Gene: L3mbtl1 (L3MBTL histone methyl-lysine binding protein 1) Rattus norvegicus
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Symbol: L3mbtl1
Name: L3MBTL histone methyl-lysine binding protein 1
Description: ENCODES a protein that exhibits chromatin binding (ortholog); histone binding (ortholog); identical protein binding (ortholog); INVOLVED IN chromatin organization (ortholog); hemopoiesis (ortholog); negative regulation of transcription, DNA-templated (ortholog); PARTICIPATES IN ataxia telangiectasia-mutated (ATM) signaling pathway; histone modification pathway; ASSOCIATED WITH breast cancer (ortholog); FOUND IN chromatin (ortholog); condensed chromosome (ortholog); nucleoplasm (ortholog); INTERACTS WITH bisphenol A; lead diacetate; methamphetamine
AGR Description: Predicted to have SAM domain binding activity, histone binding activity, and identical protein binding activity; predicted to be involved in several processes, including chromatin organization, hemopoiesis, and negative regulation of transcription, DNA-templated; predicted to localize to the intracellular organelle and plasma membrane; orthologous to human L3MBTL1 (L3MBTL histone methyl-lysine binding protein 1).
Merged Description: Predicted to have SAM domain binding activity, histone binding activity, and identical protein binding activity; predicted to be involved in several processes, including chromatin organization, hemopoiesis, and negative regulation of transcription, DNA-templated; predicted to localize to the intracellular organelle and plasma membrane; orthologous to human L3MBTL1 (L3MBTL histone methyl-lysine binding protein 1); PARTICIPATES IN ataxia telangiectasia-mutated (ATM) signaling pathway; histone modification pathway; INTERACTS WITH bisphenol A; lead diacetate; methamphetamine.
Type: protein-coding
RefSeq Status: MODEL
Also known as: H-l(3)mbt protein; L(3)mbt protein homolog; l(3)mbt-like (Drosophila); l(3)mbt-like 1; l(3)mbt-like 1 (Drosophila); L3mbtl; L3MBTL histone methyl-lysine binding protein 1; L3mbtl1; L3MBTL1, histone methyl-lysine binding protein; lethal(3)malignant brain tumor-like protein; lethal(3)malignant brain tumor-like protein 1; LOC311613; RGD1307316; similar to KIAA0681 protein
Orthologs:
Homo sapiens (human) : L3MBTL1 (L3MBTL histone methyl-lysine binding protein 1)  HGNC  Alliance
Mus musculus (house mouse) : L3mbtl1 (L3MBTL1 histone methyl-lysine binding protein)  MGI  Alliance
Chinchilla lanigera (long-tailed chinchilla) : L3mbtl1 (L3MBTL histone methyl-lysine binding protein 1)
Pan paniscus (bonobo/pygmy chimpanzee) : L3MBTL1 (L3MBTL histone methyl-lysine binding protein 1)
Canis lupus familiaris (dog) : L3MBTL1 (L3MBTL1, histone methyl-lysine binding protein)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : L3mbtl1 (L3MBTL histone methyl-lysine binding protein 1)
Sus scrofa (pig) : L3MBTL1 (L3MBTL histone methyl-lysine binding protein 1)
more info ...
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.03159,316,580 - 159,348,914 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.03165,513,621 - 165,545,362 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43153,811,334 - 153,836,990 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.13153,713,787 - 153,743,026 (+)NCBI
Celera3150,258,873 - 150,290,717 (+)NCBICelera
Cytogenetic Map3q42NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model

Annotation    (Toggle Annotation Detail/Summary View)

Disease Annotations
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References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Rnor_6.0)
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome

Strain Variation

Strain Sequence Variants (Rnor 5.0)

Additional Information

External Database Links
Nomenclature History
  
More on L3mbtl1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1307316
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2019-04-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.