probably damaging |
Het |
Gm3099 |
A |
T |
14: 15,346,488 (GRCm39) |
N118I |
probably damaging |
Het |
Heg1 |
G |
A |
16: 33,581,160 (GRCm39) |
A13T |
possibly damaging |
Het |
Ifi209 |
A |
T |
1: 173,470,156 (GRCm39) |
Y248F |
possibly damaging |
Het |
Irag1 |
T |
C |
7: 110,498,931 (GRCm39) |
T367A |
possibly damaging |
Het |
Itgb3bp |
C |
G |
4: 99,657,758 (GRCm39) |
E169Q |
probably damaging |
Het |
Kcna2 |
A |
G |
3: 107,012,066 (GRCm39) |
T216A |
probably benign |
Het |
Kcnj6 |
A |
T |
16: 94,742,042 (GRCm39) |
M10K |
probably benign |
Het |
Krt17 |
T |
G |
11: 100,148,163 (GRCm39) |
Q397P |
probably benign |
Het |
Lrtm1 |
T |
A |
14: 28,744,075 (GRCm39) |
M181K |
probably damaging |
Het |
Map3k5 |
A |
G |
10: 19,975,301 (GRCm39) |
H741R |
probably damaging |
Het |
Mier1 |
T |
A |
4: 102,996,599 (GRCm39) |
Y120* |
probably null |
Het |
Myh14 |
T |
A |
7: 44,279,415 (GRCm39) |
T922S |
probably benign |
Het |
Nfkbie |
A |
T |
17: 45,871,067 (GRCm39) |
I240F |
possibly damaging |
Het |
Npas3 |
C |
A |
12: 54,115,824 (GRCm39) |
H915Q |
probably damaging |
Het |
Nrg2 |
A |
T |
18: 36,178,994 (GRCm39) |
V314E |
probably benign |
Het |
Or2z9 |
T |
A |
8: 72,854,190 (GRCm39) |
Y195* |
probably null |
Het |
Pds5a |
T |
C |
5: 65,777,077 (GRCm39) |
N28S |
probably damaging |
Het |
Pira1 |
T |
C |
7: 3,740,493 (GRCm39) |
T243A |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,361,878 (GRCm39) |
N517I |
possibly damaging |
Het |
Plekhb1 |
T |
C |
7: 100,294,874 (GRCm39) |
Y99C |
probably benign |
Het |
Plpp6 |
T |
C |
19: 28,941,617 (GRCm39) |
S73P |
probably benign |
Het |
Polb |
T |
C |
8: 23,129,975 (GRCm39) |
N199S |
probably benign |
Het |
Ppp1r13b |
T |
C |
12: 111,838,840 (GRCm39) |
N13D |
possibly damaging |
Het |
Prorp |
A |
G |
12: 55,351,429 (GRCm39) |
D246G |
probably damaging |
Het |
Ptprn2 |
T |
A |
12: 117,212,164 (GRCm39) |
V862D |
probably damaging |
Het |
Rassf4 |
T |
C |
6: 116,617,278 (GRCm39) |
I242M |
probably damaging |
Het |
Rnf19a |
G |
A |
15: 36,254,598 (GRCm39) |
T320I |
probably damaging |
Het |
Sctr |
A |
T |
1: 119,949,970 (GRCm39) |
E53V |
probably damaging |
Het |
Srcin1 |
T |
C |
11: 97,442,519 (GRCm39) |
D103G |
probably benign |
Het |
St3gal3 |
T |
C |
4: 117,814,633 (GRCm39) |
Q220R |
|
Het |
Stk40 |
G |
A |
4: 126,019,483 (GRCm39) |
E86K |
probably benign |
Het |
Tas2r104 |
T |
A |
6: 131,662,005 (GRCm39) |
I235F |
possibly damaging |
Het |
Terf2ip |
T |
C |
8: 112,738,280 (GRCm39) |
V56A |
possibly damaging |
Het |
Thsd7b |
A |
G |
1: 130,030,890 (GRCm39) |
N1075S |
probably benign |
Het |
Trak1 |
A |
G |
9: 121,245,278 (GRCm39) |
Y51C |
probably benign |
Het |
Trav16n |
T |
A |
14: 53,588,859 (GRCm39) |
V45E |
probably benign |
Het |
Ttc6 |
T |
C |
12: 57,622,837 (GRCm39) |
S79P |
probably damaging |
Het |
Unc79 |
C |
T |
12: 103,029,449 (GRCm39) |
T484M |
probably damaging |
Het |
Usp49 |
T |
C |
17: 47,983,796 (GRCm39) |
V267A |
possibly damaging |
Het |
Vldlr |
T |
A |
19: 27,216,004 (GRCm39) |
D305E |
possibly damaging |
Het |
Vmn1r226 |
G |
T |
17: 20,908,011 (GRCm39) |
C81F |
probably damaging |
Het |
Vmn1r73 |
T |
C |
7: 11,490,824 (GRCm39) |
V214A |
probably damaging |
Het |
Vmn2r5 |
T |
C |
3: 64,411,671 (GRCm39) |
N299S |
probably damaging |
Het |
Vwa3b |
T |
C |
1: 37,203,586 (GRCm39) |
L55S |
probably damaging |
Het |
Wdr90 |
T |
C |
17: 26,070,480 (GRCm39) |
D1105G |
probably benign |
Het |
Zbtb38 |
A |
G |
9: 96,569,480 (GRCm39) |
S535P |
probably damaging |
Het |
Zfp329 |
T |
C |
7: 12,544,826 (GRCm39) |
I233V |
probably damaging |
Het |
Zfp579 |
T |
A |
7: 4,997,582 (GRCm39) |
T110S |
probably benign |
Het |
|
Other mutations in Gtse1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Gtse1
|
APN |
15 |
85,753,018 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01344:Gtse1
|
APN |
15 |
85,746,267 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01541:Gtse1
|
APN |
15 |
85,759,855 (GRCm39) |
nonsense |
probably null |
|
IGL01621:Gtse1
|
APN |
15 |
85,759,283 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01945:Gtse1
|
APN |
15 |
85,755,748 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02193:Gtse1
|
APN |
15 |
85,746,531 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02215:Gtse1
|
APN |
15 |
85,746,799 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02494:Gtse1
|
APN |
15 |
85,751,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02879:Gtse1
|
APN |
15 |
85,753,264 (GRCm39) |
splice site |
probably benign |
|
R0009:Gtse1
|
UTSW |
15 |
85,746,636 (GRCm39) |
missense |
probably benign |
0.06 |
R0047:Gtse1
|
UTSW |
15 |
85,746,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Gtse1
|
UTSW |
15 |
85,746,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R0576:Gtse1
|
UTSW |
15 |
85,753,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Gtse1
|
UTSW |
15 |
85,746,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R1442:Gtse1
|
UTSW |
15 |
85,744,303 (GRCm39) |
splice site |
probably benign |
|
R1623:Gtse1
|
UTSW |
15 |
85,751,779 (GRCm39) |
missense |
probably benign |
|
R1925:Gtse1
|
UTSW |
15 |
85,757,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1928:Gtse1
|
UTSW |
15 |
85,746,264 (GRCm39) |
splice site |
probably benign |
|
R4565:Gtse1
|
UTSW |
15 |
85,759,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5170:Gtse1
|
UTSW |
15 |
85,748,465 (GRCm39) |
critical splice donor site |
probably null |
|
R5310:Gtse1
|
UTSW |
15 |
85,757,993 (GRCm39) |
missense |
probably benign |
0.04 |
R5428:Gtse1
|
UTSW |
15 |
85,746,340 (GRCm39) |
missense |
probably benign |
0.12 |
R5748:Gtse1
|
UTSW |
15 |
85,751,778 (GRCm39) |
missense |
probably benign |
|
R5996:Gtse1
|
UTSW |
15 |
85,748,381 (GRCm39) |
missense |
probably benign |
0.00 |
R6179:Gtse1
|
UTSW |
15 |
85,753,158 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6379:Gtse1
|
UTSW |
15 |
85,748,425 (GRCm39) |
missense |
probably benign |
0.01 |
R6381:Gtse1
|
UTSW |
15 |
85,746,349 (GRCm39) |
missense |
probably benign |
0.00 |
R6434:Gtse1
|
UTSW |
15 |
85,759,370 (GRCm39) |
missense |
probably benign |
0.21 |
R7086:Gtse1
|
UTSW |
15 |
85,759,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Gtse1
|
UTSW |
15 |
85,752,901 (GRCm39) |
missense |
probably benign |
0.04 |
R7580:Gtse1
|
UTSW |
15 |
85,746,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7856:Gtse1
|
UTSW |
15 |
85,748,342 (GRCm39) |
missense |
probably benign |
0.09 |
R8496:Gtse1
|
UTSW |
15 |
85,746,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8674:Gtse1
|
UTSW |
15 |
85,746,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Gtse1
|
UTSW |
15 |
85,753,109 (GRCm39) |
missense |
probably benign |
0.00 |
R9491:Gtse1
|
UTSW |
15 |
85,755,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Gtse1
|
UTSW |
15 |
85,751,697 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Gtse1
|
UTSW |
15 |
85,752,947 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Gtse1
|
UTSW |
15 |
85,759,938 (GRCm39) |
missense |
probably damaging |
0.96 |
|