FAM135A - family with sequence similarity 135 member A Gene

Also Known as KIAA1411

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57579

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

DUF3657: Protein FAM135 (69 - 130)

DUF3657

DUF3657: Protein FAM135 (297 - 349)

DUF676

DUF676: Putative serine esterase (DUF676) (1032 - 1226)

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  • 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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS04683 FAM135A Human Pre-designed siRNA Set A Pre-designed Set / 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