1. Gene
  2. NELFE - negative elongation factor complex member E Gene

NELFE - negative elongation factor complex member E Gene

Homo sapiens

Also known as RD; RDP; RDBP; D6S45; NELF-E

Gene ID: 7936 | Gene type: protein coding

About NELFE

Cytogenetic location: 6p21.33 Genomic coordinates (GRCh38): 6:31,952,087-31,958,971 (from NCBI)

This gene has 14 transcripts (splice variants), 1 gene allele and 193 orthologues. Ubiquitous expression in testis (RPKM 52.1), ovary (RPKM 20.1) and 25 other tissues.

Summary

The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]

NELFE Products(1)

mRNA Protein Name
NM_002904.6 NP_002895.3 negative elongation factor E

NELFE Protein Structure

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (269 - 323)

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Protein Preferred Names Protein Names

negative elongation factor E

RD RNA-binding protein

Related Diseases

Diseases Alias
Immunodeficiency 12

Combined Immunodeficiency Due To Malt1 Deficiency

IMD12

Immunodeficiency, Type 12

Hairy Tongue

Overgrowth Of Filiform Papillae

Tongue, Hairy

Benign Pleural Mesothelioma

Mesothelioma Of Pleura

Benign Neoplasm Of Mesothelial Tissue Of Pleura

Pleural Malignant Mesothelioma

Wolf-Hirschhorn Syndrome

Pitt-Rogers-Danks Syndrome

WHS

Chromosome 4p16.3 Deletion Syndrome

Wittwer Syndrome

4p- Syndrome

Pitt Syndrome

4p Deletion Syndrome

Distal Deletion 4p

Distal Monosomy 4p

Telomeric Deletion 4p

Prds

4p Syndrome

Chromosome 4p Syndrome

Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation

Wolf Syndrome

Chromosome 4p Deletion Syndrome

Chromosome 4p Monosomy

Del Syndrome

Monosomy 4p

Partial Monosomy 4p

Chromosome 4 Short Arm Deletion

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
Rattus norvegicus NELFE RGD RGD:1303325
Macaca mulatta NELFE VGNC VGNC:83437
Bos taurus NELFE VGNC VGNC:32002
Felis catus NELFE VGNC VGNC:63774
Mus musculus NELFE MGD MGI:102744