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Reactome (instancebrowser)
Reactome: A Curated Pathway Database
Class:IdReferenceGeneProduct:153454
_displayNameUniProt:Q9NRA2 SLC17A5
_timestamp2014-09-22 15:58:49
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.SIMILARITY Belongs to the major facilitator superfamily. Sodium/anion cotransporter family.
created[InstanceEdit:143527] Schmidt, EE, 2004-11-12 07:45:10
crossReference[DatabaseIdentifier:6613098] PRO:Q9NRA2
[DatabaseIdentifier:6625757] GeneCards:Q9NRA2
[DatabaseIdentifier:6649945] UCSC human:Q9NRA2
[DatabaseIdentifier:6653615] RefSeq:NP_036566
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:6348050] Croft, D
[InstanceEdit:6379983] Croft, D
[InstanceEdit:6413044] Croft, D
[InstanceEdit:6446105] Croft, D
[InstanceEdit:6479166] Croft, D
[InstanceEdit:6512227] Croft, D
[InstanceEdit:6618954] Croft, D
[InstanceEdit:6636231] Croft, D
[InstanceEdit:6643142] Croft, D
[InstanceEdit:6650745] Croft, D
[InstanceEdit:6682804] Croft, D
[InstanceEdit:6698332] Croft, D
nameSLC17A5
otherIdentifierMIM:604322
10581036
AAH20961
NP_036566
PH_hs_0006462
223441_at
11758156_s_at
uc003phn.4
IPR011701
2960968
0001230066
HPA044479
AL590428
BC020961
88617_at
Hs.703047
ILMN_3251399
2960961
A_33_P3416321
2960995
XP_005248767
8127549
A_23_P110896
2960980
GE58496
AF244577
11753191_a_at
8198127
26503
AL121972
SLC17A5
2960979
2960971
2960959
11723477_x_at
PF07690
2960983
SLC17A5-001
2960982
g6912665_3p_a_at
11723476_at
OTTHUMP00000016747
XM_005248710
EntrezGene:26503
2960994
2960970
2960978
2960964
CAI15635
ILMN_1684434
A_33_P3265270
EAW48756
221041_s_at
Hs.597422
2960996
ENSG00000119899
2960962
2960972
CH471051
CAB62540
H0UI05
AJ387747
2960977
BAC11546
XP_005248768
EAW48757
ENSP00000348019
UPI000003B2DE
ILMN_1771317
2960960
HGNC:10933
65644_at
CCDS4981
2960963
NM_012434
2960997
AK075320
MIM:604369
MIM:269920
AAF97769
IPR020846
17020823
Hs.117865.1.S2_3p_at
11752119_x_at
CAI20417
IPR016196
referenceDatabase[ReferenceDatabase:2] UniProt
referenceGene[ReferenceDNASequence:6707593] KEGG Gene:26503 solute carrier family 17 (acidic sugar transporter), member 5 [Homo sapiens]
[ReferenceDNASequence:6351126] ENSEMBL:ENSG00000119899 [Homo sapiens]
[ReferenceDNASequence:6383090] NCBI Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6443127] BioGPS Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6476188] CTD Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6509249] dbSNP Gene:26503 [Homo sapiens]
[ReferenceDNASequence:6637479] OMIM:269920 [Homo sapiens]
[ReferenceDNASequence:6637480] OMIM:604369 [Homo sapiens]
[ReferenceDNASequence:6637481] OMIM:604322 [Homo sapiens]
[ReferenceDNASequence:6723172] Orphanet:15303 [Homo sapiens]
referenceTranscript[ReferenceRNASequence:6685572] RefSeq:NM_012434
secondaryIdentifierS17A5_HUMAN
Q5SZ76
Q8NBR5
Q9UGH0
sequenceLength495
species[Species:48887] Homo sapiens
(referenceEntity)[EntityWithAccessionedSequence:428624] SLC17A5 [lysosomal membrane] [Homo sapiens]
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