KEGG   Homo sapiens (human): 10205
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)
SSDB
Motif
Pfam: V-set ig Ig_3 I-set Ig_2 TMEM154 DUF4381 ASFV_J13L
Other DBs
NCBI-GeneID: 10205
NCBI-ProteinID: NP_005788
OMIM: 604873
HGNC: 3496
Ensembl: ENSG00000149573
UniProt: O60487
Position
11:complement(118253416..118264297)
AA seq 215 aa
MYGKSSTRAVLLLLGIQLTALWPIAAVEIYTSRVLEAVNGTDARLKCTFSSFAPVGDALT
VTWNFRPLDGGPEQFVFYYHIDPFQPMSGRFKDRVSWDGNPERYDASILLWKLQFDDNGT
YTCQVKNPPDVDGVIGEIRLSVVHTVRFSEIHFLALAIGSACALMIIIVIVVVLFQHYRK
KRWAERAHKVVEIKSKEEERLNQEKKVSVYLEDTD
NT seq 648 nt   +upstreamnt  +downstreamnt
atgtatggcaagagctctactcgtgcggtgcttcttctccttggcatacagctcacagct
ctttggcctatagcagctgtggaaatttatacctcccgggtgctggaggctgttaatggg
acagatgctcggttaaaatgcactttctccagctttgcccctgtgggtgatgctctaaca
gtgacctggaattttcgtcctctagacgggggacctgagcagtttgtattctactaccac
atagatcccttccaacccatgagtgggcggtttaaggaccgggtgtcttgggatgggaat
cctgagcggtacgatgcctccatccttctctggaaactgcagttcgacgacaatgggaca
tacacctgccaggtgaagaacccacctgatgttgatggggtgataggggagatccggctc
agcgtcgtgcacactgtacgcttctctgagatccacttcctggctctggccattggctct
gcctgtgcactgatgatcataatagtaattgtagtggtcctcttccagcattaccggaaa
aagcgatgggccgaaagagctcataaagtggtggagataaaatcaaaagaagaggaaagg
ctcaaccaagagaaaaaggtctctgtttatttagaagacacagactaa

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