Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
T |
C |
7: 27,271,088 (GRCm39) |
V135A |
probably damaging |
Het |
Ankrd42 |
T |
C |
7: 92,273,282 (GRCm39) |
N115S |
possibly damaging |
Het |
Baz1a |
T |
C |
12: 55,021,922 (GRCm39) |
E120G |
probably damaging |
Het |
Calcrl |
A |
T |
2: 84,169,658 (GRCm39) |
V341E |
probably damaging |
Het |
Card6 |
T |
C |
15: 5,129,564 (GRCm39) |
R611G |
probably benign |
Het |
Cd70 |
A |
T |
17: 57,453,311 (GRCm39) |
S118T |
probably damaging |
Het |
Chil5 |
T |
A |
3: 105,927,248 (GRCm39) |
I188F |
probably damaging |
Het |
Clca4b |
C |
T |
3: 144,621,269 (GRCm39) |
V602I |
probably benign |
Het |
Cldn10 |
G |
A |
14: 119,025,725 (GRCm39) |
G53S |
possibly damaging |
Het |
Col6a4 |
A |
G |
9: 105,867,977 (GRCm39) |
|
probably benign |
Het |
Cox8b |
T |
C |
7: 140,479,001 (GRCm39) |
E38G |
probably damaging |
Het |
Cx3cl1 |
C |
G |
8: 95,507,053 (GRCm39) |
L353V |
probably damaging |
Het |
Cyp2a4 |
G |
T |
7: 26,006,786 (GRCm39) |
Q48H |
probably damaging |
Het |
Defb8 |
T |
C |
8: 19,497,603 (GRCm39) |
I3V |
probably benign |
Het |
Dip2a |
A |
T |
10: 76,155,390 (GRCm39) |
L65* |
probably null |
Het |
Dnaaf4 |
A |
G |
9: 72,867,960 (GRCm39) |
T74A |
possibly damaging |
Het |
Dsg2 |
A |
T |
18: 20,734,578 (GRCm39) |
D852V |
probably benign |
Het |
Edar |
T |
C |
10: 58,441,915 (GRCm39) |
R326G |
probably damaging |
Het |
Egfr |
A |
G |
11: 16,831,493 (GRCm39) |
E554G |
possibly damaging |
Het |
Eif2b3 |
A |
C |
4: 116,923,589 (GRCm39) |
K268T |
probably benign |
Het |
Enox1 |
A |
T |
14: 77,738,875 (GRCm39) |
|
probably benign |
Het |
Enpp3 |
C |
A |
10: 24,683,436 (GRCm39) |
M260I |
probably benign |
Het |
Espn |
A |
T |
4: 152,220,040 (GRCm39) |
M361K |
possibly damaging |
Het |
Fam107a |
T |
C |
14: 8,299,514 (GRCm38) |
N108S |
possibly damaging |
Het |
Fbn2 |
A |
T |
18: 58,205,703 (GRCm39) |
V1125D |
probably damaging |
Het |
Fbxo30 |
T |
A |
10: 11,166,507 (GRCm39) |
S410T |
probably damaging |
Het |
Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
Fcsk |
G |
A |
8: 111,614,435 (GRCm39) |
A618V |
probably damaging |
Het |
Gm10715 |
T |
G |
9: 3,038,073 (GRCm39) |
|
probably benign |
Het |
Gm10722 |
A |
C |
9: 3,001,041 (GRCm39) |
Y39S |
probably benign |
Het |
Gm17416 |
C |
A |
2: 152,411,427 (GRCm39) |
P57Q |
probably damaging |
Het |
Gm27013 |
A |
T |
6: 130,653,501 (GRCm39) |
C654S |
probably damaging |
Het |
Gon4l |
G |
T |
3: 88,807,305 (GRCm39) |
E1666D |
probably damaging |
Het |
Gypa |
T |
A |
8: 81,222,964 (GRCm39) |
S23T |
unknown |
Het |
Gys1 |
C |
A |
7: 45,100,968 (GRCm39) |
|
probably benign |
Het |
Hdac10 |
T |
A |
15: 89,008,143 (GRCm39) |
Q569L |
possibly damaging |
Het |
Icos |
A |
G |
1: 61,032,941 (GRCm39) |
T47A |
possibly damaging |
Het |
Igfn1 |
T |
A |
1: 135,882,404 (GRCm39) |
I2814F |
probably damaging |
Het |
Kif27 |
A |
G |
13: 58,440,957 (GRCm39) |
S1153P |
probably damaging |
Het |
Lin28a |
A |
C |
4: 133,746,028 (GRCm39) |
F9V |
possibly damaging |
Het |
Lrriq3 |
T |
A |
3: 154,893,695 (GRCm39) |
N465K |
probably benign |
Het |
Lsm14a |
T |
C |
7: 34,074,799 (GRCm39) |
E47G |
probably damaging |
Het |
Mmel1 |
A |
G |
4: 154,969,967 (GRCm39) |
K177R |
probably benign |
Het |
Ncstn |
T |
A |
1: 171,899,087 (GRCm39) |
N348I |
possibly damaging |
Het |
Ninl |
A |
G |
2: 150,795,284 (GRCm39) |
I619T |
probably damaging |
Het |
Npb |
T |
C |
11: 120,499,401 (GRCm39) |
Y23H |
probably damaging |
Het |
Npepps |
A |
G |
11: 97,096,933 (GRCm39) |
|
probably benign |
Het |
Or8k30 |
T |
C |
2: 86,339,699 (GRCm39) |
Y299H |
probably benign |
Het |
Otop1 |
G |
A |
5: 38,451,892 (GRCm39) |
|
probably null |
Het |
Pcyt1a |
A |
G |
16: 32,270,660 (GRCm39) |
|
probably benign |
Het |
Pdpr |
G |
T |
8: 111,841,400 (GRCm39) |
V211F |
probably damaging |
Het |
Pip4k2b |
T |
C |
11: 97,613,261 (GRCm39) |
N245S |
possibly damaging |
Het |
Platr26 |
G |
A |
2: 71,561,214 (GRCm39) |
|
noncoding transcript |
Het |
Plek |
A |
G |
11: 16,933,194 (GRCm39) |
|
probably null |
Het |
Potefam3c |
G |
C |
8: 69,906,010 (GRCm39) |
N13K |
probably benign |
Het |
Prdm15 |
A |
T |
16: 97,595,689 (GRCm39) |
D1046E |
probably damaging |
Het |
Prr29 |
T |
G |
11: 106,267,779 (GRCm39) |
C175G |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,504,196 (GRCm39) |
V1097A |
probably damaging |
Het |
Ramp2 |
T |
A |
11: 101,138,247 (GRCm39) |
|
probably benign |
Het |
Rap1gap |
A |
G |
4: 137,455,595 (GRCm39) |
D381G |
possibly damaging |
Het |
Rbbp6 |
T |
A |
7: 122,589,549 (GRCm39) |
D412E |
probably benign |
Het |
Rgs4 |
C |
T |
1: 169,572,802 (GRCm39) |
V45I |
probably benign |
Het |
Ryr2 |
C |
T |
13: 11,658,781 (GRCm39) |
R3614Q |
probably damaging |
Het |
Shc3 |
G |
A |
13: 51,596,856 (GRCm39) |
|
probably null |
Het |
Shmt2 |
A |
T |
10: 127,354,139 (GRCm39) |
C412S |
probably damaging |
Het |
Slc25a45 |
A |
T |
19: 5,934,945 (GRCm39) |
N265Y |
probably damaging |
Het |
Slc4a10 |
G |
C |
2: 62,074,783 (GRCm39) |
E316Q |
probably benign |
Het |
Slc5a8 |
T |
C |
10: 88,743,919 (GRCm39) |
|
probably null |
Het |
Snx31 |
A |
G |
15: 36,539,513 (GRCm39) |
V121A |
probably damaging |
Het |
Socs3 |
T |
C |
11: 117,858,542 (GRCm39) |
E172G |
probably damaging |
Het |
Tg |
A |
G |
15: 66,545,899 (GRCm39) |
D207G |
probably damaging |
Het |
Them4 |
G |
T |
3: 94,237,088 (GRCm39) |
V183F |
probably damaging |
Het |
Tkt |
G |
A |
14: 30,287,499 (GRCm39) |
W136* |
probably null |
Het |
Tlcd3b |
C |
T |
7: 126,426,795 (GRCm39) |
R73C |
probably damaging |
Het |
Tmc3 |
C |
A |
7: 83,271,529 (GRCm39) |
R894S |
probably benign |
Het |
Tmem132a |
G |
T |
19: 10,836,305 (GRCm39) |
P742T |
probably benign |
Het |
Tmem202 |
A |
G |
9: 59,432,129 (GRCm39) |
L66P |
probably damaging |
Het |
Trbc1 |
G |
A |
6: 41,516,270 (GRCm39) |
|
probably benign |
Het |
Trhr2 |
A |
G |
8: 123,085,511 (GRCm39) |
F158L |
probably benign |
Het |
Ttc13 |
A |
T |
8: 125,406,795 (GRCm39) |
N595K |
probably damaging |
Het |
Ucp1 |
A |
G |
8: 84,024,484 (GRCm39) |
|
probably null |
Het |
Zbtb4 |
C |
T |
11: 69,669,497 (GRCm39) |
T740I |
probably benign |
Het |
Zfp69 |
A |
T |
4: 120,804,522 (GRCm39) |
D116E |
possibly damaging |
Het |
Zfp879 |
A |
G |
11: 50,728,796 (GRCm39) |
L66S |
probably damaging |
Het |
Zfp955b |
T |
A |
17: 33,524,125 (GRCm39) |
|
probably benign |
Het |
Zfyve1 |
T |
C |
12: 83,594,839 (GRCm39) |
I718V |
possibly damaging |
Het |
|
Other mutations in Pcdha1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00714:Pcdha1
|
APN |
18 |
37,065,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R0062:Pcdha1
|
UTSW |
18 |
37,139,681 (GRCm39) |
missense |
probably benign |
0.08 |
R0108:Pcdha1
|
UTSW |
18 |
37,131,809 (GRCm39) |
missense |
probably benign |
|
R0543:Pcdha1
|
UTSW |
18 |
37,318,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1599:Pcdha1
|
UTSW |
18 |
37,318,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R1717:Pcdha1
|
UTSW |
18 |
37,065,237 (GRCm39) |
missense |
probably benign |
0.01 |
R2301:Pcdha1
|
UTSW |
18 |
37,289,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R3038:Pcdha1
|
UTSW |
18 |
37,064,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R3086:Pcdha1
|
UTSW |
18 |
37,064,001 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3693:Pcdha1
|
UTSW |
18 |
37,065,361 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3783:Pcdha1
|
UTSW |
18 |
37,063,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R3881:Pcdha1
|
UTSW |
18 |
37,064,454 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4012:Pcdha1
|
UTSW |
18 |
37,064,189 (GRCm39) |
missense |
probably benign |
0.02 |
R4540:Pcdha1
|
UTSW |
18 |
37,064,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R4597:Pcdha1
|
UTSW |
18 |
37,064,959 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4678:Pcdha1
|
UTSW |
18 |
37,063,965 (GRCm39) |
missense |
probably benign |
0.00 |
R5466:Pcdha1
|
UTSW |
18 |
37,065,312 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5518:Pcdha1
|
UTSW |
18 |
37,065,415 (GRCm39) |
missense |
probably benign |
0.23 |
R5673:Pcdha1
|
UTSW |
18 |
37,063,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R5925:Pcdha1
|
UTSW |
18 |
37,063,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5942:Pcdha1
|
UTSW |
18 |
37,063,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R5963:Pcdha1
|
UTSW |
18 |
37,064,224 (GRCm39) |
missense |
probably damaging |
0.99 |
R6034:Pcdha1
|
UTSW |
18 |
37,063,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Pcdha1
|
UTSW |
18 |
37,063,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R6107:Pcdha1
|
UTSW |
18 |
37,065,354 (GRCm39) |
missense |
probably benign |
0.00 |
R6329:Pcdha1
|
UTSW |
18 |
37,065,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6479:Pcdha1
|
UTSW |
18 |
37,064,509 (GRCm39) |
missense |
probably benign |
0.28 |
R6503:Pcdha1
|
UTSW |
18 |
37,064,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Pcdha1
|
UTSW |
18 |
37,064,124 (GRCm39) |
missense |
probably benign |
0.01 |
R7011:Pcdha1
|
UTSW |
18 |
37,063,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R7030:Pcdha1
|
UTSW |
18 |
37,292,326 (GRCm39) |
missense |
probably damaging |
0.97 |
R7314:Pcdha1
|
UTSW |
18 |
37,064,553 (GRCm39) |
missense |
probably damaging |
0.99 |
R7343:Pcdha1
|
UTSW |
18 |
37,063,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Pcdha1
|
UTSW |
18 |
37,064,115 (GRCm39) |
missense |
probably damaging |
0.98 |
R7700:Pcdha1
|
UTSW |
18 |
37,064,115 (GRCm39) |
missense |
probably damaging |
0.98 |
R7768:Pcdha1
|
UTSW |
18 |
37,065,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R7780:Pcdha1
|
UTSW |
18 |
37,065,511 (GRCm39) |
missense |
probably benign |
0.28 |
R7800:Pcdha1
|
UTSW |
18 |
37,064,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R7917:Pcdha1
|
UTSW |
18 |
37,065,254 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8325:Pcdha1
|
UTSW |
18 |
37,063,867 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8699:Pcdha1
|
UTSW |
18 |
37,064,076 (GRCm39) |
missense |
probably benign |
0.00 |
R9400:Pcdha1
|
UTSW |
18 |
37,064,760 (GRCm39) |
missense |
probably benign |
0.43 |
R9513:Pcdha1
|
UTSW |
18 |
37,065,286 (GRCm39) |
missense |
probably benign |
0.26 |
R9746:Pcdha1
|
UTSW |
18 |
37,065,713 (GRCm39) |
missense |
probably benign |
|
|