SEC14L1 - SEC14 like lipid binding 1 Gene

Homo sapiens

Also known as SEC14L; PRELID4A

Gene ID: 6397 | Gene type: protein coding

About SEC14L1

Cytogenetic location: 17q25.2-q25.3 Genomic coordinates (GRCh38): 17:77,088,685-77,217,101 (from NCBI)

This gene has 23 transcripts (splice variants), 213 orthologues and 6 paralogues. Ubiquitous expression in placenta (RPKM 29.8), testis (RPKM 26.1) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the SEC14 cytosolic factor family. It has similarity to yeast SEC14 and to Japanese flying squid RALBP which suggests a possible role of the gene product in an intracellular transport system. Multiple alternatively spliced transcript variants have been found for this gene; some variants represent read-through transcripts that include exons from the upstream gene C17orf86. [provided by RefSeq, Feb 2011]

SEC14L1 Products(7)

mRNA	Protein	Name
NM_001039573.3	NP_001034662.3	SEC14-like protein 1 isoform b
NM_001143998.2	NP_001137470.2	SEC14-like protein 1 isoform a
NM_001143999.2	NP_001137471.2	SEC14-like protein 1 isoform a
NM_001144001.2	NP_001137473.2	SEC14-like protein 1 isoform c
NM_001204408.2	NP_001191337.2	SEC14-like protein 1 isoform b
NM_001204410.2	NP_001191339.2	SEC14-like protein 1 isoform a
NM_003003.4	NP_002994.4	SEC14-like protein 1 isoform a

SEC14L1 Protein Structure

PRELI

CRAL_TRIO_N

CRAL_TRIO

0
200
400
600
715 a.a.

Protein Preferred Names

Protein Names

SEC14-like protein 1

Related Diseases

Diseases

Alias

Complement Component 7 Deficiency

C7 Deficiency

C7D

Tylosis With Esophageal Cancer

Palmoplantar Keratoderma-Esophageal Carcinoma Syndrome	TOC
Keratosis Palmaris Et Plantaris With Esophageal Cancer	Bennion-Patterson Syndrome
Howell-Evans Syndrome	Keratosis Palmoplantaris-Esophageal Carcinoma Syndrome
Palmoplantar Hyperkeratosis-Esophageal Carcinoma Syndrome	Tylosis-Oesophageal Carcinoma Syndrome
Palmoplantar Keratoderma With Esophageal Cancer	Howel-Evans Syndrome
Keratosis Palmoplantaris With Esophageal Cancer	Tylosis - Oesophageal Carcinoma
Howel-Evans' Syndrome

Phlyctenulosis

Phlyctenular Keratoconjunctivitis

Strumous Ophthalmia

Amyotrophic Neuralgia

Neuralgic Amyotrophy	Brachial Plexus Neuritis
Neuralgic Shoulder Amyotrophy	Acute Brachial Plexus Neuritis
Immune Brachial Plexus Neuropathy	Mononeuritis Multiplex With Brachial Predilection
Parsonage-Turner Syndrome

Brachial Plexus Neuropathy

Brachial Plexopathy	Brachial Plexus Neuropathies
Brachial Plexus Disorder	Bpn - [Brachial Plexus Neuropathy]
Brachial Plexus Disease	Neuropathic Plexus Brachialis
Brachial Plexus Syndrome	Brachial Plexus Irritation
Brachial Plexus Lesion	Brachial Plexus Pressure
Compression Of Brachial Plexus

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-RS12606	SEC14L1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	SEC14L1	VGNC	VGNC:64961
Bos taurus	SEC14L1	VGNC	VGNC:34404
Mus musculus	SEC14L1	MGD	MGI:1921386
Macaca mulatta	SEC14L1	VGNC	VGNC:99226
Rattus norvegicus	SEC14L1	RGD	RGD:1563123
Canis familiaris	SEC14L1	VGNC	VGNC:45963

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