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HEPACAM (hepatic and glial cell adhesion molecule)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
220296
Gene nameGene Name - the full gene name approved by the HGNC.
Hepatic and glial cell adhesion molecule
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
HEPACAM
SynonymsGene synonyms aliases
GlialCAM, HEPN1, MLC2A, MLC2B
ChromosomeChromosome number
11
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q24.2
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a single-pass type I membrane protein that localizes to the cytoplasmic side of the cell membrane. The encoded protein acts as a homodimer and is involved in cell motility and cell-matrix interactions. The expression of
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1044227 hsa-miR-124 CLIP-seq
MIRT1044228 hsa-miR-154 CLIP-seq
MIRT1044229 hsa-miR-2909 CLIP-seq
MIRT1044230 hsa-miR-3622b-5p CLIP-seq
MIRT1044231 hsa-miR-4278 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IEA
GO:0005911 Component Cell-cell junction IDA 21419380
GO:0007050 Process Cell cycle arrest IEA
GO:0007155 Process Cell adhesion IEA
GO:0016021 Component Integral component of membrane IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q14CZ8
Protein name Hepatic and glial cell adhesion molecule (glialCAM) (Hepatocyte cell adhesion molecule) (Protein hepaCAM)
Protein function Involved in regulating cell motility and cell-matrix interactions. May inhibit cell growth through suppression of cell proliferation (PubMed:15885354, PubMed:15917256). In glia, associates and targets CLCN2 at astrocytic processes and myelinated
PDB 7UQC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07686 V-set
38 142
Immunoglobulin V-set domain
Domain
PF13927 Ig_3
147 221
Domain
Sequence
MKRERGALSRASRALRLAPFVYLLLIQTDPLEGVNITSPVRLIHGTVGKSALLSVQYSST
SSDRPVVKWQLKRDKPVTVVQSIGTEVIGTLRPDYRDRIRLFENGSLLLSDLQLADEGTY
EVEISITDDTFTGEKTINLTVD
VPISRPQVLVASTTVLELSEAFTLNCSHENGTKPSYTW
LKDGKPLLNDSRMLLSPDQKVLTITRVLMEDDDLYSCMVEN
PISQGRSLPVKITVYRRSS
LYIILSTGGIFLLVTLVTVCACWKPSKRKQKKLEKQNSLEYMDQNDDRLKPEADTLPRSG
EQERKNPMALYILKDKDSPETEENPAPEPRSATEPGPPGYSVSPAVPGRSPGLPIRSARR
YPRSPARSPATGRTHSSPPRAPSSPGRSRSASRTLRTAGVHIIREQDEAGPVEISA
Sequence length 416
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Autism spectrum disorder Autism Spectrum Disorders rs724159978, rs75184679, rs119103221, rs9332964, rs121912562, rs1594344233, rs727504317, rs111033204, rs1801086, rs587784464, rs724159948, rs764659822, rs794727977, rs796052733, rs796052728, rs762292772, rs864321694, rs869312878, rs758432471, rs750896617, rs886039692, rs886039770, rs201037487, rs200483989, rs1057518198, rs1057517708, rs780267761, rs1555910143, rs1057519632, rs775225727, rs751037529, rs1064794848, rs1064795655, rs1131691548, rs1135401811, rs1553248081, rs1454466097, rs1554480537, rs1553578503, rs1553518509, rs774152851, rs1554481395, rs1554464807, rs1554401434, rs1452048149, rs370498156, rs756691187, rs1557863430, rs1557863440, rs1557863546, rs769581210, rs202098093, rs1276388879, rs778792467, rs760059077, rs373783340, rs1557867853, rs772572695, rs753214391, rs749270162, rs548226228, rs1557870645, rs1557874046, rs749548928, rs754532606, rs1557901347, rs1557902023, rs1557909572, rs574335012, rs1557909821, rs1372713010, rs561369202, rs1476293577, rs1557910728, rs1557911386, rs375045125, rs998675361, rs1557916296, rs1557935477, rs866632178, rs1561824498, rs1396313317, rs1564801388, rs1564801473, rs1564950387, rs1565527302, rs1569513495, rs1569305431, rs143944436, rs1563183492, rs1561846159, rs1565819425, rs1562957809, rs1585645641, rs1585016242, rs1595127294, rs1585667374, rs1585653028, rs1585653240, rs1592919048, rs1585645384, rs1789927813 30763456
Macrocephaly Macrocephaly rs786204854, rs764333096, rs1557739557
Macrocephaly autism syndrome MACROCEPHALY/AUTISM SYNDROME rs121909219, rs121909224, rs121909227, rs121909231, rs121909238, rs121909239, rs121909240, rs397514559, rs397514560, rs398123323, rs146650273, rs398123329, rs398123317, rs587776667, rs786204863, rs797045066, rs797045904, rs1057519368, rs876660082, rs786204858, rs1057524874, rs1114167637, rs398123325, rs1114167667, rs1554890348, rs1564568303, rs1564830522, rs1564814427, rs1257124719, rs1589659492, rs1859977029 21419380
Megalencephalic leukoencephalopathy with subcortical cysts MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS, MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A rs80358245, rs1183818307, rs121908343, rs121908344, rs121908345, rs267607236, rs80358242, rs80358241, rs80358243, rs387907049, rs387907050, rs387907051, rs387907052, rs387907053, rs387907055, rs281875309, rs281875311, rs281875317, rs281875315, rs281875313, rs761620701, rs786204747, rs794729233, rs1114167286, rs1057516465, rs755271052, rs1057517375, rs769135961, rs1057517090, rs1057516336, rs1057516766, rs1057516286, rs1057517228, rs1555963392, rs1555962581, rs1555967668, rs765879182, rs1555968785, rs764754702, rs764669598, rs1555967227, rs1565339091, rs1569242061, rs1602063709, rs1602049346, rs781004589, rs281875316, rs752428321, rs1436214826 21419380, 25655951, 24357685
Unknown
Disease name Disease term dbSNP ID References
Cerebellar atrophy Cerebellar atrophy
Cerebral atrophy Cerebral atrophy
Dysarthria Dysarthria
Macrocephaly-intellectual disability-autism syndrome Macrocephaly-intellectual disability-autism syndrome

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