| NCBI GeneID : 51162 | NCBI : NM_016215.5 | NCBI : NP_057299.1 |
|---|---|---|
| Chromosome : 9 | Strand : + | |
| MANE Select : ENST00000308874 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | EGFL7 | ENSG00000172889 | 136662916 | 136672678 |
|---|---|---|---|---|
| GTEx V8 | EGFL7 | ENSG00000172889 | 136658855 | 136672678 |
| Gencode v40 | EGFL7 | ENSG00000172889 | 136658855 | 136672678 |
| Gencode v26 (GTEx V8) | Gencode v40 | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| V8 |
Transcript ID | Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
Exp Tx% |
Exp Rank |
MANE Match |
APPRIS | Transcript ID | Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
MANE Match |
APPRIS |
| ☉ | ENST00000406555 | 10 | 1529 | 3 | 822 | 1 | 47.30 | 1 | P:1 | ENST00000406555 | 10 | 1529 | 3 | 822 | 1 | P:1 | ||
| ENST00000371698 | 9 | 1282 | 4 | 822 | 1 | 42.12 | 2 | P:1 | ENST00000371698 | 9 | 1282 | 4 | 822 | 1 | P:1 | |||
| ENST00000490469 | 4 | 456 | 7 | 0 | 6 | 7.89 | 3 | ENST00000490469 | 4 | 456 | 7 | 0 | 6 | |||||
| ENST00000308874 | 11 | 1747 | 2 | 822 | 1 | 1.43 | 4 | ☀ | P:1 | ENST00000308874 | 11 | 1759 | 2 | 822 | 1 | ☀ | P:1 | |
| ENST00000492862 | 5 | 723 | 5 | 197 | 5 | 0.59 | 5 | ENST00000492862 | 5 | 723 | 5 | 197 | 5 | |||||
| ENST00000371699 | 10 | 2125 | 1 | 822 | 1 | 0.52 | 6 | P:1 | ENST00000371699 | 10 | 2125 | 1 | 822 | 1 | P:1 | |||
| ENST00000492002 | 7 | 654 | 6 | 0 | 6 | 0.15 | 7 | ENST00000492002 | 7 | 654 | 6 | 0 | 6 | |||||