Incidental Mutation 'IGL00467:Tas2r109'
ID |
45054 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Tas2r109
|
Ensembl Gene |
ENSMUSG00000062528 |
Gene Name |
taste receptor, type 2, member 109 |
Synonyms |
mt2r62, T2R09, mGR09, Tas2r9 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.048)
|
Stock # |
IGL00467
|
Quality Score |
|
Status
|
|
Chromosome |
6 |
Chromosomal Location |
132956978-132957928 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 132956986 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Leucine
at position 315
(V315L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000069300
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000067539]
|
AlphaFold |
Q7M707 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000067539
AA Change: V315L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000069300 Gene: ENSMUSG00000062528 AA Change: V315L
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
9 |
309 |
4.3e-81 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
C |
11: 110,036,496 (GRCm39) |
|
probably benign |
Het |
Acvrl1 |
C |
A |
15: 101,041,221 (GRCm39) |
|
probably null |
Het |
Ahnak |
T |
A |
19: 8,984,587 (GRCm39) |
M1957K |
probably damaging |
Het |
Brinp3 |
A |
G |
1: 146,777,512 (GRCm39) |
D653G |
probably damaging |
Het |
Dcstamp |
T |
A |
15: 39,617,812 (GRCm39) |
C74S |
probably benign |
Het |
Esrrg |
A |
G |
1: 187,943,107 (GRCm39) |
E360G |
probably damaging |
Het |
Fam13a |
C |
T |
6: 58,917,098 (GRCm39) |
|
probably benign |
Het |
Glipr1l1 |
A |
G |
10: 111,914,286 (GRCm39) |
T216A |
probably benign |
Het |
Lama2 |
T |
A |
10: 27,343,193 (GRCm39) |
|
probably benign |
Het |
Men1 |
G |
A |
19: 6,387,237 (GRCm39) |
|
probably null |
Het |
Mta3 |
T |
A |
17: 84,063,113 (GRCm39) |
|
probably benign |
Het |
Nfu1 |
A |
G |
6: 86,997,755 (GRCm39) |
M213V |
possibly damaging |
Het |
Pam |
A |
T |
1: 97,852,152 (GRCm39) |
|
probably benign |
Het |
Pcca |
A |
T |
14: 122,820,041 (GRCm39) |
M62L |
probably benign |
Het |
Phf6 |
A |
G |
X: 52,020,523 (GRCm39) |
Y25C |
probably damaging |
Het |
Phlpp2 |
C |
T |
8: 110,652,422 (GRCm39) |
H589Y |
probably benign |
Het |
Ppp1r13b |
A |
G |
12: 111,795,804 (GRCm39) |
I956T |
probably damaging |
Het |
Prkcd |
G |
A |
14: 30,324,379 (GRCm39) |
|
probably benign |
Het |
Rapgef4 |
A |
T |
2: 72,086,656 (GRCm39) |
N973I |
possibly damaging |
Het |
Rnf20 |
G |
T |
4: 49,655,480 (GRCm39) |
E905* |
probably null |
Het |
Slc26a6 |
T |
A |
9: 108,733,088 (GRCm39) |
D22E |
probably benign |
Het |
Sp2 |
C |
T |
11: 96,845,387 (GRCm39) |
R578H |
probably damaging |
Het |
Taf6l |
A |
T |
19: 8,760,752 (GRCm39) |
N57K |
probably benign |
Het |
Tasor |
A |
G |
14: 27,170,121 (GRCm39) |
N350S |
probably benign |
Het |
Tex9 |
T |
C |
9: 72,385,117 (GRCm39) |
T240A |
probably benign |
Het |
Trank1 |
G |
A |
9: 111,193,734 (GRCm39) |
|
probably benign |
Het |
Trim30c |
A |
T |
7: 104,031,389 (GRCm39) |
Y475* |
probably null |
Het |
Trim60 |
T |
C |
8: 65,453,371 (GRCm39) |
T293A |
possibly damaging |
Het |
Ttc21b |
T |
C |
2: 66,018,708 (GRCm39) |
Y1233C |
probably damaging |
Het |
Wdr75 |
A |
G |
1: 45,841,235 (GRCm39) |
I106V |
probably benign |
Het |
Zkscan16 |
T |
C |
4: 58,957,709 (GRCm39) |
S664P |
possibly damaging |
Het |
|
Other mutations in Tas2r109 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01837:Tas2r109
|
APN |
6 |
132,957,477 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02094:Tas2r109
|
APN |
6 |
132,957,202 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0788:Tas2r109
|
UTSW |
6 |
132,957,264 (GRCm39) |
missense |
probably benign |
0.01 |
R0849:Tas2r109
|
UTSW |
6 |
132,957,856 (GRCm39) |
missense |
probably benign |
0.00 |
R1542:Tas2r109
|
UTSW |
6 |
132,957,873 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1583:Tas2r109
|
UTSW |
6 |
132,957,389 (GRCm39) |
missense |
probably benign |
0.01 |
R2035:Tas2r109
|
UTSW |
6 |
132,957,423 (GRCm39) |
missense |
probably benign |
|
R3845:Tas2r109
|
UTSW |
6 |
132,957,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R4060:Tas2r109
|
UTSW |
6 |
132,957,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Tas2r109
|
UTSW |
6 |
132,957,144 (GRCm39) |
missense |
probably benign |
|
R5353:Tas2r109
|
UTSW |
6 |
132,957,594 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5860:Tas2r109
|
UTSW |
6 |
132,957,664 (GRCm39) |
missense |
probably benign |
0.06 |
R6211:Tas2r109
|
UTSW |
6 |
132,957,587 (GRCm39) |
nonsense |
probably null |
|
R6378:Tas2r109
|
UTSW |
6 |
132,957,844 (GRCm39) |
missense |
probably benign |
0.00 |
R6861:Tas2r109
|
UTSW |
6 |
132,957,048 (GRCm39) |
missense |
probably benign |
0.43 |
R7319:Tas2r109
|
UTSW |
6 |
132,957,663 (GRCm39) |
missense |
probably benign |
0.33 |
R8553:Tas2r109
|
UTSW |
6 |
132,957,171 (GRCm39) |
missense |
probably benign |
0.33 |
R9447:Tas2r109
|
UTSW |
6 |
132,957,270 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Tas2r109
|
UTSW |
6 |
132,957,264 (GRCm39) |
missense |
probably benign |
0.07 |
|
Posted On |
2013-06-11 |