Incidental Mutation 'IGL02011:Taar9'
ID |
183362 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Taar9
|
Ensembl Gene |
ENSMUSG00000037424 |
Gene Name |
trace amine-associated receptor 9 |
Synonyms |
Tar3, Trar3, Ta3 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.128)
|
Stock # |
IGL02011
|
Quality Score |
|
Status
|
|
Chromosome |
10 |
Chromosomal Location |
23984386-23985432 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 23984477 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Histidine
at position 319
(R319H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000043552
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041180]
|
AlphaFold |
Q5QD04 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000041180
AA Change: R319H
PolyPhen 2
Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000043552 Gene: ENSMUSG00000037424 AA Change: R319H
Domain | Start | End | E-Value | Type |
Pfam:7TM_GPCR_Srsx
|
43 |
326 |
7.3e-13 |
PFAM |
Pfam:7tm_1
|
49 |
311 |
8.4e-61 |
PFAM |
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] TAAR9 is a member of a large family of rhodopsin G protein-coupled receptors (GPCRs, or GPRs). GPCRs contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins.[supplied by OMIM, Jul 2005]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap5m1 |
T |
A |
14: 49,318,592 (GRCm39) |
|
probably benign |
Het |
Arg1 |
T |
C |
10: 24,792,275 (GRCm39) |
T215A |
probably benign |
Het |
Arhgap15 |
A |
T |
2: 43,670,767 (GRCm39) |
K50N |
probably damaging |
Het |
Ctdsp1 |
C |
T |
1: 74,433,175 (GRCm39) |
|
probably benign |
Het |
Cwc22 |
A |
T |
2: 77,751,366 (GRCm39) |
D363E |
possibly damaging |
Het |
Drd2 |
G |
T |
9: 49,318,258 (GRCm39) |
C400F |
probably damaging |
Het |
Eef1akmt1 |
A |
T |
14: 57,795,555 (GRCm39) |
Y65N |
probably damaging |
Het |
Gbp10 |
C |
A |
5: 105,368,967 (GRCm39) |
G291W |
probably damaging |
Het |
Lrit1 |
T |
A |
14: 36,784,280 (GRCm39) |
V536E |
probably damaging |
Het |
Or4d1 |
C |
A |
11: 87,805,708 (GRCm39) |
W8L |
probably benign |
Het |
Or52ab4 |
G |
T |
7: 102,988,056 (GRCm39) |
R265L |
probably damaging |
Het |
Or9s15 |
T |
A |
1: 92,524,621 (GRCm39) |
Y127N |
probably damaging |
Het |
Pcdh12 |
C |
T |
18: 38,414,473 (GRCm39) |
G884D |
probably damaging |
Het |
Pih1d1 |
G |
T |
7: 44,806,156 (GRCm39) |
A31S |
probably damaging |
Het |
Plcxd2 |
T |
C |
16: 45,785,454 (GRCm39) |
D317G |
probably damaging |
Het |
Prkaca |
T |
C |
8: 84,717,565 (GRCm39) |
F231S |
probably damaging |
Het |
Raet1d |
T |
A |
10: 22,247,473 (GRCm39) |
I183K |
probably damaging |
Het |
Scaper |
A |
G |
9: 55,487,606 (GRCm39) |
F752S |
probably damaging |
Het |
Shisa9 |
C |
T |
16: 12,062,502 (GRCm39) |
T241I |
possibly damaging |
Het |
Unkl |
T |
A |
17: 25,437,565 (GRCm39) |
V365E |
probably damaging |
Het |
Usp34 |
C |
T |
11: 23,421,554 (GRCm39) |
S3077F |
probably damaging |
Het |
Vps16 |
A |
G |
2: 130,283,399 (GRCm39) |
I566V |
probably benign |
Het |
Vrk2 |
T |
A |
11: 26,421,717 (GRCm39) |
T414S |
probably benign |
Het |
Xpnpep1 |
A |
T |
19: 52,990,896 (GRCm39) |
|
probably benign |
Het |
Zfp804a |
A |
G |
2: 82,087,035 (GRCm39) |
Q288R |
probably damaging |
Het |
|
Other mutations in Taar9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00955:Taar9
|
APN |
10 |
23,985,429 (GRCm39) |
missense |
probably benign |
|
IGL02883:Taar9
|
APN |
10 |
23,985,378 (GRCm39) |
missense |
probably benign |
0.08 |
R1468:Taar9
|
UTSW |
10 |
23,985,382 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1468:Taar9
|
UTSW |
10 |
23,985,382 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1598:Taar9
|
UTSW |
10 |
23,985,305 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2072:Taar9
|
UTSW |
10 |
23,984,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R2471:Taar9
|
UTSW |
10 |
23,985,289 (GRCm39) |
missense |
probably benign |
0.00 |
R2519:Taar9
|
UTSW |
10 |
23,985,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Taar9
|
UTSW |
10 |
23,984,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4793:Taar9
|
UTSW |
10 |
23,985,408 (GRCm39) |
missense |
probably benign |
|
R4801:Taar9
|
UTSW |
10 |
23,984,741 (GRCm39) |
missense |
probably damaging |
0.97 |
R4802:Taar9
|
UTSW |
10 |
23,984,741 (GRCm39) |
missense |
probably damaging |
0.97 |
R5457:Taar9
|
UTSW |
10 |
23,985,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R6450:Taar9
|
UTSW |
10 |
23,985,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Taar9
|
UTSW |
10 |
23,984,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Taar9
|
UTSW |
10 |
23,984,910 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7179:Taar9
|
UTSW |
10 |
23,984,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R7480:Taar9
|
UTSW |
10 |
23,984,843 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8200:Taar9
|
UTSW |
10 |
23,985,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R9311:Taar9
|
UTSW |
10 |
23,985,152 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Taar9
|
UTSW |
10 |
23,984,863 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Taar9
|
UTSW |
10 |
23,985,039 (GRCm39) |
missense |
probably benign |
0.01 |
|
Posted On |
2014-05-07 |