Homo sapiens (human): 84065 Help Entry 84065             CDS       T01001                                  Symbol TMEM222, C1orf160, NEDMOSBA Name (RefSeq) transmembrane protein 222   KO K20726   transmembrane protein 222 Organism hsa  Homo sapiens (human) Disease H02459   Syndromic neurodevelopmental disorder SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RTE1 Motif Other DBs NCBI-GeneID:  84065 NCBI-ProteinID:  NP_115501 OMIM:  619469 HGNC:  25363 Ensembl:  ENSG00000186501 UniProt:  Q9H0R3 LinkDB All DBs Position 1:27322163..27336400 Genome browser AA seq 208 aa AA seqDB search MAEAEGSSLLLLPPPPPPPRMAEVEAPTAAETDMKQYQGSGGVAMDVERSRFPYCVVWTP IPVLTWFFPIIGHMGICTSTGVIRDFAGPYFVSEDNMAFGKPAKYWKLDPAQVYASGPNA WDTAVHDASEEYKHRMHNLCCDNCHSHVALALNLMRYNNSTNWNMVTLCFFCLLYGKYVS VGAFVKTWLPFILLLGIILTVSLVFNLR NT seq 627 nt NT seq  +upstreamnt  +downstreamnt atggcggaagcggaagggagttctctgctcttgttgccgccgccgccacccccgcccagg atggcggaagtggaggcgccgacggcggccgagacggacatgaagcaatatcaaggctcc ggcggcgtcgccatggatgtggaacggagtcgcttcccctactgcgtggtgtggacgccc atcccggtgctcacgtggtttttccccatcatcggccacatgggcatctgcacatccaca ggagtcattcgggacttcgcgggcccctactttgtctcagaggacaacatggcctttgga aagcctgccaagtactggaagttggaccctgctcaggtctatgctagcgggcccaacgca tgggacacggctgtgcacgacgcctctgaggagtacaagcaccgcatgcacaatctctgc tgtgacaactgccactcgcacgtggcattggccctgaatctgatgcgctacaacaacagc accaactggaatatggtgacgctctgcttcttctgcctgctctacgggaagtacgtcagc gttggggccttcgtgaagacctggctgcccttcatccttctcctgggcatcatcctcacc gtcagcctggtctttaacctccggtga

DBGET integrated database retrieval system