Incidental Mutation 'R1505:Or8g52'
| ID |
169121 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or8g52
|
| Ensembl Gene |
ENSMUSG00000095839 |
| Gene Name |
olfactory receptor family 8 subfamily G member 52 |
| Synonyms |
MOR171-28, Olfr965, GA_x6K02T2PVTD-33416730-33417668 |
| MMRRC Submission |
040868-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.075)
|
| Stock # |
R1505 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
39630525-39631463 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 39630774 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Aspartic acid
at position 84
(N84D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150401
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000069342]
[ENSMUST00000213335]
[ENSMUST00000215164]
|
| AlphaFold |
Q7TRA7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000069342
AA Change: N84D
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000069696
Gene: ENSMUSG00000095839
AA Change: N84D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.4e-47 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
4.2e-24 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000213335
AA Change: N84D
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000214875
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215164
AA Change: N84D
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.8%
- 10x: 94.5%
- 20x: 86.3%
|
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcg3 |
T |
A |
5: 105,099,431 (GRCm39) |
R444W |
probably damaging |
Het |
| Adnp |
A |
G |
2: 168,025,661 (GRCm39) |
S545P |
possibly damaging |
Het |
| Ankrd17 |
T |
C |
5: 90,447,885 (GRCm39) |
R219G |
possibly damaging |
Het |
| Ap2m1 |
C |
G |
16: 20,361,447 (GRCm39) |
P372A |
probably benign |
Het |
| Calml3 |
T |
A |
13: 3,854,071 (GRCm39) |
T45S |
probably benign |
Het |
| Casp8 |
A |
G |
1: 58,868,081 (GRCm39) |
E174G |
probably damaging |
Het |
| Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
| Cfap221 |
A |
C |
1: 119,881,358 (GRCm39) |
L368R |
probably benign |
Het |
| Chd9 |
A |
G |
8: 91,733,123 (GRCm39) |
|
probably null |
Het |
| Cnot1 |
A |
T |
8: 96,455,295 (GRCm39) |
I2035N |
probably damaging |
Het |
| Cyp2c67 |
T |
C |
19: 39,637,408 (GRCm39) |
R23G |
probably benign |
Het |
| Dnah10 |
A |
C |
5: 124,831,303 (GRCm39) |
H777P |
possibly damaging |
Het |
| Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
| Fam162b |
G |
A |
10: 51,463,298 (GRCm39) |
A123V |
probably damaging |
Het |
| Golgb1 |
T |
A |
16: 36,740,005 (GRCm39) |
N2781K |
possibly damaging |
Het |
| Hs2st1 |
C |
A |
3: 144,140,322 (GRCm39) |
R333L |
probably benign |
Het |
| Kmt2e |
A |
G |
5: 23,705,533 (GRCm39) |
H1319R |
probably null |
Het |
| Necab1 |
A |
T |
4: 14,960,047 (GRCm39) |
M300K |
probably benign |
Het |
| Ntrk3 |
T |
A |
7: 78,110,272 (GRCm39) |
I321F |
probably damaging |
Het |
| Or5p60 |
A |
G |
7: 107,724,200 (GRCm39) |
V90A |
probably benign |
Het |
| Or7e169 |
A |
T |
9: 19,757,084 (GRCm39) |
M277K |
probably benign |
Het |
| Or8k41 |
A |
T |
2: 86,313,557 (GRCm39) |
H176Q |
possibly damaging |
Het |
| Osbpl6 |
T |
C |
2: 76,409,586 (GRCm39) |
S483P |
probably damaging |
Het |
| Pcdhb17 |
A |
C |
18: 37,619,875 (GRCm39) |
N555T |
probably damaging |
Het |
| Pdgfc |
G |
A |
3: 81,116,543 (GRCm39) |
R299H |
possibly damaging |
Het |
| Ptpn7 |
A |
T |
1: 135,062,302 (GRCm39) |
T83S |
probably benign |
Het |
| Rapgef5 |
T |
C |
12: 117,652,354 (GRCm39) |
V79A |
possibly damaging |
Het |
| Rexo5 |
T |
A |
7: 119,398,826 (GRCm39) |
C54* |
probably null |
Het |
| Riok3 |
A |
G |
18: 12,285,935 (GRCm39) |
K418R |
probably benign |
Het |
| Robo4 |
G |
A |
9: 37,314,523 (GRCm39) |
G170D |
probably damaging |
Het |
| Rpl8 |
A |
G |
15: 76,788,610 (GRCm39) |
D33G |
possibly damaging |
Het |
| Rspo2 |
T |
C |
15: 42,939,239 (GRCm39) |
T184A |
probably damaging |
Het |
| Ryr2 |
A |
T |
13: 11,569,478 (GRCm39) |
M4942K |
possibly damaging |
Het |
| Sel1l |
T |
C |
12: 91,780,736 (GRCm39) |
Y585C |
probably damaging |
Het |
| Slc25a11 |
G |
T |
11: 70,537,650 (GRCm39) |
D13E |
probably benign |
Het |
| Slc5a6 |
G |
T |
5: 31,194,455 (GRCm39) |
H584N |
probably benign |
Het |
| Snrpf |
A |
G |
10: 93,419,381 (GRCm39) |
V69A |
possibly damaging |
Het |
| Sorbs3 |
T |
A |
14: 70,428,251 (GRCm39) |
K475* |
probably null |
Het |
| Speg |
G |
A |
1: 75,352,186 (GRCm39) |
V35I |
probably benign |
Het |
| Tlk2 |
T |
G |
11: 105,151,121 (GRCm39) |
V468G |
probably damaging |
Het |
| Trim6 |
T |
A |
7: 103,881,771 (GRCm39) |
W341R |
probably damaging |
Het |
| Ttll5 |
T |
A |
12: 85,926,184 (GRCm39) |
I326N |
probably damaging |
Het |
| Vipas39 |
T |
C |
12: 87,292,934 (GRCm39) |
Y318C |
probably damaging |
Het |
| Vmn1r185 |
T |
A |
7: 26,310,903 (GRCm39) |
I201F |
probably damaging |
Het |
| Vwce |
A |
G |
19: 10,641,608 (GRCm39) |
H778R |
probably benign |
Het |
| Zbtb14 |
C |
G |
17: 69,694,759 (GRCm39) |
I152M |
probably benign |
Het |
|
| Other mutations in Or8g52 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01705:Or8g52
|
APN |
9 |
39,630,877 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02365:Or8g52
|
APN |
9 |
39,631,396 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02365:Or8g52
|
APN |
9 |
39,630,970 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
IGL03062:Or8g52
|
APN |
9 |
39,631,331 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL03330:Or8g52
|
APN |
9 |
39,630,784 (GRCm39) |
missense |
probably benign |
0.08 |
|
R0011:Or8g52
|
UTSW |
9 |
39,630,923 (GRCm39) |
missense |
probably benign |
0.26 |
|
R0462:Or8g52
|
UTSW |
9 |
39,630,706 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1995:Or8g52
|
UTSW |
9 |
39,630,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2049:Or8g52
|
UTSW |
9 |
39,631,411 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2110:Or8g52
|
UTSW |
9 |
39,631,018 (GRCm39) |
missense |
probably benign |
0.30 |
|
R3817:Or8g52
|
UTSW |
9 |
39,631,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4152:Or8g52
|
UTSW |
9 |
39,631,296 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4153:Or8g52
|
UTSW |
9 |
39,631,296 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4351:Or8g52
|
UTSW |
9 |
39,630,865 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4377:Or8g52
|
UTSW |
9 |
39,631,103 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4667:Or8g52
|
UTSW |
9 |
39,631,005 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5526:Or8g52
|
UTSW |
9 |
39,630,892 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5816:Or8g52
|
UTSW |
9 |
39,630,526 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R7113:Or8g52
|
UTSW |
9 |
39,630,973 (GRCm39) |
missense |
probably benign |
|
|
R7336:Or8g52
|
UTSW |
9 |
39,630,906 (GRCm39) |
missense |
probably benign |
0.28 |
|
R8153:Or8g52
|
UTSW |
9 |
39,630,954 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R8291:Or8g52
|
UTSW |
9 |
39,630,841 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8779:Or8g52
|
UTSW |
9 |
39,630,636 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9617:Or8g52
|
UTSW |
9 |
39,630,678 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R9631:Or8g52
|
UTSW |
9 |
39,631,161 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATCTACTTGTTCACGGAGCTGGGG -3'
(R):5'- CTCAAGATTGTCAGCATTGGCACAC -3'
Sequencing Primer
(F):5'- GGAACCTGGGCATGGTC -3'
(R):5'- CCTCATTGACAAATGTGCTGGAG -3'
|
| Posted On |
2014-04-13 |
Incidental Mutation