Incidental Mutation 'IGL01390:Gm10110'
ID |
79170 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gm10110
|
Ensembl Gene |
ENSMUSG00000062093 |
Gene Name |
predicted gene 10110 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.215)
|
Stock # |
IGL01390
|
Quality Score |
|
Status
|
|
Chromosome |
14 |
Chromosomal Location |
90133664-90136883 bp(-) (GRCm39) |
Type of Mutation |
exon |
DNA Base Change (assembly) |
C to A
at 90135677 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081204]
|
AlphaFold |
no structure available at present |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000081204
|
SMART Domains |
Protein: ENSMUSP00000079967 Gene: ENSMUSG00000062093
Domain | Start | End | E-Value | Type |
RRM
|
12 |
85 |
1.47e-21 |
SMART |
RRM
|
100 |
171 |
2.91e-25 |
SMART |
RRM
|
192 |
264 |
1.27e-25 |
SMART |
RRM
|
295 |
366 |
1.92e-25 |
SMART |
low complexity region
|
478 |
493 |
N/A |
INTRINSIC |
low complexity region
|
503 |
516 |
N/A |
INTRINSIC |
PolyA
|
534 |
597 |
4.49e-41 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000228705
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp6v0a1 |
A |
G |
11: 100,934,628 (GRCm39) |
K565R |
probably benign |
Het |
Cacna2d3 |
T |
C |
14: 28,665,548 (GRCm39) |
T158A |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,411,686 (GRCm39) |
D3685G |
probably benign |
Het |
Dock1 |
T |
C |
7: 134,346,776 (GRCm39) |
I236T |
possibly damaging |
Het |
Dock6 |
A |
G |
9: 21,714,341 (GRCm39) |
V1803A |
probably damaging |
Het |
Epb41 |
T |
C |
4: 131,731,048 (GRCm39) |
I178V |
probably benign |
Het |
H2ac6 |
T |
C |
13: 23,867,499 (GRCm39) |
|
probably benign |
Het |
Hoxb7 |
A |
C |
11: 96,177,837 (GRCm39) |
N95T |
probably benign |
Het |
Ikzf2 |
C |
A |
1: 69,609,801 (GRCm39) |
C116F |
probably damaging |
Het |
Ints8 |
A |
T |
4: 11,218,679 (GRCm39) |
|
probably benign |
Het |
Itprid1 |
C |
T |
6: 55,874,983 (GRCm39) |
P311L |
probably benign |
Het |
Man2a1 |
T |
C |
17: 65,017,700 (GRCm39) |
Y649H |
probably benign |
Het |
Mcm8 |
T |
C |
2: 132,679,998 (GRCm39) |
|
probably benign |
Het |
Msi1 |
T |
A |
5: 115,576,780 (GRCm39) |
D137E |
possibly damaging |
Het |
Or8u10 |
T |
C |
2: 85,915,984 (GRCm39) |
I46V |
probably benign |
Het |
Pde6c |
A |
G |
19: 38,150,376 (GRCm39) |
Y507C |
probably benign |
Het |
Prl7d1 |
A |
G |
13: 27,894,149 (GRCm39) |
V140A |
possibly damaging |
Het |
Rb1 |
T |
A |
14: 73,532,439 (GRCm39) |
I132F |
probably benign |
Het |
Rgl1 |
A |
G |
1: 152,447,339 (GRCm39) |
|
probably benign |
Het |
Rpl18a |
G |
T |
8: 71,348,154 (GRCm39) |
|
probably benign |
Het |
Sf3b1 |
T |
C |
1: 55,026,588 (GRCm39) |
I1274V |
probably benign |
Het |
Slc9a3 |
A |
C |
13: 74,298,880 (GRCm39) |
I100L |
probably benign |
Het |
Sorcs3 |
T |
A |
19: 48,778,570 (GRCm39) |
Y996N |
probably damaging |
Het |
Sra1 |
A |
G |
18: 36,803,134 (GRCm39) |
L37P |
probably damaging |
Het |
Stim1 |
A |
G |
7: 102,076,369 (GRCm39) |
Q440R |
possibly damaging |
Het |
Tacc3 |
C |
T |
5: 33,825,405 (GRCm39) |
|
probably benign |
Het |
Tas2r104 |
T |
A |
6: 131,662,448 (GRCm39) |
Y87F |
probably benign |
Het |
Tbl2 |
T |
C |
5: 135,185,217 (GRCm39) |
|
probably benign |
Het |
Vsig10l |
C |
T |
7: 43,115,889 (GRCm39) |
S410F |
probably damaging |
Het |
|
Other mutations in Gm10110 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02308:Gm10110
|
APN |
14 |
90,135,031 (GRCm39) |
exon |
noncoding transcript |
|
IGL02977:Gm10110
|
APN |
14 |
90,134,768 (GRCm39) |
exon |
noncoding transcript |
|
IGL03230:Gm10110
|
APN |
14 |
90,135,733 (GRCm39) |
exon |
noncoding transcript |
|
R0966:Gm10110
|
UTSW |
14 |
90,135,555 (GRCm39) |
exon |
noncoding transcript |
|
R1466:Gm10110
|
UTSW |
14 |
90,135,511 (GRCm39) |
exon |
noncoding transcript |
|
R1466:Gm10110
|
UTSW |
14 |
90,135,511 (GRCm39) |
exon |
noncoding transcript |
|
R1640:Gm10110
|
UTSW |
14 |
90,135,679 (GRCm39) |
exon |
noncoding transcript |
|
R1762:Gm10110
|
UTSW |
14 |
90,134,825 (GRCm39) |
exon |
noncoding transcript |
|
R1839:Gm10110
|
UTSW |
14 |
90,135,272 (GRCm39) |
exon |
noncoding transcript |
|
R2679:Gm10110
|
UTSW |
14 |
90,134,852 (GRCm39) |
exon |
noncoding transcript |
|
R3907:Gm10110
|
UTSW |
14 |
90,135,583 (GRCm39) |
exon |
noncoding transcript |
|
R4512:Gm10110
|
UTSW |
14 |
90,135,151 (GRCm39) |
exon |
noncoding transcript |
|
R4513:Gm10110
|
UTSW |
14 |
90,135,151 (GRCm39) |
exon |
noncoding transcript |
|
R4590:Gm10110
|
UTSW |
14 |
90,134,982 (GRCm39) |
exon |
noncoding transcript |
|
R4877:Gm10110
|
UTSW |
14 |
90,134,785 (GRCm39) |
exon |
noncoding transcript |
|
R5771:Gm10110
|
UTSW |
14 |
90,134,675 (GRCm39) |
exon |
noncoding transcript |
|
R6333:Gm10110
|
UTSW |
14 |
90,135,733 (GRCm39) |
exon |
noncoding transcript |
|
R6341:Gm10110
|
UTSW |
14 |
90,134,144 (GRCm39) |
exon |
noncoding transcript |
|
R8235:Gm10110
|
UTSW |
14 |
90,135,677 (GRCm39) |
missense |
noncoding transcript |
|
R8236:Gm10110
|
UTSW |
14 |
90,135,677 (GRCm39) |
missense |
noncoding transcript |
|
R8237:Gm10110
|
UTSW |
14 |
90,135,677 (GRCm39) |
missense |
noncoding transcript |
|
R8281:Gm10110
|
UTSW |
14 |
90,135,677 (GRCm39) |
missense |
noncoding transcript |
|
R8282:Gm10110
|
UTSW |
14 |
90,135,677 (GRCm39) |
missense |
noncoding transcript |
|
R8283:Gm10110
|
UTSW |
14 |
90,135,677 (GRCm39) |
missense |
noncoding transcript |
|
|
Posted On |
2013-11-05 |