Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl5 |
T |
C |
19: 55,268,933 (GRCm39) |
V198A |
possibly damaging |
Het |
Adam34l |
T |
G |
8: 44,078,949 (GRCm39) |
N425T |
probably benign |
Het |
Adgra2 |
A |
T |
8: 27,609,193 (GRCm39) |
M805L |
probably benign |
Het |
Arhgap39 |
T |
C |
15: 76,620,712 (GRCm39) |
S630G |
probably damaging |
Het |
Bcl3 |
T |
A |
7: 19,546,409 (GRCm39) |
N142I |
probably damaging |
Het |
Cfap210 |
C |
T |
2: 69,602,398 (GRCm39) |
E338K |
possibly damaging |
Het |
Chuk |
A |
T |
19: 44,085,431 (GRCm39) |
D238E |
probably benign |
Het |
Cnga4 |
T |
G |
7: 105,056,906 (GRCm39) |
Y336* |
probably null |
Het |
Cyp2j8 |
A |
T |
4: 96,395,427 (GRCm39) |
L66Q |
possibly damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dst |
T |
A |
1: 34,227,253 (GRCm39) |
D1290E |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,075,235 (GRCm39) |
I583T |
probably benign |
Het |
Eif1ad13 |
A |
T |
12: 87,762,351 (GRCm39) |
R24* |
probably null |
Het |
Fbxl2 |
T |
A |
9: 113,815,516 (GRCm39) |
D249V |
probably damaging |
Het |
Fbxo30 |
A |
T |
10: 11,165,602 (GRCm39) |
Y108F |
possibly damaging |
Het |
Fibin |
G |
T |
2: 110,193,041 (GRCm39) |
H34N |
probably damaging |
Het |
Gabrr1 |
A |
G |
4: 33,161,632 (GRCm39) |
I319V |
probably benign |
Het |
Gfm1 |
G |
T |
3: 67,375,215 (GRCm39) |
L559F |
possibly damaging |
Het |
Gm5134 |
T |
A |
10: 75,821,859 (GRCm39) |
L231Q |
possibly damaging |
Het |
Grm5 |
A |
G |
7: 87,251,638 (GRCm39) |
|
probably benign |
Het |
Hbs1l |
T |
A |
10: 21,183,657 (GRCm39) |
|
probably null |
Het |
Hsf5 |
C |
G |
11: 87,508,120 (GRCm39) |
T8S |
probably benign |
Het |
Hspa4 |
C |
T |
11: 53,153,766 (GRCm39) |
E702K |
probably benign |
Het |
Inpp4b |
A |
G |
8: 82,678,813 (GRCm39) |
Q281R |
probably damaging |
Het |
Krt40 |
G |
A |
11: 99,433,920 (GRCm39) |
A22V |
possibly damaging |
Het |
Ldlrap1 |
C |
T |
4: 134,486,345 (GRCm39) |
R38Q |
possibly damaging |
Het |
Lepr |
A |
G |
4: 101,671,588 (GRCm39) |
|
probably null |
Het |
Map3k12 |
A |
G |
15: 102,412,081 (GRCm39) |
S328P |
probably damaging |
Het |
Mrpl2 |
T |
C |
17: 46,958,356 (GRCm39) |
V46A |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,568,294 (GRCm39) |
N1408K |
unknown |
Het |
Myh7 |
T |
A |
14: 55,226,753 (GRCm39) |
Q366L |
probably benign |
Het |
Nbeal2 |
A |
G |
9: 110,467,802 (GRCm39) |
V462A |
probably damaging |
Het |
Nradd |
G |
T |
9: 110,450,655 (GRCm39) |
T174N |
probably damaging |
Het |
Nup155 |
T |
C |
15: 8,138,963 (GRCm39) |
S12P |
probably benign |
Het |
Obscn |
C |
A |
11: 58,943,337 (GRCm39) |
E4832* |
probably null |
Het |
Opn3 |
G |
A |
1: 175,490,669 (GRCm39) |
R331W |
probably damaging |
Het |
Or2ag15 |
A |
T |
7: 106,340,761 (GRCm39) |
C127S |
probably damaging |
Het |
Or2w3 |
T |
A |
11: 58,556,757 (GRCm39) |
V124E |
possibly damaging |
Het |
Or4a66 |
G |
T |
2: 88,531,161 (GRCm39) |
H171N |
probably benign |
Het |
Or52ae9 |
T |
A |
7: 103,389,661 (GRCm39) |
H262L |
probably damaging |
Het |
Or5b120 |
G |
A |
19: 13,480,427 (GRCm39) |
C240Y |
probably damaging |
Het |
Or6b2 |
T |
C |
1: 92,408,305 (GRCm39) |
I13V |
probably benign |
Het |
Phip |
A |
G |
9: 82,785,234 (GRCm39) |
V827A |
probably benign |
Het |
Phldb1 |
G |
A |
9: 44,607,414 (GRCm39) |
R1264W |
probably damaging |
Het |
Pibf1 |
T |
G |
14: 99,424,014 (GRCm39) |
I529S |
probably benign |
Het |
Pkp1 |
T |
A |
1: 135,814,599 (GRCm39) |
I241F |
probably benign |
Het |
Pla2g4f |
G |
T |
2: 120,132,702 (GRCm39) |
D711E |
possibly damaging |
Het |
Pold1 |
A |
G |
7: 44,190,266 (GRCm39) |
|
probably null |
Het |
Pold2 |
T |
C |
11: 5,823,691 (GRCm39) |
S287G |
probably benign |
Het |
Prg4 |
T |
C |
1: 150,331,567 (GRCm39) |
|
probably benign |
Het |
Prl8a1 |
T |
C |
13: 27,759,557 (GRCm39) |
E160G |
possibly damaging |
Het |
Rfc4 |
C |
T |
16: 22,932,840 (GRCm39) |
|
probably benign |
Het |
Robo3 |
T |
G |
9: 37,332,225 (GRCm39) |
Y891S |
probably damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Homo |
Rsph14 |
G |
A |
10: 74,797,520 (GRCm39) |
R156W |
probably benign |
Het |
Sec61a1 |
T |
C |
6: 88,482,150 (GRCm39) |
Y457C |
probably benign |
Het |
Sec63 |
T |
A |
10: 42,704,861 (GRCm39) |
|
probably null |
Het |
Sphkap |
T |
A |
1: 83,258,200 (GRCm39) |
E181V |
probably damaging |
Het |
Stau2 |
C |
T |
1: 16,445,035 (GRCm39) |
A298T |
probably benign |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Tbc1d23 |
T |
C |
16: 56,990,796 (GRCm39) |
I661V |
probably benign |
Het |
Thoc6 |
A |
C |
17: 23,889,295 (GRCm39) |
|
probably null |
Het |
Trpv1 |
T |
A |
11: 73,141,636 (GRCm39) |
M553K |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,641,579 (GRCm39) |
I11760V |
probably benign |
Het |
Vmn1r61 |
G |
A |
7: 5,613,850 (GRCm39) |
H155Y |
probably damaging |
Het |
Vmn2r41 |
A |
G |
7: 8,153,214 (GRCm39) |
|
probably null |
Het |
Vmn2r74 |
A |
G |
7: 85,607,498 (GRCm39) |
I75T |
possibly damaging |
Het |
Wwp2 |
C |
A |
8: 108,232,977 (GRCm39) |
T205K |
probably benign |
Het |
Zfp1003 |
A |
T |
2: 177,546,195 (GRCm39) |
T40S |
probably benign |
Het |
Zfp747 |
C |
T |
7: 126,973,306 (GRCm39) |
G288D |
probably damaging |
Het |
Zfp871 |
CCACAC |
CC |
17: 32,994,494 (GRCm39) |
|
probably null |
Het |
Zfp953 |
G |
A |
13: 67,491,161 (GRCm39) |
L264F |
possibly damaging |
Het |
|
Other mutations in Spen |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01133:Spen
|
APN |
4 |
141,217,212 (GRCm39) |
missense |
unknown |
|
IGL01357:Spen
|
APN |
4 |
141,244,424 (GRCm39) |
missense |
unknown |
|
IGL02184:Spen
|
APN |
4 |
141,214,917 (GRCm39) |
missense |
unknown |
|
IGL02226:Spen
|
APN |
4 |
141,205,457 (GRCm39) |
missense |
unknown |
|
IGL02321:Spen
|
APN |
4 |
141,244,441 (GRCm39) |
missense |
unknown |
|
IGL02350:Spen
|
APN |
4 |
141,204,890 (GRCm39) |
missense |
unknown |
|
IGL02357:Spen
|
APN |
4 |
141,204,890 (GRCm39) |
missense |
unknown |
|
IGL02627:Spen
|
APN |
4 |
141,200,326 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02683:Spen
|
APN |
4 |
141,198,956 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02945:Spen
|
APN |
4 |
141,221,624 (GRCm39) |
missense |
unknown |
|
IGL02950:Spen
|
APN |
4 |
141,196,819 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Spen
|
APN |
4 |
141,203,448 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03019:Spen
|
APN |
4 |
141,206,227 (GRCm39) |
missense |
unknown |
|
IGL03038:Spen
|
APN |
4 |
141,265,550 (GRCm39) |
missense |
unknown |
|
IGL03334:Spen
|
APN |
4 |
141,197,280 (GRCm39) |
missense |
probably damaging |
1.00 |
filtered
|
UTSW |
4 |
141,204,683 (GRCm39) |
missense |
unknown |
|
mentholated
|
UTSW |
4 |
141,196,711 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0105:Spen
|
UTSW |
4 |
141,197,121 (GRCm39) |
splice site |
probably benign |
|
R0268:Spen
|
UTSW |
4 |
141,204,868 (GRCm39) |
missense |
unknown |
|
R0359:Spen
|
UTSW |
4 |
141,244,181 (GRCm39) |
missense |
unknown |
|
R0394:Spen
|
UTSW |
4 |
141,201,514 (GRCm39) |
missense |
probably benign |
0.03 |
R0423:Spen
|
UTSW |
4 |
141,206,647 (GRCm39) |
missense |
unknown |
|
R0433:Spen
|
UTSW |
4 |
141,211,069 (GRCm39) |
missense |
unknown |
|
R0462:Spen
|
UTSW |
4 |
141,200,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0687:Spen
|
UTSW |
4 |
141,215,339 (GRCm39) |
missense |
unknown |
|
R0699:Spen
|
UTSW |
4 |
141,201,702 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0865:Spen
|
UTSW |
4 |
141,199,181 (GRCm39) |
missense |
probably benign |
0.11 |
R0918:Spen
|
UTSW |
4 |
141,212,875 (GRCm39) |
missense |
unknown |
|
R1034:Spen
|
UTSW |
4 |
141,203,063 (GRCm39) |
missense |
probably benign |
0.33 |
R1341:Spen
|
UTSW |
4 |
141,196,711 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1401:Spen
|
UTSW |
4 |
141,199,132 (GRCm39) |
missense |
probably damaging |
0.98 |
R1509:Spen
|
UTSW |
4 |
141,202,946 (GRCm39) |
missense |
probably benign |
0.00 |
R1509:Spen
|
UTSW |
4 |
141,203,011 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1561:Spen
|
UTSW |
4 |
141,199,694 (GRCm39) |
nonsense |
probably null |
|
R1589:Spen
|
UTSW |
4 |
141,215,335 (GRCm39) |
missense |
unknown |
|
R1640:Spen
|
UTSW |
4 |
141,196,254 (GRCm39) |
missense |
probably damaging |
0.98 |
R1758:Spen
|
UTSW |
4 |
141,203,686 (GRCm39) |
missense |
unknown |
|
R1764:Spen
|
UTSW |
4 |
141,200,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Spen
|
UTSW |
4 |
141,200,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Spen
|
UTSW |
4 |
141,197,654 (GRCm39) |
missense |
probably benign |
0.17 |
R1916:Spen
|
UTSW |
4 |
141,199,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Spen
|
UTSW |
4 |
141,200,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R2295:Spen
|
UTSW |
4 |
141,204,584 (GRCm39) |
missense |
unknown |
|
R2379:Spen
|
UTSW |
4 |
141,244,238 (GRCm39) |
missense |
unknown |
|
R2404:Spen
|
UTSW |
4 |
141,205,216 (GRCm39) |
missense |
unknown |
|
R3719:Spen
|
UTSW |
4 |
141,244,494 (GRCm39) |
missense |
unknown |
|
R3889:Spen
|
UTSW |
4 |
141,205,192 (GRCm39) |
missense |
unknown |
|
R3945:Spen
|
UTSW |
4 |
141,204,664 (GRCm39) |
missense |
unknown |
|
R4227:Spen
|
UTSW |
4 |
141,249,458 (GRCm39) |
missense |
unknown |
|
R4326:Spen
|
UTSW |
4 |
141,204,683 (GRCm39) |
missense |
unknown |
|
R4382:Spen
|
UTSW |
4 |
141,200,450 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4542:Spen
|
UTSW |
4 |
141,204,097 (GRCm39) |
missense |
unknown |
|
R4757:Spen
|
UTSW |
4 |
141,200,390 (GRCm39) |
nonsense |
probably null |
|
R4771:Spen
|
UTSW |
4 |
141,199,907 (GRCm39) |
missense |
probably benign |
0.14 |
R5072:Spen
|
UTSW |
4 |
141,249,613 (GRCm39) |
missense |
unknown |
|
R5121:Spen
|
UTSW |
4 |
141,203,410 (GRCm39) |
missense |
probably benign |
0.00 |
R5176:Spen
|
UTSW |
4 |
141,203,587 (GRCm39) |
missense |
unknown |
|
R5290:Spen
|
UTSW |
4 |
141,201,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R5291:Spen
|
UTSW |
4 |
141,215,390 (GRCm39) |
missense |
unknown |
|
R5293:Spen
|
UTSW |
4 |
141,199,717 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5347:Spen
|
UTSW |
4 |
141,198,796 (GRCm39) |
missense |
probably benign |
0.26 |
R5511:Spen
|
UTSW |
4 |
141,244,149 (GRCm39) |
missense |
unknown |
|
R5511:Spen
|
UTSW |
4 |
141,202,375 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5772:Spen
|
UTSW |
4 |
141,205,495 (GRCm39) |
missense |
unknown |
|
R5834:Spen
|
UTSW |
4 |
141,199,154 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5858:Spen
|
UTSW |
4 |
141,201,182 (GRCm39) |
missense |
probably benign |
0.05 |
R6214:Spen
|
UTSW |
4 |
141,206,423 (GRCm39) |
missense |
unknown |
|
R6345:Spen
|
UTSW |
4 |
141,198,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6419:Spen
|
UTSW |
4 |
141,203,621 (GRCm39) |
missense |
unknown |
|
R6455:Spen
|
UTSW |
4 |
141,202,820 (GRCm39) |
missense |
probably damaging |
0.97 |
R6979:Spen
|
UTSW |
4 |
141,205,374 (GRCm39) |
missense |
unknown |
|
R6994:Spen
|
UTSW |
4 |
141,220,770 (GRCm39) |
missense |
unknown |
|
R7018:Spen
|
UTSW |
4 |
141,220,755 (GRCm39) |
missense |
unknown |
|
R7040:Spen
|
UTSW |
4 |
141,221,693 (GRCm39) |
missense |
unknown |
|
R7127:Spen
|
UTSW |
4 |
141,203,419 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7218:Spen
|
UTSW |
4 |
141,199,961 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7234:Spen
|
UTSW |
4 |
141,206,446 (GRCm39) |
missense |
unknown |
|
R7316:Spen
|
UTSW |
4 |
141,204,365 (GRCm39) |
missense |
unknown |
|
R7350:Spen
|
UTSW |
4 |
141,206,696 (GRCm39) |
missense |
unknown |
|
R7356:Spen
|
UTSW |
4 |
141,199,235 (GRCm39) |
nonsense |
probably null |
|
R7400:Spen
|
UTSW |
4 |
141,201,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7470:Spen
|
UTSW |
4 |
141,206,605 (GRCm39) |
missense |
unknown |
|
R7698:Spen
|
UTSW |
4 |
141,200,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R7858:Spen
|
UTSW |
4 |
141,215,442 (GRCm39) |
splice site |
probably null |
|
R8033:Spen
|
UTSW |
4 |
141,199,057 (GRCm39) |
missense |
probably benign |
0.03 |
R8064:Spen
|
UTSW |
4 |
141,203,011 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8159:Spen
|
UTSW |
4 |
141,202,314 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8187:Spen
|
UTSW |
4 |
141,200,216 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8463:Spen
|
UTSW |
4 |
141,249,590 (GRCm39) |
missense |
unknown |
|
R8557:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8558:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8672:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8673:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8674:Spen
|
UTSW |
4 |
141,197,681 (GRCm39) |
missense |
probably benign |
0.14 |
R8714:Spen
|
UTSW |
4 |
141,215,314 (GRCm39) |
missense |
unknown |
|
R8735:Spen
|
UTSW |
4 |
141,197,129 (GRCm39) |
missense |
probably benign |
0.32 |
R8762:Spen
|
UTSW |
4 |
141,200,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8877:Spen
|
UTSW |
4 |
141,199,137 (GRCm39) |
nonsense |
probably null |
|
R8878:Spen
|
UTSW |
4 |
141,204,520 (GRCm39) |
missense |
unknown |
|
R8937:Spen
|
UTSW |
4 |
141,201,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R8939:Spen
|
UTSW |
4 |
141,202,969 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8968:Spen
|
UTSW |
4 |
141,197,701 (GRCm39) |
missense |
probably benign |
0.02 |
R8971:Spen
|
UTSW |
4 |
141,201,889 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9016:Spen
|
UTSW |
4 |
141,200,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Spen
|
UTSW |
4 |
141,203,702 (GRCm39) |
missense |
unknown |
|
R9073:Spen
|
UTSW |
4 |
141,203,702 (GRCm39) |
missense |
unknown |
|
R9120:Spen
|
UTSW |
4 |
141,200,233 (GRCm39) |
missense |
|
|
R9136:Spen
|
UTSW |
4 |
141,249,623 (GRCm39) |
missense |
unknown |
|
R9138:Spen
|
UTSW |
4 |
141,196,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R9150:Spen
|
UTSW |
4 |
141,244,468 (GRCm39) |
missense |
unknown |
|
R9225:Spen
|
UTSW |
4 |
141,202,943 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9492:Spen
|
UTSW |
4 |
141,199,098 (GRCm39) |
missense |
probably benign |
0.26 |
R9537:Spen
|
UTSW |
4 |
141,244,156 (GRCm39) |
small deletion |
probably benign |
|
R9537:Spen
|
UTSW |
4 |
141,199,015 (GRCm39) |
missense |
probably benign |
0.15 |
R9602:Spen
|
UTSW |
4 |
141,205,183 (GRCm39) |
missense |
unknown |
|
R9609:Spen
|
UTSW |
4 |
141,215,419 (GRCm39) |
missense |
unknown |
|
R9686:Spen
|
UTSW |
4 |
141,199,946 (GRCm39) |
missense |
probably benign |
0.27 |
R9697:Spen
|
UTSW |
4 |
141,196,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9713:Spen
|
UTSW |
4 |
141,244,331 (GRCm39) |
missense |
unknown |
|
T0722:Spen
|
UTSW |
4 |
141,201,664 (GRCm39) |
missense |
probably benign |
0.33 |
T0975:Spen
|
UTSW |
4 |
141,201,664 (GRCm39) |
missense |
probably benign |
0.33 |
Z1088:Spen
|
UTSW |
4 |
141,205,287 (GRCm39) |
missense |
unknown |
|
Z1088:Spen
|
UTSW |
4 |
141,205,288 (GRCm39) |
missense |
unknown |
|
|