| NCBI GeneID : 150864 | NCBI : NM_173511.4 | NCBI : NP_775782.2 |
|---|---|---|
| Chromosome : 2 | Strand : + | |
| MANE Select : ENST00000392238 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | FAM117B | ENSG00000138439 | 202634969 | 202769757 |
|---|---|---|---|---|
| GTEx V9 | FAM117B | ENSG00000138439 | 202635187 | 202769757 |
| Gencode v40 | FAM117B | ENSG00000138439 | 202634968 | 202769757 |
| Gencode v26 (GTEx V9) | Gencode v40 | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| V9 |
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 |
| ☉ | ENST00000392238 | 8 | 5763 | 1 | 1770 | 1 | 99.58 | 1 | ☀ | P:1 | ENST00000392238 | 8 | 5982 | 1 | 1770 | 1 | ☀ | P:1 |
| ENST00000481658 | 3 | 768 | 2 | 0 | 2 | 0.42 | 2 | ENST00000481658 | 3 | 768 | 2 | 0 | 2 | |||||