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UniProtKB/Swiss-Prot Q9BZR6: Variant p.Arg292His

Reticulon-4 receptor
Gene: RTN4R
Variant information

Variant position:  292
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  LP/P [Disclaimer]
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 Arginine (R) to Histidine (H) at position 292 (R292H, p.Arg292His).
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 large size and basic (R) to medium size and polar (H)
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  0
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

Variant description:  In SCZD; associated with disease susceptibility; unable to mediate down-regulation of axonal growth.
Any additional useful information about the variant.

Other resources:  
Links to websites of interest for the variant.



Sequence information

Variant position:  292
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  473
The length of the canonical sequence.

Location on the sequence:   WAWLQKFRGSSSEVPCSLPQ  R LAGRDLKRLAANDLQGCAVA
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                         WAWLQKFRGSSSEVPCSLPQRLAGRDLKRLAANDLQGCAVA

Mouse                         WAWLQKFRGSSSEVPCNLPQRLADRDLKRLAASDLEGCAVA

Rat                           WAWLQKFRGSSSEVPCNLPQRLAGRDLKRLAASDLEGCAVA

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.

TypePositionsDescription
Chain 27 – 447 Reticulon-4 receptor
Domain 260 – 310 LRRCT
Disulfide bond 266 – 335
Mutagenesis 277 – 277 K -> A. No effect on interaction with MAG.
Mutagenesis 277 – 277 K -> D. Decreases interaction with MAG; when associated with D-279.
Mutagenesis 279 – 279 R -> A. Mildly decreases interaction with MAG.
Mutagenesis 279 – 279 R -> D. Decreases interaction with MAG; when associated with D-277.
Mutagenesis 279 – 279 R -> E. Impaired ganglioside binding.
Helix 291 – 293


Literature citations

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.
Kimura H.; Fujita Y.; Kawabata T.; Ishizuka K.; Wang C.; Iwayama Y.; Okahisa Y.; Kushima I.; Morikawa M.; Uno Y.; Okada T.; Ikeda M.; Inada T.; Branko A.; Mori D.; Yoshikawa T.; Iwata N.; Nakamura H.; Yamashita T.; Ozaki N.;
Transl. Psychiatry 7:E1214-E1214(2017)
Cited for: FUNCTION; VARIANTS HIS-68; ASN-259 AND MET-363; INVOLVEMENT IN SCZD; VARIANT SCZD HIS-292; CHARACTERIZATION OF VARIANT SCZD HIS-292;

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.