Incidental Mutation 'IGL01927:Gm5862'
ID |
279136 |
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 # |
IGL01927
|
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: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
A |
G |
2: 35,266,026 (GRCm39) |
Y215H |
probably damaging |
Het |
Acsm2 |
T |
C |
7: 119,177,435 (GRCm39) |
F317L |
possibly damaging |
Het |
Akr1d1 |
A |
G |
6: 37,541,394 (GRCm39) |
D297G |
probably benign |
Het |
Atp10b |
A |
G |
11: 43,150,231 (GRCm39) |
|
probably benign |
Het |
Atp8b4 |
T |
C |
2: 126,164,896 (GRCm39) |
Y1140C |
probably damaging |
Het |
Cap2 |
T |
A |
13: 46,789,109 (GRCm39) |
S105T |
probably benign |
Het |
Cspg5 |
A |
T |
9: 110,091,152 (GRCm39) |
I414F |
probably damaging |
Het |
Dipk1b |
A |
G |
2: 26,526,127 (GRCm39) |
M354V |
probably benign |
Het |
Ereg |
T |
A |
5: 91,234,671 (GRCm39) |
V28E |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Ift81 |
G |
A |
5: 122,731,192 (GRCm39) |
T321M |
probably benign |
Het |
Kcnip2 |
T |
A |
19: 45,784,044 (GRCm39) |
Q95L |
probably damaging |
Het |
Meis1 |
C |
T |
11: 18,831,811 (GRCm39) |
R409H |
probably benign |
Het |
Opa1 |
T |
C |
16: 29,405,813 (GRCm39) |
I126T |
probably benign |
Het |
Osbpl8 |
T |
C |
10: 111,106,477 (GRCm39) |
Y295H |
probably benign |
Het |
Ppip5k2 |
A |
T |
1: 97,640,848 (GRCm39) |
V1005E |
probably damaging |
Het |
Prdm10 |
A |
G |
9: 31,246,694 (GRCm39) |
|
probably benign |
Het |
Rptor |
T |
A |
11: 119,548,500 (GRCm39) |
V58E |
probably damaging |
Het |
Togaram1 |
C |
T |
12: 65,023,476 (GRCm39) |
A687V |
probably benign |
Het |
Vmn2r1 |
T |
C |
3: 63,989,105 (GRCm39) |
F15L |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r82 |
T |
C |
10: 79,213,906 (GRCm39) |
L164P |
probably damaging |
Het |
Zfp623 |
T |
A |
15: 75,819,354 (GRCm39) |
N103K |
possibly 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 |
|
IGL01881: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 |
|
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 |