instancebrowser | sectioned | sidebarwithdynamichierarchy
Reactome (instancebrowser)
Reactome: A Curated Pathway Database
Class:IdReferenceGeneProduct:153454
_displayNameUniProt:Q9NRA2 SLC17A5
_timestamp2014-11-25 17:11:00
checksum5C6C154B3E93A19E
commentDISEASE Infantile sialic acid storage disorder is associated with non-immune hydrops fetalis, a generalized edema of the fetus with fluid accumulation in the body cavities due to non-immune causes. Non-immune hydrops fetalis is not a diagnosis in itself but a symptom, a feature of many genetic disorders, and the end-stage of a wide variety of disorders.
created[InstanceEdit:143527] Schmidt, EE, 2004-11-12 07:45:10
crossReference[DatabaseIdentifier:6603515] PRO:Q9NRA2
[DatabaseIdentifier:6616075] GeneCards:Q9NRA2
[DatabaseIdentifier:6640618] UCSC human:Q9NRA2
[DatabaseIdentifier:6644296] RefSeq:NP_036566
[DatabaseIdentifier:6715202] HMDB_protein:HMDBP02797
descriptionrecommendedName: Sialin alternativeName: H(+)/nitrate cotransporter alternativeName: H(+)/sialic acid cotransporter shortName:AST alternativeName: Membrane glycoprotein HP59 alternativeName: Solute carrier family 17 member 5 alternativeName: Vesicular H(+)/Aspartate-glutamate cotransporter
geneNameSLC17A5
identifierQ9NRA2
isSequenceChangedFALSE
keywordAlternative splicing
Amino-acid transport
Cell junction
Cell membrane
Complete proteome
Cytoplasmic vesicle
Disease mutation
Glycoprotein
Lysosome
Membrane
Reference proteome
Symport
Synapse
Transmembrane
Transmembrane helix
Transport
modified[InstanceEdit:217385] Schmidt, EE, 2008-03-27 06:23:53
[InstanceEdit:354386] Schmidt, EE, 2008-06-18 04:45:12
[InstanceEdit:384350] Kanapin, AA, 2008-11-26 14:00:39
[InstanceEdit:392885] Kanapin, AA, 2009-03-09 12:07:18
[InstanceEdit:400710] Schmidt, EE, 2009-03-25 05:33:35
[InstanceEdit:423310] Kanapin, AA
[InstanceEdit:435478] Kanapin, AA
[InstanceEdit:435871] Kanapin, AA
[InstanceEdit:447347] Kanapin, AA
[InstanceEdit:525883] Kanapin, AA
[InstanceEdit:613449] Kanapin, AA
[InstanceEdit:797602] Kanapin, AA
[InstanceEdit:937368] Yung, CK
[InstanceEdit:1042053] Yung, CK
[InstanceEdit:1220657] Yung, CK
[InstanceEdit:1300696] Yung, CK
[InstanceEdit:1301627] Yung, CK
[InstanceEdit:1551960] Weiser, JD
[InstanceEdit:1995863] Weiser, JD
[InstanceEdit:2132304] Weiser, JD
[InstanceEdit:2265580] Weiser, JD
[InstanceEdit:3132113] Weiser, JD
[InstanceEdit:3445779] Weiser, JD
[InstanceEdit:4341137] Weiser, JD
[InstanceEdit:5433710] Weiser, JD
[InstanceEdit:5618415] Weiser, JD
[InstanceEdit:5634237] Weiser, JD
[InstanceEdit:6348073] Croft, D
[InstanceEdit:6378953] Croft, D
[InstanceEdit:6410971] Croft, D
[InstanceEdit:6442989] Croft, D
[InstanceEdit:6475007] Croft, D
[InstanceEdit:6507025] Croft, D
[InstanceEdit:6609128] Croft, D
[InstanceEdit:6626660] Croft, D
[InstanceEdit:6633671] Croft, D
[InstanceEdit:6641434] Croft, D
[InstanceEdit:6672501] Croft, D
[InstanceEdit:6688369] Croft, D
[InstanceEdit:6715121] Croft, D
nameSLC17A5
otherIdentifier0001230066
11723476_at
11723477_x_at
11752119_x_at
11753191_a_at
11758156_s_at
17020823
221041_s_at
223441_at
26503
2960959
2960961
2960962
2960964
2960968
2960971
2960977
2960978
2960982
2960994
2960995
2960996
65644_at
8127549
88617_at
A_23_P110896
A_33_P3265270
A_33_P3416321
AF244577
AJ387747
AK075320
AL121972
AL590428
BC020961
CCDS4981
CH471051
ENSG00000119899
ENSP00000348019
ENST00000355773
EntrezGene:26503
g6912665_3p_a_at
GE58496
H0UI05
HGNC:10933
HPA044479
Hs.117865.1.S2_3p_at
Hs.597422
Hs.703047
ILMN_1684434
ILMN_1771317
ILMN_3251399
IPR011701
IPR016196
IPR020846
MIM:269920
MIM:604322
MIM:604369
NM_012434
NP_036566
OTTHUMP00000016747
PF07690
PH_hs_0006462
SLC17A5
SLC17A5-001
TC06001876.hg
uc003phn.4
UPI000003B2DE
XM_005248710
XP_005248767
XP_005248768
referenceDatabase[ReferenceDatabase:2] UniProt
referenceGene[ReferenceDNASequence:6697780] KEGG Gene:26503 solute carrier family 17 (acidic sugar transporter), member 5 [Homo sapiens]
[ReferenceDNASequence:6351080] ENSEMBL:ENSG00000119899 [Homo sapiens]
[ReferenceDNASequence:6381948] NCBI Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6440145] BioGPS Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6472163] CTD Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6504181] dbSNP Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6627927] OMIM:269920 [Homo sapiens]
[ReferenceDNASequence:6627928] OMIM:604369 [Homo sapiens]
[ReferenceDNASequence:6627929] OMIM:604322 [Homo sapiens]
[ReferenceDNASequence:6700621] Orphanet:15303 [Homo sapiens]
referenceTranscript[ReferenceRNASequence:6675335] RefSeq:NM_012434
secondaryIdentifierS17A5_HUMAN
Q5SZ76
Q8NBR5
Q9UGH0
sequenceLength495
species[Species:48887] Homo sapiens
(referenceEntity)[EntityWithAccessionedSequence:428624] SLC17A5 [lysosomal membrane] [Homo sapiens]
[Change default viewing format]