Incidental Mutation 'IGL01550:Or7e175'
| ID |
90568 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or7e175
|
| Ensembl Gene |
ENSMUSG00000058491 |
| Gene Name |
olfactory receptor family 7 subfamily E member 175 |
| Synonyms |
Olfr869, MOR145-6, GA_x6K02T2PVTD-13878275-13879204 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.061)
|
| Stock # |
IGL01550
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
20040305-20050059 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 20048750 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Serine
at position 113
(T113S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000154723
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000075717]
[ENSMUST00000213024]
|
| AlphaFold |
A0A2I3BRV7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000075717
AA Change: T113S
PolyPhen 2
Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000075135
Gene: ENSMUSG00000049028
AA Change: T113S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
45 |
321 |
6.2e-43 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
49 |
309 |
3e-8 |
PFAM |
|
Pfam:7tm_1
|
55 |
304 |
1.5e-20 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000212969
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000213024
AA Change: T113S
PolyPhen 2
Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)
|
| 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: 28 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930556J24Rik |
T |
G |
11: 3,887,974 (GRCm39) |
R137S |
unknown |
Het |
| Epha8 |
G |
T |
4: 136,659,051 (GRCm39) |
Q868K |
possibly damaging |
Het |
| Erc1 |
T |
A |
6: 119,760,355 (GRCm39) |
M386L |
probably damaging |
Het |
| Gfpt2 |
T |
A |
11: 49,715,150 (GRCm39) |
|
probably null |
Het |
| Gpr142 |
T |
A |
11: 114,695,152 (GRCm39) |
L39Q |
probably damaging |
Het |
| Hmcn1 |
A |
T |
1: 150,474,148 (GRCm39) |
W4765R |
probably damaging |
Het |
| Hmcn2 |
A |
T |
2: 31,314,264 (GRCm39) |
E3603V |
possibly damaging |
Het |
| Hsp90b1 |
C |
T |
10: 86,540,234 (GRCm39) |
D26N |
probably benign |
Het |
| Kmt2c |
T |
C |
5: 25,486,274 (GRCm39) |
T4760A |
probably damaging |
Het |
| Lmo7 |
C |
A |
14: 102,163,576 (GRCm39) |
|
probably benign |
Het |
| Mup4 |
A |
T |
4: 59,960,120 (GRCm39) |
I48K |
probably damaging |
Het |
| Mylk3 |
T |
A |
8: 86,091,718 (GRCm39) |
D29V |
probably damaging |
Het |
| Myo1b |
A |
G |
1: 51,823,690 (GRCm39) |
F405S |
probably damaging |
Het |
| Nbea |
T |
C |
3: 55,712,669 (GRCm39) |
D2136G |
possibly damaging |
Het |
| Or1l4b |
A |
T |
2: 37,036,986 (GRCm39) |
Y254F |
probably damaging |
Het |
| Or52a20 |
T |
G |
7: 103,366,204 (GRCm39) |
H134Q |
probably damaging |
Het |
| Or5g27 |
T |
A |
2: 85,409,875 (GRCm39) |
C97* |
probably null |
Het |
| Psmg2 |
G |
A |
18: 67,786,293 (GRCm39) |
V218I |
probably benign |
Het |
| Rpp40 |
T |
C |
13: 36,090,183 (GRCm39) |
|
probably null |
Het |
| Samd7 |
T |
A |
3: 30,819,399 (GRCm39) |
S383T |
probably damaging |
Het |
| Tbc1d10c |
T |
C |
19: 4,234,823 (GRCm39) |
T413A |
probably damaging |
Het |
| Tlr12 |
A |
G |
4: 128,509,535 (GRCm39) |
L905P |
probably damaging |
Het |
| Tnr |
A |
G |
1: 159,701,828 (GRCm39) |
K643R |
probably benign |
Het |
| Vmn2r124 |
T |
C |
17: 18,283,617 (GRCm39) |
|
probably null |
Het |
| Vwf |
A |
T |
6: 125,656,252 (GRCm39) |
I2606F |
probably benign |
Het |
| Wbp4 |
T |
C |
14: 79,703,774 (GRCm39) |
T258A |
probably benign |
Het |
| Zfp1005 |
T |
A |
2: 150,108,363 (GRCm39) |
|
probably benign |
Het |
| Zfp758 |
T |
C |
17: 22,594,021 (GRCm39) |
L137S |
probably damaging |
Het |
|
| Other mutations in Or7e175 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00966:Or7e175
|
APN |
9 |
20,048,531 (GRCm39) |
missense |
probably benign |
|
|
IGL02247:Or7e175
|
APN |
9 |
20,048,516 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02448:Or7e175
|
APN |
9 |
20,048,937 (GRCm39) |
nonsense |
probably null |
|
|
IGL03076:Or7e175
|
APN |
9 |
20,049,023 (GRCm39) |
missense |
probably benign |
0.25 |
|
R0045:Or7e175
|
UTSW |
9 |
20,048,487 (GRCm39) |
missense |
probably benign |
0.25 |
|
R0962:Or7e175
|
UTSW |
9 |
20,048,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4588:Or7e175
|
UTSW |
9 |
20,049,383 (GRCm39) |
makesense |
probably null |
|
|
R4931:Or7e175
|
UTSW |
9 |
20,048,858 (GRCm39) |
missense |
probably benign |
0.19 |
|
R5030:Or7e175
|
UTSW |
9 |
20,049,363 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5759:Or7e175
|
UTSW |
9 |
20,049,228 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5780:Or7e175
|
UTSW |
9 |
20,048,793 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6440:Or7e175
|
UTSW |
9 |
20,048,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6599:Or7e175
|
UTSW |
9 |
20,049,239 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6710:Or7e175
|
UTSW |
9 |
20,049,378 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6953:Or7e175
|
UTSW |
9 |
20,049,299 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7288:Or7e175
|
UTSW |
9 |
20,048,737 (GRCm39) |
nonsense |
probably null |
|
|
R7585:Or7e175
|
UTSW |
9 |
20,040,307 (GRCm39) |
|
|
|
|
R7860:Or7e175
|
UTSW |
9 |
20,048,871 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8025:Or7e175
|
UTSW |
9 |
20,048,928 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8178:Or7e175
|
UTSW |
9 |
20,048,571 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8794:Or7e175
|
UTSW |
9 |
20,048,630 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8954:Or7e175
|
UTSW |
9 |
20,048,664 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9116:Or7e175
|
UTSW |
9 |
20,048,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9162:Or7e175
|
UTSW |
9 |
20,040,457 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9269:Or7e175
|
UTSW |
9 |
20,048,757 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-12-09 |
Incidental Mutation