Incidental Mutation 'IGL02041:Or6c6c'
| ID |
184750 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or6c6c
|
| Ensembl Gene |
ENSMUSG00000095401 |
| Gene Name |
olfactory receptor family 6 subfamily C member 6C |
| Synonyms |
GA_x6K02T2PULF-11383575-11384519, MOR110-7, Olfr804 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.090)
|
| Stock # |
IGL02041
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
10 |
| Chromosomal Location |
129540749-129541693 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 129541104 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 119
(D119G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150132
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077312]
[ENSMUST00000213331]
|
| AlphaFold |
Q7TRH7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000077312
AA Change: D119G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000076540
Gene: ENSMUSG00000095401
AA Change: D119G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
6e-48 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
3.3e-23 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000213331
AA Change: D119G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000216747
|
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcc2 |
A |
T |
19: 43,772,674 (GRCm39) |
Q28L |
probably damaging |
Het |
| Abtb3 |
G |
A |
10: 85,223,418 (GRCm39) |
D76N |
unknown |
Het |
| Afg1l |
A |
G |
10: 42,330,376 (GRCm39) |
V97A |
probably damaging |
Het |
| Akap6 |
A |
C |
12: 53,187,436 (GRCm39) |
S1617R |
probably damaging |
Het |
| Aldh1a3 |
T |
C |
7: 66,057,579 (GRCm39) |
N285D |
probably damaging |
Het |
| Arhgap20 |
A |
T |
9: 51,757,490 (GRCm39) |
N494I |
possibly damaging |
Het |
| Atg9a |
G |
T |
1: 75,159,748 (GRCm39) |
Q712K |
possibly damaging |
Het |
| Cdcp2 |
G |
A |
4: 106,964,386 (GRCm39) |
|
probably benign |
Het |
| Cds2 |
T |
A |
2: 132,136,363 (GRCm39) |
I84N |
possibly damaging |
Het |
| Clcn3 |
T |
C |
8: 61,376,187 (GRCm39) |
I596V |
probably damaging |
Het |
| Ctxn1 |
A |
G |
8: 4,308,514 (GRCm39) |
L39P |
probably damaging |
Het |
| Efhb |
A |
T |
17: 53,733,287 (GRCm39) |
V528D |
probably damaging |
Het |
| Fmod |
T |
G |
1: 133,968,001 (GRCm39) |
S14A |
probably benign |
Het |
| Foxh1 |
A |
G |
15: 76,553,120 (GRCm39) |
F198S |
probably damaging |
Het |
| Gcc2 |
A |
G |
10: 58,105,103 (GRCm39) |
E77G |
probably damaging |
Het |
| Gm5420 |
G |
T |
10: 21,566,933 (GRCm39) |
|
noncoding transcript |
Het |
| Gm6434 |
T |
G |
7: 25,581,655 (GRCm39) |
|
noncoding transcript |
Het |
| Il1b |
A |
T |
2: 129,211,662 (GRCm39) |
N19K |
possibly damaging |
Het |
| Lama2 |
T |
A |
10: 26,860,322 (GRCm39) |
D3055V |
probably damaging |
Het |
| Lcn3 |
G |
A |
2: 25,655,636 (GRCm39) |
V18I |
probably benign |
Het |
| Lpcat2 |
A |
G |
8: 93,644,809 (GRCm39) |
S533G |
probably benign |
Het |
| Map4k2 |
G |
A |
19: 6,401,348 (GRCm39) |
R606Q |
probably benign |
Het |
| Mtnr1b |
T |
C |
9: 15,774,589 (GRCm39) |
T157A |
probably benign |
Het |
| Myo15a |
G |
A |
11: 60,397,689 (GRCm39) |
E2705K |
probably damaging |
Het |
| Ncf2 |
A |
G |
1: 152,711,871 (GRCm39) |
|
probably benign |
Het |
| Nfkbil1 |
G |
A |
17: 35,439,934 (GRCm39) |
T193M |
probably benign |
Het |
| Nmi |
T |
G |
2: 51,850,641 (GRCm39) |
K9T |
possibly damaging |
Het |
| Or2d4 |
T |
C |
7: 106,543,320 (GRCm39) |
D296G |
possibly damaging |
Het |
| Or5p69 |
T |
C |
7: 107,966,742 (GRCm39) |
F15S |
probably damaging |
Het |
| Osbpl7 |
T |
A |
11: 96,951,334 (GRCm39) |
C502S |
probably benign |
Het |
| Pex5 |
A |
T |
6: 124,382,240 (GRCm39) |
|
probably benign |
Het |
| Pkhd1l1 |
T |
A |
15: 44,356,452 (GRCm39) |
|
probably null |
Het |
| Prmt3 |
C |
T |
7: 49,478,711 (GRCm39) |
T424M |
possibly damaging |
Het |
| Rapgef4 |
G |
A |
2: 72,029,140 (GRCm39) |
G404D |
probably damaging |
Het |
| Rbm5 |
C |
T |
9: 107,633,045 (GRCm39) |
|
probably benign |
Het |
| Rfc2 |
T |
A |
5: 134,623,098 (GRCm39) |
F238L |
probably benign |
Het |
| Rsl1 |
A |
G |
13: 67,324,612 (GRCm39) |
E46G |
probably damaging |
Het |
| Sall1 |
A |
G |
8: 89,758,097 (GRCm39) |
F669S |
probably damaging |
Het |
| Sipa1l2 |
A |
G |
8: 126,218,558 (GRCm39) |
S260P |
probably benign |
Het |
| Slc26a8 |
A |
G |
17: 28,861,225 (GRCm39) |
Y820H |
probably damaging |
Het |
| Tas2r115 |
A |
G |
6: 132,714,430 (GRCm39) |
F174L |
probably benign |
Het |
| Terb1 |
A |
C |
8: 105,221,746 (GRCm39) |
C185G |
probably damaging |
Het |
| Vmn2r108 |
A |
T |
17: 20,683,398 (GRCm39) |
V602E |
probably damaging |
Het |
| Vmn2r58 |
T |
A |
7: 41,514,703 (GRCm39) |
I89F |
probably damaging |
Het |
| Vps13b |
G |
T |
15: 35,423,391 (GRCm39) |
R237L |
probably damaging |
Het |
| Zfp865 |
T |
C |
7: 5,034,372 (GRCm39) |
S786P |
probably benign |
Het |
|
| Other mutations in Or6c6c |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01613:Or6c6c
|
APN |
10 |
129,541,492 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02245:Or6c6c
|
APN |
10 |
129,541,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02341:Or6c6c
|
APN |
10 |
129,541,358 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02433:Or6c6c
|
APN |
10 |
129,541,445 (GRCm39) |
missense |
probably benign |
0.01 |
|
authen
|
UTSW |
10 |
129,541,668 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0111:Or6c6c
|
UTSW |
10 |
129,541,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0309:Or6c6c
|
UTSW |
10 |
129,541,008 (GRCm39) |
missense |
probably benign |
0.38 |
|
R0326:Or6c6c
|
UTSW |
10 |
129,541,638 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R0374:Or6c6c
|
UTSW |
10 |
129,541,516 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1573:Or6c6c
|
UTSW |
10 |
129,541,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1663:Or6c6c
|
UTSW |
10 |
129,541,160 (GRCm39) |
missense |
probably benign |
0.44 |
|
R1778:Or6c6c
|
UTSW |
10 |
129,541,574 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1789:Or6c6c
|
UTSW |
10 |
129,541,476 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R1906:Or6c6c
|
UTSW |
10 |
129,541,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2108:Or6c6c
|
UTSW |
10 |
129,541,490 (GRCm39) |
missense |
probably benign |
|
|
R2211:Or6c6c
|
UTSW |
10 |
129,541,320 (GRCm39) |
missense |
probably benign |
|
|
R2432:Or6c6c
|
UTSW |
10 |
129,540,794 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2902:Or6c6c
|
UTSW |
10 |
129,541,320 (GRCm39) |
missense |
probably benign |
|
|
R4114:Or6c6c
|
UTSW |
10 |
129,541,668 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5149:Or6c6c
|
UTSW |
10 |
129,541,377 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5153:Or6c6c
|
UTSW |
10 |
129,541,026 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5846:Or6c6c
|
UTSW |
10 |
129,540,756 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6553:Or6c6c
|
UTSW |
10 |
129,540,932 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7676:Or6c6c
|
UTSW |
10 |
129,541,155 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R8161:Or6c6c
|
UTSW |
10 |
129,540,753 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9266:Or6c6c
|
UTSW |
10 |
129,541,547 (GRCm39) |
missense |
probably benign |
0.17 |
|
R9318:Or6c6c
|
UTSW |
10 |
129,541,283 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9334:Or6c6c
|
UTSW |
10 |
129,541,683 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9746:Or6c6c
|
UTSW |
10 |
129,541,208 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Posted On |
2014-05-07 |
Incidental Mutation