Incidental Mutation 'R2399:Or7g16'
| ID |
248632 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or7g16
|
| Ensembl Gene |
ENSMUSG00000078116 |
| Gene Name |
olfactory receptor family 7 subfamily G member 16 |
| Synonyms |
GA_x6K02T2PVTD-12559294-12558356, Olfr828, MOR149-1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.136)
|
| Stock # |
R2399 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
18726650-18727588 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 18727323 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 89
(D89V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148853
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000104914]
[ENSMUST00000213018]
[ENSMUST00000215380]
|
| AlphaFold |
Q8VFM8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000104914
AA Change: D89V
PolyPhen 2
Score 0.067 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000100514
Gene: ENSMUSG00000078116
AA Change: D89V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
310 |
1e-48 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
1.4e-5 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.1e-21 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000213018
AA Change: D89V
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215380
AA Change: D89V
PolyPhen 2
Score 0.067 (Sensitivity: 0.94; Specificity: 0.84)
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.8%
- 20x: 93.4%
|
| 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: 18 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310003L06Rik |
A |
G |
5: 88,120,338 (GRCm39) |
E365G |
probably damaging |
Het |
| Abtb1 |
G |
A |
6: 88,815,720 (GRCm39) |
T221M |
possibly damaging |
Het |
| Atp2b1 |
T |
A |
10: 98,835,785 (GRCm39) |
I510N |
probably benign |
Het |
| Atr |
T |
A |
9: 95,753,652 (GRCm39) |
H751Q |
probably benign |
Het |
| Cacna1d |
T |
C |
14: 29,774,444 (GRCm39) |
D1650G |
probably benign |
Het |
| Cd93 |
A |
G |
2: 148,284,071 (GRCm39) |
I425T |
probably benign |
Het |
| Dpep2 |
A |
G |
8: 106,716,224 (GRCm39) |
S135P |
probably damaging |
Het |
| Gm10717 |
A |
G |
9: 3,025,532 (GRCm39) |
Y39C |
probably benign |
Het |
| Heatr4 |
T |
C |
12: 84,027,107 (GRCm39) |
H50R |
probably benign |
Het |
| Itga6 |
T |
C |
2: 71,650,358 (GRCm39) |
Y135H |
probably damaging |
Het |
| Kat6b |
AGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGA |
14: 21,712,417 (GRCm39) |
|
probably benign |
Het |
| Myh15 |
T |
C |
16: 48,957,952 (GRCm39) |
I923T |
probably damaging |
Het |
| Or5b108 |
T |
A |
19: 13,168,709 (GRCm39) |
I226K |
probably benign |
Het |
| Or7e170 |
C |
T |
9: 19,795,220 (GRCm39) |
C127Y |
probably damaging |
Het |
| Styxl1 |
C |
T |
5: 135,776,635 (GRCm39) |
E318K |
possibly damaging |
Het |
| Tmcc1 |
C |
CAT |
6: 116,019,831 (GRCm39) |
|
probably null |
Het |
| Zc3h7a |
G |
A |
16: 10,965,265 (GRCm39) |
R623C |
probably damaging |
Het |
| Zfp608 |
T |
C |
18: 55,030,974 (GRCm39) |
K989E |
probably damaging |
Het |
|
| Other mutations in Or7g16 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02088:Or7g16
|
APN |
9 |
18,727,219 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02103:Or7g16
|
APN |
9 |
18,727,005 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02792:Or7g16
|
APN |
9 |
18,727,254 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02964:Or7g16
|
APN |
9 |
18,727,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03087:Or7g16
|
APN |
9 |
18,727,380 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03105:Or7g16
|
APN |
9 |
18,726,685 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0330:Or7g16
|
UTSW |
9 |
18,726,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0335:Or7g16
|
UTSW |
9 |
18,727,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0862:Or7g16
|
UTSW |
9 |
18,727,002 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1226:Or7g16
|
UTSW |
9 |
18,727,266 (GRCm39) |
missense |
probably benign |
0.34 |
|
R2004:Or7g16
|
UTSW |
9 |
18,726,801 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2005:Or7g16
|
UTSW |
9 |
18,726,801 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2006:Or7g16
|
UTSW |
9 |
18,726,801 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2199:Or7g16
|
UTSW |
9 |
18,727,219 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2230:Or7g16
|
UTSW |
9 |
18,727,021 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5652:Or7g16
|
UTSW |
9 |
18,726,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5738:Or7g16
|
UTSW |
9 |
18,727,125 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6416:Or7g16
|
UTSW |
9 |
18,727,188 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6813:Or7g16
|
UTSW |
9 |
18,727,188 (GRCm39) |
missense |
probably benign |
0.21 |
|
R7092:Or7g16
|
UTSW |
9 |
18,727,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7109:Or7g16
|
UTSW |
9 |
18,726,904 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7292:Or7g16
|
UTSW |
9 |
18,727,486 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7429:Or7g16
|
UTSW |
9 |
18,726,650 (GRCm39) |
makesense |
probably null |
|
|
R7430:Or7g16
|
UTSW |
9 |
18,726,650 (GRCm39) |
makesense |
probably null |
|
|
R7490:Or7g16
|
UTSW |
9 |
18,727,229 (GRCm39) |
nonsense |
probably null |
|
|
R7835:Or7g16
|
UTSW |
9 |
18,727,105 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8016:Or7g16
|
UTSW |
9 |
18,727,588 (GRCm39) |
start codon destroyed |
probably null |
0.56 |
|
R8809:Or7g16
|
UTSW |
9 |
18,726,919 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8859:Or7g16
|
UTSW |
9 |
18,726,992 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9036:Or7g16
|
UTSW |
9 |
18,727,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9079:Or7g16
|
UTSW |
9 |
18,726,731 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9177:Or7g16
|
UTSW |
9 |
18,726,742 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9182:Or7g16
|
UTSW |
9 |
18,726,742 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9184:Or7g16
|
UTSW |
9 |
18,727,138 (GRCm39) |
missense |
probably benign |
0.10 |
|
RF003:Or7g16
|
UTSW |
9 |
18,726,778 (GRCm39) |
missense |
probably benign |
0.03 |
|
X0026:Or7g16
|
UTSW |
9 |
18,727,059 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
Z1176:Or7g16
|
UTSW |
9 |
18,727,276 (GRCm39) |
frame shift |
probably null |
|
|
Z1177:Or7g16
|
UTSW |
9 |
18,727,444 (GRCm39) |
missense |
probably benign |
0.09 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTAGCTTGATGACTTGAGCAAG -3'
(R):5'- AGCCCCTCATCTTCAGCATG -3'
Sequencing Primer
(F):5'- GATTTCTAAGTTTGTGCAGAAGGAC -3'
(R):5'- AGCATGTTCACCTCCATGTAC -3'
|
| Posted On |
2014-11-11 |
Incidental Mutation