Homo sapiens (human): 55997 Help Entry 55997             CDS       T01001                                  Symbol CFC1, CFC1B, CRYPTIC, DTGA2, HTX2 Name (RefSeq) cryptic, EGF-CFC family member 1   KO K25454   cryptic protein Organism hsa  Homo sapiens (human) Disease H00550   Complete transposition of the great arteries H00632   Heterotaxy H00918   Double-outlet right ventricle Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09193 Unclassified: signaling and cellular processes    99995 Signaling proteins     55997 (CFC1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  CFC hEGF EGF_2 EGF Motif Other DBs NCBI-GeneID:  55997 NCBI-ProteinID:  NP_115934 OMIM:  605194 HGNC:  18292 Ensembl:  ENSG00000136698 UniProt:  P0CG37 LinkDB All DBs Position 2:complement(130592165..130599575) Genome browser AA seq 223 aa AA seqDB search MTWRHHVRLLFTVSLALQIINLGNSYQREKHNGGREEVTKVATQKHRQSPLNWTSSHFGE VTGSAEGWGPEEPLPYSRAFGEGASARPRCCRNGGTCVLGSFCVCPAHFTGRYCEHDQRR SECGALEHGAWTLRACHLCRCIFGALHCLPLQTPDRCDPKDFLASHAHGPSAGGAPSLLL LLPCALLHRLLRPDAPAHPRSLVPSVLQRERRPCGRPGLGHRL NT seq 672 nt NT seq  +upstreamnt  +downstreamnt atgacctggaggcaccatgtcaggcttctgtttacggtcagtttggcattacagatcatc aatttgggaaacagctatcaaagagagaaacataacggcggtagagaggaagtcaccaag gttgccactcagaagcaccgacagtcaccgctcaactggacctccagtcatttcggagag gtgactgggagcgccgagggctgggggccggaggagccgctcccctactcccgggctttc ggagagggtgcgtccgcgcggccgcgctgctgcaggaacggcggtacctgcgtgctgggc agcttctgcgtgtgcccggcccacttcaccggccgctactgcgagcatgaccagaggcgc agtgaatgcggcgccctggagcacggagcctggaccctccgcgcctgccacctctgcagg tgcatcttcggggccctgcactgcctccccctccagacgcctgaccgctgtgacccgaaa gacttcctggcctcccacgctcacgggccgagcgccgggggcgcgcccagcctgctactc ttgctgccctgcgcactcctgcaccgcctcctgcgcccggatgcgcccgcgcaccctcgg tccctggtcccttccgtcctccagcgggagcggcgcccctgcggaaggccgggacttggg catcgcctttaa

DBGET integrated database retrieval system