Incidental Mutation 'IGL02396:Or10ag57'
| ID |
294365 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or10ag57
|
| Ensembl Gene |
ENSMUSG00000047594 |
| Gene Name |
olfactory receptor family 10 subfamily AG member 57 |
| Synonyms |
GA_x6K02T2Q125-48880078-48881058, Olfr1122, MOR264-1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.101)
|
| Stock # |
IGL02396
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
87218051-87219031 bp(+) (GRCm39) |
| Type of Mutation |
utr 5 prime |
| DNA Base Change (assembly) |
A to T
at 87218049 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149403
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000056435]
[ENSMUST00000215371]
|
| AlphaFold |
Q8VGT9 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000056435
|
| SMART Domains |
Protein: ENSMUSP00000052190
Gene: ENSMUSG00000047594
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
43 |
319 |
6.3e-51 |
PFAM |
|
Pfam:7tm_1
|
53 |
302 |
5.8e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215371
|
| 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: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acin1 |
C |
T |
14: 54,882,256 (GRCm39) |
|
probably benign |
Het |
| Bhmt1b |
A |
G |
18: 87,774,780 (GRCm39) |
E101G |
possibly damaging |
Het |
| Bmp3 |
C |
A |
5: 99,020,578 (GRCm39) |
Q334K |
possibly damaging |
Het |
| Bnc2 |
G |
T |
4: 84,194,246 (GRCm39) |
S1026R |
probably benign |
Het |
| Bsn |
C |
T |
9: 107,993,245 (GRCm39) |
G836S |
possibly damaging |
Het |
| Cand2 |
A |
G |
6: 115,768,149 (GRCm39) |
|
probably benign |
Het |
| Ccdc24 |
T |
C |
4: 117,726,826 (GRCm39) |
T296A |
possibly damaging |
Het |
| Ccdc38 |
A |
G |
10: 93,409,994 (GRCm39) |
N271S |
possibly damaging |
Het |
| Ccdc81 |
T |
G |
7: 89,530,857 (GRCm39) |
I362L |
probably benign |
Het |
| Cdhr3 |
T |
A |
12: 33,095,195 (GRCm39) |
I625F |
possibly damaging |
Het |
| Col12a1 |
T |
A |
9: 79,569,865 (GRCm39) |
R1568S |
probably benign |
Het |
| Cpeb4 |
T |
A |
11: 31,875,441 (GRCm39) |
S547T |
probably benign |
Het |
| Dennd4c |
T |
A |
4: 86,743,237 (GRCm39) |
N1075K |
probably damaging |
Het |
| Esrra |
C |
A |
19: 6,889,373 (GRCm39) |
V339L |
probably benign |
Het |
| Ghr |
A |
T |
15: 3,487,480 (GRCm39) |
M1K |
probably null |
Het |
| Gm4987 |
T |
A |
X: 45,544,991 (GRCm39) |
|
noncoding transcript |
Het |
| Golga2 |
G |
T |
2: 32,188,656 (GRCm39) |
|
probably benign |
Het |
| Gys1 |
T |
A |
7: 45,089,012 (GRCm39) |
I137N |
probably damaging |
Het |
| Hs3st5 |
A |
T |
10: 36,704,699 (GRCm39) |
M1L |
probably benign |
Het |
| Hsd3b5 |
T |
A |
3: 98,529,343 (GRCm39) |
T96S |
probably benign |
Het |
| Ighv6-3 |
T |
C |
12: 114,355,356 (GRCm39) |
D111G |
probably damaging |
Het |
| Immp1l |
T |
A |
2: 105,767,351 (GRCm39) |
I70N |
probably damaging |
Het |
| Ints4 |
G |
A |
7: 97,187,107 (GRCm39) |
V866I |
possibly damaging |
Het |
| Large2 |
G |
T |
2: 92,196,668 (GRCm39) |
Y529* |
probably null |
Het |
| Maf1 |
C |
A |
15: 76,237,457 (GRCm39) |
Y166* |
probably null |
Het |
| Manba |
T |
A |
3: 135,250,525 (GRCm39) |
M384K |
probably damaging |
Het |
| Mapk4 |
C |
A |
18: 74,067,068 (GRCm39) |
|
probably null |
Het |
| Mc5r |
T |
C |
18: 68,472,537 (GRCm39) |
S299P |
possibly damaging |
Het |
| Mdn1 |
T |
A |
4: 32,700,120 (GRCm39) |
N1404K |
probably damaging |
Het |
| Milr1 |
C |
A |
11: 106,656,065 (GRCm39) |
Y212* |
probably null |
Het |
| Ncor2 |
A |
G |
5: 125,114,978 (GRCm39) |
S1115P |
probably damaging |
Het |
| Or4f61 |
C |
A |
2: 111,922,812 (GRCm39) |
C78F |
probably benign |
Het |
| Osbpl7 |
T |
G |
11: 96,946,377 (GRCm39) |
L158R |
probably damaging |
Het |
| Psmd4 |
A |
T |
3: 94,943,221 (GRCm39) |
L61Q |
probably damaging |
Het |
| Rassf9 |
A |
T |
10: 102,381,554 (GRCm39) |
N310I |
possibly damaging |
Het |
| Rpl21-ps6 |
A |
G |
17: 56,222,400 (GRCm39) |
|
noncoding transcript |
Het |
| Slc31a2 |
T |
C |
4: 62,215,310 (GRCm39) |
I119T |
probably damaging |
Het |
| Srgap2 |
C |
A |
1: 131,220,413 (GRCm39) |
C187F |
probably damaging |
Het |
| Tekt5 |
C |
A |
16: 10,196,931 (GRCm39) |
A307S |
probably benign |
Het |
| Tmem214 |
G |
A |
5: 31,030,090 (GRCm39) |
A296T |
probably benign |
Het |
| Ttn |
A |
G |
2: 76,775,432 (GRCm39) |
V1916A |
unknown |
Het |
| Wee1 |
T |
G |
7: 109,741,300 (GRCm39) |
V641G |
probably damaging |
Het |
| Zfand6 |
G |
A |
7: 84,267,111 (GRCm39) |
P157L |
probably damaging |
Het |
|
| Other mutations in Or10ag57 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01783:Or10ag57
|
APN |
2 |
87,218,182 (GRCm39) |
missense |
probably benign |
0.39 |
|
IGL01783:Or10ag57
|
APN |
2 |
87,218,187 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL03338:Or10ag57
|
APN |
2 |
87,218,470 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03373:Or10ag57
|
APN |
2 |
87,218,577 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0594:Or10ag57
|
UTSW |
2 |
87,218,298 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1245:Or10ag57
|
UTSW |
2 |
87,218,553 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1376:Or10ag57
|
UTSW |
2 |
87,218,162 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1376:Or10ag57
|
UTSW |
2 |
87,218,162 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1471:Or10ag57
|
UTSW |
2 |
87,218,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1681:Or10ag57
|
UTSW |
2 |
87,218,964 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1995:Or10ag57
|
UTSW |
2 |
87,218,175 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2246:Or10ag57
|
UTSW |
2 |
87,218,195 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2341:Or10ag57
|
UTSW |
2 |
87,218,084 (GRCm39) |
missense |
probably benign |
|
|
R4008:Or10ag57
|
UTSW |
2 |
87,218,924 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4009:Or10ag57
|
UTSW |
2 |
87,218,924 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4011:Or10ag57
|
UTSW |
2 |
87,218,924 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4119:Or10ag57
|
UTSW |
2 |
87,218,187 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4547:Or10ag57
|
UTSW |
2 |
87,218,504 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4665:Or10ag57
|
UTSW |
2 |
87,218,220 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4666:Or10ag57
|
UTSW |
2 |
87,218,220 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4801:Or10ag57
|
UTSW |
2 |
87,218,553 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4802:Or10ag57
|
UTSW |
2 |
87,218,553 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5049:Or10ag57
|
UTSW |
2 |
87,219,002 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5070:Or10ag57
|
UTSW |
2 |
87,218,507 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7594:Or10ag57
|
UTSW |
2 |
87,218,613 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7684:Or10ag57
|
UTSW |
2 |
87,218,372 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8064:Or10ag57
|
UTSW |
2 |
87,218,853 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8218:Or10ag57
|
UTSW |
2 |
87,218,922 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8282:Or10ag57
|
UTSW |
2 |
87,218,852 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8335:Or10ag57
|
UTSW |
2 |
87,218,204 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9800:Or10ag57
|
UTSW |
2 |
87,218,508 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation