Homo sapiens family with sequence similarity 177 member A1 (FAM177A1), - Nucleotide

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Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder. [Genet Med. 2024]
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder.
Kohler JN, Legro NR, Baldridge D, Shin J, Bowman A, Ugur B, Jackstadt MM, Shriver LP, Patti GJ, Zhang B, et al. Genet Med. 2024 Sep; 26(9):101166. Epub 2024 May 17.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing. [Neuro Oncol. 2023]
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing.
Demirdizen E, Al-Ali R, Narayanan A, Sun X, Varga JP, Steffl B, Brom M, Krunic D, Schmidt C, Schmidt G, et al. Neuro Oncol. 2023 Jun 2; 25(6):1031-1043.
FAM177A1 Inhibits IL-1β-Induced Signaling by Impairing TRAF6-Ubc13 Association. [J Immunol. 2021]
FAM177A1 Inhibits IL-1β-Induced Signaling by Impairing TRAF6-Ubc13 Association.
Liao BW, Zhang HY, Du WT, Ran Y, Wang YY, Xu ZS. J Immunol. 2021 Dec 15; 207(12):3090-3097. Epub 2021 Nov 19.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the FAM177A1 gene.

NHERF4[gene] (75)
ClinVar
protein FAM177A1 isoform 2 [Homo sapiens]
protein FAM177A1 isoform 2 [Homo sapiens]
gi|573459759|ref|NP_001275951.1|

Protein
Na(+)/H(+) exchange regulatory cofactor NHE-RF4 isoform X7 [Homo sapiens]
Na(+)/H(+) exchange regulatory cofactor NHE-RF4 isoform X7 [Homo sapiens]
gi|2462527704|ref|XP_054225974.1|

Protein
PREDICTED: Homo sapiens NHERF family PDZ scaffold protein 4 (NHERF4), transcript...
PREDICTED: Homo sapiens NHERF family PDZ scaffold protein 4 (NHERF4), transcript variant X3, mRNA
gi|2217284747|ref|XM_011543005.3|

Nucleotide
cytochrome b (mitochondrion) [Rhipidura maculipectus]
cytochrome b (mitochondrion) [Rhipidura maculipectus]
gi|2371279688|gb|WAB21746.1|

Protein

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Nucleotide