Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI837181 |
GCG |
GCGCCG |
19: 5,475,246 (GRCm39) |
|
probably benign |
Het |
Blm |
CTCCTCCTCCTCCTCCTCCTCCTC |
CTCCTCCTCCTCTTCCTCCTCCTCCTCCTCCTCCTC |
7: 80,162,654 (GRCm39) |
|
probably benign |
Het |
Blm |
CCTCCTCCTCC |
CCTCCTCCTCCTGCTCCTCCTCC |
7: 80,162,671 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
GGGA |
GGGATGTGACAGACACACTGCCCATGGA |
9: 86,922,498 (GRCm39) |
|
probably benign |
Het |
Dcdc2b |
GCTGC |
GCTGCCAGGACTGC |
4: 129,503,444 (GRCm39) |
|
probably benign |
Het |
Dclre1a |
CTTTGCT |
C |
19: 56,532,564 (GRCm39) |
|
probably benign |
Het |
Dctn6 |
AAATCATGGCTTGCGATCT |
A |
8: 34,572,236 (GRCm39) |
|
probably null |
Het |
Elovl5 |
G |
T |
9: 77,888,755 (GRCm39) |
|
probably null |
Het |
Ermn |
AACT |
AACTACT |
2: 57,938,078 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
G |
GCGTGTGCTGGTC |
5: 110,526,017 (GRCm39) |
|
probably benign |
Het |
Fgd6 |
ATT |
A |
10: 93,880,187 (GRCm39) |
|
probably null |
Het |
Flywch1 |
TCACTCACCCACTCCTGGTGT |
TCACTCACCCACTCCTGGTGTGGGGAGGCTACGCACTCACCCACTCCTGGTGT |
17: 23,981,132 (GRCm39) |
|
probably null |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,602 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TTC |
TTCATC |
X: 74,043,607 (GRCm39) |
|
probably benign |
Het |
Gab3 |
CTT |
CTTATT |
X: 74,043,603 (GRCm39) |
|
probably null |
Het |
Gm11060 |
CTGTGTG |
CTG |
2: 104,922,385 (GRCm39) |
|
probably null |
Het |
Gm5475 |
GGTGGAAGGAAAG |
GG |
15: 100,325,029 (GRCm39) |
|
probably null |
Het |
Heatr3 |
TAT |
TATTAAT |
8: 88,883,085 (GRCm39) |
|
probably benign |
Het |
Ivl |
GCTGCTGCTGCTGC |
G |
3: 92,479,625 (GRCm39) |
|
probably null |
Het |
Kif12 |
GGC |
GGCCTCCACCCGGCGTGC |
4: 63,089,662 (GRCm39) |
|
probably benign |
Het |
L1td1 |
AGGAGGAGGAGGAGGAGGAGGAGGGGGAGGAGGAG |
AGGAGGAGGAG |
4: 98,625,026 (GRCm39) |
|
probably benign |
Het |
Lca5l |
CCCTGGCCCCGGCC |
CCC |
16: 95,960,504 (GRCm39) |
|
probably null |
Het |
Loricrin |
ATAGCCG |
A |
3: 91,989,183 (GRCm39) |
|
probably benign |
Het |
Mapk7 |
GGGGCA |
GGGGCACGGGCA |
11: 61,381,060 (GRCm39) |
|
probably benign |
Het |
Nf2 |
AAAAG |
A |
11: 4,779,936 (GRCm39) |
|
probably null |
Het |
Nlrp3 |
GGGTA |
G |
11: 59,449,378 (GRCm39) |
|
probably null |
Het |
Nolc1 |
CAGCAGC |
CAGCAGCAGGAGCAGC |
19: 46,069,810 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
TTTT |
TTTTGTTTTTGATTT |
4: 134,006,685 (GRCm39) |
|
probably null |
Het |
Phldb3 |
CGCCCCCG |
C |
7: 24,325,918 (GRCm39) |
|
probably null |
Het |
Setd1a |
GGTGGTAGT |
GGTGGTAGTAGTGGTAGT |
7: 127,384,483 (GRCm39) |
|
probably benign |
Het |
Spmap2l |
CCCCAGTCCCGCAAGGCCAG |
CCCCAGTCCCGCAAGGCCAGCGATCCTACCCAGTCCCGCAAGGCCAG |
5: 77,164,257 (GRCm39) |
|
probably benign |
Het |
Strn |
CTTACCCCAGTC |
CTTACCCCAGTCCGTGCTCCCTTACCCCAGTCCGTGATCCATTACCCCAGTC |
17: 78,984,706 (GRCm39) |
|
probably null |
Het |
Tcof1 |
TTCCCAGAGATCCCCTTGGC |
TTCCCAGAGATCCCCTTGGCTGCTGAGATGGGCACTATCCCAGAGATCCCCTTGGC |
18: 60,966,637 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
AGC |
AGCGGC |
18: 60,968,817 (GRCm39) |
|
probably benign |
Het |
Tedc2 |
AGGAACCCT |
AGGAACCCTGGAACCCT |
17: 24,435,213 (GRCm39) |
|
probably benign |
Het |
Tmem59 |
T |
TGTTTGTTG |
4: 107,047,729 (GRCm39) |
|
probably benign |
Het |
Zfhx3 |
C |
CCGCAGCAAA |
8: 109,682,730 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
TCGTCGTC |
TCGTCGTCGTC |
2: 164,749,383 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Iqcf4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Iqcf4
|
APN |
9 |
106,447,832 (GRCm39) |
missense |
probably benign |
0.12 |
R0781:Iqcf4
|
UTSW |
9 |
106,445,860 (GRCm39) |
missense |
probably benign |
0.06 |
R1764:Iqcf4
|
UTSW |
9 |
106,445,893 (GRCm39) |
missense |
probably benign |
0.12 |
R4525:Iqcf4
|
UTSW |
9 |
106,447,827 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4703:Iqcf4
|
UTSW |
9 |
106,445,519 (GRCm39) |
splice site |
probably null |
|
R5823:Iqcf4
|
UTSW |
9 |
106,445,800 (GRCm39) |
missense |
probably benign |
0.00 |
R6298:Iqcf4
|
UTSW |
9 |
106,445,874 (GRCm39) |
missense |
probably benign |
0.25 |
R7773:Iqcf4
|
UTSW |
9 |
106,445,812 (GRCm39) |
missense |
probably benign |
0.08 |
R7780:Iqcf4
|
UTSW |
9 |
106,445,860 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7818:Iqcf4
|
UTSW |
9 |
106,447,738 (GRCm39) |
nonsense |
probably null |
|
R8694:Iqcf4
|
UTSW |
9 |
106,448,111 (GRCm39) |
start gained |
probably benign |
|
R9435:Iqcf4
|
UTSW |
9 |
106,445,652 (GRCm39) |
missense |
possibly damaging |
0.95 |
RF003:Iqcf4
|
UTSW |
9 |
106,447,806 (GRCm39) |
small insertion |
probably benign |
|
RF007:Iqcf4
|
UTSW |
9 |
106,447,808 (GRCm39) |
small insertion |
probably benign |
|
RF016:Iqcf4
|
UTSW |
9 |
106,447,808 (GRCm39) |
small insertion |
probably benign |
|
RF028:Iqcf4
|
UTSW |
9 |
106,447,813 (GRCm39) |
small insertion |
probably benign |
|
RF036:Iqcf4
|
UTSW |
9 |
106,447,810 (GRCm39) |
small insertion |
probably benign |
|
RF041:Iqcf4
|
UTSW |
9 |
106,447,812 (GRCm39) |
nonsense |
probably null |
|
RF042:Iqcf4
|
UTSW |
9 |
106,447,804 (GRCm39) |
small insertion |
probably benign |
|
RF043:Iqcf4
|
UTSW |
9 |
106,447,812 (GRCm39) |
small insertion |
probably benign |
|
RF045:Iqcf4
|
UTSW |
9 |
106,447,809 (GRCm39) |
small insertion |
probably benign |
|
RF046:Iqcf4
|
UTSW |
9 |
106,447,809 (GRCm39) |
small insertion |
probably benign |
|
RF047:Iqcf4
|
UTSW |
9 |
106,447,811 (GRCm39) |
small insertion |
probably benign |
|
RF063:Iqcf4
|
UTSW |
9 |
106,447,816 (GRCm39) |
small insertion |
probably benign |
|
|