Expasy logo

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot O43156: Variant p.Asp921Asn

TELO2-interacting protein 1 homolog
Gene: TTI1
Feedback?
Variant information Variant position: help 921 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help 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: help From Aspartate (D) to Asparagine (N) at position 921 (D921N, p.Asp921Asn). 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: help Change from medium size and acidic (D) to medium size and polar (N) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 1 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: help In NEDMIM; likely pathogenic; affects signal transduction in response to DNA damage. Any additional useful information about the variant.


Sequence information Variant position: help 921 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1089 The length of the canonical sequence.
Location on the sequence: help NQLLPLAHQAWPSLVHRLTR D APLAVLRAFKVLRTLGSKCG 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         NQLLPLAHQAWPSLVHRLTRDAPLAVLRAFKVLRTLGSKCG

Mouse                         NQLLPLAHRAWPSLVHRLTSDDPLAVLRAFKVLQTLGSRCG

Baker's yeast                 NLLIREVASTWDSIIQCVLCSDYSIVQPACSCVEQMIKYSG

Fission yeast                 NTFYPAINTFWPLVVIQLDTDNELLVECALETIYQVCALAD
Sequence annotation in neighborhood: help 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 – 1089 TELO2-interacting protein 1 homolog



Literature citations
Genes that affect brain structure and function identified by rare variant analyses of mendelian neurologic disease.
Karaca E.; Harel T.; Pehlivan D.; Jhangiani S.N.; Gambin T.; Coban Akdemir Z.; Gonzaga-Jauregui C.; Erdin S.; Bayram Y.; Campbell I.M.; Hunter J.V.; Atik M.M.; Van Esch H.; Yuan B.; Wiszniewski W.; Isikay S.; Yesil G.; Yuregir O.O.; Tug Bozdogan S.; Aslan H.; Aydin H.; Tos T.; Aksoy A.; De Vivo D.C.; Jain P.; Geckinli B.B.; Sezer O.; Gul D.; Durmaz B.; Cogulu O.; Ozkinay F.; Topcu V.; Candan S.; Cebi A.H.; Ikbal M.; Yilmaz Gulec E.; Gezdirici A.; Koparir E.; Ekici F.; Coskun S.; Cicek S.; Karaer K.; Koparir A.; Duz M.B.; Kirat E.; Fenercioglu E.; Ulucan H.; Seven M.; Guran T.; Elcioglu N.; Yildirim M.S.; Aktas D.; Alikasifoglu M.; Ture M.; Yakut T.; Overton J.D.; Yuksel A.; Ozen M.; Muzny D.M.; Adams D.R.; Boerwinkle E.; Chung W.K.; Gibbs R.A.; Lupski J.R.;
Neuron 88:499-513(2015)
Cited for: VARIANT NEDMIM ASN-921;
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly.
Serey-Gaut M.; Cortes M.; Makrythanasis P.; Suri M.; Taylor A.M.R.; Sullivan J.A.; Asleh A.N.; Mitra J.; Dar M.A.; McNamara A.; Shashi V.; Dugan S.; Song X.; Rosenfeld J.A.; Cabrol C.; Iwaszkiewicz J.; Zoete V.; Pehlivan D.; Akdemir Z.C.; Roeder E.R.; Littlejohn R.O.; Dibra H.K.; Byrd P.J.; Stewart G.S.; Geckinli B.B.; Posey J.; Westman R.; Jungbluth C.; Eason J.; Sachdev R.; Evans C.A.; Lemire G.; VanNoy G.E.; O'Donnell-Luria A.; Mau-Them F.T.; Juven A.; Piard J.; Nixon C.Y.; Zhu Y.; Ha T.; Buckley M.F.; Thauvin C.; Essien Umanah G.K.; Van Maldergem L.; Lupski J.R.; Roscioli T.; Dawson V.L.; Dawson T.M.; Antonarakis S.E.;
Am. J. Hum. Genet. 110:499-515(2023)
Cited for: VARIANTS NEDMIM 36-ARG--GLN-1089 DEL; GLU-123; GLY-279; PRO-402; ARG-424; 490-GLN--GLN-1089 DEL; THR-634; SER-767; LEU-838; GLU-887; ASN-921; ARG-993; ARG-1000 AND MET-1081; INVOLVEMENT IN NEDMIM; CHARACTERIZATION OF VARIANTS NEDMIM GLU-123; PRO-402; SER-767; LEU-838; GLU-887 AND ASN-921; IDENTIFICATION IN THE MTORC1 COMPLEX; IDENTIFICATION IN THE MTORC2 COMPLEX; FUNCTION;
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.