Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030458C11Rik |
G |
T |
15: 12,818,031 (GRCm39) |
D138E |
probably benign |
Het |
Atp13a5 |
A |
G |
16: 29,140,480 (GRCm39) |
S359P |
possibly damaging |
Het |
Bcam |
T |
C |
7: 19,494,331 (GRCm39) |
D355G |
probably damaging |
Het |
Bmp8a |
C |
A |
4: 123,236,476 (GRCm39) |
W9L |
unknown |
Het |
Cacul1 |
A |
T |
19: 60,517,904 (GRCm39) |
Y334* |
probably null |
Het |
Ccdc178 |
A |
T |
18: 22,242,933 (GRCm39) |
N227K |
probably benign |
Het |
Ceacam2 |
T |
C |
7: 25,217,561 (GRCm39) |
N318S |
possibly damaging |
Het |
Cntrl |
T |
A |
2: 35,019,833 (GRCm39) |
S553R |
possibly damaging |
Het |
Ctsa |
T |
A |
2: 164,679,284 (GRCm39) |
M331K |
probably benign |
Het |
Cyp2c38 |
T |
A |
19: 39,426,748 (GRCm39) |
Q184H |
probably benign |
Het |
Cyp2c70 |
C |
T |
19: 40,172,364 (GRCm39) |
E93K |
possibly damaging |
Het |
D430041D05Rik |
C |
T |
2: 104,071,500 (GRCm39) |
V1267M |
probably damaging |
Het |
Ddias |
C |
T |
7: 92,508,773 (GRCm39) |
A381T |
possibly damaging |
Het |
Dnhd1 |
G |
A |
7: 105,352,935 (GRCm39) |
C2696Y |
probably benign |
Het |
Efr3a |
G |
A |
15: 65,701,679 (GRCm39) |
V198I |
probably benign |
Het |
Farp2 |
T |
C |
1: 93,497,738 (GRCm39) |
F256S |
probably damaging |
Het |
Fga |
A |
G |
3: 82,938,219 (GRCm39) |
Y198C |
probably damaging |
Het |
Gabpa |
T |
A |
16: 84,657,387 (GRCm39) |
C421S |
probably damaging |
Het |
Gm21798 |
A |
T |
15: 64,689,714 (GRCm39) |
|
probably benign |
Het |
Gm21798 |
A |
T |
15: 64,689,716 (GRCm39) |
|
probably benign |
Het |
Gm7145 |
A |
C |
1: 117,913,874 (GRCm39) |
N252T |
possibly damaging |
Het |
H2-Q6 |
T |
C |
17: 35,647,335 (GRCm39) |
*327R |
probably null |
Het |
H6pd |
T |
C |
4: 150,066,919 (GRCm39) |
D489G |
probably benign |
Het |
Htra2 |
A |
G |
6: 83,030,812 (GRCm39) |
|
probably benign |
Het |
Ice1 |
T |
G |
13: 70,751,421 (GRCm39) |
E1555A |
possibly damaging |
Het |
Inpp5d |
T |
A |
1: 87,609,402 (GRCm39) |
|
probably null |
Het |
Itih2 |
T |
C |
2: 10,120,077 (GRCm39) |
D320G |
probably damaging |
Het |
Kif1a |
T |
G |
1: 92,967,524 (GRCm39) |
H1129P |
possibly damaging |
Het |
Kmt2a |
G |
A |
9: 44,729,704 (GRCm39) |
|
probably benign |
Het |
L3mbtl4 |
G |
A |
17: 69,084,915 (GRCm39) |
D609N |
probably damaging |
Het |
Lgals9 |
A |
T |
11: 78,856,832 (GRCm39) |
D248E |
probably benign |
Het |
Lhx9 |
ACC |
ACCC |
1: 138,769,544 (GRCm39) |
|
probably null |
Het |
Msh3 |
A |
G |
13: 92,449,080 (GRCm39) |
|
probably null |
Het |
Mtus2 |
A |
G |
5: 148,043,821 (GRCm39) |
K803R |
probably damaging |
Het |
Oas1a |
T |
A |
5: 121,045,491 (GRCm39) |
I17L |
possibly damaging |
Het |
Or2h2c |
G |
A |
17: 37,422,400 (GRCm39) |
T158I |
probably benign |
Het |
Or5b121 |
T |
A |
19: 13,507,295 (GRCm39) |
I130K |
possibly damaging |
Het |
Or5k15 |
C |
T |
16: 58,710,121 (GRCm39) |
S154N |
possibly damaging |
Het |
Or5k15 |
T |
A |
16: 58,710,122 (GRCm39) |
S154C |
probably damaging |
Het |
Or7g32 |
T |
G |
9: 19,408,102 (GRCm39) |
Y19* |
probably null |
Het |
Otof |
T |
C |
5: 30,545,583 (GRCm39) |
D539G |
probably damaging |
Het |
Pabpc4 |
T |
C |
4: 123,188,536 (GRCm39) |
Y382H |
possibly damaging |
Het |
Rag1 |
T |
C |
2: 101,472,566 (GRCm39) |
T859A |
probably damaging |
Het |
Ralbp1 |
C |
T |
17: 66,159,751 (GRCm39) |
R504H |
possibly damaging |
Het |
Sdk2 |
A |
G |
11: 113,671,755 (GRCm39) |
F2131S |
probably damaging |
Het |
Sik1 |
A |
T |
17: 32,073,180 (GRCm39) |
|
probably null |
Het |
Sis |
A |
G |
3: 72,798,759 (GRCm39) |
I1763T |
possibly damaging |
Het |
Slc39a6 |
A |
G |
18: 24,732,376 (GRCm39) |
I304T |
possibly damaging |
Het |
Slc5a12 |
A |
G |
2: 110,454,539 (GRCm39) |
S367G |
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,743,738 (GRCm39) |
W476R |
probably damaging |
Het |
Spag17 |
T |
C |
3: 99,920,551 (GRCm39) |
Y429H |
possibly damaging |
Het |
Stt3a |
G |
A |
9: 36,653,023 (GRCm39) |
S553F |
possibly damaging |
Het |
Supt6 |
T |
C |
11: 78,123,656 (GRCm39) |
E38G |
possibly damaging |
Het |
Tenm4 |
G |
A |
7: 96,486,502 (GRCm39) |
G990R |
possibly damaging |
Het |
Thop1 |
T |
C |
10: 80,911,495 (GRCm39) |
|
probably null |
Het |
Thumpd2 |
C |
A |
17: 81,372,459 (GRCm39) |
D11Y |
possibly damaging |
Het |
Tmf1 |
T |
G |
6: 97,145,810 (GRCm39) |
I574L |
probably damaging |
Het |
Tnfaip3 |
A |
G |
10: 18,879,499 (GRCm39) |
V623A |
probably benign |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Ush2a |
T |
G |
1: 188,643,434 (GRCm39) |
Y4265* |
probably null |
Het |
Vamp5 |
G |
A |
6: 72,357,424 (GRCm39) |
|
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,240,771 (GRCm39) |
L114Q |
probably damaging |
Het |
Vmn2r98 |
A |
T |
17: 19,286,063 (GRCm39) |
Y187F |
probably benign |
Het |
|
Other mutations in Sult2a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00896:Sult2a1
|
APN |
7 |
13,566,565 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00990:Sult2a1
|
APN |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
IGL01322:Sult2a1
|
APN |
7 |
13,566,604 (GRCm39) |
nonsense |
probably null |
|
IGL02558:Sult2a1
|
APN |
7 |
13,566,520 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03033:Sult2a1
|
APN |
7 |
13,566,635 (GRCm39) |
splice site |
probably benign |
|
IGL03199:Sult2a1
|
APN |
7 |
13,566,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Sult2a1
|
UTSW |
7 |
13,535,351 (GRCm39) |
missense |
probably benign |
0.01 |
R1903:Sult2a1
|
UTSW |
7 |
13,569,900 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2295:Sult2a1
|
UTSW |
7 |
13,569,884 (GRCm39) |
critical splice donor site |
probably null |
|
R4207:Sult2a1
|
UTSW |
7 |
13,535,472 (GRCm39) |
missense |
probably benign |
0.00 |
R5444:Sult2a1
|
UTSW |
7 |
13,569,944 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6233:Sult2a1
|
UTSW |
7 |
13,566,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Sult2a1
|
UTSW |
7 |
13,569,945 (GRCm39) |
missense |
probably benign |
0.00 |
R7098:Sult2a1
|
UTSW |
7 |
13,549,978 (GRCm39) |
splice site |
probably null |
|
R8948:Sult2a1
|
UTSW |
7 |
13,530,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R8950:Sult2a1
|
UTSW |
7 |
13,530,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R9207:Sult2a1
|
UTSW |
7 |
13,566,627 (GRCm39) |
missense |
probably benign |
0.40 |
Z1088:Sult2a1
|
UTSW |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
Z1088:Sult2a1
|
UTSW |
7 |
13,535,360 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Sult2a1
|
UTSW |
7 |
13,535,339 (GRCm39) |
missense |
probably benign |
|
Z1176:Sult2a1
|
UTSW |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
Z1176:Sult2a1
|
UTSW |
7 |
13,535,360 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Sult2a1
|
UTSW |
7 |
13,535,339 (GRCm39) |
missense |
probably benign |
|
Z1176:Sult2a1
|
UTSW |
7 |
13,569,892 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sult2a1
|
UTSW |
7 |
13,535,360 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Sult2a1
|
UTSW |
7 |
13,535,339 (GRCm39) |
missense |
probably benign |
|
Z1177:Sult2a1
|
UTSW |
7 |
13,530,288 (GRCm39) |
frame shift |
probably null |
|
Z1177:Sult2a1
|
UTSW |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
|