Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
G |
A |
10: 100,448,722 (GRCm39) |
V400I |
probably damaging |
Het |
Abcb1b |
A |
G |
5: 8,848,782 (GRCm39) |
N14S |
probably damaging |
Het |
Adamts14 |
A |
G |
10: 61,034,439 (GRCm39) |
Y1150H |
probably benign |
Het |
Adgrg3 |
A |
G |
8: 95,759,997 (GRCm39) |
N72S |
probably benign |
Het |
Akain1 |
T |
A |
17: 69,746,527 (GRCm39) |
F3I |
possibly damaging |
Het |
Akr1c21 |
T |
C |
13: 4,627,452 (GRCm39) |
L182P |
probably damaging |
Het |
Arhgap21 |
A |
T |
2: 20,886,659 (GRCm39) |
Y12N |
probably damaging |
Het |
Aup1 |
A |
T |
6: 83,032,226 (GRCm39) |
H131L |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,363,928 (GRCm39) |
T812A |
possibly damaging |
Het |
Bmp2k |
A |
G |
5: 97,211,392 (GRCm39) |
Y520C |
unknown |
Het |
Calm4 |
T |
G |
13: 3,888,302 (GRCm39) |
V136G |
probably damaging |
Het |
Catsper2 |
A |
G |
2: 121,230,523 (GRCm39) |
|
probably null |
Het |
Cc2d2a |
A |
G |
5: 43,896,713 (GRCm39) |
T1537A |
possibly damaging |
Het |
Cntn2 |
A |
T |
1: 132,454,049 (GRCm39) |
V319D |
possibly damaging |
Het |
Cux1 |
G |
A |
5: 136,304,235 (GRCm39) |
R1314* |
probably null |
Het |
Cxcl12 |
A |
G |
6: 117,150,508 (GRCm39) |
I79V |
probably damaging |
Het |
Cyp2j6 |
T |
C |
4: 96,412,014 (GRCm39) |
D418G |
probably benign |
Het |
Ddx28 |
G |
C |
8: 106,737,190 (GRCm39) |
D289E |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam135a |
A |
C |
1: 24,068,887 (GRCm39) |
S448A |
probably benign |
Het |
Fbxo33 |
G |
T |
12: 59,251,626 (GRCm39) |
N30K |
possibly damaging |
Het |
Fgf12 |
A |
C |
16: 28,217,093 (GRCm39) |
Y21D |
probably damaging |
Het |
Galntl5 |
C |
T |
5: 25,415,432 (GRCm39) |
S288L |
probably benign |
Het |
Gart |
G |
T |
16: 91,422,237 (GRCm39) |
A760D |
probably damaging |
Het |
Gba2 |
A |
T |
4: 43,573,869 (GRCm39) |
|
probably benign |
Het |
Gm10518 |
C |
A |
1: 179,631,357 (GRCm39) |
S139* |
probably null |
Het |
Gm4781 |
A |
T |
10: 100,232,837 (GRCm39) |
|
noncoding transcript |
Het |
Gm9790 |
A |
G |
3: 85,823,156 (GRCm39) |
|
noncoding transcript |
Het |
Gmps |
G |
A |
3: 63,893,075 (GRCm39) |
G127R |
probably damaging |
Het |
Golim4 |
A |
T |
3: 75,802,443 (GRCm39) |
V283E |
probably benign |
Het |
Gprc5a |
A |
T |
6: 135,055,918 (GRCm39) |
I122F |
possibly damaging |
Het |
Gzmc |
T |
C |
14: 56,471,341 (GRCm39) |
K67E |
probably benign |
Het |
Hapln3 |
C |
A |
7: 78,771,638 (GRCm39) |
V84L |
probably benign |
Het |
Hif3a |
T |
A |
7: 16,778,789 (GRCm39) |
N377Y |
possibly damaging |
Het |
Ifi211 |
G |
A |
1: 173,726,969 (GRCm39) |
H392Y |
probably damaging |
Het |
Iqgap3 |
T |
A |
3: 88,015,663 (GRCm39) |
|
probably benign |
Het |
Itga10 |
T |
A |
3: 96,559,141 (GRCm39) |
F410Y |
probably damaging |
Het |
Jup |
T |
C |
11: 100,263,260 (GRCm39) |
Y705C |
probably damaging |
Het |
Khsrp |
C |
T |
17: 57,332,597 (GRCm39) |
A228T |
probably benign |
Het |
Lmntd2 |
C |
T |
7: 140,790,998 (GRCm39) |
G445D |
probably damaging |
Het |
Lyst |
T |
C |
13: 13,809,290 (GRCm39) |
V320A |
possibly damaging |
Het |
Magel2 |
T |
A |
7: 62,027,988 (GRCm39) |
H297Q |
possibly damaging |
Het |
Mbd6 |
T |
C |
10: 127,123,286 (GRCm39) |
E33G |
probably damaging |
Het |
Mob3b |
A |
G |
4: 34,985,910 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
T |
C |
1: 88,162,334 (GRCm39) |
|
probably null |
Het |
Mroh2a |
C |
T |
1: 88,158,402 (GRCm39) |
R150* |
probably null |
Het |
Mymk |
A |
T |
2: 26,952,346 (GRCm39) |
W174R |
probably damaging |
Het |
Nckap1 |
C |
T |
2: 80,348,286 (GRCm39) |
S889N |
probably benign |
Het |
Nipal3 |
T |
C |
4: 135,174,599 (GRCm39) |
Y384C |
possibly damaging |
Het |
Nt5c3b |
A |
G |
11: 100,330,920 (GRCm39) |
|
probably benign |
Het |
Obox6 |
T |
A |
7: 15,567,750 (GRCm39) |
L232F |
probably damaging |
Het |
Obscn |
A |
C |
11: 58,997,113 (GRCm39) |
|
probably benign |
Het |
Or7g12 |
T |
C |
9: 18,899,839 (GRCm39) |
L185P |
probably damaging |
Het |
Phkb |
A |
G |
8: 86,748,278 (GRCm39) |
I706V |
probably benign |
Het |
Plcb2 |
A |
G |
2: 118,546,168 (GRCm39) |
|
probably benign |
Het |
Plek2 |
T |
C |
12: 78,941,184 (GRCm39) |
D216G |
probably damaging |
Het |
Plxnb2 |
T |
C |
15: 89,046,665 (GRCm39) |
Y855C |
probably damaging |
Het |
Psma7 |
A |
T |
2: 179,679,215 (GRCm39) |
D184E |
probably benign |
Het |
Rai14 |
T |
A |
15: 10,592,282 (GRCm39) |
L204F |
probably damaging |
Het |
Ralgapa2 |
A |
G |
2: 146,199,920 (GRCm39) |
V1208A |
probably benign |
Het |
Rapgef6 |
A |
G |
11: 54,582,458 (GRCm39) |
R67G |
possibly damaging |
Het |
Ryr2 |
C |
T |
13: 11,618,665 (GRCm39) |
|
probably benign |
Het |
Satb1 |
T |
C |
17: 52,047,027 (GRCm39) |
S763G |
probably benign |
Het |
Sdk1 |
A |
T |
5: 142,020,292 (GRCm39) |
H690L |
probably benign |
Het |
Sfrp5 |
A |
C |
19: 42,190,143 (GRCm39) |
V103G |
possibly damaging |
Het |
Six6 |
A |
G |
12: 72,988,451 (GRCm39) |
E208G |
probably benign |
Het |
Sspo |
A |
T |
6: 48,437,334 (GRCm39) |
H1364L |
probably benign |
Het |
Stard9 |
A |
T |
2: 120,529,973 (GRCm39) |
T2077S |
probably benign |
Het |
Tacr3 |
T |
C |
3: 134,535,254 (GRCm39) |
L74P |
probably damaging |
Het |
Tep1 |
T |
C |
14: 51,074,245 (GRCm39) |
E1880G |
probably benign |
Het |
Tgfb3 |
A |
T |
12: 86,116,517 (GRCm39) |
|
probably benign |
Het |
Thap7 |
G |
A |
16: 17,346,576 (GRCm39) |
P136S |
probably damaging |
Het |
Thoc2l |
T |
A |
5: 104,667,789 (GRCm39) |
Y770* |
probably null |
Het |
Tmc2 |
T |
C |
2: 130,098,036 (GRCm39) |
V717A |
possibly damaging |
Het |
Usp43 |
T |
A |
11: 67,778,593 (GRCm39) |
S446C |
probably damaging |
Het |
Vwa3a |
C |
T |
7: 120,379,371 (GRCm39) |
S492L |
probably damaging |
Het |
Wdhd1 |
T |
A |
14: 47,493,672 (GRCm39) |
N16I |
probably damaging |
Het |
Wdr95 |
A |
T |
5: 149,516,566 (GRCm39) |
D327V |
probably damaging |
Het |
Zfp128 |
T |
G |
7: 12,624,563 (GRCm39) |
Y310* |
probably null |
Het |
|
Other mutations in Prkcz |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Prkcz
|
APN |
4 |
155,378,858 (GRCm39) |
splice site |
probably benign |
|
IGL02114:Prkcz
|
APN |
4 |
155,356,047 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02582:Prkcz
|
APN |
4 |
155,355,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03010:Prkcz
|
APN |
4 |
155,371,262 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03199:Prkcz
|
APN |
4 |
155,357,441 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03225:Prkcz
|
APN |
4 |
155,352,652 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03229:Prkcz
|
APN |
4 |
155,346,963 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03299:Prkcz
|
APN |
4 |
155,371,247 (GRCm39) |
missense |
possibly damaging |
0.78 |
PIT4403001:Prkcz
|
UTSW |
4 |
155,377,613 (GRCm39) |
critical splice donor site |
probably null |
|
R0389:Prkcz
|
UTSW |
4 |
155,353,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R0443:Prkcz
|
UTSW |
4 |
155,353,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Prkcz
|
UTSW |
4 |
155,374,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Prkcz
|
UTSW |
4 |
155,374,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Prkcz
|
UTSW |
4 |
155,346,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:Prkcz
|
UTSW |
4 |
155,374,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Prkcz
|
UTSW |
4 |
155,374,981 (GRCm39) |
missense |
probably benign |
0.00 |
R3162:Prkcz
|
UTSW |
4 |
155,374,981 (GRCm39) |
missense |
probably benign |
0.00 |
R4399:Prkcz
|
UTSW |
4 |
155,353,534 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4780:Prkcz
|
UTSW |
4 |
155,374,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R4923:Prkcz
|
UTSW |
4 |
155,441,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R5160:Prkcz
|
UTSW |
4 |
155,377,689 (GRCm39) |
missense |
probably benign |
0.22 |
R5510:Prkcz
|
UTSW |
4 |
155,357,393 (GRCm39) |
splice site |
probably null |
|
R6278:Prkcz
|
UTSW |
4 |
155,352,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R6290:Prkcz
|
UTSW |
4 |
155,440,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R6881:Prkcz
|
UTSW |
4 |
155,353,513 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7055:Prkcz
|
UTSW |
4 |
155,374,091 (GRCm39) |
missense |
probably benign |
0.01 |
R7108:Prkcz
|
UTSW |
4 |
155,371,250 (GRCm39) |
nonsense |
probably null |
|
R7241:Prkcz
|
UTSW |
4 |
155,353,516 (GRCm39) |
missense |
probably benign |
0.00 |
R7355:Prkcz
|
UTSW |
4 |
155,441,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Prkcz
|
UTSW |
4 |
155,356,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7522:Prkcz
|
UTSW |
4 |
155,355,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7618:Prkcz
|
UTSW |
4 |
155,346,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Prkcz
|
UTSW |
4 |
155,357,425 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8079:Prkcz
|
UTSW |
4 |
155,441,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Prkcz
|
UTSW |
4 |
155,352,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R8523:Prkcz
|
UTSW |
4 |
155,346,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R8824:Prkcz
|
UTSW |
4 |
155,429,285 (GRCm39) |
start gained |
probably benign |
|
R9753:Prkcz
|
UTSW |
4 |
155,377,659 (GRCm39) |
missense |
probably benign |
0.01 |
X0067:Prkcz
|
UTSW |
4 |
155,439,161 (GRCm39) |
missense |
probably benign |
0.25 |
Z1176:Prkcz
|
UTSW |
4 |
155,440,925 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Prkcz
|
UTSW |
4 |
155,439,137 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Prkcz
|
UTSW |
4 |
155,385,461 (GRCm39) |
missense |
probably damaging |
1.00 |
|