Homo sapiens gem (nuclear organelle) associated protein 5, mRNA (cDNA - Nucleotide

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Expanding the clinical phenotype and genetic spectrum of GEMIN5 disorders: Early-infantile developmental and epileptic encephalopathies. [Brain Behav. 2024]
Expanding the clinical phenotype and genetic spectrum of GEMIN5 disorders: Early-infantile developmental and epileptic encephalopathies.
Zhang J, Liu X, Zhu G, Wan L, Liang Y, Li N, Huang M, Yang G. Brain Behav. 2024 May; 14(5):e3535.
Mutations of GEMIN5 are associated with coenzyme Q(10) deficiency: long-term follow-up after treatment. [Eur J Hum Genet. 2024]
Mutations of GEMIN5 are associated with coenzyme Q(10) deficiency: long-term follow-up after treatment.
Cascajo-Almenara MV, Juliá-Palacios N, Urreizti R, Sánchez-Cuesta A, Fernández-Ayala DM, García-Díaz E, Oliva C, O Callaghan MDM, Paredes-Fuentes AJ, Moreno-Lozano PJ, et al. Eur J Hum Genet. 2024 Apr; 32(4):426-434. Epub 2024 Feb 5.
SRCAP complex promotes lung cancer progression by reprograming the oncogenic transcription of Hippo-YAP/TAZ signaling pathway. [Cancer Lett. 2024]
SRCAP complex promotes lung cancer progression by reprograming the oncogenic transcription of Hippo-YAP/TAZ signaling pathway.
Zhang H, Li S, Zhou R, Dong T, Zhang X, Yu M, Lin J, Shi M, Geng E, Li J, et al. Cancer Lett. 2024 Mar 31; 585:216667. Epub 2024 Jan 26.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the GEMIN5 gene.

RecName: Full=Solute carrier organic anion transporter family member 2A1; Short=...
RecName: Full=Solute carrier organic anion transporter family member 2A1; Short=SLCO2A1; AltName: Full=Matrin F/G 1; AltName: Full=OATP2A1; AltName: Full=PHOAR2; AltName: Full=Prostaglandin transporter; Short=PGT; AltName: Full=Solute carrier family 21 member 2; Short=SLC21A2
gi|357529156|sp|Q00910.3|SO2A1_RAT

Protein
Mus musculus ATP-binding cassette, sub-family A member 4 (Abca4), mRNA
Mus musculus ATP-binding cassette, sub-family A member 4 (Abca4), mRNA
gi|6671494|ref|NM_007378.1|

Nucleotide

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Nucleotide