Incidental Mutation 'R5824:Or6c65'
| ID |
450076 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or6c65
|
| Ensembl Gene |
ENSMUSG00000049894 |
| Gene Name |
olfactory receptor family 6 subfamily C member 65 |
| Synonyms |
GA_x6K02T2PULF-11446184-11447122, Olfr808, MOR112-2 |
| MMRRC Submission |
043216-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.063)
|
| Stock # |
R5824 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
10 |
| Chromosomal Location |
129603367-129604305 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 129604250 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 295
(V295A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000145315
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000060636]
[ENSMUST00000203236]
|
| AlphaFold |
Q8VGI8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000060636
AA Change: V295A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000059714
Gene: ENSMUSG00000049894
AA Change: V295A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
308 |
1.8e-53 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
7.7e-25 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000203236
AA Change: V295A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000145315
Gene: ENSMUSG00000049894
AA Change: V295A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
308 |
1.8e-53 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
7.7e-25 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.3%
- 20x: 95.2%
|
| 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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Agtpbp1 |
A |
T |
13: 59,613,913 (GRCm39) |
H66Q |
probably damaging |
Het |
| Ap1g1 |
T |
A |
8: 110,565,544 (GRCm39) |
|
probably null |
Het |
| Ap4b1 |
A |
T |
3: 103,720,701 (GRCm39) |
I124F |
probably benign |
Het |
| Arhgap10 |
A |
T |
8: 78,085,181 (GRCm39) |
Y462* |
probably null |
Het |
| Btnl10 |
G |
T |
11: 58,814,266 (GRCm39) |
M315I |
probably benign |
Het |
| Cep295 |
A |
G |
9: 15,236,952 (GRCm39) |
V1994A |
possibly damaging |
Het |
| Cherp |
G |
A |
8: 73,216,102 (GRCm39) |
|
probably benign |
Het |
| Ckap5 |
G |
A |
2: 91,389,481 (GRCm39) |
A318T |
probably benign |
Het |
| Cma1 |
T |
C |
14: 56,179,182 (GRCm39) |
K238E |
possibly damaging |
Het |
| Cspg4b |
T |
A |
13: 113,505,154 (GRCm39) |
H2094Q |
probably damaging |
Het |
| Ctif |
T |
C |
18: 75,743,749 (GRCm39) |
D141G |
possibly damaging |
Het |
| Ctnna1 |
T |
C |
18: 35,312,939 (GRCm39) |
S264P |
probably benign |
Het |
| Dnah12 |
G |
T |
14: 26,492,475 (GRCm39) |
|
probably null |
Het |
| Dnah5 |
A |
G |
15: 28,313,967 (GRCm39) |
T1928A |
probably benign |
Het |
| Etfdh |
G |
A |
3: 79,517,252 (GRCm39) |
P379L |
probably damaging |
Het |
| Gfra3 |
T |
C |
18: 34,844,264 (GRCm39) |
N92S |
probably damaging |
Het |
| Gpr161 |
C |
A |
1: 165,138,560 (GRCm39) |
T382K |
possibly damaging |
Het |
| Gspt2 |
T |
C |
X: 93,680,071 (GRCm39) |
V70A |
possibly damaging |
Het |
| Hmcn1 |
A |
G |
1: 150,868,774 (GRCm39) |
V10A |
probably benign |
Het |
| Iqgap2 |
C |
T |
13: 95,811,880 (GRCm39) |
R707H |
probably damaging |
Het |
| Kpna1 |
A |
G |
16: 35,840,575 (GRCm39) |
D205G |
possibly damaging |
Het |
| Man2a2 |
T |
G |
7: 80,002,780 (GRCm39) |
D1067A |
probably benign |
Het |
| Map3k4 |
G |
A |
17: 12,448,526 (GRCm39) |
H1551Y |
probably damaging |
Het |
| Moxd1 |
A |
T |
10: 24,162,995 (GRCm39) |
I486F |
probably damaging |
Het |
| Notch3 |
G |
T |
17: 32,372,835 (GRCm39) |
R579S |
possibly damaging |
Het |
| Or2r3 |
C |
A |
6: 42,448,906 (GRCm39) |
V69L |
probably benign |
Het |
| Or8b4 |
A |
G |
9: 37,830,861 (GRCm39) |
T308A |
probably benign |
Het |
| Pira13 |
T |
C |
7: 3,827,753 (GRCm39) |
T135A |
probably damaging |
Het |
| Recql4 |
C |
T |
15: 76,592,785 (GRCm39) |
C302Y |
probably damaging |
Het |
| Reg3b |
G |
A |
6: 78,349,104 (GRCm39) |
V77I |
possibly damaging |
Het |
| Terb1 |
T |
C |
8: 105,212,079 (GRCm39) |
T301A |
probably benign |
Het |
| Tmem260 |
G |
A |
14: 48,742,785 (GRCm39) |
C540Y |
probably damaging |
Het |
| Tmprss15 |
A |
T |
16: 78,831,201 (GRCm39) |
F385I |
probably damaging |
Het |
| Trbv12-2 |
G |
A |
6: 41,095,774 (GRCm39) |
|
probably benign |
Het |
| Upk3bl |
T |
A |
5: 136,089,133 (GRCm39) |
Y196* |
probably null |
Het |
| Vmn1r199 |
A |
T |
13: 22,567,748 (GRCm39) |
K304N |
probably benign |
Het |
|
| Other mutations in Or6c65 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00965:Or6c65
|
APN |
10 |
129,603,455 (GRCm39) |
missense |
probably null |
0.99 |
|
IGL01313:Or6c65
|
APN |
10 |
129,603,464 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01923:Or6c65
|
APN |
10 |
129,603,973 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02010:Or6c65
|
APN |
10 |
129,604,136 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL02393:Or6c65
|
APN |
10 |
129,603,662 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL03026:Or6c65
|
APN |
10 |
129,603,910 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1181:Or6c65
|
UTSW |
10 |
129,604,033 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1760:Or6c65
|
UTSW |
10 |
129,603,417 (GRCm39) |
missense |
probably benign |
0.06 |
|
R1844:Or6c65
|
UTSW |
10 |
129,603,725 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2697:Or6c65
|
UTSW |
10 |
129,603,793 (GRCm39) |
missense |
probably benign |
0.09 |
|
R3025:Or6c65
|
UTSW |
10 |
129,603,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3414:Or6c65
|
UTSW |
10 |
129,604,301 (GRCm39) |
missense |
probably benign |
|
|
R6260:Or6c65
|
UTSW |
10 |
129,603,389 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6723:Or6c65
|
UTSW |
10 |
129,604,284 (GRCm39) |
missense |
probably benign |
0.38 |
|
R6758:Or6c65
|
UTSW |
10 |
129,603,920 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7305:Or6c65
|
UTSW |
10 |
129,603,720 (GRCm39) |
nonsense |
probably null |
|
|
R7422:Or6c65
|
UTSW |
10 |
129,604,136 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8393:Or6c65
|
UTSW |
10 |
129,604,304 (GRCm39) |
makesense |
probably null |
|
|
R8444:Or6c65
|
UTSW |
10 |
129,603,794 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8702:Or6c65
|
UTSW |
10 |
129,604,284 (GRCm39) |
missense |
probably benign |
0.38 |
|
R8717:Or6c65
|
UTSW |
10 |
129,604,127 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8797:Or6c65
|
UTSW |
10 |
129,603,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9356:Or6c65
|
UTSW |
10 |
129,604,035 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R9596:Or6c65
|
UTSW |
10 |
129,603,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGATACCTTCTGCAGAGCAAAG -3'
(R):5'- AACGACTGTGAGTTATTTAGGTAGG -3'
Sequencing Primer
(F):5'- GAAAAAGGCCTTTTCCACTTGTTC -3'
(R):5'- GTTGCTGATTCCTAGTTACTAAAAGC -3'
|
| Posted On |
2016-12-20 |
Incidental Mutation