Transcript ID | C166 | Tie2+ EC | mES |
---|---|---|---|
ENSMUST00000034776 | 25.272±1.58 | 3.733±2.27 | 13.345±5.21 |
Gene Info | |||||
---|---|---|---|---|---|
Description: | |||||
Gene Accession | Gene Name | Tax ID | Strand | Position | Gene Biotype |
ENSMUSG00000032245 | Cln6 | 10090 | + | 9:62838785-62852006 | protein_coding |
Transcript Accession | Transcript Name | Position | Transcript Biotype | ||
ENSMUST00000034776 | Cln6-001 | 62838785-62852006 | protein_coding | ||
ENSMUST00000124984 | Cln6-004 | 62847033-62851162 | protein_coding | ||
ENSMUST00000138276 | Cln6-003 | 62846015-62850711 | nonsense_mediated_decay | ||
ENSMUST00000141821 | Cln6-002 | 62838792-62846018 | nonsense_mediated_decay | ||
Expression Patterns
|
Conserved Regions | ||
---|---|---|
Region ID | Sub-Region | Region Type |
CIL_0003W4 | CIL_0003W4_0002 | CGP |
CIL_0008FO | CIL_0008FO_0002 | VISTA |
CIL_00098T | CIL_00098T_0002 | VISTA |
CIL_0004FC | CIL_0004FC_0003 | CGP |
Gene Ontology |
||
---|---|---|
GO ID | Evidence Type | GO Description |
GO:0001573 | ISS | ganglioside metabolic process |
GO:0005515 | IEA | protein binding |
GO:0005634 | IEA | nucleus |
GO:0005783 | ISS | endoplasmic reticulum |
GO:0005788 | ISS | endoplasmic reticulum lumen |
GO:0007040 | IMP | lysosome organization |
GO:0007042 | ISS | lysosomal lumen acidification |
GO:0007601 | IMP | visual perception |
GO:0008203 | ISS | cholesterol metabolic process |
GO:0016020 | IEA | membrane |
GO:0030203 | ISS | glycosaminoglycan metabolic process |
GO:0031987 | IMP | locomotion involved in locomotory behavior |
GO:0042803 | ISS | protein homodimerization activity |
GO:0043231 | IEA | intracellular membrane-bounded organelle |
GO:0044265 | IMP | cellular macromolecule catabolic process |
GO:0045862 | ISS | positive regulation of proteolysis |
Homologs | |||||
ENSEMBL Accession | Gene Name | Description | Biotype | Species | |
ENSDARG00000077584 | cln6a | protein_coding | Danio_rerio | ||
ENSDARG00000090002 | cln6b | protein_coding | Danio_rerio | ||
ENSG00000128973 | CLN6 | ceroid-lipofuscinosis, neuronal 6, late infantile, variant | protein_coding | Homo_sapiens |