Incidental Mutation 'IGL01063:Or6x1'
| ID |
51856 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or6x1
|
| Ensembl Gene |
ENSMUSG00000051095 |
| Gene Name |
olfactory receptor family 6 subfamily X member 1 |
| Synonyms |
MOR104-3, GA_x6K02T2PVTD-33886895-33887833, Olfr986 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.122)
|
| Stock # |
IGL01063
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
40098375-40099390 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 40099052 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 214
(I214F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000152019
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000026693]
[ENSMUST00000062229]
[ENSMUST00000168691]
[ENSMUST00000168832]
[ENSMUST00000214763]
[ENSMUST00000216720]
[ENSMUST00000218134]
|
| AlphaFold |
Q8VFN6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000026693
|
| SMART Domains |
Protein: ENSMUSP00000026693
Gene: ENSMUSG00000025602
| Domain | Start | End | E-Value | Type |
|---|
|
SCAN
|
42 |
154 |
1.19e-75 |
SMART |
|
KRAB
|
237 |
297 |
1.7e-17 |
SMART |
|
ZnF_C2H2
|
391 |
413 |
9.44e-2 |
SMART |
|
ZnF_C2H2
|
419 |
441 |
6.42e-4 |
SMART |
|
ZnF_C2H2
|
473 |
495 |
3.44e-4 |
SMART |
|
ZnF_C2H2
|
501 |
523 |
1.47e-3 |
SMART |
|
ZnF_C2H2
|
529 |
551 |
1.64e-1 |
SMART |
|
ZnF_C2H2
|
557 |
579 |
3.11e-2 |
SMART |
|
ZnF_C2H2
|
585 |
607 |
8.47e-4 |
SMART |
|
ZnF_C2H2
|
613 |
635 |
3.39e-3 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000062229
AA Change: I214F
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
| SMART Domains |
Protein: ENSMUSP00000056713
Gene: ENSMUSG00000051095
AA Change: I214F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
5.1e-54 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
3.7e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000168691
|
| SMART Domains |
Protein: ENSMUSP00000130163
Gene: ENSMUSG00000025602
| Domain | Start | End | E-Value | Type |
|---|
|
SCAN
|
42 |
132 |
1.03e-56 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000168832
|
| SMART Domains |
Protein: ENSMUSP00000132131
Gene: ENSMUSG00000025602
| Domain | Start | End | E-Value | Type |
|---|
|
SCAN
|
42 |
154 |
1.19e-75 |
SMART |
|
KRAB
|
237 |
277 |
5.32e-2 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214763
AA Change: I214F
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216720
AA Change: I214F
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000218134
AA Change: I214F
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
| 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: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110038F14Rik |
G |
A |
15: 76,834,475 (GRCm39) |
V124I |
probably damaging |
Het |
| 4930444P10Rik |
A |
T |
1: 16,148,870 (GRCm39) |
L61* |
probably null |
Het |
| Abca7 |
T |
C |
10: 79,847,131 (GRCm39) |
I1705T |
probably damaging |
Het |
| Ablim1 |
T |
A |
19: 57,049,760 (GRCm39) |
I393F |
probably damaging |
Het |
| Adamts5 |
A |
G |
16: 85,696,722 (GRCm39) |
L145P |
probably damaging |
Het |
| Ano6 |
T |
C |
15: 95,846,310 (GRCm39) |
I537T |
probably damaging |
Het |
| AU018091 |
T |
C |
7: 3,212,153 (GRCm39) |
I190V |
possibly damaging |
Het |
| Camk1 |
T |
A |
6: 113,315,333 (GRCm39) |
D155V |
probably damaging |
Het |
| Cdh6 |
A |
C |
15: 13,064,581 (GRCm39) |
I103S |
probably damaging |
Het |
| Cntnap1 |
A |
G |
11: 101,072,614 (GRCm39) |
D537G |
probably benign |
Het |
| Col6a3 |
T |
C |
1: 90,730,054 (GRCm39) |
K1144E |
probably damaging |
Het |
| Cpeb1 |
T |
A |
7: 81,021,929 (GRCm39) |
E71D |
probably benign |
Het |
| Cps1 |
T |
C |
1: 67,234,325 (GRCm39) |
L904P |
possibly damaging |
Het |
| Cyfip1 |
T |
A |
7: 55,553,958 (GRCm39) |
F700I |
probably damaging |
Het |
| Dmp1 |
G |
A |
5: 104,354,965 (GRCm39) |
M1I |
probably null |
Het |
| Efcab6 |
A |
T |
15: 83,938,713 (GRCm39) |
M1K |
probably null |
Het |
| Extl2 |
A |
T |
3: 115,821,131 (GRCm39) |
H312L |
possibly damaging |
Het |
| Fat4 |
C |
A |
3: 38,944,728 (GRCm39) |
A1207D |
possibly damaging |
Het |
| Flnb |
T |
C |
14: 7,926,518 (GRCm38) |
|
probably benign |
Het |
| Hdac10 |
G |
T |
15: 89,008,071 (GRCm39) |
A593E |
possibly damaging |
Het |
| Hdhd2 |
T |
C |
18: 77,052,969 (GRCm39) |
|
probably null |
Het |
| Kcnq2 |
A |
G |
2: 180,751,582 (GRCm39) |
|
probably benign |
Het |
| Kdm7a |
A |
G |
6: 39,142,064 (GRCm39) |
F405L |
probably damaging |
Het |
| Lypd6b |
C |
A |
2: 49,833,642 (GRCm39) |
|
probably benign |
Het |
| Mki67 |
A |
T |
7: 135,296,651 (GRCm39) |
D2794E |
possibly damaging |
Het |
| Mtmr14 |
T |
A |
6: 113,243,287 (GRCm39) |
F40I |
probably damaging |
Het |
| Or2y3 |
G |
T |
17: 38,393,544 (GRCm39) |
S108R |
possibly damaging |
Het |
| Or5p55 |
A |
T |
7: 107,566,741 (GRCm39) |
I46F |
probably damaging |
Het |
| Or6d13 |
T |
A |
6: 116,517,968 (GRCm39) |
C185S |
probably damaging |
Het |
| Ppargc1a |
C |
A |
5: 51,631,664 (GRCm39) |
V322L |
probably benign |
Het |
| Ppfibp1 |
T |
A |
6: 146,931,195 (GRCm39) |
M917K |
probably benign |
Het |
| Prkg2 |
C |
T |
5: 99,117,795 (GRCm39) |
|
probably null |
Het |
| Rfx4 |
A |
G |
10: 84,704,246 (GRCm39) |
E296G |
possibly damaging |
Het |
| Rfx8 |
T |
A |
1: 39,722,110 (GRCm39) |
K292* |
probably null |
Het |
| Scamp3 |
C |
A |
3: 89,084,973 (GRCm39) |
|
probably benign |
Het |
| Scn4a |
A |
T |
11: 106,221,190 (GRCm39) |
I823N |
possibly damaging |
Het |
| Sdk2 |
A |
G |
11: 113,721,668 (GRCm39) |
V1316A |
probably damaging |
Het |
| Setd2 |
T |
C |
9: 110,402,741 (GRCm39) |
V1794A |
probably damaging |
Het |
| Stard8 |
G |
T |
X: 98,116,694 (GRCm39) |
R983L |
probably damaging |
Het |
| Tbc1d23 |
A |
T |
16: 57,013,038 (GRCm39) |
D311E |
probably benign |
Het |
| Tex21 |
T |
C |
12: 76,245,592 (GRCm39) |
H568R |
probably benign |
Het |
| Tex35 |
T |
C |
1: 156,932,667 (GRCm39) |
|
probably benign |
Het |
| Tgs1 |
T |
A |
4: 3,591,292 (GRCm39) |
F442I |
possibly damaging |
Het |
| Traf2 |
C |
A |
2: 25,414,931 (GRCm39) |
C303F |
probably benign |
Het |
| Trim56 |
A |
T |
5: 137,143,354 (GRCm39) |
V54D |
possibly damaging |
Het |
| Yars2 |
C |
T |
16: 16,124,406 (GRCm39) |
R338* |
probably null |
Het |
| Zfp668 |
A |
T |
7: 127,465,454 (GRCm39) |
C577S |
probably damaging |
Het |
|
| Other mutations in Or6x1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02342:Or6x1
|
APN |
9 |
40,098,823 (GRCm39) |
missense |
probably benign |
|
|
IGL02961:Or6x1
|
APN |
9 |
40,098,897 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0379:Or6x1
|
UTSW |
9 |
40,098,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1411:Or6x1
|
UTSW |
9 |
40,098,435 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1712:Or6x1
|
UTSW |
9 |
40,099,161 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1818:Or6x1
|
UTSW |
9 |
40,098,558 (GRCm39) |
missense |
probably benign |
|
|
R2249:Or6x1
|
UTSW |
9 |
40,098,980 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R3162:Or6x1
|
UTSW |
9 |
40,098,901 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3162:Or6x1
|
UTSW |
9 |
40,098,901 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5071:Or6x1
|
UTSW |
9 |
40,098,960 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5464:Or6x1
|
UTSW |
9 |
40,099,080 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5475:Or6x1
|
UTSW |
9 |
40,099,005 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R5695:Or6x1
|
UTSW |
9 |
40,098,897 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5878:Or6x1
|
UTSW |
9 |
40,098,867 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6978:Or6x1
|
UTSW |
9 |
40,099,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7252:Or6x1
|
UTSW |
9 |
40,098,657 (GRCm39) |
missense |
probably benign |
0.25 |
|
R8040:Or6x1
|
UTSW |
9 |
40,098,717 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8410:Or6x1
|
UTSW |
9 |
40,098,732 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8726:Or6x1
|
UTSW |
9 |
40,098,663 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8829:Or6x1
|
UTSW |
9 |
40,099,209 (GRCm39) |
missense |
probably benign |
0.42 |
|
| Posted On |
2013-06-21 |
Incidental Mutation