FAM107B - family with sequence similarity 107 member B Gene

Homo sapiens

Also known as HITS; C10orf45

Gene ID: 83641 | Gene type: protein coding

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

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04677	FAM107B Human Pre-designed siRNA Set A	Pre-designed Sets	/	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

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