Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
T |
C |
8: 13,601,676 (GRCm39) |
D230G |
probably benign |
Het |
Abhd13 |
A |
G |
8: 10,037,561 (GRCm39) |
I53V |
probably benign |
Het |
Adgrl2 |
A |
C |
3: 148,544,821 (GRCm39) |
|
probably null |
Het |
Aldh16a1 |
G |
A |
7: 44,794,088 (GRCm39) |
A596V |
probably damaging |
Het |
Aldh3b2 |
T |
A |
19: 4,029,414 (GRCm39) |
Y262* |
probably null |
Het |
Ambn |
A |
G |
5: 88,615,831 (GRCm39) |
Q420R |
possibly damaging |
Het |
Arhgap9 |
C |
A |
10: 127,165,407 (GRCm39) |
H430Q |
probably benign |
Het |
Arhgef25 |
C |
T |
10: 127,019,933 (GRCm39) |
G435E |
probably damaging |
Het |
Armc12 |
A |
T |
17: 28,751,366 (GRCm39) |
D120V |
possibly damaging |
Het |
Asxl3 |
G |
A |
18: 22,649,738 (GRCm39) |
E576K |
possibly damaging |
Het |
Bcdin3d |
T |
C |
15: 99,368,776 (GRCm39) |
E141G |
probably benign |
Het |
Bmpr1b |
G |
A |
3: 141,546,437 (GRCm39) |
T483M |
probably damaging |
Het |
Caprin2 |
C |
T |
6: 148,744,452 (GRCm39) |
S991N |
probably damaging |
Het |
Cd96 |
T |
C |
16: 45,892,129 (GRCm39) |
I286M |
possibly damaging |
Het |
Cdcp1 |
G |
T |
9: 123,009,237 (GRCm39) |
F480L |
probably benign |
Het |
Clca3b |
A |
G |
3: 144,547,226 (GRCm39) |
S304P |
probably benign |
Het |
Cmya5 |
A |
T |
13: 93,232,108 (GRCm39) |
H993Q |
probably benign |
Het |
Cnbp |
A |
T |
6: 87,822,746 (GRCm39) |
C6S |
probably damaging |
Het |
Col14a1 |
C |
T |
15: 55,360,907 (GRCm39) |
R1605W |
probably damaging |
Het |
Cops7a |
T |
C |
6: 124,941,817 (GRCm39) |
N11S |
probably benign |
Het |
Cpvl |
T |
C |
6: 53,909,485 (GRCm39) |
H217R |
possibly damaging |
Het |
Cyp2c66 |
A |
G |
19: 39,130,369 (GRCm39) |
Y68C |
probably damaging |
Het |
Dicer1 |
G |
A |
12: 104,668,710 (GRCm39) |
T1324M |
probably benign |
Het |
Dlgap2 |
A |
G |
8: 14,777,562 (GRCm39) |
D268G |
probably benign |
Het |
Dnm1 |
T |
A |
2: 32,207,001 (GRCm39) |
M535L |
possibly damaging |
Het |
Dock7 |
A |
T |
4: 98,850,517 (GRCm39) |
F1575Y |
probably benign |
Het |
Dpp10 |
T |
A |
1: 123,326,275 (GRCm39) |
H403L |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,616,285 (GRCm39) |
D3112G |
possibly damaging |
Het |
Eno3 |
A |
G |
11: 70,548,761 (GRCm39) |
E21G |
probably null |
Het |
Fam120b |
T |
A |
17: 15,643,186 (GRCm39) |
V655D |
probably damaging |
Het |
Fkbp5 |
A |
T |
17: 28,647,426 (GRCm39) |
D136E |
probably benign |
Het |
Gfer |
A |
G |
17: 24,913,277 (GRCm39) |
W192R |
probably damaging |
Het |
Golgb1 |
C |
T |
16: 36,695,992 (GRCm39) |
Q164* |
probably null |
Het |
Gpnmb |
A |
G |
6: 49,024,276 (GRCm39) |
N197S |
probably damaging |
Het |
Gtf2f1 |
G |
A |
17: 57,310,802 (GRCm39) |
T414M |
probably benign |
Het |
Helz2 |
C |
T |
2: 180,872,223 (GRCm39) |
R2539Q |
probably damaging |
Het |
Hsd17b12 |
T |
A |
2: 93,988,160 (GRCm39) |
I19F |
probably benign |
Het |
Incenp |
T |
C |
19: 9,871,114 (GRCm39) |
T172A |
unknown |
Het |
Jmy |
A |
G |
13: 93,578,126 (GRCm39) |
Y681H |
probably benign |
Het |
Kbtbd11 |
A |
G |
8: 15,077,508 (GRCm39) |
T36A |
probably benign |
Het |
Kcnh4 |
T |
C |
11: 100,646,525 (GRCm39) |
D267G |
probably damaging |
Het |
Krt40 |
T |
A |
11: 99,429,568 (GRCm39) |
E335D |
probably damaging |
Het |
Krt86 |
T |
A |
15: 101,374,454 (GRCm39) |
Y282* |
probably null |
Het |
Lgi3 |
C |
T |
14: 70,772,255 (GRCm39) |
R267* |
probably null |
Het |
Lrp1b |
T |
A |
2: 40,888,195 (GRCm39) |
H2355L |
probably benign |
Het |
Lrrc8e |
G |
A |
8: 4,285,401 (GRCm39) |
R542H |
probably benign |
Het |
Mast4 |
G |
A |
13: 102,990,350 (GRCm39) |
S57F |
probably damaging |
Het |
Mia2 |
T |
C |
12: 59,155,642 (GRCm39) |
Y452H |
probably damaging |
Het |
Mmachc |
C |
T |
4: 116,561,738 (GRCm39) |
R132Q |
probably damaging |
Het |
Mroh2a |
C |
A |
1: 88,170,142 (GRCm39) |
A685D |
possibly damaging |
Het |
Mtbp |
T |
A |
15: 55,440,882 (GRCm39) |
N356K |
possibly damaging |
Het |
Myo5b |
A |
G |
18: 74,794,787 (GRCm39) |
H552R |
possibly damaging |
Het |
Niban1 |
A |
G |
1: 151,593,967 (GRCm39) |
D884G |
probably benign |
Het |
Noxred1 |
A |
G |
12: 87,273,753 (GRCm39) |
V96A |
probably benign |
Het |
Nr1d2 |
T |
A |
14: 18,211,933 (GRCm38) |
D390V |
possibly damaging |
Het |
Odad2 |
A |
T |
18: 7,211,516 (GRCm39) |
V786D |
probably damaging |
Het |
Or1r1 |
T |
C |
11: 73,874,538 (GRCm39) |
S299G |
probably benign |
Het |
Or6c1b |
T |
A |
10: 129,273,217 (GRCm39) |
Y179N |
probably damaging |
Het |
Otog |
G |
T |
7: 45,916,805 (GRCm39) |
C914F |
probably damaging |
Het |
Pank2 |
G |
T |
2: 131,122,117 (GRCm39) |
C214F |
probably damaging |
Het |
Pcdhb1 |
T |
A |
18: 37,399,788 (GRCm39) |
S580T |
probably benign |
Het |
Pdia3 |
T |
C |
2: 121,244,592 (GRCm39) |
S2P |
probably damaging |
Het |
Peli1 |
G |
T |
11: 21,092,602 (GRCm39) |
R83L |
probably damaging |
Het |
Pla2g3 |
T |
A |
11: 3,441,935 (GRCm39) |
C366* |
probably null |
Het |
Pon3 |
T |
A |
6: 5,240,860 (GRCm39) |
D107V |
probably benign |
Het |
Ppip5k2 |
A |
G |
1: 97,668,816 (GRCm39) |
C532R |
probably damaging |
Het |
Psd3 |
A |
G |
8: 68,210,738 (GRCm39) |
M270T |
probably damaging |
Het |
Pus1 |
A |
T |
5: 110,927,664 (GRCm39) |
H30Q |
probably benign |
Het |
Pwwp3a |
T |
C |
10: 80,070,092 (GRCm39) |
S354P |
probably benign |
Het |
Rab7 |
A |
T |
6: 87,982,114 (GRCm39) |
V87E |
probably damaging |
Het |
Reln |
A |
G |
5: 22,147,595 (GRCm39) |
|
probably null |
Het |
S1pr3 |
A |
G |
13: 51,572,938 (GRCm39) |
T40A |
probably benign |
Het |
Senp7 |
T |
A |
16: 55,999,884 (GRCm39) |
I853N |
probably damaging |
Het |
Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
Shroom1 |
T |
G |
11: 53,356,312 (GRCm39) |
|
probably null |
Het |
Slc24a3 |
T |
C |
2: 145,448,584 (GRCm39) |
I376T |
probably benign |
Het |
Slc46a1 |
T |
C |
11: 78,359,493 (GRCm39) |
I375T |
possibly damaging |
Het |
Slc4a9 |
T |
C |
18: 36,666,733 (GRCm39) |
F527S |
probably damaging |
Het |
Slc4a9 |
T |
A |
18: 36,674,286 (GRCm39) |
I924N |
probably damaging |
Het |
Slx4 |
T |
A |
16: 3,804,816 (GRCm39) |
E666V |
probably damaging |
Het |
Sorcs1 |
C |
T |
19: 50,216,659 (GRCm39) |
G640E |
probably damaging |
Het |
Spmap2l |
G |
T |
5: 77,164,152 (GRCm39) |
E52* |
probably null |
Het |
Sptan1 |
A |
T |
2: 29,908,413 (GRCm39) |
M1725L |
probably benign |
Het |
Sync |
G |
A |
4: 129,187,514 (GRCm39) |
R182K |
probably damaging |
Het |
Syne2 |
G |
A |
12: 76,144,808 (GRCm39) |
G1586S |
probably damaging |
Het |
Sytl1 |
G |
T |
4: 132,980,768 (GRCm39) |
T522K |
probably damaging |
Het |
Tex2 |
T |
A |
11: 106,410,781 (GRCm39) |
K414* |
probably null |
Het |
Thsd7a |
G |
A |
6: 12,503,915 (GRCm39) |
T413I |
probably benign |
Het |
Tm9sf1 |
C |
T |
14: 55,875,392 (GRCm39) |
A451T |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,656,496 (GRCm39) |
|
probably benign |
Het |
Uba2 |
T |
C |
7: 33,854,054 (GRCm39) |
I140V |
possibly damaging |
Het |
Ushbp1 |
C |
A |
8: 71,842,762 (GRCm39) |
G361* |
probably null |
Het |
Wbp2nl |
C |
T |
15: 82,197,988 (GRCm39) |
A175V |
probably benign |
Het |
Zc3h12d |
A |
G |
10: 7,738,330 (GRCm39) |
E212G |
probably damaging |
Het |
|
Other mutations in Celf5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01295:Celf5
|
APN |
10 |
81,302,914 (GRCm39) |
unclassified |
probably benign |
|
IGL02193:Celf5
|
APN |
10 |
81,306,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02199:Celf5
|
APN |
10 |
81,318,318 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0012:Celf5
|
UTSW |
10 |
81,305,346 (GRCm39) |
missense |
probably damaging |
0.99 |
R0207:Celf5
|
UTSW |
10 |
81,306,532 (GRCm39) |
missense |
probably null |
1.00 |
R0242:Celf5
|
UTSW |
10 |
81,300,243 (GRCm39) |
missense |
probably benign |
0.00 |
R0607:Celf5
|
UTSW |
10 |
81,301,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1165:Celf5
|
UTSW |
10 |
81,307,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Celf5
|
UTSW |
10 |
81,303,138 (GRCm39) |
unclassified |
probably benign |
|
R1796:Celf5
|
UTSW |
10 |
81,303,053 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2291:Celf5
|
UTSW |
10 |
81,302,881 (GRCm39) |
missense |
probably damaging |
0.98 |
R4812:Celf5
|
UTSW |
10 |
81,306,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R5367:Celf5
|
UTSW |
10 |
81,303,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R6323:Celf5
|
UTSW |
10 |
81,305,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Celf5
|
UTSW |
10 |
81,298,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R7226:Celf5
|
UTSW |
10 |
81,303,863 (GRCm39) |
missense |
probably damaging |
0.98 |
R7454:Celf5
|
UTSW |
10 |
81,318,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Celf5
|
UTSW |
10 |
81,303,925 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Celf5
|
UTSW |
10 |
81,302,783 (GRCm39) |
missense |
probably damaging |
1.00 |
|