Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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5362 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Plexin A2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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PLXNA2 |
SynonymsGene synonyms aliases
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OCT, PLXN2 |
ChromosomeChromosome number
|
1 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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1q32.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the plexin-A family of semaphorin co-receptors. Semaphorins are a large family of secreted or membrane-bound proteins that mediate repulsive effects on axon pathfinding during nervous system development. A subset of semaphori |
SNPsSNP information provided by dbSNP.
|
SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs1553277591 |
C>T |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
O75051 |
Protein name |
Plexin-A2 (Semaphorin receptor OCT) |
Protein function |
Coreceptor for SEMA3A and SEMA6A. Necessary for signaling by SEMA6A and class 3 semaphorins and subsequent remodeling of the cytoskeleton. Plays a role in axon guidance, invasive growth and cell migration. Class 3 semaphorins bind to a complex c |
PDB |
3Q3J
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF01403 |
Sema |
52 → 489 |
Sema domain |
Family |
PF01437 |
PSI |
510 → 560 |
Plexin repeat |
Family |
PF17960 |
TIG_plexin |
565 → 654 |
TIG domain |
Domain |
PF18020 |
TIG_2 |
708 → 802 |
TIG domain found in plexin |
Domain |
PF01437 |
PSI |
803 → 856 |
Plexin repeat |
Family |
PF01833 |
TIG |
858 → 951 |
IPT/TIG domain |
Domain |
PF01833 |
TIG |
954 → 1037 |
IPT/TIG domain |
Domain |
PF01833 |
TIG |
1041 → 1139 |
IPT/TIG domain |
Domain |
PF01833 |
TIG |
1143 → 1228 |
IPT/TIG domain |
Domain |
PF08337 |
Plexin_cytopl |
1311 → 1864 |
Plexin cytoplasmic RasGAP domain |
Family |
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Sequence |
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Sequence length |
1894 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Leukemia |
Leukemia, Myelocytic, Acute |
rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297, rs11978267, rs4132601 |
27903959 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
18583979 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Mixed anxiety and depressive disorder |
Mixed anxiety and depressive disorder |
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17339520 |
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