Incidental Mutation 'R3965:Or10g9'
ID |
312308 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Or10g9
|
Ensembl Gene |
ENSMUSG00000059473 |
Gene Name |
olfactory receptor family 10 subfamily G member 9 |
Synonyms |
MOR223-1, Olfr979, GA_x6K02T2PVTD-33699706-33698771 |
MMRRC Submission |
040934-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.084)
|
Stock # |
R3965 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
9 |
Chromosomal Location |
39911502-39912546 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 39911767 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Glutamic Acid
at position 252
(V252E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148903
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080835]
[ENSMUST00000215523]
[ENSMUST00000216463]
|
AlphaFold |
Q8VH10 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000080835
AA Change: V252E
PolyPhen 2
Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000079648 Gene: ENSMUSG00000059473 AA Change: V252E
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
29 |
304 |
7.9e-58 |
PFAM |
Pfam:7tm_1
|
39 |
287 |
5.2e-22 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215523
AA Change: V252E
PolyPhen 2
Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000216463
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.0%
- 20x: 94.0%
|
Validation Efficiency |
100% (49/49) |
MGI Phenotype |
FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
C1galt1c1 |
A |
T |
X: 37,720,453 (GRCm39) |
V181E |
probably benign |
Het |
Ccdc121 |
T |
A |
5: 31,645,335 (GRCm39) |
C363S |
probably benign |
Het |
Cep70 |
T |
A |
9: 99,180,587 (GRCm39) |
F581I |
probably damaging |
Het |
Cfap74 |
T |
A |
4: 155,531,174 (GRCm39) |
M809K |
probably damaging |
Het |
Clic6 |
T |
C |
16: 92,295,732 (GRCm39) |
S131P |
probably benign |
Het |
Ctc1 |
T |
A |
11: 68,921,954 (GRCm39) |
V800D |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dlec1 |
A |
G |
9: 118,957,649 (GRCm39) |
I878V |
probably benign |
Het |
Elapor1 |
T |
C |
3: 108,365,765 (GRCm39) |
D998G |
probably damaging |
Het |
Esyt3 |
T |
A |
9: 99,202,375 (GRCm39) |
D512V |
probably damaging |
Het |
Ewsr1 |
T |
C |
11: 5,033,476 (GRCm39) |
Y232C |
unknown |
Het |
Exoc2 |
G |
A |
13: 31,061,565 (GRCm39) |
S492L |
probably benign |
Het |
Gprc6a |
CAAA |
CA |
10: 51,491,776 (GRCm39) |
|
probably null |
Het |
Grin2c |
G |
A |
11: 115,151,820 (GRCm39) |
R47W |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,895,557 (GRCm39) |
T1670A |
probably benign |
Het |
Med31 |
C |
T |
11: 72,102,755 (GRCm39) |
A118T |
probably benign |
Het |
Mia2 |
T |
A |
12: 59,223,158 (GRCm39) |
S489T |
probably damaging |
Het |
Mov10l1 |
A |
G |
15: 88,896,366 (GRCm39) |
I737V |
probably benign |
Het |
Muc2 |
G |
A |
7: 141,286,233 (GRCm39) |
R120H |
probably benign |
Het |
Nckap1l |
T |
A |
15: 103,373,016 (GRCm39) |
C276* |
probably null |
Het |
Nrap |
T |
C |
19: 56,330,576 (GRCm39) |
S1126G |
probably damaging |
Het |
Oas1c |
A |
G |
5: 120,946,783 (GRCm39) |
F16L |
probably damaging |
Het |
Or1ab2 |
G |
A |
8: 72,864,108 (GRCm39) |
G233R |
probably damaging |
Het |
Or5b123 |
T |
C |
19: 13,596,565 (GRCm39) |
L13P |
probably damaging |
Het |
Or8b51 |
G |
A |
9: 38,569,023 (GRCm39) |
L222F |
probably benign |
Het |
Pik3c2g |
A |
G |
6: 139,801,018 (GRCm39) |
M388V |
possibly damaging |
Het |
Pls1 |
T |
C |
9: 95,667,665 (GRCm39) |
Q81R |
probably benign |
Het |
Pole |
A |
G |
5: 110,460,648 (GRCm39) |
K1143E |
probably damaging |
Het |
Ppp6r2 |
A |
G |
15: 89,143,317 (GRCm39) |
K155E |
probably benign |
Het |
Rxra |
T |
A |
2: 27,642,318 (GRCm39) |
|
probably benign |
Het |
Susd5 |
A |
G |
9: 113,925,260 (GRCm39) |
E381G |
possibly damaging |
Het |
Svs5 |
T |
C |
2: 164,079,662 (GRCm39) |
T82A |
possibly damaging |
Het |
Syt14 |
A |
T |
1: 192,584,175 (GRCm39) |
H413Q |
probably benign |
Het |
Tg |
T |
A |
15: 66,556,039 (GRCm39) |
D910E |
probably benign |
Het |
Timd5 |
T |
A |
11: 46,426,340 (GRCm39) |
V149D |
possibly damaging |
Het |
Tpcn1 |
G |
T |
5: 120,694,640 (GRCm39) |
T143K |
probably damaging |
Het |
Trbv5 |
G |
T |
6: 41,039,342 (GRCm39) |
|
probably benign |
Het |
Trhr |
T |
A |
15: 44,061,095 (GRCm39) |
I205N |
possibly damaging |
Het |
Trp73 |
A |
G |
4: 154,146,493 (GRCm39) |
V422A |
probably benign |
Het |
Trpc6 |
G |
A |
9: 8,626,622 (GRCm39) |
C324Y |
probably damaging |
Het |
Upf1 |
C |
T |
8: 70,791,110 (GRCm39) |
R544H |
probably damaging |
Het |
Zfhx4 |
G |
T |
3: 5,468,907 (GRCm39) |
V3022F |
probably damaging |
Het |
Zswim8 |
G |
A |
14: 20,763,141 (GRCm39) |
V347I |
probably benign |
Het |
|
Other mutations in Or10g9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02718:Or10g9
|
APN |
9 |
39,912,182 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Or10g9
|
APN |
9 |
39,912,194 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02991:Or10g9
|
UTSW |
9 |
39,911,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R1388:Or10g9
|
UTSW |
9 |
39,911,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R1572:Or10g9
|
UTSW |
9 |
39,912,490 (GRCm39) |
missense |
probably benign |
0.35 |
R2089:Or10g9
|
UTSW |
9 |
39,912,500 (GRCm39) |
missense |
probably benign |
0.01 |
R2091:Or10g9
|
UTSW |
9 |
39,912,500 (GRCm39) |
missense |
probably benign |
0.01 |
R2091:Or10g9
|
UTSW |
9 |
39,912,500 (GRCm39) |
missense |
probably benign |
0.01 |
R2179:Or10g9
|
UTSW |
9 |
39,912,220 (GRCm39) |
missense |
probably benign |
0.44 |
R3424:Or10g9
|
UTSW |
9 |
39,911,830 (GRCm39) |
missense |
probably damaging |
0.97 |
R3964:Or10g9
|
UTSW |
9 |
39,911,767 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4111:Or10g9
|
UTSW |
9 |
39,912,194 (GRCm39) |
nonsense |
probably null |
|
R4537:Or10g9
|
UTSW |
9 |
39,911,616 (GRCm39) |
missense |
probably benign |
0.01 |
R4737:Or10g9
|
UTSW |
9 |
39,911,718 (GRCm39) |
missense |
probably damaging |
0.96 |
R4926:Or10g9
|
UTSW |
9 |
39,912,319 (GRCm39) |
splice site |
probably null |
|
R5303:Or10g9
|
UTSW |
9 |
39,911,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Or10g9
|
UTSW |
9 |
39,911,917 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6387:Or10g9
|
UTSW |
9 |
39,912,148 (GRCm39) |
missense |
probably damaging |
0.99 |
R6394:Or10g9
|
UTSW |
9 |
39,912,001 (GRCm39) |
missense |
probably benign |
0.04 |
R6765:Or10g9
|
UTSW |
9 |
39,912,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R7312:Or10g9
|
UTSW |
9 |
39,912,106 (GRCm39) |
missense |
probably benign |
0.22 |
R7463:Or10g9
|
UTSW |
9 |
39,911,860 (GRCm39) |
missense |
probably benign |
0.07 |
R7486:Or10g9
|
UTSW |
9 |
39,912,181 (GRCm39) |
missense |
probably benign |
0.39 |
R7581:Or10g9
|
UTSW |
9 |
39,911,718 (GRCm39) |
missense |
probably damaging |
0.96 |
R8364:Or10g9
|
UTSW |
9 |
39,911,660 (GRCm39) |
missense |
probably benign |
0.22 |
R8414:Or10g9
|
UTSW |
9 |
39,912,241 (GRCm39) |
missense |
probably benign |
0.19 |
R9049:Or10g9
|
UTSW |
9 |
39,911,919 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9567:Or10g9
|
UTSW |
9 |
39,912,367 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9632:Or10g9
|
UTSW |
9 |
39,912,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Or10g9
|
UTSW |
9 |
39,912,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGTTACTGGCTCTGAGAATATGC -3'
(R):5'- AGCATTATTTCTGTGATGCACCTC -3'
Sequencing Primer
(F):5'- ACTGGCTCTGAGAATATGCTACTTTG -3'
(R):5'- TCAGCCAATGAGATGGTCATC -3'
|
Posted On |
2015-04-29 |