Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aebp2 |
T |
A |
6: 140,587,954 (GRCm39) |
H341Q |
probably damaging |
Het |
Apob |
G |
A |
12: 8,030,635 (GRCm39) |
A125T |
probably damaging |
Het |
Bace2 |
G |
T |
16: 97,158,059 (GRCm39) |
A20S |
unknown |
Het |
Bcar1 |
T |
C |
8: 112,442,341 (GRCm39) |
Y238C |
probably damaging |
Het |
Brinp3 |
A |
T |
1: 146,777,827 (GRCm39) |
D758V |
possibly damaging |
Het |
Btnl10 |
T |
C |
11: 58,811,345 (GRCm39) |
S223P |
probably damaging |
Het |
Cckar |
C |
T |
5: 53,864,587 (GRCm39) |
|
probably null |
Het |
Cdhr2 |
A |
G |
13: 54,861,801 (GRCm39) |
N66S |
probably benign |
Het |
Chd9 |
A |
G |
8: 91,757,270 (GRCm39) |
M1890V |
probably benign |
Het |
Col6a5 |
C |
T |
9: 105,755,837 (GRCm39) |
G2196R |
probably damaging |
Het |
Col9a1 |
T |
G |
1: 24,224,175 (GRCm39) |
M119R |
unknown |
Het |
Cryaa |
A |
G |
17: 31,898,642 (GRCm39) |
H123R |
probably damaging |
Het |
Cux1 |
A |
T |
5: 136,398,989 (GRCm39) |
D171E |
probably damaging |
Het |
Dgkz |
T |
A |
2: 91,764,144 (GRCm39) |
T1067S |
probably benign |
Het |
Dnah11 |
C |
T |
12: 117,991,251 (GRCm39) |
E2372K |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,448,480 (GRCm39) |
M4181T |
possibly damaging |
Het |
Dnajb14 |
A |
G |
3: 137,614,145 (GRCm39) |
E352G |
possibly damaging |
Het |
Dnmt3l |
T |
A |
10: 77,892,586 (GRCm39) |
|
probably null |
Het |
Dph6 |
T |
C |
2: 114,399,995 (GRCm39) |
I117V |
probably damaging |
Het |
Dsg1a |
A |
G |
18: 20,473,228 (GRCm39) |
D767G |
probably damaging |
Het |
Edn3 |
C |
T |
2: 174,603,482 (GRCm39) |
P77S |
possibly damaging |
Het |
Fbln7 |
A |
C |
2: 128,737,168 (GRCm39) |
S328R |
probably null |
Het |
Fbn2 |
T |
C |
18: 58,192,428 (GRCm39) |
R1518G |
probably damaging |
Het |
Foxi2 |
A |
T |
7: 135,013,525 (GRCm39) |
T252S |
probably benign |
Het |
Foxred2 |
A |
G |
15: 77,836,206 (GRCm39) |
S384P |
probably damaging |
Het |
Gdpd1 |
G |
A |
11: 86,936,009 (GRCm39) |
H174Y |
probably benign |
Het |
Gm10542 |
A |
C |
18: 44,337,705 (GRCm39) |
D61A |
possibly damaging |
Het |
Gm10563 |
TTCCTCCTCCTCCTCCTCCTCTTCCTCCTCCTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTCCTCCTCCTC |
4: 155,720,307 (GRCm39) |
|
probably benign |
Het |
H2-Ab1 |
A |
G |
17: 34,483,981 (GRCm39) |
E114G |
probably damaging |
Het |
Htt |
C |
T |
5: 34,976,367 (GRCm39) |
T723M |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,903,695 (GRCm39) |
V348I |
probably damaging |
Het |
Itpr1 |
T |
A |
6: 108,466,810 (GRCm39) |
L2173Q |
probably damaging |
Het |
Lamp5 |
A |
G |
2: 135,901,521 (GRCm39) |
Y115C |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,430,850 (GRCm39) |
K400* |
probably null |
Het |
Man2a2 |
C |
T |
7: 80,010,868 (GRCm39) |
V708I |
probably benign |
Het |
Matr3 |
T |
C |
18: 35,720,774 (GRCm39) |
S746P |
probably benign |
Het |
Me1 |
C |
T |
9: 86,480,847 (GRCm39) |
V353M |
probably benign |
Het |
Mideas |
A |
C |
12: 84,199,661 (GRCm39) |
F1020V |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,317,839 (GRCm39) |
D1925E |
probably damaging |
Het |
Oca2 |
T |
A |
7: 55,966,168 (GRCm39) |
F387I |
probably damaging |
Het |
Opn3 |
G |
T |
1: 175,490,655 (GRCm39) |
N335K |
probably benign |
Het |
Or5d36 |
T |
A |
2: 87,900,778 (GRCm39) |
H316L |
probably benign |
Het |
Or5k17 |
T |
G |
16: 58,746,485 (GRCm39) |
I150L |
probably benign |
Het |
Or5k17 |
G |
T |
16: 58,746,486 (GRCm39) |
F149L |
probably benign |
Het |
Or6d12 |
T |
A |
6: 116,493,315 (GRCm39) |
N192K |
probably benign |
Het |
Or6k2 |
T |
C |
1: 173,986,456 (GRCm39) |
I39T |
probably benign |
Het |
Or8b48 |
T |
A |
9: 38,493,373 (GRCm39) |
S267T |
probably benign |
Het |
Otop2 |
T |
C |
11: 115,219,912 (GRCm39) |
Y251H |
probably damaging |
Het |
Pappa |
T |
C |
4: 65,074,612 (GRCm39) |
S389P |
possibly damaging |
Het |
Polr1d |
C |
T |
5: 147,038,068 (GRCm39) |
A19V |
probably damaging |
Het |
Ptchd4 |
G |
A |
17: 42,814,276 (GRCm39) |
V726M |
probably benign |
Het |
Pzp |
T |
A |
6: 128,473,626 (GRCm39) |
D731V |
probably benign |
Het |
Rgl2 |
A |
T |
17: 34,155,002 (GRCm39) |
I669F |
probably damaging |
Het |
Rpl38 |
T |
C |
11: 114,563,114 (GRCm39) |
*71R |
probably null |
Het |
Rufy1 |
G |
A |
11: 50,289,301 (GRCm39) |
R514W |
probably damaging |
Het |
Ruvbl2 |
G |
A |
7: 45,083,741 (GRCm39) |
|
probably benign |
Het |
Scn9a |
T |
G |
2: 66,363,657 (GRCm39) |
I874L |
probably damaging |
Het |
Slc14a2 |
A |
G |
18: 78,238,951 (GRCm39) |
S85P |
probably benign |
Het |
Slc17a1 |
A |
G |
13: 24,062,794 (GRCm39) |
I287V |
probably benign |
Het |
Slc35f3 |
T |
A |
8: 127,115,928 (GRCm39) |
I285N |
probably damaging |
Het |
Slx4 |
A |
G |
16: 3,805,927 (GRCm39) |
S542P |
possibly damaging |
Het |
Sox30 |
A |
T |
11: 45,908,180 (GRCm39) |
L782F |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,432,806 (GRCm39) |
N894S |
probably benign |
Het |
Syne1 |
G |
A |
10: 5,152,013 (GRCm39) |
Q5765* |
probably null |
Het |
Taar7e |
T |
C |
10: 23,913,972 (GRCm39) |
I154T |
probably benign |
Het |
Tars1 |
A |
G |
15: 11,397,265 (GRCm39) |
|
probably null |
Het |
Thap1 |
CAGCATCTGCTCGGAGCA |
CAGCA |
8: 26,650,884 (GRCm39) |
|
probably null |
Het |
Tmem198b |
A |
T |
10: 128,639,057 (GRCm39) |
C29S |
probably damaging |
Het |
Tnr |
A |
C |
1: 159,722,617 (GRCm39) |
M1021L |
probably benign |
Het |
Tom1l1 |
G |
A |
11: 90,548,644 (GRCm39) |
P309L |
probably damaging |
Het |
Traf4 |
A |
G |
11: 78,051,927 (GRCm39) |
S186P |
probably benign |
Het |
Trpm1 |
T |
G |
7: 63,890,319 (GRCm39) |
V974G |
possibly damaging |
Het |
Tsga10 |
T |
A |
1: 37,880,359 (GRCm39) |
|
probably benign |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Vmn2r93 |
A |
T |
17: 18,524,281 (GRCm39) |
I92F |
probably damaging |
Het |
Zfp457 |
A |
T |
13: 67,441,965 (GRCm39) |
D203E |
probably benign |
Het |
Zfp518b |
G |
A |
5: 38,831,501 (GRCm39) |
S168F |
probably damaging |
Het |
Zfp7 |
TGCGGGAAAGGTTTCCACCTGAGCG |
TGCG |
15: 76,774,800 (GRCm39) |
|
probably benign |
Het |
Zfp777 |
G |
A |
6: 48,002,521 (GRCm39) |
T523M |
probably benign |
Het |
|
Other mutations in Osm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02007:Osm
|
APN |
11 |
4,189,470 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02477:Osm
|
APN |
11 |
4,189,604 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02478:Osm
|
APN |
11 |
4,189,507 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02699:Osm
|
APN |
11 |
4,189,723 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL03328:Osm
|
APN |
11 |
4,188,426 (GRCm39) |
missense |
unknown |
|
R0212:Osm
|
UTSW |
11 |
4,188,465 (GRCm39) |
missense |
probably benign |
0.12 |
R0667:Osm
|
UTSW |
11 |
4,189,918 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2237:Osm
|
UTSW |
11 |
4,188,505 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4790:Osm
|
UTSW |
11 |
4,188,435 (GRCm39) |
missense |
probably benign |
0.01 |
R6621:Osm
|
UTSW |
11 |
4,189,541 (GRCm39) |
missense |
probably benign |
0.03 |
R7148:Osm
|
UTSW |
11 |
4,189,936 (GRCm39) |
missense |
probably benign |
0.02 |
R8669:Osm
|
UTSW |
11 |
4,189,665 (GRCm39) |
missense |
probably benign |
0.04 |
R8805:Osm
|
UTSW |
11 |
4,189,839 (GRCm39) |
missense |
probably benign |
0.18 |
R9673:Osm
|
UTSW |
11 |
4,189,926 (GRCm39) |
missense |
probably benign |
0.00 |
T0975:Osm
|
UTSW |
11 |
4,189,588 (GRCm39) |
missense |
probably benign |
0.02 |
|