Incidental Mutation 'R8155:Or7g32'
| ID |
633267 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or7g32
|
| Ensembl Gene |
ENSMUSG00000052625 |
| Gene Name |
olfactory receptor family 7 subfamily G member 32 |
| Synonyms |
MOR155-1, GA_x6K02T2PVTD-13234278-13235216, Olfr851 |
| MMRRC Submission |
067581-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.127)
|
| Stock # |
R8155 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
19404591-19414111 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 19389453 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Aspartic acid
at position 31
(V31D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000076569
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077347]
[ENSMUST00000211832]
|
| AlphaFold |
Q7TRG0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000077347
AA Change: V31D
PolyPhen 2
Score 0.166 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000076569
Gene: ENSMUSG00000094535
AA Change: V31D
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
21 |
N/A |
INTRINSIC |
|
Pfam:7tm_4
|
34 |
311 |
1.8e-51 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
38 |
304 |
1e-6 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
5.1e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000211832
AA Change: V28D
PolyPhen 2
Score 0.166 (Sensitivity: 0.92; Specificity: 0.87)
|
| Meta Mutation Damage Score |
0.0846 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.5%
- 20x: 98.9%
|
| Validation Efficiency |
100% (62/62) |
| 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: 62 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca12 |
G |
A |
1: 71,330,497 (GRCm39) |
T1386I |
probably damaging |
Het |
| Abcb6 |
A |
T |
1: 75,151,413 (GRCm39) |
V504E |
probably damaging |
Het |
| Abtb3 |
G |
A |
10: 85,476,473 (GRCm39) |
|
probably null |
Het |
| Adprhl1 |
C |
T |
8: 13,271,764 (GRCm39) |
A1665T |
probably damaging |
Het |
| Arhgap32 |
T |
A |
9: 32,093,196 (GRCm39) |
L183H |
probably damaging |
Het |
| Arhgef12 |
A |
G |
9: 42,953,958 (GRCm39) |
L24S |
probably damaging |
Het |
| B3gnt4 |
C |
T |
5: 123,649,426 (GRCm39) |
H264Y |
possibly damaging |
Het |
| Cfi |
A |
G |
3: 129,648,739 (GRCm39) |
T208A |
probably benign |
Het |
| Chd4 |
T |
A |
6: 125,082,287 (GRCm39) |
F605Y |
probably benign |
Het |
| Cimap1d |
A |
T |
10: 79,481,466 (GRCm39) |
V21E |
probably benign |
Het |
| Clip1 |
A |
G |
5: 123,751,699 (GRCm39) |
L694P |
|
Het |
| Crybb3 |
A |
T |
5: 113,225,466 (GRCm39) |
D135E |
probably damaging |
Het |
| Ddx60 |
T |
A |
8: 62,470,205 (GRCm39) |
S1398T |
possibly damaging |
Het |
| Dusp5 |
T |
A |
19: 53,529,537 (GRCm39) |
Y313* |
probably null |
Het |
| Eloa |
A |
G |
4: 135,734,438 (GRCm39) |
V689A |
probably benign |
Het |
| Ep300 |
T |
A |
15: 81,505,269 (GRCm39) |
Y630N |
unknown |
Het |
| Galnt5 |
A |
T |
2: 57,889,427 (GRCm39) |
K342N |
probably benign |
Het |
| Gm4841 |
A |
G |
18: 60,403,409 (GRCm39) |
V228A |
probably damaging |
Het |
| Gna14 |
A |
T |
19: 16,576,338 (GRCm39) |
D115V |
probably benign |
Het |
| Gpx5 |
T |
C |
13: 21,472,917 (GRCm39) |
D139G |
probably damaging |
Het |
| Hmcn1 |
G |
T |
1: 150,480,705 (GRCm39) |
N4490K |
probably damaging |
Het |
| Hsp90aa1 |
T |
C |
12: 110,661,828 (GRCm39) |
S63G |
unknown |
Het |
| Itpkb |
T |
C |
1: 180,159,913 (GRCm39) |
I13T |
possibly damaging |
Het |
| Itprid2 |
T |
C |
2: 79,475,177 (GRCm39) |
S379P |
probably benign |
Het |
| Lamb2 |
C |
T |
9: 108,357,845 (GRCm39) |
R123W |
probably damaging |
Het |
| Ldha |
A |
G |
7: 46,503,508 (GRCm39) |
H300R |
probably damaging |
Het |
| Lrp2 |
A |
G |
2: 69,313,342 (GRCm39) |
L2463P |
possibly damaging |
Het |
| Morf4l1 |
A |
G |
9: 89,977,225 (GRCm39) |
I232T |
probably damaging |
Het |
| Mtg1 |
A |
G |
7: 139,724,622 (GRCm39) |
H166R |
probably benign |
Het |
| Or14a260 |
A |
G |
7: 85,985,386 (GRCm39) |
S73P |
probably damaging |
Het |
| Or2ad1 |
A |
G |
13: 21,327,062 (GRCm39) |
L55P |
probably damaging |
Het |
| Or52r1 |
C |
T |
7: 102,536,452 (GRCm39) |
D303N |
probably benign |
Het |
| Or5d46 |
A |
G |
2: 88,170,296 (GRCm39) |
N129S |
probably damaging |
Het |
| Or6d12 |
T |
A |
6: 116,492,813 (GRCm39) |
V25E |
probably benign |
Het |
| Papss2 |
A |
G |
19: 32,618,742 (GRCm39) |
T267A |
probably benign |
Het |
| Park7 |
G |
A |
4: 150,991,547 (GRCm39) |
R48C |
possibly damaging |
Het |
| Pecr |
A |
G |
1: 72,309,443 (GRCm39) |
V199A |
probably damaging |
Het |
| Pla2g10 |
G |
A |
16: 13,543,048 (GRCm39) |
R80W |
probably damaging |
Het |
| Plek2 |
G |
A |
12: 78,943,066 (GRCm39) |
R77* |
probably null |
Het |
| Psg23 |
A |
G |
7: 18,346,179 (GRCm39) |
L172P |
probably damaging |
Het |
| Psg25 |
A |
C |
7: 18,260,445 (GRCm39) |
F151C |
probably benign |
Het |
| Ptpn3 |
G |
T |
4: 57,232,336 (GRCm39) |
H433Q |
probably benign |
Het |
| Rasal3 |
A |
G |
17: 32,616,381 (GRCm39) |
V294A |
possibly damaging |
Het |
| Rnf6 |
T |
C |
5: 146,147,815 (GRCm39) |
D401G |
probably damaging |
Het |
| Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
| Sema3d |
T |
C |
5: 12,498,148 (GRCm39) |
|
probably null |
Het |
| Serpinb1c |
A |
T |
13: 33,081,038 (GRCm39) |
L15Q |
probably damaging |
Het |
| Slfn3 |
T |
A |
11: 83,103,611 (GRCm39) |
Y161N |
probably damaging |
Het |
| Spns2 |
T |
C |
11: 72,347,394 (GRCm39) |
M404V |
possibly damaging |
Het |
| Stk39 |
T |
A |
2: 68,097,410 (GRCm39) |
I479L |
probably damaging |
Het |
| Tbx15 |
C |
A |
3: 99,259,886 (GRCm39) |
Q586K |
possibly damaging |
Het |
| Thap11 |
C |
T |
8: 106,582,854 (GRCm39) |
R288* |
probably null |
Het |
| Tm7sf2 |
T |
A |
19: 6,114,125 (GRCm39) |
D236V |
probably damaging |
Het |
| Tmem214 |
T |
C |
5: 31,029,136 (GRCm39) |
S192P |
possibly damaging |
Het |
| Tnfaip3 |
A |
G |
10: 18,880,439 (GRCm39) |
S543P |
possibly damaging |
Het |
| Traf3ip3 |
A |
G |
1: 192,860,524 (GRCm39) |
L466P |
probably damaging |
Het |
| Tspan18 |
C |
T |
2: 93,040,357 (GRCm39) |
|
probably null |
Het |
| Vmn1r229 |
T |
A |
17: 21,035,472 (GRCm39) |
L239Q |
probably damaging |
Het |
| Vsig2 |
T |
C |
9: 37,455,329 (GRCm39) |
V293A |
possibly damaging |
Het |
| Wdfy4 |
A |
T |
14: 32,884,776 (GRCm39) |
V42D |
|
Het |
| Wnk2 |
G |
A |
13: 49,192,577 (GRCm39) |
P2055S |
unknown |
Het |
| Zfp953 |
C |
A |
13: 67,491,535 (GRCm39) |
C139F |
probably damaging |
Het |
|
| Other mutations in Or7g32 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00094:Or7g32
|
APN |
9 |
19,408,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01992:Or7g32
|
APN |
9 |
19,408,070 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02455:Or7g32
|
APN |
9 |
19,408,559 (GRCm39) |
nonsense |
probably null |
|
|
IGL02468:Or7g32
|
APN |
9 |
19,408,473 (GRCm39) |
missense |
probably benign |
|
|
IGL02685:Or7g32
|
APN |
9 |
19,408,098 (GRCm39) |
missense |
probably benign |
|
|
IGL02723:Or7g32
|
APN |
9 |
19,388,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03294:Or7g32
|
APN |
9 |
19,389,285 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
PIT4305001:Or7g32
|
UTSW |
9 |
19,389,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0153:Or7g32
|
UTSW |
9 |
19,408,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0364:Or7g32
|
UTSW |
9 |
19,389,268 (GRCm39) |
nonsense |
probably null |
|
|
R0379:Or7g32
|
UTSW |
9 |
19,388,776 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R0449:Or7g32
|
UTSW |
9 |
19,389,388 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R0682:Or7g32
|
UTSW |
9 |
19,388,645 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0693:Or7g32
|
UTSW |
9 |
19,389,268 (GRCm39) |
nonsense |
probably null |
|
|
R0789:Or7g32
|
UTSW |
9 |
19,408,458 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R1484:Or7g32
|
UTSW |
9 |
19,389,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1599:Or7g32
|
UTSW |
9 |
19,389,517 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1626:Or7g32
|
UTSW |
9 |
19,389,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1742:Or7g32
|
UTSW |
9 |
19,389,337 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2041:Or7g32
|
UTSW |
9 |
19,408,131 (GRCm39) |
missense |
probably benign |
|
|
R2060:Or7g32
|
UTSW |
9 |
19,408,533 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4232:Or7g32
|
UTSW |
9 |
19,389,022 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4237:Or7g32
|
UTSW |
9 |
19,388,893 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4474:Or7g32
|
UTSW |
9 |
19,408,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5081:Or7g32
|
UTSW |
9 |
19,408,557 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5116:Or7g32
|
UTSW |
9 |
19,389,094 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R5643:Or7g32
|
UTSW |
9 |
19,388,853 (GRCm39) |
missense |
probably benign |
0.22 |
|
R6271:Or7g32
|
UTSW |
9 |
19,389,337 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6815:Or7g32
|
UTSW |
9 |
19,389,061 (GRCm39) |
missense |
probably benign |
0.20 |
|
R6853:Or7g32
|
UTSW |
9 |
19,408,102 (GRCm39) |
nonsense |
probably null |
|
|
R7150:Or7g32
|
UTSW |
9 |
19,408,145 (GRCm39) |
missense |
probably benign |
0.44 |
|
R7222:Or7g32
|
UTSW |
9 |
19,388,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7378:Or7g32
|
UTSW |
9 |
19,408,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7456:Or7g32
|
UTSW |
9 |
19,408,844 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7527:Or7g32
|
UTSW |
9 |
19,408,685 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7587:Or7g32
|
UTSW |
9 |
19,408,818 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7592:Or7g32
|
UTSW |
9 |
19,389,128 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8215:Or7g32
|
UTSW |
9 |
19,408,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8220:Or7g32
|
UTSW |
9 |
19,408,317 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8296:Or7g32
|
UTSW |
9 |
19,408,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8732:Or7g32
|
UTSW |
9 |
19,408,098 (GRCm39) |
missense |
probably benign |
|
|
R8813:Or7g32
|
UTSW |
9 |
19,389,477 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R9152:Or7g32
|
UTSW |
9 |
19,408,448 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9187:Or7g32
|
UTSW |
9 |
19,389,166 (GRCm39) |
missense |
probably benign |
|
|
R9528:Or7g32
|
UTSW |
9 |
19,389,444 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9789:Or7g32
|
UTSW |
9 |
19,389,382 (GRCm39) |
missense |
probably benign |
0.35 |
|
R9795:Or7g32
|
UTSW |
9 |
19,408,412 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF034:Or7g32
|
UTSW |
9 |
19,388,928 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
X0058:Or7g32
|
UTSW |
9 |
19,389,519 (GRCm39) |
missense |
probably benign |
0.10 |
|
Z1177:Or7g32
|
UTSW |
9 |
19,388,633 (GRCm39) |
frame shift |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GGCAGCCTTTGTATGTAATGC -3'
(R):5'- ACTTCAGACTTCAGGAATACTACTC -3'
Sequencing Primer
(F):5'- CAGCCTTTGTATGTAATGCTTTGAC -3'
(R):5'- CTACTCCAAAAAGGTCTTAGGTGTGG -3'
|
| Posted On |
2020-06-30 |
Incidental Mutation