Incidental Mutation 'R2925:Or8k32'
| ID |
255689 |
| 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 |
040510-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.070)
|
| Stock # |
R2925 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
86368310-86369257 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 86368891 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Asparagine
at position 121
(D121N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151072
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099882]
[ENSMUST00000111582]
[ENSMUST00000216480]
|
| AlphaFold |
Q8VF52 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000099882
AA Change: D123N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000097467
Gene: ENSMUSG00000075179
AA Change: D123N
| 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 |
probably damaging
Transcript: ENSMUST00000111582
AA Change: D121N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000107208
Gene: ENSMUSG00000075179
AA Change: D121N
| 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 |
probably damaging
Transcript: ENSMUST00000216480
AA Change: D121N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Meta Mutation Damage Score |
0.1666 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.2%
|
| 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: 41 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930503E14Rik |
T |
C |
14: 44,407,755 (GRCm39) |
T93A |
probably damaging |
Het |
| Acte1 |
A |
T |
7: 143,437,736 (GRCm39) |
R147* |
probably null |
Het |
| Akr1c21 |
A |
G |
13: 4,626,349 (GRCm39) |
|
probably null |
Het |
| Alk |
A |
G |
17: 72,910,202 (GRCm39) |
V168A |
probably benign |
Het |
| Ap4b1 |
A |
G |
3: 103,727,997 (GRCm39) |
E337G |
probably damaging |
Het |
| Bltp1 |
G |
T |
3: 37,061,271 (GRCm39) |
A3327S |
probably damaging |
Het |
| Btn2a2 |
A |
G |
13: 23,665,984 (GRCm39) |
S283P |
probably damaging |
Het |
| Ctcfl |
C |
T |
2: 172,936,489 (GRCm39) |
E628K |
probably damaging |
Het |
| Cul9 |
G |
A |
17: 46,821,907 (GRCm39) |
T1856M |
probably benign |
Het |
| Defb41 |
T |
C |
1: 18,330,857 (GRCm39) |
D30G |
probably damaging |
Het |
| Dnai1 |
A |
T |
4: 41,597,919 (GRCm39) |
I74F |
probably damaging |
Het |
| Ecpas |
T |
A |
4: 58,833,928 (GRCm39) |
K851* |
probably null |
Het |
| Fbln2 |
T |
A |
6: 91,242,837 (GRCm39) |
C846S |
probably damaging |
Het |
| Fuom |
T |
C |
7: 139,679,862 (GRCm39) |
T110A |
probably benign |
Het |
| Hsp90aa1 |
C |
A |
12: 110,662,115 (GRCm39) |
|
probably null |
Het |
| Hsp90aa1 |
T |
A |
12: 110,662,114 (GRCm39) |
M1L |
possibly damaging |
Het |
| Il12a |
TCAC |
TC |
3: 68,605,320 (GRCm39) |
|
probably null |
Het |
| Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
| Lyz3 |
C |
T |
10: 117,070,336 (GRCm39) |
R147Q |
probably benign |
Het |
| Man2b2 |
A |
G |
5: 36,981,446 (GRCm39) |
F224L |
probably benign |
Het |
| Mtbp |
G |
A |
15: 55,483,210 (GRCm39) |
R429Q |
probably benign |
Het |
| Ncapg2 |
C |
A |
12: 116,402,349 (GRCm39) |
T727K |
probably benign |
Het |
| Nek4 |
G |
A |
14: 30,673,667 (GRCm39) |
G29S |
probably benign |
Het |
| Nsf |
C |
T |
11: 103,821,578 (GRCm39) |
E26K |
possibly damaging |
Het |
| Nup214 |
A |
G |
2: 31,888,015 (GRCm39) |
K15E |
probably damaging |
Het |
| Or5ac24 |
A |
T |
16: 59,165,706 (GRCm39) |
Y119* |
probably null |
Het |
| Or5m11b |
T |
A |
2: 85,806,125 (GRCm39) |
C179* |
probably null |
Het |
| Or9a4 |
T |
A |
6: 40,548,342 (GRCm39) |
S7R |
probably benign |
Het |
| P2ry13 |
G |
A |
3: 59,116,801 (GRCm39) |
H326Y |
probably benign |
Het |
| Plec |
A |
G |
15: 76,062,452 (GRCm39) |
F2563S |
probably damaging |
Het |
| Rc3h1 |
A |
G |
1: 160,782,546 (GRCm39) |
Y675C |
probably damaging |
Het |
| Samd3 |
T |
A |
10: 26,127,785 (GRCm39) |
S288T |
probably benign |
Het |
| Scaf4 |
G |
T |
16: 90,047,177 (GRCm39) |
P400Q |
unknown |
Het |
| Selplg |
T |
C |
5: 113,958,240 (GRCm39) |
D22G |
possibly damaging |
Het |
| Slc30a6 |
T |
C |
17: 74,708,999 (GRCm39) |
|
probably benign |
Het |
| Syt3 |
T |
A |
7: 44,045,222 (GRCm39) |
V518E |
probably damaging |
Het |
| Tnks |
G |
A |
8: 35,432,815 (GRCm39) |
A2V |
unknown |
Het |
| Upk3a |
A |
G |
15: 84,902,350 (GRCm39) |
Y59C |
probably benign |
Het |
| Usp4 |
T |
C |
9: 108,245,055 (GRCm39) |
L331P |
probably damaging |
Het |
| Zbed5 |
A |
G |
5: 129,932,039 (GRCm39) |
T663A |
possibly damaging |
Het |
| Zbtb11 |
G |
A |
16: 55,794,447 (GRCm39) |
R8Q |
probably benign |
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 |
|
R4370:Or8k32
|
UTSW |
2 |
86,368,764 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
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'- TATCAAGGGAAGACCATCACAG -3'
(R):5'- GGAATCAAGGCTGCAAACAC -3'
Sequencing Primer
(F):5'- CCATCACAGTAGAAATGAGGGATGAC -3'
(R):5'- GGCTGCAAACACCTATGTACTTC -3'
|
| Posted On |
2014-12-29 |
Incidental Mutation