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Protein-coding gene in the species Homo sapiens
Nesprin-2 is a protein that in humans is encoded by the SYNE2 gene. The human SYNE2 gene consists of 116 exons and encodes nesprin-2, a member of the
SYNE2
Medical condition
Entry – * 608442 – SPECTRIN REPEAT-CONTAINING NUCLEAR ENVELOPE PROTEIN 2; SYNE2". www.omim.org. Archived from the original on 28 September 2015. Retrieved
Emery–Dreifuss muscular dystrophy
Emery–Dreifuss_muscular_dystrophy
syndrome 11, 22 partial trisomy Emery–Dreifuss syndrome EMD, LMNA, SYNE1, SYNE2, FHL1, TMEM43 Epidermolysis bullosa KRT5, KRT14, DSP, PKP1, JUP, PLEC1,
List_of_genetic_disorders
Protein family
the cell's ability to sense and respond to mechanical challenges. SYNE1 SYNE2 Spectrin repeat containing nuclear envelope family member 3 Zhang Q, Skepper
Nesprin
Protein family
MACF1; MCF2L; SPTA1; SPTAN1; SPTB; SPTBN1; SPTBN2; SPTBN4; SPTBN5; SYNE1; SYNE2; TRIO; UTRN; Pascual J, Pfuhl M, Walther D, Saraste M, Nilges M (October
Spectrin_repeat
Protein domain
SMTNL2, SPECC1, SPECC1L, SPNB4, SPTB, SPTBN1, SPTBN2, SPTBN4, SPTBN5, SYNE1, SYNE2, TAGLN, TAGLN2, TAGLN3, UTRN, and VAV1, VAV2, VAV3 PDB: 2RR8; Umemoto R
Calponin_homology_domain
nesprin proteins: nesprin -1 (encoded by SYNE1), nesprin -2 (encoded by SYNE2), nesprin -3 (encoded by SYNE3), and nesprin -4 (encoded by SYNE4); The
LINC_complex
Protein-coding gene in humans
interact with: ACTA1, ACTG2, BANF1, BCLAF1, CTNNB1, GMCL1, LMNA, PSME1, SYNE1, SYNE2, TMEM43, and YTHDC1. GRCh38: Ensembl release 89: ENSG00000102119 – Ensembl
Emerin
16160 SYNDIG1L HGNC:32388; A6NDD5 16161 SYNE1 HGNC:17089; Q8NF91 16162 SYNE2 HGNC:17084; Q8WXH0 16163 SYNE3 HGNC:19861; Q6ZMZ3 16164 SYNE4 HGNC:26703;
List of human protein-coding genes 8
List_of_human_protein-coding_genes_8
dystrophy 4; 612998; SYNE1 Emery–Dreifuss muscular dystrophy 5; 612999; SYNE2 Emery–Dreifuss muscular dystrophy 6; 300696; FHL1 Emery–Dreifuss muscular
List_of_OMIM_disorder_codes
SYNE2
SYNE2
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SYNE2
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SYNE2