Incidental Mutation 'IGL01109:Or8k32'
| ID |
50536 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or8k32
|
| Ensembl Gene |
ENSMUSG00000075179 |
| Gene Name |
olfactory receptor family 8 subfamily K member 32 |
| Synonyms |
GA_x6K02T2Q125-48024195-48023254, MOR189-1, Olfr1079 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.070)
|
| Stock # |
IGL01109
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
86368310-86369257 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 86368674 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 195
(D195V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097467
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099882]
[ENSMUST00000111582]
[ENSMUST00000216480]
|
| AlphaFold |
Q8VF52 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099882
AA Change: D195V
PolyPhen 2
Score 0.121 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000097467
Gene: ENSMUSG00000075179
AA Change: D195V
| 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 benign
Transcript: ENSMUST00000111582
AA Change: D193V
PolyPhen 2
Score 0.099 (Sensitivity: 0.93; Specificity: 0.85)
|
| SMART Domains |
Protein: ENSMUSP00000107208
Gene: ENSMUSG00000075179
AA Change: D193V
| 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 benign
Transcript: ENSMUST00000216480
AA Change: D193V
PolyPhen 2
Score 0.099 (Sensitivity: 0.93; Specificity: 0.85)
|
| Coding Region Coverage |
|
| 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: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Alpk2 |
T |
C |
18: 65,440,211 (GRCm39) |
D861G |
probably benign |
Het |
| Anapc4 |
A |
G |
5: 53,005,970 (GRCm39) |
T326A |
probably damaging |
Het |
| Atm |
T |
C |
9: 53,401,593 (GRCm39) |
I1425M |
probably damaging |
Het |
| Bend5 |
T |
C |
4: 111,305,838 (GRCm39) |
L294P |
probably damaging |
Het |
| Casp7 |
T |
A |
19: 56,425,177 (GRCm39) |
D193E |
probably benign |
Het |
| Cdc16 |
T |
C |
8: 13,814,606 (GRCm39) |
V130A |
probably benign |
Het |
| Chl1 |
T |
G |
6: 103,692,354 (GRCm39) |
Y331D |
probably damaging |
Het |
| Cntn1 |
C |
A |
15: 92,237,458 (GRCm39) |
Y1017* |
probably null |
Het |
| Cyb5d1 |
C |
A |
11: 69,284,610 (GRCm39) |
|
probably null |
Het |
| Cyp2c38 |
A |
G |
19: 39,451,329 (GRCm39) |
|
probably null |
Het |
| Dzip3 |
T |
C |
16: 48,750,037 (GRCm39) |
M827V |
probably benign |
Het |
| Ehd1 |
T |
A |
19: 6,348,177 (GRCm39) |
M385K |
possibly damaging |
Het |
| Eya3 |
C |
A |
4: 132,420,311 (GRCm39) |
Y52* |
probably null |
Het |
| Itsn1 |
C |
T |
16: 91,603,089 (GRCm39) |
|
probably benign |
Het |
| Ktn1 |
A |
T |
14: 47,952,178 (GRCm39) |
N983I |
probably damaging |
Het |
| Lrrk2 |
T |
A |
15: 91,623,035 (GRCm39) |
N1068K |
probably damaging |
Het |
| Mup6 |
T |
A |
4: 60,006,001 (GRCm39) |
N156K |
probably damaging |
Het |
| Nedd9 |
T |
A |
13: 41,469,710 (GRCm39) |
H481L |
probably benign |
Het |
| Obscn |
T |
C |
11: 59,024,588 (GRCm39) |
D484G |
probably damaging |
Het |
| Ogdh |
T |
C |
11: 6,298,790 (GRCm39) |
V674A |
probably damaging |
Het |
| Or4a27 |
T |
C |
2: 88,559,409 (GRCm39) |
D178G |
probably damaging |
Het |
| Or4f54 |
G |
A |
2: 111,122,864 (GRCm39) |
D84N |
probably benign |
Het |
| Or5b113 |
A |
G |
19: 13,342,063 (GRCm39) |
I24V |
probably benign |
Het |
| Or5d38 |
T |
C |
2: 87,955,023 (GRCm39) |
Q102R |
probably damaging |
Het |
| Or8g53 |
T |
C |
9: 39,683,293 (GRCm39) |
M268V |
probably benign |
Het |
| Osbpl6 |
A |
G |
2: 76,379,871 (GRCm39) |
T154A |
probably damaging |
Het |
| P2rx1 |
T |
C |
11: 72,899,041 (GRCm39) |
V84A |
probably damaging |
Het |
| Pcdh11x |
G |
A |
X: 119,310,611 (GRCm39) |
V685I |
possibly damaging |
Het |
| Ppp4r3b |
T |
A |
11: 29,138,288 (GRCm39) |
V212E |
probably damaging |
Het |
| Prune2 |
A |
G |
19: 17,101,243 (GRCm39) |
D2249G |
probably benign |
Het |
| Slc5a8 |
T |
A |
10: 88,742,254 (GRCm39) |
S317T |
possibly damaging |
Het |
| Ssc5d |
T |
A |
7: 4,940,111 (GRCm39) |
L822* |
probably null |
Het |
| Swt1 |
A |
G |
1: 151,286,890 (GRCm39) |
S201P |
probably damaging |
Het |
| Tet1 |
T |
A |
10: 62,715,553 (GRCm39) |
M81L |
probably benign |
Het |
| Tex9 |
T |
A |
9: 72,395,349 (GRCm39) |
N39I |
probably damaging |
Het |
| Ttc4 |
T |
C |
4: 106,520,360 (GRCm39) |
Y378C |
probably damaging |
Het |
| Ubap2 |
T |
C |
4: 41,195,155 (GRCm39) |
N1131S |
probably damaging |
Het |
| Ugt2b35 |
C |
T |
5: 87,156,165 (GRCm39) |
T419I |
probably damaging |
Het |
| Ugt3a1 |
T |
G |
15: 9,367,354 (GRCm39) |
F366V |
probably damaging |
Het |
| Zfp324 |
A |
G |
7: 12,703,362 (GRCm39) |
T95A |
probably benign |
Het |
|
| Other mutations in Or8k32 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
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 |
|
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 |
|
| Posted On |
2013-06-21 |
Incidental Mutation