Incidental Mutation 'IGL00321:Or2t43'
| ID |
13662 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| 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 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.051)
|
| Stock # |
IGL00321
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
58456682-58461379 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 58457593 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Aspartic acid
at position 193
(Y193D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000104450
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081102]
[ENSMUST00000108822]
[ENSMUST00000215322]
[ENSMUST00000216758]
[ENSMUST00000217009]
|
| AlphaFold |
M9MMJ7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000081102
AA Change: Y193D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000079881
Gene: ENSMUSG00000059279
AA Change: Y193D
| 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 |
probably damaging
Transcript: ENSMUST00000108822
AA Change: Y193D
PolyPhen 2
Score 1.000 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000104450
Gene: ENSMUSG00000064252
AA Change: Y193D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
1.1e-47 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
33 |
299 |
5.1e-7 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
4.6e-28 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215322
AA Change: Y193D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216758
AA Change: Y193D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000217009
AA Change: Y193D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| 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: 28 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam34l |
A |
G |
8: 44,078,418 (GRCm39) |
I602T |
probably benign |
Het |
| Adam39 |
A |
G |
8: 41,279,783 (GRCm39) |
R725G |
possibly damaging |
Het |
| Arid2 |
A |
G |
15: 96,186,970 (GRCm39) |
E74G |
probably damaging |
Het |
| Carf |
T |
A |
1: 60,164,001 (GRCm39) |
|
probably benign |
Het |
| Cit |
A |
T |
5: 115,984,524 (GRCm39) |
Q32L |
probably damaging |
Het |
| Dennd4b |
A |
G |
3: 90,178,514 (GRCm39) |
T526A |
possibly damaging |
Het |
| Dnhd1 |
A |
G |
7: 105,327,202 (GRCm39) |
E717G |
probably damaging |
Het |
| Ercc6 |
T |
A |
14: 32,290,029 (GRCm39) |
I968N |
probably damaging |
Het |
| Fcrl1 |
A |
T |
3: 87,296,942 (GRCm39) |
Y297F |
probably damaging |
Het |
| Gas2l3 |
A |
G |
10: 89,249,489 (GRCm39) |
L543P |
probably benign |
Het |
| Hid1 |
A |
T |
11: 115,249,895 (GRCm39) |
D84E |
probably benign |
Het |
| Ifit1bl2 |
C |
T |
19: 34,597,319 (GRCm39) |
S99N |
probably benign |
Het |
| Kpna3 |
A |
G |
14: 61,629,302 (GRCm39) |
|
probably benign |
Het |
| Myadm |
C |
A |
7: 3,345,739 (GRCm39) |
P167Q |
possibly damaging |
Het |
| Ociad1 |
C |
T |
5: 73,461,886 (GRCm39) |
|
probably benign |
Het |
| Pcdh11x |
A |
T |
X: 119,502,265 (GRCm39) |
K1029N |
probably benign |
Het |
| Pcdhb11 |
A |
G |
18: 37,555,026 (GRCm39) |
T119A |
probably benign |
Het |
| Phldb2 |
T |
C |
16: 45,592,617 (GRCm39) |
R926G |
probably damaging |
Het |
| Ppwd1 |
A |
G |
13: 104,353,651 (GRCm39) |
F369S |
probably damaging |
Het |
| Rreb1 |
T |
A |
13: 38,100,472 (GRCm39) |
M201K |
probably benign |
Het |
| Ryr1 |
A |
T |
7: 28,802,235 (GRCm39) |
I795N |
probably damaging |
Het |
| Slc3a1 |
T |
C |
17: 85,368,261 (GRCm39) |
W510R |
probably damaging |
Het |
| Slc44a5 |
T |
C |
3: 153,968,576 (GRCm39) |
L589P |
probably damaging |
Het |
| Tfr2 |
A |
G |
5: 137,572,717 (GRCm39) |
D176G |
probably null |
Het |
| Tom1 |
T |
A |
8: 75,778,802 (GRCm39) |
S24T |
probably benign |
Het |
| Vmn2r66 |
T |
A |
7: 84,656,299 (GRCm39) |
Q239L |
probably benign |
Het |
| Ythdc2 |
A |
G |
18: 44,993,040 (GRCm39) |
T149A |
probably benign |
Het |
| Zc3h3 |
A |
G |
15: 75,651,162 (GRCm39) |
I686T |
probably damaging |
Het |
|
| Other mutations in Or2t43 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
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 |
|
R6699:Or2t43
|
UTSW |
11 |
58,458,031 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
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 |
|
| Posted On |
2012-12-06 |
Incidental Mutation