Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
A |
13: 77,480,429 (GRCm39) |
L1153* |
probably null |
Het |
Adamts2 |
T |
C |
11: 50,683,550 (GRCm39) |
I944T |
possibly damaging |
Het |
Aqp9 |
A |
T |
9: 71,045,485 (GRCm39) |
C67* |
probably null |
Het |
Armt1 |
G |
T |
10: 4,404,150 (GRCm39) |
G412W |
probably damaging |
Het |
B4galt1 |
T |
C |
4: 40,807,243 (GRCm39) |
D381G |
probably benign |
Het |
Bmp5 |
A |
T |
9: 75,780,579 (GRCm39) |
H292L |
probably benign |
Het |
Brpf1 |
T |
C |
6: 113,299,510 (GRCm39) |
F1181S |
probably damaging |
Het |
Btbd7 |
C |
A |
12: 102,779,025 (GRCm39) |
G414C |
probably damaging |
Het |
Ccdc65 |
A |
T |
15: 98,616,723 (GRCm39) |
K204* |
probably null |
Het |
Cdk5 |
T |
A |
5: 24,627,379 (GRCm39) |
K88M |
probably damaging |
Het |
Cdrt4 |
T |
A |
11: 62,883,634 (GRCm39) |
L112Q |
probably damaging |
Het |
Cenpb |
T |
C |
2: 131,020,547 (GRCm39) |
E417G |
unknown |
Het |
Cep135 |
T |
C |
5: 76,754,576 (GRCm39) |
I351T |
possibly damaging |
Het |
Ces1d |
A |
T |
8: 93,914,383 (GRCm39) |
S226R |
probably damaging |
Het |
CN725425 |
T |
C |
15: 91,130,090 (GRCm39) |
C318R |
possibly damaging |
Het |
Cnga3 |
T |
A |
1: 37,300,460 (GRCm39) |
D393E |
probably benign |
Het |
Cplane1 |
A |
T |
15: 8,230,765 (GRCm39) |
H1014L |
possibly damaging |
Het |
Cpsf1 |
G |
A |
15: 76,486,169 (GRCm39) |
R358* |
probably null |
Het |
Cyp2b23 |
G |
A |
7: 26,378,963 (GRCm39) |
P167L |
probably damaging |
Het |
Cyp2c70 |
A |
T |
19: 40,142,059 (GRCm39) |
H477Q |
probably benign |
Het |
D930020B18Rik |
A |
C |
10: 121,490,721 (GRCm39) |
Y107S |
probably damaging |
Het |
Dhrs1 |
A |
T |
14: 55,978,192 (GRCm39) |
F216I |
probably benign |
Het |
Dmgdh |
A |
T |
13: 93,845,767 (GRCm39) |
K474* |
probably null |
Het |
Dsp |
T |
C |
13: 38,335,596 (GRCm39) |
I11T |
possibly damaging |
Het |
Erh |
G |
T |
12: 80,684,282 (GRCm39) |
A65E |
probably benign |
Het |
Fmnl1 |
AGGCTCTGG |
AGG |
11: 103,077,444 (GRCm39) |
|
probably benign |
Het |
Grid2 |
A |
C |
6: 64,643,139 (GRCm39) |
H967P |
probably benign |
Het |
Hc |
A |
G |
2: 34,922,317 (GRCm39) |
I503T |
possibly damaging |
Het |
Herc3 |
T |
C |
6: 58,867,183 (GRCm39) |
L824S |
probably damaging |
Het |
Hfm1 |
T |
C |
5: 107,065,439 (GRCm39) |
D80G |
probably benign |
Het |
Hjurp |
CTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCT |
C |
1: 88,193,999 (GRCm39) |
|
probably benign |
Het |
Hspa1l |
A |
G |
17: 35,196,230 (GRCm39) |
K90E |
possibly damaging |
Het |
Impa2 |
G |
A |
18: 67,451,497 (GRCm39) |
V264I |
probably benign |
Het |
Ipmk |
C |
T |
10: 71,199,333 (GRCm39) |
R65W |
probably damaging |
Het |
Klhl38 |
C |
T |
15: 58,185,500 (GRCm39) |
V410I |
probably benign |
Het |
Lcn4 |
A |
G |
2: 26,558,360 (GRCm39) |
I175T |
possibly damaging |
Het |
Lipo2 |
C |
A |
19: 33,726,917 (GRCm39) |
W40L |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,734,745 (GRCm39) |
|
probably null |
Het |
Myo16 |
T |
A |
8: 10,619,700 (GRCm39) |
I1417N |
unknown |
Het |
Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
Or4a66 |
T |
A |
2: 88,531,137 (GRCm39) |
I179F |
probably benign |
Het |
Or52e19b |
A |
T |
7: 103,032,667 (GRCm39) |
C181S |
probably damaging |
Het |
Or5j3 |
G |
A |
2: 86,128,526 (GRCm39) |
R122H |
probably benign |
Het |
Pcdha11 |
A |
G |
18: 37,145,307 (GRCm39) |
N466S |
probably damaging |
Het |
Pif1 |
C |
T |
9: 65,499,076 (GRCm39) |
T432M |
probably damaging |
Het |
Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,341,589 (GRCm39) |
|
probably null |
Het |
Pkd1l3 |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
8: 110,350,420 (GRCm39) |
|
probably benign |
Het |
Pole |
T |
C |
5: 110,459,949 (GRCm39) |
S1118P |
possibly damaging |
Het |
Ppp4r4 |
T |
C |
12: 103,566,706 (GRCm39) |
M652T |
probably benign |
Het |
Prex2 |
A |
T |
1: 11,180,562 (GRCm39) |
K376* |
probably null |
Het |
Prps1l1 |
A |
T |
12: 35,035,205 (GRCm39) |
I107F |
probably damaging |
Het |
Resf1 |
T |
A |
6: 149,228,664 (GRCm39) |
V570D |
probably damaging |
Het |
Rfc1 |
C |
T |
5: 65,432,778 (GRCm39) |
V761I |
probably benign |
Het |
Ripk4 |
T |
C |
16: 97,547,203 (GRCm39) |
E353G |
probably benign |
Het |
Robo2 |
C |
A |
16: 73,767,941 (GRCm39) |
|
probably null |
Het |
Rrm1 |
C |
T |
7: 102,117,545 (GRCm39) |
A745V |
probably benign |
Het |
Sash1 |
A |
T |
10: 8,606,179 (GRCm39) |
V737D |
probably benign |
Het |
Sel1l2 |
T |
C |
2: 140,127,209 (GRCm39) |
K101E |
probably benign |
Het |
Selenbp2 |
A |
T |
3: 94,607,337 (GRCm39) |
I253F |
probably benign |
Het |
Setd1a |
C |
T |
7: 127,385,279 (GRCm39) |
P662L |
possibly damaging |
Het |
Slc16a6 |
C |
T |
11: 109,345,776 (GRCm39) |
V496I |
possibly damaging |
Het |
Slc4a4 |
A |
T |
5: 89,232,512 (GRCm39) |
M239L |
probably benign |
Het |
Slc7a8 |
G |
C |
14: 55,018,750 (GRCm39) |
A12G |
probably benign |
Het |
Snx30 |
T |
C |
4: 59,886,517 (GRCm39) |
S309P |
possibly damaging |
Het |
Spen |
T |
C |
4: 141,197,701 (GRCm39) |
N3389S |
probably benign |
Het |
Spg11 |
T |
C |
2: 121,922,687 (GRCm39) |
T921A |
probably damaging |
Het |
Tanc2 |
T |
A |
11: 105,758,400 (GRCm39) |
D720E |
possibly damaging |
Het |
Tmprss9 |
A |
T |
10: 80,730,163 (GRCm39) |
I688F |
possibly damaging |
Het |
Trap1 |
A |
G |
16: 3,862,490 (GRCm39) |
V596A |
possibly damaging |
Het |
Ttc32 |
G |
T |
12: 9,080,187 (GRCm39) |
R44L |
probably benign |
Het |
Tusc3 |
T |
A |
8: 39,597,898 (GRCm39) |
N288K |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,127,956 (GRCm39) |
G656E |
probably damaging |
Het |
Vill |
T |
C |
9: 118,892,671 (GRCm39) |
|
probably null |
Het |
Vmn1r5 |
A |
T |
6: 56,963,182 (GRCm39) |
R286* |
probably null |
Het |
Vmn2r14 |
T |
C |
5: 109,365,533 (GRCm39) |
T514A |
probably benign |
Het |
Vmn2r32 |
G |
A |
7: 7,477,204 (GRCm39) |
H396Y |
probably benign |
Het |
Vmn2r75 |
A |
T |
7: 85,820,765 (GRCm39) |
Y56* |
probably null |
Het |
Wdfy3 |
C |
T |
5: 102,011,983 (GRCm39) |
S2668N |
probably benign |
Het |
Wdr72 |
G |
A |
9: 74,059,729 (GRCm39) |
D392N |
probably benign |
Het |
Zfp518a |
A |
C |
19: 40,901,870 (GRCm39) |
K600Q |
possibly damaging |
Het |
|
Other mutations in Cfap97 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Cfap97
|
APN |
8 |
46,623,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01335:Cfap97
|
APN |
8 |
46,623,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02327:Cfap97
|
APN |
8 |
46,623,179 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02457:Cfap97
|
APN |
8 |
46,623,315 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4289:Cfap97
|
UTSW |
8 |
46,645,698 (GRCm39) |
missense |
probably benign |
0.03 |
R4777:Cfap97
|
UTSW |
8 |
46,648,334 (GRCm39) |
nonsense |
probably null |
|
R4844:Cfap97
|
UTSW |
8 |
46,622,712 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5369:Cfap97
|
UTSW |
8 |
46,622,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Cfap97
|
UTSW |
8 |
46,623,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Cfap97
|
UTSW |
8 |
46,634,895 (GRCm39) |
missense |
probably damaging |
0.97 |
R6227:Cfap97
|
UTSW |
8 |
46,644,769 (GRCm39) |
critical splice donor site |
probably null |
|
R6790:Cfap97
|
UTSW |
8 |
46,623,113 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7409:Cfap97
|
UTSW |
8 |
46,645,733 (GRCm39) |
missense |
probably benign |
0.13 |
R7964:Cfap97
|
UTSW |
8 |
46,623,237 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8077:Cfap97
|
UTSW |
8 |
46,623,482 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8960:Cfap97
|
UTSW |
8 |
46,623,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9186:Cfap97
|
UTSW |
8 |
46,644,665 (GRCm39) |
missense |
possibly damaging |
0.91 |
|