Incidental Mutation 'R2438:Or4k49'
| ID |
249694 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4k49
|
| Ensembl Gene |
ENSMUSG00000109219 |
| Gene Name |
olfactory receptor family 4 subfamily K member 49 |
| Synonyms |
Olfr1299, GA_x6K02T2Q125-72715642-72716580, MOR248-8 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.166)
|
| Stock # |
R2438 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
111491798-111495511 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 111495096 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 175
(D175V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149299
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000207228]
[ENSMUST00000208175]
[ENSMUST00000213511]
|
| AlphaFold |
Q7TQX5 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000099610
AA Change: D175V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000097205
Gene: ENSMUSG00000074957
AA Change: D175V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
304 |
1.4e-47 |
PFAM |
|
Pfam:7tm_1
|
41 |
287 |
2.6e-19 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000207228
AA Change: D175V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000208175
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000208983
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000213511
AA Change: D175V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.2%
- 20x: 94.6%
|
| 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: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acap2 |
A |
G |
16: 30,936,133 (GRCm39) |
V318A |
probably damaging |
Het |
| B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
| Cd8b1 |
A |
G |
6: 71,306,740 (GRCm39) |
K156E |
probably damaging |
Het |
| Ckap5 |
T |
C |
2: 91,425,753 (GRCm39) |
M1262T |
possibly damaging |
Het |
| Crebbp |
A |
G |
16: 3,972,722 (GRCm39) |
M324T |
possibly damaging |
Het |
| Cwf19l1 |
G |
A |
19: 44,099,002 (GRCm39) |
R523C |
probably benign |
Het |
| Defb21 |
A |
T |
2: 152,416,695 (GRCm39) |
Y57F |
possibly damaging |
Het |
| Ebf2 |
T |
A |
14: 67,625,391 (GRCm39) |
V233D |
probably damaging |
Het |
| Gfpt1 |
A |
T |
6: 87,034,727 (GRCm39) |
E175V |
probably null |
Het |
| Gga1 |
T |
C |
15: 78,769,498 (GRCm39) |
F157S |
probably damaging |
Het |
| Impdh2 |
A |
T |
9: 108,437,815 (GRCm39) |
D28V |
probably benign |
Het |
| Itgav |
A |
G |
2: 83,606,886 (GRCm39) |
D409G |
probably damaging |
Het |
| Krt5 |
T |
C |
15: 101,620,093 (GRCm39) |
N208S |
probably benign |
Het |
| Matcap2 |
T |
C |
9: 22,342,979 (GRCm39) |
V291A |
probably damaging |
Het |
| Myo15a |
A |
T |
11: 60,373,878 (GRCm39) |
I1242F |
probably damaging |
Het |
| Myo1g |
A |
T |
11: 6,461,542 (GRCm39) |
N636K |
probably damaging |
Het |
| Nrros |
T |
C |
16: 31,962,929 (GRCm39) |
|
probably null |
Het |
| Nrros |
C |
T |
16: 31,963,117 (GRCm39) |
G264D |
probably benign |
Het |
| Nsun4 |
A |
G |
4: 115,905,794 (GRCm39) |
V54A |
probably benign |
Het |
| Or5b105 |
A |
T |
19: 13,079,785 (GRCm39) |
D294E |
probably benign |
Het |
| Pilrb2 |
T |
A |
5: 137,869,175 (GRCm39) |
I142L |
probably benign |
Het |
| Ryr2 |
A |
G |
13: 11,816,734 (GRCm39) |
S596P |
probably damaging |
Het |
| Sema5a |
G |
T |
15: 32,550,399 (GRCm39) |
S146I |
possibly damaging |
Het |
| Setx |
GTGGCT |
GT |
2: 29,044,073 (GRCm39) |
1814 |
probably null |
Het |
| Slc43a2 |
A |
T |
11: 75,453,957 (GRCm39) |
E290V |
possibly damaging |
Het |
| Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
| Zfp456 |
A |
T |
13: 67,515,073 (GRCm39) |
I211N |
probably damaging |
Het |
|
| Other mutations in Or4k49 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00946:Or4k49
|
APN |
2 |
111,495,489 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02090:Or4k49
|
APN |
2 |
111,495,333 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02213:Or4k49
|
APN |
2 |
111,495,020 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0603:Or4k49
|
UTSW |
2 |
111,495,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1598:Or4k49
|
UTSW |
2 |
111,495,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1802:Or4k49
|
UTSW |
2 |
111,495,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1803:Or4k49
|
UTSW |
2 |
111,495,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1885:Or4k49
|
UTSW |
2 |
111,495,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1887:Or4k49
|
UTSW |
2 |
111,495,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1962:Or4k49
|
UTSW |
2 |
111,495,234 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2024:Or4k49
|
UTSW |
2 |
111,495,168 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R5132:Or4k49
|
UTSW |
2 |
111,495,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5938:Or4k49
|
UTSW |
2 |
111,494,708 (GRCm39) |
missense |
probably benign |
|
|
R6115:Or4k49
|
UTSW |
2 |
111,494,987 (GRCm39) |
nonsense |
probably null |
|
|
R6336:Or4k49
|
UTSW |
2 |
111,494,964 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6418:Or4k49
|
UTSW |
2 |
111,494,817 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7196:Or4k49
|
UTSW |
2 |
111,495,042 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7539:Or4k49
|
UTSW |
2 |
111,494,778 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8262:Or4k49
|
UTSW |
2 |
111,494,587 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8331:Or4k49
|
UTSW |
2 |
111,494,727 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9765:Or4k49
|
UTSW |
2 |
111,495,230 (GRCm39) |
missense |
probably benign |
0.12 |
|
| Predicted Primers |
PCR Primer
(F):5'- CATATGACCGCTATGTGGCC -3'
(R):5'- GTGATGTTGAGGGGCCAAAC -3'
Sequencing Primer
(F):5'- GCTATGTGGCCATCTGTAAAC -3'
(R):5'- CTTAGATGCCCCAGCCTTAGAG -3'
|
| Posted On |
2014-11-12 |
Incidental Mutation