Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578G10Rik |
T |
C |
4: 42,812,473 (GRCm39) |
|
probably benign |
Het |
Abcc2 |
T |
A |
19: 43,825,947 (GRCm39) |
|
probably null |
Het |
Adamts12 |
C |
T |
15: 11,215,759 (GRCm39) |
T260M |
possibly damaging |
Het |
Adamts20 |
C |
T |
15: 94,231,556 (GRCm39) |
V878I |
possibly damaging |
Het |
Adgrl4 |
A |
G |
3: 151,144,953 (GRCm39) |
E34G |
probably damaging |
Het |
Asah1 |
A |
T |
8: 41,796,803 (GRCm39) |
I293N |
probably damaging |
Het |
Atosa |
G |
A |
9: 74,916,619 (GRCm39) |
S413N |
probably benign |
Het |
B3galt2 |
A |
T |
1: 143,522,839 (GRCm39) |
E325V |
possibly damaging |
Het |
Baz1b |
T |
A |
5: 135,271,348 (GRCm39) |
H1310Q |
probably benign |
Het |
Ccdc125 |
T |
A |
13: 100,826,834 (GRCm39) |
N204K |
probably damaging |
Het |
Cd36 |
C |
T |
5: 18,002,150 (GRCm39) |
D284N |
probably benign |
Het |
Cdh12 |
T |
C |
15: 21,520,483 (GRCm39) |
L316S |
probably damaging |
Het |
Cenpv |
T |
C |
11: 62,416,008 (GRCm39) |
K247R |
probably benign |
Het |
Cldn18 |
T |
C |
9: 99,574,801 (GRCm39) |
H257R |
possibly damaging |
Het |
Cnot8 |
T |
A |
11: 58,004,891 (GRCm39) |
Y197N |
probably damaging |
Het |
Cog3 |
A |
T |
14: 75,962,178 (GRCm39) |
C554* |
probably null |
Het |
Col4a4 |
A |
G |
1: 82,444,207 (GRCm39) |
|
probably null |
Het |
Cops5 |
G |
A |
1: 10,103,532 (GRCm39) |
T158I |
probably damaging |
Het |
Dhh |
A |
G |
15: 98,792,282 (GRCm39) |
F242S |
probably damaging |
Het |
Dot1l |
T |
C |
10: 80,627,315 (GRCm39) |
V1512A |
possibly damaging |
Het |
Dstn |
T |
G |
2: 143,781,907 (GRCm39) |
I116S |
possibly damaging |
Het |
Egfem1 |
G |
A |
3: 29,711,398 (GRCm39) |
D326N |
probably damaging |
Het |
Enpp3 |
A |
T |
10: 24,684,089 (GRCm39) |
Y52N |
probably damaging |
Het |
Gabra2 |
A |
G |
5: 71,119,426 (GRCm39) |
S359P |
probably benign |
Het |
Gbp7 |
G |
A |
3: 142,252,214 (GRCm39) |
G599E |
probably benign |
Het |
Gcat |
T |
G |
15: 78,920,264 (GRCm39) |
I198S |
probably damaging |
Het |
Gm8439 |
A |
G |
4: 120,466,755 (GRCm39) |
K82R |
unknown |
Het |
Grin2b |
A |
G |
6: 135,717,965 (GRCm39) |
F709S |
probably damaging |
Het |
Grm3 |
T |
C |
5: 9,620,201 (GRCm39) |
N348D |
probably damaging |
Het |
Hdgfl1 |
G |
A |
13: 26,954,075 (GRCm39) |
|
probably benign |
Het |
Hmgxb3 |
G |
T |
18: 61,285,296 (GRCm39) |
D564E |
possibly damaging |
Het |
Igkv4-61 |
C |
A |
6: 69,394,138 (GRCm39) |
A31S |
possibly damaging |
Het |
Impg1 |
A |
G |
9: 80,287,300 (GRCm39) |
V305A |
probably benign |
Het |
Ints7 |
T |
A |
1: 191,334,414 (GRCm39) |
S313T |
possibly damaging |
Het |
Knl1 |
T |
A |
2: 118,899,484 (GRCm39) |
I395K |
probably benign |
Het |
Lactb2 |
A |
T |
1: 13,708,459 (GRCm39) |
Y196* |
probably null |
Het |
Lad1 |
T |
C |
1: 135,759,630 (GRCm39) |
S509P |
possibly damaging |
Het |
Ltf |
T |
C |
9: 110,860,090 (GRCm39) |
F504L |
possibly damaging |
Het |
Med4 |
A |
T |
14: 73,751,363 (GRCm39) |
D104V |
probably damaging |
Het |
Mrpl58 |
A |
T |
11: 115,301,073 (GRCm39) |
N128Y |
probably damaging |
Het |
Ndufs2 |
T |
C |
1: 171,068,668 (GRCm39) |
T54A |
probably benign |
Het |
Notch2 |
G |
T |
3: 98,007,705 (GRCm39) |
|
probably null |
Het |
Ntng1 |
A |
T |
3: 109,690,169 (GRCm39) |
N424K |
possibly damaging |
Het |
Ntrk2 |
G |
A |
13: 59,009,113 (GRCm39) |
W301* |
probably null |
Het |
Or5b116 |
T |
A |
19: 13,423,131 (GRCm39) |
S252T |
probably benign |
Het |
Otud6b |
A |
G |
4: 14,822,766 (GRCm39) |
S113P |
possibly damaging |
Het |
Pcdhb20 |
A |
G |
18: 37,638,608 (GRCm39) |
N378S |
probably damaging |
Het |
Polr3b |
T |
C |
10: 84,473,975 (GRCm39) |
S185P |
possibly damaging |
Het |
Ptprn |
G |
A |
1: 75,240,681 (GRCm39) |
R31C |
probably benign |
Het |
Rgsl1 |
C |
T |
1: 153,698,117 (GRCm39) |
V478M |
probably damaging |
Het |
Sema6b |
A |
T |
17: 56,439,784 (GRCm39) |
L19* |
probably null |
Het |
Slfn8 |
A |
G |
11: 82,894,881 (GRCm39) |
|
probably null |
Het |
Syne2 |
T |
C |
12: 76,143,740 (GRCm39) |
F1522L |
probably damaging |
Het |
Tarbp1 |
C |
T |
8: 127,185,783 (GRCm39) |
A470T |
possibly damaging |
Het |
Tent4a |
A |
C |
13: 69,658,785 (GRCm39) |
M350R |
possibly damaging |
Het |
Tiam1 |
C |
A |
16: 89,694,912 (GRCm39) |
E182* |
probably null |
Het |
Tmem231 |
G |
A |
8: 112,653,524 (GRCm39) |
|
probably benign |
Het |
Trip12 |
C |
T |
1: 84,771,591 (GRCm39) |
A186T |
probably damaging |
Het |
Ufc1 |
C |
T |
1: 171,116,529 (GRCm39) |
A147T |
probably damaging |
Het |
Vmn1r199 |
A |
G |
13: 22,567,777 (GRCm39) |
K314R |
possibly damaging |
Het |
Vmn2r13 |
A |
T |
5: 109,323,085 (GRCm39) |
I68K |
possibly damaging |
Het |
Vmn2r77 |
A |
T |
7: 86,460,767 (GRCm39) |
I698F |
probably damaging |
Het |
Vmn2r86 |
T |
C |
10: 130,282,795 (GRCm39) |
K607R |
probably damaging |
Het |
Vwa3b |
T |
C |
1: 37,196,457 (GRCm39) |
V28A |
probably benign |
Het |
Wdr19 |
A |
G |
5: 65,373,236 (GRCm39) |
N166S |
possibly damaging |
Het |
Wfdc17 |
G |
A |
11: 83,595,634 (GRCm39) |
G33R |
probably damaging |
Het |
Zfp330 |
T |
G |
8: 83,491,545 (GRCm39) |
K209N |
probably benign |
Het |
Zfp493 |
A |
G |
13: 67,934,526 (GRCm39) |
T160A |
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,610,940 (GRCm39) |
C262S |
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 |
|
R6232:Spen
|
UTSW |
4 |
141,244,333 (GRCm39) |
missense |
unknown |
|
R6345:Spen
|
UTSW |
4 |
141,198,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
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 |
|
|