Incidental Mutation 'IGL01633:Tbxas1'
| ID |
93616 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Tbxas1
|
| Ensembl Gene |
ENSMUSG00000029925 |
| Gene Name |
thromboxane A synthase 1, platelet |
| Synonyms |
TXS, CYP5, TXAS, CYP5A1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.064)
|
| Stock # |
IGL01633
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
38852338-39061519 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 38959125 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Aspartic acid
at position 103
(N103D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000003017
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000003017]
[ENSMUST00000160963]
|
| AlphaFold |
P36423 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000003017
AA Change: N103D
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000003017
Gene: ENSMUSG00000029925
AA Change: N103D
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
16 |
28 |
N/A |
INTRINSIC |
|
Pfam:p450
|
44 |
530 |
1.5e-95 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159226
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160963
AA Change: N89D
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000124640
Gene: ENSMUSG00000029925
AA Change: N89D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:p450
|
30 |
134 |
3.6e-16 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161360
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161781
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162656
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000201966
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. However, this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity. This endoplasmic reticulum membrane protein catalyzes the conversion of prostglandin H2 to thromboxane A2, a potent vasoconstrictor and inducer of platelet aggregation. The enzyme plays a role in several pathophysiological processes including hemostasis, cardiovascular disease, and stroke. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]
PHENOTYPE: Homozygous null mice display increased bleeding time and decreased platelet response to arachidonic acid. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 49 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca2 |
T |
A |
2: 25,334,406 (GRCm39) |
S1868T |
possibly damaging |
Het |
| Abca3 |
G |
A |
17: 24,616,327 (GRCm39) |
W923* |
probably null |
Het |
| Abca8b |
A |
G |
11: 109,827,580 (GRCm39) |
M1476T |
probably damaging |
Het |
| Abi3bp |
T |
C |
16: 56,498,163 (GRCm39) |
F729S |
probably damaging |
Het |
| Acacb |
T |
C |
5: 114,356,919 (GRCm39) |
|
probably benign |
Het |
| Aldh3a2 |
A |
G |
11: 61,139,731 (GRCm39) |
L467P |
probably benign |
Het |
| Appl1 |
T |
C |
14: 26,684,795 (GRCm39) |
T85A |
probably damaging |
Het |
| Aspm |
T |
A |
1: 139,408,574 (GRCm39) |
I2487N |
possibly damaging |
Het |
| Bcl2a1c |
G |
A |
9: 114,159,290 (GRCm39) |
V23I |
probably benign |
Het |
| C2cd2 |
T |
A |
16: 97,676,323 (GRCm39) |
|
probably benign |
Het |
| Carmil3 |
A |
T |
14: 55,731,684 (GRCm39) |
H170L |
possibly damaging |
Het |
| Ccdc141 |
C |
T |
2: 76,919,593 (GRCm39) |
V305I |
probably benign |
Het |
| Ccdc174 |
G |
A |
6: 91,857,343 (GRCm39) |
|
probably null |
Het |
| Cep126 |
T |
G |
9: 8,103,320 (GRCm39) |
Q230P |
possibly damaging |
Het |
| Chrm1 |
T |
C |
19: 8,655,859 (GRCm39) |
I188T |
probably benign |
Het |
| Depdc5 |
T |
C |
5: 33,081,544 (GRCm39) |
S569P |
probably damaging |
Het |
| Drc1 |
G |
A |
5: 30,503,007 (GRCm39) |
E177K |
probably damaging |
Het |
| Duox1 |
A |
G |
2: 122,164,279 (GRCm39) |
E913G |
probably benign |
Het |
| Fbxw9 |
T |
C |
8: 85,791,055 (GRCm39) |
S241P |
probably damaging |
Het |
| Fez2 |
C |
A |
17: 78,712,147 (GRCm39) |
|
probably benign |
Het |
| Fga |
G |
T |
3: 82,937,606 (GRCm39) |
R161L |
possibly damaging |
Het |
| Fn3krp |
G |
T |
11: 121,320,533 (GRCm39) |
G293* |
probably null |
Het |
| Gfra1 |
C |
T |
19: 58,255,479 (GRCm39) |
E318K |
probably benign |
Het |
| Gli3 |
C |
T |
13: 15,823,219 (GRCm39) |
P314S |
probably damaging |
Het |
| Gm5114 |
A |
T |
7: 39,057,490 (GRCm39) |
S710T |
probably benign |
Het |
| Gpr141 |
T |
C |
13: 19,936,769 (GRCm39) |
D2G |
probably benign |
Het |
| Inppl1 |
G |
A |
7: 101,483,041 (GRCm39) |
Q63* |
probably null |
Het |
| Lrrc73 |
T |
A |
17: 46,566,657 (GRCm39) |
V169E |
possibly damaging |
Het |
| Lsm11 |
C |
T |
11: 45,824,615 (GRCm39) |
R304Q |
probably benign |
Het |
| Macf1 |
T |
C |
4: 123,395,964 (GRCm39) |
D788G |
probably damaging |
Het |
| Nbas |
T |
A |
12: 13,533,898 (GRCm39) |
D1844E |
probably damaging |
Het |
| Nt5c |
A |
G |
11: 115,382,161 (GRCm39) |
F73L |
probably damaging |
Het |
| Osmr |
A |
T |
15: 6,854,085 (GRCm39) |
I541N |
probably damaging |
Het |
| Phrf1 |
A |
G |
7: 140,840,413 (GRCm39) |
I1203V |
probably benign |
Het |
| Pram1 |
C |
A |
17: 33,861,109 (GRCm39) |
P510Q |
possibly damaging |
Het |
| Prepl |
A |
G |
17: 85,379,444 (GRCm39) |
Y415H |
probably benign |
Het |
| Prss27 |
A |
T |
17: 24,264,650 (GRCm39) |
H271L |
probably damaging |
Het |
| Ptpn18 |
A |
G |
1: 34,510,989 (GRCm39) |
S287G |
probably benign |
Het |
| Ptprq |
T |
C |
10: 107,535,584 (GRCm39) |
|
probably benign |
Het |
| Sars2 |
A |
G |
7: 28,446,974 (GRCm39) |
K218E |
probably benign |
Het |
| Senp6 |
G |
T |
9: 79,999,676 (GRCm39) |
S31I |
probably damaging |
Het |
| Shld2 |
G |
T |
14: 33,971,136 (GRCm39) |
T31K |
probably damaging |
Het |
| Skint6 |
C |
A |
4: 113,095,246 (GRCm39) |
V138F |
probably damaging |
Het |
| Slc4a8 |
C |
A |
15: 100,685,128 (GRCm39) |
H168N |
probably damaging |
Het |
| Tbx15 |
T |
G |
3: 99,220,358 (GRCm39) |
I150S |
probably damaging |
Het |
| Tmc5 |
A |
G |
7: 118,222,809 (GRCm39) |
N170D |
probably damaging |
Het |
| Tmem108 |
A |
T |
9: 103,361,950 (GRCm39) |
N545K |
probably benign |
Het |
| Trub1 |
A |
G |
19: 57,441,616 (GRCm39) |
K80E |
possibly damaging |
Het |
| Tulp3 |
A |
T |
6: 128,302,923 (GRCm39) |
Y299N |
probably damaging |
Het |
|
| Other mutations in Tbxas1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01080:Tbxas1
|
APN |
6 |
38,998,115 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01319:Tbxas1
|
APN |
6 |
38,994,907 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL01712:Tbxas1
|
APN |
6 |
39,057,994 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01860:Tbxas1
|
APN |
6 |
38,925,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01964:Tbxas1
|
APN |
6 |
39,060,748 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02036:Tbxas1
|
APN |
6 |
38,998,091 (GRCm39) |
missense |
probably benign |
|
|
IGL02335:Tbxas1
|
APN |
6 |
39,000,014 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02615:Tbxas1
|
APN |
6 |
39,004,800 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0245:Tbxas1
|
UTSW |
6 |
39,004,702 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1677:Tbxas1
|
UTSW |
6 |
38,994,822 (GRCm39) |
splice site |
probably benign |
|
|
R1975:Tbxas1
|
UTSW |
6 |
38,925,575 (GRCm39) |
splice site |
probably benign |
|
|
R1977:Tbxas1
|
UTSW |
6 |
38,925,575 (GRCm39) |
splice site |
probably benign |
|
|
R2308:Tbxas1
|
UTSW |
6 |
39,004,595 (GRCm39) |
missense |
probably benign |
0.08 |
|
R4394:Tbxas1
|
UTSW |
6 |
39,004,713 (GRCm39) |
missense |
probably benign |
0.19 |
|
R4702:Tbxas1
|
UTSW |
6 |
39,060,791 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4703:Tbxas1
|
UTSW |
6 |
39,060,791 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4705:Tbxas1
|
UTSW |
6 |
39,060,791 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4935:Tbxas1
|
UTSW |
6 |
38,999,981 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5424:Tbxas1
|
UTSW |
6 |
39,004,839 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R5704:Tbxas1
|
UTSW |
6 |
38,998,067 (GRCm39) |
missense |
probably benign |
0.20 |
|
R6358:Tbxas1
|
UTSW |
6 |
38,929,046 (GRCm39) |
intron |
probably benign |
|
|
R6455:Tbxas1
|
UTSW |
6 |
38,929,079 (GRCm39) |
intron |
probably benign |
|
|
R6823:Tbxas1
|
UTSW |
6 |
38,896,087 (GRCm39) |
start codon destroyed |
possibly damaging |
0.94 |
|
R6868:Tbxas1
|
UTSW |
6 |
39,061,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6888:Tbxas1
|
UTSW |
6 |
38,929,008 (GRCm39) |
intron |
probably benign |
|
|
R7500:Tbxas1
|
UTSW |
6 |
38,959,146 (GRCm39) |
nonsense |
probably null |
|
|
R8026:Tbxas1
|
UTSW |
6 |
39,004,830 (GRCm39) |
missense |
probably benign |
0.12 |
|
R8351:Tbxas1
|
UTSW |
6 |
39,004,850 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R8729:Tbxas1
|
UTSW |
6 |
38,978,272 (GRCm39) |
missense |
probably benign |
0.33 |
|
R8837:Tbxas1
|
UTSW |
6 |
39,048,364 (GRCm39) |
missense |
|
|
|
R9161:Tbxas1
|
UTSW |
6 |
38,999,989 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Tbxas1
|
UTSW |
6 |
38,998,038 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2013-12-09 |
Incidental Mutation