Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap3 |
GCATCCTGGGCTGCT |
GCATCCTGGGCTGCTACATCCTGGGCTGCT |
4: 155,989,549 (GRCm39) |
|
probably benign |
Het |
Alpk3 |
GAGAAGGCAC |
G |
7: 80,742,162 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
T |
TTATTATGATTATTAC |
3: 37,104,909 (GRCm39) |
|
probably benign |
Het |
Cox7a2l |
GGA |
GGATGGGGA |
17: 83,810,151 (GRCm39) |
|
probably benign |
Het |
Cpne1 |
TCCAC |
TC |
2: 155,915,430 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
CCCAGGGATGTGACAGACACACTG |
CCCAGGGATGTGACAGACACACTGACCAGGGATGTGACAGACACACTG |
9: 86,922,470 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
GA |
GATGTGACAGACACACTGCCCAGGTA |
9: 86,922,500 (GRCm39) |
|
probably null |
Het |
Defb22 |
TGCGGCA |
TGCGGCAGGGCTGGCCTTTGCGGCA |
2: 152,327,752 (GRCm39) |
|
probably benign |
Het |
Dnmt1 |
GGGCGGAGCACAGTTCCTACCTCGTT |
GGGCGGAGCACAGTTCCTACCTCGTTTTGGTGGCGGAGCACAGTTCCTACCTCGTT |
9: 20,821,416 (GRCm39) |
|
probably null |
Het |
Fbrsl1 |
GTG |
GTGCGTGTGCTGTTG |
5: 110,526,015 (GRCm39) |
|
probably benign |
Het |
Frem3 |
GATC |
GATCATC |
8: 81,341,867 (GRCm39) |
|
probably benign |
Het |
Gabre |
GCTC |
GCTCTGTCTC |
X: 71,314,368 (GRCm39) |
|
probably benign |
Het |
Garin5a |
GGGTCTGAGGGAGGA |
GGGTCTGAGGGAGGAAGGCTGGATCCTGGATACCTAGGTCTGAGGGAGGA |
7: 44,149,947 (GRCm39) |
|
probably null |
Het |
Gm15155 |
CAA |
CAACAACAAA |
X: 155,128,636 (GRCm39) |
|
probably null |
Het |
Igf1r |
GGAGATGGAGC |
GGAGATGGAGCTAGAGATGGAGC |
7: 67,875,924 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CACCACAGC |
CACCACAGCCACAGCGACCACAGC |
1: 83,020,003 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
AGC |
AGCGGC |
X: 70,162,441 (GRCm39) |
|
probably benign |
Het |
Map1a |
CCAGCTCCAGCTCCA |
CCAGCTCCAGCTCCAGCTACAGCTCCAGATACAGCTCCAGCTCCA |
2: 121,136,785 (GRCm39) |
|
probably benign |
Het |
Map1a |
GCTCCAGCTCCA |
GCTCCAGCTCCAGCTCCAGCTCCAGCTCCATCTCCAGCTCCA |
2: 121,136,788 (GRCm39) |
|
probably benign |
Het |
Neu1 |
TCTTCTA |
T |
17: 35,151,534 (GRCm39) |
|
probably benign |
Het |
Nolc1 |
CAGCAGC |
CAGCAGCAGAAGCAGC |
19: 46,069,810 (GRCm39) |
|
probably benign |
Het |
Or7g32 |
G |
T |
9: 19,388,928 (GRCm39) |
A206E |
possibly damaging |
Het |
Pdik1l |
TTTT |
TTTTGTTTTTGGTTT |
4: 134,006,685 (GRCm39) |
|
probably null |
Het |
Rassf6 |
CACTCATGGTCCTGTAGAGCAATGGGGATTC |
CACTCATGGTCCTGTAGAGCAATGGGGATTCTGCCTGACTCATGGTCCTGTAGAGCAATGGGGATTC |
5: 90,756,771 (GRCm39) |
|
probably benign |
Het |
Rassf6 |
CTGTAGAGCAATGGGGATTC |
CTGTAGAGCAATGGGGATTCTGCCTCACTCATGGTCATGTAGAGCAATGGGGATTC |
5: 90,756,782 (GRCm39) |
|
probably benign |
Het |
Rassf6 |
ATGGTCCTGTAGAGCAATGGGGATTC |
ATGGTCCTGTAGAGCAATGGGGATTCTGCCTCACTCGTGGTCCTGTAGAGCAATGGGGATTC |
5: 90,756,776 (GRCm39) |
|
probably benign |
Het |
Rpgrip1 |
AGAGGAGGA |
AGA |
14: 52,386,983 (GRCm39) |
|
probably benign |
Het |
Rprd2 |
AGAGCCTGTGGTGCTCGCAGGGGAGGCTGTGGTGCTC |
AGAGGCTGTGGTGCTC |
3: 95,673,632 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
CG |
CGAGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Rtbdn |
GCGGC |
GCGGCATCGGC |
8: 85,682,804 (GRCm39) |
|
probably benign |
Het |
Smarca2 |
CA |
CACCAAGA |
19: 26,608,411 (GRCm39) |
|
probably benign |
Het |
Tfeb |
GCA |
GCACCA |
17: 48,097,022 (GRCm39) |
|
probably benign |
Het |
Tfeb |
CAG |
CAGTAG |
17: 48,097,023 (GRCm39) |
|
probably null |
Het |
Tmed6 |
AGC |
AGCTGGC |
8: 107,788,228 (GRCm39) |
|
probably null |
Het |
Tomm5 |
TCTTCCGC |
TCTTCCGCAGCTTCCGC |
4: 45,107,976 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
TG |
TGATGCTGCTGCTGCGG |
15: 72,673,147 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in A030005L19Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
RF001:A030005L19Rik
|
UTSW |
1 |
82,891,311 (GRCm39) |
small insertion |
probably benign |
|
RF005:A030005L19Rik
|
UTSW |
1 |
82,891,306 (GRCm39) |
small insertion |
probably benign |
|
RF011:A030005L19Rik
|
UTSW |
1 |
82,891,307 (GRCm39) |
small insertion |
probably benign |
|
RF011:A030005L19Rik
|
UTSW |
1 |
82,891,294 (GRCm39) |
small insertion |
probably benign |
|
RF011:A030005L19Rik
|
UTSW |
1 |
82,891,290 (GRCm39) |
small insertion |
probably benign |
|
RF016:A030005L19Rik
|
UTSW |
1 |
82,891,298 (GRCm39) |
small insertion |
probably benign |
|
RF018:A030005L19Rik
|
UTSW |
1 |
82,891,293 (GRCm39) |
small insertion |
probably benign |
|
RF021:A030005L19Rik
|
UTSW |
1 |
82,891,290 (GRCm39) |
small insertion |
probably benign |
|
RF023:A030005L19Rik
|
UTSW |
1 |
82,891,117 (GRCm39) |
small deletion |
probably benign |
|
RF028:A030005L19Rik
|
UTSW |
1 |
82,891,301 (GRCm39) |
small insertion |
probably benign |
|
RF028:A030005L19Rik
|
UTSW |
1 |
82,891,299 (GRCm39) |
small insertion |
probably benign |
|
RF035:A030005L19Rik
|
UTSW |
1 |
82,891,310 (GRCm39) |
small insertion |
probably benign |
|
RF038:A030005L19Rik
|
UTSW |
1 |
82,891,301 (GRCm39) |
small insertion |
probably benign |
|
RF040:A030005L19Rik
|
UTSW |
1 |
82,891,311 (GRCm39) |
small insertion |
probably benign |
|
RF040:A030005L19Rik
|
UTSW |
1 |
82,891,298 (GRCm39) |
small insertion |
probably benign |
|
RF042:A030005L19Rik
|
UTSW |
1 |
82,891,305 (GRCm39) |
small insertion |
probably benign |
|
RF044:A030005L19Rik
|
UTSW |
1 |
82,891,310 (GRCm39) |
small insertion |
probably benign |
|
RF053:A030005L19Rik
|
UTSW |
1 |
82,891,294 (GRCm39) |
small insertion |
probably benign |
|
RF059:A030005L19Rik
|
UTSW |
1 |
82,891,300 (GRCm39) |
small insertion |
probably benign |
|
RF060:A030005L19Rik
|
UTSW |
1 |
82,891,308 (GRCm39) |
small insertion |
probably benign |
|
RF060:A030005L19Rik
|
UTSW |
1 |
82,891,300 (GRCm39) |
nonsense |
probably null |
|
RF060:A030005L19Rik
|
UTSW |
1 |
82,891,117 (GRCm39) |
small deletion |
probably benign |
|
|