Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam4 |
A |
T |
12: 81,466,428 (GRCm39) |
L731H |
probably damaging |
Het |
Adora2b |
C |
T |
11: 62,139,995 (GRCm39) |
A23V |
probably benign |
Het |
Ankrd17 |
T |
C |
5: 90,411,857 (GRCm39) |
I1336V |
probably damaging |
Het |
Asxl1 |
G |
A |
2: 153,239,442 (GRCm39) |
R410H |
probably damaging |
Het |
Atp8a2 |
T |
C |
14: 60,260,593 (GRCm39) |
E419G |
probably benign |
Het |
Atxn1l |
A |
T |
8: 110,459,016 (GRCm39) |
N415K |
probably damaging |
Het |
Bcl2l12 |
T |
A |
7: 44,646,025 (GRCm39) |
T65S |
probably benign |
Het |
Bdh2 |
A |
G |
3: 134,996,774 (GRCm39) |
I90V |
probably benign |
Het |
Cd96 |
T |
C |
16: 45,938,153 (GRCm39) |
Y104C |
possibly damaging |
Het |
Chdh |
T |
C |
14: 29,753,570 (GRCm39) |
W160R |
probably damaging |
Het |
Clock |
A |
G |
5: 76,393,365 (GRCm39) |
F193L |
probably damaging |
Het |
Copz1 |
A |
G |
15: 103,204,958 (GRCm39) |
|
probably null |
Het |
Cyp2c38 |
T |
C |
19: 39,379,500 (GRCm39) |
T450A |
probably damaging |
Het |
Cyp2d34 |
A |
T |
15: 82,501,751 (GRCm39) |
I253K |
probably benign |
Het |
Dhrs13 |
G |
T |
11: 77,927,789 (GRCm39) |
A212S |
probably damaging |
Het |
Ecsit |
T |
C |
9: 21,987,796 (GRCm39) |
N81S |
probably benign |
Het |
Efl1 |
A |
G |
7: 82,301,094 (GRCm39) |
T33A |
probably damaging |
Het |
Emid1 |
T |
C |
11: 5,093,866 (GRCm39) |
R92G |
probably damaging |
Het |
Ermp1 |
A |
G |
19: 29,609,941 (GRCm39) |
|
probably benign |
Het |
Fn1 |
A |
T |
1: 71,634,968 (GRCm39) |
|
probably null |
Het |
Hps5 |
A |
G |
7: 46,432,893 (GRCm39) |
|
probably null |
Het |
Hsd17b3 |
T |
C |
13: 64,236,882 (GRCm39) |
M21V |
probably benign |
Het |
Kat6b |
T |
C |
14: 21,718,849 (GRCm39) |
V1176A |
probably benign |
Het |
Midn |
A |
G |
10: 79,992,336 (GRCm39) |
K463E |
probably damaging |
Het |
Mier1 |
A |
G |
4: 102,996,631 (GRCm39) |
E103G |
probably damaging |
Het |
Muc15 |
A |
G |
2: 110,564,160 (GRCm39) |
N232S |
possibly damaging |
Het |
Ncoa2 |
T |
A |
1: 13,294,875 (GRCm39) |
E15V |
probably damaging |
Het |
Or10a5 |
A |
T |
7: 106,635,889 (GRCm39) |
N176Y |
probably damaging |
Het |
Or2n1d |
A |
G |
17: 38,646,735 (GRCm39) |
K229R |
probably benign |
Het |
Or52n2b |
T |
A |
7: 104,565,841 (GRCm39) |
T221S |
probably benign |
Het |
Pate14 |
C |
T |
9: 36,549,176 (GRCm39) |
G28E |
probably benign |
Het |
Pigf |
A |
T |
17: 87,327,923 (GRCm39) |
F115I |
probably benign |
Het |
Prpsap1 |
A |
T |
11: 116,362,317 (GRCm39) |
V355E |
probably damaging |
Het |
Ptprk |
G |
T |
10: 28,359,294 (GRCm39) |
|
probably benign |
Het |
Rae1 |
G |
A |
2: 172,846,957 (GRCm39) |
R67H |
probably damaging |
Het |
Sema3a |
G |
A |
5: 13,606,494 (GRCm39) |
|
probably null |
Het |
Slc22a22 |
T |
C |
15: 57,126,758 (GRCm39) |
T104A |
probably benign |
Het |
Slc38a2 |
A |
T |
15: 96,593,168 (GRCm39) |
L137* |
probably null |
Het |
Smgc |
A |
G |
15: 91,725,670 (GRCm39) |
|
probably benign |
Het |
Syce3 |
A |
G |
15: 89,274,648 (GRCm39) |
|
probably benign |
Het |
Syt9 |
T |
A |
7: 107,024,343 (GRCm39) |
W79R |
probably damaging |
Het |
Tgoln1 |
A |
C |
6: 72,592,974 (GRCm39) |
S169A |
probably benign |
Het |
Thnsl1 |
A |
G |
2: 21,216,477 (GRCm39) |
D77G |
probably benign |
Het |
Tsr1 |
T |
A |
11: 74,798,767 (GRCm39) |
V712E |
probably damaging |
Het |
Wdr12 |
C |
T |
1: 60,128,525 (GRCm39) |
|
probably benign |
Het |
Xdh |
T |
A |
17: 74,250,886 (GRCm39) |
N22I |
probably damaging |
Het |
Zfp3 |
T |
A |
11: 70,662,395 (GRCm39) |
L118Q |
probably benign |
Het |
Zfp592 |
A |
G |
7: 80,687,623 (GRCm39) |
N883D |
probably benign |
Het |
Zfp609 |
T |
A |
9: 65,638,483 (GRCm39) |
M250L |
probably benign |
Het |
Zfp94 |
A |
T |
7: 24,002,495 (GRCm39) |
S316T |
probably damaging |
Het |
Zfp955b |
A |
G |
17: 33,521,947 (GRCm39) |
N472S |
probably benign |
Het |
|
Other mutations in Bsph1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03131:Bsph1
|
APN |
7 |
13,207,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Bsph1
|
UTSW |
7 |
13,184,864 (GRCm39) |
nonsense |
probably null |
|
R0701:Bsph1
|
UTSW |
7 |
13,206,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Bsph1
|
UTSW |
7 |
13,184,839 (GRCm39) |
start codon destroyed |
probably benign |
0.33 |
R1087:Bsph1
|
UTSW |
7 |
13,206,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R2189:Bsph1
|
UTSW |
7 |
13,204,254 (GRCm39) |
critical splice donor site |
probably null |
|
R3427:Bsph1
|
UTSW |
7 |
13,206,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Bsph1
|
UTSW |
7 |
13,192,201 (GRCm39) |
critical splice donor site |
probably null |
|
R4718:Bsph1
|
UTSW |
7 |
13,206,107 (GRCm39) |
nonsense |
probably null |
|
R4726:Bsph1
|
UTSW |
7 |
13,206,920 (GRCm39) |
missense |
probably benign |
0.00 |
R5571:Bsph1
|
UTSW |
7 |
13,184,840 (GRCm39) |
start codon destroyed |
probably null |
0.86 |
R6852:Bsph1
|
UTSW |
7 |
13,204,255 (GRCm39) |
critical splice donor site |
probably null |
|
R6903:Bsph1
|
UTSW |
7 |
13,192,183 (GRCm39) |
missense |
probably damaging |
1.00 |
|