TMEM164 - transmembrane protein 164 Gene

Also Known as bB360B22.3

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 84187

About TMEM164

This gene has 8 transcripts (splice variants) and 206 orthologues. Ubiquitous expression in lung (RPKM 5.4), fat (RPKM 5.2) and 25 other tissues.

Summary

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

TMEM164 Products (6)

mRNA	Protein	Name
NM_001353849.2	NP_001340778.1	transmembrane protein 164 isoform b
NM_001353850.2	NP_001340779.1	transmembrane protein 164 isoform c
NM_001353851.2	NP_001340780.1	transmembrane protein 164 isoform c
NM_001410717.1	NP_001397646.1	transmembrane protein 164 isoform d
NM_017698.3	NP_060168.2	transmembrane protein 164 isoform a precursor
NM_032227.4	NP_115603.2	transmembrane protein 164 isoform b

Gene Ontology

Biological Process

Biological Process GO Annotation	Evidence	References	Source
involved in positive regulation of ferroptosis	IDA IDA: Inferred from direct assay	35947500	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TMEM164 Protein Structure

TMEM164

0
100
200
297 a.a.

Protein Preferred Names	Protein Names
transmembrane protein 164	RP13-360B22.2

Related Diseases

Diseases	Alias
Amme Complex	Alport Syndrome, Mental Retardation, Midface Hypoplasia, And Elliptocytosis ATS-MR Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome Chromosome Xq22.3 Telomeric Deletion Syndrome Amme Syndrome Alport Syndrome With Intellectual Disability, Midface Hypoplasia And Elliptocytosis
X-Linked Alport Syndrome	Nephropathy And Deafness, X-Linked
Alport Syndrome	Hereditary Nephritis Alport Syndrome, X-Linked Hemorrhagic Hereditary Nephritis Congenital Hereditary Hematuria Hemorrhagic Familial Nephritis Familial Nephritis Thin Basement Membrane Disease Thin Basement Membrane Nephropathy Hematuria-Nephropathy-Deafness Syndrome Hematuric Hereditary Nephritis Hereditary Familial Congenital Hemorrhagic Nephritis Hereditary Hematuria Syndrome Hereditary Interstitial Pyelonephritis Alport Deafness-Nephropathy Alport Hearing Loss-Nephropathy Alports Syndrome Nephritis, Hereditary
Non-Syndromic X-Linked Intellectual Disability	X-Linked Non-Syndromic Intellectual Disability Non-Specific X-Linked Mental Retardation X-Linked Non-Specific Intellectual Disability

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-RS14678	TMEM164 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	TMEM164	MGD	MGI:2148020
Canis familiaris	TMEM164	VGNC	VGNC:47491
Macaca mulatta	TMEM164	VGNC	VGNC:79589
Bos taurus	TMEM164	VGNC	VGNC:35989
Rattus norvegicus	TMEM164	RGD	RGD:1563286
Others	TMEM164	NCBI