Incidental Mutation 'IGL01901:Or4c10b'
| ID |
179514 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4c10b
|
| Ensembl Gene |
ENSMUSG00000049057 |
| Gene Name |
olfactory receptor family 4 subfamily C member 10B |
| Synonyms |
MOR232-1, Olfr1257, GA_x6K02T2Q125-51319458-51320387 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.071)
|
| Stock # |
IGL01901
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
89709708-89712147 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 89711826 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 219
(I219V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000107144
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000060795]
[ENSMUST00000111519]
|
| AlphaFold |
Q8VGP0 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000060795
AA Change: I219V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000056439
Gene: ENSMUSG00000049057
AA Change: I219V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
39 |
285 |
2.6e-31 |
PFAM |
|
Pfam:7tm_4
|
137 |
278 |
8e-42 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000111519
AA Change: I219V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000107144
Gene: ENSMUSG00000049057
AA Change: I219V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
303 |
1.5e-49 |
PFAM |
|
Pfam:7tm_1
|
39 |
285 |
3.9e-18 |
PFAM |
|
| 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: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam2 |
A |
G |
14: 66,272,678 (GRCm39) |
|
probably benign |
Het |
| Aldh1a7 |
T |
G |
19: 20,695,103 (GRCm39) |
Y154S |
probably damaging |
Het |
| Casc3 |
A |
G |
11: 98,713,947 (GRCm39) |
D393G |
probably damaging |
Het |
| Cd180 |
A |
G |
13: 102,842,936 (GRCm39) |
I661V |
probably benign |
Het |
| Cdh1 |
T |
C |
8: 107,384,392 (GRCm39) |
S287P |
probably damaging |
Het |
| Clnk |
T |
C |
5: 38,952,321 (GRCm39) |
N6S |
probably damaging |
Het |
| Cstdc6 |
C |
A |
16: 36,154,625 (GRCm39) |
A11S |
probably damaging |
Het |
| Cyp17a1 |
C |
T |
19: 46,659,531 (GRCm39) |
V100M |
possibly damaging |
Het |
| Ddhd2 |
A |
G |
8: 26,238,621 (GRCm39) |
V53A |
probably damaging |
Het |
| Elovl7 |
T |
A |
13: 108,410,927 (GRCm39) |
|
probably null |
Het |
| Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
| Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
| Gm14180 |
A |
G |
11: 99,625,053 (GRCm39) |
S22P |
unknown |
Het |
| Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
| Golga5 |
G |
A |
12: 102,446,061 (GRCm39) |
|
probably null |
Het |
| Gpr162 |
A |
T |
6: 124,838,370 (GRCm39) |
F93L |
possibly damaging |
Het |
| Kcnh8 |
G |
A |
17: 53,201,148 (GRCm39) |
|
probably benign |
Het |
| Lamp3 |
A |
T |
16: 19,492,169 (GRCm39) |
F358L |
probably damaging |
Het |
| Mdn1 |
T |
G |
4: 32,669,591 (GRCm39) |
D409E |
probably damaging |
Het |
| Ms4a10 |
T |
C |
19: 10,940,374 (GRCm39) |
D211G |
probably benign |
Het |
| Ms4a3 |
T |
C |
19: 11,616,630 (GRCm39) |
E4G |
possibly damaging |
Het |
| Myo15a |
A |
G |
11: 60,418,260 (GRCm39) |
|
probably benign |
Het |
| Or2ag16 |
A |
G |
7: 106,351,752 (GRCm39) |
V281A |
possibly damaging |
Het |
| Or51aa2 |
A |
T |
7: 103,188,177 (GRCm39) |
L88Q |
probably damaging |
Het |
| Or51q1c |
A |
G |
7: 103,653,274 (GRCm39) |
H264R |
probably damaging |
Het |
| Or5b12 |
T |
C |
19: 12,896,947 (GRCm39) |
H242R |
probably damaging |
Het |
| Or6c217 |
A |
G |
10: 129,737,722 (GRCm39) |
F286L |
probably benign |
Het |
| Penk |
T |
C |
4: 4,134,465 (GRCm39) |
I61V |
probably benign |
Het |
| Pkhd1 |
T |
A |
1: 20,290,307 (GRCm39) |
K2860N |
probably benign |
Het |
| Prtg |
C |
T |
9: 72,762,348 (GRCm39) |
P492S |
probably damaging |
Het |
| Spata31e2 |
A |
G |
1: 26,721,665 (GRCm39) |
F1172L |
probably benign |
Het |
| Tdrd7 |
T |
C |
4: 45,989,225 (GRCm39) |
|
probably benign |
Het |
| Terf2ip |
A |
G |
8: 112,738,700 (GRCm39) |
N196S |
probably benign |
Het |
| Tgtp1 |
T |
C |
11: 48,878,382 (GRCm39) |
N108D |
possibly damaging |
Het |
| Thumpd3 |
A |
G |
6: 113,036,932 (GRCm39) |
H277R |
probably benign |
Het |
| Tshz2 |
T |
A |
2: 169,727,456 (GRCm39) |
L215Q |
possibly damaging |
Het |
| Ube3c |
T |
A |
5: 29,873,005 (GRCm39) |
V1015E |
probably damaging |
Het |
| Utrn |
T |
A |
10: 12,516,672 (GRCm39) |
K2307N |
probably damaging |
Het |
| Vmn1r75 |
A |
G |
7: 11,614,739 (GRCm39) |
Y157C |
probably damaging |
Het |
| Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Or4c10b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01600:Or4c10b
|
APN |
2 |
89,712,006 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01641:Or4c10b
|
APN |
2 |
89,711,952 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01668:Or4c10b
|
APN |
2 |
89,711,443 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02401:Or4c10b
|
APN |
2 |
89,711,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02472:Or4c10b
|
APN |
2 |
89,711,755 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02631:Or4c10b
|
APN |
2 |
89,711,599 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
PIT4354001:Or4c10b
|
UTSW |
2 |
89,711,852 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0552:Or4c10b
|
UTSW |
2 |
89,711,235 (GRCm39) |
nonsense |
probably null |
|
|
R0616:Or4c10b
|
UTSW |
2 |
89,711,935 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0943:Or4c10b
|
UTSW |
2 |
89,711,305 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1146:Or4c10b
|
UTSW |
2 |
89,711,550 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1146:Or4c10b
|
UTSW |
2 |
89,711,550 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1314:Or4c10b
|
UTSW |
2 |
89,711,221 (GRCm39) |
missense |
probably benign |
0.35 |
|
R1641:Or4c10b
|
UTSW |
2 |
89,711,745 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1763:Or4c10b
|
UTSW |
2 |
89,711,473 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1836:Or4c10b
|
UTSW |
2 |
89,711,629 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2125:Or4c10b
|
UTSW |
2 |
89,711,982 (GRCm39) |
missense |
probably benign |
|
|
R4322:Or4c10b
|
UTSW |
2 |
89,712,078 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4897:Or4c10b
|
UTSW |
2 |
89,711,476 (GRCm39) |
missense |
probably benign |
0.39 |
|
R5446:Or4c10b
|
UTSW |
2 |
89,711,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5456:Or4c10b
|
UTSW |
2 |
89,711,602 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6415:Or4c10b
|
UTSW |
2 |
89,711,206 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6905:Or4c10b
|
UTSW |
2 |
89,712,052 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7170:Or4c10b
|
UTSW |
2 |
89,711,397 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R7170:Or4c10b
|
UTSW |
2 |
89,711,185 (GRCm39) |
missense |
probably benign |
0.12 |
|
R7411:Or4c10b
|
UTSW |
2 |
89,711,605 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8171:Or4c10b
|
UTSW |
2 |
89,711,409 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8490:Or4c10b
|
UTSW |
2 |
89,711,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9176:Or4c10b
|
UTSW |
2 |
89,711,515 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9204:Or4c10b
|
UTSW |
2 |
89,711,482 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9751:Or4c10b
|
UTSW |
2 |
89,711,956 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Posted On |
2014-05-07 |
Incidental Mutation