Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkbh6 |
A |
G |
7: 30,013,413 (GRCm39) |
T161A |
probably benign |
Het |
Alox12e |
A |
G |
11: 70,211,725 (GRCm39) |
|
probably benign |
Het |
Ap1g2 |
A |
G |
14: 55,339,149 (GRCm39) |
|
probably benign |
Het |
Arid2 |
A |
T |
15: 96,276,848 (GRCm39) |
|
probably benign |
Het |
Bmp2k |
A |
T |
5: 97,216,314 (GRCm39) |
H604L |
unknown |
Het |
Cacna1a |
A |
T |
8: 85,338,914 (GRCm39) |
M1705L |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,794,062 (GRCm39) |
D1526E |
probably damaging |
Het |
Ccdc171 |
A |
G |
4: 83,467,975 (GRCm39) |
R107G |
possibly damaging |
Het |
Cklf |
T |
C |
8: 104,988,207 (GRCm39) |
|
probably benign |
Het |
Crabp1 |
A |
G |
9: 54,672,210 (GRCm39) |
K9E |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,793,423 (GRCm39) |
D386G |
probably damaging |
Het |
Cyp3a41b |
G |
A |
5: 145,515,014 (GRCm39) |
|
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,464,684 (GRCm39) |
V393E |
probably damaging |
Het |
Ednrb |
C |
T |
14: 104,057,449 (GRCm39) |
G371D |
probably damaging |
Het |
Efcab5 |
T |
C |
11: 76,994,353 (GRCm39) |
|
probably benign |
Het |
Exoc2 |
A |
T |
13: 31,061,608 (GRCm39) |
|
probably benign |
Het |
Fbn2 |
G |
A |
18: 58,183,362 (GRCm39) |
|
probably benign |
Het |
Foxo6 |
T |
C |
4: 120,126,199 (GRCm39) |
S199G |
probably benign |
Het |
Fpr1 |
T |
A |
17: 18,097,618 (GRCm39) |
I124F |
probably damaging |
Het |
Gk5 |
A |
T |
9: 96,063,823 (GRCm39) |
|
probably null |
Het |
Gys1 |
A |
T |
7: 45,086,143 (GRCm39) |
|
probably benign |
Het |
Igfbp1 |
T |
C |
11: 7,148,103 (GRCm39) |
S49P |
probably damaging |
Het |
Incenp |
A |
T |
19: 9,871,357 (GRCm39) |
S91T |
unknown |
Het |
Itpkc |
G |
A |
7: 26,913,968 (GRCm39) |
R498* |
probably null |
Het |
Kat6a |
A |
G |
8: 23,429,819 (GRCm39) |
T1725A |
unknown |
Het |
Kiz |
T |
A |
2: 146,705,730 (GRCm39) |
C97S |
probably benign |
Het |
Kri1 |
A |
G |
9: 21,187,848 (GRCm39) |
|
probably benign |
Het |
Lipn |
A |
G |
19: 34,058,106 (GRCm39) |
S276G |
possibly damaging |
Het |
Llgl1 |
A |
G |
11: 60,602,967 (GRCm39) |
T881A |
probably damaging |
Het |
Man1a2 |
T |
C |
3: 100,592,102 (GRCm39) |
H26R |
probably damaging |
Het |
Map3k5 |
T |
A |
10: 19,876,359 (GRCm39) |
F173I |
probably damaging |
Het |
Miox |
C |
T |
15: 89,220,477 (GRCm39) |
L189F |
possibly damaging |
Het |
Mipol1 |
A |
G |
12: 57,503,855 (GRCm39) |
Q341R |
probably damaging |
Het |
Mllt6 |
G |
T |
11: 97,569,431 (GRCm39) |
A928S |
probably benign |
Het |
Ncoa6 |
TGC |
TGCGC |
2: 155,250,211 (GRCm39) |
|
probably null |
Het |
Nipsnap3a |
C |
T |
4: 52,997,178 (GRCm39) |
T150I |
probably benign |
Het |
Nsl1 |
A |
G |
1: 190,797,427 (GRCm39) |
E97G |
probably damaging |
Het |
Or11j4 |
G |
A |
14: 50,630,452 (GRCm39) |
V80M |
probably damaging |
Het |
Or4f54 |
T |
C |
2: 111,122,931 (GRCm39) |
V106A |
probably benign |
Het |
Or7g18 |
A |
T |
9: 18,786,848 (GRCm39) |
Y72F |
probably benign |
Het |
Or8c11 |
G |
A |
9: 38,289,880 (GRCm39) |
M234I |
probably benign |
Het |
Pakap |
T |
C |
4: 57,855,207 (GRCm39) |
F220L |
probably damaging |
Het |
Pdcd6ip |
A |
G |
9: 113,491,572 (GRCm39) |
L552S |
probably damaging |
Het |
Plekhf2 |
T |
C |
4: 10,990,595 (GRCm39) |
|
probably benign |
Het |
Prdm1 |
T |
C |
10: 44,332,622 (GRCm39) |
E96G |
probably damaging |
Het |
Prpf40a |
T |
A |
2: 53,040,659 (GRCm39) |
E608D |
probably damaging |
Het |
Prpf40b |
A |
T |
15: 99,214,274 (GRCm39) |
|
probably benign |
Het |
Rag2 |
T |
C |
2: 101,460,464 (GRCm39) |
V258A |
probably damaging |
Het |
S100a5 |
A |
G |
3: 90,518,881 (GRCm39) |
I68V |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,530,648 (GRCm39) |
|
probably null |
Het |
Slc24a4 |
T |
C |
12: 102,226,740 (GRCm39) |
V492A |
probably damaging |
Het |
Spmip6 |
T |
G |
4: 41,507,538 (GRCm39) |
E150A |
probably damaging |
Het |
Synpo2 |
C |
T |
3: 122,873,383 (GRCm39) |
W211* |
probably null |
Het |
Tgtp1 |
A |
G |
11: 48,877,970 (GRCm39) |
V245A |
probably benign |
Het |
Tmem144 |
G |
A |
3: 79,746,580 (GRCm39) |
|
probably benign |
Het |
Trerf1 |
A |
G |
17: 47,630,471 (GRCm39) |
|
noncoding transcript |
Het |
Ttn |
G |
C |
2: 76,677,048 (GRCm39) |
|
probably benign |
Het |
Vmn1r28 |
G |
A |
6: 58,242,702 (GRCm39) |
A182T |
probably benign |
Het |
Vps13d |
A |
T |
4: 144,871,372 (GRCm39) |
M1900K |
probably benign |
Het |
Vps41 |
A |
T |
13: 19,037,610 (GRCm39) |
D691V |
probably damaging |
Het |
Zfp518b |
T |
C |
5: 38,829,083 (GRCm39) |
Y974C |
probably damaging |
Het |
Zscan29 |
A |
T |
2: 120,997,214 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Spag6l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00864:Spag6l
|
APN |
16 |
16,598,597 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00928:Spag6l
|
APN |
16 |
16,584,877 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL00929:Spag6l
|
APN |
16 |
16,584,877 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01793:Spag6l
|
APN |
16 |
16,599,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02380:Spag6l
|
APN |
16 |
16,581,033 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03271:Spag6l
|
APN |
16 |
16,598,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0394:Spag6l
|
UTSW |
16 |
16,598,493 (GRCm39) |
missense |
probably benign |
|
R0720:Spag6l
|
UTSW |
16 |
16,584,960 (GRCm39) |
splice site |
probably benign |
|
R1205:Spag6l
|
UTSW |
16 |
16,605,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Spag6l
|
UTSW |
16 |
16,598,478 (GRCm39) |
splice site |
probably benign |
|
R1707:Spag6l
|
UTSW |
16 |
16,598,492 (GRCm39) |
missense |
probably benign |
0.00 |
R1926:Spag6l
|
UTSW |
16 |
16,580,921 (GRCm39) |
missense |
probably benign |
0.00 |
R2255:Spag6l
|
UTSW |
16 |
16,595,203 (GRCm39) |
missense |
probably damaging |
0.96 |
R2330:Spag6l
|
UTSW |
16 |
16,646,949 (GRCm39) |
missense |
probably benign |
|
R3755:Spag6l
|
UTSW |
16 |
16,580,884 (GRCm39) |
critical splice donor site |
probably null |
|
R3796:Spag6l
|
UTSW |
16 |
16,580,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R4093:Spag6l
|
UTSW |
16 |
16,646,888 (GRCm39) |
missense |
probably benign |
0.05 |
R4324:Spag6l
|
UTSW |
16 |
16,605,099 (GRCm39) |
missense |
probably benign |
0.00 |
R4725:Spag6l
|
UTSW |
16 |
16,610,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Spag6l
|
UTSW |
16 |
16,595,254 (GRCm39) |
missense |
probably benign |
0.03 |
R4877:Spag6l
|
UTSW |
16 |
16,599,622 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5753:Spag6l
|
UTSW |
16 |
16,584,831 (GRCm39) |
critical splice donor site |
probably null |
|
R5958:Spag6l
|
UTSW |
16 |
16,580,885 (GRCm39) |
critical splice donor site |
probably null |
|
R6107:Spag6l
|
UTSW |
16 |
16,599,652 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6894:Spag6l
|
UTSW |
16 |
16,601,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R7329:Spag6l
|
UTSW |
16 |
16,584,883 (GRCm39) |
missense |
probably benign |
|
R7634:Spag6l
|
UTSW |
16 |
16,595,278 (GRCm39) |
missense |
probably damaging |
0.97 |
R8240:Spag6l
|
UTSW |
16 |
16,580,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Spag6l
|
UTSW |
16 |
16,580,898 (GRCm39) |
missense |
probably damaging |
0.97 |
R9207:Spag6l
|
UTSW |
16 |
16,598,492 (GRCm39) |
missense |
probably benign |
0.00 |
R9682:Spag6l
|
UTSW |
16 |
16,646,981 (GRCm39) |
critical splice acceptor site |
probably null |
|
|