KEGG T01001: 1811

Homo sapiens (human): 1811

Entry

1811 CDS T01001

Gene name

SLC26A3, CLD, DRA

Definition

solute carrier family 26, member 3

Orthology

K14078

solute carrier family 26 (chloride anion exchanger), member 3

Organism

hsa Homo sapiens (human)

Pathway

hsa04972	Pancreatic secretion
hsa04978	Mineral absorption

Disease

H01174

Congenital diarrhea

Class

Organismal Systems; Digestive system; Pancreatic secretion [PATH:hsa04972]
Organismal Systems; Digestive system; Mineral absorption [PATH:hsa04978]

SSDB

Motif

Pfam:

Sulfate_transp STAS Sulfate_tra_GLY

Other DBs

NCBI-GI:

NCBI-GeneID:

OMIM:

HGNC:

HPRD:

Ensembl:

Vega:

UniProt:

Position

7q31

AA seq 764 aa
MIEPFGNQYIVARPVYSTNAFEENHKKTGRHHKTFLDHLKVCCSCSPQKAKRIVLSLFPI
ASWLPAYRLKEWLLSDIVSGISTGIVAVLQGLAFALLVDIPPVYGLYASFFPAIIYLFFG
TSRHISVGPFPILSMMVGLAVSGAVSKAVPDRNATTLGLPNNSNNSSLLDDERVRVAAAA
SVTVLSGIIQLAFGILRIGFVVIYLSESLISGFTTAAAVHVLVSQLKFIFQLTVPSHTDP
VSIFKVLYSVFSQIEKTNIADLVTALIVLLVVSIVKEINQRFKDKLPVPIPIEFIMTVIA
AGVSYGCDFKNRFKVAVVGDMNPGFQPPITPDVETFQNTVGDCFGIAMVAFAVAFSVASV
YSLKYDYPLDGNQELIALGLGNIVCGVFRGFAGSTALSRSAVQESTGGKTQIAGLIGAII
VLIVVLAIGFLLAPLQKSVLAALALGNLKGMLMQFAEIGRLWRKDKYDCLIWIMTFIFTI
VLGLGLGLAASVAFQLLTIVFRTQFPKCSTLANIGRTNIYKNKKDYYDMYEPEGVKIFRC
PSPIYFANIGFFRRKLIDAVGFSPLRILRKRNKALRKIRKLQKQGLLQVTPKGFICTVDT
IKDSDEELDNNQIEVLDQPINTTDLPFHIDWNDDLPLNIEVPKISLHSLILDFSAVSFLD
VSSVRGLKSILQEFIRIKVDVYIVGTDDDFIEKLNRYEFFDGEVKSSIFFLTIHDAVLHI
LMKKDYSTSKFNPSQEKDGKIDFTINTNGGLRNRVYEVPVETKF

NT seq 2295 nt +upstreamnt +downstreamnt
atgattgaaccctttgggaatcagtatattgtggccaggccagtgtattctacaaatgct
tttgaggaaaatcataaaaagacaggaagacatcataagacatttctggatcatctcaaa
gtgtgttgtagctgttccccacaaaaggccaagagaattgtcctctctttgttccccata
gcatcttggttgccagcataccggcttaaagaatggttgctcagtgatattgtttctggt
atcagcacagggattgtggccgtactacaaggtttagcatttgctctgctggtcgacatt
cccccagtctatgggttgtatgcatcctttttcccagccataatctaccttttcttcggc
acttccagacacatatccgtgggtccgtttccgattctgagtatgatggtgggactagca
gtttcaggagcagtttcaaaagcagtcccagatcgcaatgcaactactttgggattgcct
aacaactcgaataattcttcactactggatgacgagagggtgagggtggcggcggcggca
tcagtcacagtgctttctggaatcatccagttggcttttgggattctgcggattggattt
gtagtgatatacctgtctgagtccctcatcagtggcttcactactgctgctgctgttcat
gttttggtttcccaactcaaattcatttttcagttgacagtcccgtcacacactgatcca
gtttcaattttcaaagtactatactctgtattctcacaaatagagaagactaatattgca
gacctggtgacagctctgattgtccttttggttgtatccattgttaaagaaataaatcag
cgcttcaaagacaaacttccagtgcccattccaatcgaattcattatgaccgtgattgca
gcaggtgtatcctacggctgtgactttaaaaacaggtttaaagtggctgtggttggggac
atgaatcctggatttcagccccctattacacctgacgtggagactttccaaaacaccgta
ggagattgcttcggcatcgcaatggttgcatttgcagtggccttttcagttgccagcgtc
tattccctcaaatacgattatccacttgatggcaatcaggagttaatagccttgggactg
ggtaacatagtctgtggagtattcagaggatttgctgggagtactgccctctccagatca
gcagttcaggagagcacaggaggcaaaacacagattgctgggcttattggtgccatcatc
gtgctgattgtcgttctagccattggatttctcctggcgcctctacaaaagtccgtcctg
gcagctttagcattgggaaacttaaagggaatgctgatgcagtttgctgaaataggcaga
ttgtggcgaaaggacaaatatgattgtttaatttggatcatgaccttcatcttcaccatt
gtcctgggactcgggttaggcctggcagctagtgtggcatttcaactgctaaccatcgtg
ttcaggacccaatttccaaaatgcagcacgctggctaatattggaagaaccaacatctat
aagaataaaaaagattattatgatatgtatgagccagaaggagtgaaaattttcagatgt
ccatctcctatctactttgcaaacattggtttctttaggcggaaacttatcgatgctgtt
ggctttagtccacttcgaattctacgcaagcgcaacaaagctttgaggaaaatccgaaaa
ctgcagaagcaaggcttgctacaagtgacaccaaaaggatttatatgtactgttgacacc
ataaaagattctgacgaagagctggacaacaatcagatagaagtactggaccagccaatc
aataccacagacctgcctttccacattgactggaatgatgatcttcctctcaacattgag
gtccccaaaatcagcctccacagcctcattcttgacttttcagcagtgtcctttcttgat
gtttcttcagtgaggggccttaaatcgattttgcaagaatttatcaggatcaaggtagat
gtgtatatcgttggaactgatgatgacttcattgagaagcttaaccggtatgaatttttt
gatggtgaagtgaaaagctcaatatttttcttaacaatccatgatgctgttttgcatatt
ttgatgaagaaagattacagtacttcaaagtttaatcccagtcaggaaaaagatggaaaa
attgattttaccataaatacaaatggaggattacgtaatcgggtatatgaggtgccagtt
gaaacaaaattctaa

All links

Ontology (1)   
   KEGG BRITE (1)   
Pathway (2)   
   KEGG PATHWAY (2)   
Disease (2)   
   KEGG DISEASE (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (15)   
   KEGG ORTHOLOGY (1)   
   NCBI-Gene (1)   
   NCBI-GI (7)   
   UniGene (1)   
   HGNC (1)   
   HPRD (1)   
   ENSEMBL-HSA (1)   
   OC (1)   
   VEGA (1)   
Protein sequence (2)   
   UniProt (1)   
   RefSeq(pep) (1)   
DNA sequence (15)   
   RefSeq(nuc) (1)   
   GenBank (7)   
   EMBL (7)   
Protein domain (3)   
   Pfam (3)   
All databases (41)   

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