Incidental Mutation 'IGL00562:Tas2r134'
ID |
277759 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Tas2r134
|
Ensembl Gene |
ENSMUSG00000056115 |
Gene Name |
taste receptor, type 2, member 134 |
Synonyms |
Tas2r34, T2R134 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.056)
|
Stock # |
IGL00562
|
Quality Score |
|
Status
|
|
Chromosome |
2 |
Chromosomal Location |
51517523-51518419 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 51518100 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 193
(I193T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000064657
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000070028]
|
AlphaFold |
Q7TQB0 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000070028
AA Change: I193T
PolyPhen 2
Score 0.899 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000064657 Gene: ENSMUSG00000056115 AA Change: I193T
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
1 |
291 |
1.4e-75 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500035N22Rik |
T |
C |
5: 25,202,619 (GRCm39) |
|
probably benign |
Het |
AU016765 |
C |
A |
17: 64,826,877 (GRCm39) |
|
noncoding transcript |
Het |
Chaf1b |
T |
C |
16: 93,697,079 (GRCm39) |
|
probably benign |
Het |
Clstn2 |
A |
G |
9: 97,464,505 (GRCm39) |
|
probably benign |
Het |
Crip1 |
T |
A |
12: 113,117,232 (GRCm39) |
|
probably null |
Het |
Cubn |
A |
G |
2: 13,299,041 (GRCm39) |
S3211P |
probably benign |
Het |
Dlx6 |
C |
T |
6: 6,865,143 (GRCm39) |
R172W |
probably damaging |
Het |
Fktn |
A |
T |
4: 53,747,007 (GRCm39) |
|
probably null |
Het |
Focad |
T |
A |
4: 88,267,046 (GRCm39) |
M1019K |
unknown |
Het |
Fuca2 |
A |
T |
10: 13,381,651 (GRCm39) |
D188V |
probably damaging |
Het |
Kcna3 |
A |
G |
3: 106,944,046 (GRCm39) |
D103G |
probably damaging |
Het |
Mrpl19 |
A |
G |
6: 81,942,853 (GRCm39) |
V19A |
probably benign |
Het |
Ndufb3 |
T |
A |
1: 58,634,958 (GRCm39) |
H103Q |
possibly damaging |
Het |
Pkd1l3 |
T |
C |
8: 110,382,779 (GRCm39) |
V1675A |
possibly damaging |
Het |
Ptger4 |
A |
T |
15: 5,272,614 (GRCm39) |
S2T |
probably benign |
Het |
Saxo1 |
C |
T |
4: 86,363,809 (GRCm39) |
E225K |
probably damaging |
Het |
Sftpb |
G |
T |
6: 72,286,845 (GRCm39) |
A228S |
probably benign |
Het |
Slc22a29 |
T |
A |
19: 8,138,993 (GRCm39) |
T490S |
probably benign |
Het |
Slc29a1 |
T |
C |
17: 45,900,918 (GRCm39) |
N50S |
probably damaging |
Het |
Smc6 |
T |
A |
12: 11,351,532 (GRCm39) |
S854T |
probably benign |
Het |
Smim23 |
T |
C |
11: 32,771,893 (GRCm39) |
T58A |
probably benign |
Het |
Thsd7a |
G |
T |
6: 12,379,658 (GRCm39) |
|
probably null |
Het |
Trav13n-4 |
T |
G |
14: 53,601,423 (GRCm39) |
V64G |
possibly damaging |
Het |
Trmt10a |
G |
A |
3: 137,853,177 (GRCm39) |
E13K |
probably damaging |
Het |
Txndc11 |
T |
C |
16: 10,922,496 (GRCm39) |
S239G |
probably damaging |
Het |
Vmn2r96 |
T |
A |
17: 18,804,077 (GRCm39) |
N442K |
probably benign |
Het |
Vps13a |
C |
T |
19: 16,712,078 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Tas2r134 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00563:Tas2r134
|
APN |
2 |
51,518,100 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01121:Tas2r134
|
APN |
2 |
51,518,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01122:Tas2r134
|
APN |
2 |
51,517,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01128:Tas2r134
|
APN |
2 |
51,517,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01132:Tas2r134
|
APN |
2 |
51,517,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01312:Tas2r134
|
APN |
2 |
51,518,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Tas2r134
|
APN |
2 |
51,517,759 (GRCm39) |
nonsense |
probably null |
|
IGL01774:Tas2r134
|
APN |
2 |
51,518,160 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02735:Tas2r134
|
APN |
2 |
51,517,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R0799:Tas2r134
|
UTSW |
2 |
51,518,385 (GRCm39) |
missense |
probably benign |
0.00 |
R1205:Tas2r134
|
UTSW |
2 |
51,517,998 (GRCm39) |
missense |
probably benign |
0.00 |
R2267:Tas2r134
|
UTSW |
2 |
51,518,249 (GRCm39) |
missense |
probably benign |
0.01 |
R3736:Tas2r134
|
UTSW |
2 |
51,517,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R5254:Tas2r134
|
UTSW |
2 |
51,517,559 (GRCm39) |
missense |
probably benign |
0.39 |
R5752:Tas2r134
|
UTSW |
2 |
51,517,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Tas2r134
|
UTSW |
2 |
51,517,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R6940:Tas2r134
|
UTSW |
2 |
51,518,148 (GRCm39) |
missense |
probably benign |
0.00 |
R6954:Tas2r134
|
UTSW |
2 |
51,517,782 (GRCm39) |
missense |
probably benign |
0.00 |
R6996:Tas2r134
|
UTSW |
2 |
51,517,601 (GRCm39) |
missense |
probably benign |
0.00 |
R7206:Tas2r134
|
UTSW |
2 |
51,518,120 (GRCm39) |
missense |
probably benign |
0.02 |
R7303:Tas2r134
|
UTSW |
2 |
51,518,145 (GRCm39) |
missense |
probably benign |
0.01 |
R7348:Tas2r134
|
UTSW |
2 |
51,518,414 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7479:Tas2r134
|
UTSW |
2 |
51,517,541 (GRCm39) |
missense |
not run |
|
R7575:Tas2r134
|
UTSW |
2 |
51,518,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Tas2r134
|
UTSW |
2 |
51,518,255 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8721:Tas2r134
|
UTSW |
2 |
51,517,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Tas2r134
|
UTSW |
2 |
51,518,034 (GRCm39) |
missense |
probably damaging |
0.97 |
R9622:Tas2r134
|
UTSW |
2 |
51,518,358 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
Posted On |
2015-04-16 |