Incidental Mutation 'R5188:Or8k1'
| ID |
398004 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or8k1
|
| Ensembl Gene |
ENSMUSG00000075197 |
| Gene Name |
olfactory receptor family 8 subfamily K member 1 |
| Synonyms |
MOR194-1, GA_x6K02T2Q125-47692494-47691544, Olfr1046 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.113)
|
| Stock # |
R5188 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
86046319-86048055 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 86047521 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Arginine
at position 178
(S178R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148873
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099902]
[ENSMUST00000213987]
|
| AlphaFold |
Q7TR79 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099902
AA Change: S178R
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000097486
Gene: ENSMUSG00000075197
AA Change: S178R
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
311 |
2.2e-50 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
4e-20 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213987
AA Change: S178R
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.6%
|
| 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: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
| 2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
| Abca12 |
T |
A |
1: 71,330,651 (GRCm39) |
I1335F |
probably benign |
Het |
| Amigo3 |
C |
A |
9: 107,931,882 (GRCm39) |
A435E |
probably damaging |
Het |
| Atr |
T |
A |
9: 95,803,778 (GRCm39) |
N1871K |
probably benign |
Het |
| Ctsw |
C |
T |
19: 5,517,120 (GRCm39) |
A71T |
probably damaging |
Het |
| Decr1 |
C |
T |
4: 15,924,270 (GRCm39) |
V217M |
probably damaging |
Het |
| Golgb1 |
A |
G |
16: 36,738,827 (GRCm39) |
T2389A |
probably benign |
Het |
| Gpr151 |
A |
G |
18: 42,711,820 (GRCm39) |
M286T |
probably benign |
Het |
| Katnbl1 |
T |
A |
2: 112,240,499 (GRCm39) |
I262N |
probably damaging |
Het |
| Lrp1 |
A |
G |
10: 127,443,821 (GRCm39) |
C149R |
probably damaging |
Het |
| Mpc1 |
A |
T |
17: 8,515,215 (GRCm39) |
|
probably benign |
Het |
| Ndufv1 |
A |
T |
19: 4,059,988 (GRCm39) |
N37K |
probably damaging |
Het |
| Or1n1b |
T |
A |
2: 36,780,405 (GRCm39) |
I152L |
probably benign |
Het |
| Or5af2 |
C |
A |
11: 58,708,146 (GRCm39) |
T104K |
probably damaging |
Het |
| Or8g50 |
T |
C |
9: 39,648,531 (GRCm39) |
V140A |
probably benign |
Het |
| Pnpla7 |
C |
A |
2: 24,887,312 (GRCm39) |
P52Q |
probably benign |
Het |
| Prh1 |
A |
G |
6: 132,548,670 (GRCm39) |
Q59R |
unknown |
Het |
| Ren1 |
A |
G |
1: 133,278,351 (GRCm39) |
|
probably benign |
Het |
| Rnf148 |
T |
C |
6: 23,654,139 (GRCm39) |
T286A |
probably damaging |
Het |
| Sdk1 |
T |
C |
5: 141,942,015 (GRCm39) |
|
probably null |
Het |
| Srp72 |
T |
A |
5: 77,122,598 (GRCm39) |
S10T |
possibly damaging |
Het |
| Stk11 |
G |
T |
10: 79,962,113 (GRCm39) |
G215V |
probably damaging |
Het |
| Stk4 |
T |
C |
2: 163,930,828 (GRCm39) |
M143T |
possibly damaging |
Het |
| Supt20 |
T |
A |
3: 54,617,849 (GRCm39) |
S318T |
possibly damaging |
Het |
| Tchh |
G |
C |
3: 93,353,986 (GRCm39) |
R1142P |
unknown |
Het |
| Vipas39 |
G |
T |
12: 87,301,021 (GRCm39) |
R161S |
probably benign |
Het |
|
| Other mutations in Or8k1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01335:Or8k1
|
APN |
2 |
86,047,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01613:Or8k1
|
APN |
2 |
86,047,505 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03327:Or8k1
|
APN |
2 |
86,047,618 (GRCm39) |
nonsense |
probably null |
|
|
R0183:Or8k1
|
UTSW |
2 |
86,047,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1738:Or8k1
|
UTSW |
2 |
86,048,060 (GRCm39) |
splice site |
probably null |
|
|
R2279:Or8k1
|
UTSW |
2 |
86,047,148 (GRCm39) |
missense |
probably benign |
|
|
R4677:Or8k1
|
UTSW |
2 |
86,048,032 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4828:Or8k1
|
UTSW |
2 |
86,047,877 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R6244:Or8k1
|
UTSW |
2 |
86,047,566 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8097:Or8k1
|
UTSW |
2 |
86,048,010 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8420:Or8k1
|
UTSW |
2 |
86,047,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8806:Or8k1
|
UTSW |
2 |
86,047,200 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9269:Or8k1
|
UTSW |
2 |
86,047,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTACTGTCAGATGAGAGCTGC -3'
(R):5'- AACTGTTTATCCTCTCAGCCATGG -3'
Sequencing Primer
(F):5'- TGGAGAAGGCTTTGGACCTCC -3'
(R):5'- CCATGGCTTATGACCGCTATGTAG -3'
|
| Posted On |
2016-07-06 |
Incidental Mutation