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11146 GLMN

11146

GLMN

glomulin, FKBP associated protein

protein-coding

Homo sapiens

基因描述

Type Description
Definition glomulin, FKBP associated protein

研究结论

Date Results Publications
2019-03-30 11:37:00 In summary, we present a case of congenital plaquetype GVM and a case of familial disseminated cutaneous GVM, both with the same glomulin gene mutation (c.157_161delAAGAA), but with different clinical expression. 30325312
2015-07-25 10:52:00 Our report contributes to document the possible association between the c.395-1G>C mutation of GLMN gene and glomuvenous malformations. 24961656
2013-02-09 11:00:00 FAP48 adipocyte expression plays a key role in HIV-associated lipodystrophy. 22678819
2012-10-27 10:12:00 Structural and biochemical analyses reveal that GLMN adopts a HEAT-like repeat fold that tightly binds the E2-interacting surface of RBX1, inhibiting CRL-mediated chain formation by the E2 CDC34. 22748924
2012-07-14 10:34:00 These data identify glomulin as a permissivity factor for VACV infection and as a potential therapeutic target for inhibition of vaccinia virus (VACV) infection. 22280104

名称对应

Type IDs
Synonymous FAP, FAP48, FAP68, FKBPAP, GLML, GVM, VMGLOM
Gene
UniProtKB-ID: GLMN_HUMAN, B4DJ85_HUMAN
UniprotKB: Q92990, B4DJ85
UniParc: UPI0000D4DC57, UPI0000040A53, UPI000012AB7C
EMBL: AJ302728, AJ302734, AJ347709, AJ302730, AK295971, AJ302733, AJ302731, AJ302729, U73704, CH471097, AJ302735, AJ302727, AL451010, AJ302732, BC001257
Ensembl: ENSG00000174842
KO: hsa:11146
Nucleutide sequences
EMBL-CDS: AAH01257.1, CAC88124.1, CAC82938.1, AAC50908.1, CAC69882.1, EAW73098.1, BAG58747.1
Ensembl_TRS: ENST00000495106, ENST00000370360
Protein sequencees
Ensembl_PRO: ENSP00000359385, ENSP00000436829
RefSeq: XP_016855629.1, XP_016855627.1, XP_016855626.1, XP_016855628.1, NP_444504.1, XP_016855630.1, XP_016855632.1, XP_016855633.1, XP_016855631.1, XP_006710372.1, XP_005270458.1, XP_011538848.1, NP_001306612.1
Others
UniRef100: UniRef100_Q92990, UniRef100_B4DJ85
UniRef90: UniRef90_Q92990
UniRef50: UniRef50_Q92990
UniGene: Hs.49105
CCDS: CCDS738.1

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