GediPNet logo

AASS (aminoadipate-semialdehyde synthase)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10157
Gene nameGene Name - the full gene name approved by the HGNC.
Aminoadipate-semialdehyde synthase
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
AASS
SynonymsGene synonyms aliases
LKR/SDH, LKRSDH, LORSDH
ChromosomeChromosome number
7
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q31.32
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activit
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs387906333 CTTGTTTAC>- Pathogenic Non coding transcript variant, coding sequence variant, inframe indel, stop gained
rs587777121 CTTAC>AA Pathogenic Intron variant, splice donor variant
rs587777122 T>C Pathogenic Coding sequence variant, non coding transcript variant, missense variant
rs587777123 TG>- Pathogenic Coding sequence variant, frameshift variant, non coding transcript variant
rs587777124 G>C Pathogenic Coding sequence variant, stop gained, non coding transcript variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT527611 hsa-miR-591 PAR-CLIP 22012620
MIRT527610 hsa-miR-653-5p PAR-CLIP 22012620
MIRT527611 hsa-miR-591 PAR-CLIP 22012620
MIRT527610 hsa-miR-653-5p PAR-CLIP 22012620
MIRT757550 hsa-miR-1262 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II ISS
GO:0003714 Function Transcription corepressor activity ISS
GO:0004753 Function Saccharopine dehydrogenase activity IBA 21873635
GO:0004754 Function Saccharopine dehydrogenase (NAD+, L-lysine-forming) activity ISS
GO:0005634 Component Nucleus ISS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q9UDR5
Protein name Alpha-aminoadipic semialdehyde synthase, mitochondrial (LKR/SDH) [Includes: Lysine ketoglutarate reductase (LKR) (LOR) (EC 1.5.1.8); Saccharopine dehydrogenase (SDH) (EC 1.5.1.9)]
Protein function Bifunctional enzyme that catalyzes the first two steps in lysine degradation.
PDB 5L76 , 5L78 , 5O1N , 5O1O , 5O1P , 8DDA , 8E8T , 8E8U , 8E8V
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05222 AlaDh_PNT_N
27 157
Alanine dehydrogenase/PNT, N-terminal domain
Domain
PF03435 Sacchrp_dh_NADP
483 598
Saccharopine dehydrogenase NADP binding domain
Family
PF16653 Sacchrp_dh_C
602 916
Saccharopine dehydrogenase C-terminal domain
Domain
Sequence
MLQVHRTGLGRLGVSLSKGLHHKAVLAVRREDVNAWERRAPLAPKHIKGITNLGYKVLIQ
PSNRRAIHDKDYVKAGGILQEDISEACLILGVKRPPEEKLMSRKTYAFFSHTIKAQEANM
GLLDEILKQEIRLIDYEKMVDHRGVRVVAFGQWAGVA
GMINILHGMGLRLLALGHHTPFM
HIGMAHNYRNSSQAVQAVRDAGYEISLGLMPKSIGPLTFVFTGTGNVSKGAQAIFNELPC
EYVEPHELKEVSQTGDLRKVYGTVLSRHHHLVRKTDAVYDPAEYDKHPERYISRFNTDIA
PYTTCLINGIYWEQNTPRLLTRQDAQSLLAPGKFSPAGVEGCPALPHKLVAICDISADTG
GSIEFMTECTTIEHPFCMYDADQHIIHDSVEGSGILMCSIDNLPAQLPIEATECFGDMLY
PYVEEMILSDATQPLESQNFSPVVRDAVITSNGTLPDKYKYIQTLRESRERAQSLSMGTR
RKVLVLGSGYISEPVLEYLSRDGNIEITVGSDMKNQIEQLGKKYNINPVSMDICKQEEKL
GFLVAKQDLVISLLPYVLHPLVAKACITNKVNMVTASYITPALKELEKSVEDAGITII
GE
LGLDPGLDHMLAMETIDKAKEVGATIESYISYCGGLPAPEHSNNPLRYKFSWSPVGVLMN
VMQSATYLLDGKVVNVAGGISFLDAVTSMDFFPGLNLEGYPNRDSTKYAEIYGISSAHTL
LRGTLRYKGYMKALNGFVKLGLINREALPAFRPEANPLTWKQLLCDLVGISPSSEHDVLK
EAVLKKLGGDNTQLEAAEWLGLLGDEQVPQAESILDALSKHLVMKLSYGPEEKDMIVMRD
SFGIRHPSGHLEHKTIDLVAYGDINGFSAMAKTVGLPTAMAAKMLLDGEIGAKGLMGPFS
KEIYGPILERIKAEGI
IYTTQSTIKP
Sequence length 926
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Lysine degradation
Metabolic pathways
  Lysine catabolism
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Anemia Anemia rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505
Citrullinemia Citrullinemia rs80338722, rs80338725, rs80338719, rs80338723, rs80338726, rs121908636, rs121908638, rs121908639, rs121908640, rs121908641, rs121908642, rs121908643, rs121908644, rs121908645, rs121908646, rs121908647, rs80338721, rs80338724, rs80338715, rs80338727, rs80338729, rs80338716, rs80338717, rs398122839, rs398123130, rs192838388, rs148918985, rs398123131, rs371265106, rs727503814, rs786204648, rs770362721, rs786204537, rs786204460, rs751930594, rs771937610, rs777828000, rs80338720, rs1085307056, rs746155190, rs575001023, rs763389916, rs886039853, rs372128852, rs1057516960, rs1057516648, rs1057516544, rs1057516339, rs1057517259, rs982830431, rs762387914, rs1057516338, rs1057517402, rs763191789, rs1057520659, rs1060499612, rs765338121, rs758827458, rs1554725034, rs1439911743, rs936192871, rs1554725677, rs1554982237, rs756859126, rs1554982809, rs1554983719, rs1396766124, rs750780742, rs1554982824, rs1554722453, rs1554723160, rs1554723625, rs1554725033, rs1554982243, rs770944877, rs750214431, rs1213378896, rs1554982847, rs201623252, rs1554983717, rs1301613270, rs775791516, rs1564903969, rs1262020902, rs1562831765, rs962082210, rs748264993, rs1004492719, rs1261058897, rs771794639, rs761370420, rs768922690, rs1588475891, rs745404241, rs775305020, rs770585183, rs1313340299, rs374586230, rs1588495489, rs1588496214, rs1588508532, rs1312396424, rs1482630982, rs1846142146, rs549085827, rs1488840592
Ectopia lentis Ectopia Lentis rs118203985, rs137854464, rs137854480, rs587776927, rs199473693, rs794726688, rs368482584, rs794726689, rs747160538, rs397514558, rs397515793, rs757318536, rs781691587, rs363806
Hyperlysinemia Hyperlysinemias, Hyperlysinemia, type I, Hyperlysinemia rs387906333, rs587777121, rs587777122, rs587777123, rs587777124, rs587777125, rs587777126 23890588, 10775527, 23570448, 27604308, 27626380, 4385118, 10775527, 27604308
Unknown
Disease name Disease term dbSNP ID References
Alpha-aminoadipic semialdehyde deficiency disease Alpha-Aminoadipic Semialdehyde Deficiency Disease
Dwarfism Dwarfism
Histidine transport defect Histidinuria renal tubular defect
Impaired cognition Impaired cognition

| © 2021, Biomedical Informatics Centre, NIRRH |
ICMR-National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400012
Tel: +91-22-24192104, Fax No: +91-22-24139412