Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
C |
6: 128,535,257 (GRCm39) |
T818A |
probably benign |
Het |
Aasdh |
A |
G |
5: 77,036,629 (GRCm39) |
V304A |
probably benign |
Het |
Angptl3 |
G |
A |
4: 98,922,702 (GRCm39) |
A248T |
probably benign |
Het |
Ap2b1 |
T |
A |
11: 83,215,391 (GRCm39) |
C112S |
possibly damaging |
Het |
Aqr |
A |
T |
2: 113,967,368 (GRCm39) |
I549N |
probably damaging |
Het |
Barhl1 |
C |
T |
2: 28,801,562 (GRCm39) |
D161N |
possibly damaging |
Het |
Col28a1 |
A |
G |
6: 8,014,942 (GRCm39) |
V821A |
probably damaging |
Het |
Dclk2 |
G |
A |
3: 86,827,342 (GRCm39) |
P46S |
probably damaging |
Het |
Dnah1 |
A |
G |
14: 31,037,105 (GRCm39) |
L247P |
possibly damaging |
Het |
Dpysl2 |
T |
A |
14: 67,071,819 (GRCm39) |
H107L |
probably damaging |
Het |
Dzip3 |
A |
G |
16: 48,757,426 (GRCm39) |
L869S |
probably damaging |
Het |
Efs |
T |
C |
14: 55,157,552 (GRCm39) |
Y160C |
probably damaging |
Het |
Enam |
A |
T |
5: 88,652,306 (GRCm39) |
N1197Y |
possibly damaging |
Het |
Fam184b |
A |
G |
5: 45,740,157 (GRCm39) |
V343A |
possibly damaging |
Het |
Fbxw26 |
A |
T |
9: 109,572,828 (GRCm39) |
Y105* |
probably null |
Het |
Fiz1 |
A |
G |
7: 5,011,171 (GRCm39) |
L449P |
probably benign |
Het |
Foxi2 |
T |
A |
7: 135,012,180 (GRCm39) |
C23S |
possibly damaging |
Het |
Gdf2 |
G |
A |
14: 33,666,914 (GRCm39) |
R212Q |
probably damaging |
Het |
Gm5105 |
C |
A |
3: 137,755,449 (GRCm39) |
A46S |
unknown |
Het |
Grik5 |
C |
T |
7: 24,721,996 (GRCm39) |
A581T |
probably benign |
Het |
Gse1 |
C |
G |
8: 121,299,481 (GRCm39) |
|
probably benign |
Het |
Hsp90aa1 |
T |
A |
12: 110,662,114 (GRCm39) |
M1L |
possibly damaging |
Het |
Hsp90aa1 |
C |
A |
12: 110,662,115 (GRCm39) |
|
probably null |
Het |
Krt25 |
A |
C |
11: 99,208,124 (GRCm39) |
V368G |
possibly damaging |
Het |
Lacc1 |
A |
G |
14: 77,270,727 (GRCm39) |
V269A |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,126,896 (GRCm39) |
K417E |
probably damaging |
Het |
Miip |
A |
G |
4: 147,950,371 (GRCm39) |
M75T |
probably benign |
Het |
Nlrp10 |
A |
G |
7: 108,523,683 (GRCm39) |
F599S |
probably benign |
Het |
Nlrp12 |
T |
A |
7: 3,289,205 (GRCm39) |
M436L |
probably benign |
Het |
Or4b13 |
T |
C |
2: 90,082,753 (GRCm39) |
E193G |
possibly damaging |
Het |
Pafah1b1 |
G |
A |
11: 74,581,058 (GRCm39) |
S57F |
probably damaging |
Het |
Pla2g2e |
G |
A |
4: 138,607,685 (GRCm39) |
V22I |
probably benign |
Het |
Plekhd1 |
A |
G |
12: 80,764,044 (GRCm39) |
E202G |
probably damaging |
Het |
Prss21 |
A |
G |
17: 24,091,805 (GRCm39) |
T258A |
probably benign |
Het |
Prss34 |
A |
G |
17: 25,517,820 (GRCm39) |
E65G |
probably benign |
Het |
Psap |
A |
G |
10: 60,130,383 (GRCm39) |
N149S |
probably benign |
Het |
Ptprf |
C |
T |
4: 118,095,080 (GRCm39) |
A275T |
probably benign |
Het |
Sem1 |
A |
G |
6: 6,578,520 (GRCm39) |
L12P |
probably damaging |
Het |
Sf3b3 |
A |
G |
8: 111,571,155 (GRCm39) |
Y4H |
probably damaging |
Het |
Sh3bp4 |
G |
T |
1: 89,065,427 (GRCm39) |
R7L |
probably damaging |
Het |
Slc16a1 |
T |
A |
3: 104,560,886 (GRCm39) |
L397Q |
probably damaging |
Het |
Smg5 |
A |
G |
3: 88,243,758 (GRCm39) |
S10G |
possibly damaging |
Het |
Spata31e5 |
T |
C |
1: 28,815,656 (GRCm39) |
D792G |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,971,864 (GRCm39) |
N399S |
probably benign |
Het |
Tas2r102 |
C |
T |
6: 132,739,781 (GRCm39) |
Q230* |
probably null |
Het |
Tdo2 |
A |
G |
3: 81,882,735 (GRCm39) |
Y13H |
possibly damaging |
Het |
Tmem231 |
C |
T |
8: 112,644,945 (GRCm39) |
R187H |
possibly damaging |
Het |
Tmem30b |
A |
G |
12: 73,592,353 (GRCm39) |
M254T |
probably damaging |
Het |
Trpm1 |
G |
A |
7: 63,893,318 (GRCm39) |
G1057R |
probably damaging |
Het |
Tusc3 |
A |
T |
8: 39,617,879 (GRCm39) |
K347N |
probably damaging |
Het |
Usp36 |
C |
T |
11: 118,167,585 (GRCm39) |
|
probably null |
Het |
Vash2 |
T |
C |
1: 190,702,616 (GRCm39) |
Y117C |
probably damaging |
Het |
Vrk2 |
A |
G |
11: 26,439,866 (GRCm39) |
I235T |
possibly damaging |
Het |
Wdr20 |
A |
G |
12: 110,760,373 (GRCm39) |
T420A |
probably benign |
Het |
|
Other mutations in Espl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00821:Espl1
|
APN |
15 |
102,208,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00839:Espl1
|
APN |
15 |
102,228,982 (GRCm39) |
unclassified |
probably benign |
|
IGL00919:Espl1
|
APN |
15 |
102,207,064 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01125:Espl1
|
APN |
15 |
102,231,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01366:Espl1
|
APN |
15 |
102,228,271 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01488:Espl1
|
APN |
15 |
102,207,174 (GRCm39) |
missense |
probably benign |
|
IGL01554:Espl1
|
APN |
15 |
102,221,660 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01810:Espl1
|
APN |
15 |
102,206,640 (GRCm39) |
missense |
probably benign |
|
IGL01959:Espl1
|
APN |
15 |
102,214,097 (GRCm39) |
splice site |
probably benign |
|
IGL02267:Espl1
|
APN |
15 |
102,224,099 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02452:Espl1
|
APN |
15 |
102,208,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02469:Espl1
|
APN |
15 |
102,222,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02500:Espl1
|
APN |
15 |
102,224,235 (GRCm39) |
missense |
probably benign |
|
IGL02630:Espl1
|
APN |
15 |
102,205,253 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02687:Espl1
|
APN |
15 |
102,221,613 (GRCm39) |
splice site |
probably benign |
|
IGL02868:Espl1
|
APN |
15 |
102,222,425 (GRCm39) |
nonsense |
probably null |
|
IGL02926:Espl1
|
APN |
15 |
102,208,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R0019:Espl1
|
UTSW |
15 |
102,214,754 (GRCm39) |
missense |
probably null |
0.01 |
R0129:Espl1
|
UTSW |
15 |
102,225,083 (GRCm39) |
missense |
probably benign |
0.00 |
R0184:Espl1
|
UTSW |
15 |
102,207,651 (GRCm39) |
missense |
probably benign |
0.01 |
R0240:Espl1
|
UTSW |
15 |
102,220,976 (GRCm39) |
missense |
probably benign |
0.00 |
R0240:Espl1
|
UTSW |
15 |
102,220,976 (GRCm39) |
missense |
probably benign |
0.00 |
R0267:Espl1
|
UTSW |
15 |
102,221,452 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0423:Espl1
|
UTSW |
15 |
102,212,421 (GRCm39) |
nonsense |
probably null |
|
R0587:Espl1
|
UTSW |
15 |
102,212,382 (GRCm39) |
splice site |
probably benign |
|
R0726:Espl1
|
UTSW |
15 |
102,231,033 (GRCm39) |
missense |
probably benign |
|
R1186:Espl1
|
UTSW |
15 |
102,212,474 (GRCm39) |
missense |
probably benign |
0.05 |
R1282:Espl1
|
UTSW |
15 |
102,223,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1428:Espl1
|
UTSW |
15 |
102,214,120 (GRCm39) |
missense |
probably benign |
0.06 |
R1467:Espl1
|
UTSW |
15 |
102,228,293 (GRCm39) |
missense |
probably benign |
0.09 |
R1467:Espl1
|
UTSW |
15 |
102,228,293 (GRCm39) |
missense |
probably benign |
0.09 |
R1473:Espl1
|
UTSW |
15 |
102,228,878 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1570:Espl1
|
UTSW |
15 |
102,206,802 (GRCm39) |
missense |
probably damaging |
0.98 |
R1639:Espl1
|
UTSW |
15 |
102,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Espl1
|
UTSW |
15 |
102,221,656 (GRCm39) |
missense |
probably benign |
0.08 |
R1748:Espl1
|
UTSW |
15 |
102,206,964 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1845:Espl1
|
UTSW |
15 |
102,207,448 (GRCm39) |
missense |
probably benign |
|
R1938:Espl1
|
UTSW |
15 |
102,213,477 (GRCm39) |
missense |
probably benign |
0.00 |
R1954:Espl1
|
UTSW |
15 |
102,206,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R2009:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R2014:Espl1
|
UTSW |
15 |
102,231,149 (GRCm39) |
nonsense |
probably null |
|
R2067:Espl1
|
UTSW |
15 |
102,207,525 (GRCm39) |
missense |
probably damaging |
0.96 |
R2084:Espl1
|
UTSW |
15 |
102,205,286 (GRCm39) |
critical splice donor site |
probably null |
|
R2164:Espl1
|
UTSW |
15 |
102,228,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Espl1
|
UTSW |
15 |
102,214,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R2220:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R2237:Espl1
|
UTSW |
15 |
102,224,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R2314:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3107:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3108:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3114:Espl1
|
UTSW |
15 |
102,231,639 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3115:Espl1
|
UTSW |
15 |
102,231,639 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3616:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3732:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3732:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3733:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3958:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3959:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R3960:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4062:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4063:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4064:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4165:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4166:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4349:Espl1
|
UTSW |
15 |
102,228,039 (GRCm39) |
missense |
probably benign |
0.26 |
R4373:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4376:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4377:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4516:Espl1
|
UTSW |
15 |
102,231,671 (GRCm39) |
missense |
probably benign |
0.00 |
R4595:Espl1
|
UTSW |
15 |
102,207,159 (GRCm39) |
missense |
probably benign |
0.01 |
R4884:Espl1
|
UTSW |
15 |
102,232,505 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4894:Espl1
|
UTSW |
15 |
102,230,758 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4921:Espl1
|
UTSW |
15 |
102,223,676 (GRCm39) |
missense |
probably damaging |
0.98 |
R4931:Espl1
|
UTSW |
15 |
102,214,165 (GRCm39) |
missense |
probably benign |
0.02 |
R4936:Espl1
|
UTSW |
15 |
102,213,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Espl1
|
UTSW |
15 |
102,206,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R5220:Espl1
|
UTSW |
15 |
102,207,012 (GRCm39) |
missense |
probably benign |
0.03 |
R5329:Espl1
|
UTSW |
15 |
102,220,953 (GRCm39) |
missense |
probably damaging |
0.97 |
R5501:Espl1
|
UTSW |
15 |
102,225,565 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5788:Espl1
|
UTSW |
15 |
102,232,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R5848:Espl1
|
UTSW |
15 |
102,231,011 (GRCm39) |
missense |
probably benign |
0.03 |
R5906:Espl1
|
UTSW |
15 |
102,205,286 (GRCm39) |
critical splice donor site |
probably null |
|
R5978:Espl1
|
UTSW |
15 |
102,224,209 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6111:Espl1
|
UTSW |
15 |
102,208,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R6313:Espl1
|
UTSW |
15 |
102,224,247 (GRCm39) |
missense |
probably benign |
0.00 |
R6414:Espl1
|
UTSW |
15 |
102,223,995 (GRCm39) |
missense |
probably damaging |
0.96 |
R6484:Espl1
|
UTSW |
15 |
102,231,935 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6784:Espl1
|
UTSW |
15 |
102,207,660 (GRCm39) |
missense |
probably benign |
|
R6928:Espl1
|
UTSW |
15 |
102,207,342 (GRCm39) |
missense |
probably benign |
0.28 |
R6995:Espl1
|
UTSW |
15 |
102,212,535 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7053:Espl1
|
UTSW |
15 |
102,225,328 (GRCm39) |
critical splice donor site |
probably null |
|
R7062:Espl1
|
UTSW |
15 |
102,207,331 (GRCm39) |
missense |
probably benign |
0.00 |
R7135:Espl1
|
UTSW |
15 |
102,227,959 (GRCm39) |
nonsense |
probably null |
|
R7154:Espl1
|
UTSW |
15 |
102,232,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Espl1
|
UTSW |
15 |
102,221,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R7522:Espl1
|
UTSW |
15 |
102,213,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:Espl1
|
UTSW |
15 |
102,224,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Espl1
|
UTSW |
15 |
102,212,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R8275:Espl1
|
UTSW |
15 |
102,211,188 (GRCm39) |
splice site |
probably benign |
|
R8752:Espl1
|
UTSW |
15 |
102,214,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R9160:Espl1
|
UTSW |
15 |
102,206,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R9310:Espl1
|
UTSW |
15 |
102,205,285 (GRCm39) |
critical splice donor site |
probably null |
|
R9385:Espl1
|
UTSW |
15 |
102,207,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R9532:Espl1
|
UTSW |
15 |
102,228,260 (GRCm39) |
nonsense |
probably null |
|
R9563:Espl1
|
UTSW |
15 |
102,228,233 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9565:Espl1
|
UTSW |
15 |
102,228,233 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9723:Espl1
|
UTSW |
15 |
102,229,170 (GRCm39) |
missense |
probably benign |
0.43 |
X0062:Espl1
|
UTSW |
15 |
102,206,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|