SMCR5_HUMAN
ID SMCR5_HUMAN Reviewed; 140 AA.
AC Q8TEV8;
DT 23-OCT-2007, integrated into UniProtKB/Swiss-Prot.
DT 01-JUN-2002, sequence version 1.
DT 25-MAY-2022, entry version 78.
DE RecName: Full=Smith-Magenis syndrome chromosomal region candidate gene 5 protein;
GN Name=SMCR5;
OS Homo sapiens (Human).
OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC Homo.
OX NCBI_TaxID=9606;
RN [1]
RP NUCLEOTIDE SEQUENCE [MRNA], AND TISSUE SPECIFICITY.
RX PubMed=11997338; DOI=10.1101/gr.73702;
RA Bi W., Yan J., Stankiewicz P., Park S.-S., Walz K., Boerkoel C.F.,
RA Potocki L., Shaffer L.G., Devriendt K., Nowaczyk M.J.M., Inoue K.,
RA Lupski J.R.;
RT "Genes in a refined Smith-Magenis syndrome critical deletion interval on
RT chromosome 17p11.2 and the syntenic region of the mouse.";
RL Genome Res. 12:713-728(2002).
CC -!- TISSUE SPECIFICITY: Widely expressed. {ECO:0000269|PubMed:11997338}.
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DR EMBL; AF467442; AAL78339.1; -; mRNA.
DR AlphaFoldDB; Q8TEV8; -.
DR BioMuta; HGNC:17918; -.
DR PRIDE; Q8TEV8; -.
DR GeneCards; SMCR5; -.
DR HGNC; HGNC:17918; SMCR5.
DR neXtProt; NX_Q8TEV8; -.
DR InParanoid; Q8TEV8; -.
DR PhylomeDB; Q8TEV8; -.
DR PathwayCommons; Q8TEV8; -.
DR Pharos; Q8TEV8; Tdark.
DR PRO; PR:Q8TEV8; -.
DR Proteomes; UP000005640; Unplaced.
DR RNAct; Q8TEV8; protein.
PE 2: Evidence at transcript level;
KW Reference proteome.
FT CHAIN 1..140
FT /note="Smith-Magenis syndrome chromosomal region candidate
FT gene 5 protein"
FT /id="PRO_0000307803"
FT REGION 43..77
FT /note="Disordered"
FT /evidence="ECO:0000256|SAM:MobiDB-lite"
SQ SEQUENCE 140 AA; 15285 MW; 38986E68C5C9F406 CRC64;
MRRCLRVKTR RGQLGLASSC FEQHSCFSPR VNRILSAVQN TLCTGPSSQA PPQPPQASPP
AAADHSRTPS LLASSHSASG GESLFQLYIA SLAWPQNCCV LESCRRIPLG GLSSMENRRP
LLRKGRLLRG QIHHSQTNEL