Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
A |
G |
16: 20,187,214 (GRCm39) |
M924T |
probably benign |
Het |
Afg2a |
A |
G |
3: 37,512,465 (GRCm39) |
|
probably benign |
Het |
B3gat2 |
A |
G |
1: 23,854,360 (GRCm39) |
Y218C |
probably damaging |
Het |
Bcs1l |
T |
C |
1: 74,629,620 (GRCm39) |
|
probably null |
Het |
Cd109 |
T |
A |
9: 78,568,995 (GRCm39) |
I358N |
probably damaging |
Het |
Cd276 |
T |
C |
9: 58,444,719 (GRCm39) |
D84G |
possibly damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,412 (GRCm39) |
F549S |
probably damaging |
Het |
Clca3a2 |
T |
C |
3: 144,787,024 (GRCm39) |
N549S |
probably benign |
Het |
Col23a1 |
G |
A |
11: 51,452,743 (GRCm39) |
|
probably null |
Het |
Ctps1 |
A |
T |
4: 120,420,021 (GRCm39) |
I131K |
probably benign |
Het |
Cyp2w1 |
T |
C |
5: 139,342,628 (GRCm39) |
L441P |
probably damaging |
Het |
Dnajc21 |
A |
G |
15: 10,461,441 (GRCm39) |
Y170H |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,761,164 (GRCm39) |
L648Q |
probably damaging |
Het |
Eif3l |
T |
A |
15: 78,959,477 (GRCm39) |
D6E |
probably benign |
Het |
Fam228a |
A |
T |
12: 4,781,484 (GRCm39) |
L125Q |
probably damaging |
Het |
Foxa2 |
A |
G |
2: 147,886,045 (GRCm39) |
C263R |
possibly damaging |
Het |
Gm17455 |
A |
G |
10: 60,239,107 (GRCm39) |
E124G |
possibly damaging |
Het |
Gpc6 |
T |
G |
14: 117,163,394 (GRCm39) |
L16R |
probably damaging |
Het |
Hdac9 |
A |
G |
12: 34,443,273 (GRCm39) |
|
probably benign |
Het |
Herc3 |
A |
G |
6: 58,845,679 (GRCm39) |
N400S |
probably benign |
Het |
Herc4 |
G |
A |
10: 63,152,586 (GRCm39) |
|
probably null |
Het |
Il12b |
A |
G |
11: 44,301,180 (GRCm39) |
|
probably null |
Het |
Lama4 |
A |
G |
10: 38,932,920 (GRCm39) |
R599G |
probably null |
Het |
Lrp1b |
T |
A |
2: 41,561,069 (GRCm39) |
E286V |
|
Het |
Mink1 |
C |
T |
11: 70,501,176 (GRCm39) |
P784S |
probably damaging |
Het |
Musk |
T |
C |
4: 58,366,921 (GRCm39) |
F513S |
probably benign |
Het |
Nfasc |
T |
A |
1: 132,538,186 (GRCm39) |
D474V |
probably damaging |
Het |
Nhsl3 |
C |
T |
4: 129,117,104 (GRCm39) |
R565H |
probably damaging |
Het |
Nos2 |
T |
G |
11: 78,831,170 (GRCm39) |
F420V |
probably damaging |
Het |
Or52ab2 |
A |
T |
7: 102,970,058 (GRCm39) |
I147L |
probably benign |
Het |
Pcdhb14 |
A |
G |
18: 37,582,904 (GRCm39) |
Y670C |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,944,899 (GRCm39) |
E65G |
probably damaging |
Het |
Ppp1r10 |
T |
G |
17: 36,238,904 (GRCm39) |
|
probably null |
Het |
Prag1 |
C |
T |
8: 36,606,655 (GRCm39) |
R799C |
probably damaging |
Het |
Prb1c |
T |
A |
6: 132,340,008 (GRCm39) |
|
probably null |
Het |
Ptch1 |
T |
C |
13: 63,681,421 (GRCm39) |
N485S |
probably benign |
Het |
Rgsl1 |
T |
C |
1: 153,683,454 (GRCm39) |
T19A |
probably damaging |
Het |
Sgpl1 |
A |
C |
10: 60,937,507 (GRCm39) |
S507A |
probably benign |
Het |
Sgpp2 |
A |
G |
1: 78,393,819 (GRCm39) |
D274G |
probably benign |
Het |
Skap1 |
A |
G |
11: 96,603,843 (GRCm39) |
D211G |
possibly damaging |
Het |
Smc3 |
A |
G |
19: 53,627,189 (GRCm39) |
T830A |
probably benign |
Het |
Smpd2 |
G |
A |
10: 41,364,074 (GRCm39) |
T215I |
possibly damaging |
Het |
Sntg2 |
T |
G |
12: 30,276,891 (GRCm39) |
Y387S |
possibly damaging |
Het |
Sorl1 |
T |
G |
9: 41,948,355 (GRCm39) |
D810A |
probably damaging |
Het |
Spop |
T |
A |
11: 95,372,909 (GRCm39) |
I217N |
probably damaging |
Het |
Stac2 |
T |
C |
11: 97,934,345 (GRCm39) |
R120G |
possibly damaging |
Het |
Stau1 |
A |
T |
2: 166,791,266 (GRCm39) |
*496R |
probably null |
Het |
Tmeff2 |
C |
T |
1: 50,967,206 (GRCm39) |
R34C |
probably damaging |
Het |
Treml2 |
C |
T |
17: 48,609,739 (GRCm39) |
A57V |
possibly damaging |
Het |
Vmn2r15 |
T |
C |
5: 109,445,250 (GRCm39) |
D58G |
probably benign |
Het |
Vmn2r7 |
T |
C |
3: 64,598,666 (GRCm39) |
I721M |
possibly damaging |
Het |
Vmn2r70 |
C |
A |
7: 85,208,295 (GRCm39) |
M727I |
probably benign |
Het |
Vwa8 |
T |
A |
14: 79,162,702 (GRCm39) |
C161S |
probably benign |
Het |
|
Other mutations in Cma1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01070:Cma1
|
APN |
14 |
56,180,154 (GRCm39) |
missense |
probably benign |
0.26 |
R0026:Cma1
|
UTSW |
14 |
56,179,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Cma1
|
UTSW |
14 |
56,181,191 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2060:Cma1
|
UTSW |
14 |
56,181,155 (GRCm39) |
critical splice donor site |
probably null |
|
R4994:Cma1
|
UTSW |
14 |
56,179,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R5275:Cma1
|
UTSW |
14 |
56,179,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R5794:Cma1
|
UTSW |
14 |
56,181,977 (GRCm39) |
missense |
probably benign |
|
R5824:Cma1
|
UTSW |
14 |
56,179,182 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5955:Cma1
|
UTSW |
14 |
56,181,226 (GRCm39) |
missense |
probably benign |
0.20 |
R5958:Cma1
|
UTSW |
14 |
56,179,113 (GRCm39) |
makesense |
probably null |
|
R6075:Cma1
|
UTSW |
14 |
56,179,771 (GRCm39) |
missense |
probably damaging |
0.97 |
R6139:Cma1
|
UTSW |
14 |
56,180,157 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7088:Cma1
|
UTSW |
14 |
56,181,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R7139:Cma1
|
UTSW |
14 |
56,181,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R7220:Cma1
|
UTSW |
14 |
56,180,120 (GRCm39) |
missense |
probably benign |
|
R7988:Cma1
|
UTSW |
14 |
56,181,989 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9171:Cma1
|
UTSW |
14 |
56,181,189 (GRCm39) |
missense |
probably benign |
0.28 |
R9627:Cma1
|
UTSW |
14 |
56,181,289 (GRCm39) |
missense |
probably benign |
0.07 |
R9803:Cma1
|
UTSW |
14 |
56,179,186 (GRCm39) |
missense |
probably benign |
0.07 |
|