Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700109H08Rik |
A |
C |
5: 3,632,194 (GRCm39) |
*25C |
probably null |
Het |
Abca13 |
T |
C |
11: 9,349,387 (GRCm39) |
Y3654H |
probably damaging |
Het |
Ankle1 |
T |
C |
8: 71,861,636 (GRCm39) |
F438S |
probably damaging |
Het |
Atp10a |
A |
T |
7: 58,469,390 (GRCm39) |
R1080S |
probably damaging |
Het |
Ccdc51 |
A |
T |
9: 108,921,252 (GRCm39) |
N380Y |
probably damaging |
Het |
Ccr8 |
A |
T |
9: 119,923,724 (GRCm39) |
I280F |
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,107,786 (GRCm39) |
T535A |
probably benign |
Het |
Cep162 |
G |
T |
9: 87,107,779 (GRCm39) |
T537N |
probably benign |
Het |
Cfap52 |
T |
C |
11: 67,844,964 (GRCm39) |
D35G |
probably benign |
Het |
Cmip |
G |
A |
8: 118,175,827 (GRCm39) |
S530N |
probably damaging |
Het |
Col9a3 |
A |
T |
2: 180,248,599 (GRCm39) |
|
probably null |
Het |
Csf3r |
T |
C |
4: 125,931,928 (GRCm39) |
|
probably benign |
Het |
Csk |
C |
T |
9: 57,537,546 (GRCm39) |
E123K |
probably benign |
Het |
Csrnp3 |
G |
A |
2: 65,852,573 (GRCm39) |
E322K |
probably damaging |
Het |
Ddx11 |
A |
T |
17: 66,455,667 (GRCm39) |
I663F |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 30,996,336 (GRCm39) |
M2667L |
possibly damaging |
Het |
Foxred1 |
T |
C |
9: 35,121,429 (GRCm39) |
K40E |
probably damaging |
Het |
Gata2 |
C |
T |
6: 88,176,762 (GRCm39) |
P74S |
probably benign |
Het |
Gdf10 |
T |
G |
14: 33,645,937 (GRCm39) |
C29G |
probably benign |
Het |
Hectd4 |
A |
G |
5: 121,482,848 (GRCm39) |
E3133G |
probably benign |
Het |
Ints8 |
G |
A |
4: 11,218,771 (GRCm39) |
R784W |
probably damaging |
Het |
Lrriq1 |
T |
C |
10: 102,982,144 (GRCm39) |
E1392G |
probably damaging |
Het |
Muc19 |
T |
C |
15: 91,781,816 (GRCm39) |
|
noncoding transcript |
Het |
Myom2 |
A |
T |
8: 15,164,237 (GRCm39) |
D1044V |
probably benign |
Het |
Nphp4 |
G |
T |
4: 152,639,988 (GRCm39) |
R958L |
probably damaging |
Het |
Nup205 |
C |
T |
6: 35,166,859 (GRCm39) |
P293S |
probably damaging |
Het |
Or10ag60 |
T |
C |
2: 87,437,903 (GRCm39) |
I57T |
probably benign |
Het |
Or1e17 |
A |
T |
11: 73,831,651 (GRCm39) |
H193L |
probably benign |
Het |
Plxdc2 |
A |
G |
2: 16,674,409 (GRCm39) |
|
probably benign |
Het |
Pwp2 |
T |
C |
10: 78,014,899 (GRCm39) |
S362G |
probably damaging |
Het |
Siglec1 |
G |
T |
2: 130,916,915 (GRCm39) |
S1113R |
possibly damaging |
Het |
Sirpa |
A |
G |
2: 129,471,989 (GRCm39) |
E472G |
probably damaging |
Het |
Slc39a4 |
G |
T |
15: 76,498,403 (GRCm39) |
L345M |
probably damaging |
Het |
Snx27 |
C |
T |
3: 94,410,188 (GRCm39) |
R496Q |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,527,388 (GRCm39) |
H1215R |
possibly damaging |
Het |
Stau1 |
A |
G |
2: 166,792,768 (GRCm39) |
Y371H |
probably benign |
Het |
Syt16 |
A |
T |
12: 74,281,832 (GRCm39) |
K319* |
probably null |
Het |
Tcf7 |
T |
A |
11: 52,144,797 (GRCm39) |
|
probably benign |
Het |
Tfdp1 |
A |
G |
8: 13,419,546 (GRCm39) |
N92D |
possibly damaging |
Het |
Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
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 |
|
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 |
R6853:Sult2a1
|
UTSW |
7 |
13,535,412 (GRCm39) |
missense |
possibly damaging |
0.50 |
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 |
|
|