Incidental Mutation 'R6613:Or5k1'
| ID |
523803 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5k1
|
| Ensembl Gene |
ENSMUSG00000049362 |
| Gene Name |
olfactory receptor family 5 subfamily K member 1 |
| Synonyms |
MOR184-3, GA_x54KRFPKG5P-54960233-54959268, Olfr173 |
| MMRRC Submission |
044736-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.068)
|
| Stock # |
R6613 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
58617142-58618305 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 58617894 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Phenylalanine
at position 105
(C105F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000145946
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049940]
[ENSMUST00000206205]
|
| AlphaFold |
E9QAT7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000049940
AA Change: C105F
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000052798
Gene: ENSMUSG00000049362
AA Change: C105F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
5.7e-52 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
9.7e-19 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000206205
AA Change: C105F
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.5%
- 10x: 97.9%
- 20x: 93.9%
|
| Validation Efficiency |
97% (37/38) |
| 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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ano2 |
G |
A |
6: 125,783,619 (GRCm39) |
|
probably null |
Het |
| Arfgef1 |
A |
T |
1: 10,264,621 (GRCm39) |
I475N |
possibly damaging |
Het |
| Atg16l2 |
C |
T |
7: 100,939,788 (GRCm39) |
|
probably null |
Het |
| Atp2c2 |
T |
G |
8: 120,482,760 (GRCm39) |
L874R |
probably damaging |
Het |
| C2cd3 |
T |
A |
7: 100,044,448 (GRCm39) |
S343R |
possibly damaging |
Het |
| C4b |
A |
T |
17: 34,952,539 (GRCm39) |
S1167T |
probably damaging |
Het |
| Cacna1i |
G |
A |
15: 80,205,460 (GRCm39) |
G139S |
probably damaging |
Het |
| Chil6 |
A |
T |
3: 106,297,191 (GRCm39) |
F317I |
probably benign |
Het |
| Cngb1 |
A |
T |
8: 95,992,638 (GRCm39) |
V199E |
possibly damaging |
Het |
| Dcn |
A |
T |
10: 97,330,902 (GRCm39) |
T79S |
probably benign |
Het |
| Dcxr |
A |
G |
11: 120,617,832 (GRCm39) |
V48A |
probably benign |
Het |
| Dnajc13 |
A |
T |
9: 104,091,076 (GRCm39) |
D668E |
probably benign |
Het |
| Dnajc28 |
C |
A |
16: 91,413,246 (GRCm39) |
E357* |
probably null |
Het |
| Dock7 |
A |
G |
4: 98,866,197 (GRCm39) |
Y1198H |
probably damaging |
Het |
| Flot1 |
A |
G |
17: 36,136,703 (GRCm39) |
D167G |
probably damaging |
Het |
| Gpn1 |
T |
C |
5: 31,654,696 (GRCm39) |
|
probably null |
Het |
| Hyou1 |
A |
T |
9: 44,293,795 (GRCm39) |
I242F |
probably damaging |
Het |
| Igfbpl1 |
T |
C |
4: 45,813,447 (GRCm39) |
N256S |
probably benign |
Het |
| Kif20b |
C |
T |
19: 34,914,384 (GRCm39) |
Q390* |
probably null |
Het |
| Lhfpl2 |
T |
A |
13: 94,311,003 (GRCm39) |
F91Y |
probably damaging |
Het |
| Magi1 |
G |
A |
6: 93,722,654 (GRCm39) |
T408I |
probably damaging |
Het |
| Mttp |
T |
C |
3: 137,814,839 (GRCm39) |
N479D |
probably damaging |
Het |
| Myom3 |
T |
C |
4: 135,539,770 (GRCm39) |
V1339A |
possibly damaging |
Het |
| Nin |
T |
C |
12: 70,077,728 (GRCm39) |
K1733E |
probably damaging |
Het |
| Pdzrn4 |
T |
C |
15: 92,575,455 (GRCm39) |
I287T |
probably damaging |
Het |
| Ptprt |
A |
G |
2: 161,372,367 (GRCm39) |
V1435A |
probably damaging |
Het |
| Rpap3 |
T |
C |
15: 97,579,722 (GRCm39) |
|
probably null |
Het |
| Scin |
A |
G |
12: 40,129,714 (GRCm39) |
Y360H |
probably benign |
Het |
| Sfxn5 |
A |
G |
6: 85,246,890 (GRCm39) |
|
probably null |
Het |
| Sgo1 |
A |
G |
17: 53,986,085 (GRCm39) |
S369P |
probably damaging |
Het |
| Skil |
T |
A |
3: 31,152,029 (GRCm39) |
C184S |
probably null |
Het |
| Srcin1 |
A |
G |
11: 97,424,653 (GRCm39) |
M607T |
possibly damaging |
Het |
| Ssc5d |
C |
T |
7: 4,936,292 (GRCm39) |
P513S |
possibly damaging |
Het |
| Trip10 |
A |
G |
17: 57,562,197 (GRCm39) |
|
probably null |
Het |
| Vmn2r114 |
T |
A |
17: 23,529,220 (GRCm39) |
Q294L |
possibly damaging |
Het |
| Zc3h12c |
A |
G |
9: 52,027,412 (GRCm39) |
V650A |
possibly damaging |
Het |
|
| Other mutations in Or5k1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02649:Or5k1
|
APN |
16 |
58,617,713 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02728:Or5k1
|
APN |
16 |
58,617,843 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL02893:Or5k1
|
APN |
16 |
58,618,020 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0035:Or5k1
|
UTSW |
16 |
58,617,485 (GRCm39) |
nonsense |
probably null |
|
|
R0480:Or5k1
|
UTSW |
16 |
58,617,684 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1101:Or5k1
|
UTSW |
16 |
58,617,615 (GRCm39) |
missense |
probably benign |
0.27 |
|
R1434:Or5k1
|
UTSW |
16 |
58,617,811 (GRCm39) |
missense |
probably benign |
0.06 |
|
R1992:Or5k1
|
UTSW |
16 |
58,617,309 (GRCm39) |
missense |
probably benign |
|
|
R2220:Or5k1
|
UTSW |
16 |
58,617,987 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R2436:Or5k1
|
UTSW |
16 |
58,617,607 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4212:Or5k1
|
UTSW |
16 |
58,617,732 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4910:Or5k1
|
UTSW |
16 |
58,617,805 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5666:Or5k1
|
UTSW |
16 |
58,617,424 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R5670:Or5k1
|
UTSW |
16 |
58,617,424 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R5896:Or5k1
|
UTSW |
16 |
58,618,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6182:Or5k1
|
UTSW |
16 |
58,617,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6723:Or5k1
|
UTSW |
16 |
58,617,795 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7051:Or5k1
|
UTSW |
16 |
58,617,538 (GRCm39) |
missense |
probably benign |
0.21 |
|
R7141:Or5k1
|
UTSW |
16 |
58,617,771 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7179:Or5k1
|
UTSW |
16 |
58,617,250 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7602:Or5k1
|
UTSW |
16 |
58,617,343 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R8425:Or5k1
|
UTSW |
16 |
58,617,966 (GRCm39) |
missense |
probably benign |
0.11 |
|
Z1176:Or5k1
|
UTSW |
16 |
58,618,036 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1176:Or5k1
|
UTSW |
16 |
58,617,786 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTAGTCTAAATAATAGCCCCACATG -3'
(R):5'- GAAGGGCCTTCTGTTTGCAG -3'
Sequencing Primer
(F):5'- GAACCATAGAATGCAGGTTTCC -3'
(R):5'- CTGGTGATTCTGATTTCCAAAGAACG -3'
|
| Posted On |
2018-06-22 |
Incidental Mutation