Incidental Mutation 'W0251:Gm4559'
ID |
166607 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Gm4559
|
Ensembl Gene |
ENSMUSG00000056885 |
Gene Name |
predicted gene 4559 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.150)
|
Stock # |
W0251 (G3R)
of strain
daniel_gray
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
141827501-141828100 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to C
at 141827535 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Glycine
at position 189
(A189G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000079498
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080669]
|
AlphaFold |
A4IF42 |
Predicted Effect |
unknown
Transcript: ENSMUST00000080669
AA Change: A189G
|
SMART Domains |
Protein: ENSMUSP00000079498 Gene: ENSMUSG00000056885 AA Change: A189G
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
199 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.0%
- 10x: 95.5%
- 20x: 90.3%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 14 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bcl2a1b |
T |
A |
9: 89,081,636 (GRCm39) |
M75K |
probably damaging |
Het |
Btaf1 |
G |
A |
19: 36,980,904 (GRCm39) |
R1575H |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,183,862 (GRCm39) |
M2507V |
probably benign |
Het |
Dcc |
T |
C |
18: 71,959,154 (GRCm39) |
D206G |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,155,501 (GRCm39) |
I705F |
possibly damaging |
Het |
Entpd1 |
A |
T |
19: 40,714,697 (GRCm39) |
I269F |
probably damaging |
Het |
Ipo5 |
T |
A |
14: 121,176,197 (GRCm39) |
M648K |
probably benign |
Het |
Kdelr1 |
A |
G |
7: 45,531,045 (GRCm39) |
Y96C |
probably damaging |
Het |
Mmp17 |
C |
T |
5: 129,672,591 (GRCm39) |
A181V |
probably benign |
Het |
Muc20 |
T |
C |
16: 32,614,223 (GRCm39) |
I385V |
possibly damaging |
Het |
Or13c7 |
C |
T |
4: 43,855,058 (GRCm39) |
L250F |
probably benign |
Het |
Pik3r6 |
A |
G |
11: 68,424,697 (GRCm39) |
Y434C |
probably benign |
Het |
Pura |
T |
C |
18: 36,420,843 (GRCm39) |
V210A |
probably benign |
Het |
Spic |
C |
T |
10: 88,515,766 (GRCm39) |
D19N |
probably damaging |
Het |
|
Other mutations in Gm4559 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03184:Gm4559
|
APN |
7 |
141,828,046 (GRCm39) |
missense |
unknown |
|
R1493:Gm4559
|
UTSW |
7 |
141,828,050 (GRCm39) |
nonsense |
probably null |
|
R1879:Gm4559
|
UTSW |
7 |
141,827,998 (GRCm39) |
missense |
unknown |
|
R2299:Gm4559
|
UTSW |
7 |
141,827,572 (GRCm39) |
missense |
unknown |
|
R2330:Gm4559
|
UTSW |
7 |
141,827,833 (GRCm39) |
missense |
unknown |
|
R2495:Gm4559
|
UTSW |
7 |
141,827,557 (GRCm39) |
missense |
unknown |
|
R6475:Gm4559
|
UTSW |
7 |
141,827,887 (GRCm39) |
missense |
unknown |
|
R6785:Gm4559
|
UTSW |
7 |
141,827,845 (GRCm39) |
missense |
unknown |
|
R7576:Gm4559
|
UTSW |
7 |
141,827,677 (GRCm39) |
missense |
unknown |
|
R7651:Gm4559
|
UTSW |
7 |
141,827,553 (GRCm39) |
missense |
unknown |
|
R7837:Gm4559
|
UTSW |
7 |
141,827,553 (GRCm39) |
missense |
unknown |
|
R8077:Gm4559
|
UTSW |
7 |
141,827,553 (GRCm39) |
missense |
unknown |
|
R8080:Gm4559
|
UTSW |
7 |
141,827,553 (GRCm39) |
missense |
unknown |
|
R8317:Gm4559
|
UTSW |
7 |
141,827,553 (GRCm39) |
small deletion |
probably benign |
|
R8355:Gm4559
|
UTSW |
7 |
141,827,694 (GRCm39) |
missense |
unknown |
|
R8455:Gm4559
|
UTSW |
7 |
141,827,694 (GRCm39) |
missense |
unknown |
|
R8801:Gm4559
|
UTSW |
7 |
141,827,553 (GRCm39) |
small deletion |
probably benign |
|
Z1177:Gm4559
|
UTSW |
7 |
141,827,771 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- TGCAGAGGGGAATTTGTTAGCTCAC -3'
(R):5'- TGTCAATCTAGCTGCTGCAAGCC -3'
Sequencing Primer
(F):5'- CCAAATCTGAGTTGAAGCTGTG -3'
(R):5'- ccctgctgctgccagtc -3'
|
Posted On |
2014-04-13 |