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gene exp galnt12 hs00226436 m1  (Thermo Fisher)


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    Structured Review

    Thermo Fisher gene exp galnt12 hs00226436 m1
    Top-ranking up- and down- regulated 1,25D-activated VDR target genes in human fibroblasts (CO).
    Gene Exp Galnt12 Hs00226436 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/total+human+1%2E2+cdna+microarray/Gene+Exp%2E+GALNT12%2C+Hs00226436_m1/pmc06523947-110-45-9
    Average 95 stars, based on 1 article reviews
    gene exp galnt12 hs00226436 m1 - by Bioz Stars, 2026-10
    95/100 stars

    Images

    1) Product Images from "Transcriptomic Response to 1,25-Dihydroxyvitamin D in Human Fibroblasts with or without a Functional Vitamin D Receptor (VDR): Novel Target Genes and Insights into VDR Basal Transcriptional Activity"

    Article Title: Transcriptomic Response to 1,25-Dihydroxyvitamin D in Human Fibroblasts with or without a Functional Vitamin D Receptor (VDR): Novel Target Genes and Insights into VDR Basal Transcriptional Activity

    Journal: Cells

    doi: 10.3390/cells8040318

    Top-ranking up- and down- regulated 1,25D-activated VDR target genes in human fibroblasts (CO).
    Figure Legend Snippet: Top-ranking up- and down- regulated 1,25D-activated VDR target genes in human fibroblasts (CO).

    Techniques Used:

    Quantitative RT-PCR validation of differential gene expression findings.
    Figure Legend Snippet: Quantitative RT-PCR validation of differential gene expression findings.

    Techniques Used: Quantitative RT-PCR, Biomarker Discovery, Gene Expression, Quantitative Proteomics, Microarray

    Related Articles

    Quantitative RT-PCR:

    Article Title: The Role of Dimethyl Sulfoxide (DMSO) in Gene Expression Modulation and Glycosaminoglycan Metabolism in Lysosomal Storage Disorders on an Example of Mucopolysaccharidosis
    Article Snippet: Total RNA was reverse-transcribed into cDNA using Transcriptor First Strand cDNA Synthesis Kit (Roche Applied Science, Indianapolis, IN, USA), according to the manufacturer’s instructions. .. Real-time qRT-PCR was carried out with TaqMan Gene Expression Assays (Thermo Fisher Scientific, Foster City, CA, USA) with catalog numbers as follows: #4426961 (Hs00904548_m1, ALG2 ), #4331182 (Hs00970128_m1, ALG12 ), #4331182 (Hs00406036_m1, ARSK ), #4331182 (Hs00155245_m1, B4GALT1 ), #4331182 (Hs01921028_s1, CHST2 ), #4331182 (Hs00248144_m1, CHST15 ), #4331182 (Hs00609162_m1, EXT1 ), #4331182 (Hs00975732_m1, GALNS ), #4331182 (Hs00189537_m1, GALNT2 ), #4331182 (Hs00559726_s1, GALNT4 ), #4331182 (Hs99999909_m1, GALNT6 ), #4331182 (Hs00226436_m1, GALNT12 ), #4448892 (Hs00166197_m1, GM2A ), #4331182 (Hs00428900_m1, MAN2C1 ), #4331182 (Hs01100653_m1, MCOLN1 ), #4331182 (Hs00393705_m1, SGPL1 ), #4331182 (Hs01001189_m1, SLC7A5 ), #4331182 (Hs01027014_m1, SPTLC2 ), #4331182 (Hs00217867_m1, SPTLC3 ), #4331182 (Hs01105377_m1, ST3GAL5 ), #4331182 (Hs00383244_m1, ZKSCAN3 ), using the Light Cycler 480 II detection system (Roche Applied Science, Indianapolis, IN, USA). ..

    Gene Expression:

    Article Title: The Role of Dimethyl Sulfoxide (DMSO) in Gene Expression Modulation and Glycosaminoglycan Metabolism in Lysosomal Storage Disorders on an Example of Mucopolysaccharidosis
    Article Snippet: Total RNA was reverse-transcribed into cDNA using Transcriptor First Strand cDNA Synthesis Kit (Roche Applied Science, Indianapolis, IN, USA), according to the manufacturer’s instructions. .. Real-time qRT-PCR was carried out with TaqMan Gene Expression Assays (Thermo Fisher Scientific, Foster City, CA, USA) with catalog numbers as follows: #4426961 (Hs00904548_m1, ALG2 ), #4331182 (Hs00970128_m1, ALG12 ), #4331182 (Hs00406036_m1, ARSK ), #4331182 (Hs00155245_m1, B4GALT1 ), #4331182 (Hs01921028_s1, CHST2 ), #4331182 (Hs00248144_m1, CHST15 ), #4331182 (Hs00609162_m1, EXT1 ), #4331182 (Hs00975732_m1, GALNS ), #4331182 (Hs00189537_m1, GALNT2 ), #4331182 (Hs00559726_s1, GALNT4 ), #4331182 (Hs99999909_m1, GALNT6 ), #4331182 (Hs00226436_m1, GALNT12 ), #4448892 (Hs00166197_m1, GM2A ), #4331182 (Hs00428900_m1, MAN2C1 ), #4331182 (Hs01100653_m1, MCOLN1 ), #4331182 (Hs00393705_m1, SGPL1 ), #4331182 (Hs01001189_m1, SLC7A5 ), #4331182 (Hs01027014_m1, SPTLC2 ), #4331182 (Hs00217867_m1, SPTLC3 ), #4331182 (Hs01105377_m1, ST3GAL5 ), #4331182 (Hs00383244_m1, ZKSCAN3 ), using the Light Cycler 480 II detection system (Roche Applied Science, Indianapolis, IN, USA). ..

    Article Title: Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production.
    Article Snippet: SuperScript II RNase H- Reverse Transcriptase and random primers (Thermo Fisher Scientific) were used to synthesize first-strand cDNAs from 5 mg of total RNA. .. TaqMan real-time RTPCR assay on a 7300 Fast Real-Time PCR System (Thermo Fisher Scientific) were performed for relative quantification of the target mRNA following the manufacturer’s instructions using the TaqMan Universal PCR Master Mix and TaqMan Gene Expression Assays: GalNAc-T1, Hs00234919_m1; GalNAc-T2, Hs00189537_m1; GalNAc-T3, Hs00237084_m1; GalNAc-T4, Hs00236809_s1; GalNAc-T5, Hs00294826_m1; GalNAc-T6, Hs00200529_m1, GalNAc-T7, Hs00213624_m1; GalNAc-T8, Hs00213610_m1; GalNAc-T9, Hs00222357_m1; GalNAc-T10, Hs00213903_m1; GalNAc-T11, Hs00254410_m1; GalNAc-T12, Hs00226436_m1; GalNAc-T13, Hs00287613_m1; GalNAc-T14, Hs00226180_m1; GalNAc-T15 (GalNAc-TL5), Hs00377152_m1; GalNAc-T16 (GalNAc-TL1), Hs00857466_m1; endogenous control, the TaqMan Ribosomal RNA Control Reagents VIC Probe. ..

    Polymerase Chain Reaction:

    Article Title: The GalNAc-T Activation Pathway (GALA) is not a general mechanism for regulating mucin-type O-glycosylation
    Article Snippet: RT-qPCR was performed using Taqman ® Gene expression assay (ThermoFisher Scientific, Waltham, MA) following manufacturer procedure. .. The PCR was performed using TaqMan ® Universal PCR Master Mix (ThermoFisher Scientific, Waltham, MA), with 50 ng of cDNA and the following probes: Actin B (Hs99999903_m1) was used as a positive control, and used to normalization for the relative expression of GalNAc-T1 (Hs00234919_m1), GalNAc-T2 (Hs00189537_m1), GalNAc-T3 (Hs00237084_m1), GalNAc-T4 (Hs00559726_s1), GalNAc-T5 (Hs00294826_m1), GalNAc-T6 (Hs00200529_m1), GalNAc-T7 (Hs00213624_m1), GalNAc-T8 (Hs00213610_m1), GalNAc-T9 (Hs00222357_m1), GalNAc-T10 (Hs00213903_m1), GalNAc-T11 (Hs00757865_m1), GalNAc-T12 (Hs00226436_m1) and CD3e (Hs01062241_m1). .. To determine if growth factor treatment effects the localization of endogenous GalNAc-T1 and -T2 we treated HeLa CCL-2 cells (acquired from ATCC) with EGF or PDGF, using conditions previously reported as sufficient to cause redistribution of GalNAc-T from the Golgi complex (Gill et al., 2010).

    Article Title: Growth Factors do not regulate Golgi Complex-to-ER relocation of GalNAc-Ts in HeLa cells
    Article Snippet: RT-qPCR was performed using Taqman ® Gene expression assay (ThermoFisher Scientific, Waltham, MA) following manufacturer procedure. .. The PCR was performed using TaqMan ® Universal PCR Master Mix (ThermoFisher Scientific, Waltham, MA), with 50 ng of cDNA and the following probes: Actin B (Hs99999903_m1) was used as a positive control, and used to normalization for the relative expression of GalNAc-T1 (Hs00234919_m 1), GalNAc-T2 (Hs00189537_m1), GalNAc-T3 (Hs00237084_m1), GalNAc-T4 (Hs00559726_s1), GalNAc-T5 (Hs00294826_m1), GalNAc-T6 (Hs00200529_m1), GalNAc-T7 (Hs00213624_m1), GalNAc-T8 (Hs00213610_m1), GalNAc-T9 (Hs00222357_m1), GalNAc-T10 (Hs00213903_m 1), GalNAc-T11 (Hs00757865_m1), GalNAc-T12 (Hs00226436_m1) and CD3e (Hs01062241_m1). ..

    Article Title: Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production.
    Article Snippet: SuperScript II RNase H- Reverse Transcriptase and random primers (Thermo Fisher Scientific) were used to synthesize first-strand cDNAs from 5 mg of total RNA. .. TaqMan real-time RTPCR assay on a 7300 Fast Real-Time PCR System (Thermo Fisher Scientific) were performed for relative quantification of the target mRNA following the manufacturer’s instructions using the TaqMan Universal PCR Master Mix and TaqMan Gene Expression Assays: GalNAc-T1, Hs00234919_m1; GalNAc-T2, Hs00189537_m1; GalNAc-T3, Hs00237084_m1; GalNAc-T4, Hs00236809_s1; GalNAc-T5, Hs00294826_m1; GalNAc-T6, Hs00200529_m1, GalNAc-T7, Hs00213624_m1; GalNAc-T8, Hs00213610_m1; GalNAc-T9, Hs00222357_m1; GalNAc-T10, Hs00213903_m1; GalNAc-T11, Hs00254410_m1; GalNAc-T12, Hs00226436_m1; GalNAc-T13, Hs00287613_m1; GalNAc-T14, Hs00226180_m1; GalNAc-T15 (GalNAc-TL5), Hs00377152_m1; GalNAc-T16 (GalNAc-TL1), Hs00857466_m1; endogenous control, the TaqMan Ribosomal RNA Control Reagents VIC Probe. ..

    Positive Control:

    Article Title: The GalNAc-T Activation Pathway (GALA) is not a general mechanism for regulating mucin-type O-glycosylation
    Article Snippet: RT-qPCR was performed using Taqman ® Gene expression assay (ThermoFisher Scientific, Waltham, MA) following manufacturer procedure. .. The PCR was performed using TaqMan ® Universal PCR Master Mix (ThermoFisher Scientific, Waltham, MA), with 50 ng of cDNA and the following probes: Actin B (Hs99999903_m1) was used as a positive control, and used to normalization for the relative expression of GalNAc-T1 (Hs00234919_m1), GalNAc-T2 (Hs00189537_m1), GalNAc-T3 (Hs00237084_m1), GalNAc-T4 (Hs00559726_s1), GalNAc-T5 (Hs00294826_m1), GalNAc-T6 (Hs00200529_m1), GalNAc-T7 (Hs00213624_m1), GalNAc-T8 (Hs00213610_m1), GalNAc-T9 (Hs00222357_m1), GalNAc-T10 (Hs00213903_m1), GalNAc-T11 (Hs00757865_m1), GalNAc-T12 (Hs00226436_m1) and CD3e (Hs01062241_m1). .. To determine if growth factor treatment effects the localization of endogenous GalNAc-T1 and -T2 we treated HeLa CCL-2 cells (acquired from ATCC) with EGF or PDGF, using conditions previously reported as sufficient to cause redistribution of GalNAc-T from the Golgi complex (Gill et al., 2010).

    Article Title: Growth Factors do not regulate Golgi Complex-to-ER relocation of GalNAc-Ts in HeLa cells
    Article Snippet: RT-qPCR was performed using Taqman ® Gene expression assay (ThermoFisher Scientific, Waltham, MA) following manufacturer procedure. .. The PCR was performed using TaqMan ® Universal PCR Master Mix (ThermoFisher Scientific, Waltham, MA), with 50 ng of cDNA and the following probes: Actin B (Hs99999903_m1) was used as a positive control, and used to normalization for the relative expression of GalNAc-T1 (Hs00234919_m 1), GalNAc-T2 (Hs00189537_m1), GalNAc-T3 (Hs00237084_m1), GalNAc-T4 (Hs00559726_s1), GalNAc-T5 (Hs00294826_m1), GalNAc-T6 (Hs00200529_m1), GalNAc-T7 (Hs00213624_m1), GalNAc-T8 (Hs00213610_m1), GalNAc-T9 (Hs00222357_m1), GalNAc-T10 (Hs00213903_m 1), GalNAc-T11 (Hs00757865_m1), GalNAc-T12 (Hs00226436_m1) and CD3e (Hs01062241_m1). ..

    Expressing:

    Article Title: The GalNAc-T Activation Pathway (GALA) is not a general mechanism for regulating mucin-type O-glycosylation
    Article Snippet: RT-qPCR was performed using Taqman ® Gene expression assay (ThermoFisher Scientific, Waltham, MA) following manufacturer procedure. .. The PCR was performed using TaqMan ® Universal PCR Master Mix (ThermoFisher Scientific, Waltham, MA), with 50 ng of cDNA and the following probes: Actin B (Hs99999903_m1) was used as a positive control, and used to normalization for the relative expression of GalNAc-T1 (Hs00234919_m1), GalNAc-T2 (Hs00189537_m1), GalNAc-T3 (Hs00237084_m1), GalNAc-T4 (Hs00559726_s1), GalNAc-T5 (Hs00294826_m1), GalNAc-T6 (Hs00200529_m1), GalNAc-T7 (Hs00213624_m1), GalNAc-T8 (Hs00213610_m1), GalNAc-T9 (Hs00222357_m1), GalNAc-T10 (Hs00213903_m1), GalNAc-T11 (Hs00757865_m1), GalNAc-T12 (Hs00226436_m1) and CD3e (Hs01062241_m1). .. To determine if growth factor treatment effects the localization of endogenous GalNAc-T1 and -T2 we treated HeLa CCL-2 cells (acquired from ATCC) with EGF or PDGF, using conditions previously reported as sufficient to cause redistribution of GalNAc-T from the Golgi complex (Gill et al., 2010).

    Article Title: Growth Factors do not regulate Golgi Complex-to-ER relocation of GalNAc-Ts in HeLa cells
    Article Snippet: RT-qPCR was performed using Taqman ® Gene expression assay (ThermoFisher Scientific, Waltham, MA) following manufacturer procedure. .. The PCR was performed using TaqMan ® Universal PCR Master Mix (ThermoFisher Scientific, Waltham, MA), with 50 ng of cDNA and the following probes: Actin B (Hs99999903_m1) was used as a positive control, and used to normalization for the relative expression of GalNAc-T1 (Hs00234919_m 1), GalNAc-T2 (Hs00189537_m1), GalNAc-T3 (Hs00237084_m1), GalNAc-T4 (Hs00559726_s1), GalNAc-T5 (Hs00294826_m1), GalNAc-T6 (Hs00200529_m1), GalNAc-T7 (Hs00213624_m1), GalNAc-T8 (Hs00213610_m1), GalNAc-T9 (Hs00222357_m1), GalNAc-T10 (Hs00213903_m 1), GalNAc-T11 (Hs00757865_m1), GalNAc-T12 (Hs00226436_m1) and CD3e (Hs01062241_m1). ..

    Reverse Transcription Polymerase Chain Reaction:

    Article Title: Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production.
    Article Snippet: SuperScript II RNase H- Reverse Transcriptase and random primers (Thermo Fisher Scientific) were used to synthesize first-strand cDNAs from 5 mg of total RNA. .. TaqMan real-time RTPCR assay on a 7300 Fast Real-Time PCR System (Thermo Fisher Scientific) were performed for relative quantification of the target mRNA following the manufacturer’s instructions using the TaqMan Universal PCR Master Mix and TaqMan Gene Expression Assays: GalNAc-T1, Hs00234919_m1; GalNAc-T2, Hs00189537_m1; GalNAc-T3, Hs00237084_m1; GalNAc-T4, Hs00236809_s1; GalNAc-T5, Hs00294826_m1; GalNAc-T6, Hs00200529_m1, GalNAc-T7, Hs00213624_m1; GalNAc-T8, Hs00213610_m1; GalNAc-T9, Hs00222357_m1; GalNAc-T10, Hs00213903_m1; GalNAc-T11, Hs00254410_m1; GalNAc-T12, Hs00226436_m1; GalNAc-T13, Hs00287613_m1; GalNAc-T14, Hs00226180_m1; GalNAc-T15 (GalNAc-TL5), Hs00377152_m1; GalNAc-T16 (GalNAc-TL1), Hs00857466_m1; endogenous control, the TaqMan Ribosomal RNA Control Reagents VIC Probe. ..

    Real-time Polymerase Chain Reaction:

    Article Title: Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production.
    Article Snippet: SuperScript II RNase H- Reverse Transcriptase and random primers (Thermo Fisher Scientific) were used to synthesize first-strand cDNAs from 5 mg of total RNA. .. TaqMan real-time RTPCR assay on a 7300 Fast Real-Time PCR System (Thermo Fisher Scientific) were performed for relative quantification of the target mRNA following the manufacturer’s instructions using the TaqMan Universal PCR Master Mix and TaqMan Gene Expression Assays: GalNAc-T1, Hs00234919_m1; GalNAc-T2, Hs00189537_m1; GalNAc-T3, Hs00237084_m1; GalNAc-T4, Hs00236809_s1; GalNAc-T5, Hs00294826_m1; GalNAc-T6, Hs00200529_m1, GalNAc-T7, Hs00213624_m1; GalNAc-T8, Hs00213610_m1; GalNAc-T9, Hs00222357_m1; GalNAc-T10, Hs00213903_m1; GalNAc-T11, Hs00254410_m1; GalNAc-T12, Hs00226436_m1; GalNAc-T13, Hs00287613_m1; GalNAc-T14, Hs00226180_m1; GalNAc-T15 (GalNAc-TL5), Hs00377152_m1; GalNAc-T16 (GalNAc-TL1), Hs00857466_m1; endogenous control, the TaqMan Ribosomal RNA Control Reagents VIC Probe. ..

    Article Title: Transcriptomic Response to 1,25-Dihydroxyvitamin D in Human Fibroblasts with or without a Functional Vitamin D Receptor (VDR): Novel Target Genes and Insights into VDR Basal Transcriptional Activity
    Article Snippet: .. First-strand cDNA was generated using SuperScript III reverse transcriptase (Thermo Fisher) and quantitative PCR performed in a StepOnePlus Real-Time PCR System (Thermo Fisher) using the following inventoried TaqMan® assays (Thermo Fisher): CYP24A1 Hs00167999 _m1, TGFB2 Hs00234244_m1, RASSF2 Hs00248129_m1, CILP Hs00173647_m1, STC1 Hs00174970_m1, SPP1 Hs00959010_m1, GALNT12 Hs00226436_m1, HBEGF Hs00181813_m1, EFNB2 Hs00187950_m1, and EGR1 Hs00152928_m1. ..

    Quantitative Proteomics:

    Article Title: Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production.
    Article Snippet: SuperScript II RNase H- Reverse Transcriptase and random primers (Thermo Fisher Scientific) were used to synthesize first-strand cDNAs from 5 mg of total RNA. .. TaqMan real-time RTPCR assay on a 7300 Fast Real-Time PCR System (Thermo Fisher Scientific) were performed for relative quantification of the target mRNA following the manufacturer’s instructions using the TaqMan Universal PCR Master Mix and TaqMan Gene Expression Assays: GalNAc-T1, Hs00234919_m1; GalNAc-T2, Hs00189537_m1; GalNAc-T3, Hs00237084_m1; GalNAc-T4, Hs00236809_s1; GalNAc-T5, Hs00294826_m1; GalNAc-T6, Hs00200529_m1, GalNAc-T7, Hs00213624_m1; GalNAc-T8, Hs00213610_m1; GalNAc-T9, Hs00222357_m1; GalNAc-T10, Hs00213903_m1; GalNAc-T11, Hs00254410_m1; GalNAc-T12, Hs00226436_m1; GalNAc-T13, Hs00287613_m1; GalNAc-T14, Hs00226180_m1; GalNAc-T15 (GalNAc-TL5), Hs00377152_m1; GalNAc-T16 (GalNAc-TL1), Hs00857466_m1; endogenous control, the TaqMan Ribosomal RNA Control Reagents VIC Probe. ..

    Control:

    Article Title: Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production.
    Article Snippet: SuperScript II RNase H- Reverse Transcriptase and random primers (Thermo Fisher Scientific) were used to synthesize first-strand cDNAs from 5 mg of total RNA. .. TaqMan real-time RTPCR assay on a 7300 Fast Real-Time PCR System (Thermo Fisher Scientific) were performed for relative quantification of the target mRNA following the manufacturer’s instructions using the TaqMan Universal PCR Master Mix and TaqMan Gene Expression Assays: GalNAc-T1, Hs00234919_m1; GalNAc-T2, Hs00189537_m1; GalNAc-T3, Hs00237084_m1; GalNAc-T4, Hs00236809_s1; GalNAc-T5, Hs00294826_m1; GalNAc-T6, Hs00200529_m1, GalNAc-T7, Hs00213624_m1; GalNAc-T8, Hs00213610_m1; GalNAc-T9, Hs00222357_m1; GalNAc-T10, Hs00213903_m1; GalNAc-T11, Hs00254410_m1; GalNAc-T12, Hs00226436_m1; GalNAc-T13, Hs00287613_m1; GalNAc-T14, Hs00226180_m1; GalNAc-T15 (GalNAc-TL5), Hs00377152_m1; GalNAc-T16 (GalNAc-TL1), Hs00857466_m1; endogenous control, the TaqMan Ribosomal RNA Control Reagents VIC Probe. ..

    Generated:

    Article Title: Transcriptomic Response to 1,25-Dihydroxyvitamin D in Human Fibroblasts with or without a Functional Vitamin D Receptor (VDR): Novel Target Genes and Insights into VDR Basal Transcriptional Activity
    Article Snippet: .. First-strand cDNA was generated using SuperScript III reverse transcriptase (Thermo Fisher) and quantitative PCR performed in a StepOnePlus Real-Time PCR System (Thermo Fisher) using the following inventoried TaqMan® assays (Thermo Fisher): CYP24A1 Hs00167999 _m1, TGFB2 Hs00234244_m1, RASSF2 Hs00248129_m1, CILP Hs00173647_m1, STC1 Hs00174970_m1, SPP1 Hs00959010_m1, GALNT12 Hs00226436_m1, HBEGF Hs00181813_m1, EFNB2 Hs00187950_m1, and EGR1 Hs00152928_m1. ..

    Reverse Transcription:

    Article Title: Transcriptomic Response to 1,25-Dihydroxyvitamin D in Human Fibroblasts with or without a Functional Vitamin D Receptor (VDR): Novel Target Genes and Insights into VDR Basal Transcriptional Activity
    Article Snippet: .. First-strand cDNA was generated using SuperScript III reverse transcriptase (Thermo Fisher) and quantitative PCR performed in a StepOnePlus Real-Time PCR System (Thermo Fisher) using the following inventoried TaqMan® assays (Thermo Fisher): CYP24A1 Hs00167999 _m1, TGFB2 Hs00234244_m1, RASSF2 Hs00248129_m1, CILP Hs00173647_m1, STC1 Hs00174970_m1, SPP1 Hs00959010_m1, GALNT12 Hs00226436_m1, HBEGF Hs00181813_m1, EFNB2 Hs00187950_m1, and EGR1 Hs00152928_m1. ..



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