Incidental Mutation 'IGL00895:Or4c111'
| ID |
26810 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4c111
|
| Ensembl Gene |
ENSMUSG00000075107 |
| Gene Name |
olfactory receptor family 4 subfamily C member 111 |
| Synonyms |
Olfr1216, MOR233-9, GA_x6K02T2Q125-50494588-50493653 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.057)
|
| Stock # |
IGL00895
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
88843471-88844406 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 88843953 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Leucine
at position 152
(F152L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149441
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099800]
[ENSMUST00000216000]
[ENSMUST00000217000]
|
| AlphaFold |
Q7TR05 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099800
AA Change: F152L
PolyPhen 2
Score 0.131 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000097388
Gene: ENSMUSG00000075107
AA Change: F152L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
303 |
1.8e-46 |
PFAM |
|
Pfam:7tm_1
|
39 |
286 |
4.2e-17 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216000
AA Change: F152L
PolyPhen 2
Score 0.131 (Sensitivity: 0.93; Specificity: 0.86)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217000
AA Change: F152L
PolyPhen 2
Score 0.131 (Sensitivity: 0.93; Specificity: 0.86)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000218738
|
| 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: 25 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arl6ip6 |
T |
A |
2: 53,092,936 (GRCm39) |
W154R |
probably damaging |
Het |
| Ccnc |
T |
A |
4: 21,742,642 (GRCm39) |
Y156* |
probably null |
Het |
| Clca3a1 |
A |
C |
3: 144,730,357 (GRCm39) |
W163G |
probably damaging |
Het |
| Cntnap5b |
C |
T |
1: 100,311,310 (GRCm39) |
T972I |
probably damaging |
Het |
| Cpn2 |
C |
T |
16: 30,079,338 (GRCm39) |
S121N |
probably benign |
Het |
| Dcc |
T |
C |
18: 71,943,871 (GRCm39) |
E260G |
probably damaging |
Het |
| Dnah6 |
A |
T |
6: 73,133,333 (GRCm39) |
N1091K |
possibly damaging |
Het |
| Dpp9 |
G |
T |
17: 56,512,240 (GRCm39) |
F249L |
probably damaging |
Het |
| Dscaml1 |
A |
G |
9: 45,662,551 (GRCm39) |
D1839G |
probably damaging |
Het |
| Esr1 |
C |
T |
10: 4,997,890 (GRCm38) |
R481L |
probably benign |
Het |
| Frem2 |
G |
T |
3: 53,493,016 (GRCm39) |
D1833E |
probably damaging |
Het |
| Ftdc2 |
A |
T |
16: 58,458,059 (GRCm39) |
Y81N |
probably benign |
Het |
| Ica1 |
T |
C |
6: 8,653,514 (GRCm39) |
D343G |
probably benign |
Het |
| Il27 |
T |
C |
7: 126,188,555 (GRCm39) |
H206R |
probably benign |
Het |
| Med14 |
A |
G |
X: 12,547,039 (GRCm39) |
V723A |
probably damaging |
Het |
| Msh3 |
C |
A |
13: 92,481,472 (GRCm39) |
G347C |
probably damaging |
Het |
| Nfasc |
T |
A |
1: 132,501,536 (GRCm39) |
K1262* |
probably null |
Het |
| Nlrp9a |
A |
T |
7: 26,258,103 (GRCm39) |
M485L |
probably benign |
Het |
| Or4f60 |
A |
G |
2: 111,902,100 (GRCm39) |
V276A |
probably damaging |
Het |
| Pcdhb5 |
T |
G |
18: 37,454,036 (GRCm39) |
L139V |
probably benign |
Het |
| Rbfox1 |
A |
T |
16: 7,187,698 (GRCm39) |
K43N |
probably benign |
Het |
| Scn5a |
G |
T |
9: 119,342,170 (GRCm39) |
|
probably null |
Het |
| Senp7 |
G |
T |
16: 55,902,740 (GRCm39) |
R21L |
probably damaging |
Het |
| Ssb |
G |
A |
2: 69,696,606 (GRCm39) |
V47I |
probably benign |
Het |
| Ttll8 |
T |
A |
15: 88,817,731 (GRCm39) |
S221C |
probably damaging |
Het |
|
| Other mutations in Or4c111 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00341:Or4c111
|
APN |
2 |
88,844,268 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL01634:Or4c111
|
APN |
2 |
88,843,788 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01844:Or4c111
|
APN |
2 |
88,843,814 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02036:Or4c111
|
APN |
2 |
88,843,823 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02102:Or4c111
|
APN |
2 |
88,843,470 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL02194:Or4c111
|
APN |
2 |
88,844,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02483:Or4c111
|
APN |
2 |
88,843,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02745:Or4c111
|
APN |
2 |
88,844,232 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02829:Or4c111
|
APN |
2 |
88,844,021 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03113:Or4c111
|
APN |
2 |
88,844,379 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03324:Or4c111
|
APN |
2 |
88,843,903 (GRCm39) |
nonsense |
probably null |
|
|
R0102:Or4c111
|
UTSW |
2 |
88,844,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0304:Or4c111
|
UTSW |
2 |
88,843,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1184:Or4c111
|
UTSW |
2 |
88,844,057 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1484:Or4c111
|
UTSW |
2 |
88,843,713 (GRCm39) |
nonsense |
probably null |
|
|
R1560:Or4c111
|
UTSW |
2 |
88,843,550 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1823:Or4c111
|
UTSW |
2 |
88,843,722 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1911:Or4c111
|
UTSW |
2 |
88,843,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2245:Or4c111
|
UTSW |
2 |
88,843,493 (GRCm39) |
missense |
probably benign |
|
|
R2331:Or4c111
|
UTSW |
2 |
88,844,265 (GRCm39) |
missense |
probably benign |
|
|
R3859:Or4c111
|
UTSW |
2 |
88,844,405 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R4579:Or4c111
|
UTSW |
2 |
88,843,488 (GRCm39) |
missense |
probably benign |
|
|
R5022:Or4c111
|
UTSW |
2 |
88,844,387 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5353:Or4c111
|
UTSW |
2 |
88,844,099 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5894:Or4c111
|
UTSW |
2 |
88,844,399 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6240:Or4c111
|
UTSW |
2 |
88,843,970 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7101:Or4c111
|
UTSW |
2 |
88,844,324 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7652:Or4c111
|
UTSW |
2 |
88,843,893 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8243:Or4c111
|
UTSW |
2 |
88,844,051 (GRCm39) |
missense |
probably benign |
0.39 |
|
R8752:Or4c111
|
UTSW |
2 |
88,844,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9062:Or4c111
|
UTSW |
2 |
88,843,548 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9472:Or4c111
|
UTSW |
2 |
88,843,517 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R9628:Or4c111
|
UTSW |
2 |
88,843,670 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Posted On |
2013-04-17 |
Incidental Mutation