ALX4 ELISA Kit for Human(Homo sapiens) | EIAab.comALX4 ELISA Kit for Human(Homo sapiens)

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Index > Protein center > ALX4(Gene name) > Human

ALX4 (Gene name),

Homeobox protein aristaless-like 4 (Protein name ), ALX4_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

ALX4(KIAA1788);

Protein name:

Homeobox protein aristaless-like 4;

Alternative:

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

Binds DNA.

Function:

Transcription factor involved in skull and limb development. Plays an essential role in craniofacial development, skin and hair follicle development.

Subcellular Location:

Nucleus

Protein Attributes:

Sequence length:

411

Sequence:

50:

100:

150:

200:

250:

300:

350:

400:

411:

KEHSAAISWA | T

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

STRING:

9606.ENSP00000332744

SMR:

Q9H161

String:

Q9H161

MIM:

601224

UniGene:

Hs.436055

KEGG:

hsa:60529

Pfam:

PF00046

Uniprot:

Q9H161

FOR

ELISA Kit for Human Homeobox protein aristaless-like 4

CLIA Kit for Human Homeobox protein aristaless-like 4

Polyclonal Antibody for Human Homeobox protein aristaless-like 4

Monoclonal Antibody for Human Homeobox protein aristaless-like 4

Protein for Human Homeobox protein aristaless-like 4

R&D Technical Data

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Precision

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Recovery

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Linearity

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

References

1.

"Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome."
Wu Y.-Q. , Badano J.L. , McCaskill C. , Vogel H. , Potocki L. , Shaffer L.G.
Am. J. Hum. Genet.67:1327-1332(2000) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA]
2.

"The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)."
Wuyts W. , Cleiren E. , Homfray T. , Rasore-Quartino A. , Vanhoenacker F. , Van Hul W.
J. Med. Genet.37:916-920(2000) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA];VARIANT THR-35;VARIANT PFM2 PRO-272
3.

"Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects."
Mavrogiannis L.A. , Antonopoulou I. , Baxova A. , Kutilek S. , Kim C.A. , Sugayama S.M. , Salamanca A. , Wall S.A. , Morriss-Kay G.M. , Wilkie A.O.M.
Nat. Genet.27:17-18(2001) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA];VARIANTS THR-35 AND SER-102;VARIANT PFM2 GLN-218
4.

"Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro."
Nagase T. , Nakayama M. , Nakajima D. , Kikuno R. , Ohara O.
DNA Res.8:85-95(2001) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]
tissue: Brain.
5.

"ALX4 dysfunction disrupts craniofacial and epidermal development."
Kayserili H. , Uz E. , Niessen C. , Vargel I. , Alanay Y. , Tuncbilek G. , Yigit G. , Uyguner O. , Candan S. , Okur H. , Kaygin S. , Balci S. , Mavili E. , Alikasifoglu M. , Haase I. , Wollnik B. , Akarsu N.A.
Hum. Mol. Genet.18:4357-4366(2009) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: INVOLVEMENT IN FND2;FUNCTION;SUBCELLULAR LOCATION
6.

"ALX4 gain-of-function mutations in nonsyndromic craniosynostosis."
Yagnik G. , Ghuman A. , Kim S. , Stevens C.G. , Kimonis V. , Stoler J. , Sanchez-Lara P.A. , Bernstein J.A. , Naydenov C. , Drissi H. , Cunningham M.L. , Kim J. , Boyadjiev S.A.
Hum. Mutat.33:1626-1629(2012) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS CRS5 PHE-7 AND GLU-211;VARIANT LEU-306;CHARACTERIZATION OF VARIANTS CRS5 PHE-7 AND GLU-211;CHARACTERIZATION OF VARIANT LEU-306

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