Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat3 |
T |
A |
17: 13,159,176 (GRCm39) |
R4S |
probably benign |
Het |
Adamdec1 |
A |
T |
14: 68,814,547 (GRCm39) |
C143* |
probably null |
Het |
Adck5 |
A |
G |
15: 76,460,612 (GRCm39) |
|
probably benign |
Het |
Aebp2 |
A |
G |
6: 140,579,441 (GRCm39) |
D226G |
probably damaging |
Het |
Ascc3 |
A |
G |
10: 50,630,175 (GRCm39) |
I1755V |
possibly damaging |
Het |
Aspm |
C |
T |
1: 139,419,266 (GRCm39) |
T2977M |
probably damaging |
Het |
Cacna1a |
A |
G |
8: 85,276,152 (GRCm39) |
S582G |
probably damaging |
Het |
Card14 |
T |
C |
11: 119,231,835 (GRCm39) |
F801S |
probably damaging |
Het |
Casp16 |
T |
A |
17: 23,771,003 (GRCm39) |
D134V |
probably damaging |
Het |
Cmya5 |
A |
G |
13: 93,234,108 (GRCm39) |
S327P |
possibly damaging |
Het |
Cutc |
A |
T |
19: 43,755,727 (GRCm39) |
D229V |
possibly damaging |
Het |
Cyp21a1 |
C |
A |
17: 35,023,419 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,859,423 (GRCm39) |
K2130R |
probably damaging |
Het |
Dsc1 |
C |
T |
18: 20,234,904 (GRCm39) |
S250N |
probably benign |
Het |
Edc4 |
T |
C |
8: 106,611,778 (GRCm39) |
|
probably null |
Het |
Efcab8 |
G |
C |
2: 153,646,861 (GRCm39) |
V397L |
unknown |
Het |
Ehmt1 |
A |
T |
2: 24,729,635 (GRCm39) |
I642K |
possibly damaging |
Het |
Gjd2 |
T |
C |
2: 113,842,039 (GRCm39) |
Q146R |
probably benign |
Het |
Gm26661 |
A |
G |
14: 7,791,936 (GRCm38) |
H117R |
unknown |
Het |
H2-Oa |
T |
A |
17: 34,313,505 (GRCm39) |
D185E |
probably damaging |
Het |
Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
Hyal6 |
A |
G |
6: 24,734,585 (GRCm39) |
R173G |
possibly damaging |
Het |
Ica1 |
A |
T |
6: 8,659,921 (GRCm39) |
V125D |
probably benign |
Het |
Ift172 |
T |
C |
5: 31,442,867 (GRCm39) |
T140A |
probably benign |
Het |
Ighv9-4 |
T |
A |
12: 114,263,883 (GRCm39) |
I17F |
probably benign |
Het |
Igkv4-92 |
G |
T |
6: 68,732,248 (GRCm39) |
T42N |
probably damaging |
Het |
Kctd16 |
C |
A |
18: 40,392,069 (GRCm39) |
P219Q |
probably damaging |
Het |
Kdm5b |
A |
T |
1: 134,530,323 (GRCm39) |
I445F |
probably benign |
Het |
Ksr2 |
A |
G |
5: 117,841,319 (GRCm39) |
T598A |
probably benign |
Het |
Lrrn1 |
C |
T |
6: 107,544,568 (GRCm39) |
T122I |
probably damaging |
Het |
Mars2 |
A |
G |
1: 55,276,721 (GRCm39) |
D108G |
possibly damaging |
Het |
Ms4a14 |
A |
G |
19: 11,281,038 (GRCm39) |
W507R |
|
Het |
Ncoa3 |
A |
G |
2: 165,910,381 (GRCm39) |
T1266A |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,083,256 (GRCm39) |
K5650E |
possibly damaging |
Het |
Nlrp4f |
T |
A |
13: 65,332,883 (GRCm39) |
K92* |
probably null |
Het |
Nme4 |
G |
T |
17: 26,314,389 (GRCm39) |
A13E |
probably benign |
Het |
Nova1 |
G |
T |
12: 46,865,524 (GRCm39) |
A4E |
unknown |
Het |
Nphs1 |
G |
T |
7: 30,160,092 (GRCm39) |
E124* |
probably null |
Het |
Or10d4 |
T |
A |
9: 39,580,974 (GRCm39) |
I207N |
possibly damaging |
Het |
Or10d4b |
T |
A |
9: 39,534,809 (GRCm39) |
L128* |
probably null |
Het |
Or5d14 |
T |
C |
2: 87,880,782 (GRCm39) |
Y62C |
probably damaging |
Het |
Pde8a |
C |
T |
7: 80,982,619 (GRCm39) |
T746I |
probably damaging |
Het |
Peg3 |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
7: 6,712,167 (GRCm39) |
|
probably benign |
Het |
Ranbp2 |
T |
C |
10: 58,313,050 (GRCm39) |
S1257P |
probably damaging |
Het |
Ranbp3 |
T |
C |
17: 57,003,791 (GRCm39) |
|
probably null |
Het |
Rasgrf1 |
A |
G |
9: 89,793,600 (GRCm39) |
T126A |
probably benign |
Het |
Rhobtb3 |
A |
G |
13: 76,020,512 (GRCm39) |
Y597H |
probably damaging |
Het |
Riox1 |
C |
G |
12: 83,998,221 (GRCm39) |
Y252* |
probably null |
Het |
Sh2d3c |
T |
C |
2: 32,634,778 (GRCm39) |
Y186H |
possibly damaging |
Het |
Slc16a7 |
T |
A |
10: 125,066,536 (GRCm39) |
T368S |
probably benign |
Het |
Slc25a26 |
G |
A |
6: 94,511,143 (GRCm39) |
V107I |
|
Het |
Slc4a5 |
A |
T |
6: 83,203,217 (GRCm39) |
Y39F |
possibly damaging |
Het |
Smarcad1 |
A |
G |
6: 65,049,035 (GRCm39) |
K254E |
probably damaging |
Het |
Sspo |
G |
T |
6: 48,434,747 (GRCm39) |
V1080L |
possibly damaging |
Het |
Thsd7b |
A |
T |
1: 129,843,382 (GRCm39) |
T865S |
probably benign |
Het |
Top1 |
C |
T |
2: 160,545,591 (GRCm39) |
Q320* |
probably null |
Het |
Trank1 |
T |
A |
9: 111,220,770 (GRCm39) |
N2502K |
possibly damaging |
Het |
Urad |
T |
C |
5: 147,252,251 (GRCm39) |
H67R |
probably damaging |
Het |
Vamp5 |
A |
C |
6: 72,357,362 (GRCm39) |
|
probably null |
Het |
Vmn1r62 |
A |
G |
7: 5,679,062 (GRCm39) |
I248V |
probably benign |
Het |
Wwc2 |
G |
T |
8: 48,305,007 (GRCm39) |
Q873K |
unknown |
Het |
Zcchc2 |
C |
A |
1: 105,958,535 (GRCm39) |
S1002Y |
probably damaging |
Het |
Zdhhc14 |
G |
A |
17: 5,803,283 (GRCm39) |
R462H |
probably benign |
Het |
Zfp788 |
A |
G |
7: 41,299,484 (GRCm39) |
N707D |
|
Het |
Zfp964 |
A |
G |
8: 70,115,783 (GRCm39) |
T128A |
probably benign |
Het |
Zkscan16 |
T |
C |
4: 58,957,722 (GRCm39) |
L668S |
possibly damaging |
Het |
|
Other mutations in Rexo5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01308:Rexo5
|
APN |
7 |
119,433,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R0347:Rexo5
|
UTSW |
7 |
119,423,119 (GRCm39) |
critical splice donor site |
probably null |
|
R0442:Rexo5
|
UTSW |
7 |
119,442,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R0589:Rexo5
|
UTSW |
7 |
119,444,606 (GRCm39) |
missense |
probably benign |
0.00 |
R0980:Rexo5
|
UTSW |
7 |
119,423,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Rexo5
|
UTSW |
7 |
119,400,581 (GRCm39) |
critical splice donor site |
probably null |
|
R1465:Rexo5
|
UTSW |
7 |
119,400,581 (GRCm39) |
critical splice donor site |
probably null |
|
R1505:Rexo5
|
UTSW |
7 |
119,398,826 (GRCm39) |
nonsense |
probably null |
|
R1775:Rexo5
|
UTSW |
7 |
119,444,634 (GRCm39) |
missense |
probably benign |
0.00 |
R1911:Rexo5
|
UTSW |
7 |
119,398,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1996:Rexo5
|
UTSW |
7 |
119,423,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R4168:Rexo5
|
UTSW |
7 |
119,426,621 (GRCm39) |
intron |
probably benign |
|
R4169:Rexo5
|
UTSW |
7 |
119,426,621 (GRCm39) |
intron |
probably benign |
|
R4402:Rexo5
|
UTSW |
7 |
119,433,599 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4486:Rexo5
|
UTSW |
7 |
119,424,800 (GRCm39) |
missense |
probably benign |
0.00 |
R4620:Rexo5
|
UTSW |
7 |
119,426,526 (GRCm39) |
missense |
probably benign |
0.37 |
R4621:Rexo5
|
UTSW |
7 |
119,418,722 (GRCm39) |
missense |
probably benign |
0.19 |
R4865:Rexo5
|
UTSW |
7 |
119,400,553 (GRCm39) |
nonsense |
probably null |
|
R4884:Rexo5
|
UTSW |
7 |
119,424,774 (GRCm39) |
nonsense |
probably null |
|
R5171:Rexo5
|
UTSW |
7 |
119,423,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Rexo5
|
UTSW |
7 |
119,433,522 (GRCm39) |
nonsense |
probably null |
|
R5266:Rexo5
|
UTSW |
7 |
119,443,660 (GRCm39) |
missense |
probably benign |
0.00 |
R5463:Rexo5
|
UTSW |
7 |
119,433,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Rexo5
|
UTSW |
7 |
119,433,626 (GRCm39) |
critical splice donor site |
probably null |
|
R6163:Rexo5
|
UTSW |
7 |
119,404,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R6305:Rexo5
|
UTSW |
7 |
119,427,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Rexo5
|
UTSW |
7 |
119,404,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Rexo5
|
UTSW |
7 |
119,417,636 (GRCm39) |
missense |
probably damaging |
0.97 |
R8143:Rexo5
|
UTSW |
7 |
119,433,484 (GRCm39) |
splice site |
probably null |
|
R8379:Rexo5
|
UTSW |
7 |
119,433,508 (GRCm39) |
missense |
probably benign |
0.03 |
R8550:Rexo5
|
UTSW |
7 |
119,400,568 (GRCm39) |
missense |
probably benign |
0.01 |
R8841:Rexo5
|
UTSW |
7 |
119,448,011 (GRCm39) |
missense |
probably benign |
0.00 |
R9287:Rexo5
|
UTSW |
7 |
119,402,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R9404:Rexo5
|
UTSW |
7 |
119,400,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R9499:Rexo5
|
UTSW |
7 |
119,404,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|