Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
C |
T |
5: 144,982,183 (GRCm39) |
T256I |
probably damaging |
Het |
2700097O09Rik |
C |
T |
12: 55,104,136 (GRCm39) |
G161D |
probably damaging |
Het |
Acvr1 |
G |
A |
2: 58,352,961 (GRCm39) |
A333V |
probably damaging |
Het |
Adamtsl1 |
A |
C |
4: 86,166,263 (GRCm39) |
S209R |
|
Het |
Akr1c18 |
T |
C |
13: 4,187,194 (GRCm39) |
K207E |
possibly damaging |
Het |
Anapc1 |
T |
G |
2: 128,527,748 (GRCm39) |
Q70P |
probably benign |
Het |
Arhgef33 |
A |
G |
17: 80,680,615 (GRCm39) |
E585G |
probably damaging |
Het |
Baz1b |
T |
G |
5: 135,271,343 (GRCm39) |
S1309A |
probably benign |
Het |
Bdp1 |
T |
C |
13: 100,240,307 (GRCm39) |
R14G |
probably damaging |
Het |
Bltp1 |
T |
A |
3: 37,090,066 (GRCm39) |
Y745N |
|
Het |
Ccdc150 |
A |
C |
1: 54,407,132 (GRCm39) |
Q1058H |
probably damaging |
Het |
Cdk5rap2 |
A |
G |
4: 70,298,510 (GRCm39) |
F74S |
probably damaging |
Het |
CK137956 |
C |
T |
4: 127,844,739 (GRCm39) |
E335K |
possibly damaging |
Het |
Cyp2c66 |
A |
T |
19: 39,151,884 (GRCm39) |
I200F |
probably benign |
Het |
Dmbt1 |
T |
A |
7: 130,659,984 (GRCm39) |
W412R |
unknown |
Het |
Dsel |
A |
T |
1: 111,790,468 (GRCm39) |
C22* |
probably null |
Het |
Ep400 |
A |
G |
5: 110,868,685 (GRCm39) |
M949T |
unknown |
Het |
Gcc1 |
A |
T |
6: 28,418,739 (GRCm39) |
Y531* |
probably null |
Het |
Gm10277 |
T |
C |
11: 77,676,405 (GRCm39) |
R189G |
unknown |
Het |
Gm17078 |
T |
A |
14: 51,848,687 (GRCm39) |
R17* |
probably null |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Grip1 |
A |
G |
10: 119,835,809 (GRCm39) |
I502V |
probably benign |
Het |
Hcls1 |
T |
C |
16: 36,781,821 (GRCm39) |
L310P |
probably benign |
Het |
Hsd17b11 |
T |
A |
5: 104,169,584 (GRCm39) |
I8F |
probably benign |
Het |
Iftap |
T |
C |
2: 101,440,916 (GRCm39) |
E29G |
probably damaging |
Het |
Ildr2 |
A |
T |
1: 166,097,102 (GRCm39) |
D107V |
probably damaging |
Het |
Ivl |
TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
3: 92,479,608 (GRCm39) |
|
probably benign |
Het |
Josd2 |
T |
C |
7: 44,120,640 (GRCm39) |
W126R |
probably damaging |
Het |
Ltbp2 |
T |
A |
12: 84,850,578 (GRCm39) |
D912V |
probably benign |
Het |
Mdc1 |
A |
G |
17: 36,161,383 (GRCm39) |
I765M |
probably benign |
Het |
Mroh1 |
A |
G |
15: 76,312,550 (GRCm39) |
E579G |
probably benign |
Het |
Nmur2 |
T |
C |
11: 55,931,654 (GRCm39) |
N19S |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,946,909 (GRCm39) |
Y4075C |
probably damaging |
Het |
Ogfr |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
2: 180,236,850 (GRCm39) |
|
probably benign |
Het |
Or4k40 |
C |
T |
2: 111,250,958 (GRCm39) |
V113I |
probably benign |
Het |
Or8b51 |
T |
A |
9: 38,569,047 (GRCm39) |
I214L |
probably benign |
Het |
Orm1 |
G |
A |
4: 63,264,578 (GRCm39) |
V167M |
probably damaging |
Het |
Phf14 |
A |
G |
6: 11,990,034 (GRCm39) |
N688D |
probably damaging |
Het |
Phlpp2 |
A |
G |
8: 110,631,012 (GRCm39) |
K219E |
probably damaging |
Het |
Prdm2 |
T |
C |
4: 142,838,310 (GRCm39) |
T1683A |
probably benign |
Het |
Ptprh |
T |
A |
7: 4,554,022 (GRCm39) |
Q815L |
probably benign |
Het |
Rag1 |
A |
T |
2: 101,472,968 (GRCm39) |
Y725N |
probably damaging |
Het |
Rp1 |
T |
A |
1: 4,416,628 (GRCm39) |
I1495F |
probably benign |
Het |
Scn3a |
A |
G |
2: 65,356,047 (GRCm39) |
V229A |
possibly damaging |
Het |
Siglech |
A |
G |
7: 55,418,362 (GRCm39) |
D110G |
probably benign |
Het |
St8sia2 |
A |
T |
7: 73,593,092 (GRCm39) |
D321E |
probably damaging |
Het |
Stxbp3 |
A |
G |
3: 108,709,425 (GRCm39) |
|
probably benign |
Het |
Tbccd1 |
A |
T |
16: 22,641,208 (GRCm39) |
S390T |
possibly damaging |
Het |
Tg |
T |
A |
15: 66,566,802 (GRCm39) |
|
probably benign |
Het |
Trio |
T |
A |
15: 27,748,324 (GRCm39) |
N2443Y |
possibly damaging |
Het |
Ube2s |
C |
T |
7: 4,813,577 (GRCm39) |
M62I |
probably benign |
Het |
Ugt2b37 |
T |
C |
5: 87,390,240 (GRCm39) |
D402G |
possibly damaging |
Het |
Vmn2r80 |
A |
G |
10: 79,004,069 (GRCm39) |
N94S |
probably damaging |
Het |
Wapl |
T |
A |
14: 34,414,549 (GRCm39) |
S470R |
possibly damaging |
Het |
Xrra1 |
A |
G |
7: 99,555,752 (GRCm39) |
E373G |
probably damaging |
Het |
Zfp335 |
A |
G |
2: 164,734,113 (GRCm39) |
Y1329H |
probably damaging |
Het |
Zfp689 |
C |
A |
7: 127,044,084 (GRCm39) |
C182F |
probably benign |
Het |
Zfp933 |
T |
A |
4: 147,911,249 (GRCm39) |
S116C |
probably benign |
Het |
|
Other mutations in H2-M9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01808:H2-M9
|
APN |
17 |
36,952,711 (GRCm39) |
splice site |
probably null |
|
IGL02133:H2-M9
|
APN |
17 |
36,952,629 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02323:H2-M9
|
APN |
17 |
36,951,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02957:H2-M9
|
APN |
17 |
36,953,049 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03127:H2-M9
|
APN |
17 |
36,951,714 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0025:H2-M9
|
UTSW |
17 |
36,952,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:H2-M9
|
UTSW |
17 |
36,952,419 (GRCm39) |
splice site |
probably benign |
|
R0926:H2-M9
|
UTSW |
17 |
36,952,665 (GRCm39) |
missense |
probably damaging |
0.98 |
R1171:H2-M9
|
UTSW |
17 |
36,952,545 (GRCm39) |
missense |
probably benign |
0.14 |
R1264:H2-M9
|
UTSW |
17 |
36,953,484 (GRCm39) |
missense |
probably benign |
|
R1995:H2-M9
|
UTSW |
17 |
36,952,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R4622:H2-M9
|
UTSW |
17 |
36,952,716 (GRCm39) |
splice site |
probably null |
|
R4737:H2-M9
|
UTSW |
17 |
36,951,631 (GRCm39) |
nonsense |
probably null |
|
R4808:H2-M9
|
UTSW |
17 |
36,951,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R5176:H2-M9
|
UTSW |
17 |
36,952,523 (GRCm39) |
missense |
probably damaging |
0.98 |
R6756:H2-M9
|
UTSW |
17 |
36,953,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:H2-M9
|
UTSW |
17 |
36,953,125 (GRCm39) |
missense |
probably damaging |
0.99 |
R7216:H2-M9
|
UTSW |
17 |
36,951,594 (GRCm39) |
missense |
probably benign |
|
R7464:H2-M9
|
UTSW |
17 |
36,953,303 (GRCm39) |
splice site |
probably null |
|
R8079:H2-M9
|
UTSW |
17 |
36,953,025 (GRCm39) |
missense |
probably benign |
0.39 |
R9174:H2-M9
|
UTSW |
17 |
36,953,181 (GRCm39) |
missense |
probably damaging |
0.99 |
X0018:H2-M9
|
UTSW |
17 |
36,952,614 (GRCm39) |
missense |
probably benign |
0.01 |
|