Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | MYT1L | contributors: mct/npt - updated : 03-05-2010 |
HGNC name | myelin transcription factor 1-like |
HGNC id | 7623 |
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Corresponding disease |
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Location | 2p25.3 Physical location : 1.792.886 - 2.335.045 | ||
Synonym name | |||
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Synonym symbol(s) | KIAA1106, NZF1, MyT1-L |
DNA |
TYPE | functioning gene |
STRUCTURE | 542.16 kb 25 Exon(s) |
10 Kb 5' upstream gene genomic sequence study |
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MAPPING | cloned | Y | linked | N | status | provisional |
RNA |
TRANSCRIPTS | type | messenger |
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EXPRESSION |
Type |
expressed in | (based on citations) | ||||||||||||||||||||||||||||||||||||||||
organ(s) |
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tissue |
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cells |
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cell lineage
cell lines
| fluid/secretion
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at STAGE |
physiological period | embryo |
Text | neurons early stage of differentiation |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
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motifs/domains
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HOMOLOGY |
interspecies | homolog to murine Myt1l (93.5pc) |
homolog to rattus Myt1l (92.9pc) |
intraspecies | paralog to MYT1 |
Homologene |
FAMILY |
CATEGORY | transcription factor |
SUBCELLULAR LOCALIZATION | intracellular |
intracellular,nucleus |
CELLULAR PROCESS | nucleotide, transcription |
PHYSIOLOGICAL PROCESS | development |
text | developing nervous system |
PATHWAY |
metabolism |
signaling |
a component |
INTERACTION |
DNA |
RNA |
small molecule |
protein |
cell & other |
REGULATION |
ASSOCIATED DISORDERS |
corresponding disease(s) | DEL2P25 |
Susceptibility | to schizophrenia |
Variant & Polymorphism other | disrupted by rare CNVs in schizophrenia patients |
Candidate gene | for intellectual disability in patients with 2p25.3 (2pter) deletions. | |
Marker
Therapy target
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ANIMAL & CELL MODELS |