Incidental Mutation 'IGL01869:Or10q12'
| ID |
178642 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or10q12
|
| Ensembl Gene |
ENSMUSG00000047207 |
| Gene Name |
olfactory receptor family 10 subfamily Q member 12 |
| Synonyms |
Olfr1495, GA_x6K02T2RE5P-4101369-4102328, MOR266-9 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.126)
|
| Stock # |
IGL01869
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
19 |
| Chromosomal Location |
13745708-13746667 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 13746534 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 276
(D276G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150205
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061669]
[ENSMUST00000215930]
[ENSMUST00000216980]
|
| AlphaFold |
Q8VEZ4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000061669
AA Change: D276G
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000057468
Gene: ENSMUSG00000047207
AA Change: D276G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
312 |
1.4e-52 |
PFAM |
|
Pfam:7tm_1
|
45 |
295 |
1.7e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215930
AA Change: D276G
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216980
AA Change: D276G
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| 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 |
|---|
| 1700026F02Rik |
A |
G |
8: 71,495,689 (GRCm39) |
|
noncoding transcript |
Het |
| Adam29 |
T |
C |
8: 56,324,732 (GRCm39) |
H574R |
probably damaging |
Het |
| Arap1 |
C |
A |
7: 101,049,490 (GRCm39) |
T984K |
probably damaging |
Het |
| Ccdc146 |
A |
T |
5: 21,521,837 (GRCm39) |
S396T |
probably benign |
Het |
| Col6a3 |
T |
C |
1: 90,700,770 (GRCm39) |
K2587E |
unknown |
Het |
| Cyp3a44 |
A |
G |
5: 145,727,496 (GRCm39) |
S278P |
probably damaging |
Het |
| Daw1 |
T |
G |
1: 83,159,965 (GRCm39) |
|
probably benign |
Het |
| Dnah17 |
T |
C |
11: 117,943,502 (GRCm39) |
K3200R |
probably benign |
Het |
| Efhd2 |
A |
G |
4: 141,601,913 (GRCm39) |
F89S |
probably damaging |
Het |
| Fras1 |
A |
G |
5: 96,856,642 (GRCm39) |
|
probably benign |
Het |
| Ggps1 |
T |
C |
13: 14,228,979 (GRCm39) |
D68G |
probably damaging |
Het |
| Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
| Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
| Gm3604 |
A |
T |
13: 62,517,954 (GRCm39) |
C134S |
probably damaging |
Het |
| Gpaa1 |
A |
G |
15: 76,217,198 (GRCm39) |
T178A |
probably benign |
Het |
| Lama3 |
A |
G |
18: 12,657,820 (GRCm39) |
N312S |
possibly damaging |
Het |
| Npepps |
T |
C |
11: 97,126,948 (GRCm39) |
I437M |
probably damaging |
Het |
| Or11i1 |
C |
T |
3: 106,729,342 (GRCm39) |
D178N |
probably benign |
Het |
| Rcor1 |
C |
A |
12: 111,070,193 (GRCm39) |
T330K |
possibly damaging |
Het |
| Sbno2 |
A |
G |
10: 79,896,226 (GRCm39) |
|
probably null |
Het |
| Sema3g |
A |
G |
14: 30,945,624 (GRCm39) |
E478G |
probably damaging |
Het |
| Smg9 |
A |
G |
7: 24,115,949 (GRCm39) |
D280G |
probably damaging |
Het |
| Smtnl1 |
A |
T |
2: 84,641,741 (GRCm39) |
*460R |
probably null |
Het |
| Syde1 |
A |
G |
10: 78,424,753 (GRCm39) |
C360R |
possibly damaging |
Het |
| Szt2 |
A |
G |
4: 118,256,268 (GRCm39) |
V197A |
possibly damaging |
Het |
| Tnrc6c |
T |
C |
11: 117,646,274 (GRCm39) |
V1405A |
possibly damaging |
Het |
| Ttbk1 |
A |
G |
17: 46,757,989 (GRCm39) |
S882P |
probably damaging |
Het |
| Tubgcp4 |
T |
A |
2: 121,006,269 (GRCm39) |
H116Q |
possibly damaging |
Het |
| Vmn1r192 |
T |
A |
13: 22,371,750 (GRCm39) |
N157Y |
probably damaging |
Het |
| Vmn1r60 |
C |
T |
7: 5,547,228 (GRCm39) |
V291M |
probably benign |
Het |
| Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
| Xpo5 |
C |
T |
17: 46,553,133 (GRCm39) |
P1184L |
possibly damaging |
Het |
| Zfp946 |
T |
G |
17: 22,673,684 (GRCm39) |
I146S |
probably benign |
Het |
|
| Other mutations in Or10q12 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01542:Or10q12
|
APN |
19 |
13,745,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02088:Or10q12
|
APN |
19 |
13,746,030 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1583:Or10q12
|
UTSW |
19 |
13,745,874 (GRCm39) |
missense |
probably benign |
0.10 |
|
R1713:Or10q12
|
UTSW |
19 |
13,746,659 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1859:Or10q12
|
UTSW |
19 |
13,746,088 (GRCm39) |
nonsense |
probably null |
|
|
R3717:Or10q12
|
UTSW |
19 |
13,746,428 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3718:Or10q12
|
UTSW |
19 |
13,746,428 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3881:Or10q12
|
UTSW |
19 |
13,746,144 (GRCm39) |
missense |
probably benign |
|
|
R4370:Or10q12
|
UTSW |
19 |
13,746,315 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4873:Or10q12
|
UTSW |
19 |
13,746,126 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4875:Or10q12
|
UTSW |
19 |
13,746,126 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6335:Or10q12
|
UTSW |
19 |
13,746,144 (GRCm39) |
missense |
probably benign |
|
|
R6352:Or10q12
|
UTSW |
19 |
13,745,828 (GRCm39) |
missense |
probably benign |
|
|
R7038:Or10q12
|
UTSW |
19 |
13,745,715 (GRCm39) |
missense |
probably benign |
|
|
R7107:Or10q12
|
UTSW |
19 |
13,746,525 (GRCm39) |
missense |
probably benign |
0.22 |
|
R7504:Or10q12
|
UTSW |
19 |
13,746,096 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7626:Or10q12
|
UTSW |
19 |
13,745,709 (GRCm39) |
start codon destroyed |
probably null |
0.92 |
|
R7812:Or10q12
|
UTSW |
19 |
13,746,380 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7852:Or10q12
|
UTSW |
19 |
13,745,874 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7860:Or10q12
|
UTSW |
19 |
13,745,716 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8183:Or10q12
|
UTSW |
19 |
13,746,086 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8357:Or10q12
|
UTSW |
19 |
13,745,721 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8457:Or10q12
|
UTSW |
19 |
13,745,721 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8716:Or10q12
|
UTSW |
19 |
13,746,185 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1088:Or10q12
|
UTSW |
19 |
13,745,780 (GRCm39) |
missense |
probably benign |
0.22 |
|
| Posted On |
2014-05-07 |
Incidental Mutation