Sequence information
Variant position: 163 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 442 The length of the canonical sequence.
Location on the sequence:
LAGREQYGRAGFAGSYSSPY
P AYMADVGASWAAAAAASAGP
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human LAGREQYGRAGFAGSYSSPYP AYMA-DVGASWAAAAAASAGP
LAGREQYGRAGFAGSYSSPYP AYMA-DVGASWAAAAAASAG
Mouse LAGREQYGRPGFAGSYSSPYP AYMA-DVGASWAAAAAASAG
Rat LAGREQYGRPGFAGSYSSPYP AYMA-DVGASWAAAAAASAG
Xenopus laevis ANGREQYSR-GLGATYASPYP AYMSPDMGAAWTAS------
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
Chain
1 – 442
Transcription factor GATA-4
Literature citations
Spectrum of heart disease associated with murine and human GATA4 mutation.
Rajagopal S.K.; Ma Q.; Obler D.; Shen J.; Manichaikul A.; Tomita-Mitchell A.; Boardman K.; Briggs C.; Garg V.; Srivastava D.; Goldmuntz E.; Broman K.W.; Benson D.W.; Smoot L.B.; Pu W.T.;
J. Mol. Cell. Cardiol. 43:677-685(2007)
Cited for: VARIANTS ASD2 CYS-296 AND MET-403; VARIANTS AVSD4 SER-163 AND VAL-346;
GATA4 mutations in 486 Chinese patients with congenital heart disease.
Zhang W.; Li X.; Shen A.; Jiao W.; Guan X.; Li Z.;
Eur. J. Med. Genet. 51:527-535(2008)
Cited for: VARIANTS VSD1 VAL-6; SER-46 DEL; SER-163; LYS-359; THR-429 AND VAL-442; VARIANTS TOF ALA-118 INS AND GLN-407;
Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease.
Peng T.; Wang L.; Zhou S.F.; Li X.;
Genetica 138:1231-1240(2010)
Cited for: VARIANT VSD1 GLN-407; VARIANT TOF SER-163;
Disclaimer:
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.