KEGG T01001: 25839

Homo sapiens (human): 25839

Entry

25839 CDS T01001

Gene name

COG4, CDG2J, COD1

Definition

component of oligomeric golgi complex 4

Organism

hsa Homo sapiens (human)

Disease

H00119

Congenital disorders of glycosylation (CDG) type II

Class

SSDB

Motif

Pfam:

COG4 Bac_thur_toxin

Other DBs

NCBI-GI:

NCBI-GeneID:

OMIM:

HGNC:

HPRD:

Ensembl:

Vega:

UniProt:

Structure

PDB:

3HR0

Position

16q22.1

AA seq 768 aa
MGTKMADLDSPPKLSGVQQPSEGVGGGRCSEISAELIRSLTELQELEAVYERLCGEEKVV
ERELDALLEQQNTIESKMVTLHRMGPNLQLIEGDAKQLAGMITFTCNLAENVSSKVRQLD
LAKNRLYQAIQRADDILDLKFCMDGVQTALRSEDYEQAAAHTHRYLCLDKSVIELSRQGK
EGSMIDANLKLLQEAEQRLKAIVAEKFAIATKEGDLPQVERFFKIFPLLGLHEEGLRKFS
EYLCKQVASKAEENLLMVLGTDMSDRRAAVIFADTLTLLFEGIARIVETHQPIVETYYGP
GRLYTLIKYLQVECDRQVEKVVDKFIKQRDYHQQFRHVQNNLMRNSTTEKIEPRELDPIL
TEVTLMNARSELYLRFLKKRISSDFEVGDSMASEEVKQEHQKCLDKLLNNCLLSCTMQEL
IGLYVTMEEYFMRETVNKAVALDTYEKGQLTSSMVDDVFYIVKKCIGRALSSSSIDCLCA
MINLATTELESDFRDVLCNKLRMGFPATTFQDIQRGVTSAVNIMHSSLQQGKFDTKGIES
TDEAKMSFLSDCTKLFSQGIGGEQAQAKFDSCLSDLAAVSNKFRDLLQEGLTELNSTAIK
PQVQPWINSFFSVSHNIEEEEFNDYEANDPWVQQFILNLEQQMAEFKASLSPVIYDSLTG
LMTSLVAVELEKVVLKSTFNRLGGLQFDKELRSLIAYLTTVTTWTIRDKFARLSQMATIL
NLERVTEILDYWGPNSGPLTWRLTPAEVRQVLALRIDFRSEDIKRLRL

NT seq 2307 nt +upstreamnt +downstreamnt
atggggaccaagatggcggaccttgattcgcctccgaagctgtcaggggtgcagcagccg
tctgagggggtgggaggtggccgctgctccgaaatctccgctgagctcattcgctccctg
acagagctgcaggagctggaggctgtatacgaacggctctgcggcgaggagaaagtggtg
gagagagagctggatgctcttttggaacagcaaaacaccattgaaagtaagatggtcact
ctccaccgaatgggtcctaatctgcagctgattgagggagatgcaaagcagctggctgga
atgatcacctttacctgcaacctggctgagaatgtgtccagcaaagttcgtcagcttgac
ctggccaagaaccgcctctatcaggccattcagagagctgatgacatcttggacctgaag
ttctgcatggatggagttcagactgctttgaggagtgaagattatgagcaggctgcagca
catactcatcgctacttgtgcctggacaagtcggtcattgagctcagccgacagggcaaa
gaggggagcatgattgatgccaacctgaaattgctgcaggaagctgagcaacgtctcaaa
gccattgtggcagagaagtttgccattgccaccaaggaaggtgatctgccccaggtggag
cgcttcttcaagatcttcccactgctgggtttgcatgaggagggattaagaaagttctcg
gagtacctttgcaagcaggtggccagtaaagctgaggagaatctgctcatggtgctgggg
acagacatgagtgatcggagagctgcagtcatctttgcagatacacttactcttctgttt
gaagggattgcccgcattgtggagacccaccagccaatagtggagacctattatgggcca
gggagactctataccctgatcaaatatctgcaggtggaatgtgacagacaggtggagaag
gtggtagacaagttcatcaagcaaagggactaccaccagcagttccggcatgttcagaac
aacctgatgagaaattctacaacagaaaaaatcgaaccaagagaactggaccccatcctg
actgaggtcaccctgatgaatgcccgcagtgagctatacttacgcttcctcaagaagagg
attagctctgattttgaggtgggagactccatggcctcagaggaagtaaagcaagagcac
cagaagtgtctggacaaactcctcaataactgccttttgagctgtaccatgcaggagcta
attggcttatatgttaccatggaggagtacttcatgagggagactgtcaataaggctgtg
gctctggacacctatgagaagggccagctgacatccagcatggtggatgatgtcttctac
attgttaagaagtgcattgggcgggctctgtccagctccagcattgactgtctctgtgcc
atgatcaacctcgccaccacagagctggagtctgacttcagggatgttctgtgtaataag
ctgcggatgggctttcctgccaccaccttccaggacatccagcgcggggtgacaagtgcc
gtgaacatcatgcacagcagcctccagcaaggcaaatttgacacaaaaggcatcgagagt
actgacgaggcgaagatgtccttcctgagtgactgcaccaagctcttcagccagggcatt
ggaggggagcaggcccaggccaagtttgacagctgcctttctgacttggccgccgtgtcc
aacaaattccgagacctcttgcaggaagggctgacggagctcaacagcacagccatcaag
ccacaggtgcagccttggatcaacagctttttctccgtctcccacaacatcgaggaggaa
gaattcaatgactatgaggccaacgacccttgggtacaacagttcatccttaacctggag
cagcaaatggcagagttcaaggccagcctgtccccggtcatctacgacagcctaaccggc
ctcatgactagccttgttgccgtcgagttggagaaagtggtgctgaaatccacctttaac
cggctgggtggtctgcagtttgacaaggagctgaggtcgctcattgcctaccttaccacg
gtgaccacctggaccatccgagacaagtttgcccggctctcccagatggccaccatcctc
aatctggagcgggtgaccgagatcctcgattactggggacccaattccggcccattgacg
tggcgcctcacccctgctgaagtgcgccaggtgctggccctgcggatagacttccgcagt
gaagatatcaagaggctgcgcctgtag

All links

Ontology (1)   
   KEGG BRITE (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (22)   
   NCBI-Gene (1)   
   NCBI-GI (15)   
   UniGene (1)   
   HGNC (1)   
   HPRD (1)   
   ENSEMBL-HSA (1)   
   OC (1)   
   VEGA (1)   
Protein sequence (5)   
   UniProt (3)   
   RefSeq(pep) (2)   
DNA sequence (36)   
   RefSeq(nuc) (2)   
   GenBank (17)   
   EMBL (17)   
3D Structure (1)   
   PDB (1)   
Protein domain (2)   
   Pfam (2)   
All databases (71)   

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