Incidental Mutation 'R1035:Or5ac19'
| ID |
95571 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5ac19
|
| Ensembl Gene |
ENSMUSG00000074995 |
| Gene Name |
olfactory receptor family 5 subfamily AC member 19 |
| Synonyms |
Olfr201, MOR182-2, GA_x54KRFPKG5P-55483936-55483010 |
| MMRRC Submission |
039134-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.170)
|
| Stock # |
R1035 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
59089102-59090028 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 59089307 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Tyrosine
at position 241
(C241Y)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150660
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099656]
[ENSMUST00000216834]
|
| AlphaFold |
Q7TS38 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000099656
AA Change: C241Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000097248
Gene: ENSMUSG00000074995
AA Change: C241Y
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.2e-46 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
8e-18 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216834
AA Change: C241Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Meta Mutation Damage Score |
0.6467 |
| Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 94.9%
- 20x: 88.4%
|
| Validation Efficiency |
97% (36/37) |
| 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: 30 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aasdh |
G |
A |
5: 77,024,130 (GRCm39) |
T174M |
probably damaging |
Het |
| Ap3b2 |
A |
T |
7: 81,113,659 (GRCm39) |
L850Q |
unknown |
Het |
| Asxl3 |
T |
C |
18: 22,658,106 (GRCm39) |
S2039P |
probably damaging |
Het |
| Cadm2 |
A |
T |
16: 66,612,235 (GRCm39) |
M109K |
probably damaging |
Het |
| Caskin1 |
A |
G |
17: 24,724,011 (GRCm39) |
N933S |
probably damaging |
Het |
| Cbln4 |
T |
C |
2: 171,883,989 (GRCm39) |
N77S |
possibly damaging |
Het |
| Chek1 |
A |
G |
9: 36,627,769 (GRCm39) |
I256T |
probably damaging |
Het |
| Col5a3 |
A |
T |
9: 20,704,795 (GRCm39) |
|
probably benign |
Het |
| Cyp2b10 |
C |
T |
7: 25,616,473 (GRCm39) |
S360L |
probably benign |
Het |
| Dctn1 |
T |
C |
6: 83,167,202 (GRCm39) |
S222P |
probably damaging |
Het |
| Dnah7b |
A |
G |
1: 46,163,608 (GRCm39) |
I471V |
probably benign |
Het |
| Ear2 |
A |
T |
14: 44,340,344 (GRCm39) |
M1L |
possibly damaging |
Het |
| Entpd6 |
T |
A |
2: 150,606,112 (GRCm39) |
|
probably benign |
Het |
| Extl1 |
TGCGTTGCACCGATACCGGG |
TG |
4: 134,084,988 (GRCm39) |
|
probably benign |
Het |
| Fam98b |
C |
T |
2: 117,101,120 (GRCm39) |
R311W |
possibly damaging |
Het |
| Ggt7 |
A |
T |
2: 155,348,347 (GRCm39) |
C102S |
probably damaging |
Het |
| Myo15a |
T |
C |
11: 60,401,384 (GRCm39) |
|
probably benign |
Het |
| Nlrp9c |
C |
T |
7: 26,070,702 (GRCm39) |
|
probably benign |
Het |
| Nrxn1 |
A |
T |
17: 90,471,302 (GRCm39) |
N1234K |
probably damaging |
Het |
| Pcsk1 |
T |
C |
13: 75,280,238 (GRCm39) |
S688P |
probably benign |
Het |
| Polr1a |
T |
C |
6: 71,944,900 (GRCm39) |
F1319L |
probably benign |
Het |
| Ppig |
T |
C |
2: 69,579,803 (GRCm39) |
Y446H |
unknown |
Het |
| Spmap2 |
G |
A |
10: 79,419,684 (GRCm39) |
T182M |
probably damaging |
Het |
| Stk17b |
T |
C |
1: 53,801,758 (GRCm39) |
T88A |
probably benign |
Het |
| Tas2r143 |
A |
T |
6: 42,377,199 (GRCm39) |
I10F |
probably benign |
Het |
| Tmprss12 |
G |
A |
15: 100,183,081 (GRCm39) |
R141Q |
probably benign |
Het |
| Trpa1 |
A |
G |
1: 14,961,527 (GRCm39) |
|
probably null |
Het |
| Txndc16 |
A |
G |
14: 45,410,020 (GRCm39) |
S187P |
possibly damaging |
Het |
| Vmn2r98 |
T |
C |
17: 19,301,011 (GRCm39) |
I671T |
possibly damaging |
Het |
| Zfp78 |
G |
T |
7: 6,381,660 (GRCm39) |
V237F |
probably damaging |
Het |
|
| Other mutations in Or5ac19 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01734:Or5ac19
|
APN |
16 |
59,089,213 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL01985:Or5ac19
|
APN |
16 |
59,089,442 (GRCm39) |
missense |
probably benign |
|
|
IGL02618:Or5ac19
|
APN |
16 |
59,089,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02830:Or5ac19
|
APN |
16 |
59,089,416 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
PIT4449001:Or5ac19
|
UTSW |
16 |
59,089,493 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0047:Or5ac19
|
UTSW |
16 |
59,089,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0047:Or5ac19
|
UTSW |
16 |
59,089,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1037:Or5ac19
|
UTSW |
16 |
59,089,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1163:Or5ac19
|
UTSW |
16 |
59,089,518 (GRCm39) |
missense |
probably benign |
0.23 |
|
R1225:Or5ac19
|
UTSW |
16 |
59,089,587 (GRCm39) |
missense |
probably benign |
|
|
R1519:Or5ac19
|
UTSW |
16 |
59,089,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1583:Or5ac19
|
UTSW |
16 |
59,089,394 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2075:Or5ac19
|
UTSW |
16 |
59,089,274 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R4591:Or5ac19
|
UTSW |
16 |
59,089,776 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5547:Or5ac19
|
UTSW |
16 |
59,089,479 (GRCm39) |
missense |
probably benign |
0.35 |
|
R6132:Or5ac19
|
UTSW |
16 |
59,089,367 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6737:Or5ac19
|
UTSW |
16 |
59,089,175 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R6872:Or5ac19
|
UTSW |
16 |
59,089,961 (GRCm39) |
missense |
probably benign |
0.20 |
|
R8001:Or5ac19
|
UTSW |
16 |
59,089,472 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8525:Or5ac19
|
UTSW |
16 |
59,089,571 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9003:Or5ac19
|
UTSW |
16 |
59,089,263 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9260:Or5ac19
|
UTSW |
16 |
59,089,677 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9584:Or5ac19
|
UTSW |
16 |
59,089,580 (GRCm39) |
missense |
probably benign |
0.05 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTGCTACAAGAACTTCACTGAACCC -3'
(R):5'- CTTGGTGTTCTGCACTTGGCAATTC -3'
Sequencing Primer
(F):5'- GAGGATACTGACCCTCCAGTAAAATG -3'
(R):5'- GTTTGTTACTTAGACTGACTTTCTGC -3'
|
| Posted On |
2014-01-05 |
Incidental Mutation