| Type | Description |
|---|---|
| Definition | scleraxis bHLH transcription factor a |
| Date | Results | Publications |
|---|---|---|
| 2020-06-06 13:05:00 | Although scxb mutants show no obvious phenotype, scxa mutant embryos have defects in cranial tendon maturation and muscle misalignment. Mutation of both scleraxis genes results in more severe defects in cranial tendon differentiation, muscle and cartilage dysmorphogenesis and paralysis, and lethality by 2-5 wk, which indicates an essential function of scleraxis for craniofacial development. | 31100023 |
| Type | IDs |
|---|---|
| Synonymous | TCF15, si:ch211-251g8.3 |
| Gene | |
| Nucleutide sequences | |
| Protein sequencees |
RefSeq:
NP_001076538.2
|
| Others |
UniGene:
Dr.134169
|
| {{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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