1. Gene
  2. FER1L6 - fer-1 like family member 6 Gene

FER1L6 - fer-1 like family member 6 Gene

Homo sapiens

Also known as C8ORFK23

Gene ID: 654463 | Gene type: protein coding

About FER1L6

This gene has 1 transcript (splice variant), 194 orthologues and 4 paralogues. Biased expression in stomach (RPKM 17.6), colon (RPKM 3.5) and 5 other tissues.

Summary

Predicted to enable metal ion binding activity. Predicted to be involved in plasma membrane organization. Predicted to act upstream of or within response to bacterium. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

FER1L6 Products(1)

mRNA Protein Name
NM_001039112.2 NP_001034201.2 fer-1-like protein 6

FER1L6 Protein Structure

C2

C2: C2 domain (87 - 164)

FerI

FerI: FerI (NUC094) domain (166 - 236)

C2

C2: C2 domain (247 - 333)

FerB

FerB: FerB (NUC096) domain (712 - 784)

C2

C2: C2 domain (828 - 916)

C2

C2: C2 domain (1017 - 1080)

C2

C2: C2 domain (1359 - 1440)

C2

C2: C2 domain (1599 - 1661)

C2

C2: C2 domain (1679 - 1711)

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  • 1857 a.a.
Protein Preferred Names Protein Names

fer-1-like protein 6

fer-1-like 6

Related Diseases

Diseases Alias
Miyoshi Muscular Dystrophy

Distal Myopathy

Distal Muscular Dystrophy

Miyoshi Myopathy

Distal Myopathies

Dystrophy, Muscular, Miyoshi

Myopathy, Distal

Distal Muscular Dystrophies

Deafness, Autosomal Recessive 9

Auditory Neuropathy, Autosomal Recessive, 1

Neurosensory Nonsyndromic Recessive Deafness 9

DFNB9

Nsrd9

Autosomal Recessive Nonsyndromic Deafness 9

Autosomal Recessive Deafness 9

Nrsd9

AUNB1

Nonsyndromic Auditory Neuropathy Autosomal Recessive

Nsran

Deafness, Autosomal Recessive, 9

Deafness Neurosensory Autosomal Recessive 9

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 9

Non-Syndromic Recessive Hearing Loss 9

Deafness, Autosomal Recessive, Type 9

Auditory Neuropathy, Nonsyndromic Recessive

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b

Lgmd2b

Lgmd3

Limb-Girdle Muscular Dystrophy Due To Dysferlin Deficiency

Limb-Girdle Muscular Dystrophy Type 3

Muscular Dystrophy, Limb-Girdle, Type 2b

Autosomal Recessive Limb-Girdle Muscular Dystrophy

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive

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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus FER1L6 RGD RGD:1564703
Mus musculus FER1L6 MGD MGI:3645398
Macaca mulatta FER1L6 VGNC VGNC:72585
Bos taurus FER1L6 VGNC VGNC:28950
Canis familiaris FER1L6 VGNC VGNC:40820
Felis catus FER1L6 VGNC VGNC:62227