Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
T |
A |
12: 118,891,139 (GRCm39) |
I453F |
probably damaging |
Het |
Anpep |
C |
T |
7: 79,488,720 (GRCm39) |
W402* |
probably null |
Het |
Apcdd1 |
T |
C |
18: 63,070,134 (GRCm39) |
S134P |
probably damaging |
Het |
Ccdc154 |
T |
C |
17: 25,382,183 (GRCm39) |
V34A |
probably benign |
Het |
Cntn3 |
A |
T |
6: 102,397,377 (GRCm39) |
N65K |
probably damaging |
Het |
Cntn6 |
G |
T |
6: 104,812,706 (GRCm39) |
V663F |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,344,955 (GRCm39) |
W2100R |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 7,011,290 (GRCm39) |
S3634R |
probably benign |
Het |
Entrep2 |
T |
A |
7: 64,425,579 (GRCm39) |
H171L |
probably damaging |
Het |
Gucy1a2 |
T |
C |
9: 3,865,460 (GRCm39) |
F645L |
probably damaging |
Het |
Hs6st3 |
G |
T |
14: 120,106,738 (GRCm39) |
R382L |
probably damaging |
Het |
Il27 |
T |
A |
7: 126,191,786 (GRCm39) |
T89S |
possibly damaging |
Het |
Iqgap2 |
C |
T |
13: 95,811,880 (GRCm39) |
R707H |
probably damaging |
Het |
Klhl23 |
T |
A |
2: 69,654,613 (GRCm39) |
I161N |
probably benign |
Het |
Lrrk2 |
G |
A |
15: 91,640,152 (GRCm39) |
E1566K |
probably damaging |
Het |
Mia3 |
A |
G |
1: 183,113,713 (GRCm39) |
V437A |
probably benign |
Het |
Ncoa6 |
G |
T |
2: 155,247,419 (GRCm39) |
H1962N |
possibly damaging |
Het |
Nox4 |
C |
T |
7: 86,988,172 (GRCm39) |
T361I |
probably damaging |
Het |
Pappa2 |
T |
C |
1: 158,544,584 (GRCm39) |
Y1748C |
probably damaging |
Het |
Phyhip |
T |
C |
14: 70,699,369 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
A |
G |
1: 20,447,632 (GRCm39) |
F2254L |
probably benign |
Het |
Plxnb1 |
A |
G |
9: 108,935,518 (GRCm39) |
Y1018C |
probably damaging |
Het |
Pnoc |
C |
T |
14: 65,648,671 (GRCm39) |
V8I |
probably benign |
Het |
Prss29 |
A |
G |
17: 25,541,408 (GRCm39) |
D256G |
probably benign |
Het |
Scrn3 |
T |
C |
2: 73,161,349 (GRCm39) |
F312L |
probably damaging |
Het |
Sephs1 |
A |
G |
2: 4,904,339 (GRCm39) |
E239G |
possibly damaging |
Het |
Tti1 |
A |
G |
2: 157,842,593 (GRCm39) |
L812P |
probably damaging |
Het |
Wdr1 |
A |
G |
5: 38,694,518 (GRCm39) |
S62P |
probably benign |
Het |
Zfp106 |
A |
G |
2: 120,346,487 (GRCm39) |
S1659P |
probably damaging |
Het |
Zng1 |
A |
G |
19: 24,932,769 (GRCm39) |
V88A |
possibly damaging |
Het |
|
Other mutations in Crisp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00839:Crisp3
|
APN |
17 |
40,550,147 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2082:Crisp3
|
UTSW |
17 |
40,536,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R2357:Crisp3
|
UTSW |
17 |
40,533,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R3704:Crisp3
|
UTSW |
17 |
40,546,848 (GRCm39) |
splice site |
probably benign |
|
R5111:Crisp3
|
UTSW |
17 |
40,536,695 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5723:Crisp3
|
UTSW |
17 |
40,546,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R6502:Crisp3
|
UTSW |
17 |
40,546,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Crisp3
|
UTSW |
17 |
40,536,693 (GRCm39) |
critical splice donor site |
probably null |
|
R7531:Crisp3
|
UTSW |
17 |
40,545,629 (GRCm39) |
missense |
probably benign |
0.02 |
R8051:Crisp3
|
UTSW |
17 |
40,543,451 (GRCm39) |
missense |
probably benign |
0.13 |
R8270:Crisp3
|
UTSW |
17 |
40,546,813 (GRCm39) |
missense |
probably benign |
0.01 |
R9472:Crisp3
|
UTSW |
17 |
40,539,676 (GRCm39) |
critical splice donor site |
probably null |
|
|