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SGPL1

SGPL1

Enzyme

Sphingosine-1-phosphate lyase 1 is an enzyme that, in humans, is encoded by the SGPL1 gene. A mutation in the gene can lead to sphingosine phosphate lyase insufficiency

SGPL1

ISLR

Protein-coding gene in the species Homo sapiens

ISLR with Rho GTP-family (RHOBTB3), BMP7, Sphingose-1-Phosphate Lyase (SGPL1), Carnitine-acylcarnitine translocase (SLC25A20), Canopy FGF Signaling regulator

ISLR

Alpha oxidation

Metabolic pathway

by SPHK2. PHS-1P is converted to 2-hydroxypalmital (2-OH C16:0-CHO) by SGPL1. 2-OH C16:0-CHO is converted to 2-hydroxypalmitate (2-OH C16:0-COOH) by

Alpha oxidation

Alpha_oxidation

Chromosome 10

Human chromosome

encoding protein Schizophrenia susceptibility locus, chromosome 10q-related SGPL1: sphingosine-1-phosphate lyase 1 SHTN1: encoding protein Shootin 1 SLC16A12:

Chromosome 10

Chromosome_10

TMEM242

Protein-coding gene in the species Homo sapiens

ARID1B, SIAE, EDARADD, URB1, ZDHHC14, KIF11, RRM2, KCTD13, TMEM31, NDUFA3, SGPL1, CNR2, and GJA8. All of the listed proteins have known functions. The tmem242

TMEM242

List of human protein-coding genes 7

Q8NHU3 14683 SGO1 HGNC:25088; Q5FBB7 14684 SGO2 HGNC:30812; Q562F6 14685 SGPL1 HGNC:10817; O95470 14686 SGPP1 HGNC:17720; Q9BX95 14687 SGPP2 HGNC:19953;

List of human protein-coding genes 7

List_of_human_protein-coding_genes_7

Sphingosine phosphate lyase insufficiency syndrome

Medical condition

(SPLIS) is a rare autosomal recessive disorder caused by mutations in the SGPL1 gene located on human chromosome 10. It is also known as Renal, Endocrine

Sphingosine phosphate lyase insufficiency syndrome

Sphingosine_phosphate_lyase_insufficiency_syndrome

FAM177A1

Protein-coding gene in the species Homo sapiens

human proteins: Aquaporin-6 Caspase 6 DPM3 ELOVL4 FATE1 JAGN1 LAMP2 PBX3 SGPL1 SH3GLB1 TMX2 GRCh38: Ensembl release 89: ENSG00000151327 – Ensembl, May

FAM177A1