FAM135A - family with sequence similarity 135 member A Gene

Homo sapiens

Also known as KIAA1411

Gene ID: 57579 | Gene type: protein coding

About FAM135A

This gene has 16 transcripts (splice variants), 213 orthologues and 1 paralogue. Broad expression in esophagus (RPKM 17.6), prostate (RPKM 12.9) and 22 other tissues.

Summary

Predicted to be involved in cellular lipid metabolic process. [provided by Alliance of Genome Resources, Apr 2022]

FAM135A Products(21)

mRNA	Protein	Name
NM_001105531.3	NP_001099001.1	protein FAM135A isoform a
NM_001162529.3	NP_001156001.1	protein FAM135A isoform c
NM_001330995.3	NP_001317924.1	protein FAM135A isoform d
NM_001330996.3	NP_001317925.1	protein FAM135A isoform e
NM_001330997.3	NP_001317926.1	protein FAM135A isoform a
NM_001330998.3	NP_001317927.1	protein FAM135A isoform f
NM_001330999.3	NP_001317928.1	protein FAM135A isoform e
NM_001331000.3	NP_001317929.1	protein FAM135A isoform g
NM_001331001.3	NP_001317930.1	protein FAM135A isoform a
NM_001331002.3	NP_001317931.1	protein FAM135A isoform a
NM_001331003.3	NP_001317932.1	protein FAM135A isoform f
NM_001331004.3	NP_001317933.1	protein FAM135A isoform h
NM_001331005.3	NP_001317934.1	protein FAM135A isoform i
NM_001331006.3	NP_001317935.1	protein FAM135A isoform j
NM_001351599.2	NP_001338528.1	protein FAM135A isoform e
NM_001351600.2	NP_001338529.1	protein FAM135A isoform c
NM_001351602.2	NP_001338531.1	protein FAM135A isoform c
NM_001351607.2	NP_001338536.1	protein FAM135A isoform c
NM_001351608.2	NP_001338537.1	protein FAM135A isoform k
NM_001351609.2	NP_001338538.1	protein FAM135A isoform l
NM_020819.5	NP_065870.3	protein FAM135A isoform b

FAM135A Protein Structure

DUF3657

DUF676

0
200
400
600
800
1000
1200
1302 a.a.

Protein Preferred Names

Protein Names

protein FAM135A

Related Diseases

Diseases

Alias

Myeloma, Multiple

Multiple Myeloma	Plasma Cell Myeloma
Kahler Disease	Myelomatosis
Medullary Plasmacytoma	Multiple Myeloma, Resistance To
Myeloma	Plasma Cell Dyscrasia
Kahler'S Disease	Multiple Myeloma, Susceptibility To
Myeloma - Multiple	Kahler-Bozzolo Disease
Plasma Cell Myelomas	MM
Plasma Cell Neoplasm	Primary Systemic Amyloidosis
Primary Amyloidosis	Immunoglobulin Deposition Disease
Plasmacytic Myeloma	Multiple Myelomata
Multiple Myeloma Nos	Multiple Myeloma Without Mention Of Remission
Monostotic Plasma Cell Myeloma	Mm - [Multiple Myeloma]

Linear Skin Defects With Multiple Congenital Anomalies 1

Midas Syndrome	Mcops7
Mls Syndrome	Microphthalmia, Syndromic 7
Microphthalmia With Linear Skin Defects Syndrome	Microphthalmia With Linear Skin Defects
Microphthalmia-Dermal Aplasia-Sclerocornea Syndrome	Syndromic Microphthalmia Type 7
LSDMCA1	Mls
Microphthalmia, Dermal Aplasia, And Sclerocornea	Microphthalmia With Linear Skin Defect Syndrome
Syndromic Microphthalmia 7	Linear Skin Defects With Multiple Congenital Anomalies
Microphthalmia, Dermal Aplasia, Sclerocornea Syndrome	Microphthalmia Dermal Aplasia And Sclerocornea Syndrome
Micropthalmia Syndromic 7	Microphthalmia Syndromic 7
Microphthalmia With Linear Skin Lesions Syndrome	Syndromic Microphthalmia-7
Microphthalmia, Dermal Aplasia And Sclerocornea	Microphthalmia, Syndromic, 7
Midas

Hypotonia-Cystinuria Syndrome

Cystinuria With Mitochondrial Disease	2p21 Microdeletion Syndrome
HCS	Homozygous 2p16 Deletion Syndrome, Formerly
2p21 Deletion Syndrome	Del(2)(P21)
Monosomy 2p21	Atypical Hypotonia-Cystinuria Syndrome
Atypical Hcs

Retinitis Pigmentosa

RP	Rod-Cone Dystrophy
Autosomal Recessive Retinitis Pigmentosa	Non-Syndromic Retinitis Pigmentosa
Pericentral Pigmentary Retinopathy	Pigmentary Retinopathy
Tapetoretinal Degeneration	Rcd
Retinitis Pigmentosa Autosomal Recessive	ARRP
Retinitis Pigmentosa, Autosomal Recessive	Retinitis Pigmentosa 1

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-RS04683	FAM135A Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	FAM135A	VGNC	VGNC:40594
Felis catus	FAM135A	VGNC	VGNC:62062
Macaca mulatta	FAM135A	VGNC	VGNC:72310
Rattus norvegicus	FAM135A	RGD	RGD:1304927
Bos taurus	FAM135A	VGNC	VGNC:28730
Mus musculus	FAM135A	MGD	MGI:1915437

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