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 |
Rexo5 |
T |
G |
7: 119,444,667 (GRCm39) |
L714R |
probably damaging |
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 |
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 Zcchc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00587:Zcchc2
|
APN |
1 |
105,957,993 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01339:Zcchc2
|
APN |
1 |
105,957,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01981:Zcchc2
|
APN |
1 |
105,955,229 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02172:Zcchc2
|
APN |
1 |
105,928,664 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02864:Zcchc2
|
APN |
1 |
105,943,814 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02993:Zcchc2
|
APN |
1 |
105,957,898 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03163:Zcchc2
|
APN |
1 |
105,958,841 (GRCm39) |
missense |
probably damaging |
1.00 |
P0042:Zcchc2
|
UTSW |
1 |
105,958,727 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0200:Zcchc2
|
UTSW |
1 |
105,931,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Zcchc2
|
UTSW |
1 |
105,958,000 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0501:Zcchc2
|
UTSW |
1 |
105,943,821 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0689:Zcchc2
|
UTSW |
1 |
105,958,234 (GRCm39) |
nonsense |
probably null |
|
R1799:Zcchc2
|
UTSW |
1 |
105,958,017 (GRCm39) |
missense |
probably benign |
0.00 |
R2016:Zcchc2
|
UTSW |
1 |
105,931,851 (GRCm39) |
splice site |
probably null |
|
R2153:Zcchc2
|
UTSW |
1 |
105,949,453 (GRCm39) |
splice site |
probably null |
|
R2175:Zcchc2
|
UTSW |
1 |
105,955,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R2999:Zcchc2
|
UTSW |
1 |
105,957,754 (GRCm39) |
missense |
probably benign |
0.00 |
R3113:Zcchc2
|
UTSW |
1 |
105,918,752 (GRCm39) |
missense |
unknown |
|
R4571:Zcchc2
|
UTSW |
1 |
105,958,987 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4670:Zcchc2
|
UTSW |
1 |
105,917,996 (GRCm39) |
unclassified |
probably benign |
|
R5067:Zcchc2
|
UTSW |
1 |
105,958,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Zcchc2
|
UTSW |
1 |
105,958,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R5499:Zcchc2
|
UTSW |
1 |
105,958,322 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5522:Zcchc2
|
UTSW |
1 |
105,951,426 (GRCm39) |
missense |
probably benign |
0.00 |
R5526:Zcchc2
|
UTSW |
1 |
105,957,984 (GRCm39) |
nonsense |
probably null |
|
R5571:Zcchc2
|
UTSW |
1 |
105,951,402 (GRCm39) |
missense |
probably benign |
|
R5599:Zcchc2
|
UTSW |
1 |
105,959,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R6133:Zcchc2
|
UTSW |
1 |
105,947,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Zcchc2
|
UTSW |
1 |
105,917,900 (GRCm39) |
unclassified |
probably benign |
|
R6194:Zcchc2
|
UTSW |
1 |
105,918,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6246:Zcchc2
|
UTSW |
1 |
105,957,796 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7089:Zcchc2
|
UTSW |
1 |
105,958,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R7626:Zcchc2
|
UTSW |
1 |
105,928,742 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7749:Zcchc2
|
UTSW |
1 |
105,946,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Zcchc2
|
UTSW |
1 |
105,931,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Zcchc2
|
UTSW |
1 |
105,945,982 (GRCm39) |
missense |
probably damaging |
0.99 |
R7982:Zcchc2
|
UTSW |
1 |
105,958,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R8316:Zcchc2
|
UTSW |
1 |
105,959,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R8351:Zcchc2
|
UTSW |
1 |
105,958,662 (GRCm39) |
missense |
probably damaging |
0.98 |
R8451:Zcchc2
|
UTSW |
1 |
105,958,662 (GRCm39) |
missense |
probably damaging |
0.98 |
R8697:Zcchc2
|
UTSW |
1 |
105,958,494 (GRCm39) |
missense |
probably damaging |
0.98 |
R8862:Zcchc2
|
UTSW |
1 |
105,958,998 (GRCm39) |
makesense |
probably null |
|
R9421:Zcchc2
|
UTSW |
1 |
105,950,987 (GRCm39) |
missense |
probably benign |
|
RF022:Zcchc2
|
UTSW |
1 |
105,939,472 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Zcchc2
|
UTSW |
1 |
105,918,856 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zcchc2
|
UTSW |
1 |
105,957,555 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Zcchc2
|
UTSW |
1 |
105,931,866 (GRCm39) |
missense |
possibly damaging |
0.74 |
|