Incidental Mutation 'R6135:Or5b97'
| ID |
488326 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5b97
|
| Ensembl Gene |
ENSMUSG00000060303 |
| Gene Name |
olfactory receptor family 5 subfamily B member 97 |
| Synonyms |
MOR202-3, Olfr1447, GA_x6K02T2RE5P-3231251-3230331 |
| MMRRC Submission |
044282-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.063)
|
| Stock # |
R6135 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
12878213-12879142 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 12878803 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Aspartic acid
at position 114
(Y114D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149392
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071484]
[ENSMUST00000208343]
[ENSMUST00000216989]
|
| AlphaFold |
Q8VFX3 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000071484
AA Change: Y114D
PolyPhen 2
Score 0.969 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000071419
Gene: ENSMUSG00000060303
AA Change: Y114D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
32 |
309 |
5.3e-50 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
36 |
306 |
2.1e-7 |
PFAM |
|
Pfam:7tm_1
|
42 |
291 |
7.4e-20 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000208343
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216989
AA Change: Y114D
PolyPhen 2
Score 0.969 (Sensitivity: 0.77; Specificity: 0.95)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000218013
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000220222
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.2%
- 20x: 94.7%
|
| Validation Efficiency |
100% (55/55) |
| 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: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
A |
G |
13: 77,402,335 (GRCm39) |
E95G |
probably damaging |
Het |
| Abca4 |
C |
T |
3: 121,932,096 (GRCm39) |
T250I |
possibly damaging |
Het |
| Ahi1 |
G |
A |
10: 20,845,020 (GRCm39) |
R375H |
probably benign |
Het |
| Aimp1 |
T |
C |
3: 132,377,844 (GRCm39) |
K174E |
probably benign |
Het |
| Aire |
A |
G |
10: 77,878,801 (GRCm39) |
L82P |
probably damaging |
Het |
| Akap13 |
T |
A |
7: 75,259,656 (GRCm39) |
V760D |
possibly damaging |
Het |
| Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
| Carf |
C |
T |
1: 60,187,122 (GRCm39) |
S540F |
probably damaging |
Het |
| Ccdc171 |
T |
A |
4: 83,473,087 (GRCm39) |
M172K |
probably benign |
Het |
| Chpt1 |
A |
T |
10: 88,318,145 (GRCm39) |
V199E |
possibly damaging |
Het |
| Cldn16 |
G |
A |
16: 26,293,018 (GRCm39) |
D65N |
possibly damaging |
Het |
| Cnga3 |
G |
A |
1: 37,271,318 (GRCm39) |
|
probably benign |
Het |
| Col14a1 |
A |
G |
15: 55,244,246 (GRCm39) |
T440A |
unknown |
Het |
| Creb3l3 |
A |
G |
10: 80,921,552 (GRCm39) |
I331T |
probably benign |
Het |
| Cul9 |
T |
C |
17: 46,832,379 (GRCm39) |
T1410A |
probably benign |
Het |
| Dnm1 |
T |
A |
2: 32,223,075 (GRCm39) |
|
probably null |
Het |
| Fhl5 |
A |
T |
4: 25,214,716 (GRCm39) |
Y20* |
probably null |
Het |
| Fignl1 |
T |
C |
11: 11,752,557 (GRCm39) |
D166G |
probably benign |
Het |
| Ghr |
T |
C |
15: 3,355,447 (GRCm39) |
I279V |
probably benign |
Het |
| Gm1979 |
T |
G |
5: 26,205,298 (GRCm39) |
S180R |
probably damaging |
Het |
| Hydin |
T |
C |
8: 111,189,292 (GRCm39) |
V1232A |
possibly damaging |
Het |
| Ifnar1 |
A |
G |
16: 91,298,508 (GRCm39) |
|
probably null |
Het |
| Inpp5d |
A |
G |
1: 87,548,119 (GRCm39) |
|
probably null |
Het |
| Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
| Kcnh2 |
T |
A |
5: 24,526,791 (GRCm39) |
S1002C |
probably damaging |
Het |
| Krt87 |
T |
A |
15: 101,385,415 (GRCm39) |
E319V |
probably damaging |
Het |
| Lbp |
A |
G |
2: 158,159,469 (GRCm39) |
I201V |
probably benign |
Het |
| Man1a2 |
G |
A |
3: 100,592,248 (GRCm39) |
|
probably benign |
Het |
| Myh8 |
A |
G |
11: 67,188,326 (GRCm39) |
T996A |
possibly damaging |
Het |
| Nat10 |
A |
G |
2: 103,573,661 (GRCm39) |
L319P |
probably damaging |
Het |
| Nelfa |
A |
G |
5: 34,056,620 (GRCm39) |
|
probably null |
Het |
| Pcdha11 |
T |
A |
18: 37,138,870 (GRCm39) |
N166K |
probably damaging |
Het |
| Pcdha6 |
C |
A |
18: 37,102,269 (GRCm39) |
N487K |
probably damaging |
Het |
| Pcsk2 |
A |
G |
2: 143,415,460 (GRCm39) |
D91G |
possibly damaging |
Het |
| Pigp |
A |
G |
16: 94,171,065 (GRCm39) |
F22L |
probably benign |
Het |
| Pnpla8 |
A |
C |
12: 44,329,670 (GRCm39) |
N74T |
probably benign |
Het |
| Ppargc1b |
T |
C |
18: 61,448,980 (GRCm39) |
K114R |
probably damaging |
Het |
| Ppfia2 |
A |
G |
10: 106,693,430 (GRCm39) |
D645G |
probably damaging |
Het |
| Rnf213 |
G |
A |
11: 119,332,854 (GRCm39) |
V2688I |
probably benign |
Het |
| Rnf43 |
A |
G |
11: 87,622,951 (GRCm39) |
H557R |
probably damaging |
Het |
| Rp1l1 |
C |
T |
14: 64,267,545 (GRCm39) |
P1044S |
probably damaging |
Het |
| Rrp9 |
G |
A |
9: 106,360,221 (GRCm39) |
D210N |
probably damaging |
Het |
| Scin |
G |
T |
12: 40,129,807 (GRCm39) |
Q329K |
possibly damaging |
Het |
| Scn7a |
T |
A |
2: 66,534,244 (GRCm39) |
H477L |
probably benign |
Het |
| Slc26a8 |
A |
T |
17: 28,888,914 (GRCm39) |
M195K |
probably benign |
Het |
| Spata13 |
A |
G |
14: 60,993,877 (GRCm39) |
K1110E |
probably damaging |
Het |
| Spata24 |
T |
A |
18: 35,793,503 (GRCm39) |
E103V |
probably damaging |
Het |
| Srek1 |
T |
C |
13: 103,910,894 (GRCm39) |
N25S |
probably damaging |
Het |
| Strada |
T |
C |
11: 106,064,140 (GRCm39) |
Y59C |
probably damaging |
Het |
| Tnrc6c |
T |
C |
11: 117,626,831 (GRCm39) |
W1143R |
probably damaging |
Het |
| Trip12 |
A |
T |
1: 84,738,559 (GRCm39) |
D765E |
probably benign |
Het |
| Ttbk2 |
G |
A |
2: 120,580,798 (GRCm39) |
R444C |
probably damaging |
Het |
| Ush2a |
T |
A |
1: 188,644,303 (GRCm39) |
I4555N |
possibly damaging |
Het |
| Vcan |
C |
T |
13: 89,838,045 (GRCm39) |
E2500K |
probably benign |
Het |
| Vps16 |
A |
G |
2: 130,280,573 (GRCm39) |
Y200C |
possibly damaging |
Het |
| Wdfy4 |
T |
A |
14: 32,693,668 (GRCm39) |
H2719L |
probably damaging |
Het |
| Zfhx2 |
T |
C |
14: 55,311,653 (GRCm39) |
D347G |
possibly damaging |
Het |
| Zfp653 |
G |
A |
9: 21,969,558 (GRCm39) |
T236I |
probably damaging |
Het |
| Zscan4-ps1 |
A |
T |
7: 10,799,913 (GRCm39) |
H325Q |
probably benign |
Het |
|
| Other mutations in Or5b97 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00944:Or5b97
|
APN |
19 |
12,878,719 (GRCm39) |
missense |
probably benign |
0.40 |
|
IGL01704:Or5b97
|
APN |
19 |
12,879,103 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01767:Or5b97
|
APN |
19 |
12,879,112 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL01969:Or5b97
|
APN |
19 |
12,878,416 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
IGL02435:Or5b97
|
APN |
19 |
12,878,391 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02666:Or5b97
|
APN |
19 |
12,878,221 (GRCm39) |
missense |
probably benign |
|
|
IGL03034:Or5b97
|
APN |
19 |
12,879,121 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL03221:Or5b97
|
APN |
19 |
12,878,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0315:Or5b97
|
UTSW |
19 |
12,878,598 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R0550:Or5b97
|
UTSW |
19 |
12,879,164 (GRCm39) |
splice site |
probably null |
|
|
R0729:Or5b97
|
UTSW |
19 |
12,878,259 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1381:Or5b97
|
UTSW |
19 |
12,878,320 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1669:Or5b97
|
UTSW |
19 |
12,878,652 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R1775:Or5b97
|
UTSW |
19 |
12,878,599 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1918:Or5b97
|
UTSW |
19 |
12,878,215 (GRCm39) |
makesense |
probably null |
|
|
R2377:Or5b97
|
UTSW |
19 |
12,878,217 (GRCm39) |
missense |
possibly damaging |
0.45 |
|
R2406:Or5b97
|
UTSW |
19 |
12,878,991 (GRCm39) |
missense |
probably benign |
0.11 |
|
R2471:Or5b97
|
UTSW |
19 |
12,878,679 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2484:Or5b97
|
UTSW |
19 |
12,879,005 (GRCm39) |
missense |
probably benign |
0.06 |
|
R2656:Or5b97
|
UTSW |
19 |
12,879,030 (GRCm39) |
missense |
probably benign |
0.37 |
|
R3888:Or5b97
|
UTSW |
19 |
12,878,497 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4250:Or5b97
|
UTSW |
19 |
12,878,368 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4545:Or5b97
|
UTSW |
19 |
12,878,632 (GRCm39) |
nonsense |
probably null |
|
|
R4895:Or5b97
|
UTSW |
19 |
12,878,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4956:Or5b97
|
UTSW |
19 |
12,878,963 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4991:Or5b97
|
UTSW |
19 |
12,878,815 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5044:Or5b97
|
UTSW |
19 |
12,878,365 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5165:Or5b97
|
UTSW |
19 |
12,878,564 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6025:Or5b97
|
UTSW |
19 |
12,879,034 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6459:Or5b97
|
UTSW |
19 |
12,878,369 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6733:Or5b97
|
UTSW |
19 |
12,878,605 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6789:Or5b97
|
UTSW |
19 |
12,878,653 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6923:Or5b97
|
UTSW |
19 |
12,878,676 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7310:Or5b97
|
UTSW |
19 |
12,878,637 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8552:Or5b97
|
UTSW |
19 |
12,879,096 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8699:Or5b97
|
UTSW |
19 |
12,878,828 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R8735:Or5b97
|
UTSW |
19 |
12,878,274 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8955:Or5b97
|
UTSW |
19 |
12,878,578 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9626:Or5b97
|
UTSW |
19 |
12,878,600 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9631:Or5b97
|
UTSW |
19 |
12,878,502 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R9694:Or5b97
|
UTSW |
19 |
12,879,021 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATGATGGATCACATTGGACTTGC -3'
(R):5'- ACCTAGGGATGATCCTGCTG -3'
Sequencing Primer
(F):5'- TCACATTGGACTTGCAGAAGG -3'
(R):5'- ATGATCCTGCTGATTGTCCTGGAC -3'
|
| Posted On |
2017-10-10 |
Incidental Mutation