Incidental Mutation 'IGL02287:Gm1818'
| ID |
289996 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Gm1818
|
| Ensembl Gene |
ENSMUSG00000091277 |
| Gene Name |
predicted gene 1818 |
| Synonyms |
LOC217536 |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.899)
|
| Stock # |
IGL02287
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
12 |
| Chromosomal Location |
48602091-48606668 bp(-) (GRCm39) |
| Type of Mutation |
exon |
| DNA Base Change (assembly) |
A to T
at 48602505 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000169406
|
| SMART Domains |
Protein: ENSMUSP00000131939
Gene: ENSMUSG00000091277
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
1 |
22 |
N/A |
INTRINSIC |
|
Pfam:RrnaAD
|
78 |
377 |
4.3e-23 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 8 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2810021J22Rik |
A |
G |
11: 58,771,418 (GRCm39) |
D300G |
probably benign |
Het |
| Dot1l |
A |
G |
10: 80,600,443 (GRCm39) |
H30R |
possibly damaging |
Het |
| Isca2 |
G |
T |
12: 84,820,114 (GRCm39) |
V14F |
probably benign |
Het |
| Or4a80 |
A |
T |
2: 89,582,958 (GRCm39) |
Y71* |
probably null |
Het |
| Ppp4r4 |
A |
T |
12: 103,553,747 (GRCm39) |
T402S |
probably benign |
Het |
| Slc25a13 |
T |
C |
6: 6,216,992 (GRCm39) |
|
probably benign |
Het |
| Trrap |
T |
C |
5: 144,769,348 (GRCm39) |
W2618R |
probably damaging |
Het |
| Uba7 |
A |
G |
9: 107,855,426 (GRCm39) |
M368V |
probably benign |
Het |
|
| Other mutations in Gm1818 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01456:Gm1818
|
APN |
12 |
48,602,583 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01472:Gm1818
|
APN |
12 |
48,603,072 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01634:Gm1818
|
APN |
12 |
48,602,992 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01874:Gm1818
|
APN |
12 |
48,602,973 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL02805:Gm1818
|
APN |
12 |
48,602,518 (GRCm39) |
exon |
noncoding transcript |
|
|
R1174:Gm1818
|
UTSW |
12 |
48,602,982 (GRCm39) |
exon |
noncoding transcript |
|
|
R1175:Gm1818
|
UTSW |
12 |
48,602,982 (GRCm39) |
exon |
noncoding transcript |
|
|
R1636:Gm1818
|
UTSW |
12 |
48,602,550 (GRCm39) |
exon |
noncoding transcript |
|
|
R4797:Gm1818
|
UTSW |
12 |
48,602,393 (GRCm39) |
exon |
noncoding transcript |
|
|
R4828:Gm1818
|
UTSW |
12 |
48,602,409 (GRCm39) |
exon |
noncoding transcript |
|
|
R4937:Gm1818
|
UTSW |
12 |
48,606,607 (GRCm39) |
exon |
noncoding transcript |
|
|
R5022:Gm1818
|
UTSW |
12 |
48,602,318 (GRCm39) |
exon |
noncoding transcript |
|
|
R5023:Gm1818
|
UTSW |
12 |
48,602,318 (GRCm39) |
exon |
noncoding transcript |
|
|
R5952:Gm1818
|
UTSW |
12 |
48,602,719 (GRCm39) |
exon |
noncoding transcript |
|
|
R6057:Gm1818
|
UTSW |
12 |
48,602,346 (GRCm39) |
exon |
noncoding transcript |
|
|
R6131:Gm1818
|
UTSW |
12 |
48,602,319 (GRCm39) |
exon |
noncoding transcript |
|
|
Z1088:Gm1818
|
UTSW |
12 |
48,602,907 (GRCm39) |
exon |
noncoding transcript |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation