Incidental Mutation 'IGL01881:Gm5862'
ID |
278990 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gm5862
|
Ensembl Gene |
ENSMUSG00000067700 |
Gene Name |
predicted gene 5862 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.196)
|
Stock # |
IGL01881
|
Quality Score |
|
Status
|
|
Chromosome |
5 |
Chromosomal Location |
26223419-26227889 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 26227769 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tryptophan to Glycine
at position 41
(W41G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000072133
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072286]
|
AlphaFold |
K7N5V5 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000072286
AA Change: W41G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000072133 Gene: ENSMUSG00000067700 AA Change: W41G
Domain | Start | End | E-Value | Type |
Pfam:Takusan
|
50 |
134 |
1.6e-25 |
PFAM |
low complexity region
|
154 |
168 |
N/A |
INTRINSIC |
low complexity region
|
235 |
259 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 13 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asl |
A |
T |
5: 130,047,379 (GRCm39) |
|
probably benign |
Het |
Cd3g |
A |
T |
9: 44,882,566 (GRCm39) |
Y160N |
probably damaging |
Het |
Exoc8 |
T |
A |
8: 125,623,090 (GRCm39) |
R426W |
probably damaging |
Het |
Fam216a |
A |
G |
5: 122,505,698 (GRCm39) |
Y114H |
probably damaging |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm3402 |
A |
T |
5: 146,451,408 (GRCm39) |
I89F |
possibly damaging |
Het |
Mterf4 |
A |
G |
1: 93,232,363 (GRCm39) |
S163P |
probably damaging |
Het |
Myo7b |
G |
A |
18: 32,133,320 (GRCm39) |
|
probably benign |
Het |
Pde6b |
A |
T |
5: 108,569,366 (GRCm39) |
M358L |
probably benign |
Het |
Ppp1cb |
A |
G |
5: 32,635,487 (GRCm39) |
I44V |
probably benign |
Het |
Slitrk3 |
T |
C |
3: 72,956,639 (GRCm39) |
E711G |
probably benign |
Het |
Trappc9 |
A |
T |
15: 72,871,841 (GRCm39) |
L492Q |
probably damaging |
Het |
Tulp2 |
C |
T |
7: 45,170,219 (GRCm39) |
R297W |
probably damaging |
Het |
|
Other mutations in Gm5862 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01606:Gm5862
|
APN |
5 |
26,224,514 (GRCm39) |
missense |
probably benign |
|
IGL01863:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01868:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01873:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01902:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01905:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01909:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01917:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01924:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01927:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01951:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL03374:Gm5862
|
APN |
5 |
26,224,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R2475:Gm5862
|
UTSW |
5 |
26,224,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R3828:Gm5862
|
UTSW |
5 |
26,224,345 (GRCm39) |
missense |
probably benign |
0.27 |
R4591:Gm5862
|
UTSW |
5 |
26,224,486 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6916:Gm5862
|
UTSW |
5 |
26,224,346 (GRCm39) |
missense |
probably benign |
|
R8291:Gm5862
|
UTSW |
5 |
26,224,444 (GRCm39) |
missense |
probably benign |
0.32 |
R8927:Gm5862
|
UTSW |
5 |
26,226,678 (GRCm39) |
missense |
probably damaging |
0.98 |
R8928:Gm5862
|
UTSW |
5 |
26,226,678 (GRCm39) |
missense |
probably damaging |
0.98 |
R9074:Gm5862
|
UTSW |
5 |
26,226,624 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Gm5862
|
UTSW |
5 |
26,223,485 (GRCm39) |
frame shift |
probably null |
|
|
Posted On |
2015-04-16 |