Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933407L21Rik |
T |
A |
1: 85,868,273 (GRCm39) |
|
probably null |
Het |
Adam17 |
G |
A |
12: 21,375,588 (GRCm39) |
R744C |
probably damaging |
Het |
Adss2 |
A |
G |
1: 177,595,335 (GRCm39) |
Y402H |
probably damaging |
Het |
Ccdc73 |
A |
T |
2: 104,821,688 (GRCm39) |
T546S |
possibly damaging |
Het |
Cd22 |
T |
C |
7: 30,569,532 (GRCm39) |
D354G |
possibly damaging |
Het |
Chchd6 |
T |
C |
6: 89,444,433 (GRCm39) |
E183G |
probably damaging |
Het |
Col6a5 |
A |
G |
9: 105,808,129 (GRCm39) |
L973P |
unknown |
Het |
Cp |
T |
C |
3: 20,043,275 (GRCm39) |
L1021P |
probably damaging |
Het |
Cplane1 |
T |
A |
15: 8,201,289 (GRCm39) |
V22E |
probably damaging |
Het |
Cps1 |
C |
A |
1: 67,204,659 (GRCm39) |
T493K |
possibly damaging |
Het |
D630045J12Rik |
A |
G |
6: 38,119,633 (GRCm39) |
V1703A |
possibly damaging |
Het |
Dennd1a |
T |
C |
2: 37,748,089 (GRCm39) |
N376S |
possibly damaging |
Het |
Dmxl1 |
T |
A |
18: 50,011,326 (GRCm39) |
M1161K |
probably damaging |
Het |
Ect2l |
C |
T |
10: 18,044,206 (GRCm39) |
V310M |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,679,465 (GRCm39) |
Y511C |
probably damaging |
Het |
Foxd2 |
T |
C |
4: 114,765,483 (GRCm39) |
H179R |
unknown |
Het |
Gm8674 |
T |
C |
13: 50,056,199 (GRCm39) |
|
noncoding transcript |
Het |
Ice1 |
T |
C |
13: 70,753,489 (GRCm39) |
T866A |
probably benign |
Het |
Jade2 |
C |
T |
11: 51,721,326 (GRCm39) |
V201I |
possibly damaging |
Het |
Kcnb2 |
T |
C |
1: 15,780,639 (GRCm39) |
S504P |
probably damaging |
Het |
Kcng4 |
T |
C |
8: 120,359,986 (GRCm39) |
K130R |
probably benign |
Het |
Lcor |
T |
A |
19: 41,546,795 (GRCm39) |
S126R |
probably damaging |
Het |
Lct |
T |
C |
1: 128,231,963 (GRCm39) |
M629V |
probably damaging |
Het |
Lrch2 |
C |
G |
X: 146,256,003 (GRCm39) |
A437P |
probably damaging |
Het |
Lrrk1 |
C |
T |
7: 65,942,112 (GRCm39) |
V709I |
probably damaging |
Het |
Mdh1 |
A |
G |
11: 21,509,832 (GRCm39) |
V181A |
probably damaging |
Het |
Or10g7 |
A |
G |
9: 39,905,835 (GRCm39) |
H243R |
probably damaging |
Het |
Or4a71 |
T |
A |
2: 89,358,076 (GRCm39) |
H226L |
possibly damaging |
Het |
Ppp1r3a |
A |
C |
6: 14,719,911 (GRCm39) |
D334E |
possibly damaging |
Het |
Pramel17 |
T |
C |
4: 101,692,920 (GRCm39) |
K360R |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rbm45 |
A |
G |
2: 76,205,768 (GRCm39) |
S207G |
probably benign |
Het |
Relch |
A |
G |
1: 105,619,938 (GRCm39) |
N331S |
probably benign |
Het |
Robo3 |
G |
A |
9: 37,333,477 (GRCm39) |
Q723* |
probably null |
Het |
Rreb1 |
G |
A |
13: 38,082,482 (GRCm39) |
|
probably null |
Het |
Slitrk5 |
T |
A |
14: 111,917,229 (GRCm39) |
C284* |
probably null |
Het |
Snapc4 |
G |
A |
2: 26,255,510 (GRCm39) |
Q1005* |
probably null |
Het |
Tent4b |
C |
A |
8: 88,927,043 (GRCm39) |
A151E |
probably benign |
Het |
Tnxb |
A |
G |
17: 34,937,885 (GRCm39) |
D3896G |
probably damaging |
Het |
Tti1 |
A |
G |
2: 157,850,870 (GRCm39) |
V123A |
possibly damaging |
Het |
Usp1 |
T |
C |
4: 98,817,973 (GRCm39) |
C147R |
probably damaging |
Het |
Vill |
A |
G |
9: 118,895,782 (GRCm39) |
N106S |
probably benign |
Het |
|
Other mutations in Slc35f2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Slc35f2
|
APN |
9 |
53,705,298 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01476:Slc35f2
|
APN |
9 |
53,713,990 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01732:Slc35f2
|
APN |
9 |
53,713,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02719:Slc35f2
|
APN |
9 |
53,717,026 (GRCm39) |
splice site |
probably benign |
|
R0449:Slc35f2
|
UTSW |
9 |
53,724,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R1268:Slc35f2
|
UTSW |
9 |
53,705,197 (GRCm39) |
nonsense |
probably null |
|
R1539:Slc35f2
|
UTSW |
9 |
53,716,992 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4748:Slc35f2
|
UTSW |
9 |
53,679,069 (GRCm39) |
start codon destroyed |
probably benign |
0.23 |
R4779:Slc35f2
|
UTSW |
9 |
53,717,013 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5438:Slc35f2
|
UTSW |
9 |
53,708,302 (GRCm39) |
missense |
probably benign |
|
R7308:Slc35f2
|
UTSW |
9 |
53,705,294 (GRCm39) |
missense |
probably benign |
0.00 |
R7520:Slc35f2
|
UTSW |
9 |
53,708,385 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7680:Slc35f2
|
UTSW |
9 |
53,715,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R8293:Slc35f2
|
UTSW |
9 |
53,724,224 (GRCm39) |
missense |
probably benign |
0.27 |
R8483:Slc35f2
|
UTSW |
9 |
53,716,985 (GRCm39) |
nonsense |
probably null |
|
R9733:Slc35f2
|
UTSW |
9 |
53,708,385 (GRCm39) |
missense |
probably benign |
0.08 |
|