Incidental Mutation 'R8389:Or8g32'
| ID |
647288 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or8g32
|
| Ensembl Gene |
ENSMUSG00000094269 |
| Gene Name |
olfactory receptor family 8 subfamily G member 32 |
| Synonyms |
GA_x6K02T2PVTD-33090395-33091330, MOR171-33P, MOR171-49, Olfr951 |
| MMRRC Submission |
067754-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.074)
|
| Stock # |
R8389 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
39305089-39306033 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 39305912 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Arginine
at position 272
(K272R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150976
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078531]
[ENSMUST00000216107]
|
| AlphaFold |
Q9EQ94 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000078531
AA Change: K275R
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000077615
Gene: ENSMUSG00000094269
AA Change: K275R
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
311 |
2.5e-52 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
5e-19 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216107
AA Change: K272R
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| 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: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acadl |
C |
T |
1: 66,893,906 (GRCm39) |
G83E |
probably damaging |
Het |
| Adamtsl2 |
A |
G |
2: 26,993,136 (GRCm39) |
D722G |
possibly damaging |
Het |
| Akap11 |
A |
T |
14: 78,756,322 (GRCm39) |
D25E |
|
Het |
| Akr1c21 |
C |
T |
13: 4,626,278 (GRCm39) |
R101W |
probably damaging |
Het |
| Ano2 |
T |
C |
6: 125,957,132 (GRCm39) |
Y634H |
probably damaging |
Het |
| Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
| Cfap221 |
T |
C |
1: 119,851,301 (GRCm39) |
E820G |
probably damaging |
Het |
| Chad |
A |
G |
11: 94,458,718 (GRCm39) |
D289G |
probably benign |
Het |
| Col4a2 |
C |
A |
8: 11,498,132 (GRCm39) |
A1647E |
probably damaging |
Het |
| Dhx32 |
G |
T |
7: 133,326,935 (GRCm39) |
T522K |
possibly damaging |
Het |
| Eloa |
A |
G |
4: 135,733,622 (GRCm39) |
V707A |
probably benign |
Het |
| Fam219a |
A |
G |
4: 41,520,935 (GRCm39) |
S109P |
probably damaging |
Het |
| Ftl1 |
A |
T |
7: 45,108,651 (GRCm39) |
F36I |
probably benign |
Het |
| Furin |
C |
T |
7: 80,040,627 (GRCm39) |
R737Q |
probably benign |
Het |
| Gm40460 |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
7: 141,794,171 (GRCm39) |
|
probably benign |
Het |
| Gpt |
C |
T |
15: 76,583,242 (GRCm39) |
T393M |
probably damaging |
Het |
| Greb1l |
A |
T |
18: 10,529,613 (GRCm39) |
D865V |
probably benign |
Het |
| Ifi207 |
GTT |
GT |
1: 173,557,016 (GRCm39) |
|
probably null |
Het |
| Klk1b11 |
G |
A |
7: 43,649,120 (GRCm39) |
C219Y |
probably damaging |
Het |
| Lcn11 |
A |
T |
2: 25,669,043 (GRCm39) |
D117V |
probably damaging |
Het |
| Lrpprc |
A |
T |
17: 85,080,742 (GRCm39) |
V161D |
possibly damaging |
Het |
| Lrrk2 |
T |
C |
15: 91,584,194 (GRCm39) |
L318S |
probably damaging |
Het |
| Muc5b |
A |
G |
7: 141,415,516 (GRCm39) |
T2821A |
possibly damaging |
Het |
| Mysm1 |
A |
G |
4: 94,853,849 (GRCm39) |
M250T |
probably benign |
Het |
| Nol12 |
A |
G |
15: 78,819,268 (GRCm39) |
K27E |
probably damaging |
Het |
| Omg |
T |
A |
11: 79,393,001 (GRCm39) |
M286L |
probably benign |
Het |
| Or4c100 |
G |
A |
2: 88,355,931 (GRCm39) |
M1I |
probably null |
Het |
| Pdyn |
A |
G |
2: 129,530,357 (GRCm39) |
L104P |
probably benign |
Het |
| Pira2 |
A |
C |
7: 3,846,888 (GRCm39) |
L218R |
probably damaging |
Het |
| Pnpt1 |
A |
T |
11: 29,080,758 (GRCm39) |
M1L |
unknown |
Het |
| Pofut2 |
C |
T |
10: 77,101,785 (GRCm39) |
T274M |
probably benign |
Het |
| Pramel34 |
A |
T |
5: 93,785,587 (GRCm39) |
F231Y |
probably benign |
Het |
| Rbm12b1 |
C |
A |
4: 12,146,363 (GRCm39) |
D778E |
probably damaging |
Het |
| Srsf12 |
C |
G |
4: 33,226,070 (GRCm39) |
P111R |
probably damaging |
Het |
| Tbc1d14 |
G |
A |
5: 36,687,792 (GRCm39) |
|
probably benign |
Het |
| Tcf23 |
A |
G |
5: 31,127,464 (GRCm39) |
K89E |
probably benign |
Het |
| Tmem74 |
C |
T |
15: 43,730,315 (GRCm39) |
G243R |
probably damaging |
Het |
| Ufd1 |
T |
C |
16: 18,639,853 (GRCm39) |
V119A |
possibly damaging |
Het |
| Vmn2r72 |
A |
T |
7: 85,401,168 (GRCm39) |
Y84N |
probably damaging |
Het |
| Zfp120 |
A |
T |
2: 149,959,327 (GRCm39) |
C354S |
probably damaging |
Het |
| Zfp69 |
G |
A |
4: 120,806,549 (GRCm39) |
T28I |
possibly damaging |
Het |
| Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
| Zfp959 |
T |
C |
17: 56,204,299 (GRCm39) |
V112A |
probably benign |
Het |
| Zfr2 |
T |
A |
10: 81,081,323 (GRCm39) |
W458R |
probably benign |
Het |
|
| Other mutations in Or8g32 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01527:Or8g32
|
APN |
9 |
39,305,114 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01650:Or8g32
|
APN |
9 |
39,305,252 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02134:Or8g32
|
APN |
9 |
39,305,830 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03113:Or8g32
|
APN |
9 |
39,305,981 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0127:Or8g32
|
UTSW |
9 |
39,305,238 (GRCm39) |
missense |
probably benign |
0.16 |
|
R1730:Or8g32
|
UTSW |
9 |
39,305,518 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1783:Or8g32
|
UTSW |
9 |
39,305,518 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1924:Or8g32
|
UTSW |
9 |
39,305,163 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R3785:Or8g32
|
UTSW |
9 |
39,305,678 (GRCm39) |
missense |
probably benign |
0.07 |
|
R3787:Or8g32
|
UTSW |
9 |
39,305,678 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4607:Or8g32
|
UTSW |
9 |
39,306,031 (GRCm39) |
makesense |
probably null |
|
|
R4803:Or8g32
|
UTSW |
9 |
39,305,932 (GRCm39) |
missense |
probably benign |
0.26 |
|
R5314:Or8g32
|
UTSW |
9 |
39,305,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5338:Or8g32
|
UTSW |
9 |
39,305,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5360:Or8g32
|
UTSW |
9 |
39,305,698 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5468:Or8g32
|
UTSW |
9 |
39,305,257 (GRCm39) |
missense |
probably benign |
0.33 |
|
R6590:Or8g32
|
UTSW |
9 |
39,305,845 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6690:Or8g32
|
UTSW |
9 |
39,305,845 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6925:Or8g32
|
UTSW |
9 |
39,305,157 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6925:Or8g32
|
UTSW |
9 |
39,305,156 (GRCm39) |
missense |
probably benign |
0.32 |
|
R6982:Or8g32
|
UTSW |
9 |
39,305,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7662:Or8g32
|
UTSW |
9 |
39,305,389 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8074:Or8g32
|
UTSW |
9 |
39,305,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9444:Or8g32
|
UTSW |
9 |
39,305,365 (GRCm39) |
missense |
probably benign |
0.19 |
|
R9642:Or8g32
|
UTSW |
9 |
39,305,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTCCCAATGCTGACCATTATTAC -3'
(R):5'- GCATAAGGATCCATGTCTTCCATAC -3'
Sequencing Primer
(F):5'- CAATGCTGACCATTATTACTTCCTAC -3'
(R):5'- TCAAAGGTTTCTAGCAAATGAGC -3'
|
| Posted On |
2020-09-02 |
Incidental Mutation