Incidental Mutation 'R4370:Or8k32'
| ID |
325943 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or8k32
|
| Ensembl Gene |
ENSMUSG00000075179 |
| Gene Name |
olfactory receptor family 8 subfamily K member 32 |
| Synonyms |
GA_x6K02T2Q125-48024195-48023254, MOR189-1, Olfr1079 |
| MMRRC Submission |
041674-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.070)
|
| Stock # |
R4370 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
86368310-86369257 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 86368764 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 165
(I165N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097467
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099882]
[ENSMUST00000111582]
[ENSMUST00000216480]
|
| AlphaFold |
Q8VF52 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000099882
AA Change: I165N
PolyPhen 2
Score 0.781 (Sensitivity: 0.85; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000097467
Gene: ENSMUSG00000075179
AA Change: I165N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srsx
|
37 |
175 |
1.2e-7 |
PFAM |
|
Pfam:7tm_1
|
43 |
292 |
7.1e-32 |
PFAM |
|
Pfam:7tm_4
|
141 |
285 |
1.3e-43 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000111582
AA Change: I163N
PolyPhen 2
Score 0.740 (Sensitivity: 0.85; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000107208
Gene: ENSMUSG00000075179
AA Change: I163N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
308 |
1.6e-48 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
175 |
1.2e-7 |
PFAM |
|
Pfam:7tm_1
|
43 |
292 |
2.4e-20 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216480
AA Change: I163N
PolyPhen 2
Score 0.740 (Sensitivity: 0.85; Specificity: 0.92)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.9%
|
| 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: 34 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acoxl |
T |
A |
2: 127,720,708 (GRCm39) |
D190E |
possibly damaging |
Het |
| Alg11 |
C |
A |
8: 22,558,095 (GRCm39) |
A469E |
probably benign |
Het |
| Armc2 |
A |
T |
10: 41,793,196 (GRCm39) |
N809K |
probably benign |
Het |
| B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
| Bmal2 |
A |
T |
6: 146,711,149 (GRCm39) |
E51V |
probably damaging |
Het |
| Cage1 |
G |
A |
13: 38,209,626 (GRCm39) |
S11F |
probably damaging |
Het |
| Car15 |
T |
C |
16: 17,653,299 (GRCm39) |
I289M |
probably damaging |
Het |
| Cdhr18 |
C |
T |
14: 13,862,375 (GRCm38) |
S393N |
probably benign |
Het |
| Cfap100 |
A |
T |
6: 90,390,376 (GRCm39) |
I242N |
probably damaging |
Het |
| Dst |
GAA |
GA |
1: 34,290,809 (GRCm39) |
|
probably null |
Het |
| Epdr1 |
C |
A |
13: 19,803,576 (GRCm39) |
V53F |
probably benign |
Het |
| Igfn1 |
A |
G |
1: 135,895,844 (GRCm39) |
M1574T |
probably benign |
Het |
| Kat6a |
T |
C |
8: 23,401,945 (GRCm39) |
I438T |
possibly damaging |
Het |
| Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
| Krtap4-7 |
G |
A |
11: 99,534,543 (GRCm39) |
P107S |
unknown |
Het |
| Lrp6 |
A |
C |
6: 134,483,321 (GRCm39) |
Y461* |
probably null |
Het |
| Mecom |
T |
A |
3: 30,011,504 (GRCm39) |
E723V |
probably damaging |
Het |
| Nsd3 |
T |
A |
8: 26,138,524 (GRCm39) |
I258N |
probably benign |
Het |
| Or10q12 |
T |
C |
19: 13,746,315 (GRCm39) |
V203A |
probably benign |
Het |
| Or5k8 |
T |
A |
16: 58,644,956 (GRCm39) |
M39L |
probably benign |
Het |
| Rb1cc1 |
A |
G |
1: 6,318,771 (GRCm39) |
D730G |
probably damaging |
Het |
| Sacs |
A |
G |
14: 61,449,758 (GRCm39) |
R3935G |
probably damaging |
Het |
| Setd5 |
A |
G |
6: 113,098,766 (GRCm39) |
K800E |
probably damaging |
Het |
| Slc26a4 |
G |
T |
12: 31,579,475 (GRCm39) |
Q596K |
probably benign |
Het |
| Slc38a4 |
T |
A |
15: 96,906,965 (GRCm39) |
N258Y |
possibly damaging |
Het |
| Sntb1 |
A |
G |
15: 55,655,487 (GRCm39) |
I243T |
probably damaging |
Het |
| Sspo |
A |
G |
6: 48,443,282 (GRCm39) |
S2051G |
probably null |
Het |
| Sys1 |
T |
C |
2: 164,303,315 (GRCm39) |
W10R |
probably damaging |
Het |
| Tgm2 |
G |
A |
2: 157,966,221 (GRCm39) |
R478* |
probably null |
Het |
| Tgm6 |
T |
C |
2: 129,985,525 (GRCm39) |
Y443H |
probably benign |
Het |
| Tor2a |
T |
A |
2: 32,648,870 (GRCm39) |
D113E |
probably benign |
Het |
| Trio |
C |
A |
15: 27,748,423 (GRCm39) |
E1266* |
probably null |
Het |
| Usp40 |
T |
C |
1: 87,925,597 (GRCm39) |
I211V |
probably benign |
Het |
| Zfp791 |
C |
T |
8: 85,840,235 (GRCm39) |
V11M |
probably damaging |
Het |
|
| Other mutations in Or8k32 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01109:Or8k32
|
APN |
2 |
86,368,674 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL02289:Or8k32
|
APN |
2 |
86,368,792 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL02794:Or8k32
|
APN |
2 |
86,368,492 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R1498:Or8k32
|
UTSW |
2 |
86,368,902 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1923:Or8k32
|
UTSW |
2 |
86,368,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2195:Or8k32
|
UTSW |
2 |
86,369,247 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2211:Or8k32
|
UTSW |
2 |
86,368,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2925:Or8k32
|
UTSW |
2 |
86,368,891 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4430:Or8k32
|
UTSW |
2 |
86,368,731 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4678:Or8k32
|
UTSW |
2 |
86,369,077 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4790:Or8k32
|
UTSW |
2 |
86,369,224 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R4996:Or8k32
|
UTSW |
2 |
86,368,615 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5905:Or8k32
|
UTSW |
2 |
86,369,113 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5984:Or8k32
|
UTSW |
2 |
86,368,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6028:Or8k32
|
UTSW |
2 |
86,369,113 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6878:Or8k32
|
UTSW |
2 |
86,369,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7579:Or8k32
|
UTSW |
2 |
86,368,872 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7942:Or8k32
|
UTSW |
2 |
86,368,566 (GRCm39) |
missense |
probably benign |
0.42 |
|
R8079:Or8k32
|
UTSW |
2 |
86,368,725 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R8465:Or8k32
|
UTSW |
2 |
86,368,731 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGAAAGCCTTCCGTCTTCCC -3'
(R):5'- TGGTTATTCAACTGCTATTGGACC -3'
Sequencing Primer
(F):5'- CCTCAGCAGAGTTCATTCTGAG -3'
(R):5'- CTGCTATTGGACCTAAAATGTTAGC -3'
|
| Posted On |
2015-07-06 |
Incidental Mutation