Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,774,267 (GRCm39) |
N1152S |
probably benign |
Het |
Abcb6 |
A |
T |
1: 75,151,372 (GRCm39) |
Y518N |
possibly damaging |
Het |
Actr2 |
G |
A |
11: 20,030,745 (GRCm39) |
P168S |
probably damaging |
Het |
Adam12 |
A |
G |
7: 133,566,454 (GRCm39) |
V332A |
probably damaging |
Het |
Adam23 |
T |
C |
1: 63,620,359 (GRCm39) |
I805T |
probably benign |
Het |
Adar |
A |
G |
3: 89,654,516 (GRCm39) |
T883A |
probably benign |
Het |
Aldh3a1 |
A |
G |
11: 61,107,912 (GRCm39) |
T319A |
probably damaging |
Het |
Apcdd1 |
T |
A |
18: 63,083,269 (GRCm39) |
|
probably null |
Het |
Arhgef18 |
C |
A |
8: 3,482,718 (GRCm39) |
A141E |
possibly damaging |
Het |
Bub3 |
A |
G |
7: 131,170,428 (GRCm39) |
T317A |
probably benign |
Het |
Ccdc60 |
C |
A |
5: 116,269,265 (GRCm39) |
D452Y |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,219,381 (GRCm39) |
E125G |
probably damaging |
Het |
Ccdc68 |
A |
G |
18: 70,093,492 (GRCm39) |
E233G |
probably damaging |
Het |
Cep192 |
A |
G |
18: 67,968,525 (GRCm39) |
D973G |
probably benign |
Het |
Cox5b |
T |
A |
1: 36,730,759 (GRCm39) |
M31K |
probably benign |
Het |
Cse1l |
A |
G |
2: 166,783,386 (GRCm39) |
N780S |
probably benign |
Het |
Cyfip1 |
T |
C |
7: 55,563,277 (GRCm39) |
|
probably null |
Het |
Cyp1a1 |
C |
T |
9: 57,607,770 (GRCm39) |
P133S |
probably benign |
Het |
Dcp1a |
A |
G |
14: 30,241,497 (GRCm39) |
M436V |
probably benign |
Het |
Dcst1 |
G |
T |
3: 89,265,075 (GRCm39) |
Y258* |
probably null |
Het |
Dhx30 |
T |
C |
9: 109,914,518 (GRCm39) |
E993G |
possibly damaging |
Het |
Disc1 |
A |
T |
8: 125,814,261 (GRCm39) |
M42L |
possibly damaging |
Het |
Dnah8 |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
17: 30,979,841 (GRCm39) |
|
probably null |
Het |
Entrep3 |
A |
G |
3: 89,094,099 (GRCm39) |
D304G |
possibly damaging |
Het |
Erbb2 |
A |
T |
11: 98,318,216 (GRCm39) |
D484V |
probably benign |
Het |
Fxr2 |
A |
G |
11: 69,543,469 (GRCm39) |
N657D |
probably benign |
Het |
Gbx2 |
T |
C |
1: 89,856,635 (GRCm39) |
T252A |
probably damaging |
Het |
Gdap2 |
A |
T |
3: 100,078,264 (GRCm39) |
N76I |
probably damaging |
Het |
Gm20939 |
A |
G |
17: 95,184,666 (GRCm39) |
Y438C |
probably damaging |
Het |
Gsdma2 |
A |
G |
11: 98,540,459 (GRCm39) |
E126G |
possibly damaging |
Het |
Gsg1 |
T |
G |
6: 135,217,098 (GRCm39) |
H246P |
probably damaging |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Ighv1-62-1 |
T |
C |
12: 115,350,601 (GRCm39) |
Q22R |
possibly damaging |
Het |
Kcng3 |
A |
T |
17: 83,895,211 (GRCm39) |
F418L |
probably benign |
Het |
Lin54 |
C |
A |
5: 100,598,546 (GRCm39) |
R593L |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,410,246 (GRCm39) |
N1500I |
probably damaging |
Het |
Lvrn |
A |
C |
18: 46,999,494 (GRCm39) |
S287R |
probably benign |
Het |
Mab21l4 |
T |
C |
1: 93,087,568 (GRCm39) |
E95G |
possibly damaging |
Het |
Madd |
G |
A |
2: 91,006,026 (GRCm39) |
P390S |
probably damaging |
Het |
Mapk8ip3 |
C |
A |
17: 25,118,124 (GRCm39) |
R1281L |
probably damaging |
Het |
Masp1 |
T |
A |
16: 23,271,698 (GRCm39) |
T618S |
probably benign |
Het |
Mgat5 |
A |
G |
1: 127,248,445 (GRCm39) |
T116A |
probably benign |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mrpl39 |
A |
G |
16: 84,527,359 (GRCm39) |
F176S |
probably damaging |
Het |
Myt1l |
T |
C |
12: 29,943,441 (GRCm39) |
I953T |
unknown |
Het |
Nedd4l |
A |
G |
18: 65,343,400 (GRCm39) |
H820R |
probably damaging |
Het |
Nxpe3 |
A |
T |
16: 55,664,855 (GRCm39) |
V455D |
probably damaging |
Het |
Olfm4 |
T |
C |
14: 80,243,747 (GRCm39) |
F105S |
probably damaging |
Het |
Or10ak8 |
C |
T |
4: 118,773,851 (GRCm39) |
R271Q |
probably benign |
Het |
Patz1 |
A |
G |
11: 3,240,720 (GRCm39) |
N36S |
probably benign |
Het |
Peg3 |
T |
A |
7: 6,714,723 (GRCm39) |
K166N |
probably damaging |
Het |
Pes1 |
T |
A |
11: 3,926,118 (GRCm39) |
D302E |
probably benign |
Het |
Pierce1 |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
2: 28,356,122 (GRCm39) |
|
probably benign |
Het |
Plekhh3 |
G |
A |
11: 101,054,972 (GRCm39) |
T627M |
unknown |
Het |
Plxnd1 |
C |
T |
6: 115,940,274 (GRCm39) |
R1370Q |
possibly damaging |
Het |
Rnf20 |
T |
C |
4: 49,638,751 (GRCm39) |
V191A |
probably benign |
Het |
Scn8a |
A |
T |
15: 100,911,172 (GRCm39) |
K864M |
probably damaging |
Het |
Sema3c |
T |
C |
5: 17,919,452 (GRCm39) |
|
probably null |
Het |
Slc24a4 |
C |
T |
12: 102,097,779 (GRCm39) |
T30I |
probably benign |
Het |
Slc27a2 |
A |
G |
2: 126,420,904 (GRCm39) |
D465G |
probably damaging |
Het |
Snrnp48 |
T |
C |
13: 38,393,920 (GRCm39) |
M75T |
probably benign |
Het |
Srgap2 |
A |
G |
1: 131,272,164 (GRCm39) |
S41P |
|
Het |
St3gal5 |
A |
G |
6: 72,130,580 (GRCm39) |
T391A |
probably benign |
Het |
Stkld1 |
T |
C |
2: 26,843,297 (GRCm39) |
L628P |
possibly damaging |
Het |
Tbc1d1 |
T |
A |
5: 64,502,701 (GRCm39) |
M1074K |
probably benign |
Het |
Tent2 |
G |
T |
13: 93,322,821 (GRCm39) |
Q43K |
probably benign |
Het |
Tpsb2 |
T |
A |
17: 25,586,077 (GRCm39) |
Y98* |
probably null |
Het |
Trav6d-3 |
G |
A |
14: 52,964,144 (GRCm39) |
D36N |
probably benign |
Het |
Trim16 |
A |
G |
11: 62,731,644 (GRCm39) |
Y505C |
probably damaging |
Het |
Ttpal |
A |
G |
2: 163,457,458 (GRCm39) |
D310G |
probably benign |
Het |
Ubox5 |
A |
G |
2: 130,441,835 (GRCm39) |
I284T |
probably damaging |
Het |
Vmn2r45 |
T |
A |
7: 8,478,457 (GRCm39) |
|
probably null |
Het |
Vmn2r67 |
T |
C |
7: 84,804,941 (GRCm39) |
D57G |
probably damaging |
Het |
Wdfy4 |
T |
C |
14: 32,855,428 (GRCm39) |
T729A |
|
Het |
Wdr81 |
A |
T |
11: 75,344,349 (GRCm39) |
M306K |
probably benign |
Het |
Zfp62 |
A |
G |
11: 49,106,542 (GRCm39) |
D211G |
probably damaging |
Het |
Zfyve16 |
T |
C |
13: 92,636,763 (GRCm39) |
K1316E |
probably damaging |
Het |
|
Other mutations in Ccdc102a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Ccdc102a
|
APN |
8 |
95,638,266 (GRCm39) |
splice site |
probably null |
|
IGL01921:Ccdc102a
|
APN |
8 |
95,640,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Ccdc102a
|
APN |
8 |
95,629,978 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0413:Ccdc102a
|
UTSW |
8 |
95,629,914 (GRCm39) |
missense |
probably benign |
0.23 |
R0423:Ccdc102a
|
UTSW |
8 |
95,632,554 (GRCm39) |
splice site |
probably benign |
|
R0437:Ccdc102a
|
UTSW |
8 |
95,640,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Ccdc102a
|
UTSW |
8 |
95,632,714 (GRCm39) |
missense |
probably benign |
0.06 |
R1468:Ccdc102a
|
UTSW |
8 |
95,632,714 (GRCm39) |
missense |
probably benign |
0.06 |
R1540:Ccdc102a
|
UTSW |
8 |
95,634,341 (GRCm39) |
critical splice donor site |
probably null |
|
R1893:Ccdc102a
|
UTSW |
8 |
95,640,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2317:Ccdc102a
|
UTSW |
8 |
95,634,957 (GRCm39) |
missense |
probably null |
1.00 |
R4280:Ccdc102a
|
UTSW |
8 |
95,634,444 (GRCm39) |
nonsense |
probably null |
|
R6115:Ccdc102a
|
UTSW |
8 |
95,629,999 (GRCm39) |
missense |
probably benign |
|
R6331:Ccdc102a
|
UTSW |
8 |
95,638,144 (GRCm39) |
missense |
probably benign |
|
R6650:Ccdc102a
|
UTSW |
8 |
95,639,892 (GRCm39) |
missense |
probably benign |
0.23 |
R7019:Ccdc102a
|
UTSW |
8 |
95,636,431 (GRCm39) |
missense |
probably benign |
0.42 |
R7302:Ccdc102a
|
UTSW |
8 |
95,640,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Ccdc102a
|
UTSW |
8 |
95,629,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R7949:Ccdc102a
|
UTSW |
8 |
95,631,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Ccdc102a
|
UTSW |
8 |
95,634,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R8166:Ccdc102a
|
UTSW |
8 |
95,639,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8537:Ccdc102a
|
UTSW |
8 |
95,632,684 (GRCm39) |
missense |
probably benign |
0.00 |
R9179:Ccdc102a
|
UTSW |
8 |
95,639,748 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9297:Ccdc102a
|
UTSW |
8 |
95,638,120 (GRCm39) |
missense |
possibly damaging |
0.78 |
|