1. Gene
  2. PREB - prolactin regulatory element binding Gene

PREB - prolactin regulatory element binding Gene

Homo sapiens

Also known as SEC12

Gene ID: 10113 | Gene type: protein coding

About PREB

Cytogenetic location: 2p23.3 Genomic coordinates (GRCh38): 2:27,130,756-27,134,636 (from NCBI)

This gene has 9 transcripts (splice variants) and 205 orthologues. Ubiquitous expression in ovary (RPKM 22.2), fat (RPKM 20.3) and 25 other tissues.

Summary

This gene encodes a protein that specifically binds to a Pit1-binding element of the Prolactin (PRL) promoter. This protein may act as a transcriptional regulator and is thought to be involved in some of the developmental abnormalities observed in patients with partial trisomy 2p. This gene overlaps the abhydrolase domain containing 1 (ABHD1) gene on the opposite strand. [provided by RefSeq, Jul 2008]

PREB Products(5)

mRNA Protein Name
NM_001330484.2 NP_001317413.1 prolactin regulatory element-binding protein isoform 2
NM_001330485.2 NP_001317414.1 prolactin regulatory element-binding protein isoform 3
NM_001330486.2 NP_001317415.1 prolactin regulatory element-binding protein isoform 4
NM_001330487.2 NP_001317416.1 prolactin regulatory element-binding protein isoform 5
NM_013388.6 NP_037520.1 prolactin regulatory element-binding protein isoform 1

PREB Protein Structure

WD40

WD40: WD domain, G-beta repeat (160 - 182)

WD40

WD40: WD domain, G-beta repeat (188 - 222)

  • 0
  • 100
  • 200
  • 300
  • 417 a.a.
Protein Preferred Names Protein Names

prolactin regulatory element-binding protein

mammalian guanine nucleotide exchange factor mSec12

Related Diseases

Diseases Alias
Craniolenticulosutural Dysplasia

Boyadjiev-Jabs Syndrome

CLSD

Cranio-Lenticulo-Sutural Dysplasia

Cranio-Lenticulo-Sutural Dysplasia, Clsd

Chylomicron Retention Disease

CMRD

Anderson Disease

Lipid Transport Defect Of Intestine

Hypobetalipoproteinemia With Accumulation Of Apolipoprotein B-Like Protein In Intestinal Cells

Andd

Anderson Syndrome

Crd

Andersons Disease

Malabsorption Syndrome

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 PREB MGD MGI:1355326
Bos taurus PREB VGNC VGNC:33305
Felis catus PREB VGNC VGNC:69039
Canis familiaris PREB VGNC VGNC:44954
Macaca mulatta PREB VGNC VGNC:103847
Rattus norvegicus PREB RGD RGD:61929