Incidental Mutation 'R4195:Or11i1'
ID |
318526 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Or11i1
|
Ensembl Gene |
ENSMUSG00000043529 |
Gene Name |
olfactory receptor family 11 subfamily I member 1 |
Synonyms |
GA_x6K02T2N6GK-529983-529033, Olfr266, MOR122-2 |
MMRRC Submission |
041026-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.076)
|
Stock # |
R4195 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
106728923-106729873 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to T
at 106729328 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Stop codon
at position 182
(C182*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000150519
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000059486]
[ENSMUST00000213616]
[ENSMUST00000216610]
|
AlphaFold |
Q8VFC3 |
Predicted Effect |
probably null
Transcript: ENSMUST00000059486
AA Change: C182*
|
SMART Domains |
Protein: ENSMUSP00000054070 Gene: ENSMUSG00000043529 AA Change: C182*
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
34 |
311 |
1.2e-58 |
PFAM |
Pfam:7tm_1
|
44 |
293 |
5.4e-21 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000213616
AA Change: C182*
|
Predicted Effect |
probably null
Transcript: ENSMUST00000216610
AA Change: C182*
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.8%
|
Validation Efficiency |
98% (40/41) |
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: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acmsd |
T |
G |
1: 127,676,931 (GRCm39) |
L152R |
probably damaging |
Het |
Actg2 |
T |
G |
6: 83,500,155 (GRCm39) |
T39P |
probably damaging |
Het |
Agap1 |
A |
G |
1: 89,762,261 (GRCm39) |
E531G |
probably damaging |
Het |
Alox12b |
A |
G |
11: 69,060,426 (GRCm39) |
S661G |
probably benign |
Het |
Apod |
T |
C |
16: 31,116,392 (GRCm39) |
M113V |
probably benign |
Het |
Atl3 |
A |
G |
19: 7,495,911 (GRCm39) |
I171V |
possibly damaging |
Het |
Atrn |
C |
A |
2: 130,775,332 (GRCm39) |
T145K |
probably damaging |
Het |
Cacna1f |
A |
G |
X: 7,475,169 (GRCm39) |
H57R |
probably damaging |
Het |
Cdhr18 |
C |
A |
14: 13,829,772 (GRCm38) |
V657L |
probably benign |
Het |
Cldn9 |
T |
C |
17: 23,902,148 (GRCm39) |
E159G |
probably damaging |
Het |
Cnnm4 |
C |
A |
1: 36,538,589 (GRCm39) |
H590Q |
probably benign |
Het |
Col19a1 |
G |
A |
1: 24,573,133 (GRCm39) |
S213L |
unknown |
Het |
Cse1l |
A |
G |
2: 166,771,899 (GRCm39) |
T387A |
probably damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,193,186 (GRCm39) |
V675A |
possibly damaging |
Het |
Fbll1 |
A |
G |
11: 35,688,493 (GRCm39) |
S257P |
possibly damaging |
Het |
Fbll1 |
T |
A |
11: 35,688,699 (GRCm39) |
H188L |
possibly damaging |
Het |
Frem2 |
A |
G |
3: 53,446,689 (GRCm39) |
F2360L |
possibly damaging |
Het |
G3bp2 |
A |
G |
5: 92,203,275 (GRCm39) |
S349P |
probably damaging |
Het |
Gm2396 |
A |
G |
9: 88,799,715 (GRCm39) |
|
noncoding transcript |
Het |
Gm6569 |
C |
T |
15: 73,708,092 (GRCm39) |
P22L |
probably damaging |
Het |
Itih2 |
T |
C |
2: 10,120,096 (GRCm39) |
N314D |
probably damaging |
Het |
Lman2l |
A |
C |
1: 36,464,022 (GRCm39) |
I266M |
probably damaging |
Het |
Mrps9 |
T |
G |
1: 42,940,254 (GRCm39) |
|
probably benign |
Het |
Mtmr11 |
T |
C |
3: 96,075,207 (GRCm39) |
|
probably benign |
Het |
Neb |
G |
T |
2: 52,161,571 (GRCm39) |
R2074S |
probably damaging |
Het |
Neb |
A |
T |
2: 52,180,847 (GRCm39) |
H1226Q |
probably damaging |
Het |
Nmi |
A |
C |
2: 51,838,632 (GRCm39) |
S301A |
probably benign |
Het |
Pclo |
A |
G |
5: 14,727,577 (GRCm39) |
|
probably benign |
Het |
Pkd1l1 |
T |
A |
11: 8,859,929 (GRCm39) |
I560F |
probably damaging |
Het |
Polr1e |
T |
C |
4: 45,019,327 (GRCm39) |
Y59H |
probably damaging |
Het |
Slc30a4 |
G |
A |
2: 122,527,190 (GRCm39) |
T401M |
probably damaging |
Het |
Tas1r3 |
T |
C |
4: 155,947,442 (GRCm39) |
E81G |
probably damaging |
Het |
Zfp990 |
A |
T |
4: 145,263,547 (GRCm39) |
|
probably null |
Het |
Zzz3 |
A |
G |
3: 152,134,102 (GRCm39) |
T387A |
probably benign |
Het |
|
Other mutations in Or11i1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01869:Or11i1
|
APN |
3 |
106,729,342 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01954:Or11i1
|
APN |
3 |
106,729,311 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02371:Or11i1
|
APN |
3 |
106,729,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02792:Or11i1
|
APN |
3 |
106,729,456 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4131001:Or11i1
|
UTSW |
3 |
106,729,282 (GRCm39) |
missense |
probably benign |
0.00 |
R0540:Or11i1
|
UTSW |
3 |
106,729,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R1925:Or11i1
|
UTSW |
3 |
106,729,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R2026:Or11i1
|
UTSW |
3 |
106,729,027 (GRCm39) |
missense |
probably benign |
0.01 |
R4735:Or11i1
|
UTSW |
3 |
106,728,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Or11i1
|
UTSW |
3 |
106,729,624 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4789:Or11i1
|
UTSW |
3 |
106,729,608 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4922:Or11i1
|
UTSW |
3 |
106,729,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R6318:Or11i1
|
UTSW |
3 |
106,729,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6359:Or11i1
|
UTSW |
3 |
106,729,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R6505:Or11i1
|
UTSW |
3 |
106,729,638 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7605:Or11i1
|
UTSW |
3 |
106,729,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R8529:Or11i1
|
UTSW |
3 |
106,729,109 (GRCm39) |
nonsense |
probably null |
|
R8998:Or11i1
|
UTSW |
3 |
106,728,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R8999:Or11i1
|
UTSW |
3 |
106,728,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R9255:Or11i1
|
UTSW |
3 |
106,729,737 (GRCm39) |
missense |
probably benign |
0.00 |
R9260:Or11i1
|
UTSW |
3 |
106,729,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R9771:Or11i1
|
UTSW |
3 |
106,729,060 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1176:Or11i1
|
UTSW |
3 |
106,729,359 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- TAGGTGGCAATCAGTGTTCC -3'
(R):5'- ACCGCTACCTAGCTATCTGC -3'
Sequencing Primer
(F):5'- ACAGGTGGAGAAAGCCTTTTTCC -3'
(R):5'- ACCTAGCTATCTGCCAGCC -3'
|
Posted On |
2015-06-10 |