Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
A |
6: 86,827,044 (GRCm39) |
F4I |
probably damaging |
Het |
Adamts8 |
G |
T |
9: 30,862,684 (GRCm39) |
E296D |
probably benign |
Het |
Alg11 |
T |
C |
8: 22,555,573 (GRCm39) |
V278A |
probably damaging |
Het |
Ankfy1 |
G |
A |
11: 72,605,310 (GRCm39) |
|
probably null |
Het |
Avil |
C |
T |
10: 126,842,496 (GRCm39) |
Q92* |
probably null |
Het |
Cfap300 |
A |
T |
9: 8,026,071 (GRCm39) |
L167Q |
probably damaging |
Het |
CK137956 |
A |
T |
4: 127,864,522 (GRCm39) |
S36T |
possibly damaging |
Het |
Epb41l3 |
T |
C |
17: 69,514,883 (GRCm39) |
S7P |
probably damaging |
Het |
Fsd2 |
T |
C |
7: 81,195,608 (GRCm39) |
T434A |
probably damaging |
Het |
Gm5174 |
A |
G |
10: 86,492,797 (GRCm39) |
|
noncoding transcript |
Het |
Gpaa1 |
A |
C |
15: 76,216,667 (GRCm39) |
|
probably benign |
Het |
Grina |
T |
A |
15: 76,133,529 (GRCm39) |
L334Q |
probably damaging |
Het |
Gvin-ps5 |
T |
A |
7: 105,929,895 (GRCm39) |
|
noncoding transcript |
Het |
Igkv15-103 |
G |
T |
6: 68,414,824 (GRCm39) |
G88* |
probably null |
Het |
Ip6k2 |
G |
A |
9: 108,682,847 (GRCm39) |
R319Q |
probably benign |
Het |
Kdm3b |
A |
T |
18: 34,928,797 (GRCm39) |
I183F |
probably benign |
Het |
Kyat3 |
A |
G |
3: 142,432,066 (GRCm39) |
|
probably null |
Het |
Larp7 |
A |
G |
3: 127,330,611 (GRCm39) |
Y569H |
probably benign |
Het |
Loxhd1 |
A |
T |
18: 77,460,025 (GRCm39) |
I758F |
probably damaging |
Het |
Nr1d2 |
T |
C |
14: 18,215,446 (GRCm38) |
I189V |
probably benign |
Het |
Odad2 |
A |
T |
18: 7,217,008 (GRCm39) |
I668K |
probably damaging |
Het |
Pcdhb19 |
T |
A |
18: 37,632,243 (GRCm39) |
N679K |
probably benign |
Het |
Pigr |
G |
A |
1: 130,769,554 (GRCm39) |
D122N |
probably benign |
Het |
Prap1 |
T |
A |
7: 139,676,091 (GRCm39) |
V35E |
probably benign |
Het |
Prdm1 |
T |
A |
10: 44,317,572 (GRCm39) |
Y417F |
probably benign |
Het |
Ralgapa1 |
C |
T |
12: 55,687,429 (GRCm39) |
R2019Q |
probably damaging |
Het |
Rps3 |
T |
C |
7: 99,132,816 (GRCm39) |
I5V |
probably benign |
Het |
Sema3a |
A |
T |
5: 13,523,364 (GRCm39) |
|
probably null |
Het |
Serpina3g |
A |
T |
12: 104,206,546 (GRCm39) |
T116S |
probably benign |
Het |
Skint11 |
C |
A |
4: 114,101,856 (GRCm39) |
Q99K |
probably benign |
Het |
Slc22a28 |
A |
G |
19: 8,040,773 (GRCm39) |
S493P |
possibly damaging |
Het |
Snapc1 |
G |
T |
12: 74,029,354 (GRCm39) |
|
probably null |
Het |
Sobp |
C |
T |
10: 42,897,644 (GRCm39) |
G647D |
probably damaging |
Het |
Tomm22 |
C |
A |
15: 79,555,206 (GRCm39) |
|
probably benign |
Het |
Trappc11 |
T |
C |
8: 47,978,003 (GRCm39) |
|
probably benign |
Het |
Txnl4a |
T |
A |
18: 80,265,471 (GRCm39) |
M112K |
probably benign |
Het |
Vmn2r16 |
T |
C |
5: 109,478,427 (GRCm39) |
F61L |
possibly damaging |
Het |
Zfp709 |
C |
T |
8: 72,644,649 (GRCm39) |
Q693* |
probably null |
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 |
R3615:Espl1
|
UTSW |
15 |
102,221,424 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|