Homo sapiens (human): 84978 Help Entry 84978             CDS       T01001                                  Symbol FRMD5, NEDEMA Name (RefSeq) FERM domain containing 5   KO K23969   FERM domain-containing protein 3/5 Organism hsa  Homo sapiens (human) Disease H02397   Neurodevelopmental disorder with movement abnormalities or hypotonia Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04990 Domain-containing proteins not elsewhere classified [BR:hsa04990]     84978 (FRMD5) Domain-containing proteins not elsewhere classified [BR:hsa04990]  Other domain-containing proteins   FERM domain-containing proteins    84978 (FRMD5) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  FERM_M FERM_N FERM_C FA YcxB Motif Other DBs NCBI-GeneID:  84978 NCBI-ProteinID:  NP_116281 OMIM:  616309 HGNC:  28214 Ensembl:  ENSG00000171877 UniProt:  Q7Z6J6 LinkDB All DBs Position 15:complement(43870764..44199473) Genome browser AA seq 570 aa AA seqDB search MLSRLMSGSSRSLEREYSCTVRLLDDSEYTCTIQRDAKGQYLFDLLCHHLNLLEKDYFGI RFVDPDKQRHWLEFTKSVVKQLRSQPPFTMCFRVKFYPADPAALKEEITRYLVFLQIKRD LYHGRLLCKTSDAALLAAYILQAEIGDYDSGKHPEGYSSKFQFFPKHSEKLERKIAEIHK TELSGQTPATSELNFLRKAQTLETYGVDPHPCKDVSGNAAFLAFTPFGFVVLQGNKRVHF IKWNEVTKLKFEGKTFYLYVSQKEEKKIILTYFAPTPEACKHLWKCGIENQAFYKLEKSS QVRTVSSSNLFFKGSRFRYSGRVAKEVMESSAKIKREPPEIHRAGMVPSRSCPSITHGPR LSSVPRTRRRAVHISIMEGLESLRDSAHSTPVRSTSHGDTFLPHVRSSRTDSNERVAVIA DEAYSPADSVLPTPVAEHSLELMLLSRQINGATCSIEEEKESEASTPTATEVEALGGELR ALCQGHSGPEEEQVNKFVLSVLRLLLVTMGLLFVLLLLLIILTESDLDIAFFRDIRQTPE FEQFHYQYFCPLRRWFACKIRSVVSLLIDT NT seq 1713 nt NT seq  +upstreamnt  +downstreamnt atgctgagcaggttgatgagcggcagcagcaggagcctggagcgcgagtacagctgcacc gtgcggctgctggacgacagcgagtacacctgcaccatccagagagatgccaaaggccag tacctgtttgaccttctttgccaccatctgaacctacttgagaaagactattttggtatc cgctttgtagacccagataagcagcggcattggctggaatttacaaagtctgtggtgaaa caattgagatcccagcctccattcaccatgtgcttccgtgtgaagttttatcctgcagac cctgctgctctgaaagaagaaataaccaggtatttagtcttcctgcagatcaaaagggat ctctaccatggccgactcctctgtaaaacatcggatgctgccttgttagcagcttacatc cttcaagcggagattggggattatgactcagggaaacaccctgaaggctacagctccaag ttccagtttttccctaaacattcagagaagctggaaaggaaaattgctgagattcacaag acggaactgagtggtcaaacaccagcaacatcagagctgaacttcttaagaaaagcacag acattggaaacatatggagtggatcctcacccatgtaaggacgtgtcaggaaatgctgca tttctggccttcactccttttgggtttgttgttcttcaaggaaacaagagggtccacttc attaaatggaatgaggtgaccaagctgaaatttgaaggaaagactttctatttatacgta agtcagaaagaggaaaagaaaattattcttacatattttgctccaactcctgaagcgtgt aagcacctctggaaatgtggaatcgagaaccaagccttctacaagctggagaagtcaagc caagtccgcacagtgtccagcagcaatttattctttaaagggagccggttccgatacagt ggccgagttgcaaaggaagtcatggaatcaagtgctaagatcaaacgggagccaccggaa atacacagagcagggatggttcccagccggagctgtccctccataacccatggcccaagg ctgagcagcgtccccaggacccgcagaagagctgttcacatctccatcatggaaggccta gagtccttacgggacagtgcccattccacaccagtgcgttccacttcccatggggacacc ttcctgcctcacgtgagaagcagccggacagatagcaatgagcgagtagctgtgattgca gacgaggcctacagccctgcagacagcgtgctgcccacccctgtggctgagcacagcctg gagctgatgttgctttcccggcagatcaatggagccacctgcagcattgaggaggagaag gaatctgaagccagcaccccaactgctacagaggtggaggcccttgggggagagctgagg gccctgtgtcaggggcacagcgggcccgaggaggaacaggtgaataagtttgttctaagt gtcctccgtttgctccttgtgaccatgggactcctctttgttttgctcctcctcctgatc atccttaccgagtctgaccttgacattgcctttttccgtgatatccgccagacccccgag tttgaacaattccactatcaatacttttgtcccctcaggcgatggtttgcctgcaaaatc cgctcagtggtgagcctgctcattgacacctga

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