SLMAP - sarcolemma associated protein Gene

Also Known as SLAP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7871

About SLMAP

Cytogenetic location: 3p14.3 Genomic coordinates (GRCh38): 3:57,756,309-57,930,013 (from NCBI)

This gene has 40 transcripts (splice variants), 209 orthologues, 2 paralogues and is associated with 1 phenotype. Ubiquitous expression in heart (RPKM 29.5), esophagus (RPKM 29.0) and 24 other tissues.

Summary

This gene encodes a component of a conserved striatin-interacting Phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and Apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]

SLMAP Products (28)

mRNA Protein Name
NM_001304420.3 NP_001291349.1 sarcolemmal membrane-associated protein isoform a
NM_001304421.2 NP_001291350.1 sarcolemmal membrane-associated protein isoform c
NM_001304422.3 NP_001291351.1 sarcolemmal membrane-associated protein isoform d
NM_001304423.3 NP_001291352.1 sarcolemmal membrane-associated protein isoform e
NM_001311178.2 NP_001298107.1 sarcolemmal membrane-associated protein isoform f
NM_001311179.2 NP_001298108.1 sarcolemmal membrane-associated protein isoform g
NM_001377538.1 NP_001364467.1 sarcolemmal membrane-associated protein isoform h
NM_001377539.1 NP_001364468.1 sarcolemmal membrane-associated protein isoform i
NM_001377540.1 NP_001364469.1 sarcolemmal membrane-associated protein isoform j
NM_001377541.1 NP_001364470.1 sarcolemmal membrane-associated protein isoform k
NM_001377542.1 NP_001364471.1 sarcolemmal membrane-associated protein isoform q
NM_001377545.1 NP_001364474.1 sarcolemmal membrane-associated protein isoform l
NM_001377549.1 NP_001364478.1 sarcolemmal membrane-associated protein isoform n
NM_001377551.1 NP_001364480.1 sarcolemmal membrane-associated protein isoform aa
NM_001377552.1 NP_001364481.1 sarcolemmal membrane-associated protein isoform o
NM_001377555.1 NP_001364484.1 sarcolemmal membrane-associated protein isoform p
NM_001377557.1 NP_001364486.1 sarcolemmal membrane-associated protein isoform c
NM_001377559.1 NP_001364488.1 sarcolemmal membrane-associated protein isoform r
NM_001377562.1 NP_001364491.1 sarcolemmal membrane-associated protein isoform bb
NM_001377921.1 NP_001364850.1 sarcolemmal membrane-associated protein isoform s
NM_001377922.1 NP_001364851.1 sarcolemmal membrane-associated protein isoform t
NM_001377923.1 NP_001364852.1 sarcolemmal membrane-associated protein isoform u
NM_001377924.1 NP_001364853.1 sarcolemmal membrane-associated protein isoform v
NM_001377925.1 NP_001364854.1 sarcolemmal membrane-associated protein isoform w
NM_001377926.1 NP_001364855.1 sarcolemmal membrane-associated protein isoform x
NM_001377927.1 NP_001364856.1 sarcolemmal membrane-associated protein isoform y
NM_001377928.1 NP_001364857.1 sarcolemmal membrane-associated protein isoform z
NM_007159.5 NP_009090.2 sarcolemmal membrane-associated protein isoform b
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
23386615 GOA
enables protein-macromolecule adaptor activity IDA
IDA: Inferred from direct assay
29063833 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of hippo signaling IDA
IDA: Inferred from direct assay
29063833 GOA
involved in protein localization to plasma membrane IMP
IMP: Inferred from mutant phenotype
23064965 GOA
involved in regulation of membrane depolarization during cardiac muscle cell action potential IMP
IMP: Inferred from mutant phenotype
23064965 GOA
involved in regulation of sodium ion transmembrane transport IMP
IMP: Inferred from mutant phenotype
23064965 GOA
involved in regulation of voltage-gated sodium channel activity IMP
IMP: Inferred from mutant phenotype
23064965 GOA
Cellular Component GO Annotation Evidence References Source
part of FAR/SIN/STRIPAK complex IDA
IDA: Inferred from direct assay
29063833 GOA
is active in cytoplasm IDA
IDA: Inferred from direct assay
29063833 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

SLMAP Protein Structure

FHA

FHA: FHA domain (28 - 106)

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

sarcolemmal membrane-associated protein

SLMAP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SLMAP Q14BN4 STK4 Homo sapiens Q13043 24255178
Intra
SLMAP Q14BN4 STK4 Homo sapiens Q13043 24255178
Intra
SLMAP Q14BN4 STK4 Homo sapiens Q13043 24255178
Intra
SLMAP Q14BN4 STK4 Homo sapiens Q13043
Y2H
23386615
Intra
SLMAP Q14BN4 STK3 Homo sapiens Q13188 25416956
Intra
SLMAP Q14BN4 STK3 Homo sapiens Q13188 24255178
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Brugada Syndrome
  • Sudden Unexpected Nocturnal Death Syndrome

  • Sudden Unexplained Nocturnal Death Syndrome

  • Bangungut

  • Brugada Type Idiopathic Ventricular Fibrillation

  • Pokkuri Death Syndrome

  • Sunds

  • Idiopathic Ventricular Fibrillation, Brugada Type

  • Sudden Unexplained Death

  • Dream Disease

  • Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome

  • Sudden Unexplained Death Syndrome

  • Suds

  • Sunds - [Sudden Unexplained Nocturnal Death Syndrome]

Lung Cancer
  • Lung Carcinoma

  • Non-Small Cell Lung Carcinoma

  • Lung Cancer, Susceptibility To

  • Lung Cancer, Protection Against

  • Adenocarcinoma Of Lung, Somatic

  • Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer

  • Lung Neoplasm

  • Carcinoma Of Lung

  • Lung Non-Small Cell Carcinoma

  • Non-Small Cell Lung Cancer

  • Nsclc

  • Lung Neoplasms

  • Malignant Neoplasm Of Lung

  • Alveolar Cell Carcinoma

  • Nonsmall Cell Lung Cancer, Somatic

  • Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer, Susceptibility To

  • Lung Cancer, Somatic

  • Lung Cancer, Resistance To

  • Cancer Of Lung

  • Cancer Of Bronchus

  • Cancer Of The Lung

  • Lung Malignancies

  • Lung Malignant Tumors

  • Malignant Lung Tumor

  • Malignant Tumor Of Lung

  • Pulmonary Cancer

  • Pulmonary Carcinoma

  • Pulmonary Neoplasms

  • Respiratory Carcinoma

  • LNCR

  • Adenocarcinoma Of Lung

  • Neoplasm Of Lung

  • Cancer Lung

  • Carcinoma Non-Small Cell Lung

  • Carcinoma, Non-Small-Cell Lung

  • Lung Cancers

  • Lung Carcinomas

  • Cancer, Lung

  • Cancer, Lung, Non-Small Cell

  • Primary Malignant Neoplasm Of Lung

  • Bronchioloalveolar Adenocarcinoma

Cerebral Cavernous Malformations 3
  • Cerebral Cavernous Malformation 3

  • CCM3

  • Cerebral Cavernous Malformations-3

  • Cavernous Angiomatous Malformations

  • Cavernous Hemangioma Of The Brain

  • Cerebral Capillary Malformations

  • Cerebral Cavernoma

  • Familial Cavernous Angioma

  • Cerebral Cavernous Malformations, Type 3

Cerebral Cavernous Malformations
  • Cerebral Cavernous Malformation

  • Cavernous Malformations Of Cns And Retina

  • Cerebral Cavernous Malformation 1

  • Cavernous Angiomatous Malformations

  • Cerebral Capillary Malformations

  • CCM

  • Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations

  • Familial Cavernous Angioma

  • Cavernous Angioma

  • Familial Cerebral Cavernous Malformation

  • Cerebral Cavernous Malformations 1

  • Cavernous Angioma, Familial

  • Cam

  • Cerebral Cavernous Malformations-1

  • Cavernoma

  • Central Nervous System Cavernous Hemangioma

  • Cerebral Cavernous Hemangioma

  • Familial Cavernous Hemangioma

  • Familial Cavernous Malformation

  • Familial Cerebral Cavernous Angioma

  • Intracerebral Cavernous Hemangioma

  • CCM1

  • Cavernous Hemangioma Of The Brain

  • Cerebral Cavernoma

  • Cerebral Cavernous Malformations, Type 1

  • Hemangioma, Cavernous, Central Nervous System

  • Hemangioma, Cavernous

  • Angioma, Cavernous

Long Qt Syndrome 1
  • Romano-Ward Syndrome

  • LQT1

  • Ward-Romano Syndrome

  • Rws

  • Ventricular Fibrillation With Prolonged Qt Interval

  • Wrs

  • Long Qt Syndrome 1, Acquired, Susceptibility To

  • Long Qt Syndrome 1, Acquired

  • Romano-Ward Long Qt Syndrome

  • Long Qt Syndrome Type 1

  • Long Qt Syndrome-1

  • Acquired Susceptibility To Long Qt Syndrome 1

  • Qt Syndrome, Long, Type 1

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
Mus musculus SLMAP MGD MGI:1933549
Canis familiaris SLMAP VGNC VGNC:46513
Macaca mulatta SLMAP VGNC VGNC:77723
Felis catus SLMAP VGNC VGNC:65455
Rattus norvegicus SLMAP RGD RGD:1307674
Bos taurus SLMAP VGNC VGNC:34969
Others SLMAP NCBI