2. Gene
  3. FAM177A1 - family with sequence similarity 177 member A1 Gene

FAM177A1 - family with sequence similarity 177 member A1 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as C14orf24

Gene ID: 283635 | Gene type: protein coding

About FAM177A1

Cytogenetic location: 14q13.2 Genomic coordinates (GRCh38): 14:35,044,907-35,083,383 (from NCBI)

This gene has 14 transcripts (splice variants), 265 orthologues and 1 paralogue. Ubiquitous expression in prostate (RPKM 15.8), colon (RPKM 14.8) and 25 other tissues.

Summary

This gene encodes a member of a conserved protein family. Alternative splicing results in multiple transcript variants. This gene is thought to be associated with susceptibility to juvenile idiopathic arthritis. [provided by RefSeq, Apr 2017]

FAM177A1 Products(3)

mRNA Protein Name
NM_001079519.1 NP_001072987.1 protein FAM177A1 isoform 2
NM_001289022.3 NP_001275951.1 protein FAM177A1 isoform 2
NM_173607.5 NP_775878.2 protein FAM177A1 isoform 1 precursor

FAM177A1 Protein Structure

FAM177

FAM177: FAM177 family (37 - 156)

  • 0
  • 100
  • 200
  • 213 a.a.
Protein Preferred Names Protein Names

protein FAM177A1

Related Diseases

Diseases Alias
Myasthenic Syndrome, Congenital, 22

CMS22

Prepl Deficiency

Congenital Myasthenic Syndrome 22
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
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-RS04699 FAM177A1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus FAM177A1 RGD RGD:2323636
Bos taurus FAM177A1 VGNC VGNC:50064
Mus musculus FAM177A1 MGD MGI:1920635
Felis catus FAM177A1 VGNC VGNC:104388
Canis familiaris FAM177A1 VGNC VGNC:49745