Incidental Mutation 'IGL03260:Or6z7'
| ID |
414772 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or6z7
|
| Ensembl Gene |
ENSMUSG00000096228 |
| Gene Name |
olfactory receptor family 6 subfamily Z member 7 |
| Synonyms |
MOR103-8, Olfr5, GA_x6K02T2QGBW-3210997-3210059 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.114)
|
| Stock # |
IGL03260
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
6483215-6490013 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 6483658 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Serine
at position 166
(C166S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000147586
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086318]
[ENSMUST00000207658]
[ENSMUST00000209866]
[ENSMUST00000215302]
|
| AlphaFold |
Q60889 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000086318
AA Change: C166S
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000083498
Gene: ENSMUSG00000096228
AA Change: C166S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
311 |
2.1e-50 |
PFAM |
|
Pfam:7tm_1
|
45 |
294 |
6.9e-19 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000207658
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000209866
AA Change: C166S
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215302
|
| 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: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933406P04Rik |
A |
G |
10: 20,187,071 (GRCm39) |
|
probably benign |
Het |
| Abca12 |
A |
G |
1: 71,323,258 (GRCm39) |
L1608P |
probably damaging |
Het |
| Akr1b8 |
G |
T |
6: 34,340,394 (GRCm39) |
|
probably benign |
Het |
| Appbp2 |
A |
G |
11: 85,107,283 (GRCm39) |
V69A |
probably benign |
Het |
| Ces1e |
T |
C |
8: 93,950,545 (GRCm39) |
N79D |
probably benign |
Het |
| Cldn34b3 |
A |
G |
X: 75,310,479 (GRCm39) |
T16A |
probably damaging |
Het |
| Frmd4b |
A |
T |
6: 97,373,185 (GRCm39) |
F103Y |
probably damaging |
Het |
| Ifi47 |
T |
C |
11: 48,986,932 (GRCm39) |
F233S |
probably damaging |
Het |
| Igkv8-30 |
A |
T |
6: 70,094,339 (GRCm39) |
M24K |
probably damaging |
Het |
| Krt72 |
C |
T |
15: 101,686,708 (GRCm39) |
A413T |
probably damaging |
Het |
| Lingo4 |
A |
G |
3: 94,309,250 (GRCm39) |
T63A |
probably benign |
Het |
| Naa35 |
T |
G |
13: 59,775,699 (GRCm39) |
S125A |
probably benign |
Het |
| Or6c76 |
T |
C |
10: 129,612,521 (GRCm39) |
V261A |
probably damaging |
Het |
| Padi1 |
T |
C |
4: 140,555,505 (GRCm39) |
H240R |
probably benign |
Het |
| Ppp1r12a |
A |
G |
10: 108,097,106 (GRCm39) |
T240A |
probably benign |
Het |
| Ppp2ca |
A |
G |
11: 52,003,975 (GRCm39) |
N44S |
probably damaging |
Het |
| Prg4 |
T |
A |
1: 150,331,378 (GRCm39) |
|
probably benign |
Het |
| Rab33a |
A |
G |
X: 47,608,545 (GRCm39) |
E23G |
probably benign |
Het |
| Scarb2 |
G |
T |
5: 92,594,296 (GRCm39) |
A422E |
probably damaging |
Het |
| Scn4b |
A |
T |
9: 45,058,987 (GRCm39) |
N86I |
probably damaging |
Het |
| Serpina1d |
G |
A |
12: 103,730,108 (GRCm39) |
T358I |
probably damaging |
Het |
| Slc12a3 |
T |
A |
8: 95,059,870 (GRCm39) |
I172N |
probably damaging |
Het |
| Slc18a1 |
T |
C |
8: 69,527,766 (GRCm39) |
E15G |
probably benign |
Het |
| Snx7 |
A |
G |
3: 117,575,942 (GRCm39) |
|
probably benign |
Het |
| Srpx |
T |
A |
X: 9,921,987 (GRCm39) |
K216* |
probably null |
Het |
| Ugt2a3 |
G |
A |
5: 87,484,439 (GRCm39) |
P195L |
probably damaging |
Het |
| Unc13c |
A |
G |
9: 73,838,626 (GRCm39) |
S742P |
probably benign |
Het |
| Vmn2r104 |
C |
T |
17: 20,263,083 (GRCm39) |
C126Y |
probably benign |
Het |
| Vmn2r63 |
A |
T |
7: 42,578,616 (GRCm39) |
N92K |
probably damaging |
Het |
|
| Other mutations in Or6z7 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01336:Or6z7
|
APN |
7 |
6,483,997 (GRCm39) |
missense |
probably benign |
|
|
IGL02174:Or6z7
|
APN |
7 |
6,483,438 (GRCm39) |
missense |
probably benign |
|
|
IGL03411:Or6z7
|
APN |
7 |
6,483,435 (GRCm39) |
missense |
probably benign |
0.26 |
|
R1186:Or6z7
|
UTSW |
7 |
6,483,541 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1381:Or6z7
|
UTSW |
7 |
6,484,008 (GRCm39) |
splice site |
probably null |
|
|
R1981:Or6z7
|
UTSW |
7 |
6,483,931 (GRCm39) |
missense |
probably benign |
0.29 |
|
R1982:Or6z7
|
UTSW |
7 |
6,483,931 (GRCm39) |
missense |
probably benign |
0.29 |
|
R3876:Or6z7
|
UTSW |
7 |
6,484,131 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3907:Or6z7
|
UTSW |
7 |
6,483,678 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4422:Or6z7
|
UTSW |
7 |
6,484,037 (GRCm39) |
nonsense |
probably null |
|
|
R4654:Or6z7
|
UTSW |
7 |
6,484,045 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5605:Or6z7
|
UTSW |
7 |
6,483,325 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6962:Or6z7
|
UTSW |
7 |
6,484,008 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7524:Or6z7
|
UTSW |
7 |
6,483,586 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7576:Or6z7
|
UTSW |
7 |
6,483,330 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8306:Or6z7
|
UTSW |
7 |
6,483,868 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8947:Or6z7
|
UTSW |
7 |
6,483,246 (GRCm39) |
missense |
probably benign |
|
|
R8967:Or6z7
|
UTSW |
7 |
6,484,011 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9562:Or6z7
|
UTSW |
7 |
6,483,243 (GRCm39) |
missense |
probably null |
0.60 |
|
Z1177:Or6z7
|
UTSW |
7 |
6,483,872 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation