Incidental Mutation 'IGL03121:Or4f6'
| ID |
409976 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4f6
|
| Ensembl Gene |
ENSMUSG00000108827 |
| Gene Name |
olfactory receptor family 4 subfamily F member 6 |
| Synonyms |
Olfr1310, MOR245-3, GA_x6K02T2Q125-73056609-73055671 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.234)
|
| Stock # |
IGL03121
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
111838591-111839529 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 111838953 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 193
(Y193H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149701
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000207169]
[ENSMUST00000213559]
|
| AlphaFold |
Q8VF85 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000207169
AA Change: Y193H
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213559
AA Change: Y193H
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| 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: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700012B09Rik |
A |
G |
9: 14,672,946 (GRCm39) |
S4P |
possibly damaging |
Het |
| A2m |
A |
G |
6: 121,618,265 (GRCm39) |
N186S |
probably benign |
Het |
| Afg2a |
T |
C |
3: 37,518,800 (GRCm39) |
I778T |
probably damaging |
Het |
| Ago1 |
T |
C |
4: 126,353,796 (GRCm39) |
K261R |
probably benign |
Het |
| Alas1 |
G |
A |
9: 106,124,113 (GRCm39) |
P15L |
probably damaging |
Het |
| Aox1 |
G |
A |
1: 58,398,113 (GRCm39) |
V1285M |
probably damaging |
Het |
| Brd8 |
A |
T |
18: 34,739,740 (GRCm39) |
F678I |
probably damaging |
Het |
| Col27a1 |
T |
A |
4: 63,143,446 (GRCm39) |
M378K |
probably benign |
Het |
| Dpy19l4 |
C |
A |
4: 11,303,334 (GRCm39) |
V196F |
probably damaging |
Het |
| Dst |
G |
T |
1: 34,256,884 (GRCm39) |
|
probably benign |
Het |
| Hsd17b1 |
T |
A |
11: 100,970,870 (GRCm39) |
Y275* |
probably null |
Het |
| Kdm3b |
A |
G |
18: 34,928,762 (GRCm39) |
E171G |
probably damaging |
Het |
| Klc1 |
T |
C |
12: 111,748,076 (GRCm39) |
|
probably benign |
Het |
| Mlkl |
G |
A |
8: 112,041,612 (GRCm39) |
R443W |
probably damaging |
Het |
| Mov10 |
A |
T |
3: 104,708,318 (GRCm39) |
V477E |
probably benign |
Het |
| Nacad |
A |
G |
11: 6,550,933 (GRCm39) |
S753P |
probably damaging |
Het |
| Ncapd2 |
A |
C |
6: 125,150,575 (GRCm39) |
M842R |
probably benign |
Het |
| Nkd2 |
C |
A |
13: 73,969,498 (GRCm39) |
A311S |
probably benign |
Het |
| Nrg1 |
A |
G |
8: 32,314,608 (GRCm39) |
|
probably benign |
Het |
| Or6c68 |
A |
G |
10: 129,158,037 (GRCm39) |
I182V |
probably benign |
Het |
| Pde6h |
A |
G |
6: 136,936,280 (GRCm39) |
S8G |
probably null |
Het |
| Pik3c2b |
A |
G |
1: 133,007,483 (GRCm39) |
K616E |
probably benign |
Het |
| Pnpt1 |
A |
T |
11: 29,082,845 (GRCm39) |
R54S |
probably benign |
Het |
| Pramel38 |
T |
C |
5: 94,368,912 (GRCm39) |
V469A |
possibly damaging |
Het |
| Rttn |
A |
G |
18: 88,993,875 (GRCm39) |
D184G |
probably damaging |
Het |
| Skint5 |
T |
A |
4: 113,574,284 (GRCm39) |
I756F |
unknown |
Het |
| Slc24a2 |
T |
C |
4: 87,145,143 (GRCm39) |
T304A |
probably benign |
Het |
| Stk3 |
A |
T |
15: 35,099,572 (GRCm39) |
|
probably benign |
Het |
| Trim69 |
A |
G |
2: 121,998,128 (GRCm39) |
I33M |
probably benign |
Het |
| Ube2q2 |
A |
T |
9: 55,102,323 (GRCm39) |
|
probably benign |
Het |
| Vmn1r67 |
T |
A |
7: 10,181,394 (GRCm39) |
N158K |
probably benign |
Het |
| Wipi2 |
G |
A |
5: 142,648,857 (GRCm39) |
E252K |
probably benign |
Het |
|
| Other mutations in Or4f6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01947:Or4f6
|
APN |
2 |
111,839,361 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL02700:Or4f6
|
APN |
2 |
111,839,036 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL03008:Or4f6
|
APN |
2 |
111,838,868 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0025:Or4f6
|
UTSW |
2 |
111,839,365 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1624:Or4f6
|
UTSW |
2 |
111,838,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1851:Or4f6
|
UTSW |
2 |
111,839,036 (GRCm39) |
missense |
probably benign |
0.04 |
|
R3872:Or4f6
|
UTSW |
2 |
111,838,668 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3873:Or4f6
|
UTSW |
2 |
111,838,668 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3874:Or4f6
|
UTSW |
2 |
111,838,668 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4651:Or4f6
|
UTSW |
2 |
111,838,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4652:Or4f6
|
UTSW |
2 |
111,838,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4834:Or4f6
|
UTSW |
2 |
111,839,276 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5076:Or4f6
|
UTSW |
2 |
111,838,937 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7262:Or4f6
|
UTSW |
2 |
111,838,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7339:Or4f6
|
UTSW |
2 |
111,838,820 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7657:Or4f6
|
UTSW |
2 |
111,839,093 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7798:Or4f6
|
UTSW |
2 |
111,838,617 (GRCm39) |
missense |
probably benign |
|
|
R7875:Or4f6
|
UTSW |
2 |
111,839,192 (GRCm39) |
missense |
probably benign |
0.32 |
|
R8869:Or4f6
|
UTSW |
2 |
111,838,596 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9689:Or4f6
|
UTSW |
2 |
111,839,124 (GRCm39) |
missense |
probably benign |
0.29 |
|
X0027:Or4f6
|
UTSW |
2 |
111,839,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Or4f6
|
UTSW |
2 |
111,838,802 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation