Incidental Mutation 'R5767:Or11g1'
ID |
446347 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Or11g1
|
Ensembl Gene |
ENSMUSG00000094692 |
Gene Name |
olfactory receptor family 11 subfamily G member 1 |
Synonyms |
GA_x6K02T2PMLR-6110726-6111661, Olfr738, MOR106-3 |
MMRRC Submission |
043367-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.088)
|
Stock # |
R5767 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
50651003-50651938 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 50651235 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 78
(V78A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000150351
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058972]
[ENSMUST00000214320]
[ENSMUST00000214853]
[ENSMUST00000216949]
|
AlphaFold |
L7N1X7 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000058972
AA Change: V78A
PolyPhen 2
Score 0.551 (Sensitivity: 0.88; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000059540 Gene: ENSMUSG00000094692 AA Change: V78A
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
35 |
311 |
2.5e-50 |
PFAM |
Pfam:7TM_GPCR_Srsx
|
39 |
309 |
1.3e-5 |
PFAM |
Pfam:7tm_1
|
45 |
294 |
6.9e-22 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205382
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000214320
AA Change: V78A
PolyPhen 2
Score 0.551 (Sensitivity: 0.88; Specificity: 0.91)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000214853
AA Change: V78A
PolyPhen 2
Score 0.551 (Sensitivity: 0.88; Specificity: 0.91)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000216949
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 95.5%
|
Validation Efficiency |
98% (52/53) |
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: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr6 |
A |
T |
10: 89,562,617 (GRCm39) |
D87E |
probably damaging |
Het |
AI429214 |
TCCCTGATGAAC |
TC |
8: 37,461,383 (GRCm39) |
|
probably null |
Het |
Ano3 |
A |
T |
2: 110,491,616 (GRCm39) |
Y887N |
probably damaging |
Het |
Arid4a |
A |
G |
12: 71,106,867 (GRCm39) |
D313G |
probably damaging |
Het |
Armc2 |
A |
G |
10: 41,887,923 (GRCm39) |
V20A |
probably benign |
Het |
Bltp3b |
A |
G |
10: 89,623,061 (GRCm39) |
D312G |
possibly damaging |
Het |
C2 |
T |
A |
17: 35,095,432 (GRCm39) |
N171I |
possibly damaging |
Het |
Cdh1 |
C |
A |
8: 107,395,187 (GRCm39) |
N865K |
probably damaging |
Het |
Cep89 |
T |
A |
7: 35,117,070 (GRCm39) |
V224E |
probably damaging |
Het |
Cfap251 |
G |
A |
5: 123,436,584 (GRCm39) |
V1038I |
probably benign |
Het |
Dennd2d |
C |
T |
3: 106,395,131 (GRCm39) |
|
probably benign |
Het |
Diaph1 |
T |
A |
18: 37,986,408 (GRCm39) |
K1157N |
probably damaging |
Het |
Dsg4 |
T |
A |
18: 20,595,549 (GRCm39) |
L584* |
probably null |
Het |
Exoc4 |
G |
A |
6: 33,895,367 (GRCm39) |
A795T |
probably benign |
Het |
Fbln5 |
A |
T |
12: 101,731,468 (GRCm39) |
I242N |
probably damaging |
Het |
Gls2 |
A |
G |
10: 128,041,090 (GRCm39) |
H394R |
probably damaging |
Het |
Gm27013 |
C |
T |
6: 130,652,921 (GRCm39) |
C847Y |
possibly damaging |
Het |
Ifna5 |
C |
A |
4: 88,754,036 (GRCm39) |
T92K |
possibly damaging |
Het |
Ireb2 |
A |
G |
9: 54,807,800 (GRCm39) |
M674V |
probably benign |
Het |
Itga2 |
C |
T |
13: 114,976,106 (GRCm39) |
V1089M |
possibly damaging |
Het |
Kctd16 |
A |
T |
18: 40,391,922 (GRCm39) |
Y170F |
probably benign |
Het |
Kif15 |
A |
G |
9: 122,843,039 (GRCm39) |
N45D |
possibly damaging |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,496,901 (GRCm39) |
K420E |
possibly damaging |
Het |
Ms4a14 |
G |
T |
19: 11,279,391 (GRCm39) |
Q1056K |
probably benign |
Het |
Or5k8 |
T |
C |
16: 58,644,316 (GRCm39) |
Y252C |
probably benign |
Het |
Or8k21 |
T |
A |
2: 86,144,742 (GRCm39) |
E296V |
probably damaging |
Het |
Ovch2 |
T |
C |
7: 107,381,185 (GRCm39) |
E571G |
probably benign |
Het |
Pmel |
T |
C |
10: 128,550,250 (GRCm39) |
V95A |
probably damaging |
Het |
Ptger2 |
G |
T |
14: 45,226,599 (GRCm39) |
G60C |
probably benign |
Het |
Ranbp2 |
T |
G |
10: 58,312,647 (GRCm39) |
S1122R |
probably benign |
Het |
Rasal2 |
T |
C |
1: 157,003,732 (GRCm39) |
D309G |
probably damaging |
Het |
Rcc2 |
T |
A |
4: 140,443,230 (GRCm39) |
C303S |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Serpini1 |
C |
T |
3: 75,520,388 (GRCm39) |
|
probably benign |
Het |
Sgo2a |
G |
T |
1: 58,058,819 (GRCm39) |
E1133* |
probably null |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Smarcc1 |
G |
A |
9: 109,961,251 (GRCm39) |
|
probably benign |
Het |
Tbcd |
A |
G |
11: 121,483,518 (GRCm39) |
E749G |
probably benign |
Het |
Tmc3 |
G |
A |
7: 83,249,190 (GRCm39) |
A260T |
probably benign |
Het |
Tnfrsf21 |
A |
G |
17: 43,348,550 (GRCm39) |
Y54C |
probably damaging |
Het |
Urb1 |
T |
A |
16: 90,573,051 (GRCm39) |
M994L |
probably benign |
Het |
Usp14 |
A |
T |
18: 10,009,935 (GRCm39) |
|
probably benign |
Het |
Vps13a |
T |
C |
19: 16,641,928 (GRCm39) |
Y2233C |
probably damaging |
Het |
Wnt2 |
G |
T |
6: 17,990,027 (GRCm39) |
A290E |
probably damaging |
Het |
Zc3h8 |
A |
T |
2: 128,772,812 (GRCm39) |
C225* |
probably null |
Het |
|
Other mutations in Or11g1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01608:Or11g1
|
APN |
14 |
50,651,910 (GRCm39) |
missense |
probably benign |
|
IGL01935:Or11g1
|
APN |
14 |
50,651,012 (GRCm39) |
missense |
probably benign |
|
IGL02431:Or11g1
|
APN |
14 |
50,651,226 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Or11g1
|
UTSW |
14 |
50,651,786 (GRCm39) |
missense |
probably damaging |
0.96 |
BB018:Or11g1
|
UTSW |
14 |
50,651,786 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4480001:Or11g1
|
UTSW |
14 |
50,651,372 (GRCm39) |
missense |
probably benign |
0.14 |
R0620:Or11g1
|
UTSW |
14 |
50,651,154 (GRCm39) |
missense |
probably benign |
0.20 |
R1445:Or11g1
|
UTSW |
14 |
50,651,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R1831:Or11g1
|
UTSW |
14 |
50,651,658 (GRCm39) |
splice site |
probably null |
|
R1915:Or11g1
|
UTSW |
14 |
50,651,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Or11g1
|
UTSW |
14 |
50,651,333 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5301:Or11g1
|
UTSW |
14 |
50,651,030 (GRCm39) |
missense |
probably benign |
0.09 |
R5831:Or11g1
|
UTSW |
14 |
50,651,439 (GRCm39) |
splice site |
probably null |
|
R6173:Or11g1
|
UTSW |
14 |
50,651,654 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6176:Or11g1
|
UTSW |
14 |
50,651,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7356:Or11g1
|
UTSW |
14 |
50,651,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Or11g1
|
UTSW |
14 |
50,651,471 (GRCm39) |
missense |
probably damaging |
0.98 |
R7931:Or11g1
|
UTSW |
14 |
50,651,786 (GRCm39) |
missense |
probably damaging |
0.96 |
R8508:Or11g1
|
UTSW |
14 |
50,651,132 (GRCm39) |
missense |
probably benign |
0.00 |
R8696:Or11g1
|
UTSW |
14 |
50,651,420 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9374:Or11g1
|
UTSW |
14 |
50,651,625 (GRCm39) |
missense |
probably benign |
0.38 |
R9470:Or11g1
|
UTSW |
14 |
50,651,235 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9551:Or11g1
|
UTSW |
14 |
50,651,625 (GRCm39) |
missense |
probably benign |
0.38 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCATCATCACTGGCTTCATC -3'
(R):5'- TCACAAGGATGTTGCAGAGGC -3'
Sequencing Primer
(F):5'- ACTGGCTTCATCCTCCTGGG -3'
(R):5'- AGAGGCGCCCAGTCATGAG -3'
|
Posted On |
2016-11-21 |