KEGG   Homo sapiens (human): 57231
Entry
57231             CDS       T01001                                 
Symbol
SNX14, RGS-PX2, SCAR20
Name
(RefSeq) sorting nexin 14
  KO
K17926  sorting nexin-14
Organism
hsa  Homo sapiens (human)
Disease
H01891  Autosomal recessive spinocerebellar ataxias
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04990 Domain-containing proteins not elsewhere classified [BR:hsa04990]
    57231 (SNX14)
Domain-containing proteins not elsewhere classified [BR:hsa04990]
 Phox homology (PX) domain-containing proteins
  Sorting nexins
   57231 (SNX14)
SSDB
Motif
Pfam: PXA PX Nexin_C RGS
Other DBs
NCBI-GeneID: 57231
NCBI-ProteinID: NP_722523
OMIM: 616105
HGNC: 14977
Ensembl: ENSG00000135317
UniProt: Q9Y5W7
Structure
Position
6:complement(85505496..85593858)
AA seq 946 aa
MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVA
GVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLEN
YQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRR
IHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDE
LHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFI
DDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAV
HVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQ
RIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSK
LNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEG
IVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERND
RRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEF
QEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQH
LEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNY
FMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQ
EHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESI
RLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM
NT seq 2841 nt   +upstreamnt  +downstreamnt
atggtgccctgggtgcggacgatggggcagaagctgaagcagcggctgcgactggacgtg
ggacgcgagatctgccgccagtacccgctgttctgcttcctgctgctctgtctcagcgcc
gcctccctgcttcttaacaggtatattcatattttaatgatcttctggtcatttgttgct
ggagttgtcacattctactgctcactaggacctgattctctcttaccaaatatattcttc
acaataaaatacaaacccaagcagttaggacttcaggaattatttcctcaaggtcatagc
tgtgctgtttgtggtaaagtgaaatgtaaacgacataggccttctttgctacttgaaaac
taccagccatggctagacctgaaaatttcttccaaggttgatgcatctctctcagaggtt
cttgaattagtgttggaaaactttgtttatccgtggtacagggatgtgacagatgatgaa
tcctttgttgatgaactgagaataacattacgtttttttgcatctgtcttaataagaagg
attcacaaggtggatattccatctattataaccaagaaactattaaaagcagcaatgaag
catatagaagtgatagttaaagccagacagaaagtaaaaaatacagagtttttacagcaa
gctgctttagaagaatatggtccagagcttcatgttgctttgagaagtcgaagagatgaa
ttgcactatttaaggaaacttactgaactgctttttccttatattttgcctcctaaagca
acagactgcagatctctgaccttacttataagagagattctgtctggctctgtgttcctt
ccttctttggatttcctagctgatccagatactgtgaatcatttgcttatcatcttcata
gatgacagtccacctgaaaaagcaactgaaccggcttctcctttggttccattcttgcag
aaatttgcagaacctagaaataaaaagccatctgtgctgaagttagaattgaagcaaatc
agagagcaacaagatcttttatttcgttttatgaactttctgaaacaagaaggcgcagtg
cacgtgttgcagttttgtttgactgtggaggaatttaatgatagaattttacgaccagaa
ttatcaaatgatgaaatgctgtctcttcatgaagaattgcagaagatttataaaacatac
tgtttggatgaaagtattgacaaaattagatttgatcccttcattgtagaagagattcaa
agaattgctgaaggcccatacatagatgttgtgaaacttcaaactatgagatgtcttttt
gaagcatatgaacatgttctttcccttttggagaatgtatttactcctatgttctgccat
agtgatgagtatttcagacaacttttaagaggtgcagaatcaccaacacgcaattcaaaa
ttgaacagaggtagcctaagtttggatgattttcggaacacacagaaaaggggagaatca
tttggaatcagcagaataggtagcaaaattaaaggagtattcaaaagtaccacaatggag
ggagctatgttgcctaattatggtgtagctgaaggtgaagatgattttattgaagaaggt
attgttgtaatggaagatgattctccagtggaggctgtgagcacacctaatactccccga
aaccttgctgcatggaaaattagcattccatatgtagacttttttgaggatccctcctct
gaaaggaaggagaaaaaagaaagaattcctgtgttttgtattgatgttgaaagaaatgat
agaagagcagttggacacgagcctgaacattggtctgtctatagaagatatcttgaattc
tatgtacttgaatcaaaactaacagaatttcatggtgcatttcctgatgcccagcttcct
tctaagaggatcattggccccaaaaattatgaattcttaaagtcaaagagggaagagttc
caagaatatctacagaaacttctgcagcatccagaactgagtaatagtcaacttctggca
gactttctttcccctaatggtggggaaacacaatttcttgataagatactaccagatgta
aatcttgggaaaattataaaatctgttcctggaaaactaatgaaagagaaaggtcagcat
ttggaaccttttatcatgaatttcattaattcttgtgagtctccaaagcctaaaccaagt
agaccagaactgaccattctcagccctacttcagaaaacaacaagaagcttttcaatgat
ctgtttaaaaataatgcaaaccgtgctgaaaatacagagagaaagcaaaatcagaattat
tttatggaggtgatgactgtagaaggagtctatgattacctgatgtatgtaggacgggta
gttttccaggttcctgactggcttcatcatctcttaatgggaactcgaatcctctttaaa
aacaccctggaaatgtatactgattactatcttcagtgtaaactagaacagctatttcag
gagcaccgtttggtctcactcataacacttctcagagatgctatattctgtgaaaacact
gaacctcgctctctccaagataagcaaaaaggagcaaaacagacttttgaagaaatgatg
aattacattccagatctgttagtcaagtgtattggtgaagaaaccaagtatgaaagcatc
agacttctgtttgatggcttacagcaaccagtactcaacaagcagctgacttatgtttta
ttggacattgtgatacaggaactgtttccagagctcaataaggtacaaaaggaagttacc
tctgtgacatcttggatgtaa

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (16)   
   KEGG ORTHOLOGY (1)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (52)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (50)   
DNA sequence (92)   
   RefSeq(nuc) (56)   
   GenBank (18)   
   EMBL (18)   
3D Structure (3)   
   PDB (3)   
Protein domain (4)   
   Pfam (4)   
All databases (173)   

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