NUBP1 - NUBP iron-sulfur cluster assembly factor 1, cytosolic Gene

Homo sapiens

Also known as NBP; NBP1; CIAO5; NBP35

Gene ID: 4682 | Gene type: protein coding

About NUBP1

Cytogenetic location: 16p13.13 Genomic coordinates (GRCh38): 16:10,743,842-10,769,351 (from NCBI)

This gene has 8 transcripts (splice variants), 207 orthologues and 2 paralogues. Ubiquitous expression in adrenal (RPKM 9.0), heart (RPKM 8.6) and 25 other tissues.

Summary

NUBP1 is a member of the NUBP/MRP subfamily of ATP-binding proteins (Nakashima et al., 1999 [PubMed 10486206]).[supplied by OMIM, Mar 2008]

NUBP1 Products(6)

mRNA	Protein	Name
NM_001278506.2	NP_001265435.1	cytosolic Fe-S cluster assembly factor NUBP1 isoform 2
NM_001323594.2	NP_001310523.1	cytosolic Fe-S cluster assembly factor NUBP1 isoform 3
NM_001323595.2	NP_001310524.1	cytosolic Fe-S cluster assembly factor NUBP1 isoform 4
NM_001323596.2	NP_001310525.1	cytosolic Fe-S cluster assembly factor NUBP1 isoform 5
NM_001323597.1	NP_001310526.1	cytosolic Fe-S cluster assembly factor NUBP1 isoform 6
NM_002484.4	NP_002475.2	cytosolic Fe-S cluster assembly factor NUBP1 isoform 1

NUBP1 Protein Structure

ArsA_ATPase

ParA

0
100
200
300
320 a.a.

Protein Preferred Names

Protein Names

cytosolic Fe-S cluster assembly factor NUBP1

NBP 1

Related Diseases

Diseases

Alias

Pica Disease

Pica

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 6

Mitochondrial Dna Deletion Syndrome With Progressive Myopathy	PEOA6
Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 6	Dna2-Related Mitochondrial Dna Deletion Syndrome
Mitochondrial Dna Deletion Syndrome With Limb-Girdle Weakness	Mtdna Deletion Syndrome With Limb-Girdle Weakness
Mtdna Deletion Syndrome With Progressive Myopathy	Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 6
Progressive External Ophthalmoplegia, Autosomal Dominant 6	Autosomal Dominant Progressive External Ophthalmoplegia 6
Progressive External Ophthalmoplegia Autosomal Dominant 6	Ophthalmoplegia, External, Progressive, With Mitochondrial Dna Deletions, Autosomal Dominant, Type 6

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS09651	NUBP1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	NUBP1	VGNC	VGNC:44017
Felis catus	NUBP1	VGNC	VGNC:68584
Macaca mulatta	NUBP1	VGNC	VGNC:75546
Rattus norvegicus	NUBP1	RGD	RGD:1310514
Bos taurus	NUBP1	VGNC	VGNC:32315
Mus musculus	NUBP1	MGD	MGI:1347073

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