Incidental Mutation 'IGL02548:Or5k8'
| ID |
297906 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5k8
|
| Ensembl Gene |
ENSMUSG00000060663 |
| Gene Name |
olfactory receptor family 5 subfamily K member 8 |
| Synonyms |
GA_x54KRFPKG5P-55026345-55025418, MOR184-10P, MOR184-1, GA_x54KRFPKG5P-54993816-54992890, Olfr175-ps1, Olfr175, Olfr174 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.122)
|
| Stock # |
IGL02548
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
16 |
| Chromosomal Location |
58644144-58647124 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 58644691 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Phenylalanine
at position 127
(C127F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150202
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079955]
[ENSMUST00000215069]
|
| AlphaFold |
A0A140T8K4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000079955
AA Change: C127F
PolyPhen 2
Score 0.417 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000078873
Gene: ENSMUSG00000060663
AA Change: C127F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
1.3e-52 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
6.8e-6 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.5e-18 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215069
AA Change: C127F
PolyPhen 2
Score 0.417 (Sensitivity: 0.89; Specificity: 0.90)
|
| Coding Region Coverage |
|
| 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: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcc6 |
G |
A |
7: 45,654,686 (GRCm39) |
A545V |
probably damaging |
Het |
| Adam29 |
A |
T |
8: 56,325,902 (GRCm39) |
L184* |
probably null |
Het |
| Ap1g1 |
C |
T |
8: 110,576,254 (GRCm39) |
A432V |
probably damaging |
Het |
| Atrn |
C |
T |
2: 130,814,202 (GRCm39) |
T716I |
probably damaging |
Het |
| Bahd1 |
C |
A |
2: 118,747,526 (GRCm39) |
Q382K |
possibly damaging |
Het |
| Barhl2 |
A |
G |
5: 106,603,391 (GRCm39) |
V256A |
probably benign |
Het |
| Camta2 |
A |
G |
11: 70,561,511 (GRCm39) |
F1113L |
probably damaging |
Het |
| Cdh23 |
G |
T |
10: 60,485,901 (GRCm39) |
T38K |
probably benign |
Het |
| Cmtm3 |
T |
C |
8: 105,071,437 (GRCm39) |
L111P |
probably damaging |
Het |
| Col27a1 |
T |
C |
4: 63,236,492 (GRCm39) |
|
probably benign |
Het |
| Cyp2c29 |
G |
A |
19: 39,279,291 (GRCm39) |
G96D |
possibly damaging |
Het |
| Flt1 |
C |
A |
5: 147,576,058 (GRCm39) |
R650L |
probably benign |
Het |
| Fpr1 |
T |
A |
17: 18,096,915 (GRCm39) |
E358V |
probably benign |
Het |
| Ggnbp2 |
A |
T |
11: 84,753,112 (GRCm39) |
N42K |
possibly damaging |
Het |
| Gldc |
T |
C |
19: 30,077,299 (GRCm39) |
T958A |
probably benign |
Het |
| Gm3573 |
A |
G |
14: 42,009,452 (GRCm39) |
|
probably null |
Het |
| Hspbp1 |
T |
C |
7: 4,684,840 (GRCm39) |
|
probably benign |
Het |
| Jhy |
G |
T |
9: 40,828,471 (GRCm39) |
Y478* |
probably null |
Het |
| Kiz |
A |
G |
2: 146,712,690 (GRCm39) |
E118G |
probably damaging |
Het |
| Klhdc1 |
A |
G |
12: 69,300,492 (GRCm39) |
Y144C |
probably benign |
Het |
| Lamc3 |
A |
T |
2: 31,810,674 (GRCm39) |
Y848F |
probably benign |
Het |
| Mixl1 |
T |
C |
1: 180,522,269 (GRCm39) |
E204G |
probably benign |
Het |
| Muc2 |
T |
A |
7: 141,305,594 (GRCm39) |
C202S |
probably damaging |
Het |
| Nfatc1 |
T |
C |
18: 80,741,113 (GRCm39) |
S282G |
probably damaging |
Het |
| Or2j6 |
T |
A |
7: 139,980,575 (GRCm39) |
Y128F |
probably damaging |
Het |
| Or5b111 |
T |
C |
19: 13,291,302 (GRCm39) |
M116V |
probably damaging |
Het |
| Orc2 |
A |
T |
1: 58,505,281 (GRCm39) |
|
probably benign |
Het |
| Pcdhb10 |
T |
C |
18: 37,545,743 (GRCm39) |
I273T |
probably benign |
Het |
| Pdzph1 |
G |
A |
17: 59,280,386 (GRCm39) |
T632I |
probably benign |
Het |
| Phf1 |
A |
G |
17: 27,154,600 (GRCm39) |
Y225C |
probably damaging |
Het |
| Pramel17 |
T |
A |
4: 101,692,770 (GRCm39) |
Y410F |
probably damaging |
Het |
| Prcp |
T |
C |
7: 92,550,382 (GRCm39) |
F60L |
probably damaging |
Het |
| Psg21 |
C |
T |
7: 18,388,961 (GRCm39) |
V44I |
possibly damaging |
Het |
| Ptgdr |
C |
T |
14: 45,096,071 (GRCm39) |
V214M |
probably damaging |
Het |
| Pth1r |
G |
A |
9: 110,556,748 (GRCm39) |
R181W |
probably damaging |
Het |
| Ralgapb |
A |
G |
2: 158,286,585 (GRCm39) |
I343M |
probably damaging |
Het |
| Retreg1 |
C |
T |
15: 25,895,204 (GRCm39) |
Q128* |
probably null |
Het |
| Rrbp1 |
T |
C |
2: 143,791,679 (GRCm39) |
|
probably benign |
Het |
| Skint5 |
T |
A |
4: 113,588,273 (GRCm39) |
M726L |
unknown |
Het |
| Slc6a18 |
T |
C |
13: 73,818,114 (GRCm39) |
Y301C |
probably damaging |
Het |
| Slc8a3 |
G |
A |
12: 81,250,930 (GRCm39) |
|
probably benign |
Het |
| Tacr3 |
C |
A |
3: 134,535,232 (GRCm39) |
Q67K |
probably damaging |
Het |
| Tfrc |
A |
T |
16: 32,443,640 (GRCm39) |
K534* |
probably null |
Het |
| Timp3 |
T |
A |
10: 86,174,315 (GRCm39) |
M67K |
probably benign |
Het |
| Tmem120a |
C |
T |
5: 135,765,628 (GRCm39) |
E179K |
probably damaging |
Het |
| Tomm40l |
G |
A |
1: 171,049,216 (GRCm39) |
|
probably benign |
Het |
| Tubal3 |
A |
G |
13: 3,980,554 (GRCm39) |
R89G |
probably benign |
Het |
| Wdr35 |
A |
T |
12: 9,074,297 (GRCm39) |
N976I |
probably benign |
Het |
| Zfp292 |
T |
C |
4: 34,805,416 (GRCm39) |
T2543A |
probably damaging |
Het |
| Zfp976 |
T |
A |
7: 42,261,953 (GRCm39) |
H628L |
unknown |
Het |
| Zmynd8 |
A |
G |
2: 165,675,325 (GRCm39) |
V301A |
probably damaging |
Het |
|
| Other mutations in Or5k8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01402:Or5k8
|
APN |
16 |
58,644,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01404:Or5k8
|
APN |
16 |
58,644,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01867:Or5k8
|
APN |
16 |
58,644,337 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02073:Or5k8
|
APN |
16 |
58,644,169 (GRCm39) |
missense |
probably benign |
|
|
IGL02393:Or5k8
|
APN |
16 |
58,644,409 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02474:Or5k8
|
APN |
16 |
58,645,019 (GRCm39) |
missense |
probably benign |
|
|
IGL02948:Or5k8
|
APN |
16 |
58,644,451 (GRCm39) |
missense |
probably benign |
0.00 |
|
PIT4504001:Or5k8
|
UTSW |
16 |
58,644,671 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0553:Or5k8
|
UTSW |
16 |
58,644,518 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1191:Or5k8
|
UTSW |
16 |
58,644,922 (GRCm39) |
missense |
probably benign |
|
|
R1201:Or5k8
|
UTSW |
16 |
58,644,226 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1458:Or5k8
|
UTSW |
16 |
58,645,039 (GRCm39) |
missense |
probably null |
0.68 |
|
R1469:Or5k8
|
UTSW |
16 |
58,644,973 (GRCm39) |
missense |
probably benign |
|
|
R1469:Or5k8
|
UTSW |
16 |
58,644,973 (GRCm39) |
missense |
probably benign |
|
|
R1843:Or5k8
|
UTSW |
16 |
58,644,440 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2147:Or5k8
|
UTSW |
16 |
58,644,842 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2421:Or5k8
|
UTSW |
16 |
58,644,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4370:Or5k8
|
UTSW |
16 |
58,644,956 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4621:Or5k8
|
UTSW |
16 |
58,644,469 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4622:Or5k8
|
UTSW |
16 |
58,644,469 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4623:Or5k8
|
UTSW |
16 |
58,644,469 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4711:Or5k8
|
UTSW |
16 |
58,645,069 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
|
R5323:Or5k8
|
UTSW |
16 |
58,645,066 (GRCm39) |
missense |
probably benign |
|
|
R5447:Or5k8
|
UTSW |
16 |
58,644,846 (GRCm39) |
nonsense |
probably null |
|
|
R5457:Or5k8
|
UTSW |
16 |
58,644,796 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5546:Or5k8
|
UTSW |
16 |
58,644,516 (GRCm39) |
nonsense |
probably null |
|
|
R5623:Or5k8
|
UTSW |
16 |
58,644,706 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5767:Or5k8
|
UTSW |
16 |
58,644,316 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6270:Or5k8
|
UTSW |
16 |
58,644,782 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6449:Or5k8
|
UTSW |
16 |
58,644,889 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7356:Or5k8
|
UTSW |
16 |
58,644,718 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7521:Or5k8
|
UTSW |
16 |
58,644,257 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7638:Or5k8
|
UTSW |
16 |
58,644,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7814:Or5k8
|
UTSW |
16 |
58,644,365 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9109:Or5k8
|
UTSW |
16 |
58,644,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9276:Or5k8
|
UTSW |
16 |
58,644,734 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9681:Or5k8
|
UTSW |
16 |
58,644,176 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
X0011:Or5k8
|
UTSW |
16 |
58,645,026 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Or5k8
|
UTSW |
16 |
58,644,670 (GRCm39) |
frame shift |
probably null |
|
|
Z1177:Or5k8
|
UTSW |
16 |
58,645,061 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
| Posted On |
2015-04-16 |
Incidental Mutation