Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6997
Gene name Gene Name - the full gene name approved by the HGNC.
Cripto, EGF-CFC family member
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CRIPTO
Synonyms (NCBI Gene) Gene synonyms aliases
CR, CR-1, CRGF, TDGF1
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p21.31
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1416955 hsa-miR-3122 CLIP-seq
MIRT1416956 hsa-miR-3148 CLIP-seq
MIRT1416957 hsa-miR-3153 CLIP-seq
MIRT1416958 hsa-miR-365 CLIP-seq
MIRT1416959 hsa-miR-374a CLIP-seq
Transcription factors
Transcription factor Regulation Reference
POU5F1 Activation 17068183
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000187 Process Activation of MAPK activity IDA 9013573
GO:0001568 Process Blood vessel development IBA 21873635
GO:0001763 Process Morphogenesis of a branching structure TAS 10070255
GO:0002042 Process Cell migration involved in sprouting angiogenesis IMP 17720976
GO:0005102 Function Signaling receptor binding IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
187395 11701 ENSG00000241186
Protein
UniProt ID P13385
Protein name Protein Cripto (Cripto, EGF-CFC family member) (Cripto-1 growth factor) (CRGF) (Epidermal growth factor-like cripto protein CR1) (Teratocarcinoma-derived growth factor 1)
Protein function GPI-anchored cell membrane protein involved in Nodal signaling. Cell-associated CRIPTO acts as a Nodal coreceptor in cis. Shedding of CRIPTO by TMEM8A modulates Nodal signaling by allowing soluble CRIPTO to act as a Nodal coreceptor on other cel
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09443 CFC 115 149 Cripto_Frl-1_Cryptic (CFC) Domain
Tissue specificity TISSUE SPECIFICITY: Preferentially expressed in gastric and colorectal carcinomas than in their normal counterparts. Expressed in breast and lung. {ECO:0000269|PubMed:18835250}.
Sequence
MDCRKMARFSYSVIWIMAISKVFELGLVAGLGHQEFARPSRGYLAFRDDSIWPQEEPAIR
PRSSQRVPPMGIQHSKELNRTCCLNGGTCMLGSFCACPPSFYGRNCEHDVRKENCGSVPH
DTWLPKKCSLCKCWHGQLRCFPQAFLPGC
DGLVMDEHLVASRTPELPPSARTTTFMLVGI
CLSIQSYY
Sequence length 188
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Agenesis of corpus callosum Agenesis of corpus callosum rs754914260, rs1057519053, rs1057519056, rs1057519054, rs1057519055, rs1057519057, rs1384496494, rs1599017933
Atrial isomerism Right Atrial Isomerism rs121434422, rs606231383, rs1555702261, rs753643819 11062482
Hemangioma Hemangioma rs121917766
Heterotaxia Heterotaxy Syndrome rs200321595, rs775946081, rs1060501464, rs1560086701 11062482
Unknown
Disease term Disease name Evidence References Source
Ambiguous genitalia Ambiguous Genitalia ClinVar
Asthma Asthma ClinVar
Forebrain defects Forebrain Defects ClinVar