The TYMP gene homepage

General information
Gene symbol TYMP
Gene name thymidine phosphorylase
Chromosome 22
Chromosomal band q13.33
Imprinted Unknown
Genomic reference NG_011860.1
Transcript reference NM_001113755.3, NM_001113756.3, NM_001257988.1, NM_001257989.1, NM_001953.5
Associated with diseases MNGIE
Citation reference(s) -
Curators (1) MyHVP
Total number of public variants reported 12
Unique public DNA variants reported 3
Individuals with public variants 6
Hidden variants -
Date created June 06, 2021
Date last updated September 12, 2021
Version TYMP:210912

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 3148
Entrez Gene 1890
PubMed articles TYMP
OMIM - Gene 131222
OMIM - Diseases MNGIE (Mitochondrial Neurogastrointestinal Encephalomyopathy)
HGMD TYMP
GeneCards TYMP
GeneTests TYMP
Orphanet TYMP


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000673 22 transcript variant 1 NM_001113755.3 NP_001107227.1 11
00000674 22 transcript variant 2 NM_001953.5 NP_001944.1 1
00000675 22 transcript variant 3 NM_001113756.3 NP_001107228.1 -
00000676 22 transcript variant 4 NM_001257988.1 NP_001244917.1 -
00000677 22 transcript variant 5 NM_001257989.1 NP_001244918.1 -


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