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Home › Dataset Library › Expression Profiles of Monozygotic Twin

Dataset: Expression Profiles of Monozygotic Twin

The expression level for 15 887 transcripts in lymphoblastoid cell lines from 19 monozygotic twin pairs (10 male, 9 female) were analysed...

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The expression level for 15 887 transcripts in lymphoblastoid cell lines from 19 monozygotic twin pairs (10 male, 9 female) were analysed for the effects of genotype and sex. On an average, the effect of twin pairs explained 31% of the variance in normalized gene expression levels, consistent with previous broad sense heritability estimates. The effect of sex on gene expression levels was most noticeable on the X chromosome, which contained 15 of the 20 significantly differentially expressed genes. A high concordance was observed between the sex difference test statistics and surveys of genes escaping X chromosome inactivation. Notably, several autosomal genes showed significant differences in gene expression between the sexes despite much of the cellular environment differences being effectively removed in the cell lines. A publicly available gene expression data set from the CEPH families was used to validate the results. The heritability of gene expression levels as estimated from the two data sets showed a highly significant positive correlation, particularly when both estimates were close to one and thus had the smallest standard error. There was a large concordance between the genes significantly differentially expressed between the sexes in the two data sets. Analysis of the variability of probe binding intensities within a probe set indicated that results are robust to the possible presence of polymorphisms in the target sequences. Keywords: Monozygotic twin pair Expression Profiles Genome-wide gene expression in lymphoblastoid cell lines was determined using microarrays derived from 15 monozygotic (MZ) twin pairs (10 male, 9 female). 10 twin pair are discordant, 4 are concordant for a disease phenotype and their are 5 controls which have no disease phenotype. This data set was analyzed to interrupt replicated effects of sex and genotype, not disease characteristics. Subsets of these samples have been analyzed separately for disease characteristics, (GSE7036 – 3 MZ twins discordant for bipolar disorder) and (GSE7486 - 5 discordant and 4 concordant MZ twin pairs with idiopathic absence epilepsies and 5 unaffected MZ twin pairs).

Species:
human

Samples:
35

Source:
E-GEOD-7624

PubMed:
17164263

Updated:
Dec.12, 2014

Registered:
Sep.22, 2014


Factors: (via ArrayExpress)
Sample SAMPLE ID CLINICAL STATUS TWIN PAIR ID SEX MEDICATION AT INTERVIEW DURATION BLOOD SAMPLING MEDICATION AT BLOOD SAMPLING
GSM162903 TP10 control DCBD3.2 female None 35 not specified
GSM18137 TP11 Late onset IGE DCE1.1 male not specified 39 Epilim
GSM181372 TP12 Unaffected DCE1.2 male not specified 39 Nil
GSM181373 TP19 Childhood Absence Epilepsy + Febrile Seizures DCE2.1 female not specified 42 None
GSM181374 TP20 Unaffected DCE2.2 female not specified 42 None
GSM181375 TP29 Childhood absence epilepsy DCE3.1 male not specified 23 Epilim
GSM181376 TP30 Unaffected DCE3.2 male not specified 23 None
GSM181377 TP33 Childhood absence epilepsy DCE4.1 male not specified 26 Epilim
GSM181378 TP34 Unaffected DCE4.2 male not specified 26 None
GSM181379 TP37 Juvenile Absence Epilepsy + Febrile Seizures DCE5.1 female not specified 27 Epilim
GSM181380 TP38 Unaffected DCE5.2 female not specified 27 None
GSM18138 TP21 Childhood absence epilepsy CCE1.1 female not specified 22 Epilim
GSM181382 TP22 Childhood Absence Epilepsy + Febrile Seizures CCE1.2 female not specified 22 None
GSM181384 TP31 Childhood absence epilepsy CCE2.1 female not specified 34 None
GSM181385 TP32 Childhood absence epilepsy CCE2.2 female not specified 34 None
GSM181389 TP35 Childhood absence epilepsy CCE3.1 male not specified 57 Epilim
GSM181390 TP36 Childhood absence epilepsy CCE3.2 male not specified 57 None
GSM18139 TP39 Childhood absence epilepsy CCE4.1 male not specified 31 Epilim & Lamictal
GSM181392 TP40 Childhood absence epilepsy CCE4.2 male not specified 31 Epilim
GSM181395 TP13 Unaffected CCN1.1 male not specified 37 None
GSM181396 TP14 Unaffected CCN1.2 male not specified 37 None
GSM181399 TP15 Unaffected CCN1.1R male not specified 37 None
GSM181400 TP16 Unaffected CCN1.2R male not specified 37 None
GSM181405 TP17 Unaffected CCN2.1 male not specified 27 None
GSM181406 TP18 Unaffected CCN2.2 male not specified 27 None
GSM181409 TP23 Unaffected CCN3.1 male not specified 25 None
GSM181410 TP24 Unaffected CCN3.2 male not specified 25 None
GSM181412 TP25 Unaffected CCN4.1 female not specified 29 None
GSM181413 TP26 Unaffected CCN4.2 female not specified 29 None
GSM181416 TP27 Unaffected CCN5.1 female not specified 34 None
GSM181417 TP28 Unaffected CCN5.2 female not specified 34 None
GSM184438 TP1 Brief Psychotic Disorder - female thyroxine 61 not specified
GSM184439 TP2 Unaffected - female thyroxine 61 not specified
GSM184442 TP3 schizophrenia - female olanzapine 26 not specified
GSM184443 TP4 schizophrenia - female Nil 26 not specified

Tags

  • bipolar disorder
  • cell
  • chromosome
  • disease
  • genome
  • x chromosome

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