Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apol10a |
A |
T |
15: 77,373,068 (GRCm39) |
I235F |
probably damaging |
Het |
Aspn |
A |
T |
13: 49,712,352 (GRCm39) |
E222D |
probably benign |
Het |
Cfap221 |
A |
T |
1: 119,881,948 (GRCm39) |
V280D |
possibly damaging |
Het |
Chrd |
G |
A |
16: 20,560,316 (GRCm39) |
R922Q |
probably benign |
Het |
Cnga4 |
T |
A |
7: 105,056,172 (GRCm39) |
V361E |
probably damaging |
Het |
Col15a1 |
T |
A |
4: 47,284,467 (GRCm39) |
|
probably null |
Het |
Col6a4 |
A |
G |
9: 105,877,656 (GRCm39) |
V2107A |
possibly damaging |
Het |
Eea1 |
G |
T |
10: 95,825,493 (GRCm39) |
V63F |
probably benign |
Het |
Eml1 |
A |
G |
12: 108,504,432 (GRCm39) |
H797R |
possibly damaging |
Het |
Il1r2 |
A |
G |
1: 40,151,167 (GRCm39) |
T141A |
probably benign |
Het |
Il6st |
T |
C |
13: 112,631,832 (GRCm39) |
V457A |
probably benign |
Het |
Kif19b |
T |
A |
5: 140,461,767 (GRCm39) |
V523E |
probably damaging |
Het |
Lrrc56 |
T |
C |
7: 140,789,578 (GRCm39) |
C532R |
probably benign |
Het |
Lrrn4 |
T |
C |
2: 132,721,749 (GRCm39) |
S23G |
unknown |
Het |
Mapk8ip3 |
A |
T |
17: 25,125,148 (GRCm39) |
D498E |
probably benign |
Het |
Mcam |
T |
C |
9: 44,052,241 (GRCm39) |
F584S |
possibly damaging |
Het |
Mdga1 |
A |
T |
17: 30,188,912 (GRCm39) |
D50E |
unknown |
Het |
Mga |
T |
C |
2: 119,765,695 (GRCm39) |
S1320P |
probably damaging |
Het |
Muc5b |
G |
A |
7: 141,405,307 (GRCm39) |
G905D |
unknown |
Het |
Ncor2 |
T |
C |
5: 125,100,687 (GRCm39) |
N1297S |
|
Het |
Nisch |
A |
G |
14: 30,896,364 (GRCm39) |
V946A |
unknown |
Het |
Npc1l1 |
A |
G |
11: 6,168,320 (GRCm39) |
F957S |
probably damaging |
Het |
Nuggc |
A |
G |
14: 65,857,057 (GRCm39) |
N402S |
probably damaging |
Het |
Nup210l |
A |
G |
3: 90,025,854 (GRCm39) |
T159A |
probably benign |
Het |
Or10g6 |
A |
T |
9: 39,933,961 (GRCm39) |
I91F |
probably benign |
Het |
Otud1 |
A |
G |
2: 19,663,873 (GRCm39) |
D334G |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,731,608 (GRCm39) |
V3370A |
unknown |
Het |
Prdm16 |
A |
G |
4: 154,429,910 (GRCm39) |
L353P |
probably damaging |
Het |
Prepl |
A |
C |
17: 85,389,420 (GRCm39) |
V128G |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,478,791 (GRCm39) |
V568A |
probably damaging |
Het |
Rab10 |
G |
T |
12: 3,306,891 (GRCm39) |
S101R |
probably benign |
Het |
Rfx3 |
C |
T |
19: 27,779,858 (GRCm39) |
R435Q |
probably damaging |
Het |
Rnf213 |
A |
T |
11: 119,322,582 (GRCm39) |
|
probably null |
Het |
Sema5a |
A |
G |
15: 32,417,608 (GRCm39) |
D26G |
probably benign |
Het |
Spata31d1b |
G |
A |
13: 59,865,446 (GRCm39) |
V865I |
probably benign |
Het |
Sycp3 |
A |
T |
10: 88,305,428 (GRCm39) |
Q176H |
probably damaging |
Het |
Tdpoz8 |
G |
T |
3: 92,981,475 (GRCm39) |
M90I |
probably damaging |
Het |
Tmprss11d |
A |
T |
5: 86,485,098 (GRCm39) |
V102D |
probably damaging |
Het |
Top1mt |
A |
G |
15: 75,535,931 (GRCm39) |
V457A |
probably benign |
Het |
Tubal3 |
T |
A |
13: 3,980,675 (GRCm39) |
I129N |
probably damaging |
Het |
Ubr3 |
G |
A |
2: 69,809,677 (GRCm39) |
D1217N |
probably damaging |
Het |
Uggt1 |
A |
G |
1: 36,201,302 (GRCm39) |
I1146T |
probably damaging |
Het |
Umod |
T |
C |
7: 119,076,250 (GRCm39) |
Q172R |
probably benign |
Het |
Uqcc5 |
G |
T |
14: 30,846,555 (GRCm39) |
R55S |
probably damaging |
Het |
Zdbf2 |
C |
T |
1: 63,342,563 (GRCm39) |
A314V |
possibly damaging |
Het |
Zfp787 |
A |
T |
7: 6,136,039 (GRCm39) |
C71S |
possibly damaging |
Het |
Zhx2 |
C |
T |
15: 57,686,824 (GRCm39) |
A731V |
probably benign |
Het |
|
Other mutations in Slc49a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01125:Slc49a3
|
APN |
5 |
108,592,458 (GRCm39) |
splice site |
probably benign |
|
R0239:Slc49a3
|
UTSW |
5 |
108,591,882 (GRCm39) |
splice site |
probably benign |
|
R0551:Slc49a3
|
UTSW |
5 |
108,592,331 (GRCm39) |
splice site |
probably benign |
|
R2086:Slc49a3
|
UTSW |
5 |
108,593,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Slc49a3
|
UTSW |
5 |
108,592,573 (GRCm39) |
missense |
probably benign |
0.04 |
R4663:Slc49a3
|
UTSW |
5 |
108,590,011 (GRCm39) |
missense |
probably benign |
0.01 |
R4713:Slc49a3
|
UTSW |
5 |
108,589,945 (GRCm39) |
missense |
probably damaging |
0.97 |
R5560:Slc49a3
|
UTSW |
5 |
108,596,729 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R5950:Slc49a3
|
UTSW |
5 |
108,593,351 (GRCm39) |
missense |
probably damaging |
0.98 |
R6618:Slc49a3
|
UTSW |
5 |
108,590,964 (GRCm39) |
missense |
probably benign |
0.16 |
R7107:Slc49a3
|
UTSW |
5 |
108,596,581 (GRCm39) |
splice site |
probably null |
|
R7369:Slc49a3
|
UTSW |
5 |
108,593,394 (GRCm39) |
missense |
probably benign |
0.09 |
R7384:Slc49a3
|
UTSW |
5 |
108,593,926 (GRCm39) |
missense |
probably damaging |
0.96 |
R7502:Slc49a3
|
UTSW |
5 |
108,591,646 (GRCm39) |
splice site |
probably null |
|
R7585:Slc49a3
|
UTSW |
5 |
108,596,685 (GRCm39) |
missense |
probably benign |
|
R7863:Slc49a3
|
UTSW |
5 |
108,593,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Slc49a3
|
UTSW |
5 |
108,592,363 (GRCm39) |
missense |
probably benign |
0.09 |
R8909:Slc49a3
|
UTSW |
5 |
108,592,432 (GRCm39) |
missense |
probably benign |
0.00 |
R8976:Slc49a3
|
UTSW |
5 |
108,589,897 (GRCm39) |
missense |
probably benign |
0.01 |
R9063:Slc49a3
|
UTSW |
5 |
108,590,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R9277:Slc49a3
|
UTSW |
5 |
108,589,864 (GRCm39) |
missense |
probably benign |
|
R9797:Slc49a3
|
UTSW |
5 |
108,593,403 (GRCm39) |
missense |
probably benign |
0.01 |
|