Incidental Mutation 'IGL01563:Or8c15'
| ID |
90886 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or8c15
|
| Ensembl Gene |
ENSMUSG00000093901 |
| Gene Name |
olfactory receptor family 8 subfamily C member 15 |
| Synonyms |
GA_x6K02T2PVTD-31889215-31890153, Olfr893, MOR170-11 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.135)
|
| Stock # |
IGL01563
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
38120348-38121289 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 38120997 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 214
(I214N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148719
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000093867]
[ENSMUST00000211975]
|
| AlphaFold |
K7N678 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000093867
AA Change: I216N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000091390
Gene: ENSMUSG00000093901
AA Change: I216N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
309 |
1.2e-45 |
PFAM |
|
Pfam:7tm_1
|
43 |
292 |
8e-20 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000211975
AA Change: I214N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212815
|
| 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: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Alms1 |
A |
G |
6: 85,604,965 (GRCm39) |
E2205G |
probably damaging |
Het |
| Arid2 |
G |
A |
15: 96,270,278 (GRCm39) |
V1464I |
probably damaging |
Het |
| Axin2 |
A |
G |
11: 108,814,631 (GRCm39) |
Q173R |
probably damaging |
Het |
| Best1 |
A |
G |
19: 9,964,099 (GRCm39) |
F454L |
probably benign |
Het |
| CK137956 |
T |
G |
4: 127,864,428 (GRCm39) |
K67T |
possibly damaging |
Het |
| Col14a1 |
G |
A |
15: 55,351,337 (GRCm39) |
G1555R |
unknown |
Het |
| Csad |
G |
A |
15: 102,095,598 (GRCm39) |
S153F |
probably damaging |
Het |
| Cyp4f40 |
A |
T |
17: 32,892,930 (GRCm39) |
D315V |
probably damaging |
Het |
| Galnt3 |
G |
A |
2: 65,928,101 (GRCm39) |
A265V |
probably damaging |
Het |
| Gm5901 |
C |
A |
7: 105,026,722 (GRCm39) |
Y163* |
probably null |
Het |
| Golga4 |
A |
G |
9: 118,356,074 (GRCm39) |
|
probably benign |
Het |
| Greb1l |
A |
G |
18: 10,469,399 (GRCm39) |
D138G |
probably damaging |
Het |
| Has1 |
A |
T |
17: 18,063,924 (GRCm39) |
|
probably benign |
Het |
| Ighv1-42 |
A |
G |
12: 114,900,804 (GRCm39) |
S94P |
probably damaging |
Het |
| Katnb1 |
T |
A |
8: 95,824,787 (GRCm39) |
L569Q |
probably damaging |
Het |
| Nedd1 |
C |
T |
10: 92,534,031 (GRCm39) |
|
probably null |
Het |
| Or2b2 |
A |
G |
13: 21,887,243 (GRCm39) |
E24G |
probably benign |
Het |
| Pdcd4 |
G |
A |
19: 53,917,552 (GRCm39) |
R463H |
probably benign |
Het |
| Psmg2 |
G |
A |
18: 67,786,293 (GRCm39) |
V218I |
probably benign |
Het |
| Ro60 |
A |
G |
1: 143,637,120 (GRCm39) |
V364A |
probably benign |
Het |
| Rps19bp1 |
A |
G |
15: 80,145,532 (GRCm39) |
M84T |
probably benign |
Het |
| Sass6 |
A |
T |
3: 116,398,847 (GRCm39) |
D43V |
probably damaging |
Het |
| Senp6 |
G |
A |
9: 80,029,290 (GRCm39) |
S551N |
probably benign |
Het |
| Sh2d2a |
A |
G |
3: 87,759,432 (GRCm39) |
E273G |
probably damaging |
Het |
| Slc16a14 |
T |
C |
1: 84,889,908 (GRCm39) |
|
probably benign |
Het |
| Smcr8 |
C |
T |
11: 60,674,671 (GRCm39) |
R816C |
possibly damaging |
Het |
| Trappc8 |
A |
T |
18: 20,970,103 (GRCm39) |
N962K |
probably benign |
Het |
| Trpc6 |
A |
G |
9: 8,656,604 (GRCm39) |
E677G |
probably damaging |
Het |
| Ubap2 |
G |
T |
4: 41,195,998 (GRCm39) |
P961T |
probably damaging |
Het |
| Vmn1r23 |
A |
G |
6: 57,903,061 (GRCm39) |
V239A |
possibly damaging |
Het |
| Vps41 |
T |
C |
13: 18,966,897 (GRCm39) |
|
probably benign |
Het |
| Vwf |
A |
T |
6: 125,568,128 (GRCm39) |
D341V |
probably damaging |
Het |
| Zfp618 |
C |
T |
4: 62,998,133 (GRCm39) |
P45L |
probably benign |
Het |
|
| Other mutations in Or8c15 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00331:Or8c15
|
APN |
9 |
38,120,534 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00914:Or8c15
|
APN |
9 |
38,121,095 (GRCm39) |
splice site |
probably null |
|
|
IGL01696:Or8c15
|
APN |
9 |
38,120,345 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02064:Or8c15
|
APN |
9 |
38,120,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02605:Or8c15
|
APN |
9 |
38,120,532 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0415:Or8c15
|
UTSW |
9 |
38,121,269 (GRCm39) |
missense |
probably benign |
|
|
R0463:Or8c15
|
UTSW |
9 |
38,120,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0843:Or8c15
|
UTSW |
9 |
38,120,579 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1441:Or8c15
|
UTSW |
9 |
38,120,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1939:Or8c15
|
UTSW |
9 |
38,120,725 (GRCm39) |
nonsense |
probably null |
|
|
R2512:Or8c15
|
UTSW |
9 |
38,120,670 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4890:Or8c15
|
UTSW |
9 |
38,120,586 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5439:Or8c15
|
UTSW |
9 |
38,121,050 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6918:Or8c15
|
UTSW |
9 |
38,120,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7621:Or8c15
|
UTSW |
9 |
38,120,447 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7715:Or8c15
|
UTSW |
9 |
38,120,775 (GRCm39) |
missense |
probably benign |
0.30 |
|
R7940:Or8c15
|
UTSW |
9 |
38,120,496 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8710:Or8c15
|
UTSW |
9 |
38,121,066 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R8712:Or8c15
|
UTSW |
9 |
38,121,099 (GRCm39) |
missense |
probably benign |
0.39 |
|
R8882:Or8c15
|
UTSW |
9 |
38,120,461 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2013-12-09 |
Incidental Mutation