Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl6b |
A |
T |
5: 137,552,871 (GRCm39) |
I67F |
probably damaging |
Het |
Adam24 |
A |
T |
8: 41,134,431 (GRCm39) |
N633I |
probably benign |
Het |
Adgrg6 |
T |
C |
10: 14,344,585 (GRCm39) |
S123G |
possibly damaging |
Het |
Afdn |
T |
A |
17: 14,075,652 (GRCm39) |
F940L |
probably damaging |
Het |
Ahrr |
A |
T |
13: 74,372,987 (GRCm39) |
Y26* |
probably null |
Het |
Akap1 |
C |
A |
11: 88,735,577 (GRCm39) |
G362* |
probably null |
Het |
Aox3 |
A |
T |
1: 58,192,337 (GRCm39) |
T536S |
probably benign |
Het |
Boc |
A |
T |
16: 44,309,109 (GRCm39) |
|
probably null |
Het |
Cchcr1 |
T |
C |
17: 35,841,457 (GRCm39) |
|
probably null |
Het |
Cct2 |
A |
T |
10: 116,890,897 (GRCm39) |
|
probably benign |
Het |
Cd84 |
A |
T |
1: 171,679,685 (GRCm39) |
Y121F |
probably damaging |
Het |
Cecr2 |
T |
A |
6: 120,738,433 (GRCm39) |
C275* |
probably null |
Het |
Chchd3 |
C |
A |
6: 32,985,503 (GRCm39) |
|
probably benign |
Het |
Ckmt2 |
A |
T |
13: 92,007,971 (GRCm39) |
|
probably benign |
Het |
Col5a3 |
T |
C |
9: 20,691,253 (GRCm39) |
K1131E |
probably damaging |
Het |
Dek |
A |
T |
13: 47,241,647 (GRCm39) |
S306T |
probably benign |
Het |
Dhx32 |
T |
C |
7: 133,339,069 (GRCm39) |
E322G |
possibly damaging |
Het |
Dlg5 |
T |
A |
14: 24,204,673 (GRCm39) |
D941V |
possibly damaging |
Het |
Dnah10 |
A |
G |
5: 124,876,009 (GRCm39) |
N2559S |
probably benign |
Het |
Dnajc3 |
A |
G |
14: 119,205,518 (GRCm39) |
T171A |
probably benign |
Het |
Eftud2 |
G |
T |
11: 102,750,868 (GRCm39) |
F308L |
probably damaging |
Het |
Elp6 |
T |
C |
9: 110,143,123 (GRCm39) |
F95S |
probably damaging |
Het |
Emsy |
C |
T |
7: 98,270,613 (GRCm39) |
V450I |
possibly damaging |
Het |
Exoc3 |
A |
T |
13: 74,338,298 (GRCm39) |
M362K |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,178,637 (GRCm39) |
D1474E |
probably damaging |
Het |
Fcgbp |
T |
A |
7: 27,803,158 (GRCm39) |
C1587* |
probably null |
Het |
Fosl2 |
T |
A |
5: 32,304,329 (GRCm39) |
L88Q |
probably damaging |
Het |
Fsd2 |
T |
C |
7: 81,198,621 (GRCm39) |
D381G |
probably benign |
Het |
Golim4 |
A |
C |
3: 75,863,440 (GRCm39) |
S56A |
probably damaging |
Het |
Gpr39 |
T |
C |
1: 125,800,093 (GRCm39) |
|
probably benign |
Het |
Gucy1b2 |
T |
C |
14: 62,651,770 (GRCm39) |
I409V |
probably damaging |
Het |
Hivep1 |
A |
G |
13: 42,311,596 (GRCm39) |
T1279A |
probably benign |
Het |
Ifit1bl2 |
T |
A |
19: 34,596,569 (GRCm39) |
Q349L |
possibly damaging |
Het |
Kcnc1 |
A |
T |
7: 46,077,691 (GRCm39) |
I498F |
possibly damaging |
Het |
Kctd21 |
T |
A |
7: 96,996,704 (GRCm39) |
I59N |
probably damaging |
Het |
Lama5 |
T |
A |
2: 179,824,593 (GRCm39) |
T2577S |
probably benign |
Het |
Mief2 |
G |
T |
11: 60,621,140 (GRCm39) |
R9M |
possibly damaging |
Het |
Mmp3 |
T |
C |
9: 7,453,705 (GRCm39) |
V442A |
probably benign |
Het |
Nkapd1 |
C |
A |
9: 50,518,972 (GRCm39) |
K213N |
possibly damaging |
Het |
Nrxn3 |
C |
T |
12: 90,298,909 (GRCm39) |
R477W |
probably damaging |
Het |
Or12e7 |
A |
G |
2: 87,288,336 (GRCm39) |
T276A |
probably benign |
Het |
Or7a41 |
T |
A |
10: 78,871,122 (GRCm39) |
V164E |
possibly damaging |
Het |
Parp1 |
A |
G |
1: 180,418,807 (GRCm39) |
T656A |
probably benign |
Het |
Phlpp1 |
A |
G |
1: 106,101,142 (GRCm39) |
D470G |
possibly damaging |
Het |
Prdm1 |
T |
C |
10: 44,318,124 (GRCm39) |
E248G |
probably benign |
Het |
Prtg |
C |
T |
9: 72,818,032 (GRCm39) |
|
probably benign |
Het |
Ptpn1 |
T |
C |
2: 167,818,529 (GRCm39) |
Y424H |
probably damaging |
Het |
Ptprr |
T |
C |
10: 116,092,109 (GRCm39) |
V369A |
probably damaging |
Het |
Rai1 |
T |
G |
11: 60,076,221 (GRCm39) |
V95G |
probably benign |
Het |
Rasal3 |
T |
A |
17: 32,612,509 (GRCm39) |
|
probably null |
Het |
Rbm19 |
A |
G |
5: 120,260,961 (GRCm39) |
E195G |
probably benign |
Het |
Rhbdd3 |
T |
A |
11: 5,053,332 (GRCm39) |
L44Q |
probably damaging |
Het |
Ripply2 |
T |
C |
9: 86,901,713 (GRCm39) |
W80R |
probably damaging |
Het |
Rnf183 |
A |
G |
4: 62,346,760 (GRCm39) |
C13R |
probably damaging |
Het |
Rorb |
A |
G |
19: 18,932,417 (GRCm39) |
L367P |
probably damaging |
Het |
Rpl7a-ps5 |
C |
T |
17: 58,146,135 (GRCm39) |
|
probably benign |
Het |
Rreb1 |
A |
G |
13: 38,114,581 (GRCm39) |
N647D |
probably benign |
Het |
Rtn1 |
A |
T |
12: 72,351,187 (GRCm39) |
S341T |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,588,046 (GRCm39) |
S2632G |
probably benign |
Het |
Scube1 |
A |
G |
15: 83,499,227 (GRCm39) |
C633R |
possibly damaging |
Het |
Sdk1 |
A |
T |
5: 142,024,078 (GRCm39) |
I723F |
probably damaging |
Het |
Sec23a |
A |
T |
12: 59,048,796 (GRCm39) |
C109S |
probably damaging |
Het |
Septin11 |
T |
C |
5: 93,296,287 (GRCm39) |
F60L |
probably damaging |
Het |
Sgf29 |
G |
A |
7: 126,271,063 (GRCm39) |
|
probably null |
Het |
Skint5 |
A |
G |
4: 113,413,308 (GRCm39) |
|
probably benign |
Het |
Smo |
G |
A |
6: 29,755,482 (GRCm39) |
V385I |
possibly damaging |
Het |
Tada2a |
G |
A |
11: 84,000,837 (GRCm39) |
T76I |
probably damaging |
Het |
Tas2r118 |
T |
A |
6: 23,969,422 (GRCm39) |
H213L |
possibly damaging |
Het |
Thoc5 |
A |
T |
11: 4,861,427 (GRCm39) |
|
probably benign |
Het |
Tmem33 |
T |
A |
5: 67,424,634 (GRCm39) |
|
probably null |
Het |
Top1mt |
A |
G |
15: 75,546,247 (GRCm39) |
L78P |
probably damaging |
Het |
Uvssa |
T |
A |
5: 33,571,228 (GRCm39) |
|
probably benign |
Het |
Vmn2r50 |
A |
T |
7: 9,784,062 (GRCm39) |
C137* |
probably null |
Het |
Vmn2r81 |
A |
G |
10: 79,129,691 (GRCm39) |
T861A |
probably benign |
Het |
Wnt3 |
A |
T |
11: 103,699,077 (GRCm39) |
N61I |
probably damaging |
Het |
Zswim9 |
A |
G |
7: 13,011,144 (GRCm39) |
I68T |
possibly damaging |
Het |
Zzef1 |
T |
C |
11: 72,803,771 (GRCm39) |
I2535T |
probably damaging |
Het |
|
Other mutations in Pcdhb19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01374:Pcdhb19
|
APN |
18 |
37,631,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02070:Pcdhb19
|
APN |
18 |
37,631,597 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02348:Pcdhb19
|
APN |
18 |
37,631,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02866:Pcdhb19
|
APN |
18 |
37,632,163 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02869:Pcdhb19
|
APN |
18 |
37,631,690 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03118:Pcdhb19
|
APN |
18 |
37,632,618 (GRCm39) |
intron |
probably benign |
|
IGL03120:Pcdhb19
|
APN |
18 |
37,631,209 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03135:Pcdhb19
|
APN |
18 |
37,631,588 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03366:Pcdhb19
|
APN |
18 |
37,631,665 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0147:Pcdhb19
|
UTSW |
18 |
37,630,235 (GRCm39) |
missense |
probably benign |
0.01 |
R0148:Pcdhb19
|
UTSW |
18 |
37,630,235 (GRCm39) |
missense |
probably benign |
0.01 |
R0432:Pcdhb19
|
UTSW |
18 |
37,632,588 (GRCm39) |
missense |
probably benign |
0.01 |
R0609:Pcdhb19
|
UTSW |
18 |
37,631,005 (GRCm39) |
missense |
probably benign |
|
R2255:Pcdhb19
|
UTSW |
18 |
37,630,997 (GRCm39) |
missense |
probably benign |
0.00 |
R2265:Pcdhb19
|
UTSW |
18 |
37,630,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R3500:Pcdhb19
|
UTSW |
18 |
37,630,532 (GRCm39) |
nonsense |
probably null |
|
R3708:Pcdhb19
|
UTSW |
18 |
37,630,442 (GRCm39) |
missense |
probably benign |
0.04 |
R4165:Pcdhb19
|
UTSW |
18 |
37,632,243 (GRCm39) |
missense |
probably benign |
|
R4166:Pcdhb19
|
UTSW |
18 |
37,632,243 (GRCm39) |
missense |
probably benign |
|
R4863:Pcdhb19
|
UTSW |
18 |
37,632,161 (GRCm39) |
missense |
probably benign |
0.00 |
R5217:Pcdhb19
|
UTSW |
18 |
37,630,939 (GRCm39) |
missense |
probably benign |
0.00 |
R5770:Pcdhb19
|
UTSW |
18 |
37,631,090 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6031:Pcdhb19
|
UTSW |
18 |
37,630,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Pcdhb19
|
UTSW |
18 |
37,630,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6372:Pcdhb19
|
UTSW |
18 |
37,630,419 (GRCm39) |
missense |
probably benign |
0.04 |
R6454:Pcdhb19
|
UTSW |
18 |
37,632,322 (GRCm39) |
missense |
probably benign |
0.43 |
R6985:Pcdhb19
|
UTSW |
18 |
37,630,211 (GRCm39) |
missense |
probably benign |
0.00 |
R7658:Pcdhb19
|
UTSW |
18 |
37,632,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R7662:Pcdhb19
|
UTSW |
18 |
37,631,788 (GRCm39) |
missense |
probably damaging |
0.98 |
R7910:Pcdhb19
|
UTSW |
18 |
37,630,720 (GRCm39) |
missense |
probably benign |
0.43 |
R8041:Pcdhb19
|
UTSW |
18 |
37,630,367 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8318:Pcdhb19
|
UTSW |
18 |
37,630,999 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8989:Pcdhb19
|
UTSW |
18 |
37,631,476 (GRCm39) |
missense |
probably benign |
0.04 |
R9053:Pcdhb19
|
UTSW |
18 |
37,631,143 (GRCm39) |
missense |
probably benign |
0.01 |
R9164:Pcdhb19
|
UTSW |
18 |
37,631,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R9197:Pcdhb19
|
UTSW |
18 |
37,631,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R9309:Pcdhb19
|
UTSW |
18 |
37,631,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Pcdhb19
|
UTSW |
18 |
37,632,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Pcdhb19
|
UTSW |
18 |
37,632,532 (GRCm39) |
nonsense |
probably null |
|
R9432:Pcdhb19
|
UTSW |
18 |
37,630,628 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9553:Pcdhb19
|
UTSW |
18 |
37,631,848 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Pcdhb19
|
UTSW |
18 |
37,630,228 (GRCm39) |
missense |
probably benign |
|
Z1177:Pcdhb19
|
UTSW |
18 |
37,631,498 (GRCm39) |
missense |
probably damaging |
1.00 |
|