UniProtKB/Swiss-Prot Q96KN7: Variant p.Glu1033Gln

X-linked retinitis pigmentosa GTPase regulator-interacting protein 1
Gene: RPGRIP1
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Variant information Variant position:

1033 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

LB/B The variants are classified into three categories: LP/P, LB/B and US.

LP/P: likely pathogenic or pathogenic.
LB/B: likely benign or benign.
US: uncertain significance

Residue change:

From Glutamate (E) to Glutamine (Q) at position 1033 (E1033Q, p.Glu1033Gln). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties:

Change from medium size and acidic (E) to medium size and polar (Q) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

2 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:

Lowest score: -4 (low probability of substitution).
Highest score: 11 (high probability of substitution).

More information can be found on the following page
Other resources:

Links to websites of interest for the variant.

Variant rs3748361 [ dbSNP | Ensembl ]

Sequence information Variant position:

1033 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

1286 The length of the canonical sequence.
Location on the sequence:

VQGKNRMEYLSLNILNGNTP E QVNYTEWKFSETNSFIGDGF 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                         VQGKNRMEYLSLNILNGNTPEQVNYTEWKFSETNSFIGDGF

Mouse                         VQDKNRMEYLSCNILNGNT-QQMHYTEWKFSGLKKAEDGGL

Bovine                        LQGKNRMEYLSHNLLNGNTLQQVKYIEWKFSGLKISADHVL

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 – 1286	X-linked retinitis pigmentosa GTPase regulator-interacting protein 1
Alternative sequence	966 – 1286	Missing. In isoform 6.

Literature citations
Identification of a novel protein interacting with RPGR.
Boylan J.P.; Wright A.F.;
Hum. Mol. Genet. 9:2085-2093(2000)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 5 AND 6); INTERACTION WITH RPGR; TISSUE SPECIFICITY; VARIANT GLN-1033; Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis.
Gerber S.; Perrault I.; Hanein S.; Barbet F.; Ducroq D.; Ghazi I.; Martin-Coignard D.; Leowski C.; Homfray T.; Dufier J.-L.; Munnich A.; Kaplan J.; Rozet J.-M.;
Eur. J. Hum. Genet. 9:561-571(2001)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA] (ISOFORM 1); VARIANTS LCA6 GLU-746 AND GLY-1114; VARIANT GLN-1033; The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 4); VARIANT GLN-1033; Molecular characterization of Leber congenital amaurosis in Koreans.
Seong M.W.; Kim S.Y.; Yu Y.S.; Hwang J.M.; Kim J.Y.; Park S.S.;
Mol. Vis. 14:1429-1436(2008)
Cited for: VARIANT LCA6 PRO-631; VARIANTS GLN-96; GLU-192; PHE-432; TRP-601; GLN-1033 AND LEU-1057;

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.