Incidental Mutation 'R8387:Or4c113'
| ID |
647189 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4c113
|
| Ensembl Gene |
ENSMUSG00000075105 |
| Gene Name |
olfactory receptor family 4 subfamily C member 113 |
| Synonyms |
GA_x6K02T2Q125-50536041-50535106, Olfr1218, MOR233-12 |
| MMRRC Submission |
067876-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.071)
|
| Stock # |
R8387 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
88884833-88885768 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 88885646 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Methionine
at position 41
(I41M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149558
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099798]
[ENSMUST00000213609]
[ENSMUST00000215048]
[ENSMUST00000215054]
|
| AlphaFold |
L7MU54 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099798
AA Change: I41M
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000097386
Gene: ENSMUSG00000075105
AA Change: I41M
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
303 |
1.4e-45 |
PFAM |
|
Pfam:7tm_1
|
39 |
286 |
2.2e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213609
AA Change: I41M
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215048
AA Change: I41M
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215054
AA Change: I41M
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
98% (46/47) |
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb1b |
G |
A |
5: 8,874,698 (GRCm39) |
D453N |
probably damaging |
Het |
| Arl14ep |
T |
C |
2: 106,799,562 (GRCm39) |
D93G |
probably damaging |
Het |
| Bcl7b |
T |
C |
5: 135,197,413 (GRCm39) |
I18T |
probably damaging |
Het |
| Cdh1 |
A |
G |
8: 107,390,501 (GRCm39) |
I614V |
probably benign |
Het |
| Cpa3 |
T |
C |
3: 20,281,400 (GRCm39) |
I169V |
probably benign |
Het |
| Cpeb4 |
T |
C |
11: 31,858,877 (GRCm39) |
|
probably null |
Het |
| Csmd1 |
G |
A |
8: 16,050,484 (GRCm39) |
H2251Y |
possibly damaging |
Het |
| Dab2ip |
T |
A |
2: 35,609,870 (GRCm39) |
I695K |
probably damaging |
Het |
| Dhtkd1 |
C |
A |
2: 5,934,479 (GRCm39) |
L230F |
possibly damaging |
Het |
| Emc1 |
T |
C |
4: 139,088,600 (GRCm39) |
S353P |
probably benign |
Het |
| Erc2 |
T |
A |
14: 27,375,253 (GRCm39) |
L157Q |
possibly damaging |
Het |
| Flvcr1 |
A |
G |
1: 190,743,731 (GRCm39) |
|
probably null |
Het |
| Fryl |
A |
C |
5: 73,293,663 (GRCm39) |
|
probably null |
Het |
| Gnl2 |
T |
C |
4: 124,949,127 (GRCm39) |
*729Q |
probably null |
Het |
| Gpr63 |
G |
A |
4: 25,008,301 (GRCm39) |
V342M |
possibly damaging |
Het |
| Guf1 |
C |
T |
5: 69,723,810 (GRCm39) |
P463L |
probably damaging |
Het |
| Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
| Ifngr2 |
T |
C |
16: 91,358,535 (GRCm39) |
L245P |
probably damaging |
Het |
| Igsf10 |
A |
G |
3: 59,236,564 (GRCm39) |
F1206L |
probably damaging |
Het |
| Ktn1 |
T |
A |
14: 47,944,744 (GRCm39) |
|
probably null |
Het |
| Lekr1 |
A |
G |
3: 65,591,520 (GRCm39) |
K86E |
possibly damaging |
Het |
| Lrrc3 |
C |
T |
10: 77,737,346 (GRCm39) |
G30D |
possibly damaging |
Het |
| Mapk8ip2 |
T |
C |
15: 89,344,897 (GRCm39) |
F765L |
probably damaging |
Het |
| Myo6 |
A |
G |
9: 80,183,632 (GRCm39) |
T676A |
unknown |
Het |
| Nr4a1 |
T |
C |
15: 101,171,053 (GRCm39) |
S510P |
probably damaging |
Het |
| Or2o1 |
T |
C |
11: 49,051,497 (GRCm39) |
S219P |
probably damaging |
Het |
| Or4c11c |
G |
A |
2: 88,661,633 (GRCm39) |
M57I |
possibly damaging |
Het |
| Or51e1 |
C |
T |
7: 102,359,402 (GRCm39) |
T312I |
probably benign |
Het |
| Or5a1 |
A |
G |
19: 12,097,785 (GRCm39) |
L97P |
probably damaging |
Het |
| Pdcd1 |
G |
A |
1: 93,969,193 (GRCm39) |
L42F |
probably damaging |
Het |
| Pdzd7 |
T |
C |
19: 45,018,490 (GRCm39) |
D621G |
probably damaging |
Het |
| Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
| Pias4 |
G |
A |
10: 80,990,342 (GRCm39) |
R398C |
probably benign |
Het |
| Plekha6 |
A |
T |
1: 133,219,893 (GRCm39) |
|
probably null |
Het |
| Prkag3 |
A |
G |
1: 74,784,854 (GRCm39) |
|
probably null |
Het |
| Ptpn7 |
A |
G |
1: 135,061,606 (GRCm39) |
T23A |
probably benign |
Het |
| Ptprd |
T |
C |
4: 75,873,526 (GRCm39) |
D1069G |
probably damaging |
Het |
| Ptprr |
A |
G |
10: 116,087,030 (GRCm39) |
Y503C |
probably damaging |
Het |
| Slc26a8 |
T |
C |
17: 28,866,899 (GRCm39) |
D610G |
probably benign |
Het |
| Smyd4 |
A |
G |
11: 75,292,984 (GRCm39) |
N638S |
probably benign |
Het |
| Tenm3 |
A |
G |
8: 48,740,883 (GRCm39) |
F1200S |
probably damaging |
Het |
| Tox3 |
A |
G |
8: 90,984,595 (GRCm39) |
S195P |
probably benign |
Het |
| Trim44 |
T |
C |
2: 102,230,518 (GRCm39) |
E171G |
probably damaging |
Het |
| Vars1 |
T |
A |
17: 35,229,490 (GRCm39) |
M369K |
probably damaging |
Het |
| Vmn2r77 |
C |
A |
7: 86,450,947 (GRCm39) |
Q278K |
probably benign |
Het |
| Zfp345 |
T |
C |
2: 150,314,740 (GRCm39) |
T266A |
probably damaging |
Het |
|
| Other mutations in Or4c113 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01652:Or4c113
|
APN |
2 |
88,884,913 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03089:Or4c113
|
APN |
2 |
88,885,357 (GRCm39) |
missense |
probably benign |
0.34 |
|
IGL03387:Or4c113
|
APN |
2 |
88,885,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0350:Or4c113
|
UTSW |
2 |
88,885,700 (GRCm39) |
missense |
probably benign |
0.10 |
|
R0699:Or4c113
|
UTSW |
2 |
88,885,636 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R1609:Or4c113
|
UTSW |
2 |
88,885,688 (GRCm39) |
missense |
probably benign |
|
|
R1856:Or4c113
|
UTSW |
2 |
88,885,203 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1972:Or4c113
|
UTSW |
2 |
88,884,891 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2066:Or4c113
|
UTSW |
2 |
88,885,243 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2921:Or4c113
|
UTSW |
2 |
88,884,843 (GRCm39) |
missense |
probably benign |
0.04 |
|
R2923:Or4c113
|
UTSW |
2 |
88,884,843 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4037:Or4c113
|
UTSW |
2 |
88,885,032 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4585:Or4c113
|
UTSW |
2 |
88,885,498 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R4586:Or4c113
|
UTSW |
2 |
88,885,498 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R5041:Or4c113
|
UTSW |
2 |
88,885,265 (GRCm39) |
nonsense |
probably null |
|
|
R5124:Or4c113
|
UTSW |
2 |
88,885,431 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5138:Or4c113
|
UTSW |
2 |
88,885,291 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5415:Or4c113
|
UTSW |
2 |
88,885,240 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5501:Or4c113
|
UTSW |
2 |
88,885,230 (GRCm39) |
nonsense |
probably null |
|
|
R5941:Or4c113
|
UTSW |
2 |
88,884,963 (GRCm39) |
missense |
probably benign |
|
|
R5991:Or4c113
|
UTSW |
2 |
88,885,126 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6396:Or4c113
|
UTSW |
2 |
88,885,641 (GRCm39) |
missense |
probably benign |
0.36 |
|
R7047:Or4c113
|
UTSW |
2 |
88,885,490 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8038:Or4c113
|
UTSW |
2 |
88,885,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8403:Or4c113
|
UTSW |
2 |
88,884,948 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8794:Or4c113
|
UTSW |
2 |
88,885,477 (GRCm39) |
missense |
probably benign |
|
|
R8907:Or4c113
|
UTSW |
2 |
88,885,542 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCATGCAACAGCCAAAGGAG -3'
(R):5'- ATTCAAGAGCGTTGTACCCC -3'
Sequencing Primer
(F):5'- CAGCCAAAGGAGATGGTCTTC -3'
(R):5'- AATAGACTCCTCAATGCAAA -3'
|
| Posted On |
2020-09-02 |
Incidental Mutation