Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
C |
11: 58,880,924 (GRCm38) |
S411P |
probably damaging |
Het |
4930503L19Rik |
A |
T |
18: 70,468,476 (GRCm38) |
Y112N |
probably benign |
Het |
Abcd2 |
A |
T |
15: 91,191,274 (GRCm38) |
V112E |
probably benign |
Het |
Acadm |
A |
T |
3: 153,925,800 (GRCm38) |
Y353* |
probably null |
Het |
Adra2c |
A |
G |
5: 35,279,998 (GRCm38) |
D38G |
probably benign |
Het |
Ankrd10 |
C |
T |
8: 11,612,624 (GRCm38) |
G370R |
probably damaging |
Het |
Arfgef2 |
T |
A |
2: 166,873,608 (GRCm38) |
N1324K |
possibly damaging |
Het |
Atp6v1b2 |
A |
G |
8: 69,102,501 (GRCm38) |
T172A |
probably damaging |
Het |
BC003331 |
T |
C |
1: 150,382,290 (GRCm38) |
Y198C |
probably benign |
Het |
Bloc1s1 |
T |
A |
10: 128,922,723 (GRCm38) |
K22M |
possibly damaging |
Het |
Brpf3 |
A |
G |
17: 28,817,125 (GRCm38) |
T599A |
probably benign |
Het |
Cacna1e |
TTCCAGTCTC |
TTC |
1: 154,468,995 (GRCm38) |
|
probably null |
Het |
Casc1 |
G |
A |
6: 145,185,865 (GRCm38) |
Q351* |
probably null |
Het |
Ccdc186 |
T |
C |
19: 56,798,760 (GRCm38) |
D592G |
probably damaging |
Het |
Cfap161 |
A |
T |
7: 83,793,310 (GRCm38) |
D98E |
possibly damaging |
Het |
Cfi |
G |
A |
3: 129,875,016 (GRCm38) |
V564M |
probably damaging |
Het |
Cilp2 |
T |
A |
8: 69,881,129 (GRCm38) |
Q1073L |
probably damaging |
Het |
Cox6b1 |
A |
G |
7: 30,623,504 (GRCm38) |
C40R |
possibly damaging |
Het |
Cyp3a59 |
A |
T |
5: 146,096,333 (GRCm38) |
M172L |
probably benign |
Het |
Cyth1 |
T |
C |
11: 118,182,913 (GRCm38) |
D198G |
probably damaging |
Het |
Daam2 |
T |
C |
17: 49,460,674 (GRCm38) |
D963G |
probably damaging |
Het |
Ddi2 |
A |
T |
4: 141,705,937 (GRCm38) |
D209E |
probably benign |
Het |
Dnah12 |
G |
A |
14: 26,778,912 (GRCm38) |
|
probably null |
Het |
Dpagt1 |
G |
T |
9: 44,327,021 (GRCm38) |
|
probably benign |
Het |
Drc3 |
T |
A |
11: 60,370,554 (GRCm38) |
F177Y |
probably benign |
Het |
Dsg2 |
T |
C |
18: 20,601,863 (GRCm38) |
V966A |
probably damaging |
Het |
E430018J23Rik |
A |
G |
7: 127,391,523 (GRCm38) |
S431P |
probably benign |
Het |
E4f1 |
A |
G |
17: 24,444,578 (GRCm38) |
V633A |
probably damaging |
Het |
Eif2ak2 |
T |
A |
17: 78,858,536 (GRCm38) |
R411* |
probably null |
Het |
Frem2 |
T |
C |
3: 53,653,513 (GRCm38) |
E1191G |
probably damaging |
Het |
Fry |
T |
C |
5: 150,395,786 (GRCm38) |
V972A |
probably damaging |
Het |
Fry |
T |
A |
5: 150,491,090 (GRCm38) |
C467S |
|
Het |
Fscn1 |
T |
C |
5: 142,960,515 (GRCm38) |
Y23H |
probably damaging |
Het |
Gm16506 |
T |
A |
14: 43,724,302 (GRCm38) |
I163F |
|
Het |
Gm21103 |
T |
C |
14: 6,303,774 (GRCm38) |
Y92C |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,913,721 (GRCm38) |
H1151R |
probably benign |
Het |
Gprc5c |
T |
C |
11: 114,864,282 (GRCm38) |
Y262H |
probably damaging |
Het |
Hc |
G |
T |
2: 35,039,694 (GRCm38) |
N245K |
probably benign |
Het |
Hps6 |
T |
A |
19: 46,005,490 (GRCm38) |
L622Q |
probably damaging |
Het |
Hsd17b1 |
T |
C |
11: 101,079,209 (GRCm38) |
Y156H |
probably damaging |
Het |
Ireb2 |
T |
A |
9: 54,906,641 (GRCm38) |
F799L |
probably damaging |
Het |
Irf1 |
A |
G |
11: 53,774,412 (GRCm38) |
D205G |
probably damaging |
Het |
Kif12 |
A |
T |
4: 63,171,205 (GRCm38) |
F103L |
probably benign |
Het |
Krt12 |
C |
T |
11: 99,416,052 (GRCm38) |
V475M |
unknown |
Het |
Lca5 |
T |
A |
9: 83,423,169 (GRCm38) |
T195S |
probably benign |
Het |
Lrrc17 |
T |
C |
5: 21,575,339 (GRCm38) |
V437A |
possibly damaging |
Het |
Malt1 |
G |
T |
18: 65,464,051 (GRCm38) |
D468Y |
probably damaging |
Het |
Man2b2 |
C |
T |
5: 36,815,485 (GRCm38) |
A562T |
probably benign |
Het |
Mrc1 |
C |
T |
2: 14,304,146 (GRCm38) |
Q794* |
probably null |
Het |
Muc16 |
T |
A |
9: 18,655,233 (GRCm38) |
I1997L |
unknown |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,634,450 (GRCm38) |
|
probably null |
Het |
Mycbp2 |
A |
T |
14: 103,122,603 (GRCm38) |
F4518Y |
probably damaging |
Het |
Myo5a |
T |
A |
9: 75,129,992 (GRCm38) |
I159N |
probably damaging |
Het |
Nat1 |
T |
C |
8: 67,491,020 (GRCm38) |
V19A |
probably benign |
Het |
Ndst4 |
A |
G |
3: 125,561,471 (GRCm38) |
T343A |
probably damaging |
Het |
Nlrp9b |
A |
T |
7: 20,045,930 (GRCm38) |
L839F |
probably damaging |
Het |
Nxnl1 |
A |
G |
8: 71,566,554 (GRCm38) |
I9T |
probably benign |
Het |
Olfr1351 |
C |
A |
10: 79,017,649 (GRCm38) |
S109* |
probably null |
Het |
Olfr331 |
T |
A |
11: 58,502,554 (GRCm38) |
M7L |
probably benign |
Het |
Olfr364-ps1 |
C |
T |
2: 37,146,260 (GRCm38) |
T16I |
probably benign |
Het |
Olfr548-ps1 |
A |
T |
7: 102,541,992 (GRCm38) |
I19F |
probably damaging |
Het |
Olfr693 |
G |
A |
7: 106,678,048 (GRCm38) |
A146V |
probably benign |
Het |
Pou5f2 |
T |
C |
13: 78,025,265 (GRCm38) |
S109P |
possibly damaging |
Het |
Prr18 |
G |
T |
17: 8,341,531 (GRCm38) |
R173L |
probably damaging |
Het |
Ralgapb |
A |
T |
2: 158,494,662 (GRCm38) |
I1407F |
probably damaging |
Het |
Ralgapb |
T |
C |
2: 158,492,460 (GRCm38) |
Y1364H |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,211,009 (GRCm38) |
Y3501* |
probably null |
Het |
Sall3 |
G |
A |
18: 80,973,754 (GRCm38) |
P320S |
probably benign |
Het |
Scn8a |
A |
T |
15: 101,039,778 (GRCm38) |
H1676L |
probably benign |
Het |
Shmt1 |
T |
C |
11: 60,798,644 (GRCm38) |
D178G |
probably damaging |
Het |
Slmap |
T |
C |
14: 26,422,521 (GRCm38) |
K737R |
probably benign |
Het |
Ssh2 |
G |
A |
11: 77,454,794 (GRCm38) |
V1202I |
probably benign |
Het |
Stard7 |
A |
G |
2: 127,295,494 (GRCm38) |
D288G |
possibly damaging |
Het |
Tek |
A |
T |
4: 94,853,487 (GRCm38) |
D827V |
probably damaging |
Het |
Tfap2e |
A |
G |
4: 126,720,563 (GRCm38) |
L276P |
probably damaging |
Het |
Tns3 |
T |
C |
11: 8,437,251 (GRCm38) |
N1312S |
probably benign |
Het |
Tubd1 |
T |
A |
11: 86,557,805 (GRCm38) |
S315T |
probably damaging |
Het |
Ube2f |
T |
A |
1: 91,265,219 (GRCm38) |
C50* |
probably null |
Het |
Vmn2r109 |
T |
C |
17: 20,564,744 (GRCm38) |
I5V |
probably benign |
Het |
Vmn2r39 |
T |
C |
7: 9,023,668 (GRCm38) |
T445A |
probably damaging |
Het |
|
Other mutations in Prkcz |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Prkcz
|
APN |
4 |
155,294,401 (GRCm38) |
splice site |
probably benign |
|
IGL02114:Prkcz
|
APN |
4 |
155,271,590 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02582:Prkcz
|
APN |
4 |
155,271,256 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03010:Prkcz
|
APN |
4 |
155,286,805 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03199:Prkcz
|
APN |
4 |
155,272,984 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL03225:Prkcz
|
APN |
4 |
155,268,195 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03229:Prkcz
|
APN |
4 |
155,262,506 (GRCm38) |
missense |
probably benign |
0.19 |
IGL03299:Prkcz
|
APN |
4 |
155,286,790 (GRCm38) |
missense |
possibly damaging |
0.78 |
PIT4403001:Prkcz
|
UTSW |
4 |
155,293,156 (GRCm38) |
critical splice donor site |
probably null |
|
R0389:Prkcz
|
UTSW |
4 |
155,269,140 (GRCm38) |
missense |
probably damaging |
1.00 |
R0443:Prkcz
|
UTSW |
4 |
155,269,140 (GRCm38) |
missense |
probably damaging |
1.00 |
R1666:Prkcz
|
UTSW |
4 |
155,289,751 (GRCm38) |
missense |
probably damaging |
1.00 |
R1668:Prkcz
|
UTSW |
4 |
155,289,751 (GRCm38) |
missense |
probably damaging |
1.00 |
R1686:Prkcz
|
UTSW |
4 |
155,271,256 (GRCm38) |
missense |
probably damaging |
1.00 |
R1710:Prkcz
|
UTSW |
4 |
155,262,512 (GRCm38) |
missense |
probably damaging |
1.00 |
R2025:Prkcz
|
UTSW |
4 |
155,289,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R3162:Prkcz
|
UTSW |
4 |
155,290,524 (GRCm38) |
missense |
probably benign |
0.00 |
R3162:Prkcz
|
UTSW |
4 |
155,290,524 (GRCm38) |
missense |
probably benign |
0.00 |
R4399:Prkcz
|
UTSW |
4 |
155,269,077 (GRCm38) |
missense |
possibly damaging |
0.86 |
R4780:Prkcz
|
UTSW |
4 |
155,289,702 (GRCm38) |
missense |
probably damaging |
1.00 |
R4923:Prkcz
|
UTSW |
4 |
155,357,489 (GRCm38) |
missense |
probably damaging |
1.00 |
R5160:Prkcz
|
UTSW |
4 |
155,293,232 (GRCm38) |
missense |
probably benign |
0.22 |
R5510:Prkcz
|
UTSW |
4 |
155,272,936 (GRCm38) |
splice site |
probably null |
|
R6278:Prkcz
|
UTSW |
4 |
155,268,195 (GRCm38) |
missense |
probably damaging |
0.99 |
R6290:Prkcz
|
UTSW |
4 |
155,356,499 (GRCm38) |
missense |
probably damaging |
1.00 |
R6881:Prkcz
|
UTSW |
4 |
155,269,056 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7055:Prkcz
|
UTSW |
4 |
155,289,634 (GRCm38) |
missense |
probably benign |
0.01 |
R7241:Prkcz
|
UTSW |
4 |
155,269,059 (GRCm38) |
missense |
probably benign |
0.00 |
R7355:Prkcz
|
UTSW |
4 |
155,357,496 (GRCm38) |
missense |
probably damaging |
1.00 |
R7466:Prkcz
|
UTSW |
4 |
155,271,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R7522:Prkcz
|
UTSW |
4 |
155,271,285 (GRCm38) |
missense |
probably damaging |
1.00 |
R7618:Prkcz
|
UTSW |
4 |
155,262,482 (GRCm38) |
missense |
probably damaging |
1.00 |
R7753:Prkcz
|
UTSW |
4 |
155,272,968 (GRCm38) |
missense |
possibly damaging |
0.61 |
R8079:Prkcz
|
UTSW |
4 |
155,357,505 (GRCm38) |
missense |
probably damaging |
1.00 |
R8407:Prkcz
|
UTSW |
4 |
155,268,216 (GRCm38) |
missense |
probably damaging |
0.99 |
R8523:Prkcz
|
UTSW |
4 |
155,262,511 (GRCm38) |
missense |
probably damaging |
1.00 |
R8824:Prkcz
|
UTSW |
4 |
155,344,828 (GRCm38) |
start gained |
probably benign |
|
R9753:Prkcz
|
UTSW |
4 |
155,293,202 (GRCm38) |
missense |
probably benign |
0.01 |
X0067:Prkcz
|
UTSW |
4 |
155,354,704 (GRCm38) |
missense |
probably benign |
0.25 |
Z1176:Prkcz
|
UTSW |
4 |
155,356,468 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Prkcz
|
UTSW |
4 |
155,354,680 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Prkcz
|
UTSW |
4 |
155,301,004 (GRCm38) |
missense |
probably damaging |
1.00 |
|