Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamdec1 |
A |
T |
14: 68,806,172 (GRCm39) |
C434* |
probably null |
Het |
Adprhl1 |
A |
G |
8: 13,292,391 (GRCm39) |
|
probably benign |
Het |
Ago1 |
T |
A |
4: 126,357,499 (GRCm39) |
I59F |
possibly damaging |
Het |
Arel1 |
T |
C |
12: 84,967,467 (GRCm39) |
T786A |
probably damaging |
Het |
Arhgap26 |
A |
G |
18: 39,496,184 (GRCm39) |
K117R |
probably benign |
Het |
Atp6v0b |
C |
T |
4: 117,741,819 (GRCm39) |
G204D |
probably damaging |
Het |
Bace2 |
T |
A |
16: 97,237,973 (GRCm39) |
|
probably null |
Het |
Bltp2 |
T |
A |
11: 78,177,317 (GRCm39) |
|
probably null |
Het |
Camk4 |
G |
A |
18: 33,312,678 (GRCm39) |
|
probably null |
Het |
Cep152 |
T |
C |
2: 125,406,134 (GRCm39) |
E1466G |
probably benign |
Het |
Ces3b |
T |
C |
8: 105,819,267 (GRCm39) |
F441S |
probably damaging |
Het |
Cfap52 |
T |
C |
11: 67,817,208 (GRCm39) |
T562A |
possibly damaging |
Het |
Clca3a2 |
C |
A |
3: 144,519,659 (GRCm39) |
M238I |
possibly damaging |
Het |
Cntnap5c |
A |
T |
17: 58,409,163 (GRCm39) |
D467V |
probably damaging |
Het |
Col7a1 |
T |
A |
9: 108,801,252 (GRCm39) |
|
probably null |
Het |
Cstf1 |
A |
G |
2: 172,219,630 (GRCm39) |
N247S |
possibly damaging |
Het |
Dffb |
G |
T |
4: 154,059,072 (GRCm39) |
N68K |
probably benign |
Het |
Dnaaf10 |
T |
C |
11: 17,179,851 (GRCm39) |
L284P |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,122,341 (GRCm39) |
G595S |
probably benign |
Het |
Eftud2 |
T |
A |
11: 102,755,551 (GRCm39) |
I228F |
probably damaging |
Het |
Elmo3 |
T |
C |
8: 106,035,803 (GRCm39) |
V578A |
probably benign |
Het |
Elp2 |
A |
G |
18: 24,764,528 (GRCm39) |
D625G |
possibly damaging |
Het |
Ep300 |
C |
T |
15: 81,524,329 (GRCm39) |
P1386S |
unknown |
Het |
Fam120b |
A |
G |
17: 15,637,899 (GRCm39) |
D610G |
probably damaging |
Het |
Fastk |
A |
T |
5: 24,647,176 (GRCm39) |
|
probably benign |
Het |
Fbxl6 |
A |
G |
15: 76,421,391 (GRCm39) |
S252P |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,161,939 (GRCm39) |
K423E |
probably damaging |
Het |
Filip1 |
T |
A |
9: 79,726,744 (GRCm39) |
E625V |
possibly damaging |
Het |
Fkbp9 |
T |
A |
6: 56,833,363 (GRCm39) |
Y283* |
probably null |
Het |
Gigyf2 |
T |
A |
1: 87,306,737 (GRCm39) |
D142E |
possibly damaging |
Het |
Gm10142 |
T |
C |
10: 77,551,848 (GRCm39) |
|
probably null |
Het |
Golga5 |
T |
C |
12: 102,442,447 (GRCm39) |
V262A |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,467,668 (GRCm39) |
V2539A |
probably benign |
Het |
Ica1 |
G |
T |
6: 8,653,632 (GRCm39) |
S335* |
probably null |
Het |
Itga1 |
A |
T |
13: 115,143,433 (GRCm39) |
|
probably benign |
Het |
Itgb1 |
T |
C |
8: 129,444,166 (GRCm39) |
|
probably benign |
Het |
Itpr1 |
G |
A |
6: 108,450,550 (GRCm39) |
V1960I |
probably benign |
Het |
Kcnh4 |
C |
T |
11: 100,637,758 (GRCm39) |
G633E |
probably benign |
Het |
Kprp |
C |
T |
3: 92,732,718 (GRCm39) |
V111I |
probably benign |
Het |
Lamc3 |
T |
C |
2: 31,830,733 (GRCm39) |
I1490T |
probably damaging |
Het |
Lcp1 |
A |
T |
14: 75,464,441 (GRCm39) |
D554V |
possibly damaging |
Het |
Lgi3 |
A |
G |
14: 70,772,138 (GRCm39) |
T228A |
probably benign |
Het |
Lipa |
A |
T |
19: 34,478,941 (GRCm39) |
F260I |
probably damaging |
Het |
Lrriq1 |
C |
T |
10: 103,051,634 (GRCm39) |
E373K |
probably damaging |
Het |
Map6 |
G |
A |
7: 98,986,043 (GRCm39) |
G649D |
probably benign |
Het |
Mccc1 |
A |
G |
3: 36,044,196 (GRCm39) |
|
probably null |
Het |
Mical3 |
A |
T |
6: 120,934,683 (GRCm39) |
S1799T |
probably benign |
Het |
Mmp23 |
T |
A |
4: 155,736,589 (GRCm39) |
T151S |
probably damaging |
Het |
Myo1d |
T |
A |
11: 80,565,534 (GRCm39) |
N401I |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,774,457 (GRCm39) |
S323T |
probably damaging |
Het |
Nbn |
G |
T |
4: 15,979,353 (GRCm39) |
W446L |
probably benign |
Het |
Nedd1 |
A |
T |
10: 92,552,127 (GRCm39) |
|
probably benign |
Het |
Ngef |
C |
A |
1: 87,415,684 (GRCm39) |
|
probably benign |
Het |
Nup153 |
A |
T |
13: 46,847,412 (GRCm39) |
N672K |
probably benign |
Het |
Or10d1b |
T |
A |
9: 39,613,469 (GRCm39) |
I199F |
probably damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or4e2 |
T |
C |
14: 52,687,969 (GRCm39) |
V33A |
probably benign |
Het |
Or4f57 |
T |
C |
2: 111,791,361 (GRCm39) |
N19S |
probably benign |
Het |
Pakap |
T |
G |
4: 57,710,177 (GRCm39) |
V374G |
possibly damaging |
Het |
Pdlim3 |
C |
A |
8: 46,361,497 (GRCm39) |
|
probably benign |
Het |
Pmfbp1 |
G |
A |
8: 110,268,305 (GRCm39) |
E951K |
probably damaging |
Het |
Pop1 |
T |
A |
15: 34,516,037 (GRCm39) |
C548* |
probably null |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Ptpdc1 |
A |
T |
13: 48,739,456 (GRCm39) |
N658K |
probably benign |
Het |
Ptprk |
A |
C |
10: 28,082,221 (GRCm39) |
E63D |
possibly damaging |
Het |
Rtf1 |
C |
T |
2: 119,563,358 (GRCm39) |
R712W |
probably damaging |
Het |
Samd7 |
A |
C |
3: 30,805,222 (GRCm39) |
T2P |
probably benign |
Het |
Sft2d1 |
A |
G |
17: 8,538,254 (GRCm39) |
T52A |
probably benign |
Het |
Slc25a26 |
A |
G |
6: 94,487,814 (GRCm39) |
H91R |
probably damaging |
Het |
Slc5a4a |
A |
G |
10: 76,024,986 (GRCm39) |
E621G |
possibly damaging |
Het |
Slf1 |
A |
T |
13: 77,274,751 (GRCm39) |
L28* |
probably null |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Sorcs2 |
G |
A |
5: 36,554,897 (GRCm39) |
|
probably benign |
Het |
Tacc2 |
T |
C |
7: 130,353,555 (GRCm39) |
|
probably benign |
Het |
Tas2r140 |
A |
G |
6: 133,032,290 (GRCm39) |
V156A |
possibly damaging |
Het |
Terf2ip |
C |
A |
8: 112,744,796 (GRCm39) |
T371K |
possibly damaging |
Het |
Tifa |
C |
T |
3: 127,590,537 (GRCm39) |
L103F |
probably damaging |
Het |
Tmco3 |
A |
G |
8: 13,342,037 (GRCm39) |
N104D |
probably damaging |
Het |
Tmem259 |
T |
A |
10: 79,814,797 (GRCm39) |
D240V |
probably damaging |
Het |
Trim60 |
C |
T |
8: 65,453,700 (GRCm39) |
R183H |
probably benign |
Het |
Trps1 |
T |
C |
15: 50,528,139 (GRCm39) |
N725D |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,645,150 (GRCm39) |
V12902M |
probably damaging |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Unc79 |
A |
G |
12: 103,079,150 (GRCm39) |
K1772E |
probably damaging |
Het |
Vwde |
C |
T |
6: 13,193,125 (GRCm39) |
V405I |
probably benign |
Het |
Wdr18 |
T |
A |
10: 79,802,242 (GRCm39) |
D290E |
probably damaging |
Het |
Wwc2 |
G |
A |
8: 48,353,756 (GRCm39) |
A126V |
probably benign |
Het |
Zfp882 |
A |
T |
8: 72,667,367 (GRCm39) |
I105F |
possibly damaging |
Het |
Zfp942 |
A |
T |
17: 22,147,553 (GRCm39) |
C359S |
probably benign |
Het |
|
Other mutations in Cdh26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00846:Cdh26
|
APN |
2 |
178,123,417 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01341:Cdh26
|
APN |
2 |
178,099,240 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02636:Cdh26
|
APN |
2 |
178,091,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03144:Cdh26
|
APN |
2 |
178,109,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R0245:Cdh26
|
UTSW |
2 |
178,123,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0466:Cdh26
|
UTSW |
2 |
178,123,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0467:Cdh26
|
UTSW |
2 |
178,123,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0514:Cdh26
|
UTSW |
2 |
178,108,621 (GRCm39) |
critical splice donor site |
probably null |
|
R0610:Cdh26
|
UTSW |
2 |
178,091,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R0733:Cdh26
|
UTSW |
2 |
178,128,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R1592:Cdh26
|
UTSW |
2 |
178,091,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Cdh26
|
UTSW |
2 |
178,108,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R3756:Cdh26
|
UTSW |
2 |
178,111,794 (GRCm39) |
splice site |
probably benign |
|
R4617:Cdh26
|
UTSW |
2 |
178,102,435 (GRCm39) |
intron |
probably benign |
|
R4914:Cdh26
|
UTSW |
2 |
178,091,614 (GRCm39) |
missense |
probably benign |
0.02 |
R4915:Cdh26
|
UTSW |
2 |
178,091,614 (GRCm39) |
missense |
probably benign |
0.02 |
R4917:Cdh26
|
UTSW |
2 |
178,091,614 (GRCm39) |
missense |
probably benign |
0.02 |
R4918:Cdh26
|
UTSW |
2 |
178,091,614 (GRCm39) |
missense |
probably benign |
0.02 |
R5086:Cdh26
|
UTSW |
2 |
178,083,210 (GRCm39) |
nonsense |
probably null |
|
R5573:Cdh26
|
UTSW |
2 |
178,108,482 (GRCm39) |
missense |
probably damaging |
0.96 |
R5809:Cdh26
|
UTSW |
2 |
178,101,919 (GRCm39) |
nonsense |
probably null |
|
R5941:Cdh26
|
UTSW |
2 |
178,123,443 (GRCm39) |
nonsense |
probably null |
|
R6284:Cdh26
|
UTSW |
2 |
178,091,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6341:Cdh26
|
UTSW |
2 |
178,113,366 (GRCm39) |
splice site |
probably null |
|
R6496:Cdh26
|
UTSW |
2 |
178,091,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Cdh26
|
UTSW |
2 |
178,128,555 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7664:Cdh26
|
UTSW |
2 |
178,111,835 (GRCm39) |
missense |
probably benign |
0.02 |
R7694:Cdh26
|
UTSW |
2 |
178,101,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R7814:Cdh26
|
UTSW |
2 |
178,111,828 (GRCm39) |
missense |
probably damaging |
0.98 |
R8089:Cdh26
|
UTSW |
2 |
178,099,370 (GRCm39) |
critical splice donor site |
probably null |
|
R8103:Cdh26
|
UTSW |
2 |
178,110,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R8412:Cdh26
|
UTSW |
2 |
178,104,517 (GRCm39) |
missense |
probably damaging |
0.98 |
R8413:Cdh26
|
UTSW |
2 |
178,110,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R9025:Cdh26
|
UTSW |
2 |
178,104,409 (GRCm39) |
missense |
probably benign |
0.01 |
R9621:Cdh26
|
UTSW |
2 |
178,111,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R9628:Cdh26
|
UTSW |
2 |
178,083,213 (GRCm39) |
missense |
|
|
RF002:Cdh26
|
UTSW |
2 |
178,108,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|