Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700057G04Rik |
A |
T |
9: 92,352,649 |
I146F |
possibly damaging |
Het |
4930548H24Rik |
C |
T |
5: 31,487,550 |
Q216* |
probably null |
Het |
Acbd7 |
GTT |
GT |
2: 3,340,699 |
|
probably null |
Het |
Acp7 |
A |
T |
7: 28,614,779 |
N330K |
possibly damaging |
Het |
Adam25 |
A |
T |
8: 40,755,797 |
H700L |
probably benign |
Het |
Alg9 |
GGGTGG |
GGGTGGTGG |
9: 50,775,417 |
|
probably benign |
Het |
Atp8b3 |
A |
T |
10: 80,526,236 |
V689E |
probably benign |
Het |
Atxn2l |
A |
G |
7: 126,495,891 |
V533A |
probably benign |
Het |
C87414 |
A |
T |
5: 93,636,703 |
C301S |
probably benign |
Het |
Catsperb |
G |
A |
12: 101,575,979 |
|
probably null |
Het |
Ccdc13 |
T |
C |
9: 121,814,207 |
K376R |
probably damaging |
Het |
Ccdc170 |
C |
CCAA |
10: 4,561,030 |
|
probably benign |
Het |
Cdh9 |
G |
C |
15: 16,855,830 |
R652P |
probably damaging |
Het |
Cenpf |
A |
C |
1: 189,657,386 |
C1416W |
probably damaging |
Het |
Chga |
GCA |
GCATCA |
12: 102,561,412 |
|
probably benign |
Het |
Cyb5r4 |
TGTGACAGACACACTGCCCAGGGAAG |
TGTGACAGACACACTGCCCAGGGAAGTGACAGACACACTGCCCAGGGAAG |
9: 87,040,425 |
|
probably benign |
Het |
Cyb5r4 |
CCCAGGGA |
CCCAGGGATGTGAGAGACACGCTGGCCAGGGA |
9: 87,040,441 |
|
probably benign |
Het |
Dennd3 |
T |
C |
15: 73,547,592 |
I744T |
probably damaging |
Het |
Dnah1 |
C |
T |
14: 31,307,875 |
R491Q |
probably benign |
Het |
Eif4a2 |
A |
T |
16: 23,110,278 |
M188L |
possibly damaging |
Het |
Esf1 |
CTCCTCTTC |
CTC |
2: 140,164,374 |
|
probably benign |
Het |
Fat3 |
T |
C |
9: 15,998,617 |
I2030V |
probably benign |
Het |
Gab3 |
CTT |
CTTTTT |
X: 75,000,027 |
|
probably benign |
Het |
Gins4 |
A |
T |
8: 23,227,167 |
V195E |
possibly damaging |
Het |
Gm17402 |
TCCTCCTCC |
TCCTCCTCCCCCTCCTCC |
3: 67,365,559 |
|
probably benign |
Het |
Gm17604 |
CTCTCTTTC |
CTC |
X: 165,003,818 |
|
probably null |
Het |
Gm8369 |
GTGTGT |
GTGTGTTTGTGT |
19: 11,511,764 |
|
probably benign |
Het |
Gnpnat1 |
T |
A |
14: 45,383,443 |
|
probably null |
Het |
Inpp4a |
A |
C |
1: 37,388,827 |
N651T |
possibly damaging |
Het |
Ireb2 |
T |
C |
9: 54,881,484 |
F81L |
possibly damaging |
Het |
Kcnh3 |
T |
A |
15: 99,239,928 |
|
probably null |
Het |
Kmt2b |
CTCCTC |
CTCCTCATCCTC |
7: 30,586,377 |
|
probably benign |
Het |
Kmt2c |
TG |
TGCTGTGG |
5: 25,315,772 |
|
probably benign |
Het |
Myt1 |
T |
C |
2: 181,797,773 |
S405P |
probably damaging |
Het |
Net1 |
T |
C |
13: 3,887,406 |
T245A |
probably benign |
Het |
Nkx2-1 |
T |
C |
12: 56,533,547 |
T203A |
probably damaging |
Het |
Oas3 |
T |
C |
5: 120,774,100 |
E75G |
probably damaging |
Het |
Pappa |
T |
A |
4: 65,323,873 |
D1491E |
probably benign |
Het |
Ppp1r8 |
TCTCTCAC |
TC |
4: 132,830,617 |
|
probably benign |
Het |
Ppp2r3c |
T |
A |
12: 55,293,815 |
I157F |
probably benign |
Het |
Rspo4 |
C |
T |
2: 151,867,877 |
|
probably null |
Het |
Rtn4 |
T |
C |
11: 29,706,919 |
S358P |
possibly damaging |
Het |
Siglecg |
T |
A |
7: 43,408,864 |
Y58* |
probably null |
Het |
Slc4a1 |
C |
T |
11: 102,356,716 |
|
probably null |
Het |
Slc9b1 |
CGAAGGAACCAGAAAGGAAGGAACCAGAAAGGAAGGAACCAGAAAGGAAGGAACCAGAAAGGAAGGAACCAGAAAGGAAGG |
CGAAGGAACCAGAAAGGAAGGAACCAGAAAGGAAGGAACCAGAAAGGAAGG |
3: 135,357,542 |
|
probably benign |
Het |
Smc2 |
T |
A |
4: 52,442,276 |
D64E |
probably benign |
Het |
Spaca1 |
CTCGC |
CTCGCTATCGC |
4: 34,049,853 |
|
probably benign |
Het |
Srrm2 |
A |
G |
17: 23,812,588 |
S236G |
unknown |
Het |
Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 |
|
probably benign |
Het |
Strn |
TGCTCCCTTACCCCAGTC |
TGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCAGTCCGAGCTCCCTTACCCCAGTC |
17: 78,677,271 |
|
probably null |
Het |
Tfeb |
CAG |
CAGGAG |
17: 47,786,113 |
|
probably benign |
Het |
Tktl2 |
A |
T |
8: 66,512,852 |
E354V |
probably benign |
Het |
Tpte |
A |
G |
8: 22,306,943 |
T94A |
probably benign |
Het |
Usp40 |
A |
C |
1: 87,967,195 |
S868A |
possibly damaging |
Het |
Vmn2r24 |
G |
A |
6: 123,806,419 |
C526Y |
probably damaging |
Het |
Vmn2r58 |
CAAAATGATGTAGCACTT |
C |
7: 41,836,959 |
|
probably null |
Het |
|