| Type | Description |
|---|---|
| Definition | thioredoxin domain containing 15 |
| Date | Results | Publications |
|---|---|---|
| 2019-06-29 12:15:00 | TXNDC15 was identified as a novel causative gene of prenatally diagnosed Meckel-Gruber syndrome. | 30851085 |
| 2012-06-30 11:50:00 | Increased surface thiol isomerase activity on platelets, compared with cells of the vascular wall, may explain the platelet-selective actions of S-nitrosoglutathione and help define its antithrombotic potential | 21642008 |
| Type | IDs |
|---|---|
| Synonymous | BUG, C5orf14, UNQ335 |
| Gene |
UniProtKB-ID:
TXD15_HUMAN,
Q7Z345_HUMAN
UniprotKB:
Q96J42,
Q7Z345
UniParc:
UPI00001A9DAE,
UPI000013FC8F,
UPI00000359EE
EMBL:
BX538131,
AK056512,
AK026278,
BC001615,
BC032568,
AY358649,
CH471062
Ensembl:
ENSG00000113621
KO:
hsa:79770
|
| Nucleutide sequences |
EMBL-CDS:
AAH32568.1,
AAH01615.1,
BAB15427.1,
EAW62231.1,
BAB71199.1,
AAQ89012.1,
EAW62233.1,
CAD98032.1
Gene_ORFName:
UNQ335/PRO534
Ensembl_TRS:
ENST00000358387
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000351157
RefSeq:
NP_001337664.1,
NP_078991.3
|
| Others |
UniRef100:
UniRef100_Q7Z345,
UniRef100_Q96J42
UniRef90:
UniRef90_A0A0D9RLW6,
UniRef90_Q96J42
UniRef50:
UniRef50_Q96J42,
UniRef50_H0X5B9
UniGene:
Hs.741304
CCDS:
CCDS4180.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Location | {{protein.contigId}} ( {{protein.positionStart}}..{{protein.positionEnd}} , {{protein.orientation}} ) | |||||||
| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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