Incidental Mutation 'IGL02638:Or2z2'
| ID |
301602 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or2z2
|
| Ensembl Gene |
ENSMUSG00000043314 |
| Gene Name |
olfactory receptor family 2 subfamily Z member 2 |
| Synonyms |
MOR281-1, MTPCR07, GA_x6K02T2NKPP-957001-957948, Olfr30 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.083)
|
| Stock # |
IGL02638
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
58345741-58346806 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 58345873 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Serine
at position 301
(A301S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148907
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055204]
[ENSMUST00000064614]
[ENSMUST00000215691]
|
| AlphaFold |
Q8VGD8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000055204
AA Change: A301S
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000055961
Gene: ENSMUSG00000043314
AA Change: A301S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
32 |
308 |
1.9e-53 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
36 |
252 |
1.7e-6 |
PFAM |
|
Pfam:7tm_1
|
42 |
291 |
8.3e-25 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000064614
|
| SMART Domains |
Protein: ENSMUSP00000063665
Gene: ENSMUSG00000052642
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
Pfam:UPAR_LY6
|
47 |
124 |
1.3e-6 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215691
AA Change: A301S
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| 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: 50 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Alkbh3 |
T |
A |
2: 93,838,458 (GRCm39) |
T38S |
probably benign |
Het |
| Btbd8 |
T |
C |
5: 107,656,422 (GRCm39) |
V895A |
possibly damaging |
Het |
| Cdkn2c |
A |
G |
4: 109,522,209 (GRCm39) |
|
probably benign |
Het |
| Clca4b |
A |
C |
3: 144,631,939 (GRCm39) |
C189G |
probably damaging |
Het |
| Clec4f |
T |
A |
6: 83,629,682 (GRCm39) |
N292I |
possibly damaging |
Het |
| Dkk3 |
A |
C |
7: 111,748,234 (GRCm39) |
S123R |
probably benign |
Het |
| Dock1 |
C |
T |
7: 134,748,209 (GRCm39) |
A1557V |
probably benign |
Het |
| E130308A19Rik |
C |
T |
4: 59,719,676 (GRCm39) |
Q403* |
probably null |
Het |
| F5 |
G |
A |
1: 164,012,177 (GRCm39) |
|
probably null |
Het |
| Fam98c |
T |
A |
7: 28,852,187 (GRCm39) |
D326V |
probably damaging |
Het |
| Firrm |
G |
A |
1: 163,786,868 (GRCm39) |
Q734* |
probably null |
Het |
| Frem2 |
A |
C |
3: 53,458,767 (GRCm39) |
V2034G |
possibly damaging |
Het |
| Galnt2 |
G |
A |
8: 124,958,318 (GRCm39) |
G18D |
probably damaging |
Het |
| Grhl3 |
T |
C |
4: 135,284,176 (GRCm39) |
E222G |
probably benign |
Het |
| Hif3a |
A |
C |
7: 16,778,293 (GRCm39) |
|
probably benign |
Het |
| Ibtk |
C |
T |
9: 85,601,946 (GRCm39) |
G755D |
probably damaging |
Het |
| Laptm4b |
A |
G |
15: 34,277,630 (GRCm39) |
N187S |
probably benign |
Het |
| Lrba |
A |
G |
3: 86,232,380 (GRCm39) |
T776A |
probably damaging |
Het |
| Matcap2 |
A |
T |
9: 22,341,775 (GRCm39) |
K149* |
probably null |
Het |
| Mfhas1 |
T |
A |
8: 36,058,104 (GRCm39) |
W860R |
possibly damaging |
Het |
| Mon2 |
A |
C |
10: 122,859,844 (GRCm39) |
W811G |
probably damaging |
Het |
| Nup42 |
A |
G |
5: 24,380,505 (GRCm39) |
T167A |
probably benign |
Het |
| Or10j2 |
A |
G |
1: 173,097,898 (GRCm39) |
D52G |
probably benign |
Het |
| Or4k45 |
T |
C |
2: 111,395,249 (GRCm39) |
D180G |
probably damaging |
Het |
| Or5w10 |
T |
C |
2: 87,375,093 (GRCm39) |
Y265C |
probably damaging |
Het |
| Or8j3c |
T |
C |
2: 86,254,021 (GRCm39) |
|
probably null |
Het |
| Pgap2 |
T |
C |
7: 101,886,629 (GRCm39) |
L217P |
probably damaging |
Het |
| Pik3c2b |
T |
G |
1: 133,005,056 (GRCm39) |
|
probably benign |
Het |
| Ppfia3 |
T |
A |
7: 45,006,092 (GRCm39) |
D149V |
probably damaging |
Het |
| Prkcb |
C |
T |
7: 122,200,063 (GRCm39) |
|
probably benign |
Het |
| Prl |
A |
G |
13: 27,245,562 (GRCm39) |
D97G |
probably benign |
Het |
| Psma5-ps |
T |
C |
10: 85,149,698 (GRCm39) |
|
noncoding transcript |
Het |
| Rnf112 |
T |
C |
11: 61,340,231 (GRCm39) |
|
probably benign |
Het |
| Slc17a8 |
C |
A |
10: 89,412,465 (GRCm39) |
G323* |
probably null |
Het |
| Snx19 |
T |
C |
9: 30,343,660 (GRCm39) |
F607L |
possibly damaging |
Het |
| Suco |
A |
G |
1: 161,655,256 (GRCm39) |
S1079P |
probably damaging |
Het |
| Taf5 |
T |
C |
19: 47,056,649 (GRCm39) |
L149P |
probably benign |
Het |
| Taf6l |
T |
C |
19: 8,752,630 (GRCm39) |
M379V |
probably benign |
Het |
| Tcf25 |
T |
C |
8: 124,126,031 (GRCm39) |
F558L |
probably damaging |
Het |
| Tlcd1 |
T |
C |
11: 78,070,444 (GRCm39) |
V102A |
probably benign |
Het |
| Tmc5 |
G |
T |
7: 118,226,456 (GRCm39) |
A274S |
probably benign |
Het |
| Toporsl |
C |
T |
4: 52,611,624 (GRCm39) |
H506Y |
probably benign |
Het |
| Ubtd1 |
T |
C |
19: 42,022,109 (GRCm39) |
L127P |
possibly damaging |
Het |
| Usp24 |
A |
C |
4: 106,295,967 (GRCm39) |
|
probably benign |
Het |
| Usp24 |
C |
A |
4: 106,295,969 (GRCm39) |
|
probably benign |
Het |
| Usp43 |
T |
G |
11: 67,746,581 (GRCm39) |
D1042A |
probably benign |
Het |
| Whrn |
T |
C |
4: 63,337,709 (GRCm39) |
T48A |
possibly damaging |
Het |
| Wnt2b |
A |
G |
3: 104,862,032 (GRCm39) |
I102T |
probably benign |
Het |
| Zfp763 |
T |
C |
17: 33,238,908 (GRCm39) |
D79G |
probably benign |
Het |
| Zmat4 |
A |
G |
8: 24,287,389 (GRCm39) |
Y45C |
probably damaging |
Het |
|
| Other mutations in Or2z2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01305:Or2z2
|
APN |
11 |
58,346,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02001:Or2z2
|
APN |
11 |
58,346,335 (GRCm39) |
missense |
probably benign |
0.33 |
|
IGL02170:Or2z2
|
APN |
11 |
58,345,906 (GRCm39) |
missense |
probably damaging |
1.00 |
|
ANU22:Or2z2
|
UTSW |
11 |
58,346,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0502:Or2z2
|
UTSW |
11 |
58,346,140 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R0784:Or2z2
|
UTSW |
11 |
58,346,131 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R1300:Or2z2
|
UTSW |
11 |
58,346,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1451:Or2z2
|
UTSW |
11 |
58,346,358 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1642:Or2z2
|
UTSW |
11 |
58,346,664 (GRCm39) |
missense |
probably benign |
|
|
R1754:Or2z2
|
UTSW |
11 |
58,346,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1854:Or2z2
|
UTSW |
11 |
58,346,257 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2920:Or2z2
|
UTSW |
11 |
58,346,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3160:Or2z2
|
UTSW |
11 |
58,346,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3162:Or2z2
|
UTSW |
11 |
58,346,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4791:Or2z2
|
UTSW |
11 |
58,346,370 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R4964:Or2z2
|
UTSW |
11 |
58,346,733 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5433:Or2z2
|
UTSW |
11 |
58,346,680 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5543:Or2z2
|
UTSW |
11 |
58,345,993 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6649:Or2z2
|
UTSW |
11 |
58,346,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6653:Or2z2
|
UTSW |
11 |
58,346,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7388:Or2z2
|
UTSW |
11 |
58,346,481 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7492:Or2z2
|
UTSW |
11 |
58,346,715 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7566:Or2z2
|
UTSW |
11 |
58,346,489 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7567:Or2z2
|
UTSW |
11 |
58,345,992 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8557:Or2z2
|
UTSW |
11 |
58,346,562 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8777:Or2z2
|
UTSW |
11 |
58,346,757 (GRCm39) |
nonsense |
probably null |
|
|
R8777-TAIL:Or2z2
|
UTSW |
11 |
58,346,757 (GRCm39) |
nonsense |
probably null |
|
|
R8810:Or2z2
|
UTSW |
11 |
58,345,936 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R9139:Or2z2
|
UTSW |
11 |
58,345,999 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
Z1177:Or2z2
|
UTSW |
11 |
58,346,363 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation