Incidental Mutation 'IGL02881:Or5m13'
ID |
362804 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Or5m13
|
Ensembl Gene |
ENSMUSG00000058884 |
Gene Name |
olfactory receptor family 5 subfamily M member 13 |
Synonyms |
MOR196-5P, GA_x6K02T2Q125-47397266-47398205, Olfr1025, MOR196-6_p |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.090)
|
Stock # |
IGL02881
|
Quality Score |
|
Status
|
|
Chromosome |
2 |
Chromosomal Location |
85748271-85749097 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 85748460 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Glycine
at position 64
(S64G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000149785
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000188749]
[ENSMUST00000213474]
[ENSMUST00000217615]
[ENSMUST00000219615]
|
AlphaFold |
A0A140T8K3 |
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000076311 Gene: ENSMUSG00000058884 AA Change: S64G
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
31 |
308 |
1.5e-57 |
PFAM |
Pfam:7tm_1
|
41 |
290 |
2.6e-24 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000188749
AA Change: S64G
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000139860 Gene: ENSMUSG00000058884 AA Change: S64G
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
40 |
N/A |
INTRINSIC |
Pfam:7tm_1
|
41 |
290 |
5.7e-30 |
PFAM |
Pfam:7tm_4
|
139 |
283 |
7.8e-48 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000213474
AA Change: S64G
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000217615
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000219615
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
C |
A |
8: 13,605,999 (GRCm39) |
|
probably benign |
Het |
Aatf |
A |
G |
11: 84,362,115 (GRCm39) |
|
probably benign |
Het |
Asap3 |
A |
T |
4: 135,966,548 (GRCm39) |
H542L |
probably benign |
Het |
Cyp4v3 |
A |
T |
8: 45,761,753 (GRCm39) |
L389H |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,932,944 (GRCm39) |
E3605K |
probably damaging |
Het |
Fry |
C |
T |
5: 150,282,516 (GRCm39) |
T347M |
probably damaging |
Het |
Glul |
C |
A |
1: 153,782,862 (GRCm39) |
T191K |
probably benign |
Het |
Grsf1 |
A |
T |
5: 88,821,689 (GRCm39) |
L125Q |
probably damaging |
Het |
Hfm1 |
A |
G |
5: 107,022,118 (GRCm39) |
I976T |
probably damaging |
Het |
Itgb5 |
A |
G |
16: 33,740,275 (GRCm39) |
T462A |
probably benign |
Het |
Lmna |
G |
T |
3: 88,410,233 (GRCm39) |
R60S |
possibly damaging |
Het |
Mrpl10 |
T |
A |
11: 96,937,899 (GRCm39) |
V89D |
probably damaging |
Het |
Muc5b |
C |
T |
7: 141,411,449 (GRCm39) |
T1465I |
unknown |
Het |
Myh15 |
A |
C |
16: 48,937,628 (GRCm39) |
D743A |
possibly damaging |
Het |
Noxo1 |
C |
A |
17: 24,918,409 (GRCm39) |
L190I |
probably damaging |
Het |
Noxo1 |
T |
A |
17: 24,918,410 (GRCm39) |
L190Q |
probably damaging |
Het |
Nrn1 |
C |
A |
13: 36,914,080 (GRCm39) |
|
probably null |
Het |
Or2aj5 |
A |
T |
16: 19,425,050 (GRCm39) |
Y123N |
probably damaging |
Het |
Or4c121 |
T |
A |
2: 89,023,985 (GRCm39) |
Y131F |
probably damaging |
Het |
Or8h8 |
A |
G |
2: 86,753,057 (GRCm39) |
V273A |
possibly damaging |
Het |
Pfkfb4 |
A |
G |
9: 108,836,364 (GRCm39) |
T131A |
probably null |
Het |
Phf20l1 |
T |
C |
15: 66,466,829 (GRCm39) |
|
probably null |
Het |
Pnliprp2 |
A |
G |
19: 58,759,878 (GRCm39) |
D363G |
probably benign |
Het |
Prpf6 |
C |
T |
2: 181,273,864 (GRCm39) |
T336I |
probably benign |
Het |
Rcc1 |
C |
T |
4: 132,065,067 (GRCm39) |
R139H |
probably benign |
Het |
Sae1 |
T |
G |
7: 16,093,043 (GRCm39) |
K221N |
probably damaging |
Het |
Slc45a1 |
T |
C |
4: 150,722,987 (GRCm39) |
K299R |
probably benign |
Het |
Slco1a8 |
T |
C |
6: 141,917,969 (GRCm39) |
R636G |
probably benign |
Het |
Smad2 |
C |
A |
18: 76,432,851 (GRCm39) |
|
probably null |
Het |
Tmem117 |
T |
C |
15: 94,777,306 (GRCm39) |
F152S |
probably damaging |
Het |
Tmem232 |
C |
T |
17: 65,757,365 (GRCm39) |
C276Y |
probably damaging |
Het |
Tor1b |
A |
T |
2: 30,843,865 (GRCm39) |
K47* |
probably null |
Het |
Ttn |
A |
G |
2: 76,740,147 (GRCm39) |
V3464A |
probably benign |
Het |
Ube3b |
A |
G |
5: 114,550,945 (GRCm39) |
T870A |
possibly damaging |
Het |
Zscan25 |
T |
G |
5: 145,227,296 (GRCm39) |
L320R |
probably benign |
Het |
|
Other mutations in Or5m13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01660:Or5m13
|
APN |
2 |
85,748,908 (GRCm39) |
missense |
probably benign |
0.25 |
R0097:Or5m13
|
UTSW |
2 |
85,749,184 (GRCm39) |
missense |
probably benign |
0.00 |
R0097:Or5m13
|
UTSW |
2 |
85,749,184 (GRCm39) |
missense |
probably benign |
0.00 |
R0324:Or5m13
|
UTSW |
2 |
85,748,295 (GRCm39) |
missense |
probably benign |
0.22 |
R0392:Or5m13
|
UTSW |
2 |
85,749,106 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0765:Or5m13
|
UTSW |
2 |
85,749,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R1199:Or5m13
|
UTSW |
2 |
85,748,379 (GRCm39) |
missense |
probably benign |
0.00 |
R1894:Or5m13
|
UTSW |
2 |
85,748,599 (GRCm39) |
missense |
probably benign |
0.28 |
R2027:Or5m13
|
UTSW |
2 |
85,749,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R2141:Or5m13
|
UTSW |
2 |
85,749,171 (GRCm39) |
missense |
probably null |
|
R3871:Or5m13
|
UTSW |
2 |
85,748,926 (GRCm39) |
splice site |
probably null |
|
R4837:Or5m13
|
UTSW |
2 |
85,748,748 (GRCm39) |
missense |
probably benign |
0.00 |
R4945:Or5m13
|
UTSW |
2 |
85,748,917 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5056:Or5m13
|
UTSW |
2 |
85,748,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Or5m13
|
UTSW |
2 |
85,748,934 (GRCm39) |
missense |
probably benign |
0.01 |
R5960:Or5m13
|
UTSW |
2 |
85,749,069 (GRCm39) |
missense |
probably benign |
0.07 |
R6807:Or5m13
|
UTSW |
2 |
85,748,382 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7320:Or5m13
|
UTSW |
2 |
85,748,718 (GRCm39) |
missense |
probably benign |
0.00 |
R8523:Or5m13
|
UTSW |
2 |
85,748,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R8715:Or5m13
|
UTSW |
2 |
85,748,273 (GRCm39) |
start codon destroyed |
probably null |
0.81 |
R8734:Or5m13
|
UTSW |
2 |
85,748,993 (GRCm39) |
nonsense |
probably null |
|
R9275:Or5m13
|
UTSW |
2 |
85,749,046 (GRCm39) |
missense |
probably benign |
0.17 |
R9427:Or5m13
|
UTSW |
2 |
85,748,704 (GRCm39) |
missense |
probably benign |
0.00 |
R9728:Or5m13
|
UTSW |
2 |
85,748,887 (GRCm39) |
missense |
possibly damaging |
0.72 |
V1662:Or5m13
|
UTSW |
2 |
85,748,938 (GRCm39) |
missense |
probably benign |
0.10 |
Z1176:Or5m13
|
UTSW |
2 |
85,748,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Posted On |
2015-12-18 |