Incidental Mutation 'IGL00741:1810009J06Rik'
ID |
8430 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
1810009J06Rik
|
Ensembl Gene |
ENSMUSG00000094808 |
Gene Name |
RIKEN cDNA 1810009J06 gene |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.162)
|
Stock # |
IGL00741
|
Quality Score |
|
Status
|
|
Chromosome |
6 |
Chromosomal Location |
40941706-40945361 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to A
at 40941768 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000075935
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076638]
|
AlphaFold |
Q9CPN7 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000076638
|
SMART Domains |
Protein: ENSMUSP00000075935 Gene: ENSMUSG00000094808
Domain | Start | End | E-Value | Type |
Tryp_SPc
|
23 |
240 |
4.94e-97 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 12 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
C |
6: 142,632,956 (GRCm39) |
V262G |
probably benign |
Het |
Adamtsl1 |
T |
C |
4: 86,195,185 (GRCm39) |
V534A |
probably damaging |
Het |
Arhgap31 |
A |
G |
16: 38,423,363 (GRCm39) |
V901A |
probably damaging |
Het |
C3 |
A |
G |
17: 57,527,206 (GRCm39) |
|
probably benign |
Het |
Chd7 |
T |
C |
4: 8,839,454 (GRCm39) |
V1330A |
probably damaging |
Het |
Dop1a |
A |
G |
9: 86,404,859 (GRCm39) |
T255A |
possibly damaging |
Het |
Eef1a2 |
T |
C |
2: 180,794,803 (GRCm39) |
Q132R |
possibly damaging |
Het |
Pamr1 |
A |
C |
2: 102,416,966 (GRCm39) |
S93R |
possibly damaging |
Het |
Tacc3 |
A |
G |
5: 33,826,984 (GRCm39) |
Y531C |
probably damaging |
Het |
Tcerg1 |
A |
G |
18: 42,701,518 (GRCm39) |
E860G |
possibly damaging |
Het |
Tmco4 |
T |
A |
4: 138,723,885 (GRCm39) |
|
probably null |
Het |
Zfyve16 |
A |
G |
13: 92,660,761 (GRCm39) |
L16P |
probably damaging |
Het |
|
Other mutations in 1810009J06Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:1810009J06Rik
|
APN |
6 |
40,941,733 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01146:1810009J06Rik
|
APN |
6 |
40,943,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02815:1810009J06Rik
|
APN |
6 |
40,941,729 (GRCm39) |
missense |
probably benign |
|
R1543:1810009J06Rik
|
UTSW |
6 |
40,945,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R1708:1810009J06Rik
|
UTSW |
6 |
40,941,732 (GRCm39) |
missense |
probably benign |
|
R1964:1810009J06Rik
|
UTSW |
6 |
40,945,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:1810009J06Rik
|
UTSW |
6 |
40,945,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R6611:1810009J06Rik
|
UTSW |
6 |
40,943,713 (GRCm39) |
missense |
probably benign |
0.09 |
R7057:1810009J06Rik
|
UTSW |
6 |
40,945,181 (GRCm39) |
missense |
probably benign |
0.00 |
R9371:1810009J06Rik
|
UTSW |
6 |
40,943,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2012-12-06 |