1. Gene
  2. SEC14L1 - SEC14 like lipid binding 1 Gene

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
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables RIG-I binding IPI
IPI: Inferred from physical interaction
23843640 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17092608 GOA
enables protein sequestering activity IDA
IDA: Inferred from direct assay
23843640 GOA
Biological Process GO Annotation Evidence Reference Source
involved in choline transport IDA
IDA: Inferred from direct assay
17092608 GOA
involved in negative regulation of RIG-I signaling pathway IMP
IMP: Inferred from mutant phenotype
23843640 GOA
Cellular Component GO Annotation Evidence Reference Source
colocalizes with Golgi apparatus IDA
IDA: Inferred from direct assay
17092608 GOA
is active in cytoplasm IDA
IDA: Inferred from direct assay
23843640 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
17092608 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SEC14L1 Protein Structure

PRELI

PRELI: PRELI-like family (17 - 173)

CRAL_TRIO_N

CRAL_TRIO_N: CRAL/TRIO, N-terminal domain (259 - 296)

CRAL_TRIO

CRAL_TRIO: CRAL/TRIO domain (323 - 490)

  • 0
  • 200
  • 400
  • 600
  • 715 a.a.
Protein Preferred Names Protein Names

SEC14-like protein 1

SEC14L1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SEC14L1 Q92503 CEP70 Homo sapiens Q8NHQ1
Y2H Array
32296183
Intra
SEC14L1 Q92503 CEP70 Homo sapiens Q8NHQ1
Y2H Prey Pooling
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

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

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