UniProtKB/Swiss-Prot Q8IZD2: Variant p.Pro1376Leu

Inactive histone-lysine N-methyltransferase 2E
Gene: KMT2E
Feedback?

Variant information Variant position:

1376 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 Proline (P) to Leucine (L) at position 1376 (P1376L, p.Pro1376Leu). 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 hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-3 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 rs140764929 [ dbSNP | Ensembl ]

Sequence information Variant position:

1376 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

1858 The length of the canonical sequence.
Location on the sequence:

KPGSPGSVIPAQAHGKIFTK P DPQWDSTVSASEAENGVHLK 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                         KPGSPGSVIPAQAHGKIFTKPDPQWDSTVSASEAENGVHLK

Mouse                         KPGSPGPINPAQSHGKILTKPDSHWEATATVSEADNSVHQN

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 – 1858	Inactive histone-lysine N-methyltransferase 2E
Region	1164 – 1561	Disordered
Modified residue	1359 – 1359	Phosphoserine
Alternative sequence	610 – 1858	Missing. In isoform 3.
Alternative sequence	866 – 1858	Missing. In isoform 4.
Alternative sequence	1169 – 1858	Missing. In isoform NKp44L.

Literature citations
Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy.
O'Donnell-Luria A.H.; Pais L.S.; Faundes V.; Wood J.C.; Sveden A.; Luria V.; Abou Jamra R.; Accogli A.; Amburgey K.; Anderlid B.M.; Azzarello-Burri S.; Basinger A.A.; Bianchini C.; Bird L.M.; Buchert R.; Carre W.; Ceulemans S.; Charles P.; Cox H.; Culliton L.; Curro A.; Demurger F.; Dowling J.J.; Duban-Bedu B.; Dubourg C.; Eiset S.E.; Escobar L.F.; Ferrarini A.; Haack T.B.; Hashim M.; Heide S.; Helbig K.L.; Helbig I.; Heredia R.; Heron D.; Isidor B.; Jonasson A.R.; Joset P.; Keren B.; Kok F.; Kroes H.Y.; Lavillaureix A.; Lu X.; Maas S.M.; Maegawa G.H.B.; Marcelis C.L.M.; Mark P.R.; Masruha M.R.; McLaughlin H.M.; McWalter K.; Melchinger E.U.; Mercimek-Andrews S.; Nava C.; Pendziwiat M.; Person R.; Ramelli G.P.; Ramos L.L.P.; Rauch A.; Reavey C.; Renieri A.; Riess A.; Sanchez-Valle A.; Sattar S.; Saunders C.; Schwarz N.; Smol T.; Srour M.; Steindl K.; Syrbe S.; Taylor J.C.; Telegrafi A.; Thiffault I.; Trauner D.A.; van der Linden H. Jr.; van Koningsbruggen S.; Villard L.; Vogel I.; Vogt J.; Weber Y.G.; Wentzensen I.M.; Widjaja E.; Zak J.; Baxter S.; Banka S.; Rodan L.H.;
Am. J. Hum. Genet. 104:1210-1222(2019)
Cited for: INVOLVEMENT IN ODLURO; VARIANTS ODLURO ILE-140; 151-ARG--HIS-1858 DEL; HIS-284; 754-SER--HIS-1858 DEL; 818-ARG--HIS-1858 DEL; 874-ARG--HIS-1858 DEL; VAL-907; 1024-GLN--HIS-1858 DEL; 1185-SER--HIS-1858 DEL; 1224-TYR--HIS-1858 DEL AND SER-1376; VARIANT LEU-1376;

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.