Incidental Mutation 'IGL02103:Or7g16'
| ID |
279853 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| 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 # |
IGL02103
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
18726650-18727588 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 18727005 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Serine
at position 195
(N195S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148853
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000104914]
[ENSMUST00000213018]
[ENSMUST00000215380]
|
| AlphaFold |
Q8VFM8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000104914
AA Change: N195S
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000100514
Gene: ENSMUSG00000078116
AA Change: N195S
| 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: N195S
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215380
AA Change: N195S
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| 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: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcd4 |
G |
A |
12: 84,659,138 (GRCm39) |
T206M |
probably benign |
Het |
| Adcy3 |
T |
A |
12: 4,184,390 (GRCm39) |
V22D |
possibly damaging |
Het |
| Alb |
G |
A |
5: 90,611,990 (GRCm39) |
E140K |
probably benign |
Het |
| Aph1a |
G |
A |
3: 95,803,125 (GRCm39) |
V193I |
probably damaging |
Het |
| Asb2 |
G |
A |
12: 103,299,755 (GRCm39) |
R178* |
probably null |
Het |
| Celf3 |
A |
T |
3: 94,394,108 (GRCm39) |
Q137L |
probably damaging |
Het |
| Cmya5 |
T |
C |
13: 93,228,635 (GRCm39) |
D2151G |
probably benign |
Het |
| Cuedc1 |
T |
A |
11: 88,079,625 (GRCm39) |
S353T |
probably damaging |
Het |
| Dlg5 |
A |
C |
14: 24,194,414 (GRCm39) |
L1709R |
probably damaging |
Het |
| Dst |
T |
C |
1: 34,229,199 (GRCm39) |
I1939T |
possibly damaging |
Het |
| Emx2 |
A |
T |
19: 59,450,130 (GRCm39) |
N149I |
probably benign |
Het |
| Fancm |
A |
G |
12: 65,142,558 (GRCm39) |
D472G |
probably benign |
Het |
| Fasn |
T |
C |
11: 120,702,762 (GRCm39) |
Y1700C |
probably damaging |
Het |
| Fat2 |
T |
A |
11: 55,180,122 (GRCm39) |
R1406S |
probably damaging |
Het |
| Fat4 |
C |
A |
3: 38,943,348 (GRCm39) |
T747K |
probably damaging |
Het |
| Fer |
A |
G |
17: 64,445,923 (GRCm39) |
M795V |
probably benign |
Het |
| Gm5916 |
A |
G |
9: 36,039,970 (GRCm39) |
L6P |
probably damaging |
Het |
| Gpr139 |
A |
G |
7: 118,744,355 (GRCm39) |
F77L |
possibly damaging |
Het |
| Kcnu1 |
T |
C |
8: 26,395,976 (GRCm39) |
S654P |
possibly damaging |
Het |
| Kdm5c |
T |
A |
X: 151,031,762 (GRCm39) |
F408L |
probably damaging |
Het |
| Kel |
A |
G |
6: 41,679,323 (GRCm39) |
S147P |
probably benign |
Het |
| Klra5 |
A |
T |
6: 129,888,307 (GRCm39) |
|
probably null |
Het |
| Mastl |
A |
G |
2: 23,030,010 (GRCm39) |
S239P |
probably benign |
Het |
| Med18 |
A |
T |
4: 132,186,977 (GRCm39) |
V174D |
probably damaging |
Het |
| Mgat4a |
A |
T |
1: 37,502,007 (GRCm39) |
M247K |
possibly damaging |
Het |
| Mx2 |
A |
C |
16: 97,345,795 (GRCm39) |
D71A |
probably damaging |
Het |
| Nxt1 |
G |
T |
2: 148,517,564 (GRCm39) |
E102* |
probably null |
Het |
| Or14j1 |
A |
G |
17: 38,146,169 (GRCm39) |
Q93R |
possibly damaging |
Het |
| Or3a1 |
A |
G |
11: 74,225,862 (GRCm39) |
F65S |
probably damaging |
Het |
| Pcdhb16 |
T |
A |
18: 37,613,161 (GRCm39) |
V707E |
probably benign |
Het |
| Pdzrn4 |
T |
A |
15: 92,667,768 (GRCm39) |
V640E |
probably damaging |
Het |
| Piwil4 |
T |
C |
9: 14,637,282 (GRCm39) |
|
probably null |
Het |
| Pla2g4a |
A |
T |
1: 149,776,950 (GRCm39) |
D55E |
probably damaging |
Het |
| Plekhg2 |
C |
A |
7: 28,059,501 (GRCm39) |
R1276L |
probably damaging |
Het |
| Psd4 |
G |
A |
2: 24,290,540 (GRCm39) |
W539* |
probably null |
Het |
| Rae1 |
G |
A |
2: 172,845,306 (GRCm39) |
E33K |
probably damaging |
Het |
| Rbm12b1 |
T |
A |
4: 12,145,563 (GRCm39) |
F512I |
probably damaging |
Het |
| Rfx6 |
A |
G |
10: 51,602,952 (GRCm39) |
D823G |
possibly damaging |
Het |
| Samt3 |
A |
T |
X: 85,090,759 (GRCm39) |
Q217L |
probably damaging |
Het |
| Selenbp2 |
A |
G |
3: 94,605,438 (GRCm39) |
N134S |
probably null |
Het |
| Selenoo |
T |
C |
15: 88,984,173 (GRCm39) |
V663A |
probably damaging |
Het |
| Sp4 |
G |
T |
12: 118,263,284 (GRCm39) |
T254N |
probably damaging |
Het |
| Spdya |
A |
G |
17: 71,885,242 (GRCm39) |
K232R |
probably benign |
Het |
| Stom |
A |
T |
2: 35,210,401 (GRCm39) |
V201E |
probably benign |
Het |
| Sycp3 |
A |
G |
10: 88,302,334 (GRCm39) |
K108R |
possibly damaging |
Het |
| Usp2 |
A |
G |
9: 44,000,425 (GRCm39) |
|
probably benign |
Het |
| Vmn1r226 |
T |
C |
17: 20,907,926 (GRCm39) |
S53P |
probably damaging |
Het |
| Vmn2r14 |
C |
T |
5: 109,372,349 (GRCm39) |
G47D |
probably damaging |
Het |
| Vwf |
T |
G |
6: 125,623,318 (GRCm39) |
L1805W |
probably damaging |
Het |
| Washc3 |
A |
T |
10: 88,037,687 (GRCm39) |
Q22L |
probably damaging |
Het |
| Wdr81 |
T |
A |
11: 75,335,546 (GRCm39) |
D1761V |
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 |
|
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 |
|
R2399:Or7g16
|
UTSW |
9 |
18,727,323 (GRCm39) |
missense |
probably benign |
0.07 |
|
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 |
|
| Posted On |
2015-04-16 |
Incidental Mutation