| Display title | CYP26B1 |
| Default sort key | CYP26B1 |
| Page length (in bytes) | 9,568 |
| Namespace ID | 0 |
| Page ID | 16853993 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | Fewer than 30 watchers |
| Number of redirects to this page | 2 |
| Counted as a content page | Yes |
| Wikidata item ID | Q18042403 |
| Local description | Protein-coding gene in the species Homo sapiens |
| Central description | protein-coding gene in the species Homo sapiens |
| Page image |  |
| Page views in the past 30 days | |
| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
| Page creator | ProteinBoxBot (talk | contribs) |
| Date of page creation | 00:01, 10 April 2008 |
| Latest editor | Maxim Masiutin (talk | contribs) |
| Date of latest edit | 04:53, 15 December 2023 |
| Total number of edits | 51 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (3) | This page is a member of 3 hidden categories (help):
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| Transcluded templates (51) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - Entrez Gene ID
- UniProt protein ID
- HGNC gene symbol
- HGNC ID
- cytogenetic location
- OMIM ID
- HomoloGene ID
- Ensembl gene ID
- RefSeq protein ID
- RefSeq RNA ID
- Mouse Genome Informatics ID
- Gene Ontology ID
- metal ion binding
- endoplasmic reticulum membrane
- membrane
- intracellular membrane-bounded organelle
- oxidoreductase activity
- iron ion binding
- heme binding
- xenobiotic metabolic process
- monooxygenase activity
- oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
- sterol metabolic process
- vitamin metabolic process
- positive regulation of gene expression
- negative regulation of retinoic acid receptor signaling pathway
- inflammatory response
- response to retinoic acid
- cellular response to retinoic acid
- response to vitamin A
- embryonic limb morphogenesis
- tongue morphogenesis
- oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen
- regulation of T cell differentiation
- organelle membrane
- establishment of skin barrier
- bone morphogenesis
- retinoic acid binding
- establishment of T cell polarity
- male meiotic nuclear division
- lip
- mouse chromosome 6
- foot
- CYP26B1
- Title
- Miscellaneous (e.g. aliases, entity existence)
- Label: en
- Statement: P31
- Statement: P688
- Statement: P684
- Statement: P351
- Statement: P18
- Statement: P353
- Statement: P354
- Statement: P593
- Statement: P492
- Statement: P692
- Statement: P594
- Statement: P639
- Statement: P644
- Statement: P645
- Statement: P1057
- Statement: P4196
- Statement: P2293
- Sitelink
- Statement: P5572
- Description: en
- Cyp26b1
- Statement: P688
- Statement: P351
- Statement: P671
- Statement: P594
- Statement: P639
- Statement: P644
- Statement: P645
- Statement: P1057
- Statement: P4196
- Statement: P5572
- pons
- adipose tissue
- genome assembly GRCh38
- Miscellaneous (e.g. aliases, entity existence)
- Genome assembly GRCh37
- Miscellaneous (e.g. aliases, entity existence)
- proximal/distal pattern formation
- retinoic acid receptor signaling pathway
- cornification
- regulation of retinoic acid receptor signaling pathway
- retinoic acid 4-hydroxylase activity
- retinoic acid catabolic process
- positive regulation of tongue muscle cell differentiation
- cytochrome P450 family 26 subfamily B member 1
- Label: en
- Statement: P352
- Statement: P638
- Statement: P591
- Statement: P680
- Statement: P681
- Statement: P682
- Statement: P637
- Statement: P129
- Cytochrome P450, family 26, subfamily b, polypeptide 1
- Statement: P352
- Statement: P637
- kidney development
- decidua
- endocardial cushion
- otolith organ
- subcutaneous adipose tissue
- cerebellar vermis
- neuromere
- hand
- spermatogenesis
- rhombomere
- cell fate determination
- cerebellar hemisphere
- lethal occipital encephalocele-skeletal dysplasia syndrome
- human chromosome 2
- skin of abdomen
- skin of external ear
- skin of arm
- skin of leg
- right hemisphere of cerebellum
- gene
- cytoplasm
- endoplasmic reticulum
- utricle
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| Duplicate IDs | 1 |
| Background color inline style rule exists without a corresponding text color | 1 |
