- DNA-binding
protein RFXANK is a
protein that in
humans is
encoded by the
RFXANK gene.
Major histocompatibility (MHC)
class II
molecules are transmembrane...
- CD3gamma
chain deficiency (defective CD3G gene),
MCHII deficiency (defective
RFXANK gene), Wiskott–Aldrich
syndrome (defective WAS gene), IPEX
syndrome (defective...
- HDAC4 1
Nucleus /
cytoplasm heart,
skeletal muscle,
brain GCMA, GATA1, HP1
RFXANK Defects in
chondrocyte differentiation HDAC5 1
Nucleus /
cytoplasm heart...
- PPP1R12B; PPP1R12C; PPP1R13B; PPP1R13L; PPP1R16A; PPP1R16B; PSMD10; RAI14;
RFXANK; RIPK4; RNASEL; SHANK1; SHANK2; SHANK3; SNCAIP; TA-NFKBH; TEX14; TNKS; TNKS2;...
-
regulatory factor X5 (RFX5) RFX-****ociated
protein (RFXAP) RFX
ankyrin repeats (
RFXANK; also
known as RFXB) The
comparatively rarer BLS I, also
called "HLA class...
- been
shown to
interact with: MAPK1,
Nuclear receptor coactivator 1, RFX5,
RFXANK, XPO1, and ZXDC. MHC
class II GRCh38:
Ensembl release 89: ENSG00000179583...
-
signals have been
found for this gene.
RFXAP has been
shown to
interact with
RFXANK. GRCh38:
Ensembl release 89: ENSG00000133111 – Ensembl, May 2017 GRCm38:...
- Q8HWS3 13666 RFX7 HGNC:25777 Q2KHR2 13667 RFX8 HGNC:37253 Q6ZV50 13668
RFXANK HGNC:9987 O14593 13669
RFXAP HGNC:9988 O00287 13670 RGCC HGNC:20369 Q9H4X1...
- TAP2, TAPBP, or B2M) MHC
class II
deficiency (with
mutations in CIITA,
RFXANK, RFX5, or RFXAP) CD25
deficiency CD27
deficiency STAT5b
deficiency ITK deficiency...
- function(as
prior gene) and is
located at 1q21.3(cytogenetic location)
RFXANK(also
known as
ankyrin repeat-containing
regulatory factor X-****ociated protein)...
