Incidental Mutation 'R8920:Or7g18'
| ID |
679198 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or7g18
|
| Ensembl Gene |
ENSMUSG00000062868 |
| Gene Name |
olfactory receptor family 7 subfamily G member 18 |
| Synonyms |
GA_x6K02T2PVTD-12618399-12619337, Olfr830, MOR152-1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.122)
|
| Stock # |
R8920 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
18786256-18787572 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 18787394 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Lysine
at position 254
(T254K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148394
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078861]
[ENSMUST00000212723]
|
| AlphaFold |
Q8VFJ5 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000078861
AA Change: T257K
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000077903
Gene: ENSMUSG00000062868
AA Change: T257K
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
311 |
1.8e-51 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
1.6e-20 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000212723
AA Change: T254K
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.5%
|
| 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: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Anxa10 |
T |
A |
8: 62,527,580 (GRCm39) |
Q160L |
probably benign |
Het |
| Apc2 |
A |
T |
10: 80,149,934 (GRCm39) |
I1663L |
probably benign |
Het |
| Bahcc1 |
C |
G |
11: 120,175,331 (GRCm39) |
R1802G |
probably damaging |
Het |
| C1qtnf1 |
T |
C |
11: 118,339,068 (GRCm39) |
V246A |
possibly damaging |
Het |
| Cbl |
A |
G |
9: 44,078,570 (GRCm39) |
M267T |
probably damaging |
Het |
| Cd300lf |
T |
C |
11: 115,017,180 (GRCm39) |
K48E |
probably benign |
Het |
| Cfap46 |
G |
T |
7: 139,232,442 (GRCm39) |
N840K |
|
Het |
| Cfap54 |
T |
A |
10: 92,776,199 (GRCm39) |
|
probably null |
Het |
| Cnrip1 |
A |
C |
11: 17,005,003 (GRCm39) |
K184N |
unknown |
Het |
| Dnah11 |
A |
T |
12: 118,077,674 (GRCm39) |
L1273Q |
probably damaging |
Het |
| Dyrk1a |
T |
G |
16: 94,460,488 (GRCm39) |
I48R |
probably benign |
Het |
| Exoc7 |
T |
C |
11: 116,180,055 (GRCm39) |
E683G |
probably benign |
Het |
| Hdac1-ps |
A |
G |
17: 78,799,171 (GRCm39) |
Y54C |
probably benign |
Het |
| Igtp |
A |
T |
11: 58,096,999 (GRCm39) |
I57F |
probably damaging |
Het |
| Inhbb |
T |
C |
1: 119,345,107 (GRCm39) |
N394S |
probably damaging |
Het |
| Jag1 |
T |
C |
2: 136,931,143 (GRCm39) |
H663R |
probably benign |
Het |
| Kcna6 |
A |
G |
6: 126,716,610 (GRCm39) |
F93S |
probably damaging |
Het |
| L1td1 |
C |
A |
4: 98,624,864 (GRCm39) |
S353* |
probably null |
Het |
| Lgals12 |
T |
C |
19: 7,576,166 (GRCm39) |
I253V |
possibly damaging |
Het |
| Lgals4 |
C |
T |
7: 28,540,289 (GRCm39) |
R195C |
probably benign |
Het |
| Lrp1b |
A |
T |
2: 42,213,610 (GRCm39) |
D67E |
|
Het |
| Lrrc43 |
T |
C |
5: 123,639,194 (GRCm39) |
S408P |
probably benign |
Het |
| Madd |
T |
C |
2: 91,007,168 (GRCm39) |
I315V |
probably benign |
Het |
| Mdn1 |
T |
C |
4: 32,719,280 (GRCm39) |
F2281S |
probably damaging |
Het |
| Med13l |
A |
T |
5: 118,885,543 (GRCm39) |
K1499* |
probably null |
Het |
| Myoc |
A |
G |
1: 162,475,127 (GRCm39) |
E226G |
probably benign |
Het |
| Nmur1 |
T |
C |
1: 86,315,577 (GRCm39) |
Y96C |
probably damaging |
Het |
| Nwd2 |
A |
T |
5: 63,948,863 (GRCm39) |
D145V |
probably damaging |
Het |
| Paqr8 |
A |
T |
1: 21,005,245 (GRCm39) |
Q133L |
probably damaging |
Het |
| Plbd2 |
T |
C |
5: 120,630,915 (GRCm39) |
D230G |
probably damaging |
Het |
| Plekha7 |
A |
G |
7: 115,744,218 (GRCm39) |
I694T |
probably benign |
Het |
| Rnf139 |
C |
T |
15: 58,771,529 (GRCm39) |
T518I |
possibly damaging |
Het |
| Ryr1 |
G |
T |
7: 28,789,640 (GRCm39) |
S1498R |
possibly damaging |
Het |
| Senp6 |
T |
A |
9: 79,999,561 (GRCm39) |
S72T |
probably benign |
Het |
| Slc12a7 |
C |
T |
13: 73,946,568 (GRCm39) |
P554S |
probably damaging |
Het |
| Slc6a2 |
C |
A |
8: 93,687,990 (GRCm39) |
R39S |
probably benign |
Het |
| Snrpe |
T |
G |
1: 133,534,199 (GRCm39) |
H88P |
probably benign |
Het |
| Stard9 |
T |
A |
2: 120,533,088 (GRCm39) |
V3115E |
probably damaging |
Het |
| Stk39 |
C |
T |
2: 68,302,191 (GRCm39) |
V11I |
unknown |
Het |
| Tapbpl |
T |
C |
6: 125,205,214 (GRCm39) |
Y244C |
probably damaging |
Het |
| Tpx2 |
A |
G |
2: 152,726,214 (GRCm39) |
E393G |
probably damaging |
Het |
| Vmn2r100 |
A |
T |
17: 19,741,620 (GRCm39) |
N111Y |
probably damaging |
Het |
| Vstm4 |
C |
T |
14: 32,585,615 (GRCm39) |
R61C |
probably damaging |
Het |
| Washc2 |
T |
A |
6: 116,221,615 (GRCm39) |
F698I |
possibly damaging |
Het |
| Zfp467 |
G |
A |
6: 48,415,414 (GRCm39) |
P413S |
probably benign |
Het |
| Zfp532 |
G |
T |
18: 65,820,390 (GRCm39) |
A992S |
probably benign |
Het |
| Zfp622 |
G |
A |
15: 25,996,321 (GRCm39) |
W430* |
probably null |
Het |
|
| Other mutations in Or7g18 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00932:Or7g18
|
APN |
9 |
18,787,310 (GRCm39) |
nonsense |
probably null |
|
|
IGL00954:Or7g18
|
APN |
9 |
18,787,369 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL01090:Or7g18
|
APN |
9 |
18,787,538 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01613:Or7g18
|
APN |
9 |
18,786,617 (GRCm39) |
splice site |
probably benign |
|
|
IGL01987:Or7g18
|
APN |
9 |
18,787,003 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03018:Or7g18
|
APN |
9 |
18,787,523 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL03037:Or7g18
|
APN |
9 |
18,786,668 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0284:Or7g18
|
UTSW |
9 |
18,786,848 (GRCm39) |
missense |
probably benign |
|
|
R1322:Or7g18
|
UTSW |
9 |
18,786,817 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1715:Or7g18
|
UTSW |
9 |
18,787,090 (GRCm39) |
missense |
probably benign |
0.06 |
|
R1803:Or7g18
|
UTSW |
9 |
18,787,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4360:Or7g18
|
UTSW |
9 |
18,787,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4394:Or7g18
|
UTSW |
9 |
18,786,907 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4642:Or7g18
|
UTSW |
9 |
18,787,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4796:Or7g18
|
UTSW |
9 |
18,787,475 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4814:Or7g18
|
UTSW |
9 |
18,787,213 (GRCm39) |
missense |
probably benign |
0.30 |
|
R5210:Or7g18
|
UTSW |
9 |
18,787,103 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5375:Or7g18
|
UTSW |
9 |
18,787,442 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6072:Or7g18
|
UTSW |
9 |
18,786,718 (GRCm39) |
missense |
probably benign |
|
|
R6361:Or7g18
|
UTSW |
9 |
18,787,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6602:Or7g18
|
UTSW |
9 |
18,787,145 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6920:Or7g18
|
UTSW |
9 |
18,786,821 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7730:Or7g18
|
UTSW |
9 |
18,786,709 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7780:Or7g18
|
UTSW |
9 |
18,786,910 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8245:Or7g18
|
UTSW |
9 |
18,787,126 (GRCm39) |
missense |
probably benign |
|
|
R8274:Or7g18
|
UTSW |
9 |
18,786,795 (GRCm39) |
missense |
probably benign |
0.36 |
|
R9564:Or7g18
|
UTSW |
9 |
18,786,640 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0026:Or7g18
|
UTSW |
9 |
18,786,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GAAATTGCACAAATCCTGAAGCTTG -3'
(R):5'- ACAGAAGAGAAGCTGTCCTACC -3'
Sequencing Primer
(F):5'- AAATCCTGAAGCTTGCCTGTTCTG -3'
(R):5'- GAGAAGCTGTCCTACCAATAACTTTC -3'
|
| Posted On |
2021-08-02 |
Incidental Mutation