Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadl |
T |
C |
1: 66,876,128 (GRCm39) |
I398V |
probably benign |
Het |
Adcy4 |
A |
T |
14: 56,011,013 (GRCm39) |
C635S |
probably benign |
Het |
Aoc1l3 |
A |
G |
6: 48,964,052 (GRCm39) |
H20R |
probably benign |
Het |
Asic4 |
C |
A |
1: 75,427,967 (GRCm39) |
D164E |
possibly damaging |
Het |
C8g |
T |
A |
2: 25,388,823 (GRCm39) |
*203L |
probably null |
Het |
Cad |
T |
C |
5: 31,212,330 (GRCm39) |
V11A |
probably benign |
Het |
Cckar |
T |
C |
5: 53,860,247 (GRCm39) |
N194S |
probably damaging |
Het |
Chrm5 |
T |
C |
2: 112,310,706 (GRCm39) |
T137A |
probably damaging |
Het |
Cyp1a1 |
A |
G |
9: 57,609,724 (GRCm39) |
|
probably benign |
Het |
Dapk3 |
G |
T |
10: 81,026,437 (GRCm39) |
E187* |
probably null |
Het |
Dmtf1 |
T |
C |
5: 9,190,474 (GRCm39) |
E80G |
probably damaging |
Het |
Dusp19 |
T |
A |
2: 80,461,279 (GRCm39) |
N189K |
probably damaging |
Het |
Gfral |
A |
G |
9: 76,104,520 (GRCm39) |
V164A |
possibly damaging |
Het |
Hk1 |
A |
T |
10: 62,107,578 (GRCm39) |
V799E |
probably damaging |
Het |
Iars2 |
C |
T |
1: 185,055,013 (GRCm39) |
|
probably null |
Het |
Jcad |
T |
A |
18: 4,675,153 (GRCm39) |
Y972N |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,425,505 (GRCm39) |
D708E |
probably damaging |
Het |
Mbtd1 |
T |
A |
11: 93,815,316 (GRCm39) |
H301Q |
probably benign |
Het |
Med12 |
A |
G |
X: 100,339,461 (GRCm39) |
T2004A |
probably benign |
Het |
Mib1 |
T |
C |
18: 10,798,356 (GRCm39) |
I739T |
possibly damaging |
Het |
Mthfsd |
C |
T |
8: 121,835,018 (GRCm39) |
|
probably benign |
Het |
Mybpc3 |
T |
G |
2: 90,954,234 (GRCm39) |
F369C |
probably damaging |
Het |
Nfatc2 |
C |
T |
2: 168,376,904 (GRCm39) |
V329M |
probably damaging |
Het |
Ngef |
A |
T |
1: 87,437,114 (GRCm39) |
|
probably null |
Het |
Nlrp1b |
T |
C |
11: 71,059,685 (GRCm39) |
E759G |
probably benign |
Het |
Or10aa3 |
C |
A |
1: 173,878,191 (GRCm39) |
T84N |
probably benign |
Het |
Prdm4 |
T |
C |
10: 85,729,016 (GRCm39) |
E790G |
probably benign |
Het |
Psmd12 |
A |
G |
11: 107,376,607 (GRCm39) |
D81G |
probably benign |
Het |
Rnf144b |
A |
G |
13: 47,396,359 (GRCm39) |
H232R |
probably damaging |
Het |
Sec63 |
C |
T |
10: 42,686,905 (GRCm39) |
T475M |
possibly damaging |
Het |
Slc16a4 |
A |
T |
3: 107,208,102 (GRCm39) |
N204I |
probably benign |
Het |
Socs1 |
T |
C |
16: 10,602,404 (GRCm39) |
N111S |
probably damaging |
Het |
Srpra |
A |
G |
9: 35,126,017 (GRCm39) |
N432D |
probably damaging |
Het |
Srrm2 |
A |
G |
17: 24,034,708 (GRCm39) |
|
probably benign |
Het |
Tgoln1 |
A |
G |
6: 72,593,055 (GRCm39) |
S142P |
possibly damaging |
Het |
Trbv13-1 |
A |
G |
6: 41,093,169 (GRCm39) |
N34S |
probably benign |
Het |
Vmn2r26 |
T |
C |
6: 124,016,754 (GRCm39) |
V406A |
possibly damaging |
Het |
Vsig1 |
G |
T |
X: 139,827,088 (GRCm39) |
G79V |
probably damaging |
Het |
|
Other mutations in Cdc123 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Cdc123
|
APN |
2 |
5,809,746 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00422:Cdc123
|
APN |
2 |
5,803,260 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01860:Cdc123
|
APN |
2 |
5,808,752 (GRCm39) |
splice site |
probably benign |
|
Sinking
|
UTSW |
2 |
5,803,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0563:Cdc123
|
UTSW |
2 |
5,803,212 (GRCm39) |
missense |
probably benign |
|
R1412:Cdc123
|
UTSW |
2 |
5,808,776 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1584:Cdc123
|
UTSW |
2 |
5,808,788 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1838:Cdc123
|
UTSW |
2 |
5,799,702 (GRCm39) |
splice site |
probably null |
|
R2064:Cdc123
|
UTSW |
2 |
5,800,354 (GRCm39) |
splice site |
probably benign |
|
R2144:Cdc123
|
UTSW |
2 |
5,815,617 (GRCm39) |
missense |
probably benign |
0.19 |
R4082:Cdc123
|
UTSW |
2 |
5,815,566 (GRCm39) |
intron |
probably benign |
|
R4679:Cdc123
|
UTSW |
2 |
5,849,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Cdc123
|
UTSW |
2 |
5,809,748 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5089:Cdc123
|
UTSW |
2 |
5,809,811 (GRCm39) |
missense |
probably benign |
0.00 |
R5112:Cdc123
|
UTSW |
2 |
5,809,748 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5691:Cdc123
|
UTSW |
2 |
5,827,986 (GRCm39) |
missense |
probably benign |
0.00 |
R5914:Cdc123
|
UTSW |
2 |
5,803,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7860:Cdc123
|
UTSW |
2 |
5,808,775 (GRCm39) |
missense |
probably benign |
0.00 |
R8695:Cdc123
|
UTSW |
2 |
5,826,174 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8865:Cdc123
|
UTSW |
2 |
5,800,235 (GRCm39) |
intron |
probably benign |
|
R9018:Cdc123
|
UTSW |
2 |
5,849,683 (GRCm39) |
missense |
probably benign |
0.00 |
R9265:Cdc123
|
UTSW |
2 |
5,808,765 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Cdc123
|
UTSW |
2 |
5,809,796 (GRCm39) |
missense |
probably damaging |
0.97 |
|