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CRMP1 (collapsin response mediator protein 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1400
Gene nameGene Name - the full gene name approved by the HGNC.
Collapsin response mediator protein 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
CRMP1
SynonymsGene synonyms aliases
CRMP-1, DPYSL1, DRP-1, DRP1, ULIP-3
ChromosomeChromosome number
4
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16.2
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a member of a family of cytosolic phosphoproteins expressed exclusively in the nervous system. The encoded protein is thought to be a part of the semaphorin signal transduction pathway implicated in semaphorin-induced growth cone collaps
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT569829 hsa-miR-4781-5p PAR-CLIP 20371350
MIRT569828 hsa-miR-151a-5p PAR-CLIP 20371350
MIRT569827 hsa-miR-151b PAR-CLIP 20371350
MIRT569826 hsa-miR-3150b-3p PAR-CLIP 20371350
MIRT569825 hsa-miR-4784 PAR-CLIP 20371350
Transcription factors
Transcription factor Regulation Reference
CEBPA Unknown 18524846
NFKB1 Unknown 18782567
SP1 Unknown 18524846
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000226 Process Microtubule cytoskeleton organization IEA
GO:0004157 Function Dihydropyrimidinase activity IBA 21873635
GO:0005515 Function Protein binding IPI 15383276, 16169070, 21900206, 24722188, 25416956, 32296183, 32814053
GO:0005634 Component Nucleus IEA
GO:0005813 Component Centrosome IDA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q14194
Protein name Dihydropyrimidinase-related protein 1 (DRP-1) (Collapsin response mediator protein 1) (CRMP-1) (Inactive dihydropyrimidinase) (Unc-33-like phosphoprotein 3) (ULIP-3)
Protein function Necessary for signaling by class 3 semaphorins and subsequent remodeling of the cytoskeleton (PubMed:25358863). Plays a role in axon guidance (PubMed:25358863). During the axon guidance process, acts downstream of SEMA3A to promote FLNA dissocia
PDB 4B3Z
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01979 Amidohydro_1
64 453
Amidohydrolase family
Domain
Sequence
Sequence length 572
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.
 
Reactome
    CRMPs in Sema3A signaling
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Ellis-van creveld syndrome Ellis-Van Creveld Syndrome rs1265421045, rs137852924, rs137852925, rs137852926, rs137852927, rs794726665, rs121908424, rs121908425, rs587776619, rs121908426, rs794726666, rs1302074641, rs146538906, rs751356206, rs886037764, rs886037763, rs548681312, rs200300612, rs150814290, rs146475474, rs965707319, rs767913372, rs1553815019, rs376133710, rs769864196, rs761707323, rs748523193, rs755381180, rs765269619, rs1553891936, rs759106605, rs1017946059, rs1553876034, rs1553812417, rs1424976594, rs1553865346, rs1553876870, rs753581033, rs760066386, rs1553833239, rs767072839, rs777505711, rs1553849894, rs1553855074, rs1553855151, rs1485152854, rs1553871764, rs1553871866, rs527255616, rs1553873138, rs760607210, rs1169539647, rs770918273, rs762947212, rs1553837446, rs1553811863, rs1307502841, rs1553851870, rs781096099, rs1553818428, rs1447633595, rs749251178, rs769799880, rs992326794, rs1431987950, rs1553836169, rs772840335, rs1553867117, rs1553873969, rs909612975, rs1262933856, rs755789146, rs1553889992, rs773019082, rs1553892090, rs1305301849, rs1553850677, rs1553895755, rs778793911, rs1553851462, rs760382778, rs1007534611, rs73198165, rs1553855127, rs1490912913, rs1430962566, rs1553857801, rs1159758018, rs1553840713, rs763363403, rs1553857995, rs1294715119, rs1553871792, rs1236566474, rs1553852469, rs1214848359, rs1420414097, rs1221185345, rs1300178432, rs1477102573, rs1553876813, rs764397417, rs1553857828, rs1553891368, rs1363547577, rs1553867138, rs779915989, rs1553886849, rs753014919, rs779275317, rs1553894457, rs1553895776, rs1437174284, rs777852863, rs762795511, rs1577638781, rs1722451930, rs758841632, rs767400887 29068549, 23220543, 17024374, 10700184, 29321360, 20184732, 19810119
Polydactyly Polydactyly rs1583729398, rs121917709, rs1583734240, rs121917714, rs397507422, rs398122899, rs587776959, rs386833752, rs1057518698, rs1060499558, rs755938967, rs1375768446, rs1309855392, rs1565601979, rs748321474, rs368652620, rs1562587032, rs760694987
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 22798627
Unknown
Disease name Disease term dbSNP ID References
Majewski syndrome Majewski Syndrome
Micrognathism Micrognathism
Social anhedonia Social Anhedonia 22798627
Syndactyly of the toes Syndactyly of the toes

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