YIF1B - Yip1 interacting factor homolog B, membrane trafficking protein Gene

Also Known as FinGER8; KABAMAS

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 90522

About YIF1B

Cytogenetic location: 19q13.2 Genomic coordinates (GRCh38): 19:38,303,558-38,321,887 (from NCBI)

This gene has 16 transcripts (splice variants), 192 orthologues, 1 paralogue and is associated with 1 phenotype. Ubiquitous expression in colon (RPKM 13.5), small intestine (RPKM 9.4) and 25 other tissues.

Summary

Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport; protein targeting to membrane; and sperm axoneme assembly. Located in Golgi apparatus; endoplasmic reticulum; and endoplasmic reticulum-Golgi intermediate compartment. [provided by Alliance of Genome Resources, Apr 2022]

YIF1B Products (6)

mRNA Protein Name
NM_001039671.3 NP_001034760.1 protein YIF1B isoform 3
NM_001039672.3 NP_001034761.1 protein YIF1B isoform 5
NM_001039673.3 NP_001034762.1 protein YIF1B isoform 4
NM_001145461.2 NP_001138933.1 protein YIF1B isoform 6
NM_001145462.2 NP_001138934.1 protein YIF1B isoform 2
NM_001145463.2 NP_001138935.1 protein YIF1B isoform 7

YIF1B Protein Structure

YIF1

YIF1: YIF1 (72 - 309)

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

protein YIF1B

  • YIP1-interacting factor homolog B

YIF1B Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
YIF1B Q5BJH7 GPR37 Homo sapiens O15354
Ub Reconstruction
28298427
Intra
YIF1B Q5BJH7 CKAP4 Homo sapiens Q07065
Anti Tag CoIP
33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Kaya-Barakat-Masson Syndrome

  • KABAMAS
Dystonia

  • Dystonic Disease

  • Dystonic Disorder

  • Dystonia Disorders

  • Neuroleptic Dyskinesia
Microcephaly

  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly
Chromosome 22q11.2 Deletion Syndrome, Distal

  • 22q11.2 Deletion Syndrome

  • Autosomal Dominant Opitz G/Bbb Syndrome

  • Catch22

  • Cayler Cardiofacial Syndrome

  • Conotruncal Anomaly Face Syndrome

  • Digeorge Syndrome

  • Sedlackova Syndrome

  • Shprintzen Syndrome

  • Velocardiofacial Syndrome

  • 22q11.2 Distal Deletion Syndrome

  • Distal 22q11.2 Microdeletion Syndrome

  • 22q11.2ds

  • Vcfs

  • Velo-Cardio-Facial Syndrome

  • Distal Chromosome 22q11.2 Deletion Syndrome

  • Chromosome 22q11.2 Deletion Syndrome Distal

  • Chromosome 22q11.2 Deletion Syndrome

  • Deletion 22q11.2 Syndrome

  • 22q11ds

  • Catch 22

  • Digeorge Sequence

  • Microdeletion 22q11.2

  • Monosomy 22q11

  • Takao Syndrome

  • Distal Del(22)(Q11.2)

  • Distal Monosomy 22q11.2

  • Catch 22 Syndrome

  • Chromosome Deletion Syndrome 22q11.2, Distal
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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS15923 YIF1B Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus YIF1B VGNC VGNC:37024
Rattus norvegicus YIF1B RGD RGD:735199
Mus musculus YIF1B MGD MGI:1924504
Felis catus YIF1B VGNC VGNC:67138
Canis familiaris YIF1B VGNC VGNC:48486
Macaca mulatta YIF1B VGNC VGNC:79852