Incidental Mutation 'R4663:Or11g27'
| ID |
353045 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or11g27
|
| Ensembl Gene |
ENSMUSG00000094285 |
| Gene Name |
olfactory receptor family 11 subfamily G member 27 |
| Synonyms |
GA_x6K02T2PMLR-6243196-6244132, MOR106-8P, Olfr264, Olfr743, Olfr743-ps1, Olfr265, GA_x6K02T2N6FY-2320-2039, GA_x6K02T2N6FY-3870-3385, MOR106-14 |
| MMRRC Submission |
041921-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.086)
|
| Stock # |
R4663 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
14 |
| Chromosomal Location |
50770871-50771806 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 50771061 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Phenylalanine
at position 64
(Y64F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150946
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071294]
[ENSMUST00000215793]
|
| AlphaFold |
L7N1Y2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000071294
AA Change: Y64F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000071263
Gene: ENSMUSG00000094285
AA Change: Y64F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
311 |
1.6e-56 |
PFAM |
|
Pfam:7tm_1
|
45 |
294 |
1e-21 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215793
AA Change: Y64F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.9%
|
| 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: 72 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aqr |
A |
T |
2: 113,992,147 (GRCm39) |
Y76* |
probably null |
Het |
| Armc5 |
C |
A |
7: 127,837,717 (GRCm39) |
A140E |
probably benign |
Het |
| Auts2 |
T |
C |
5: 131,468,476 (GRCm39) |
H947R |
probably damaging |
Het |
| Bag2 |
T |
C |
1: 33,786,074 (GRCm39) |
T83A |
probably damaging |
Het |
| Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
| Bean1 |
A |
G |
8: 104,937,799 (GRCm39) |
Y126C |
probably damaging |
Het |
| Cars1 |
T |
C |
7: 143,129,697 (GRCm39) |
E330G |
probably damaging |
Het |
| Ccdc40 |
A |
G |
11: 119,122,332 (GRCm39) |
I45V |
probably benign |
Het |
| Cd320 |
G |
A |
17: 34,067,152 (GRCm39) |
G214R |
probably null |
Het |
| Ckm |
G |
A |
7: 19,153,419 (GRCm39) |
V237M |
probably damaging |
Het |
| Cplane1 |
T |
C |
15: 8,247,939 (GRCm39) |
V1496A |
probably benign |
Het |
| Cspg4 |
T |
C |
9: 56,793,960 (GRCm39) |
V565A |
possibly damaging |
Het |
| Dnaaf10 |
T |
C |
11: 17,182,853 (GRCm39) |
V338A |
probably benign |
Het |
| Eddm13 |
T |
G |
7: 6,261,624 (GRCm39) |
I35S |
possibly damaging |
Het |
| Ephb6 |
A |
G |
6: 41,594,799 (GRCm39) |
Y638C |
probably damaging |
Het |
| Fat2 |
G |
C |
11: 55,187,039 (GRCm39) |
S1269* |
probably null |
Het |
| Fbxo3 |
T |
C |
2: 103,883,820 (GRCm39) |
V348A |
probably damaging |
Het |
| Gas6 |
G |
A |
8: 13,520,254 (GRCm39) |
P478L |
probably damaging |
Het |
| Herc1 |
T |
C |
9: 66,340,660 (GRCm39) |
S1670P |
probably damaging |
Het |
| Hnrnpk |
C |
A |
13: 58,542,331 (GRCm39) |
R281L |
probably damaging |
Het |
| Ifih1 |
C |
A |
2: 62,439,563 (GRCm39) |
C488F |
probably benign |
Het |
| Ift172 |
T |
C |
5: 31,441,559 (GRCm39) |
K192E |
probably benign |
Het |
| Ighv5-9 |
T |
A |
12: 113,625,440 (GRCm39) |
Q101L |
probably benign |
Het |
| Igkv3-2 |
G |
T |
6: 70,675,863 (GRCm39) |
M57I |
probably benign |
Het |
| Insyn2a |
A |
T |
7: 134,500,877 (GRCm39) |
Y409* |
probably null |
Het |
| Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
| L3mbtl3 |
T |
C |
10: 26,213,715 (GRCm39) |
Y237C |
unknown |
Het |
| Lats1 |
G |
A |
10: 7,588,347 (GRCm39) |
C988Y |
probably damaging |
Het |
| Lgals3 |
T |
A |
14: 47,619,079 (GRCm39) |
|
probably null |
Het |
| Lrrc3b |
G |
T |
14: 15,358,220 (GRCm38) |
H129N |
probably benign |
Het |
| Lrriq1 |
T |
C |
10: 102,899,273 (GRCm39) |
H1656R |
possibly damaging |
Het |
| Lypd6 |
T |
G |
2: 50,063,623 (GRCm39) |
Y43* |
probably null |
Het |
| Mettl25b |
A |
G |
3: 87,835,055 (GRCm39) |
S82P |
probably damaging |
Het |
| Mical2 |
A |
G |
7: 111,927,884 (GRCm39) |
D674G |
possibly damaging |
Het |
| Msi1 |
G |
A |
5: 115,588,334 (GRCm39) |
R284Q |
probably damaging |
Het |
| Mybpc2 |
T |
C |
7: 44,155,066 (GRCm39) |
E947G |
probably damaging |
Het |
| Nat14 |
T |
A |
7: 4,927,446 (GRCm39) |
L206Q |
probably damaging |
Het |
| Nup88 |
A |
T |
11: 70,856,672 (GRCm39) |
|
probably null |
Het |
| Or4k15 |
A |
G |
14: 50,364,939 (GRCm39) |
R302G |
probably benign |
Het |
| Or8g19 |
A |
T |
9: 39,056,145 (GRCm39) |
I250F |
probably damaging |
Het |
| Pdcl |
T |
C |
2: 37,245,778 (GRCm39) |
E75G |
probably damaging |
Het |
| Phf14 |
A |
G |
6: 11,953,421 (GRCm39) |
I387V |
possibly damaging |
Het |
| Phf3 |
G |
A |
1: 30,860,296 (GRCm39) |
R845W |
probably damaging |
Het |
| Pm20d1 |
T |
C |
1: 131,726,340 (GRCm39) |
I59T |
probably damaging |
Het |
| Prkd1 |
C |
T |
12: 50,466,631 (GRCm39) |
|
probably null |
Het |
| Psmb2 |
T |
C |
4: 126,571,558 (GRCm39) |
L4P |
probably damaging |
Het |
| Pttg1 |
T |
A |
11: 43,315,677 (GRCm39) |
K46* |
probably null |
Het |
| Ryr2 |
T |
C |
13: 11,764,395 (GRCm39) |
H1401R |
possibly damaging |
Het |
| Septin4 |
T |
A |
11: 87,458,429 (GRCm39) |
Y268N |
probably damaging |
Het |
| Sh3d19 |
G |
A |
3: 86,030,570 (GRCm39) |
D696N |
probably benign |
Het |
| Slc16a2 |
T |
C |
X: 102,751,585 (GRCm39) |
T274A |
probably benign |
Het |
| Slc26a6 |
G |
A |
9: 108,735,106 (GRCm39) |
A335T |
probably damaging |
Het |
| Slc49a3 |
T |
C |
5: 108,590,011 (GRCm39) |
M464V |
probably benign |
Het |
| Slc6a5 |
C |
A |
7: 49,588,146 (GRCm39) |
Y493* |
probably null |
Het |
| Slf1 |
A |
T |
13: 77,274,723 (GRCm39) |
S37R |
probably damaging |
Het |
| Smoc1 |
G |
A |
12: 81,214,376 (GRCm39) |
G264S |
probably damaging |
Het |
| Snapc4 |
T |
C |
2: 26,264,193 (GRCm39) |
E280G |
possibly damaging |
Het |
| Snx25 |
G |
A |
8: 46,488,616 (GRCm39) |
T913M |
probably damaging |
Het |
| Snx7 |
T |
C |
3: 117,594,528 (GRCm39) |
T408A |
probably benign |
Het |
| Spdya |
T |
A |
17: 71,885,339 (GRCm39) |
S264R |
probably benign |
Het |
| Spg11 |
A |
T |
2: 121,928,580 (GRCm39) |
|
probably null |
Het |
| Suz12 |
T |
A |
11: 79,904,350 (GRCm39) |
L230Q |
probably damaging |
Het |
| Szt2 |
A |
G |
4: 118,234,881 (GRCm39) |
|
probably benign |
Het |
| Tenm3 |
C |
A |
8: 48,689,005 (GRCm39) |
R2194L |
probably damaging |
Het |
| Tmed8 |
T |
A |
12: 87,221,005 (GRCm39) |
I194F |
probably damaging |
Het |
| Tmem79 |
T |
A |
3: 88,240,751 (GRCm39) |
T66S |
probably damaging |
Het |
| Trappc1 |
T |
A |
11: 69,216,337 (GRCm39) |
S118T |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,569,225 (GRCm39) |
V27223I |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,606,839 (GRCm39) |
T18024A |
probably damaging |
Het |
| Vmn2r15 |
C |
T |
5: 109,441,940 (GRCm39) |
M164I |
probably benign |
Het |
| Vmn2r53 |
T |
A |
7: 12,334,901 (GRCm39) |
Y253F |
probably benign |
Het |
| Zfand6 |
C |
T |
7: 84,267,093 (GRCm39) |
R163H |
probably benign |
Het |
|
| Other mutations in Or11g27 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01128:Or11g27
|
APN |
14 |
50,771,406 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01551:Or11g27
|
APN |
14 |
50,771,618 (GRCm39) |
missense |
probably benign |
|
|
IGL02024:Or11g27
|
APN |
14 |
50,771,307 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02867:Or11g27
|
APN |
14 |
50,770,970 (GRCm39) |
missense |
probably benign |
|
|
IGL02889:Or11g27
|
APN |
14 |
50,770,970 (GRCm39) |
missense |
probably benign |
|
|
IGL03195:Or11g27
|
APN |
14 |
50,770,877 (GRCm39) |
missense |
probably benign |
|
|
IGL03296:Or11g27
|
APN |
14 |
50,771,402 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0049:Or11g27
|
UTSW |
14 |
50,771,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0049:Or11g27
|
UTSW |
14 |
50,771,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0102:Or11g27
|
UTSW |
14 |
50,771,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0556:Or11g27
|
UTSW |
14 |
50,771,381 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0626:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R0661:Or11g27
|
UTSW |
14 |
50,771,552 (GRCm39) |
missense |
probably benign |
|
|
R0759:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R0761:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R0894:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1109:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1110:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1312:Or11g27
|
UTSW |
14 |
50,771,652 (GRCm39) |
missense |
probably benign |
|
|
R1446:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1470:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1470:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1502:Or11g27
|
UTSW |
14 |
50,771,234 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R1518:Or11g27
|
UTSW |
14 |
50,771,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1529:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1624:Or11g27
|
UTSW |
14 |
50,771,100 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1646:Or11g27
|
UTSW |
14 |
50,771,040 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1687:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1795:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R2011:Or11g27
|
UTSW |
14 |
50,771,141 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2120:Or11g27
|
UTSW |
14 |
50,771,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2697:Or11g27
|
UTSW |
14 |
50,771,238 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2857:Or11g27
|
UTSW |
14 |
50,770,897 (GRCm39) |
missense |
probably benign |
0.19 |
|
R2858:Or11g27
|
UTSW |
14 |
50,770,897 (GRCm39) |
missense |
probably benign |
0.19 |
|
R3906:Or11g27
|
UTSW |
14 |
50,771,211 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4327:Or11g27
|
UTSW |
14 |
50,770,971 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4355:Or11g27
|
UTSW |
14 |
50,771,216 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5214:Or11g27
|
UTSW |
14 |
50,771,804 (GRCm39) |
makesense |
probably null |
|
|
R5964:Or11g27
|
UTSW |
14 |
50,771,655 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6148:Or11g27
|
UTSW |
14 |
50,771,778 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6167:Or11g27
|
UTSW |
14 |
50,771,612 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6301:Or11g27
|
UTSW |
14 |
50,771,711 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6616:Or11g27
|
UTSW |
14 |
50,771,364 (GRCm39) |
missense |
probably benign |
0.43 |
|
R6910:Or11g27
|
UTSW |
14 |
50,771,330 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7076:Or11g27
|
UTSW |
14 |
50,771,278 (GRCm39) |
nonsense |
probably null |
|
|
R7483:Or11g27
|
UTSW |
14 |
50,771,472 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7574:Or11g27
|
UTSW |
14 |
50,771,770 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7731:Or11g27
|
UTSW |
14 |
50,771,141 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8691:Or11g27
|
UTSW |
14 |
50,770,910 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9072:Or11g27
|
UTSW |
14 |
50,771,211 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9073:Or11g27
|
UTSW |
14 |
50,771,211 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9321:Or11g27
|
UTSW |
14 |
50,771,471 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9478:Or11g27
|
UTSW |
14 |
50,771,051 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9557:Or11g27
|
UTSW |
14 |
50,771,552 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GTGCTTTCACAGAACACAGACAG -3'
(R):5'- CGATCAAATGCCATGACTGCC -3'
Sequencing Primer
(F):5'- GACAGATGAAAACCCTCAGCAG -3'
(R):5'- CTGCCAGGAAAAAGCATTCTG -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation