Incidental Mutation 'R4862:Or2f1'
| ID |
374590 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or2f1
|
| Ensembl Gene |
ENSMUSG00000095831 |
| Gene Name |
olfactory receptor family 2 subfamily F member 1 |
| Synonyms |
MOR257-8P, Olfr453, GA_x6K02T2P3E9-4815856-4814903 |
| MMRRC Submission |
043260-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.101)
|
| Stock # |
R4862 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
6 |
| Chromosomal Location |
42720973-42721926 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 42721489 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 173
(Y173H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150467
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053647]
[ENSMUST00000213997]
|
| AlphaFold |
Q7TRV7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000053647
AA Change: Y173H
PolyPhen 2
Score 0.652 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000052043
Gene: ENSMUSG00000095831
AA Change: Y173H
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
5.6e-54 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.8e-23 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203812
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213997
AA Change: Y173H
PolyPhen 2
Score 0.652 (Sensitivity: 0.87; Specificity: 0.91)
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 95.0%
|
| Validation Efficiency |
95% (40/42) |
| 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 |
|---|
| Acox3 |
A |
G |
5: 35,747,083 (GRCm39) |
T167A |
probably benign |
Het |
| Aox1 |
T |
G |
1: 58,134,316 (GRCm39) |
D1096E |
probably damaging |
Het |
| Arid4a |
A |
T |
12: 71,122,721 (GRCm39) |
D1034V |
probably damaging |
Het |
| Ccdc168 |
G |
A |
1: 44,097,178 (GRCm39) |
P1307S |
possibly damaging |
Het |
| Chaf1b |
T |
A |
16: 93,684,022 (GRCm39) |
L91Q |
probably damaging |
Het |
| Copb2 |
G |
T |
9: 98,463,320 (GRCm39) |
D512Y |
probably damaging |
Het |
| Daam1 |
A |
G |
12: 71,988,981 (GRCm39) |
E127G |
unknown |
Het |
| Dhx16 |
A |
G |
17: 36,194,154 (GRCm39) |
I422V |
probably benign |
Het |
| Dnah6 |
C |
T |
6: 73,098,771 (GRCm39) |
V2043I |
probably damaging |
Het |
| Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
| Dync2h1 |
A |
G |
9: 7,147,717 (GRCm39) |
V971A |
probably benign |
Het |
| Elapor1 |
A |
G |
3: 108,375,149 (GRCm39) |
S573P |
probably benign |
Het |
| Elmo1 |
A |
G |
13: 20,633,682 (GRCm39) |
H448R |
probably benign |
Het |
| Fndc1 |
A |
T |
17: 7,988,567 (GRCm39) |
V1165D |
unknown |
Het |
| Hapln1 |
G |
A |
13: 89,749,571 (GRCm39) |
G39S |
possibly damaging |
Het |
| Igkv6-13 |
C |
A |
6: 70,434,765 (GRCm39) |
V27L |
probably benign |
Het |
| Krt28 |
A |
T |
11: 99,255,936 (GRCm39) |
I441N |
possibly damaging |
Het |
| Lgr5 |
A |
T |
10: 115,298,669 (GRCm39) |
D286E |
probably damaging |
Het |
| Mapkap1 |
A |
G |
2: 34,513,442 (GRCm39) |
Y448C |
probably damaging |
Het |
| Or5t9 |
T |
A |
2: 86,659,876 (GRCm39) |
V260E |
probably damaging |
Het |
| Ppt1 |
A |
C |
4: 122,738,242 (GRCm39) |
N89T |
probably damaging |
Het |
| Prss3b |
T |
G |
6: 41,009,345 (GRCm39) |
D163A |
possibly damaging |
Het |
| Ptgs1 |
G |
T |
2: 36,127,267 (GRCm39) |
R51L |
probably damaging |
Het |
| Slc47a2 |
A |
G |
11: 61,204,520 (GRCm39) |
F277S |
possibly damaging |
Het |
| Smcr8 |
A |
G |
11: 60,668,897 (GRCm39) |
E15G |
probably benign |
Het |
| Tbce |
A |
G |
13: 14,173,004 (GRCm39) |
S476P |
possibly damaging |
Het |
| Tmem131l |
A |
T |
3: 83,805,517 (GRCm39) |
|
probably benign |
Het |
| Unc5c |
T |
C |
3: 141,495,534 (GRCm39) |
Y468H |
probably damaging |
Het |
| Ush1c |
A |
T |
7: 45,878,664 (GRCm39) |
L117H |
probably damaging |
Het |
| Wdfy4 |
A |
G |
14: 32,822,860 (GRCm39) |
|
probably null |
Het |
| Zfa-ps |
G |
T |
10: 52,419,192 (GRCm39) |
|
noncoding transcript |
Het |
| Zfat |
C |
A |
15: 68,051,959 (GRCm39) |
A605S |
probably benign |
Het |
| Zfp853 |
T |
A |
5: 143,275,416 (GRCm39) |
Q68L |
unknown |
Het |
| Zfyve16 |
G |
A |
13: 92,644,764 (GRCm39) |
T1146I |
probably damaging |
Het |
|
| Other mutations in Or2f1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00934:Or2f1
|
APN |
6 |
42,721,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01642:Or2f1
|
APN |
6 |
42,721,486 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02703:Or2f1
|
APN |
6 |
42,721,010 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL03018:Or2f1
|
APN |
6 |
42,721,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1163:Or2f1
|
UTSW |
6 |
42,721,057 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1728:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1729:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1730:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1739:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1784:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R2014:Or2f1
|
UTSW |
6 |
42,721,784 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2015:Or2f1
|
UTSW |
6 |
42,721,784 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2130:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R2132:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R2133:Or2f1
|
UTSW |
6 |
42,721,069 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R3937:Or2f1
|
UTSW |
6 |
42,721,010 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4959:Or2f1
|
UTSW |
6 |
42,721,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4973:Or2f1
|
UTSW |
6 |
42,721,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5155:Or2f1
|
UTSW |
6 |
42,721,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6581:Or2f1
|
UTSW |
6 |
42,721,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7028:Or2f1
|
UTSW |
6 |
42,721,337 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7348:Or2f1
|
UTSW |
6 |
42,721,790 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7490:Or2f1
|
UTSW |
6 |
42,721,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7522:Or2f1
|
UTSW |
6 |
42,721,568 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8373:Or2f1
|
UTSW |
6 |
42,721,280 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9224:Or2f1
|
UTSW |
6 |
42,721,904 (GRCm39) |
missense |
probably benign |
0.30 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGCAATGATGGCCTATGACC -3'
(R):5'- ATACGTGAAAATGGCCATGC -3'
Sequencing Primer
(F):5'- CAATGATGGCCTATGACCGTTATG -3'
(R):5'- CCCTCTTTGGACTGGATTTTGAG -3'
|
| Posted On |
2016-03-17 |
Incidental Mutation