| Item | Value |
|---|---|
| gene id | XLOC_004518 |
| gene name | tfam |
| gene type | coding |
| species | zebrafish (Danio rerio) |
| category of species | model fish |
| Item | Value |
|---|---|
| chromosome id | NC_007123.7 |
| NCBI id | CM002896.2 |
| chromosome length | 49182954 |
| location | 7254112 ~ 7263958 (+) |
| genome version | GRCz11_2017_zebrafish_Genome |
| symbol | description |
|---|---|
| tfam | Predicted to enable DNA binding activity, bending and transcription cis-regulatory region binding activity. Predicted to be involved in transcription initiation from mitochondrial promoter. Predicted to be located in nucleus. Is expressed in brain; muscle; pericardial region; pharyngeal arch 3-7; and somite. Human ortholog(s) of this gene implicated in Alzheimer's disease; Huntington's disease; Parkinson's disease; amyotrophic lateral sclerosis; and mitochondrial DNA depletion syndrome 15. Orthologous to human TFAM (transcription factor A, mitochondrial). |
| id | name | namespace |
|---|---|---|
| GO:0006338 | chromatin remodeling | biological_process |
| GO:0006355 | regulation of transcription, DNA-templated | biological_process |
| GO:0006357 | regulation of transcription by RNA polymerase II | biological_process |
| GO:0005634 | nucleus | cellular_component |
| GO:0008134 | transcription factor binding | molecular_function |
| GO:0003677 | DNA binding | molecular_function |
| GO:0003682 | chromatin binding | molecular_function |
| GO:0008301 | DNA binding, bending | molecular_function |
| id | description |
|---|---|
| ko04371 | Apelin signaling pathway |
| ko05016 | Huntington disease |
| ko03029 | Mitochondrial biogenesis |
| id | description |
|---|---|
| ZDB-GENE-061013-552 | Predicted to enable DNA binding activity, bending and transcription cis-regulatory region binding activity. Predicted to be involved in transcription initiation from mitochondrial promoter. Predicted to be located in nucleus. Is expressed in brain; muscle; pericardial region; pharyngeal arch 3-7; and somite. Human ortholog(s) of this gene implicated in Alzheimer's disease; Huntington's disease; Parkinson's disease; amyotrophic lateral sclerosis; and mitochondrial DNA depletion syndrome 15. Orthologous to human TFAM (transcription factor A, mitochondrial). |
| ensembl_id | ENSDARG00000063145 |
| RNA id | representative | length | rna type | GC content | exon number | start site | end site |
|---|---|---|---|---|---|---|---|
| TCONS_00009010 | True | 1356 | mRNA | 0.43 | 7 | 7254112 | 7263958 |
| gene id | symbol | gene type | direction | distance | location |
|---|---|---|---|---|---|
| XLOC_004517 | CU184911.1 | coding | upstream | 545869 | 6708129 ~ 6708243 (+) |
| XLOC_004516 | dkk1b | coding | upstream | 786437 | 6465557 ~ 6467675 (+) |
| XLOC_004515 | NA | coding | upstream | 802503 | 6195170 ~ 6451609 (+) |
| XLOC_004514 | NA | coding | upstream | 1082184 | 6156963 ~ 6171928 (+) |
| XLOC_004513 | NA | coding | upstream | 1100991 | 6149007 ~ 6153121 (+) |
| XLOC_004519 | bicc1b | coding | downstream | 135445 | 7399403 ~ 7429824 (+) |
| XLOC_004520 | FP102277.2 | coding | downstream | 156074 | 7420032 ~ 7420148 (+) |
| XLOC_004521 | phyhiplb | coding | downstream | 181637 | 7445595 ~ 7513794 (+) |
| XLOC_004522 | FQ311940.1 | coding | downstream | 297107 | 7561065 ~ 7561202 (+) |
| XLOC_004523 | CABZ01050061.1 | coding | downstream | 468576 | 7732534 ~ 7732650 (+) |
| XLOC_004512 | NA | non-coding | upstream | 1101533 | 6144705 ~ 6152579 (+) |
| XLOC_004524 | NA | non-coding | downstream | 535843 | 7799801 ~ 7841013 (+) |
| XLOC_004527 | NA | non-coding | downstream | 779563 | 8043521 ~ 8046466 (+) |
| species | gene id | symbol | gene type | chromosome | NCBI id | location |
|---|---|---|---|---|---|---|
| grasscarp (Ctenopharyngodon idella) | CI01000047_01824882_01828103 | TFAM | coding | CI01000047 | null | 1824882 ~ 1828952 (-) |