Incidental Mutation 'R1132:Or12d12'
| ID |
94766 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or12d12
|
| Ensembl Gene |
ENSMUSG00000092077 |
| Gene Name |
olfactory receptor family 12 subfamily D member 12 |
| Synonyms |
Olfr101, MOR250-2, GA_x6K02T2PSCP-1761617-1760691 |
| MMRRC Submission |
039205-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.119)
|
| Stock # |
R1132 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
37610337-37611375 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 37610423 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glycine
at position 297
(R297G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149851
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058046]
[ENSMUST00000214376]
[ENSMUST00000215392]
|
| AlphaFold |
Q920Z0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000058046
AA Change: R297G
PolyPhen 2
Score 0.195 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000061042
Gene: ENSMUSG00000092077
AA Change: R297G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
3.3e-53 |
PFAM |
|
Pfam:7tm_1
|
39 |
289 |
3e-20 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214376
AA Change: R297G
PolyPhen 2
Score 0.195 (Sensitivity: 0.92; Specificity: 0.87)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215392
AA Change: R297G
PolyPhen 2
Score 0.195 (Sensitivity: 0.92; Specificity: 0.87)
|
| Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.7%
|
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Apba1 |
T |
C |
19: 23,894,917 (GRCm39) |
V451A |
possibly damaging |
Het |
| Atxn2l |
CCAGCAGCAGCAGCAGCAGC |
CCAGCAGCAGCAGCAGC |
7: 126,093,420 (GRCm39) |
|
probably benign |
Het |
| C3 |
C |
T |
17: 57,514,531 (GRCm39) |
|
probably null |
Het |
| Car9 |
G |
T |
4: 43,512,439 (GRCm39) |
|
probably null |
Het |
| Cd163 |
G |
T |
6: 124,286,055 (GRCm39) |
G202* |
probably null |
Het |
| Cdk8 |
A |
G |
5: 146,236,625 (GRCm39) |
T347A |
probably benign |
Het |
| Cep170 |
C |
A |
1: 176,577,603 (GRCm39) |
R1257L |
probably damaging |
Het |
| Cib1 |
A |
G |
7: 79,877,778 (GRCm39) |
F168S |
probably damaging |
Het |
| Cntnap5c |
G |
A |
17: 58,601,351 (GRCm39) |
G833D |
probably damaging |
Het |
| Dhx37 |
A |
T |
5: 125,498,103 (GRCm39) |
I702N |
probably damaging |
Het |
| Dnah3 |
T |
C |
7: 119,538,227 (GRCm39) |
K3586R |
possibly damaging |
Het |
| Fbxo31 |
ACGGCGCGGCG |
ACGGCGCGGCGCGGCG |
8: 122,279,015 (GRCm39) |
|
probably null |
Het |
| Fbxo31 |
CGCGG |
CGCGGAGCGG |
8: 122,279,019 (GRCm39) |
|
probably null |
Het |
| Fhod3 |
TGAGGAGGAGGAGGAGGA |
TGAGGAGGAGGAGGA |
18: 25,153,722 (GRCm39) |
|
probably benign |
Het |
| Gaa |
T |
C |
11: 119,175,885 (GRCm39) |
S953P |
probably damaging |
Het |
| Inpp5j |
T |
C |
11: 3,452,305 (GRCm39) |
E315G |
possibly damaging |
Het |
| Itsn2 |
T |
C |
12: 4,708,464 (GRCm39) |
Y840H |
probably damaging |
Het |
| Kif1a |
T |
C |
1: 92,983,743 (GRCm39) |
E653G |
probably damaging |
Het |
| Loxhd1 |
T |
C |
18: 77,517,639 (GRCm39) |
V1829A |
possibly damaging |
Het |
| Myh8 |
C |
T |
11: 67,187,957 (GRCm39) |
Q910* |
probably null |
Het |
| Or14a257 |
A |
T |
7: 86,138,425 (GRCm39) |
F111L |
probably benign |
Het |
| Or14j4 |
G |
T |
17: 37,921,333 (GRCm39) |
T103K |
possibly damaging |
Het |
| Or2ag17 |
A |
T |
7: 106,389,758 (GRCm39) |
I150N |
possibly damaging |
Het |
| Prdm4 |
A |
G |
10: 85,735,145 (GRCm39) |
S666P |
probably damaging |
Het |
| Rad50 |
T |
C |
11: 53,585,788 (GRCm39) |
K331E |
possibly damaging |
Het |
| Rbbp6 |
A |
G |
7: 122,599,336 (GRCm39) |
|
probably benign |
Het |
| Selenbp1 |
C |
G |
3: 94,844,644 (GRCm39) |
I100M |
probably benign |
Het |
| Skint6 |
A |
G |
4: 112,755,296 (GRCm39) |
|
probably null |
Het |
| Stac3 |
T |
C |
10: 127,343,128 (GRCm39) |
S208P |
probably benign |
Het |
| Tfap2a |
T |
C |
13: 40,874,867 (GRCm39) |
|
probably null |
Het |
| Trhde |
T |
C |
10: 114,248,383 (GRCm39) |
K939E |
possibly damaging |
Het |
| Vmn1r22 |
T |
C |
6: 57,877,826 (GRCm39) |
I50M |
probably benign |
Het |
| Vmn1r39 |
C |
T |
6: 66,781,428 (GRCm39) |
V260I |
probably benign |
Het |
| Zdhhc25 |
T |
C |
15: 88,484,926 (GRCm39) |
L87P |
probably damaging |
Het |
| Zfp202 |
T |
C |
9: 40,122,318 (GRCm39) |
L360P |
probably benign |
Het |
|
| Other mutations in Or12d12 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01583:Or12d12
|
APN |
17 |
37,610,629 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01584:Or12d12
|
APN |
17 |
37,610,629 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01609:Or12d12
|
APN |
17 |
37,610,629 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01739:Or12d12
|
APN |
17 |
37,610,673 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03203:Or12d12
|
APN |
17 |
37,611,317 (GRCm39) |
splice site |
probably benign |
|
|
R1122:Or12d12
|
UTSW |
17 |
37,611,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1237:Or12d12
|
UTSW |
17 |
37,611,156 (GRCm39) |
missense |
probably benign |
0.19 |
|
R3423:Or12d12
|
UTSW |
17 |
37,610,761 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3872:Or12d12
|
UTSW |
17 |
37,610,870 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3873:Or12d12
|
UTSW |
17 |
37,610,870 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3874:Or12d12
|
UTSW |
17 |
37,610,870 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4871:Or12d12
|
UTSW |
17 |
37,611,095 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5213:Or12d12
|
UTSW |
17 |
37,610,942 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5974:Or12d12
|
UTSW |
17 |
37,611,229 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R6294:Or12d12
|
UTSW |
17 |
37,610,444 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8784:Or12d12
|
UTSW |
17 |
37,610,701 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9469:Or12d12
|
UTSW |
17 |
37,610,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGGCCACAAATTAAGCTTCCTTTGC -3'
(R):5'- CATGCTCCACAAAGCTCTGTCTACC -3'
Sequencing Primer
(F):5'- AAGCTTCCTTTGCTTTAAAACATC -3'
(R):5'- ACAAAGCTCTGTCTACCTGTGC -3'
|
| Posted On |
2014-01-05 |
Incidental Mutation