Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
AACC |
A |
7: 40,993,055 |
|
probably benign |
Het |
4930548H24Rik |
GAGAAG |
GAG |
5: 31,487,373 |
|
probably benign |
Het |
4930578G10Rik |
G |
T |
4: 42,761,098 |
|
probably benign |
Het |
4932438A13Rik |
TATTATTAT |
TATTATTATTATTATCATTATTAT |
3: 37,050,752 |
|
probably benign |
Het |
7530416G11Rik |
T |
A |
15: 85,494,307 |
E45V |
unknown |
Homo |
A530032D15Rik |
A |
C |
1: 85,109,351 |
N6K |
probably damaging |
Het |
A530064D06Rik |
GTAGGAAGCTTAG |
GTAG |
17: 48,163,381 |
|
probably benign |
Homo |
Arpc1b |
CC |
CCTGGTC |
5: 145,126,792 |
|
probably null |
Het |
Arrb2 |
C |
T |
11: 70,438,671 |
T269M |
probably damaging |
Homo |
BC051142 |
CAG |
CAGTAG |
17: 34,460,060 |
|
probably null |
Het |
BC051142 |
GCA |
GCATCA |
17: 34,460,068 |
|
probably benign |
Het |
BC051142 |
GC |
GCAAC |
17: 34,460,077 |
|
probably benign |
Het |
Bcas3 |
G |
A |
11: 85,509,497 |
V431I |
probably benign |
Homo |
Blm |
ACCT |
ACCTGCCT |
7: 80,463,767 |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCGCCTCCTCCTCCTCCTCCTCCTCC |
7: 80,512,907 |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCACCTCCTCCTCCTCCTCCTCCTCC |
7: 80,512,910 |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCGCC |
8: 84,638,723 |
|
probably benign |
Het |
Cacna1f |
AGG |
AGGCGG |
X: 7,620,067 |
|
probably benign |
Het |
Calhm1 |
CTCTGTGGCTGTGGCTGTGGCTGTG |
CTCTGTGGCTGTGTCTGTGGCTGTGGCTGTGGCTGTG |
19: 47,141,251 |
|
probably benign |
Het |
Casz1 |
ACCACAGCCACAGCCACAGCCAC |
ACCACAGCCACAGCCAC |
4: 148,952,302 |
|
probably benign |
Homo |
Cd164 |
G |
T |
10: 41,521,926 |
A59S |
probably benign |
Het |
Cd22 |
C |
T |
7: 30,878,082 |
R2H |
possibly damaging |
Homo |
Cd80 |
GAA |
GAAAAA |
16: 38,486,316 |
|
probably benign |
Homo |
Col2a1 |
C |
A |
15: 97,988,981 |
|
probably null |
Het |
Col6a5 |
A |
T |
9: 105,934,174 |
N715K |
unknown |
Homo |
Crygc |
A |
T |
1: 65,071,663 |
F155Y |
probably benign |
Het |
Cul9 |
TCC |
TCCCCC |
17: 46,500,853 |
|
probably benign |
Het |
Cyp2d11 |
T |
TGGGA |
15: 82,390,022 |
|
probably null |
Homo |
D230025D16Rik |
G |
A |
8: 105,241,098 |
G207E |
probably benign |
Homo |
Dbr1 |
AGG |
AGGAGGCGG |
9: 99,583,701 |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,849,385 |
G2817V |
probably damaging |
Homo |
Dthd1 |
C |
CTTA |
5: 62,843,026 |
|
probably benign |
Homo |
Fam166b |
CAGAG |
CAG |
4: 43,427,384 |
|
probably null |
Homo |
Fam45a |
CT |
CTTTT |
19: 60,814,621 |
|
probably benign |
Homo |
Frem3 |
CT |
CTTTT |
8: 80,615,241 |
|
probably benign |
Homo |
Frmpd2 |
G |
T |
14: 33,511,021 |
L399F |
probably damaging |
Homo |
G530012D18Rik |
CACACAGAGAGAGAGAGAGAGAGAGA |
CA |
1: 85,577,152 |
|
probably benign |
Het |
Gbp2b |
A |
G |
3: 142,603,652 |
I175V |
probably benign |
Het |
Gm14393 |
T |
C |
2: 175,061,634 |
E160G |
possibly damaging |
Het |
Gm16519 |
A |
AGAAC |
17: 70,929,338 |
|
probably null |
Homo |
Gm4340 |
CAG |
CAGTAG |
10: 104,196,075 |
|
probably null |
Het |
Gm4340 |
GCAG |
GCAACAG |
10: 104,196,098 |
|
probably benign |
Het |
Gm4340 |
CAGAAG |
CAGAAGAAG |
10: 104,196,099 |
|
probably benign |
Het |
Gpatch11 |
AGGAAG |
AGGAAGGGGAAG |
17: 78,842,174 |
|
probably benign |
Het |
H2-Q4 |
G |
A |
17: 35,380,405 |
D155N |
probably damaging |
Het |
Ifi208 |
ATGGTG |
ATG |
1: 173,677,698 |
|
probably benign |
Homo |
Ighv5-9 |
C |
T |
12: 113,661,877 |
S82N |
probably benign |
Homo |
Ipo9 |
TCC |
TCCCCC |
1: 135,386,269 |
|
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,386,271 |
|
probably benign |
Het |
Isg20l2 |
AAG |
AAGTAG |
3: 87,931,712 |
|
probably null |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,586,363 |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,586,369 |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,586,375 |
|
probably benign |
Het |
Krt10 |
CAC |
CACGAC |
11: 99,386,202 |
|
probably benign |
Het |
Krt10 |
CCTCCT |
CCTCCTTCTCCT |
11: 99,389,274 |
|
probably benign |
Het |
Krt10 |
ACCG |
ACCGCCG |
11: 99,386,203 |
|
probably benign |
Homo |
Las1l |
TCCTC |
TCCTCTACCTC |
X: 95,940,622 |
|
probably benign |
Het |
Lce1a1 |
C |
T |
3: 92,646,844 |
G108S |
unknown |
Het |
Lkaaear1 |
CCAGCTCCAG |
CCAGCTCCAGCTGCAGCTCCAG |
2: 181,697,594 |
|
probably benign |
Het |
Lrit3 |
CTG |
CTGTTG |
3: 129,788,808 |
|
probably benign |
Het |
Mamld1 |
CAG |
CAGAAG |
X: 71,118,846 |
|
probably benign |
Het |
Mapk7 |
TGCTGGCGCTGGTGCTGGCGCTGG |
TGCTGGCGCTGGCGCTGGTGCTGGCGCTGG |
11: 61,490,206 |
|
probably benign |
Het |
Mast4 |
TTTT |
TTTTATTT |
13: 102,734,857 |
|
probably null |
Het |
Mast4 |
GCA |
GCAGTGTCA |
13: 102,736,317 |
|
probably benign |
Homo |
Med12l |
AGC |
AGCCGC |
3: 59,275,985 |
|
probably benign |
Het |
Mfsd5 |
G |
A |
15: 102,281,161 |
V323I |
probably benign |
Het |
Nacad |
GTC |
GTCAGGATC |
11: 6,599,761 |
|
probably benign |
Het |
Naip1 |
A |
C |
13: 100,423,076 |
M1140R |
probably benign |
Het |
Nbea |
TTTA |
T |
3: 56,009,212 |
|
probably benign |
Homo |
Nefh |
GCCTCACCTGGGGACTTGGCCTC |
GCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,941,038 |
|
probably benign |
Homo |
Nefh |
CTCACCTGGGGACTTGGCCTC |
CTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,941,040 |
|
probably benign |
Homo |
Nefh |
ACTTGGCCTCACCTGGGG |
ACTTGGCCTCACCTGGGGCCTTGGCCTCACCTGGGG |
11: 4,941,033 |
|
probably benign |
Het |
Neu1 |
TCTTCTA |
T |
17: 34,932,558 |
|
probably benign |
Het |
Nutf2 |
G |
T |
8: 105,876,570 |
D78Y |
probably damaging |
Het |
Olfr495 |
A |
G |
7: 108,395,893 |
T258A |
probably benign |
Het |
Olfr495 |
G |
A |
7: 108,395,898 |
M259I |
probably benign |
Het |
Olfr513 |
AT |
ATGATATT |
7: 108,754,954 |
|
probably benign |
Homo |
Olfr635 |
TCC |
TCCC |
7: 103,979,903 |
|
probably null |
Het |
Park2 |
G |
A |
17: 11,854,763 |
V323M |
probably damaging |
Homo |
Pdik1l |
ACCAC |
ACCACCCCCAC |
4: 134,279,512 |
|
probably benign |
Het |
Pik3c2g |
AG |
AGAGGG |
6: 139,635,656 |
|
probably null |
Homo |
Plekhs1 |
TCCAGAC |
TCCAGACCTCCCCCCAGAC |
19: 56,479,858 |
|
probably benign |
Homo |
Prag1 |
C |
CAGT |
8: 36,103,886 |
|
probably benign |
Homo |
Pramef25 |
G |
A |
4: 143,949,742 |
T264M |
probably damaging |
Het |
Raet1d |
A |
G |
10: 22,371,559 |
Q178R |
probably benign |
Het |
Serac1 |
T |
A |
17: 6,070,808 |
K70N |
probably damaging |
Homo |
Serpina3i |
CGG |
CGGTGG |
12: 104,265,164 |
|
probably benign |
Het |
Sfswap |
ACTCAGCCC |
ACTCAGCCCCCTCAGCCC |
5: 129,569,751 |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,621,356 |
|
probably benign |
Het |
Speer4a |
C |
A |
5: 26,036,748 |
E127* |
probably null |
Het |
Sry |
GCTGCTGCTGCTG |
GCTGCTGCTGCTGCTG |
Y: 2,662,824 |
|
probably benign |
Het |
St5 |
CACCACACTGGGGCAGCCCACACTGGGGCAG |
CCCCACACTGGGGCAG |
7: 109,556,921 |
|
probably benign |
Het |
Tbr1 |
A |
C |
2: 61,806,347 |
|
probably benign |
Het |
Tdpoz2 |
T |
TCC |
3: 93,651,615 |
|
probably null |
Homo |
Tdpoz4 |
GAA |
GA |
3: 93,796,880 |
|
probably null |
Het |
Tgoln1 |
AAG |
AAGCCTCAG |
6: 72,616,351 |
|
probably benign |
Homo |
Tmbim7 |
C |
T |
5: 3,670,064 |
R100C |
possibly damaging |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,214,454 |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,214,460 |
|
probably benign |
Het |
Tob1 |
CA |
CAGAA |
11: 94,214,477 |
|
probably benign |
Het |
Tomm5 |
GCATCTTCC |
GCATCTTCCACATCTTCC |
4: 45,107,973 |
|
probably benign |
Het |
Triobp |
TCGG |
TCGGCGG |
15: 78,993,390 |
|
probably benign |
Homo |
Tsen2 |
AGG |
AGGGGG |
6: 115,560,066 |
|
probably benign |
Homo |
Tsen2 |
AGG |
AGGGGG |
6: 115,560,069 |
|
probably benign |
Homo |
Ubtf |
TCC |
TCCCCC |
11: 102,306,950 |
|
probably benign |
Het |
Vmn2r87 |
C |
T |
10: 130,478,714 |
M334I |
probably benign |
Homo |
Zc3h13 |
CGGGATGTGCG |
CGGGATGTGCGGGATGTGCG |
14: 75,323,592 |
|
probably benign |
Homo |
Zfp28 |
G |
A |
7: 6,394,863 |
G766R |
probably damaging |
Het |
Zfp384 |
AAGCCCAGGCCCAGGCCCAGGCCCA |
AAGCCCAGGCCCAAGCCCAGGCCCAGGCCCAGGCCCA |
6: 125,036,463 |
|
probably benign |
Het |
Zfp428 |
G |
A |
7: 24,515,081 |
D41N |
probably damaging |
Homo |
Zfp598 |
CCACAGGC |
CC |
17: 24,679,372 |
|
probably benign |
Het |
Zfp598 |
CCACCA |
CCACCAACACCA |
17: 24,680,783 |
|
probably benign |
Het |
Zfp831 |
TCC |
TCCCCC |
2: 174,645,480 |
|
probably benign |
Het |
Zfp933 |
GCTT |
GCTTTTCTT |
4: 147,825,729 |
|
probably null |
Homo |
Zfp936 |
G |
A |
7: 43,189,489 |
G127R |
possibly damaging |
Het |
|