Incidental Mutation 'R6729:Or4d10c'
| ID |
529993 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4d10c
|
| Ensembl Gene |
ENSMUSG00000044994 |
| Gene Name |
olfactory receptor family 4 subfamily D member 10C |
| Synonyms |
Olfr1426, MOR239-1, GA_x6K02T2RE5P-2447610-2446675 |
| MMRRC Submission |
044847-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.139)
|
| Stock # |
R6729 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
12064974-12069211 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 12065860 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Leucine
at position 99
(M99L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151988
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000112952]
[ENSMUST00000208703]
[ENSMUST00000217952]
[ENSMUST00000219005]
[ENSMUST00000219155]
[ENSMUST00000219996]
[ENSMUST00000220005]
|
| AlphaFold |
Q8VG74 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000112952
AA Change: M99L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000108575
Gene: ENSMUSG00000044994
AA Change: M99L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
302 |
2.1e-49 |
PFAM |
|
Pfam:7tm_1
|
39 |
300 |
1.1e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000208703
AA Change: M99L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217952
AA Change: M99L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000219005
AA Change: M99L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000219155
AA Change: M99L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000219996
AA Change: M99L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000220005
AA Change: M99L
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.4%
- 20x: 95.5%
|
| Validation Efficiency |
100% (34/34) |
| 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: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acad12 |
A |
T |
5: 121,745,998 (GRCm39) |
H230Q |
probably damaging |
Het |
| AI182371 |
G |
T |
2: 34,974,717 (GRCm39) |
|
probably benign |
Het |
| Ank3 |
T |
C |
10: 69,644,755 (GRCm39) |
V73A |
probably damaging |
Het |
| Apbb1 |
A |
T |
7: 105,214,588 (GRCm39) |
M28K |
probably damaging |
Het |
| Atp6v1f |
A |
G |
6: 29,467,964 (GRCm39) |
D50G |
probably benign |
Het |
| Bltp3b |
T |
A |
10: 89,641,546 (GRCm39) |
S906T |
probably benign |
Het |
| Cdkal1 |
G |
A |
13: 29,658,678 (GRCm39) |
T356M |
probably damaging |
Het |
| Clca3a1 |
A |
G |
3: 144,711,727 (GRCm39) |
I756T |
probably damaging |
Het |
| Cplane1 |
T |
C |
15: 8,218,085 (GRCm39) |
|
probably null |
Het |
| Cyp17a1 |
A |
G |
19: 46,659,020 (GRCm39) |
V207A |
probably benign |
Het |
| Dnah7c |
A |
G |
1: 46,711,681 (GRCm39) |
E2636G |
possibly damaging |
Het |
| Gm13090 |
A |
T |
4: 151,174,085 (GRCm39) |
|
probably benign |
Het |
| Nceh1 |
T |
A |
3: 27,295,420 (GRCm39) |
L227* |
probably null |
Het |
| Nedd9 |
A |
G |
13: 41,469,278 (GRCm39) |
M625T |
probably damaging |
Het |
| Or10n1 |
A |
T |
9: 39,525,069 (GRCm39) |
M69L |
probably benign |
Het |
| Or4d1 |
G |
A |
11: 87,805,676 (GRCm39) |
Q19* |
probably null |
Het |
| Or8b53 |
A |
G |
9: 38,667,124 (GRCm39) |
I47V |
probably benign |
Het |
| Pcsk4 |
T |
C |
10: 80,160,935 (GRCm39) |
N297S |
probably damaging |
Het |
| Psg21 |
T |
A |
7: 18,386,516 (GRCm39) |
I157F |
probably damaging |
Het |
| Rabep2 |
T |
C |
7: 126,039,369 (GRCm39) |
V294A |
probably benign |
Het |
| Rsph1 |
A |
G |
17: 31,496,226 (GRCm39) |
S2P |
unknown |
Het |
| Sacs |
A |
G |
14: 61,447,967 (GRCm39) |
K3338E |
probably damaging |
Het |
| Slc35f4 |
T |
G |
14: 49,556,417 (GRCm39) |
N112T |
probably benign |
Het |
| Slc43a3 |
T |
C |
2: 84,768,629 (GRCm39) |
F83L |
probably damaging |
Het |
| Slc6a15 |
T |
C |
10: 103,229,775 (GRCm39) |
V154A |
probably damaging |
Het |
| Synj2 |
T |
A |
17: 6,036,289 (GRCm39) |
M1K |
probably null |
Het |
| Tcp1 |
G |
A |
17: 13,142,140 (GRCm39) |
R378Q |
probably damaging |
Het |
| Tead2 |
A |
G |
7: 44,866,658 (GRCm39) |
T6A |
probably benign |
Het |
| Tpte |
G |
T |
8: 22,845,491 (GRCm39) |
V514L |
probably damaging |
Het |
| Trpm6 |
A |
G |
19: 18,807,661 (GRCm39) |
N1069D |
probably damaging |
Het |
| Vmn2r105 |
C |
A |
17: 20,428,605 (GRCm39) |
G824C |
probably damaging |
Het |
| Yod1 |
G |
A |
1: 130,645,275 (GRCm39) |
G19S |
probably damaging |
Het |
| Zfp934 |
A |
T |
13: 62,640,746 (GRCm39) |
N2K |
probably damaging |
Het |
|
| Other mutations in Or4d10c |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00092:Or4d10c
|
APN |
19 |
12,065,357 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL01549:Or4d10c
|
APN |
19 |
12,065,329 (GRCm39) |
missense |
probably benign |
0.20 |
|
IGL02479:Or4d10c
|
APN |
19 |
12,065,269 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03065:Or4d10c
|
APN |
19 |
12,065,975 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL03092:Or4d10c
|
APN |
19 |
12,065,230 (GRCm39) |
nonsense |
probably null |
|
|
IGL03046:Or4d10c
|
UTSW |
19 |
12,065,391 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0734:Or4d10c
|
UTSW |
19 |
12,065,483 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1190:Or4d10c
|
UTSW |
19 |
12,066,051 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R1990:Or4d10c
|
UTSW |
19 |
12,065,620 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2331:Or4d10c
|
UTSW |
19 |
12,065,522 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3500:Or4d10c
|
UTSW |
19 |
12,065,421 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R3768:Or4d10c
|
UTSW |
19 |
12,065,304 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3825:Or4d10c
|
UTSW |
19 |
12,065,391 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4589:Or4d10c
|
UTSW |
19 |
12,065,305 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R5175:Or4d10c
|
UTSW |
19 |
12,065,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6436:Or4d10c
|
UTSW |
19 |
12,065,299 (GRCm39) |
missense |
probably benign |
0.24 |
|
R6965:Or4d10c
|
UTSW |
19 |
12,066,120 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7099:Or4d10c
|
UTSW |
19 |
12,065,530 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7393:Or4d10c
|
UTSW |
19 |
12,065,992 (GRCm39) |
missense |
probably benign |
0.13 |
|
R7582:Or4d10c
|
UTSW |
19 |
12,065,370 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8000:Or4d10c
|
UTSW |
19 |
12,065,358 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8803:Or4d10c
|
UTSW |
19 |
12,065,469 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8833:Or4d10c
|
UTSW |
19 |
12,065,643 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8846:Or4d10c
|
UTSW |
19 |
12,065,433 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8951:Or4d10c
|
UTSW |
19 |
12,066,056 (GRCm39) |
nonsense |
probably null |
|
|
R9469:Or4d10c
|
UTSW |
19 |
12,065,434 (GRCm39) |
missense |
probably benign |
0.20 |
|
RF011:Or4d10c
|
UTSW |
19 |
12,065,611 (GRCm39) |
missense |
probably benign |
0.09 |
|
Z1177:Or4d10c
|
UTSW |
19 |
12,065,308 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCAGCAAGAGAGAAATCTGCAC -3'
(R):5'- CTCCTGGTGTATGTGACAACTC -3'
Sequencing Primer
(F):5'- CAAGAGAGAAATCTGCACTATGG -3'
(R):5'- TATGTGACAACTCTGCTGGGGAAC -3'
|
| Posted On |
2018-08-01 |
Incidental Mutation