Incidental Mutation 'IGL02705:Or7g12'
| ID |
304293 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or7g12
|
| Ensembl Gene |
ENSMUSG00000095525 |
| Gene Name |
olfactory receptor family 7 subfamily G member 12 |
| Synonyms |
GA_x6K02T2PVTD-12724921-12725859, MOR153-2, Olfr834, MOR153-4_p |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.315)
|
| Stock # |
IGL02705
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
18899286-18900224 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 18899696 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Lysine
at position 137
(N137K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000083680
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086492]
|
| AlphaFold |
Q7TRG8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000086492
AA Change: N137K
PolyPhen 2
Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000083680
Gene: ENSMUSG00000095525
AA Change: N137K
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
7.2e-51 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
7e-6 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.9e-20 |
PFAM |
|
| 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: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700025G04Rik |
A |
G |
1: 151,791,264 (GRCm39) |
F99S |
probably damaging |
Het |
| Ankrd17 |
G |
A |
5: 90,430,974 (GRCm39) |
P937S |
probably benign |
Het |
| Apom |
T |
G |
17: 35,349,471 (GRCm39) |
|
probably null |
Het |
| Baz2b |
A |
G |
2: 59,778,604 (GRCm39) |
I752T |
possibly damaging |
Het |
| Bcat1 |
T |
C |
6: 144,964,914 (GRCm39) |
|
probably benign |
Het |
| Bcl9 |
A |
G |
3: 97,112,181 (GRCm39) |
F1425L |
possibly damaging |
Het |
| Bco1 |
G |
A |
8: 117,844,242 (GRCm39) |
V319M |
possibly damaging |
Het |
| Dmwd |
C |
A |
7: 18,814,769 (GRCm39) |
T473K |
probably benign |
Het |
| Garin4 |
T |
C |
1: 190,896,499 (GRCm39) |
Y48C |
probably damaging |
Het |
| Gata2 |
C |
T |
6: 88,182,346 (GRCm39) |
A438V |
possibly damaging |
Het |
| Ifnz |
A |
G |
4: 88,701,574 (GRCm39) |
|
probably benign |
Het |
| Myh14 |
T |
C |
7: 44,257,960 (GRCm39) |
I1859V |
possibly damaging |
Het |
| Ndn |
A |
G |
7: 61,998,856 (GRCm39) |
D234G |
probably damaging |
Het |
| Nfe2l3 |
T |
C |
6: 51,410,098 (GRCm39) |
L71P |
probably damaging |
Het |
| Nfia |
T |
G |
4: 97,671,605 (GRCm39) |
L105R |
probably damaging |
Het |
| Npy2r |
T |
A |
3: 82,448,056 (GRCm39) |
T127S |
probably benign |
Het |
| Or51a8 |
T |
C |
7: 102,550,449 (GRCm39) |
Y292H |
probably damaging |
Het |
| Ppip5k2 |
A |
T |
1: 97,686,924 (GRCm39) |
C94S |
probably damaging |
Het |
| Pramel26 |
A |
G |
4: 143,537,372 (GRCm39) |
S320P |
probably damaging |
Het |
| Slc1a6 |
T |
C |
10: 78,637,788 (GRCm39) |
V438A |
probably damaging |
Het |
| Slc6a7 |
C |
T |
18: 61,142,500 (GRCm39) |
G71R |
probably damaging |
Het |
| Styk1 |
C |
T |
6: 131,289,546 (GRCm39) |
V23I |
probably benign |
Het |
| Tmprss5 |
C |
A |
9: 49,018,447 (GRCm39) |
N92K |
probably benign |
Het |
| Trpm6 |
T |
G |
19: 18,754,097 (GRCm39) |
|
probably null |
Het |
| Ttn |
C |
T |
2: 76,677,114 (GRCm39) |
|
probably benign |
Het |
| Tut7 |
A |
G |
13: 59,937,017 (GRCm39) |
F808S |
probably damaging |
Het |
| Vmn2r109 |
G |
A |
17: 20,774,062 (GRCm39) |
A431V |
probably benign |
Het |
| Wdr17 |
C |
T |
8: 55,101,250 (GRCm39) |
|
probably null |
Het |
| Zfp407 |
G |
T |
18: 84,577,156 (GRCm39) |
S1319* |
probably null |
Het |
|
| Other mutations in Or7g12 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01804:Or7g12
|
APN |
9 |
18,900,136 (GRCm39) |
missense |
probably benign |
0.16 |
|
IGL02073:Or7g12
|
APN |
9 |
18,899,621 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02119:Or7g12
|
APN |
9 |
18,899,908 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0462:Or7g12
|
UTSW |
9 |
18,900,198 (GRCm39) |
missense |
probably benign |
|
|
R0466:Or7g12
|
UTSW |
9 |
18,899,551 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0709:Or7g12
|
UTSW |
9 |
18,899,422 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0711:Or7g12
|
UTSW |
9 |
18,899,447 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1268:Or7g12
|
UTSW |
9 |
18,899,652 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1663:Or7g12
|
UTSW |
9 |
18,900,006 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1680:Or7g12
|
UTSW |
9 |
18,899,812 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1686:Or7g12
|
UTSW |
9 |
18,899,839 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1903:Or7g12
|
UTSW |
9 |
18,900,192 (GRCm39) |
nonsense |
probably null |
|
|
R1907:Or7g12
|
UTSW |
9 |
18,899,737 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R1911:Or7g12
|
UTSW |
9 |
18,900,196 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2143:Or7g12
|
UTSW |
9 |
18,900,099 (GRCm39) |
missense |
probably benign |
0.06 |
|
R2431:Or7g12
|
UTSW |
9 |
18,899,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4014:Or7g12
|
UTSW |
9 |
18,900,178 (GRCm39) |
missense |
probably benign |
0.08 |
|
R4515:Or7g12
|
UTSW |
9 |
18,899,278 (GRCm39) |
splice site |
probably null |
|
|
R4575:Or7g12
|
UTSW |
9 |
18,900,001 (GRCm39) |
nonsense |
probably null |
|
|
R6974:Or7g12
|
UTSW |
9 |
18,899,689 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7394:Or7g12
|
UTSW |
9 |
18,900,006 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7455:Or7g12
|
UTSW |
9 |
18,900,150 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7828:Or7g12
|
UTSW |
9 |
18,900,216 (GRCm39) |
missense |
probably benign |
|
|
R7962:Or7g12
|
UTSW |
9 |
18,899,952 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8360:Or7g12
|
UTSW |
9 |
18,900,139 (GRCm39) |
missense |
probably benign |
0.28 |
|
R8812:Or7g12
|
UTSW |
9 |
18,899,812 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R8905:Or7g12
|
UTSW |
9 |
18,899,494 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8973:Or7g12
|
UTSW |
9 |
18,899,974 (GRCm39) |
nonsense |
probably null |
|
|
R8980:Or7g12
|
UTSW |
9 |
18,899,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9013:Or7g12
|
UTSW |
9 |
18,899,874 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9058:Or7g12
|
UTSW |
9 |
18,900,222 (GRCm39) |
makesense |
probably null |
|
|
R9614:Or7g12
|
UTSW |
9 |
18,899,526 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R9779:Or7g12
|
UTSW |
9 |
18,900,135 (GRCm39) |
missense |
probably benign |
0.04 |
|
| Posted On |
2015-04-16 |
Incidental Mutation