Incidental Mutation 'R6699:Or2t43'
| ID |
528692 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or2t43
|
| Ensembl Gene |
ENSMUSG00000059279 |
| Gene Name |
olfactory receptor family 2 subfamily T member 43 |
| Synonyms |
GA_x6K02T00261-652-347, Olfr224, Olfr327-ps1, GA_x6K02T2NKPP-858022-858862, MOR275-10_p, MOR275-3 |
| MMRRC Submission |
044817-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.051)
|
| Stock # |
R6699 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
58456682-58461379 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 58458031 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Leucine
at position 47
(I47L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150268
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081102]
[ENSMUST00000215322]
[ENSMUST00000216758]
[ENSMUST00000217009]
|
| AlphaFold |
M9MMJ7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000081102
AA Change: I47L
PolyPhen 2
Score 0.688 (Sensitivity: 0.86; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000079881
Gene: ENSMUSG00000059279
AA Change: I47L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srsx
|
33 |
299 |
5.1e-7 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
4.4e-35 |
PFAM |
|
Pfam:7tm_4
|
137 |
281 |
5.8e-43 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215322
AA Change: I47L
PolyPhen 2
Score 0.688 (Sensitivity: 0.86; Specificity: 0.92)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216758
AA Change: I47L
PolyPhen 2
Score 0.688 (Sensitivity: 0.86; Specificity: 0.92)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000217009
AA Change: I47L
PolyPhen 2
Score 0.688 (Sensitivity: 0.86; Specificity: 0.92)
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.2%
- 20x: 95.1%
|
| Validation Efficiency |
100% (35/35) |
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam39 |
A |
G |
8: 41,279,694 (GRCm39) |
K695R |
probably benign |
Het |
| Agfg1 |
G |
A |
1: 82,836,175 (GRCm39) |
|
probably null |
Het |
| Ankrd44 |
G |
A |
1: 54,801,604 (GRCm39) |
T241I |
probably damaging |
Het |
| Car15 |
T |
C |
16: 17,654,438 (GRCm39) |
D166G |
probably null |
Het |
| Cpne2 |
G |
A |
8: 95,290,587 (GRCm39) |
V391M |
probably damaging |
Het |
| Ddx27 |
C |
T |
2: 166,862,423 (GRCm39) |
T155I |
possibly damaging |
Het |
| F830045P16Rik |
T |
C |
2: 129,302,341 (GRCm39) |
D417G |
probably damaging |
Het |
| Fam217b |
T |
G |
2: 178,062,210 (GRCm39) |
M58R |
probably benign |
Het |
| Fcgbpl1 |
A |
G |
7: 27,843,793 (GRCm39) |
T894A |
probably damaging |
Het |
| Ftmt |
T |
C |
18: 52,464,737 (GRCm39) |
S18P |
possibly damaging |
Het |
| Gm16494 |
C |
T |
17: 47,327,834 (GRCm39) |
V17M |
probably damaging |
Het |
| Gm36864 |
A |
T |
7: 43,888,196 (GRCm39) |
I342F |
possibly damaging |
Het |
| Grid2 |
C |
G |
6: 63,908,031 (GRCm39) |
R224G |
possibly damaging |
Het |
| H4c12 |
A |
T |
13: 21,934,674 (GRCm39) |
M1K |
probably null |
Het |
| Hmgcr |
T |
C |
13: 96,796,717 (GRCm39) |
E191G |
probably damaging |
Het |
| Hrc |
A |
G |
7: 44,985,119 (GRCm39) |
D90G |
possibly damaging |
Het |
| Kbtbd7 |
A |
G |
14: 79,665,632 (GRCm39) |
E488G |
probably benign |
Het |
| Krtap26-1 |
T |
C |
16: 88,444,603 (GRCm39) |
N6S |
unknown |
Het |
| Mgat2 |
A |
G |
12: 69,231,555 (GRCm39) |
D43G |
probably damaging |
Het |
| Mrps30 |
A |
T |
13: 118,517,134 (GRCm39) |
S362T |
probably damaging |
Het |
| Or10ag58 |
A |
T |
2: 87,265,160 (GRCm39) |
I110F |
probably benign |
Het |
| Pcdhb11 |
T |
A |
18: 37,555,990 (GRCm39) |
V440E |
probably damaging |
Het |
| Pcdhb18 |
T |
A |
18: 37,625,005 (GRCm39) |
H778Q |
probably benign |
Het |
| Plekha7 |
T |
C |
7: 115,734,410 (GRCm39) |
E1025G |
probably damaging |
Het |
| Rnf39 |
T |
C |
17: 37,258,121 (GRCm39) |
W96R |
probably damaging |
Het |
| Rph3al |
A |
T |
11: 75,791,663 (GRCm39) |
|
probably benign |
Het |
| Rrm1 |
T |
A |
7: 102,110,032 (GRCm39) |
Y556N |
probably damaging |
Het |
| Saal1 |
A |
T |
7: 46,342,241 (GRCm39) |
C401S |
probably damaging |
Het |
| Sec14l3 |
T |
C |
11: 4,025,193 (GRCm39) |
S268P |
possibly damaging |
Het |
| Tmem54 |
A |
G |
4: 129,005,118 (GRCm39) |
I199M |
probably benign |
Het |
| Tomm70a |
A |
G |
16: 56,963,165 (GRCm39) |
M395V |
probably benign |
Het |
| Topors |
A |
G |
4: 40,262,300 (GRCm39) |
V328A |
probably damaging |
Het |
| Vmn2r61 |
T |
G |
7: 41,949,580 (GRCm39) |
S667A |
probably benign |
Het |
| Vmn2r68 |
G |
A |
7: 84,881,583 (GRCm39) |
A499V |
possibly damaging |
Het |
| Zcchc14 |
A |
T |
8: 122,335,355 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Or2t43 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00321:Or2t43
|
APN |
11 |
58,457,593 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02327:Or2t43
|
APN |
11 |
58,457,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02904:Or2t43
|
APN |
11 |
58,457,623 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
IGL02968:Or2t43
|
APN |
11 |
58,458,021 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1704:Or2t43
|
UTSW |
11 |
58,457,580 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2055:Or2t43
|
UTSW |
11 |
58,457,673 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3925:Or2t43
|
UTSW |
11 |
58,457,652 (GRCm39) |
missense |
probably benign |
0.34 |
|
R4093:Or2t43
|
UTSW |
11 |
58,457,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4902:Or2t43
|
UTSW |
11 |
58,457,451 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R4955:Or2t43
|
UTSW |
11 |
58,457,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4956:Or2t43
|
UTSW |
11 |
58,457,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4957:Or2t43
|
UTSW |
11 |
58,457,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5436:Or2t43
|
UTSW |
11 |
58,457,763 (GRCm39) |
missense |
probably benign |
0.34 |
|
R6825:Or2t43
|
UTSW |
11 |
58,457,476 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7467:Or2t43
|
UTSW |
11 |
58,457,288 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R7590:Or2t43
|
UTSW |
11 |
58,458,085 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7600:Or2t43
|
UTSW |
11 |
58,458,162 (GRCm39) |
missense |
probably benign |
0.17 |
|
R7725:Or2t43
|
UTSW |
11 |
58,457,593 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8438:Or2t43
|
UTSW |
11 |
58,457,665 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R8848:Or2t43
|
UTSW |
11 |
58,457,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8867:Or2t43
|
UTSW |
11 |
58,457,562 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9376:Or2t43
|
UTSW |
11 |
58,457,683 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
X0026:Or2t43
|
UTSW |
11 |
58,458,000 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
Z1186:Or2t43
|
UTSW |
11 |
58,457,920 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1186:Or2t43
|
UTSW |
11 |
58,457,521 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1186:Or2t43
|
UTSW |
11 |
58,457,388 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1187:Or2t43
|
UTSW |
11 |
58,457,920 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1187:Or2t43
|
UTSW |
11 |
58,457,521 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1187:Or2t43
|
UTSW |
11 |
58,457,388 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1188:Or2t43
|
UTSW |
11 |
58,457,920 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1188:Or2t43
|
UTSW |
11 |
58,457,521 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1188:Or2t43
|
UTSW |
11 |
58,457,388 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1189:Or2t43
|
UTSW |
11 |
58,457,920 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1189:Or2t43
|
UTSW |
11 |
58,457,521 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1189:Or2t43
|
UTSW |
11 |
58,457,388 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1190:Or2t43
|
UTSW |
11 |
58,457,920 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1190:Or2t43
|
UTSW |
11 |
58,457,521 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1190:Or2t43
|
UTSW |
11 |
58,457,388 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1191:Or2t43
|
UTSW |
11 |
58,457,521 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1191:Or2t43
|
UTSW |
11 |
58,457,388 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1191:Or2t43
|
UTSW |
11 |
58,457,920 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1192:Or2t43
|
UTSW |
11 |
58,457,920 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1192:Or2t43
|
UTSW |
11 |
58,457,521 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1192:Or2t43
|
UTSW |
11 |
58,457,388 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATAGCGGTCATAAGACATAGCAGC -3'
(R):5'- TTAGTTGCCTAGGAGACACCC -3'
Sequencing Primer
(F):5'- ATTCTGAACCTCCTAGTGACATG -3'
(R):5'- CTAGGAGACACCCAGGGAC -3'
|
| Posted On |
2018-07-24 |
Incidental Mutation