1. Gene
  2. L3MBTL3 - L3MBTL histone methyl-lysine binding protein 3 Gene

L3MBTL3 - L3MBTL histone methyl-lysine binding protein 3 Gene

Homo sapiens

Also known as MBT1; MBT-1

Gene ID: 84456 | Gene type: protein coding

About L3MBTL3

Cytogenetic location: 6q23.1 Genomic coordinates (GRCh38): 6:130,018,581-130,141,438 (from NCBI)

This gene has 10 transcripts (splice variants), 169 orthologues and 18 paralogues. Ubiquitous expression in endometrium (RPKM 5.0), spleen (RPKM 4.6) and 24 other tissues.

Summary

This gene encodes a member of the malignant brain tumor (MBT) family of chromatin interacting transcriptional repressors. Members of this family function as methyl-lysine readers, which recognize methylated lysine residues on histone protein tails, and are associated with the repression of gene expression. The encoded protein may regulate hematopoiesis. Homozygous deletion of this gene has been observed in human patients with medulloblastoma. [provided by RefSeq, Oct 2016]

L3MBTL3 Products(4)

mRNA Protein Name
NM_001007102.4 NP_001007103.1 lethal(3)malignant brain tumor-like protein 3 isoform b
NM_001346550.2 NP_001333479.1 lethal(3)malignant brain tumor-like protein 3 isoform b
NM_001346551.2 NP_001333480.1 lethal(3)malignant brain tumor-like protein 3 isoform b
NM_032438.4 NP_115814.1 lethal(3)malignant brain tumor-like protein 3 isoform a

L3MBTL3 Protein Structure

MBT

MBT: mbt repeat (268 - 340)

MBT

MBT: mbt repeat (375 - 444)

MBT

MBT: mbt repeat (479 - 543)

SAM_1

SAM_1: SAM domain (Sterile alpha motif) (706 - 770)

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  • 780 a.a.
Protein Preferred Names Protein Names

lethal(3)malignant brain tumor-like protein 3

H-l(3)mbt-like protein 3

Related Diseases

Diseases Alias
Lipodystrophy, Familial Partial, Type 1

FPLD1

Familial Partial Lipodystrophy Type 1

Familial Partial Lipodystrophy, Kobberling Type

Lipodystrophy, Familial Partial, Kobberling Type

Familial Partial Lipodystrophy Kobberling Type

Familial Partial Lipodystrophy Type Köbberling

Familial Partial Lipodystrophy, Köbberling Type

Familial Partial Lipodystrophy, Type 1

N Syndrome

NSX

Intellectual Disability, Malformations, Chromosome Breakage, And Development Of T-Cell Leukemia

Medulloblastoma

MDB

Cpnet

Localized Primitive Neuroectodermal Tumor

Classic Medulloblastoma

Medulloblastoma Predisposition Syndrome

Medulloblastoma, Somatic

Brain Medulloblastoma

Cns Pnet

Infratentorial Primitive Neuroectodermal Tumor

Neuroectodermal Tumors, Primitive

Medulloblastomas

Desmoplastic Medulloblastoma

Medulloblastoma, With Extensive Nodularity

Medulloblastoma Of Unspecified Site

Medullomyoblastoma Of Unspecified Site

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus L3MBTL3 MGD MGI:2143628
Macaca mulatta L3MBTL3 VGNC VGNC:74106
Canis familiaris L3MBTL3 VGNC VGNC:53732
Rattus norvegicus L3MBTL3 RGD RGD:1305474
Felis catus L3MBTL3 VGNC VGNC:63183
Bos taurus L3MBTL3 VGNC VGNC:50640