Homo sapiens (human): 10205 Help Entry 10205             CDS       T01001                                  Symbol MPZL2, DFNB111, EVA, EVA1 Name (RefSeq) myelin protein zero like 2   KO K27316   myelin protein zero-like protein 2 Organism hsa  Homo sapiens (human) Disease H00605   Deafness, autosomal recessive Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04515 Cell adhesion molecules [BR:hsa04515]     10205 (MPZL2) Cell adhesion molecules [BR:hsa04515]  Immunoglobulin superfamily   P0    10205 (MPZL2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  V-set ig Ig_3 I-set Ig_2 TMEM154 ASFV_J13L Motif Other DBs NCBI-GeneID:  10205 NCBI-ProteinID:  NP_005788 OMIM:  604873 HGNC:  3496 Ensembl:  ENSG00000149573 UniProt:  O60487 LinkDB All DBs Position 11:complement(118253416..118264297) Genome browser AA seq 215 aa AA seqDB search MYGKSSTRAVLLLLGIQLTALWPIAAVEIYTSRVLEAVNGTDARLKCTFSSFAPVGDALT VTWNFRPLDGGPEQFVFYYHIDPFQPMSGRFKDRVSWDGNPERYDASILLWKLQFDDNGT YTCQVKNPPDVDGVIGEIRLSVVHTVRFSEIHFLALAIGSACALMIIIVIVVVLFQHYRK KRWAERAHKVVEIKSKEEERLNQEKKVSVYLEDTD NT seq 648 nt NT seq  +upstreamnt  +downstreamnt atgtatggcaagagctctactcgtgcggtgcttcttctccttggcatacagctcacagct ctttggcctatagcagctgtggaaatttatacctcccgggtgctggaggctgttaatggg acagatgctcggttaaaatgcactttctccagctttgcccctgtgggtgatgctctaaca gtgacctggaattttcgtcctctagacgggggacctgagcagtttgtattctactaccac atagatcccttccaacccatgagtgggcggtttaaggaccgggtgtcttgggatgggaat cctgagcggtacgatgcctccatccttctctggaaactgcagttcgacgacaatgggaca tacacctgccaggtgaagaacccacctgatgttgatggggtgataggggagatccggctc agcgtcgtgcacactgtacgcttctctgagatccacttcctggctctggccattggctct gcctgtgcactgatgatcataatagtaattgtagtggtcctcttccagcattaccggaaa aagcgatgggccgaaagagctcataaagtggtggagataaaatcaaaagaagaggaaagg ctcaaccaagagaaaaaggtctctgtttatttagaagacacagactaa

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