Homo sapiens solute carrier family 25 member 36 (SLC25A36), transcript - Nucleotide

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Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation. [J Inherit Metab Dis. 2023]
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation.
Safran A, Proskorovski-Ohayon R, Eskin-Schwartz M, Yogev Y, Drabkin M, Eremenko E, Aharoni S, Freund O, Jean MM, Agam N, et al. J Inherit Metab Dis. 2023 Jul; 46(4):744-755. Epub 2023 Feb 9.
Human transcription factor protein interaction networks. [Nat Commun. 2022]
Human transcription factor protein interaction networks.
Göös H, Kinnunen M, Salokas K, Tan Z, Liu X, Yadav L, Zhang Q, Wei GH, Varjosalo M. Nat Commun. 2022 Feb 9; 13(1):766. Epub 2022 Feb 9.
PNC2 (SLC25A36) Deficiency Associated With the Hyperinsulinism/Hyperammonemia Syndrome. [J Clin Endocrinol Metab. 2022]
PNC2 (SLC25A36) Deficiency Associated With the Hyperinsulinism/Hyperammonemia Syndrome.
Shahroor MA, Lasorsa FM, Porcelli V, Dweikat I, Di Noia MA, Gur M, Agostino G, Shaag A, Rinaldi T, Gasparre G, et al. J Clin Endocrinol Metab. 2022 Apr 19; 107(5):1346-1356.

RefSeq protein product
See the reference protein sequence for solute carrier family 25 member 36 isoform b (NP_060625.2).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens solute carrier family 25 member 36 (SLC25A36), transcript variant 2...
Homo sapiens solute carrier family 25 member 36 (SLC25A36), transcript variant 2, mRNA
gi|1676319092|ref|NM_018155.3|

Nucleotide
Lwq21 liver weight QTL 21 [Mus musculus]
Lwq21 liver weight QTL 21 [Mus musculus]
Gene ID:493000

Gene

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Nucleotide