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UniProtKB/Swiss-Prot Q6N022: Variant p.Thr1367Asn

Teneurin-4
Gene: TENM4
Variant information

Variant position:  1367
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  Disease [Disclaimer]
The variants are classified into three categories: Disease, Polymorphism and Unclassified.
  • Disease: Variants implicated in disease according to literature reports.
  • Polymorphism: Variants not reported to be implicated in disease.
  • Unclassified: Variants with uncertain implication in disease according to literature reports. Evidence against or in favor of a pathogenic role is limited and/or conflicting.

Residue change:  From Threonine (T) to Asparagine (N) at position 1367 (T1367N, p.Thr1367Asn).
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:  Similar physico-chemical property. Both residues are medium size and polar.
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

Involvement in disease:  Tremor, hereditary essential 5 (ETM5) [MIM:616736]: A common movement disorder mainly characterized by postural tremor of the arms. Head, legs, trunk, voice, jaw, and facial muscles also may be involved. The condition can be aggravated by emotions, hunger, fatigue and temperature extremes, and may cause a functional disability or even incapacitation. Inheritance is autosomal dominant. {ECO:0000269|PubMed:26188006}. Note=The disease is caused by mutations affecting the gene represented in this entry.
The name and a short description of the disease associated with the variant. For more information about the disease, the user can refer to OMIM, following the link provided after the disease acronym.

Variant description:  In ETM5; dominant negative effect on central nervous myelination and axon guidance; changed localization to the plasma membrane; clustered plasma membrane localization.
Any additional useful information about the variant.

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



Sequence information

Variant position:  1367
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  2769
The length of the canonical sequence.

Location on the sequence:   LTNPRGITVDKFGLIYFVDG  T MIRRIDQNGIISTLLGSNDL
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                         LTNPRGITVDKFGLIYFVDGTMIRRIDQNGIISTLLGSNDL

Mouse                         LTNPRGITVDKFGLIYFVDGTMIRRVDQNGIISTLLGSNDL

Zebrafish                     LTNPRGITVDKYGVIFFVDGTMIRRIDQNGIISTLLGFNDL

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 1 – 2769 Teneurin-4
Topological domain 367 – 2769 Extracellular
Repeat 1334 – 1378 NHL 3


Literature citations

Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.
Hor H.; Francescatto L.; Bartesaghi L.; Ortega-Cubero S.; Kousi M.; Lorenzo-Betancor O.; Jimenez-Jimenez F.J.; Gironell A.; Clarimon J.; Drechsel O.; Agundez J.A.; Kenzelmann Broz D.; Chiquet-Ehrismann R.; Lleo A.; Coria F.; Garcia-Martin E.; Alonso-Navarro H.; Marti M.J.; Kulisevsky J.; Hor C.N.; Ossowski S.; Chrast R.; Katsanis N.; Pastor P.; Estivill X.;
Hum. Mol. Genet. 24:5677-5686(2015)
Cited for: FUNCTION; SUBCELLULAR LOCATION; INVOLVEMENT IN ETM5; VARIANTS ETM5 PRO-53; ASP-474; GLN-518; MET-1128; MET-1138; ASN-1367; THR-1442; GLN-1535; HIS-1632; ARG-1763 AND ILE-2451; CHARACTERIZATION OF VARIANTS ETM5 MET-1138; ASN-1367 AND THR-1442;

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.