MAB21L1 (mab-21 like 1)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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4081 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Mab-21 like 1 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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MAB21L1 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CAGR1, COFG, Nbla00126 |
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Chromosome
Chromosome number
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13 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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13q13.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene is similar to the MAB-21 cell fate-determining gene found in C. elegans. It may be involved in eye and cerebellum development, and it has been proposed that expansion of a trinucleotide repeat region in the 5` UTR may play a role in a variety of |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||
| UniProt ID | Q13394 | ||||||||||
| Protein name | Putative nucleotidyltransferase MAB21L1 (EC 2.7.7.-) (Protein mab-21-like 1) | ||||||||||
| Protein function | Putative nucleotidyltransferase required for several aspects of embryonic development including normal development of the eye (PubMed:27103078, PubMed:30487245). It is unclear whether it displays nucleotidyltransferase activity in vivo (PubMed:2 | ||||||||||
| PDB | 5EOG , 5EOM | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in brain, cerebellum and skeletal muscle. {ECO:0000269|PubMed:8733127}. | ||||||||||
| Sequence |
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| Sequence length | 359 | ||||||||||
| Interactions | View interactions | ||||||||||