Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
B430218F22Rik |
GGCGGCGGCGGCG |
GGCGGCGGCGGCGGCGGCG |
13: 118,523,385 (GRCm39) |
|
probably benign |
Het |
Bhlhb9 |
C |
T |
X: 134,791,239 (GRCm39) |
L484F |
possibly damaging |
Het |
Bltp1 |
TTAT |
TTATTATTATTATTAGTAT |
3: 37,104,906 (GRCm39) |
|
probably benign |
Het |
Cul1 |
A |
T |
6: 47,494,067 (GRCm39) |
D460V |
probably damaging |
Het |
Cyb5r4 |
CTGCCCAGGGATGTGACAGACACA |
CTGCCCAGGGATGTGACAGACACAATGCCCAGGGATGTGACAGACACA |
9: 86,922,467 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
CT |
CTTCCCAGGGATGTGACAGACACATT |
9: 86,922,491 (GRCm39) |
|
probably benign |
Het |
Dmkn |
GTGGTGGAAGTGGTGG |
GTGGTGGAAGTGGTGGAAGTTGTGGAATTGGTGGAAGTGGTGG |
7: 30,466,616 (GRCm39) |
|
probably benign |
Het |
Dnmt1 |
CACAGTTCCTACCTCGTT |
CACAGTTCCTACCTCGTTTTGGGGGCGGAGAACAGTTCCTACCTCGTT |
9: 20,821,424 (GRCm39) |
|
probably null |
Het |
Dnmt1 |
CTACCTCGTT |
CTACCTCGTTTTGGGGGCGGAGCACAGTTCGTACCTCGTT |
9: 20,821,432 (GRCm39) |
|
probably benign |
Het |
Dnmt1 |
CCTACCTCGTT |
CCTACCTCGTTTTGGAGGCGGAGCACAGTTGCTACCTCGTT |
9: 20,821,431 (GRCm39) |
|
probably null |
Het |
Fam171b |
AGCAGC |
AGCAGCCGCAGC |
2: 83,643,220 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,593 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TTC |
TTCGTC |
X: 74,043,616 (GRCm39) |
|
probably benign |
Het |
Gabre |
CAGGCTCA |
C |
X: 71,313,783 (GRCm39) |
|
probably null |
Het |
Garin5a |
GAGGA |
GAGGAAGGCTGGATCCTGGATACCTGGGGCTGAGGTAGGA |
7: 44,149,957 (GRCm39) |
|
probably null |
Het |
Gm16519 |
AAGCAG |
AAGCAGCAG |
17: 71,236,326 (GRCm39) |
|
probably benign |
Het |
Gm8369 |
GTGT |
GTGTTTGT |
19: 11,489,112 (GRCm39) |
|
probably null |
Het |
Gucy2d |
CTGGG |
CTGGGGGTCGTGGG |
7: 98,108,248 (GRCm39) |
|
probably benign |
Het |
Irag2 |
CACATTG |
CACATTGAGTACATTG |
6: 145,119,511 (GRCm39) |
|
probably benign |
Het |
Ivl |
CTTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
CCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
3: 92,479,607 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
TG |
TGCTCTCG,TGCGG |
5: 25,520,770 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
GCCACA |
GCCACATCCACA |
1: 83,019,851 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CACAGCCACAGCC |
CACAGCCACAGCCGCAACAGCCACAGCC |
1: 83,019,991 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
ACAGCCACCACAGCCACAGCCACCACAGC |
ACAGCCACCACAGCCCCAGCCACCACAGCCACAGCCACCACAGC |
1: 83,019,983 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
CAG |
CAGGAG |
X: 70,162,443 (GRCm39) |
|
probably benign |
Het |
Med12l |
GCA |
GCATCA |
3: 59,183,404 (GRCm39) |
|
probably benign |
Het |
Nefh |
CTCAGCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
CTCAGCTGGGGACTTGGCCTCAGCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,004 (GRCm39) |
|
probably benign |
Het |
Nelfe |
AAGACAGAGACCGGGATCGAGACAGAGAC |
AAGACAGAGACCGGGATCGAGACAGAGACAGAGACCGGGATCGAGACAGAGAC |
17: 35,073,038 (GRCm39) |
|
probably benign |
Het |
Pou3f1 |
GGCGGCAGCGGC |
GGCGGCAGCGGCAGCGGC |
4: 124,551,589 (GRCm39) |
|
probably benign |
Het |
Setd1a |
GGTGGTGGT |
GGTGGTGGTTGTGGTGGT |
7: 127,384,471 (GRCm39) |
|
probably benign |
Het |
Sgo2b |
G |
A |
8: 64,396,203 (GRCm39) |
R18C |
probably damaging |
Het |
Spata31h1 |
AATG |
AATGTCAATG |
10: 82,126,827 (GRCm39) |
|
probably benign |
Het |
Spmap2l |
CGA |
CGAACCTCCCCAGTCCCGCAAGGCCAGTGA |
5: 77,164,250 (GRCm39) |
|
probably benign |
Het |
Stard8 |
GGA |
GGAAGA |
X: 98,110,126 (GRCm39) |
|
probably benign |
Het |
Zscan18 |
GCTGGCTAGGCTCTTCCTGTTGGTTGGGTTGATCCTTCTGGCTAGGCTCTTCCTGTTGTTTGCATTGATCCTTCTGGCTAGGCTCTTCCTGTTGGTTGCATTGATCCTTCTGGCTAGGCTCTTCCTGTTGG |
GCTGGCTAGGCTCTTCCTGTTGTTTGCATTGATCCTTCTGGCTAGGCTCTTCCTGTTGGTTGCATTGATCCTTCTGGCTAGGCTCTTCCTGTTGG |
7: 12,508,352 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Osmr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Osmr
|
APN |
15 |
6,873,926 (GRCm39) |
nonsense |
probably null |
|
IGL00335:Osmr
|
APN |
15 |
6,866,504 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00497:Osmr
|
APN |
15 |
6,876,547 (GRCm39) |
missense |
probably benign |
0.26 |
IGL00510:Osmr
|
APN |
15 |
6,853,112 (GRCm39) |
nonsense |
probably null |
|
IGL00811:Osmr
|
APN |
15 |
6,845,147 (GRCm39) |
missense |
probably benign |
0.28 |
IGL00959:Osmr
|
APN |
15 |
6,854,086 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01115:Osmr
|
APN |
15 |
6,876,682 (GRCm39) |
splice site |
probably benign |
|
IGL01307:Osmr
|
APN |
15 |
6,873,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01330:Osmr
|
APN |
15 |
6,871,509 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Osmr
|
APN |
15 |
6,854,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01780:Osmr
|
APN |
15 |
6,858,144 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02164:Osmr
|
APN |
15 |
6,871,529 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02207:Osmr
|
APN |
15 |
6,876,628 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02338:Osmr
|
APN |
15 |
6,867,210 (GRCm39) |
nonsense |
probably null |
|
IGL02350:Osmr
|
APN |
15 |
6,858,144 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02357:Osmr
|
APN |
15 |
6,858,144 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02545:Osmr
|
APN |
15 |
6,853,060 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02619:Osmr
|
APN |
15 |
6,871,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02685:Osmr
|
APN |
15 |
6,845,054 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02959:Osmr
|
APN |
15 |
6,845,378 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03303:Osmr
|
APN |
15 |
6,872,289 (GRCm39) |
missense |
probably benign |
0.03 |
FR4548:Osmr
|
UTSW |
15 |
6,867,184 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Osmr
|
UTSW |
15 |
6,867,187 (GRCm39) |
nonsense |
probably null |
|
R0149:Osmr
|
UTSW |
15 |
6,871,432 (GRCm39) |
critical splice donor site |
probably null |
|
R0361:Osmr
|
UTSW |
15 |
6,871,432 (GRCm39) |
critical splice donor site |
probably null |
|
R0492:Osmr
|
UTSW |
15 |
6,853,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Osmr
|
UTSW |
15 |
6,871,419 (GRCm39) |
splice site |
probably benign |
|
R0585:Osmr
|
UTSW |
15 |
6,867,274 (GRCm39) |
missense |
probably benign |
|
R0980:Osmr
|
UTSW |
15 |
6,881,921 (GRCm39) |
missense |
probably benign |
0.00 |
R1221:Osmr
|
UTSW |
15 |
6,853,042 (GRCm39) |
nonsense |
probably null |
|
R1922:Osmr
|
UTSW |
15 |
6,873,848 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2067:Osmr
|
UTSW |
15 |
6,844,896 (GRCm39) |
missense |
probably benign |
0.00 |
R2136:Osmr
|
UTSW |
15 |
6,881,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Osmr
|
UTSW |
15 |
6,873,891 (GRCm39) |
missense |
probably benign |
0.04 |
R3683:Osmr
|
UTSW |
15 |
6,866,534 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3735:Osmr
|
UTSW |
15 |
6,851,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R3736:Osmr
|
UTSW |
15 |
6,851,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R4011:Osmr
|
UTSW |
15 |
6,854,014 (GRCm39) |
missense |
probably benign |
0.01 |
R4175:Osmr
|
UTSW |
15 |
6,882,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4555:Osmr
|
UTSW |
15 |
6,845,201 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4581:Osmr
|
UTSW |
15 |
6,872,375 (GRCm39) |
missense |
probably benign |
0.00 |
R4751:Osmr
|
UTSW |
15 |
6,872,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Osmr
|
UTSW |
15 |
6,882,036 (GRCm39) |
missense |
probably benign |
0.23 |
R4986:Osmr
|
UTSW |
15 |
6,846,061 (GRCm39) |
critical splice donor site |
probably null |
|
R4997:Osmr
|
UTSW |
15 |
6,845,120 (GRCm39) |
missense |
probably benign |
0.25 |
R5077:Osmr
|
UTSW |
15 |
6,873,874 (GRCm39) |
nonsense |
probably null |
|
R5093:Osmr
|
UTSW |
15 |
6,850,560 (GRCm39) |
missense |
probably damaging |
0.96 |
R5120:Osmr
|
UTSW |
15 |
6,856,756 (GRCm39) |
missense |
probably benign |
0.16 |
R5331:Osmr
|
UTSW |
15 |
6,872,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R5812:Osmr
|
UTSW |
15 |
6,866,540 (GRCm39) |
missense |
probably damaging |
0.99 |
R5819:Osmr
|
UTSW |
15 |
6,845,268 (GRCm39) |
missense |
probably benign |
0.00 |
R5876:Osmr
|
UTSW |
15 |
6,850,528 (GRCm39) |
missense |
probably benign |
0.07 |
R5986:Osmr
|
UTSW |
15 |
6,873,934 (GRCm39) |
missense |
probably benign |
0.36 |
R6018:Osmr
|
UTSW |
15 |
6,845,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Osmr
|
UTSW |
15 |
6,889,833 (GRCm39) |
missense |
probably benign |
0.00 |
R6217:Osmr
|
UTSW |
15 |
6,853,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R6312:Osmr
|
UTSW |
15 |
6,853,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Osmr
|
UTSW |
15 |
6,850,544 (GRCm39) |
missense |
probably benign |
0.00 |
R6898:Osmr
|
UTSW |
15 |
6,845,364 (GRCm39) |
missense |
probably damaging |
0.97 |
R7139:Osmr
|
UTSW |
15 |
6,850,569 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7412:Osmr
|
UTSW |
15 |
6,853,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Osmr
|
UTSW |
15 |
6,856,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7630:Osmr
|
UTSW |
15 |
6,846,452 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7730:Osmr
|
UTSW |
15 |
6,853,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7990:Osmr
|
UTSW |
15 |
6,881,948 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8094:Osmr
|
UTSW |
15 |
6,845,102 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8187:Osmr
|
UTSW |
15 |
6,850,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Osmr
|
UTSW |
15 |
6,844,897 (GRCm39) |
missense |
probably benign |
0.41 |
R8366:Osmr
|
UTSW |
15 |
6,850,435 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9051:Osmr
|
UTSW |
15 |
6,882,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9137:Osmr
|
UTSW |
15 |
6,856,709 (GRCm39) |
missense |
probably benign |
0.13 |
R9182:Osmr
|
UTSW |
15 |
6,850,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Osmr
|
UTSW |
15 |
6,846,086 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9260:Osmr
|
UTSW |
15 |
6,882,033 (GRCm39) |
missense |
probably benign |
|
R9559:Osmr
|
UTSW |
15 |
6,882,027 (GRCm39) |
missense |
probably damaging |
1.00 |
RF040:Osmr
|
UTSW |
15 |
6,867,182 (GRCm39) |
small insertion |
probably benign |
|
|