Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700061I17Rik |
G |
T |
3: 116,861,385 (GRCm39) |
|
noncoding transcript |
Het |
2300003K06Rik |
G |
T |
11: 99,728,793 (GRCm39) |
Q17K |
probably benign |
Het |
Abca16 |
T |
C |
7: 120,119,256 (GRCm39) |
V999A |
probably benign |
Het |
Actn3 |
C |
T |
19: 4,915,483 (GRCm39) |
|
probably benign |
Het |
Agap2 |
T |
A |
10: 126,926,981 (GRCm39) |
|
probably benign |
Het |
Ago3 |
C |
A |
4: 126,265,580 (GRCm39) |
R278L |
probably benign |
Het |
Aldh1a2 |
T |
C |
9: 71,192,492 (GRCm39) |
V449A |
possibly damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Aplnr |
A |
G |
2: 84,967,353 (GRCm39) |
Y126C |
probably damaging |
Het |
Apob |
T |
C |
12: 8,066,084 (GRCm39) |
I4351T |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 88,914,659 (GRCm39) |
L1763P |
probably benign |
Het |
Aspn |
T |
C |
13: 49,710,849 (GRCm39) |
S165P |
possibly damaging |
Het |
Atg13 |
A |
T |
2: 91,510,335 (GRCm39) |
V349E |
probably damaging |
Het |
Atp1b2 |
T |
A |
11: 69,493,309 (GRCm39) |
|
probably null |
Het |
B3glct |
A |
T |
5: 149,677,604 (GRCm39) |
D411V |
probably damaging |
Het |
Bcar3 |
A |
T |
3: 122,316,840 (GRCm39) |
I255F |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,608,148 (GRCm39) |
|
probably benign |
Het |
Cep164 |
T |
G |
9: 45,690,198 (GRCm39) |
E675A |
possibly damaging |
Het |
Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
Chst8 |
C |
A |
7: 34,447,593 (GRCm39) |
M8I |
possibly damaging |
Het |
Clec4n |
A |
G |
6: 123,212,475 (GRCm39) |
E67G |
probably benign |
Het |
Cobll1 |
A |
T |
2: 64,929,480 (GRCm39) |
D653E |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,276,579 (GRCm39) |
|
probably null |
Het |
Crip2 |
T |
C |
12: 113,107,124 (GRCm39) |
L30P |
probably damaging |
Het |
Ctbp1 |
C |
T |
5: 33,418,407 (GRCm39) |
V22I |
probably benign |
Het |
Cwc22 |
T |
C |
2: 77,747,521 (GRCm39) |
|
probably benign |
Het |
Cyp4a32 |
C |
A |
4: 115,460,147 (GRCm39) |
Y119* |
probably null |
Het |
Dido1 |
G |
T |
2: 180,313,263 (GRCm39) |
A463E |
possibly damaging |
Het |
Dnah7a |
G |
A |
1: 53,567,956 (GRCm39) |
P1880L |
probably benign |
Het |
Dock2 |
T |
A |
11: 34,189,705 (GRCm39) |
T1489S |
probably benign |
Het |
Dsp |
A |
G |
13: 38,375,907 (GRCm39) |
T1231A |
probably damaging |
Het |
Eif2ak1 |
G |
T |
5: 143,810,717 (GRCm39) |
|
probably benign |
Het |
Entrep1 |
G |
A |
19: 23,998,998 (GRCm39) |
T140M |
probably damaging |
Het |
Epc1 |
A |
T |
18: 6,452,360 (GRCm39) |
M233K |
probably damaging |
Het |
Gigyf2 |
A |
G |
1: 87,371,360 (GRCm39) |
|
probably benign |
Het |
Greb1 |
T |
G |
12: 16,757,852 (GRCm39) |
H58P |
probably damaging |
Het |
Gtpbp1 |
T |
C |
15: 79,597,649 (GRCm39) |
I348T |
possibly damaging |
Het |
Hck |
A |
T |
2: 152,970,192 (GRCm39) |
N64Y |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,818,744 (GRCm39) |
S2812P |
probably damaging |
Het |
Inpp4b |
T |
A |
8: 82,679,463 (GRCm39) |
|
probably null |
Het |
Kcnq5 |
A |
C |
1: 21,475,248 (GRCm39) |
S473A |
probably benign |
Het |
Lrat |
T |
G |
3: 82,810,676 (GRCm39) |
D115A |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,814,639 (GRCm39) |
I1131M |
possibly damaging |
Het |
Man2a2 |
T |
C |
7: 80,018,310 (GRCm39) |
D160G |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,933,688 (GRCm39) |
D1567N |
probably benign |
Het |
Mars1 |
T |
C |
10: 127,133,857 (GRCm39) |
D680G |
possibly damaging |
Het |
Mat1a |
T |
C |
14: 40,843,797 (GRCm39) |
S339P |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,042,081 (GRCm39) |
S1300P |
probably damaging |
Het |
Mga |
T |
C |
2: 119,733,179 (GRCm39) |
L9S |
probably damaging |
Het |
Mllt6 |
T |
C |
11: 97,563,277 (GRCm39) |
|
probably benign |
Het |
Mrpl37 |
A |
G |
4: 106,921,692 (GRCm39) |
L179P |
probably benign |
Het |
Mtnr1a |
G |
T |
8: 45,540,782 (GRCm39) |
V248L |
probably benign |
Het |
Mylk |
T |
C |
16: 34,635,835 (GRCm39) |
S19P |
possibly damaging |
Het |
Or11g1 |
A |
G |
14: 50,651,858 (GRCm39) |
T286A |
probably damaging |
Het |
Pacc1 |
A |
G |
1: 191,080,559 (GRCm39) |
|
probably benign |
Het |
Parp8 |
A |
T |
13: 117,161,886 (GRCm39) |
|
probably null |
Het |
Pcnx2 |
T |
C |
8: 126,479,023 (GRCm39) |
D2075G |
probably damaging |
Het |
Pigo |
A |
T |
4: 43,021,460 (GRCm39) |
I494K |
probably benign |
Het |
Pkd1l1 |
A |
T |
11: 8,820,313 (GRCm39) |
D1217E |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,369,040 (GRCm39) |
V895A |
probably benign |
Het |
Plxnb1 |
A |
G |
9: 108,937,989 (GRCm39) |
K1245R |
probably null |
Het |
Pold1 |
C |
T |
7: 44,192,181 (GRCm39) |
|
probably benign |
Het |
Ptprq |
T |
C |
10: 107,498,423 (GRCm39) |
I885V |
probably damaging |
Het |
Ptprz1 |
A |
G |
6: 23,050,473 (GRCm39) |
D1398G |
probably damaging |
Het |
Pygm |
G |
A |
19: 6,439,917 (GRCm39) |
A364T |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,035,018 (GRCm39) |
N354S |
probably benign |
Het |
Scgb2b19 |
C |
T |
7: 32,979,037 (GRCm39) |
|
probably null |
Het |
Slc26a8 |
C |
T |
17: 28,867,187 (GRCm39) |
V545M |
possibly damaging |
Het |
Slc27a1 |
T |
A |
8: 72,036,757 (GRCm39) |
|
probably null |
Het |
Smpd1 |
A |
G |
7: 105,205,881 (GRCm39) |
D416G |
possibly damaging |
Het |
Sorbs3 |
A |
G |
14: 70,431,095 (GRCm39) |
V284A |
probably benign |
Het |
Stfa2l1 |
T |
C |
16: 35,982,154 (GRCm39) |
V75A |
probably damaging |
Het |
Syndig1 |
A |
G |
2: 149,772,841 (GRCm39) |
D166G |
probably damaging |
Het |
Tcp10a |
G |
A |
17: 7,593,406 (GRCm39) |
|
probably null |
Het |
Themis2 |
T |
A |
4: 132,510,212 (GRCm39) |
I663F |
possibly damaging |
Het |
Thrap3 |
T |
C |
4: 126,070,129 (GRCm39) |
Q586R |
probably damaging |
Het |
Tinag |
C |
A |
9: 76,952,798 (GRCm39) |
C62F |
probably damaging |
Het |
Tmod1 |
T |
C |
4: 46,090,884 (GRCm39) |
Y146H |
probably damaging |
Het |
Tmprss4 |
T |
A |
9: 45,095,683 (GRCm39) |
I54F |
possibly damaging |
Het |
Tnks |
A |
C |
8: 35,301,757 (GRCm39) |
|
probably benign |
Het |
Trim43a |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
9: 88,465,042 (GRCm39) |
|
probably benign |
Het |
Trpc6 |
A |
G |
9: 8,680,538 (GRCm39) |
E844G |
probably benign |
Het |
Ubtd2 |
C |
T |
11: 32,466,125 (GRCm39) |
R115W |
probably damaging |
Het |
Ubxn6 |
T |
C |
17: 56,376,042 (GRCm39) |
D373G |
probably benign |
Het |
Upf1 |
T |
A |
8: 70,794,174 (GRCm39) |
Q244L |
probably benign |
Het |
Usp33 |
A |
G |
3: 152,074,271 (GRCm39) |
I372M |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,301,629 (GRCm39) |
E351G |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,554,318 (GRCm39) |
|
probably benign |
Het |
Vmn1r78 |
A |
G |
7: 11,886,508 (GRCm39) |
K40E |
possibly damaging |
Het |
Vmn2r7 |
T |
A |
3: 64,632,223 (GRCm39) |
M80L |
probably benign |
Het |
Vps13a |
G |
T |
19: 16,678,602 (GRCm39) |
Y1126* |
probably null |
Het |
Wfdc11 |
T |
C |
2: 164,506,366 (GRCm39) |
N60S |
probably benign |
Het |
Wnk2 |
C |
T |
13: 49,224,586 (GRCm39) |
D992N |
probably damaging |
Het |
Zpbp2 |
C |
A |
11: 98,444,670 (GRCm39) |
T66K |
probably damaging |
Het |
|
Other mutations in Plcb4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Plcb4
|
APN |
2 |
135,813,718 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01405:Plcb4
|
APN |
2 |
135,792,267 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01522:Plcb4
|
APN |
2 |
135,844,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01589:Plcb4
|
APN |
2 |
135,809,038 (GRCm39) |
missense |
probably benign |
|
IGL02090:Plcb4
|
APN |
2 |
135,789,041 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02247:Plcb4
|
APN |
2 |
135,836,245 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02259:Plcb4
|
APN |
2 |
135,752,166 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02338:Plcb4
|
APN |
2 |
135,842,100 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02625:Plcb4
|
APN |
2 |
135,803,714 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03026:Plcb4
|
APN |
2 |
135,792,349 (GRCm39) |
splice site |
probably benign |
|
IGL03111:Plcb4
|
APN |
2 |
135,818,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Plcb4
|
UTSW |
2 |
135,813,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Plcb4
|
UTSW |
2 |
135,803,689 (GRCm39) |
missense |
probably benign |
0.10 |
R0066:Plcb4
|
UTSW |
2 |
135,803,689 (GRCm39) |
missense |
probably benign |
0.10 |
R0143:Plcb4
|
UTSW |
2 |
135,818,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Plcb4
|
UTSW |
2 |
135,823,995 (GRCm39) |
missense |
probably benign |
0.00 |
R0234:Plcb4
|
UTSW |
2 |
135,823,995 (GRCm39) |
missense |
probably benign |
0.00 |
R0348:Plcb4
|
UTSW |
2 |
135,810,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Plcb4
|
UTSW |
2 |
135,796,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R0591:Plcb4
|
UTSW |
2 |
135,796,932 (GRCm39) |
splice site |
probably benign |
|
R0975:Plcb4
|
UTSW |
2 |
135,829,832 (GRCm39) |
splice site |
probably benign |
|
R1187:Plcb4
|
UTSW |
2 |
135,810,314 (GRCm39) |
missense |
probably benign |
0.36 |
R1235:Plcb4
|
UTSW |
2 |
135,814,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1562:Plcb4
|
UTSW |
2 |
135,812,367 (GRCm39) |
critical splice donor site |
probably null |
|
R1594:Plcb4
|
UTSW |
2 |
135,812,310 (GRCm39) |
splice site |
probably benign |
|
R1920:Plcb4
|
UTSW |
2 |
135,854,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Plcb4
|
UTSW |
2 |
135,780,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Plcb4
|
UTSW |
2 |
135,818,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Plcb4
|
UTSW |
2 |
135,818,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2202:Plcb4
|
UTSW |
2 |
135,844,514 (GRCm39) |
missense |
probably benign |
0.01 |
R2203:Plcb4
|
UTSW |
2 |
135,844,514 (GRCm39) |
missense |
probably benign |
0.01 |
R2204:Plcb4
|
UTSW |
2 |
135,844,514 (GRCm39) |
missense |
probably benign |
0.01 |
R2250:Plcb4
|
UTSW |
2 |
135,813,781 (GRCm39) |
critical splice donor site |
probably null |
|
R2291:Plcb4
|
UTSW |
2 |
135,781,903 (GRCm39) |
missense |
probably benign |
0.08 |
R2326:Plcb4
|
UTSW |
2 |
135,781,893 (GRCm39) |
missense |
probably damaging |
0.99 |
R2442:Plcb4
|
UTSW |
2 |
135,792,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Plcb4
|
UTSW |
2 |
135,781,123 (GRCm39) |
splice site |
probably benign |
|
R3774:Plcb4
|
UTSW |
2 |
135,800,065 (GRCm39) |
missense |
probably benign |
0.00 |
R3875:Plcb4
|
UTSW |
2 |
135,844,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R4594:Plcb4
|
UTSW |
2 |
135,844,519 (GRCm39) |
missense |
probably damaging |
0.98 |
R4673:Plcb4
|
UTSW |
2 |
135,774,191 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4812:Plcb4
|
UTSW |
2 |
135,849,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R5084:Plcb4
|
UTSW |
2 |
135,844,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Plcb4
|
UTSW |
2 |
135,809,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R5498:Plcb4
|
UTSW |
2 |
135,818,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R5923:Plcb4
|
UTSW |
2 |
135,803,734 (GRCm39) |
nonsense |
probably null |
|
R6241:Plcb4
|
UTSW |
2 |
135,752,094 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6492:Plcb4
|
UTSW |
2 |
135,814,991 (GRCm39) |
nonsense |
probably null |
|
R6514:Plcb4
|
UTSW |
2 |
135,796,916 (GRCm39) |
missense |
probably benign |
0.22 |
R6570:Plcb4
|
UTSW |
2 |
135,824,906 (GRCm39) |
missense |
probably benign |
0.13 |
R6721:Plcb4
|
UTSW |
2 |
135,752,157 (GRCm39) |
missense |
probably benign |
0.01 |
R6915:Plcb4
|
UTSW |
2 |
135,789,035 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6991:Plcb4
|
UTSW |
2 |
135,752,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R7040:Plcb4
|
UTSW |
2 |
135,774,182 (GRCm39) |
missense |
probably benign |
|
R7086:Plcb4
|
UTSW |
2 |
135,849,767 (GRCm39) |
missense |
probably benign |
|
R7114:Plcb4
|
UTSW |
2 |
135,824,043 (GRCm39) |
critical splice donor site |
probably null |
|
R7249:Plcb4
|
UTSW |
2 |
135,849,741 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7264:Plcb4
|
UTSW |
2 |
135,807,000 (GRCm39) |
missense |
probably benign |
|
R7361:Plcb4
|
UTSW |
2 |
135,818,068 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7426:Plcb4
|
UTSW |
2 |
135,842,139 (GRCm39) |
missense |
probably benign |
0.00 |
R7429:Plcb4
|
UTSW |
2 |
135,810,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Plcb4
|
UTSW |
2 |
135,810,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Plcb4
|
UTSW |
2 |
135,749,480 (GRCm39) |
missense |
probably benign |
0.00 |
R8141:Plcb4
|
UTSW |
2 |
135,781,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Plcb4
|
UTSW |
2 |
135,849,795 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9119:Plcb4
|
UTSW |
2 |
135,809,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Plcb4
|
UTSW |
2 |
135,829,817 (GRCm39) |
missense |
probably benign |
0.00 |
R9448:Plcb4
|
UTSW |
2 |
135,752,045 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9578:Plcb4
|
UTSW |
2 |
135,829,444 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Plcb4
|
UTSW |
2 |
135,800,658 (GRCm39) |
critical splice donor site |
probably null |
|
|