Homo sapiens TULP1 mRNA for tubby-related protein 1, complete cds, clo - Nucleotide

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Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG. [Acta Ophthalmol. 2023]
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG.
Majander A, Sankila EM, Falck A, Vasara LK, Seitsonen S, Kulmala M, Haavisto AK, Avela K, Turunen JA. Acta Ophthalmol. 2023 Mar; 101(2):215-221. Epub 2022 Sep 21.
TULP1 related retinal dystrophy: report of rare and novel variants with a previously undescribed phenotype in two cases. [Ophthalmic Genet. 2022]
TULP1 related retinal dystrophy: report of rare and novel variants with a previously undescribed phenotype in two cases.
Al-Hindi H, Chauhan MZ, Sanders R, Samarah H, DeBenedictis M, Traboulsi E, Uwaydat SH. Ophthalmic Genet. 2022 Apr; 43(2):277-281. Epub 2021 Dec 5.
A novel homozygous missense mutation p.P388S in TULP1 causes protein instability and retinitis pigmentosa. [Mol Vis. 2021]
A novel homozygous missense mutation p.P388S in TULP1 causes protein instability and retinitis pigmentosa.
Woodard DR, Xing C, Ganne P, Liang H, Mahindrakar A, Sankurathri C, Hulleman JD, Mootha VV. Mol Vis. 2021; 27:179-190. Epub 2021 Apr 2.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the TULP1 gene.

Homo sapiens TULP1 mRNA for tubby-related protein 1, complete cds, clone: HP0791...
Homo sapiens TULP1 mRNA for tubby-related protein 1, complete cds, clone: HP07915-RBd95E12
gi|326205368|dbj|AB593123.1|

Nucleotide
PREDICTED: Homo sapiens melanophilin (MLPH), transcript variant X2, mRNA
PREDICTED: Homo sapiens melanophilin (MLPH), transcript variant X2, mRNA
gi|2462577030|ref|XM_054343852.1|

Nucleotide
Homo sapiens cDNA FLJ60288 complete cds, highly similar to Melanophilin
Homo sapiens cDNA FLJ60288 complete cds, highly similar to Melanophilin
gi|194383941|dbj|AK296745.1|

Nucleotide

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Nucleotide