Incidental Mutation 'IGL00590:Tas2r104'
ID |
5367 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Tas2r104
|
Ensembl Gene |
ENSMUSG00000061977 |
Gene Name |
taste receptor, type 2, member 104 |
Synonyms |
mt2r45, Tas2r4, mGR04, T2R04 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.057)
|
Stock # |
IGL00590
|
Quality Score |
|
Status
|
|
Chromosome |
6 |
Chromosomal Location |
131661799-131662707 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 131662530 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tryptophan to Arginine
at position 60
(W60R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000072237
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053652]
[ENSMUST00000072404]
[ENSMUST00000080619]
|
AlphaFold |
Q7M723 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000053652
|
SMART Domains |
Protein: ENSMUSP00000058006 Gene: ENSMUSG00000051153
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
1 |
298 |
9.4e-109 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000072404
AA Change: W60R
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000072237 Gene: ENSMUSG00000061977 AA Change: W60R
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
1 |
298 |
8.3e-102 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000080619
|
SMART Domains |
Protein: ENSMUSP00000079453 Gene: ENSMUSG00000063478
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
1 |
298 |
8.1e-104 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
G |
7: 120,023,038 (GRCm39) |
F58C |
probably damaging |
Het |
Adgrf5 |
G |
T |
17: 43,764,038 (GRCm39) |
G1320V |
probably damaging |
Het |
Akap13 |
A |
G |
7: 75,260,417 (GRCm39) |
K211E |
probably benign |
Het |
Akap8l |
T |
C |
17: 32,552,071 (GRCm39) |
D402G |
possibly damaging |
Het |
Akna |
T |
C |
4: 63,290,115 (GRCm39) |
I1198V |
probably benign |
Het |
Apaf1 |
T |
A |
10: 90,859,650 (GRCm39) |
I832F |
probably damaging |
Het |
Cbl |
A |
C |
9: 44,112,495 (GRCm39) |
L67V |
probably damaging |
Het |
Chl1 |
T |
C |
6: 103,670,022 (GRCm39) |
Y471H |
probably benign |
Het |
Cystm1 |
T |
A |
18: 36,499,728 (GRCm39) |
Y48N |
unknown |
Het |
Dennd5b |
T |
C |
6: 148,969,806 (GRCm39) |
T216A |
probably benign |
Het |
Dpep2 |
A |
T |
8: 106,715,453 (GRCm39) |
M356K |
probably damaging |
Het |
Dtymk |
A |
G |
1: 93,722,446 (GRCm39) |
|
probably null |
Het |
Fam91a1 |
A |
G |
15: 58,287,565 (GRCm39) |
D4G |
possibly damaging |
Het |
Fbxl20 |
A |
G |
11: 97,983,955 (GRCm39) |
L306P |
probably damaging |
Het |
Fchsd1 |
C |
T |
18: 38,098,946 (GRCm39) |
|
probably benign |
Het |
Fndc1 |
G |
A |
17: 7,983,933 (GRCm39) |
T1331I |
unknown |
Het |
Gpatch8 |
T |
C |
11: 102,371,375 (GRCm39) |
D721G |
unknown |
Het |
Gsg1 |
A |
T |
6: 135,221,348 (GRCm39) |
I17N |
possibly damaging |
Het |
Heyl |
A |
G |
4: 123,140,423 (GRCm39) |
*327W |
probably null |
Het |
Kif13b |
G |
T |
14: 65,016,911 (GRCm39) |
R1359L |
probably damaging |
Het |
Map3k14 |
C |
T |
11: 103,128,380 (GRCm39) |
G414S |
probably damaging |
Het |
Meis2 |
C |
T |
2: 115,699,274 (GRCm39) |
A330T |
probably damaging |
Het |
Mrpl9 |
T |
C |
3: 94,351,003 (GRCm39) |
L61P |
probably damaging |
Het |
Mrps6 |
A |
G |
16: 91,896,548 (GRCm39) |
N38D |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,575,465 (GRCm39) |
T1407I |
probably benign |
Het |
Nup107 |
A |
G |
10: 117,599,708 (GRCm39) |
Y604H |
probably damaging |
Het |
Pgm2l1 |
T |
C |
7: 99,904,826 (GRCm39) |
|
probably null |
Het |
Pisd |
T |
C |
5: 32,895,756 (GRCm39) |
I441V |
probably benign |
Het |
Rb1cc1 |
T |
C |
1: 6,308,520 (GRCm39) |
F52S |
probably damaging |
Het |
Rnft1 |
T |
A |
11: 86,386,740 (GRCm39) |
W383R |
probably damaging |
Het |
Tlr11 |
A |
G |
14: 50,598,373 (GRCm39) |
T120A |
probably benign |
Het |
Tmem150b |
T |
G |
7: 4,726,896 (GRCm39) |
I71L |
probably benign |
Het |
Zfp296 |
A |
G |
7: 19,311,760 (GRCm39) |
D89G |
possibly damaging |
Het |
|
Other mutations in Tas2r104 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01390:Tas2r104
|
APN |
6 |
131,662,448 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02751:Tas2r104
|
APN |
6 |
131,662,107 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4585001:Tas2r104
|
UTSW |
6 |
131,662,521 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0218:Tas2r104
|
UTSW |
6 |
131,662,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0453:Tas2r104
|
UTSW |
6 |
131,662,304 (GRCm39) |
missense |
probably benign |
0.00 |
R0472:Tas2r104
|
UTSW |
6 |
131,662,434 (GRCm39) |
missense |
probably benign |
0.06 |
R0614:Tas2r104
|
UTSW |
6 |
131,662,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R1290:Tas2r104
|
UTSW |
6 |
131,661,808 (GRCm39) |
nonsense |
probably null |
|
R1480:Tas2r104
|
UTSW |
6 |
131,662,257 (GRCm39) |
missense |
probably benign |
0.17 |
R1698:Tas2r104
|
UTSW |
6 |
131,662,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Tas2r104
|
UTSW |
6 |
131,662,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R2229:Tas2r104
|
UTSW |
6 |
131,662,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R3824:Tas2r104
|
UTSW |
6 |
131,662,002 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3852:Tas2r104
|
UTSW |
6 |
131,661,888 (GRCm39) |
missense |
probably benign |
0.09 |
R4283:Tas2r104
|
UTSW |
6 |
131,662,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Tas2r104
|
UTSW |
6 |
131,662,398 (GRCm39) |
missense |
probably benign |
0.00 |
R4710:Tas2r104
|
UTSW |
6 |
131,662,407 (GRCm39) |
missense |
probably damaging |
0.96 |
R4954:Tas2r104
|
UTSW |
6 |
131,661,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R5559:Tas2r104
|
UTSW |
6 |
131,662,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Tas2r104
|
UTSW |
6 |
131,662,236 (GRCm39) |
missense |
probably benign |
|
R5843:Tas2r104
|
UTSW |
6 |
131,661,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R7304:Tas2r104
|
UTSW |
6 |
131,662,005 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8559:Tas2r104
|
UTSW |
6 |
131,662,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Tas2r104
|
UTSW |
6 |
131,662,632 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8951:Tas2r104
|
UTSW |
6 |
131,662,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2012-04-20 |