Results for the protein: P51508

Results for the Protein: P51508

55977803

347344

ZNF81

NCBI, UniProt

ZNF81_HUMAN RecName: Full=Zinc finger protein 81; AltName: Full=HFZ20

Known Diseases associated with this Protein:
MENTAL RETARDATION, X-LINKED 45
MENTAL RETARDATION, X-LINKED 45 (MRX45)

2

6

1

2

5

Tips:

The Domains on the Default View are decided by the Domain's E-Value.

Clicking a check box will display or hide the correlated domain.

To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic.

Default View: KRAB - smart00349 KRAB - pfam01352 KRAB_A-box - cd07765 COG5048 - COG5048 zf-C2H2 - pfam00096 ZnF_C2H2 - smart00355	Swiss-Prot Protein: P51508 Identical to: NP_009068 Default View:

Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕
KRAB	pfam01352	4.2e-26	21	61
COG5048	COG5048	0.00036	173	630
zf-C2H2	pfam00096	1.1e-06	330	352
zf-C2H2	pfam00096	3e-06	358	380
zf-C2H2	pfam00096	2e-06	386	408
zf-C2H2	pfam00096	1.1e-07	414	436
zf-C2H2	pfam00096	2e-06	442	464
zf-C2H2	pfam00096	6.1e-08	470	492
zf-C2H2	pfam00096	3.3e-08	498	520
zf-C2H2	pfam00096	4.2e-07	526	548
zf-C2H2	pfam00096	4.4e-07	554	576
zf-C2H2	pfam00096	2e-07	582	604
zf-C2H2	pfam00096	4.2e-07	610	632
zf-C2H2	pfam00096	1.7e-06	638	660
KRAB	smart00349	7.5e-39	21	81
ZnF_C2H2	smart00355	8.6e-05	330	352
ZnF_C2H2	smart00355	9.2e-06	358	380
ZnF_C2H2	smart00355	0.00013	386	408
ZnF_C2H2	smart00355	6.8e-06	414	436
ZnF_C2H2	smart00355	3.7e-05	442	464
ZnF_C2H2	smart00355	3.8e-07	470	492
ZnF_C2H2	smart00355	1.2e-06	498	520
ZnF_C2H2	smart00355	2.3e-05	526	548
ZnF_C2H2	smart00355	8.4e-05	554	576
ZnF_C2H2	smart00355	9.4e-06	582	604
ZnF_C2H2	smart00355	2.3e-05	610	632
ZnF_C2H2	smart00355	9.4e-05	638	660

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
dbSNP	rs537825	Polymorphism	p.ALA213GLU	N/A
Swiss-Prot	VAR_019939	Polymorphism	p.ALA3VAL	N/A
Swiss-Prot	VAR_019940	Polymorphism	p.ASN157SER	N/A
dbSNP	rs17147793	Polymorphism	p.GLY117VAL	N/A
Swiss-Prot	VAR_019943	Polymorphism	p.ILE499VAL	N/A
Swiss-Prot	VAR_019941	Disease	p.SER179ASN	Mental retardation, X-linked 45 (MRX45)
Swiss-Prot	VAR_019942	Polymorphism	p.SER185LEU	N/A
OMIM	314998.0001	Disease	p.SER179ASN	MENTAL RETARDATION, X-LINKED 45

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