Incidental Mutation 'IGL01072:Gm7275'
ID |
52886 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gm7275
|
Ensembl Gene |
ENSMUSG00000067716 |
Gene Name |
predicted gene 7275 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.260)
|
Stock # |
IGL01072
|
Quality Score |
|
Status
|
|
Chromosome |
16 |
Chromosomal Location |
47893360-47894545 bp(+) (GRCm39) |
Type of Mutation |
exon |
DNA Base Change (assembly) |
T to C
at 47894519 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000085634
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088296]
|
AlphaFold |
no structure available at present |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000088296
|
SMART Domains |
Protein: ENSMUSP00000085634 Gene: ENSMUSG00000067716
Domain | Start | End | E-Value | Type |
Pfam:Peptidase_C48
|
67 |
246 |
1e-43 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 19 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ccdc65 |
A |
T |
15: 98,606,277 (GRCm39) |
M1L |
unknown |
Het |
Cyp3a44 |
T |
C |
5: 145,728,438 (GRCm39) |
D262G |
probably benign |
Het |
Dmbt1 |
C |
T |
7: 130,687,098 (GRCm39) |
|
probably benign |
Het |
Dnmt3l |
A |
G |
10: 77,888,605 (GRCm39) |
N169S |
probably benign |
Het |
Fbxw26 |
A |
T |
9: 109,552,905 (GRCm39) |
F290I |
probably damaging |
Het |
Foxj3 |
A |
G |
4: 119,467,226 (GRCm39) |
M190V |
probably benign |
Het |
Ly75 |
T |
A |
2: 60,184,840 (GRCm39) |
D438V |
probably damaging |
Het |
Lzts3 |
T |
C |
2: 130,477,365 (GRCm39) |
E475G |
probably damaging |
Het |
Mon2 |
A |
T |
10: 122,846,444 (GRCm39) |
Y1375* |
probably null |
Het |
Ndufc2 |
T |
A |
7: 97,049,490 (GRCm39) |
V32D |
probably damaging |
Het |
Nf2 |
A |
C |
11: 4,739,713 (GRCm39) |
L431R |
probably null |
Het |
Niban2 |
T |
C |
2: 32,802,427 (GRCm39) |
|
probably benign |
Het |
Ptpn9 |
C |
T |
9: 56,943,987 (GRCm39) |
T287I |
possibly damaging |
Het |
Rictor |
A |
G |
15: 6,819,043 (GRCm39) |
D1422G |
probably damaging |
Het |
Rpp40 |
C |
A |
13: 36,086,017 (GRCm39) |
G115C |
probably damaging |
Het |
Rps6ka5 |
A |
G |
12: 100,540,157 (GRCm39) |
V522A |
probably benign |
Het |
Scgb1b24 |
A |
T |
7: 33,443,434 (GRCm39) |
D31V |
probably damaging |
Het |
Trrap |
C |
A |
5: 144,721,065 (GRCm39) |
|
probably benign |
Het |
Vmn1r214 |
T |
C |
13: 23,219,300 (GRCm39) |
Y265H |
possibly damaging |
Het |
|
Other mutations in Gm7275 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01603:Gm7275
|
APN |
16 |
47,893,942 (GRCm39) |
exon |
noncoding transcript |
|
IGL01939:Gm7275
|
APN |
16 |
47,893,946 (GRCm39) |
exon |
noncoding transcript |
|
IGL02269:Gm7275
|
APN |
16 |
47,894,185 (GRCm39) |
exon |
noncoding transcript |
|
IGL02403:Gm7275
|
APN |
16 |
47,893,991 (GRCm39) |
exon |
noncoding transcript |
|
R0332:Gm7275
|
UTSW |
16 |
47,894,132 (GRCm39) |
exon |
noncoding transcript |
|
R1162:Gm7275
|
UTSW |
16 |
47,894,395 (GRCm39) |
exon |
noncoding transcript |
|
R1743:Gm7275
|
UTSW |
16 |
47,894,120 (GRCm39) |
exon |
noncoding transcript |
|
R3087:Gm7275
|
UTSW |
16 |
47,894,098 (GRCm39) |
exon |
noncoding transcript |
|
R4590:Gm7275
|
UTSW |
16 |
47,893,982 (GRCm39) |
exon |
noncoding transcript |
|
R5617:Gm7275
|
UTSW |
16 |
47,894,527 (GRCm39) |
exon |
noncoding transcript |
|
R5910:Gm7275
|
UTSW |
16 |
47,893,826 (GRCm39) |
exon |
noncoding transcript |
|
|
Posted On |
2013-06-21 |