Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apobec1 |
A |
G |
6: 122,568,044 (GRCm39) |
|
probably null |
Het |
Arhgap21 |
G |
T |
2: 20,885,651 (GRCm39) |
Q348K |
probably benign |
Het |
Arl5c |
A |
G |
11: 97,883,213 (GRCm39) |
V129A |
probably benign |
Het |
Armh1 |
A |
G |
4: 117,087,189 (GRCm39) |
S159P |
probably damaging |
Het |
Asb8 |
A |
G |
15: 98,034,309 (GRCm39) |
L82P |
probably damaging |
Het |
Bahcc1 |
G |
A |
11: 120,163,009 (GRCm39) |
A436T |
possibly damaging |
Het |
Btc |
T |
C |
5: 91,550,576 (GRCm39) |
D2G |
unknown |
Het |
C1s2 |
G |
A |
6: 124,602,723 (GRCm39) |
T490M |
probably benign |
Het |
Caap1 |
C |
T |
4: 94,444,814 (GRCm39) |
G43D |
probably benign |
Het |
Ccr5 |
T |
C |
9: 123,925,000 (GRCm39) |
V201A |
probably benign |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cdhr5 |
C |
A |
7: 140,851,682 (GRCm39) |
G541C |
probably damaging |
Het |
Cep170 |
A |
G |
1: 176,583,367 (GRCm39) |
I1004T |
possibly damaging |
Het |
Chd9 |
A |
T |
8: 91,763,170 (GRCm39) |
M2332L |
probably benign |
Het |
Clk1 |
T |
A |
1: 58,453,584 (GRCm39) |
H334L |
probably benign |
Het |
Cyp4b1 |
G |
A |
4: 115,493,160 (GRCm39) |
S228F |
probably benign |
Het |
Dnah9 |
T |
C |
11: 66,003,156 (GRCm39) |
N883D |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,176,926 (GRCm39) |
L11P |
probably benign |
Het |
Ephx4 |
A |
G |
5: 107,567,717 (GRCm39) |
E225G |
probably damaging |
Het |
Erich6 |
C |
T |
3: 58,538,080 (GRCm39) |
|
probably null |
Het |
Evi2 |
T |
A |
11: 79,407,076 (GRCm39) |
K166N |
possibly damaging |
Het |
Glrx5 |
A |
G |
12: 104,999,127 (GRCm39) |
T57A |
possibly damaging |
Het |
Gnptab |
T |
A |
10: 88,255,316 (GRCm39) |
V222E |
probably damaging |
Het |
Gpr155 |
T |
C |
2: 73,200,382 (GRCm39) |
Y375C |
possibly damaging |
Het |
Hsd11b1 |
C |
G |
1: 192,922,635 (GRCm39) |
E141Q |
probably damaging |
Het |
Ildr2 |
T |
C |
1: 166,131,154 (GRCm39) |
F337L |
probably damaging |
Het |
Ino80 |
C |
T |
2: 119,277,509 (GRCm39) |
R322Q |
possibly damaging |
Het |
Lcp2 |
A |
G |
11: 34,039,601 (GRCm39) |
D467G |
probably benign |
Het |
Lmbr1 |
A |
G |
5: 29,459,556 (GRCm39) |
I229T |
probably damaging |
Het |
Lnpep |
A |
T |
17: 17,799,418 (GRCm39) |
M79K |
probably damaging |
Het |
Lpin1 |
T |
C |
12: 16,610,999 (GRCm39) |
Q564R |
possibly damaging |
Het |
Lpin2 |
T |
A |
17: 71,552,176 (GRCm39) |
L794* |
probably null |
Het |
Lrrc37 |
A |
G |
11: 103,500,764 (GRCm39) |
Y597H |
possibly damaging |
Het |
Lrrc45 |
T |
C |
11: 120,610,935 (GRCm39) |
|
probably null |
Het |
Mtus1 |
A |
G |
8: 41,529,278 (GRCm39) |
S751P |
probably damaging |
Het |
Nbr1 |
T |
C |
11: 101,455,656 (GRCm39) |
|
probably benign |
Het |
Nup107 |
A |
G |
10: 117,599,749 (GRCm39) |
F592S |
possibly damaging |
Het |
Nup133 |
T |
A |
8: 124,675,915 (GRCm39) |
M1L |
possibly damaging |
Het |
Or2a20 |
T |
C |
6: 43,194,285 (GRCm39) |
V146A |
probably benign |
Het |
Or3a10 |
A |
C |
11: 73,935,633 (GRCm39) |
F156V |
possibly damaging |
Het |
Or4n4 |
T |
G |
14: 50,518,981 (GRCm39) |
H243P |
probably damaging |
Het |
Or4p8 |
A |
C |
2: 88,727,290 (GRCm39) |
I217S |
probably damaging |
Het |
Or52b4i |
C |
A |
7: 102,191,177 (GRCm39) |
H11Q |
probably damaging |
Het |
Or8i2 |
A |
T |
2: 86,852,616 (GRCm39) |
S91T |
probably benign |
Het |
Otud7b |
T |
C |
3: 96,063,208 (GRCm39) |
C816R |
probably damaging |
Het |
Pi4k2a |
T |
C |
19: 42,089,083 (GRCm39) |
V148A |
probably benign |
Het |
Pih1d2 |
T |
C |
9: 50,532,479 (GRCm39) |
M195T |
probably benign |
Het |
Pira13 |
T |
C |
7: 3,826,060 (GRCm39) |
E311G |
probably benign |
Het |
Plpp6 |
T |
C |
19: 28,942,178 (GRCm39) |
F260L |
probably damaging |
Het |
R3hcc1l |
A |
T |
19: 42,570,393 (GRCm39) |
T663S |
probably damaging |
Het |
Rnf25 |
T |
C |
1: 74,634,426 (GRCm39) |
E199G |
probably damaging |
Het |
Scin |
G |
A |
12: 40,134,380 (GRCm39) |
|
probably benign |
Het |
Serpinb1c |
A |
T |
13: 33,080,973 (GRCm39) |
S37T |
probably benign |
Het |
Snx19 |
A |
G |
9: 30,339,639 (GRCm39) |
D259G |
probably damaging |
Het |
Sorcs3 |
A |
G |
19: 48,752,620 (GRCm39) |
K805R |
probably damaging |
Het |
Sox6 |
C |
A |
7: 115,376,358 (GRCm39) |
G125W |
probably damaging |
Het |
Spink5 |
A |
G |
18: 44,100,174 (GRCm39) |
I64V |
probably benign |
Het |
Spmip10 |
T |
A |
18: 56,727,606 (GRCm39) |
D101E |
probably benign |
Het |
St6galnac1 |
A |
G |
11: 116,657,474 (GRCm39) |
|
probably benign |
Het |
Sult1c2 |
T |
C |
17: 54,143,991 (GRCm39) |
I105V |
probably benign |
Het |
Tacr3 |
T |
G |
3: 134,535,517 (GRCm39) |
S162A |
probably damaging |
Het |
Ttc6 |
T |
C |
12: 57,721,549 (GRCm39) |
S1013P |
probably damaging |
Het |
Zbtb11 |
C |
A |
16: 55,811,178 (GRCm39) |
N445K |
probably benign |
Het |
Zfp423 |
A |
C |
8: 88,509,186 (GRCm39) |
V261G |
probably benign |
Het |
Zfp59 |
T |
C |
7: 27,553,016 (GRCm39) |
V156A |
probably benign |
Het |
Zscan2 |
C |
A |
7: 80,513,141 (GRCm39) |
A42E |
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 |
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 |
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 |
|