Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI837181 |
GGC |
GGCTGC |
19: 5,475,254 (GRCm39) |
|
probably benign |
Het |
AI837181 |
GGC |
GGCCGC |
19: 5,475,263 (GRCm39) |
|
probably benign |
Het |
Amfr |
GCC |
GCCGGCGCGAGCTCC |
8: 94,738,920 (GRCm39) |
|
probably benign |
Het |
Ankhd1 |
GCGGCG |
GCGGCGCCGGCG |
18: 36,693,966 (GRCm39) |
|
probably benign |
Het |
Ankhd1 |
GGCGGCAGC |
GGCGGCAGCGGCAGC |
18: 36,693,980 (GRCm39) |
|
probably benign |
Het |
AY761185 |
GGGCACTGTGG |
GGG |
8: 21,433,916 (GRCm39) |
|
probably null |
Het |
B430218F22Rik |
GG |
GGTCGGCG |
13: 118,523,384 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
CTGTGGCTGTGGCTGTGGCTGTGG |
CTGTGGCTGTGGATGTGGCTGTGGCTGTGGCTGTGG |
19: 47,129,692 (GRCm39) |
|
probably benign |
Het |
Cox7a2l |
GGA |
GGATAGGGA |
17: 83,810,151 (GRCm39) |
|
probably benign |
Het |
Cul9 |
CCTC |
CCTCCTC |
17: 46,811,795 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
ACACACTGCCCAGGGATGTGACAGACACACTGCCCAGGGA |
ACACACTGCCCAGGGATGTGACAGCCACACTGCCCAGGGATGTGACAGACACACTGCCCAGGGA |
9: 86,922,462 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
TGCCCAGGGATGTGACAGACACAC |
TGCCCAGGGATGTGACAGACACACGGCCCAGGGATGTGACAGACACAC |
9: 86,922,468 (GRCm39) |
|
probably benign |
Het |
Dmkn |
GTG |
GTGTTGGAAGTGGTGGAAGTGGTGGAAATG |
7: 30,466,607 (GRCm39) |
|
probably benign |
Het |
Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 72,684,217 (GRCm39) |
|
probably benign |
Het |
Eed |
C |
A |
7: 89,604,240 (GRCm39) |
A411S |
probably benign |
Het |
Fer1l4 |
GGTC |
G |
2: 155,887,449 (GRCm39) |
|
probably benign |
Het |
Frem3 |
GATC |
GATCATC |
8: 81,341,867 (GRCm39) |
|
probably benign |
Het |
Gab3 |
CTTTT |
CT |
X: 74,043,583 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,632 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TTC |
TTCGTC |
X: 74,043,631 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTCCT |
X: 74,043,614 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,611 (GRCm39) |
|
probably benign |
Het |
Gm5475 |
GAAAGGTGGAAGGAAA |
GAA |
15: 100,325,037 (GRCm39) |
|
probably null |
Het |
Gm572 |
TGGGGGGGGGGGG |
TGGGGG |
4: 148,755,850 (GRCm39) |
|
probably null |
Het |
Gucy1b2 |
CACACACACACACACACTTAC |
CAC |
14: 62,646,090 (GRCm39) |
|
probably benign |
Het |
Gucy2d |
C |
CTGGGGCCTG |
7: 98,108,241 (GRCm39) |
|
probably benign |
Het |
Hsdl2 |
CCACAGCTGCAG |
CCACAGCTGCAGCAGCAGACACAGCTGCAG |
4: 59,610,647 (GRCm39) |
|
probably benign |
Het |
Idh2 |
GGTCCCAG |
GG |
7: 79,748,077 (GRCm39) |
|
probably benign |
Het |
Il2 |
GG |
GGGCTTGAAGTGTG |
3: 37,179,991 (GRCm39) |
|
probably benign |
Het |
Il2 |
GTGG |
GTGGGGCTTGAACTGG |
3: 37,179,976 (GRCm39) |
|
probably benign |
Het |
Irag2 |
ATTG |
ATTGAGCACGTTG |
6: 145,119,514 (GRCm39) |
|
probably benign |
Het |
Irag2 |
TG |
TGAGCACATGG |
6: 145,119,516 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CTCCTC |
CTCCTCTTCCTC |
7: 30,285,802 (GRCm39) |
|
probably benign |
Het |
Lce1m |
C |
CGGCTGCTGCCAA |
3: 92,925,448 (GRCm39) |
|
probably benign |
Het |
Lce1m |
GCTGCCAC |
GCTGCCACAGCAACTTCTGCCAC |
3: 92,925,651 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
CAG |
CAGTAG |
X: 70,162,434 (GRCm39) |
|
probably null |
Het |
Map1a |
CAGCTCCA |
CAGCTCCAGCTCCAGCTCCAGCTCCAGCTCTAGCTCCA |
2: 121,136,792 (GRCm39) |
|
probably benign |
Het |
Map1a |
CA |
CAGCTCCAGCTCCAGCTCCAGCTCCAGCTCAA |
2: 121,136,798 (GRCm39) |
|
probably benign |
Het |
Med12l |
GCA |
GCATCA |
3: 59,183,410 (GRCm39) |
|
probably benign |
Het |
Morn4 |
GCAGTGAG |
GCAGTGAGTCAGTCAGTGAG |
19: 42,064,550 (GRCm39) |
|
probably null |
Het |
Pdik1l |
C |
CCACCAA |
4: 134,006,827 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
TTTTTTT |
TTTTTTTTTGTTTTTT |
15: 44,421,898 (GRCm39) |
|
probably benign |
Het |
Rfx4 |
TCTCTCTCTCTCTCT |
TCTCTCTCTCTCTCTCCCTCTCTCTCTCTCT |
10: 84,694,344 (GRCm39) |
|
probably benign |
Het |
Setd1a |
TGGTGGTGG |
TGGTGGTGGGGGTGGTGG |
7: 127,384,473 (GRCm39) |
|
probably benign |
Het |
Setd1a |
GGTGGTAGT |
GGTGGTAGTTGTGGTAGT |
7: 127,384,483 (GRCm39) |
|
probably benign |
Het |
Six5 |
CGGA |
C |
7: 18,828,725 (GRCm39) |
|
probably benign |
Het |
Spmap2l |
AGCGATCCTCCCCAGTCCCGCAAGGCC |
AGCGATCCTCCCCTGTCCCGCAAGGCCGGCGATCCTCCCCAGTCCCGCAAGGCC |
5: 77,164,248 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
CTGCTGCTGC |
CTGCTGCTGCTGC |
18: 60,968,795 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
CCAGA |
CCAGACATCCCCTTGGCTGCTGAGCTGGGCACTTTCTCAGA |
18: 60,966,640 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
ATCCCCTTGGC |
ATCCCCTTGGCTGCTGAGATGGGCACTTTCCCAGAGGTCCCCTTGGC |
18: 60,966,646 (GRCm39) |
|
probably benign |
Het |
Tfeb |
CAG |
CAGAAG |
17: 48,097,038 (GRCm39) |
|
probably benign |
Het |
Tfeb |
AGC |
AGCCGC |
17: 48,097,036 (GRCm39) |
|
probably benign |
Het |
Tfeb |
GCA |
GCACCA |
17: 48,097,037 (GRCm39) |
|
probably benign |
Het |
Tgoln1 |
TGGGCTTG |
TGGGCTTGTCAGAATCACCTCCTGCGGGCTTG |
6: 72,593,019 (GRCm39) |
|
probably benign |
Het |
Tgoln1 |
GCTTGCCAGAAT |
GCTTGCCAGAATCACCTCCCGTGGTCTTGCCAGAAT |
6: 72,593,046 (GRCm39) |
|
probably benign |
Het |
Tomm5 |
GCATCTTCC |
GCATCTTCCACATCTTCC |
4: 45,107,973 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
TGCTGCT |
TGCTGCTGCTGCTGCGGCTGCT |
15: 72,673,174 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
GGA |
GGACGA |
6: 115,537,028 (GRCm39) |
|
probably benign |
Het |
Zfp384 |
GCCCAGGCCCAG |
GCCCAGGCCCAGTCCCAGGCCCAG |
6: 125,013,446 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Wdr97 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6006:Wdr97
|
UTSW |
15 |
76,241,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Wdr97
|
UTSW |
15 |
76,239,895 (GRCm39) |
nonsense |
probably null |
|
R6464:Wdr97
|
UTSW |
15 |
76,246,977 (GRCm39) |
missense |
probably benign |
0.01 |
R6544:Wdr97
|
UTSW |
15 |
76,242,478 (GRCm39) |
missense |
probably benign |
0.00 |
R6545:Wdr97
|
UTSW |
15 |
76,247,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Wdr97
|
UTSW |
15 |
76,239,178 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6803:Wdr97
|
UTSW |
15 |
76,240,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Wdr97
|
UTSW |
15 |
76,241,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Wdr97
|
UTSW |
15 |
76,241,949 (GRCm39) |
nonsense |
probably null |
|
R7793:Wdr97
|
UTSW |
15 |
76,243,307 (GRCm39) |
missense |
|
|
R7985:Wdr97
|
UTSW |
15 |
76,245,687 (GRCm39) |
missense |
|
|
R8008:Wdr97
|
UTSW |
15 |
76,244,832 (GRCm39) |
missense |
|
|
R8170:Wdr97
|
UTSW |
15 |
76,247,819 (GRCm39) |
missense |
|
|
R8171:Wdr97
|
UTSW |
15 |
76,247,819 (GRCm39) |
missense |
|
|
R8267:Wdr97
|
UTSW |
15 |
76,240,794 (GRCm39) |
missense |
|
|
R8337:Wdr97
|
UTSW |
15 |
76,245,684 (GRCm39) |
missense |
|
|
R8478:Wdr97
|
UTSW |
15 |
76,247,629 (GRCm39) |
splice site |
probably null |
|
R8735:Wdr97
|
UTSW |
15 |
76,240,775 (GRCm39) |
missense |
|
|
R8958:Wdr97
|
UTSW |
15 |
76,245,694 (GRCm39) |
missense |
|
|
R9385:Wdr97
|
UTSW |
15 |
76,240,367 (GRCm39) |
missense |
|
|
R9440:Wdr97
|
UTSW |
15 |
76,245,064 (GRCm39) |
missense |
|
|
R9657:Wdr97
|
UTSW |
15 |
76,245,476 (GRCm39) |
missense |
|
|
R9672:Wdr97
|
UTSW |
15 |
76,240,377 (GRCm39) |
missense |
|
|
R9778:Wdr97
|
UTSW |
15 |
76,241,125 (GRCm39) |
missense |
|
|
RF004:Wdr97
|
UTSW |
15 |
76,247,373 (GRCm39) |
frame shift |
probably null |
|
RF009:Wdr97
|
UTSW |
15 |
76,247,367 (GRCm39) |
frame shift |
probably null |
|
RF016:Wdr97
|
UTSW |
15 |
76,240,172 (GRCm39) |
missense |
|
|
Z1177:Wdr97
|
UTSW |
15 |
76,247,330 (GRCm39) |
missense |
|
|
Z1177:Wdr97
|
UTSW |
15 |
76,239,130 (GRCm39) |
missense |
|
|
|