ID   Q7Z4G3_HUMAN            Unreviewed;       133 AA.
AC   Q7Z4G3;
DT   01-OCT-2003, integrated into UniProtKB/TrEMBL.
DT   01-OCT-2003, sequence version 1.
DT   27-MAR-2024, entry version 61.
DE   SubName: Full=IL1RAPL1-dystrophin fusion protein {ECO:0000313|EMBL:AAQ10304.1};
DE   Flags: Fragment;
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 {ECO:0000313|EMBL:AAQ10304.1};
RN   [1] {ECO:0000313|EMBL:AAQ10304.1}
RP   NUCLEOTIDE SEQUENCE.
RC   TISSUE=Muscle {ECO:0000313|EMBL:AAQ10304.1};
RA   Wheway J.M., Yau S.C., Nihalani V., Ellis D., Irving M., Splitt M.,
RA   Roberts R.G.;
RT   "A complex deletion-inversion-deletion event results in a chimeric
RT   IL1RAPL1-dystrophin transcript and a contiguous gene deletion syndrome.";
RL   Submitted (JUL-2002) to the EMBL/GenBank/DDBJ databases.
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DR   EMBL; AF533682; AAQ10304.1; -; mRNA.
DR   AlphaFoldDB; Q7Z4G3; -.
DR   PeptideAtlas; Q7Z4G3; -.
DR   Gene3D; 2.60.40.10; Immunoglobulins; 1.
DR   InterPro; IPR007110; Ig-like_dom.
DR   InterPro; IPR036179; Ig-like_dom_sf.
DR   InterPro; IPR013783; Ig-like_fold.
DR   SUPFAM; SSF48726; Immunoglobulin; 1.
DR   SUPFAM; SSF46966; Spectrin repeat; 1.
DR   PROSITE; PS50835; IG_LIKE; 1.
PE   2: Evidence at transcript level;
FT   DOMAIN          1..64
FT                   /note="Ig-like"
FT                   /evidence="ECO:0000259|PROSITE:PS50835"
FT   NON_TER         1
FT                   /evidence="ECO:0000313|EMBL:AAQ10304.1"
FT   NON_TER         133
FT                   /evidence="ECO:0000313|EMBL:AAQ10304.1"
SQ   SEQUENCE   133 AA;  15970 MW;  D097BA5743A7DB1E CRC64;
     DFLLPTREPE ILWYKECRTK TWRPSIVFKR DTLLIREVRE DDIGNYTCEL KYGGFVVRRT
     TELTVTVERI QNQWDEVQEH LQNRRQQLNE MLKDSTQWLE AKEEAEQVLG QARAKLESWK
     EGPYTVDAIQ KKI
//