Incidental Mutation 'IGL02486:Or11h6'
| ID |
295415 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or11h6
|
| Ensembl Gene |
ENSMUSG00000050028 |
| Gene Name |
olfactory receptor family 11 subfamily H member 6 |
| Synonyms |
GA_x6K02T2PMLR-6361495-6362481, Olfr745, MOR106-11 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.112)
|
| Stock # |
IGL02486
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
50879652-50880826 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 50880089 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Serine
at position 111
(F111S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153971
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000062534]
[ENSMUST00000213127]
[ENSMUST00000218546]
|
| AlphaFold |
Q7TRL9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000062534
AA Change: F117S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000050184
Gene: ENSMUSG00000050028
AA Change: F117S
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
5 |
27 |
N/A |
INTRINSIC |
|
Pfam:7tm_4
|
44 |
324 |
6.3e-54 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
51 |
191 |
6.6e-6 |
PFAM |
|
Pfam:7tm_1
|
57 |
306 |
1e-21 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206749
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000213127
AA Change: F111S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000216105
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000218546
|
| 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: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2010106E10Rik |
T |
A |
X: 111,424,955 (GRCm39) |
N147K |
probably benign |
Het |
| Abtb3 |
C |
A |
10: 85,476,419 (GRCm39) |
P900H |
probably damaging |
Het |
| Bcas1 |
T |
C |
2: 170,248,318 (GRCm39) |
D201G |
probably damaging |
Het |
| Bmp1 |
T |
A |
14: 70,742,216 (GRCm39) |
D333V |
possibly damaging |
Het |
| Capn6 |
T |
C |
X: 142,587,673 (GRCm39) |
E535G |
probably benign |
Het |
| Cdin1 |
T |
C |
2: 115,607,487 (GRCm39) |
V280A |
possibly damaging |
Het |
| Chac2 |
T |
C |
11: 30,927,625 (GRCm39) |
D86G |
probably damaging |
Het |
| Col14a1 |
T |
A |
15: 55,252,092 (GRCm39) |
|
probably benign |
Het |
| Daam1 |
T |
C |
12: 71,993,919 (GRCm39) |
|
probably benign |
Het |
| Elapor2 |
T |
A |
5: 9,472,323 (GRCm39) |
V340E |
probably benign |
Het |
| Eno4 |
A |
G |
19: 58,934,097 (GRCm39) |
|
probably null |
Het |
| Fat1 |
T |
C |
8: 45,478,109 (GRCm39) |
V2385A |
probably benign |
Het |
| Ffar4 |
T |
C |
19: 38,102,208 (GRCm39) |
I281T |
possibly damaging |
Het |
| Flcn |
C |
T |
11: 59,691,869 (GRCm39) |
W260* |
probably null |
Het |
| Fry |
T |
G |
5: 150,414,642 (GRCm39) |
S496A |
probably damaging |
Het |
| Gk |
T |
A |
X: 84,759,274 (GRCm39) |
I373F |
possibly damaging |
Het |
| Gpr108 |
T |
C |
17: 57,542,977 (GRCm39) |
N528S |
probably damaging |
Het |
| Hey1 |
T |
A |
3: 8,731,579 (GRCm39) |
R50W |
probably damaging |
Het |
| Hgf |
A |
G |
5: 16,807,287 (GRCm39) |
Y393C |
probably damaging |
Het |
| Hmcn2 |
A |
T |
2: 31,310,107 (GRCm39) |
E3260D |
probably damaging |
Het |
| Ift172 |
A |
G |
5: 31,414,927 (GRCm39) |
I1365T |
probably damaging |
Het |
| Letmd1 |
A |
G |
15: 100,372,992 (GRCm39) |
R31G |
probably damaging |
Het |
| Mak16 |
T |
C |
8: 31,650,614 (GRCm39) |
|
probably benign |
Het |
| Mapkapk3 |
C |
T |
9: 107,166,467 (GRCm39) |
G26D |
probably damaging |
Het |
| Mphosph8 |
T |
C |
14: 56,925,844 (GRCm39) |
V603A |
possibly damaging |
Het |
| Myom1 |
G |
T |
17: 71,406,939 (GRCm39) |
|
probably benign |
Het |
| Neb |
T |
A |
2: 52,172,615 (GRCm39) |
N1564I |
possibly damaging |
Het |
| Nox1 |
C |
T |
X: 132,993,560 (GRCm39) |
G433D |
probably damaging |
Het |
| Or2n1b |
T |
A |
17: 38,460,112 (GRCm39) |
L211Q |
probably damaging |
Het |
| Or51i2 |
T |
C |
7: 103,689,617 (GRCm39) |
S205P |
probably damaging |
Het |
| Or52m1 |
A |
T |
7: 102,289,627 (GRCm39) |
H58L |
probably damaging |
Het |
| Rcc2 |
T |
C |
4: 140,437,673 (GRCm39) |
W135R |
probably damaging |
Het |
| Rgl2 |
A |
G |
17: 34,154,954 (GRCm39) |
I205V |
probably damaging |
Het |
| Robo4 |
G |
A |
9: 37,319,670 (GRCm39) |
G640E |
probably damaging |
Het |
| Slc26a5 |
A |
G |
5: 22,051,323 (GRCm39) |
F64L |
probably damaging |
Het |
| Slc27a2 |
A |
G |
2: 126,395,270 (GRCm39) |
T66A |
probably benign |
Het |
| St18 |
T |
C |
1: 6,890,307 (GRCm39) |
S580P |
probably damaging |
Het |
| Syt15 |
G |
A |
14: 33,944,933 (GRCm39) |
R160K |
probably damaging |
Het |
| Tmem63b |
A |
G |
17: 45,984,909 (GRCm39) |
S200P |
probably damaging |
Het |
| Tnks |
T |
A |
8: 35,318,352 (GRCm39) |
N841I |
probably damaging |
Het |
| Tnr |
G |
A |
1: 159,679,664 (GRCm39) |
|
probably null |
Het |
| Unc13d |
A |
G |
11: 115,960,632 (GRCm39) |
|
probably benign |
Het |
| Usp4 |
T |
C |
9: 108,228,228 (GRCm39) |
L74P |
probably damaging |
Het |
|
| Other mutations in Or11h6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00330:Or11h6
|
APN |
14 |
50,880,625 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02316:Or11h6
|
APN |
14 |
50,879,744 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02377:Or11h6
|
APN |
14 |
50,879,975 (GRCm39) |
splice site |
probably null |
|
|
IGL02471:Or11h6
|
APN |
14 |
50,880,214 (GRCm39) |
missense |
probably benign |
0.43 |
|
IGL02517:Or11h6
|
APN |
14 |
50,880,658 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0453:Or11h6
|
UTSW |
14 |
50,880,461 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0727:Or11h6
|
UTSW |
14 |
50,880,460 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0746:Or11h6
|
UTSW |
14 |
50,880,232 (GRCm39) |
splice site |
probably null |
|
|
R1638:Or11h6
|
UTSW |
14 |
50,880,565 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1688:Or11h6
|
UTSW |
14 |
50,880,705 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1991:Or11h6
|
UTSW |
14 |
50,880,323 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R2245:Or11h6
|
UTSW |
14 |
50,880,062 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3758:Or11h6
|
UTSW |
14 |
50,880,493 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R4084:Or11h6
|
UTSW |
14 |
50,880,305 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5033:Or11h6
|
UTSW |
14 |
50,880,619 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5211:Or11h6
|
UTSW |
14 |
50,880,710 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R5302:Or11h6
|
UTSW |
14 |
50,879,776 (GRCm39) |
splice site |
probably null |
|
|
R5645:Or11h6
|
UTSW |
14 |
50,880,524 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5731:Or11h6
|
UTSW |
14 |
50,880,248 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6917:Or11h6
|
UTSW |
14 |
50,880,680 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R7408:Or11h6
|
UTSW |
14 |
50,879,852 (GRCm39) |
missense |
probably benign |
0.16 |
|
R7716:Or11h6
|
UTSW |
14 |
50,879,815 (GRCm39) |
missense |
probably benign |
0.17 |
|
R7728:Or11h6
|
UTSW |
14 |
50,879,849 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8208:Or11h6
|
UTSW |
14 |
50,880,088 (GRCm39) |
missense |
probably benign |
0.28 |
|
R8447:Or11h6
|
UTSW |
14 |
50,880,008 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8726:Or11h6
|
UTSW |
14 |
50,880,703 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8748:Or11h6
|
UTSW |
14 |
50,880,211 (GRCm39) |
missense |
probably benign |
0.19 |
|
R9279:Or11h6
|
UTSW |
14 |
50,880,493 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
| Posted On |
2015-04-16 |
Incidental Mutation