Incidental Mutation 'R5805:Or13a28'
| ID |
448451 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or13a28
|
| Ensembl Gene |
ENSMUSG00000096069 |
| Gene Name |
olfactory receptor family 13 subfamily A member 28 |
| Synonyms |
Olfr61, IH7, GA_x6K02T2PBJ9-42783826-42784758, MOR253-1 |
| MMRRC Submission |
043212-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.065)
|
| Stock # |
R5805 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
140217616-140218551 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 140218384 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Isoleucine
at position 257
(F257I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000147924
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084455]
[ENSMUST00000210241]
[ENSMUST00000210373]
[ENSMUST00000211685]
|
| AlphaFold |
Q8VGM2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000084455
AA Change: F257I
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000081493
Gene: ENSMUSG00000096069
AA Change: F257I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
32 |
308 |
3.3e-49 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
36 |
175 |
1.3e-8 |
PFAM |
|
Pfam:7tm_1
|
42 |
291 |
3.6e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000210241
AA Change: F257I
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000210373
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000211685
AA Change: F257I
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.6%
|
| 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: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca5 |
C |
T |
11: 110,170,216 (GRCm39) |
C1293Y |
probably benign |
Het |
| Adam8 |
T |
A |
7: 139,565,794 (GRCm39) |
D611V |
probably damaging |
Het |
| Arhgap33 |
T |
C |
7: 30,225,839 (GRCm39) |
T576A |
probably benign |
Het |
| Atf7 |
A |
T |
15: 102,466,022 (GRCm39) |
|
probably null |
Het |
| Baiap3 |
T |
A |
17: 25,466,489 (GRCm39) |
T464S |
probably benign |
Het |
| Ccdc40 |
T |
C |
11: 119,136,906 (GRCm39) |
|
probably null |
Het |
| Celf2 |
T |
C |
2: 6,558,598 (GRCm39) |
E430G |
probably damaging |
Het |
| Chia1 |
A |
G |
3: 106,035,792 (GRCm39) |
T211A |
probably damaging |
Het |
| Ciz1 |
T |
C |
2: 32,257,408 (GRCm39) |
F151S |
probably damaging |
Het |
| Dnm2 |
A |
G |
9: 21,378,965 (GRCm39) |
T175A |
probably damaging |
Het |
| Doc2b |
A |
G |
11: 75,663,364 (GRCm39) |
S363P |
probably damaging |
Het |
| Garem1 |
C |
T |
18: 21,281,492 (GRCm39) |
R288H |
probably benign |
Het |
| Gpr132 |
G |
A |
12: 112,816,416 (GRCm39) |
R137C |
probably damaging |
Het |
| Helz2 |
C |
A |
2: 180,882,301 (GRCm39) |
C164F |
probably damaging |
Het |
| Itfg1 |
A |
T |
8: 86,493,601 (GRCm39) |
S293T |
probably benign |
Het |
| Kcnn2 |
T |
A |
18: 45,816,198 (GRCm39) |
D336E |
probably damaging |
Het |
| Kifc2 |
C |
T |
15: 76,546,353 (GRCm39) |
A245V |
probably benign |
Het |
| Krt18 |
T |
A |
15: 101,939,735 (GRCm39) |
I311N |
probably benign |
Het |
| Lypla1 |
T |
C |
1: 4,900,517 (GRCm39) |
M7T |
possibly damaging |
Het |
| Mef2a |
T |
C |
7: 66,901,416 (GRCm39) |
M285V |
possibly damaging |
Het |
| Micu1 |
A |
C |
10: 59,663,128 (GRCm39) |
K353Q |
possibly damaging |
Het |
| Mpv17l |
A |
G |
16: 13,760,013 (GRCm39) |
|
probably benign |
Het |
| Ntrk1 |
G |
A |
3: 87,687,479 (GRCm39) |
R652W |
probably damaging |
Het |
| Or13c7 |
T |
C |
4: 43,855,152 (GRCm39) |
I281T |
probably benign |
Het |
| Or4c107 |
G |
A |
2: 88,788,985 (GRCm39) |
M58I |
possibly damaging |
Het |
| Pcdh15 |
C |
A |
10: 74,066,091 (GRCm39) |
T252K |
probably damaging |
Het |
| Pcsk5 |
T |
C |
19: 17,434,193 (GRCm39) |
M1392V |
probably benign |
Het |
| Phf20 |
T |
A |
2: 156,149,214 (GRCm39) |
V964E |
probably damaging |
Het |
| Pira13 |
G |
A |
7: 3,825,622 (GRCm39) |
L416F |
probably benign |
Het |
| Plcg2 |
T |
C |
8: 118,325,234 (GRCm39) |
|
probably null |
Het |
| Rnf10 |
A |
T |
5: 115,382,127 (GRCm39) |
C693S |
probably benign |
Het |
| Rnf19b |
A |
G |
4: 128,952,617 (GRCm39) |
Y185C |
probably damaging |
Het |
| Ros1 |
G |
T |
10: 51,999,385 (GRCm39) |
D1167E |
probably damaging |
Het |
| Sidt2 |
G |
A |
9: 45,853,497 (GRCm39) |
S701L |
probably damaging |
Het |
| Slc66a2 |
C |
T |
18: 80,306,658 (GRCm39) |
P76L |
probably damaging |
Het |
| Spag1 |
T |
C |
15: 36,200,430 (GRCm39) |
I345T |
probably damaging |
Het |
| Srcap |
T |
A |
7: 127,141,211 (GRCm39) |
S1603T |
possibly damaging |
Het |
| Stag1 |
T |
A |
9: 100,678,831 (GRCm39) |
Y251N |
probably damaging |
Het |
| Stxbp5 |
T |
C |
10: 9,776,330 (GRCm39) |
N33S |
probably benign |
Het |
| Tnrc6a |
T |
C |
7: 122,769,299 (GRCm39) |
L363P |
probably damaging |
Het |
| U2surp |
C |
T |
9: 95,361,357 (GRCm39) |
R591H |
possibly damaging |
Het |
| Usf3 |
A |
G |
16: 44,041,109 (GRCm39) |
N1863S |
possibly damaging |
Het |
| Vmn2r15 |
T |
C |
5: 109,434,806 (GRCm39) |
I633V |
possibly damaging |
Het |
| Zfp979 |
T |
C |
4: 147,698,067 (GRCm39) |
D214G |
probably damaging |
Het |
|
| Other mutations in Or13a28 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00958:Or13a28
|
APN |
7 |
140,218,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01837:Or13a28
|
APN |
7 |
140,218,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02349:Or13a28
|
APN |
7 |
140,218,384 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02713:Or13a28
|
APN |
7 |
140,217,829 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02982:Or13a28
|
APN |
7 |
140,217,865 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL03205:Or13a28
|
APN |
7 |
140,218,073 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1477:Or13a28
|
UTSW |
7 |
140,218,355 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1564:Or13a28
|
UTSW |
7 |
140,217,967 (GRCm39) |
missense |
probably benign |
0.21 |
|
R1900:Or13a28
|
UTSW |
7 |
140,218,505 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2149:Or13a28
|
UTSW |
7 |
140,217,965 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2504:Or13a28
|
UTSW |
7 |
140,218,397 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2887:Or13a28
|
UTSW |
7 |
140,218,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3787:Or13a28
|
UTSW |
7 |
140,217,748 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4628:Or13a28
|
UTSW |
7 |
140,218,297 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4775:Or13a28
|
UTSW |
7 |
140,217,829 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6019:Or13a28
|
UTSW |
7 |
140,217,925 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6244:Or13a28
|
UTSW |
7 |
140,218,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7303:Or13a28
|
UTSW |
7 |
140,218,267 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7505:Or13a28
|
UTSW |
7 |
140,217,965 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7783:Or13a28
|
UTSW |
7 |
140,217,637 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7936:Or13a28
|
UTSW |
7 |
140,217,652 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9060:Or13a28
|
UTSW |
7 |
140,217,695 (GRCm39) |
missense |
|
|
|
R9114:Or13a28
|
UTSW |
7 |
140,218,282 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1088:Or13a28
|
UTSW |
7 |
140,218,133 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ATGACACTTGTGGCAGATGC -3'
(R):5'- CTCAGGAAAGCACGTTTAGGAG -3'
Sequencing Primer
(F):5'- AGATGCCTTTTATGGGTGCATCAAC -3'
(R):5'- TCCAGGTCAGGAGAATATTCTGC -3'
|
| Posted On |
2016-12-15 |
Incidental Mutation