FAM107B - family with sequence similarity 107 member B Gene

Also Known as HITS; C10orf45

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 83641

About FAM107B

This gene has 29 transcripts (splice variants), 206 orthologues and 1 paralogue. Ubiquitous expression in lymph node (RPKM 45.0), kidney (RPKM 31.4) and 23 other tissues.

Summary

Predicted to act upstream of or within sensory perception of sound. [provided by Alliance of Genome Resources, Apr 2022]

FAM107B Products (17)

mRNA Protein Name
NM_001282695.2 NP_001269624.1 protein FAM107B isoform a
NM_001282696.2 NP_001269625.1 protein FAM107B isoform a
NM_001282697.2 NP_001269626.1 protein FAM107B isoform a
NM_001282698.2 NP_001269627.1 protein FAM107B isoform a
NM_001282699.1 NP_001269628.1 protein FAM107B isoform a
NM_001282700.2 NP_001269629.1 protein FAM107B isoform a
NM_001282701.2 NP_001269630.1 protein FAM107B isoform a
NM_001282702.2 NP_001269631.1 protein FAM107B isoform a
NM_001282703.1 NP_001269632.1 protein FAM107B isoform a
NM_001320735.2 NP_001307664.1 protein FAM107B isoform a
NM_001320736.2 NP_001307665.1 protein FAM107B isoform a
NM_001320737.1 NP_001307666.1 protein FAM107B isoform a
NM_001320738.2 NP_001307667.1 protein FAM107B isoform a
NM_001320739.2 NP_001307668.1 protein FAM107B isoform a
NM_001320740.1 NP_001307669.1 protein FAM107B isoform a
NM_001320741.2 NP_001307670.1 protein FAM107B isoform c
NM_031453.4 NP_113641.2 protein FAM107B isoform b

FAM107B Protein Structure

DUF1151

DUF1151: Protein of unknown function (DUF1151) (1 - 120)

  • 0
  • 100
  • 131 a.a.
Protein Preferred Names Protein Names

protein FAM107B

  • FAM107B/CDNF fusion

Related Diseases

Diseases Alias
Retinitis Pigmentosa-Deafness Syndrome

  • Retinitis Pigmentosa 8, Formerly

  • Rp8, Formerly

  • Retinitis Pigmentosa 21, Formerly

  • Rp21, Formerly

  • Usher Syndrome
Alzheimer Disease 13

  • AD13

  • Alzheimer Disease-13

  • Alzheimer'S Disease 13

  • Alzheimer'S Disease 13, Late Onset
Leech Infestation

  • Hirudiniasis

  • Leeches
Cardiomyopathy, Dilated, 1dd

  • Dilated Cardiomyopathy 1dd

  • CMD1DD

  • Cardiomyopathy, Dilated 1dd

  • Cardiomyopathy, Dilated, Type 1dd
Patent Foramen Ovale

  • Atrial Septal Defect Within Oval Fossa

  • Foramen Ovale Patent

  • Ostium Secundum Atrial Septal Defect

  • Atrial Septal Defect, Ostium Secundum Type

  • Foramen Ovale, Patent

  • Defect, Patent Or Persistent, Ostium Secundum

  • Ostium Secundum Type Atrial Septal Defect

  • Persistent Ostium Secundum

  • Asd Ostium Secundum Type

  • Ostium Secundum Asd

  • Osasd

  • Asd, Ostium Secundum Type

  • Pfo - [Patent Foramen Ovale]

  • Open Foramen Ovale

  • Open Oval Foramen

  • Persistent Foramen Ovale

  • Secundum Atrial Septal Defect
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-RS04677 FAM107B Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Macaca mulatta FAM107B VGNC VGNC:72323
Canis familiaris FAM107B VGNC VGNC:52133
Felis catus FAM107B VGNC VGNC:83878
Mus musculus FAM107B MGD MGI:1913790
Rattus norvegicus FAM107B RGD RGD:1561482
Bos taurus FAM107B VGNC VGNC:57007
Others FAM107B NCBI