Incidental Mutation 'R9750:Or1d2'
| ID |
732477 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or1d2
|
| Ensembl Gene |
ENSMUSG00000058275 |
| Gene Name |
olfactory receptor family 1 subfamily D member 2 |
| Synonyms |
Olfr412, GA_x6K02T2P1NL-4500587-4501525, MOR127-5P |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.265)
|
| Stock # |
R9750 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
74255497-74256435 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 74255858 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 121
(D121G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149922
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077794]
[ENSMUST00000216362]
|
| AlphaFold |
Q7TRW7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000077794
AA Change: D121G
PolyPhen 2
Score 0.842 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000076967
Gene: ENSMUSG00000058275
AA Change: D121G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
1.7e-51 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
172 |
1.8e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
289 |
3.8e-28 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216362
AA Change: D121G
PolyPhen 2
Score 0.842 (Sensitivity: 0.83; Specificity: 0.93)
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.2%
- 20x: 97.9%
|
| 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: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts2 |
G |
T |
11: 50,494,333 (GRCm39) |
V136L |
probably benign |
Het |
| Adamtsl3 |
G |
T |
7: 82,244,589 (GRCm39) |
L1348F |
probably benign |
Het |
| Amotl1 |
T |
A |
9: 14,504,102 (GRCm39) |
T369S |
probably benign |
Het |
| Anapc2 |
T |
G |
2: 25,174,982 (GRCm39) |
V700G |
possibly damaging |
Het |
| Aox3 |
C |
T |
1: 58,215,648 (GRCm39) |
Q1027* |
probably null |
Het |
| Ap5m1 |
A |
G |
14: 49,317,756 (GRCm39) |
T338A |
probably benign |
Het |
| Carf |
T |
A |
1: 60,171,158 (GRCm39) |
Y240* |
probably null |
Het |
| Ccl21a |
G |
A |
4: 42,773,875 (GRCm39) |
A15V |
probably benign |
Het |
| Dcst1 |
A |
T |
3: 89,261,462 (GRCm39) |
I429N |
probably damaging |
Het |
| Esco1 |
A |
G |
18: 10,594,510 (GRCm39) |
S259P |
probably benign |
Het |
| Esp15 |
A |
G |
17: 39,955,603 (GRCm39) |
M57V |
probably benign |
Het |
| Fat3 |
A |
G |
9: 15,915,157 (GRCm39) |
I1597T |
probably benign |
Het |
| Fbxo38 |
T |
C |
18: 62,674,061 (GRCm39) |
S7G |
probably benign |
Het |
| Gm11562 |
G |
A |
11: 99,510,856 (GRCm39) |
P115S |
unknown |
Het |
| Hectd4 |
A |
T |
5: 121,448,744 (GRCm39) |
Y364F |
probably benign |
Het |
| Kansl1l |
G |
C |
1: 66,817,150 (GRCm39) |
I403M |
probably benign |
Het |
| Kmt2a |
T |
C |
9: 44,747,499 (GRCm39) |
H1505R |
unknown |
Het |
| Krt79 |
T |
G |
15: 101,839,196 (GRCm39) |
E424D |
probably benign |
Het |
| Lpgat1 |
T |
A |
1: 191,510,587 (GRCm39) |
F391I |
probably benign |
Het |
| Ltbr |
G |
A |
6: 125,284,348 (GRCm39) |
R365W |
probably damaging |
Het |
| Mon1a |
T |
A |
9: 107,778,778 (GRCm39) |
V334E |
probably damaging |
Het |
| Ngef |
G |
A |
1: 87,431,010 (GRCm39) |
P269L |
probably damaging |
Het |
| Nup210l |
A |
T |
3: 90,117,659 (GRCm39) |
|
probably null |
Het |
| Obscn |
G |
A |
11: 59,024,682 (GRCm39) |
R453W |
probably benign |
Het |
| Pdzd8 |
A |
G |
19: 59,289,684 (GRCm39) |
V572A |
probably benign |
Het |
| Pgr |
T |
C |
9: 8,901,918 (GRCm39) |
S484P |
possibly damaging |
Het |
| Pygl |
G |
T |
12: 70,245,303 (GRCm39) |
S473R |
possibly damaging |
Het |
| Samd1 |
T |
C |
8: 84,725,989 (GRCm39) |
V410A |
probably damaging |
Het |
| Serpina3j |
T |
G |
12: 104,280,942 (GRCm39) |
H38Q |
probably benign |
Het |
| Shprh |
A |
G |
10: 11,040,204 (GRCm39) |
Y559C |
probably damaging |
Het |
| Skint5 |
T |
A |
4: 113,727,866 (GRCm39) |
D426V |
unknown |
Het |
| Slc25a21 |
T |
C |
12: 56,785,382 (GRCm39) |
K158R |
probably benign |
Het |
| Smc1b |
A |
T |
15: 85,016,106 (GRCm39) |
N11K |
probably damaging |
Het |
| St18 |
T |
C |
1: 6,873,216 (GRCm39) |
V317A |
probably benign |
Het |
| Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
| Tcap |
A |
G |
11: 98,275,228 (GRCm39) |
T121A |
probably benign |
Het |
| Tgs1 |
C |
A |
4: 3,585,869 (GRCm39) |
Q249K |
probably damaging |
Het |
| Tiam1 |
A |
T |
16: 89,695,394 (GRCm39) |
L21Q |
probably damaging |
Het |
| Tmem131l |
G |
A |
3: 83,831,358 (GRCm39) |
A858V |
probably damaging |
Het |
| Trpm3 |
G |
A |
19: 22,903,495 (GRCm39) |
R927H |
probably benign |
Het |
| Wdfy3 |
T |
A |
5: 102,077,960 (GRCm39) |
H870L |
probably benign |
Het |
| Zfp518a |
T |
A |
19: 40,903,889 (GRCm39) |
C1273S |
possibly damaging |
Het |
| Zfp960 |
A |
T |
17: 17,307,898 (GRCm39) |
H204L |
probably damaging |
Het |
|
| Other mutations in Or1d2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01327:Or1d2
|
APN |
11 |
74,255,738 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL01395:Or1d2
|
APN |
11 |
74,255,713 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01418:Or1d2
|
APN |
11 |
74,255,810 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
IGL01645:Or1d2
|
APN |
11 |
74,256,359 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02421:Or1d2
|
APN |
11 |
74,256,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02424:Or1d2
|
APN |
11 |
74,256,299 (GRCm39) |
missense |
probably benign |
0.09 |
|
R0206:Or1d2
|
UTSW |
11 |
74,255,968 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0206:Or1d2
|
UTSW |
11 |
74,255,968 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0278:Or1d2
|
UTSW |
11 |
74,256,028 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0698:Or1d2
|
UTSW |
11 |
74,255,968 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1424:Or1d2
|
UTSW |
11 |
74,255,780 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1549:Or1d2
|
UTSW |
11 |
74,256,076 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1659:Or1d2
|
UTSW |
11 |
74,255,759 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1755:Or1d2
|
UTSW |
11 |
74,255,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2031:Or1d2
|
UTSW |
11 |
74,255,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2185:Or1d2
|
UTSW |
11 |
74,255,572 (GRCm39) |
missense |
probably benign |
|
|
R3620:Or1d2
|
UTSW |
11 |
74,256,050 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4568:Or1d2
|
UTSW |
11 |
74,256,035 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4878:Or1d2
|
UTSW |
11 |
74,255,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7779:Or1d2
|
UTSW |
11 |
74,255,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8086:Or1d2
|
UTSW |
11 |
74,255,780 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9155:Or1d2
|
UTSW |
11 |
74,255,791 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9396:Or1d2
|
UTSW |
11 |
74,256,089 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTCATCATCCTGGCCATTG -3'
(R):5'- TGTAGTGGATTTTCCGAGACC -3'
Sequencing Primer
(F):5'- GCCATTGGCTCTGACTCG -3'
(R):5'- CCACAGAAGGTTACTCTGGTCATG -3'
|
| Posted On |
2022-11-14 |
Incidental Mutation