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

Homo sapiens

Also known as FinGER8; KABAMAS

Gene ID: 90522 | Gene type: protein coding

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

0
100
200
314 a.a.

Protein Preferred Names

Protein Names

protein YIF1B

YIP1-interacting factor homolog B

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15923	YIF1B Human Pre-designed siRNA Set A		/	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

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