Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl9 |
A |
G |
17: 33,652,738 (GRCm39) |
K266R |
probably benign |
Het |
Cebpd |
T |
C |
16: 15,705,327 (GRCm39) |
S47P |
possibly damaging |
Het |
Celf4 |
A |
G |
18: 25,670,811 (GRCm39) |
M124T |
probably benign |
Het |
Ckap4 |
C |
T |
10: 84,364,028 (GRCm39) |
R345H |
probably benign |
Het |
Clasp1 |
T |
C |
1: 118,395,611 (GRCm39) |
V183A |
probably damaging |
Het |
Cyp2s1 |
C |
T |
7: 25,503,379 (GRCm39) |
R424Q |
probably null |
Het |
Etl4 |
A |
G |
2: 20,344,854 (GRCm39) |
T53A |
probably benign |
Het |
Glyat |
A |
T |
19: 12,617,197 (GRCm39) |
K16N |
probably benign |
Het |
Gm6522 |
T |
C |
3: 106,206,120 (GRCm39) |
|
noncoding transcript |
Het |
Grin1 |
G |
A |
2: 25,203,465 (GRCm39) |
T182M |
probably damaging |
Het |
Hcn4 |
T |
C |
9: 58,751,331 (GRCm39) |
V319A |
unknown |
Het |
Hmgcs2 |
T |
C |
3: 98,204,793 (GRCm39) |
F317S |
possibly damaging |
Het |
Hoxd8 |
C |
T |
2: 74,536,884 (GRCm39) |
Q18* |
probably null |
Het |
Itpr2 |
C |
T |
6: 146,327,008 (GRCm39) |
V120I |
probably damaging |
Het |
Kmt2d |
G |
A |
15: 98,753,430 (GRCm39) |
T141M |
possibly damaging |
Het |
Lrp1 |
A |
G |
10: 127,407,827 (GRCm39) |
S1821P |
probably benign |
Het |
Neb |
T |
C |
2: 52,153,641 (GRCm39) |
E2428G |
probably damaging |
Het |
Nepn |
T |
C |
10: 52,276,804 (GRCm39) |
V119A |
probably benign |
Het |
Or4k41 |
G |
T |
2: 111,280,230 (GRCm39) |
L248F |
possibly damaging |
Het |
Otogl |
T |
C |
10: 107,657,786 (GRCm39) |
D1048G |
probably damaging |
Het |
Panx1 |
GTTCTTCT |
GTTCT |
9: 14,917,467 (GRCm39) |
|
probably benign |
Het |
Ppp6r3 |
A |
T |
19: 3,546,583 (GRCm39) |
V305D |
probably damaging |
Het |
Prkg2 |
G |
T |
5: 99,145,354 (GRCm39) |
T160K |
possibly damaging |
Het |
Prmt8 |
G |
A |
6: 127,709,707 (GRCm39) |
T51I |
probably benign |
Het |
Rgl3 |
T |
C |
9: 21,886,885 (GRCm39) |
|
probably benign |
Het |
Sec23ip |
C |
G |
7: 128,378,574 (GRCm39) |
T796S |
probably benign |
Het |
Selp |
T |
C |
1: 163,953,855 (GRCm39) |
S52P |
probably benign |
Het |
Slc44a2 |
T |
C |
9: 21,259,837 (GRCm39) |
I615T |
probably damaging |
Het |
Snap91 |
T |
C |
9: 86,720,183 (GRCm39) |
Y118C |
probably damaging |
Het |
Tmem106b |
A |
T |
6: 13,081,587 (GRCm39) |
N165Y |
probably damaging |
Het |
Ucp3 |
A |
G |
7: 100,131,946 (GRCm39) |
T266A |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Utrn |
T |
C |
10: 12,625,852 (GRCm39) |
I110V |
probably damaging |
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 |
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 |
|