Homo sapiens (human): 57620
Entry
57620 CDS
T01001
Gene name
STIM2
Definition
(RefSeq) stromal interaction molecule 2
KO
K18196
stromal interaction molecule 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04020
Calcium signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
57620 (STIM2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
57620 (STIM2)
Transporters [BR:
hsa02000
]
Other transporters
Pores ion channels [TC:
1
]
57620 (STIM2)
SSDB
Motif
Pfam:
SOAR
SAM_2
SAM_1
SAM_Ste50p
ESSS
DUF4446
Other DBs
NCBI-GeneID:
57620
NCBI-ProteinID:
NP_065911
OMIM:
610841
HGNC:
19205
Ensembl:
ENSG00000109689
Vega:
OTTHUMG00000097805
Pharos:
Q9P246
(Tbio)
UniProt:
Q9P246
B3KUB5
LinkDB
Structure
PDB:
2L5Y
Position
4p15.2
AA seq
746 aa
MLVLGLLVAGAADGCELVPRHLRGRRATGSAATAASSPAAAAGDSPALMTDPCMSLSPPC
FTEEDRFSLEALQTIHKQMDDDKDGGIEVEESDEFIREDMKYKDATNKHSHLHREDKHIT
IEDLWKRWKTSEVHNWTLEDTLQWLIEFVELPQYEKNFRDNNVKGTTLPRIAVHEPSFMI
SQLKISDRSHRQKLQLKALDVVLFGPLTRPPHNWMKDFILTVSIVIGVGGCWFAYTQNKT
SKEHVAKMMKDLESLQTAEQSLMDLQERLEKAQEENRNVAVEKQNLERKMMDEINYAKEE
ACRLRELREGAECELSRRQYAEQELEQVRMALKKAEKEFELRSSWSVPDALQKWLQLTHE
VEVQYYNIKRQNAEMQLAIAKDEAEKIKKKRSTVFGTLHVAHSSSLDEVDHKILEAKKAL
SELTTCLRERLFRWQQIEKICGFQIAHNSGLPSLTSSLYSDHSWVVMPRVSIPPYPIAGG
VDDLDEDTPPIVSQFPGTMAKPPGSLARSSSLCRSRRSIVPSSPQPQRAQLAPHAPHPSH
PRHPHHPQHTPHSLPSPDPDILSVSSCPALYRNEEEEEAIYFSAEKQWEVPDTASECDSL
NSSIGRKQSPPLSLEIYQTLSPRKISRDEVSLEDSSRGDSPVTVDVSWGSPDCVGLTETK
SMIFSPASKVYNGILEKSCSMNQLSSGIPVPKPRHTSCSSAGNDSKPVQEAPSVARISSI
PHDLCHNGEKSKKPSKIKSLFKKKSK
NT seq
2241 nt
+upstream
nt +downstream
nt
ttgctggtgctcgggctgctggtagccggagcggcggacggatgcgagcttgtgccccgg
cacctccgcgggcggcgggcgactggctctgccgcaactgccgcctcctctcccgccgcg
gcggccggcgatagcccggcgctcatgacagatccctgcatgtcactgagtccaccatgc
tttacagaagaagacagatttagtctggaagctcttcaaacaatacataaacaaatggat
gatgacaaagatggtggaattgaagtagaggaaagtgatgaattcatcagagaagatatg
aaatataaagatgctactaataaacacagccatctgcacagagaagataaacatataacg
attgaggatttatggaaacgatggaaaacatcagaagttcataattggacccttgaagac
actcttcagtggttgatagagtttgttgaactaccccaatatgagaagaattttagagac
aacaatgtcaaaggaacgacacttcccaggatagcagtgcacgaaccttcatttatgatc
tcccagttgaaaatcagtgaccggagtcacagacaaaaacttcagctcaaggcattggat
gtggttttgtttggacctctaacacgcccacctcataactggatgaaagattttatcctc
acagtttctatagtaattggtgttggaggctgctggtttgcttatacgcagaataagaca
tcaaaagaacatgttgcaaaaatgatgaaagatttagagagcttacaaactgcagagcaa
agtctaatggacttacaggagaggcttgaaaaggcacaggaagaaaacagaaatgttgct
gtagaaaagcaaaatttagagcgcaaaatgatggatgaaatcaattatgcaaaggaggag
gcttgtcggctgagagagctaagggagggagctgaatgtgaattgagtagacgtcagtat
gcagaacaggaattggaacaggttcgcatggctctgaaaaaggccgaaaaagaatttgaa
ctgagaagcagttggtctgttccagatgcacttcagaaatggcttcagttaacacatgaa
gtagaagtgcaatactacaatattaaaagacaaaacgctgaaatgcagctagctattgct
aaagatgaggcagaaaaaattaaaaagaagagaagcacagtctttgggactctgcacgtt
gcacacagctcctccctagatgaggtagaccacaaaattctggaagcaaagaaagctctc
tctgagttgacaacttgtttacgagaacgactttttcgctggcaacaaattgagaagatc
tgtggctttcagatagcccataactcaggactccccagcctgacctcttccctttattct
gatcacagctgggtggtgatgcccagagtctccattccaccctatccaattgctggagga
gttgatgacttagatgaagacacacccccaatagtgtcacaatttcccgggaccatggct
aaacctcctggatcattagccagaagcagcagcctgtgccgttcacgccgcagcattgtg
ccgtcctcgcctcagcctcagcgagctcagcttgctccacacgccccccacccgtcacac
cctcggcaccctcaccacccgcaacacacaccacactccttgccttcccctgatccagat
atcctctcagtgtcaagttgccctgcgctttatcgaaatgaagaggaggaagaggccatt
tacttctctgctgaaaagcaatgggaagtgccagacacagcttcagaatgtgactcctta
aattcttccattggaaggaaacagtctcctcctttaagcctcgagatataccaaacatta
tctccgcgaaagatatcaagagatgaggtgtccctagaggattcctcccgaggggattcg
cctgtaactgtggatgtgtcttggggttctcccgactgtgtaggtctgacagaaactaag
agtatgatcttcagtcctgcaagcaaagtgtacaatggcattttggagaaatcctgtagc
atgaaccagctttccagtggcatcccggtgcctaaacctcgccacacatcatgttcctca
gctggcaacgacagtaaaccagttcaggaagccccaagtgttgccagaataagcagcatc
ccacatgacctttgtcataatggagagaaaagcaaaaagccatcaaaaatcaaaagcctt
tttaagaagaaatctaagtga
Homo sapiens (human): 6786
Entry
6786 CDS
T01001
Gene name
STIM1, D11S4896E, GOK, IMD10, STRMK, TAM, TAM1
Definition
(RefSeq) stromal interaction molecule 1
KO
K16059
stromal interaction molecule 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04020
Calcium signaling pathway
hsa04611
Platelet activation
Disease
H00093
Combined immunodeficiency
H02258
Tubular aggregate myopathy
H02259
Stormorken syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
6786 (STIM1)
09150 Organismal Systems
09151 Immune system
04611 Platelet activation
6786 (STIM1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
6786 (STIM1)
Transporters [BR:
hsa02000
]
Other transporters
Pores ion channels [TC:
1
]
6786 (STIM1)
SSDB
Motif
Pfam:
SOAR
SAM_2
SAM_1
SAM_Ste50p
Prominin
Other DBs
NCBI-GeneID:
6786
NCBI-ProteinID:
NP_003147
OMIM:
605921
HGNC:
11386
Ensembl:
ENSG00000167323
Vega:
OTTHUMG00000133360
Pharos:
Q13586
(Tbio)
UniProt:
Q13586
LinkDB
Structure
PDB:
3TEQ
4O9B
2MAJ
2MAK
2K60
Position
11p15.4
AA seq
685 aa
MDVCVRLALWLLWGLLLHQGQSLSHSHSEKATGTSSGANSEESTAAEFCRIDKPLCHSED
EKLSFEAVRNIHKLMDDDANGDVDVEESDEFLREDLNYHDPTVKHSTFHGEDKLISVEDL
WKAWKSSEVYNWTVDEVVQWLITYVELPQYEETFRKLQLSGHAMPRLAVTNTTMTGTVLK
MTDRSHRQKLQLKALDTVLFGPPLLTRHNHLKDFMLVVSIVIGVGGCWFAYIQNRYSKEH
MKKMMKDLEGLHRAEQSLHDLQERLHKAQEEHRTVEVEKVHLEKKLRDEINLAKQEAQRL
KELREGTENERSRQKYAEEELEQVREALRKAEKELESHSSWYAPEALQKWLQLTHEVEVQ
YYNIKKQNAEKQLLVAKEGAEKIKKKRNTLFGTFHVAHSSSLDDVDHKILTAKQALSEVT
AALRERLHRWQQIEILCGFQIVNNPGIHSLVAALNIDPSWMGSTRPNPAHFIMTDDVDDM
DEEIVSPLSMQSPSLQSSVRQRLTEPQHGLGSQRDLTHSDSESSLHMSDRQRVAPKPPQM
SRAADEALNAMTSNGSHRLIEGVHPGSLVEKLPDSPALAKKALLALNHGLDKAHSLMELS
PSAPPGGSPHLDSSRSHSPSSPDPDTPSPVGDSRALQASRNTRIPHLAGKKAVAEEDNGS
IGEETDSSPGRKKFPLKIFKKPLKK
NT seq
2058 nt
+upstream
nt +downstream
nt
atggatgtatgcgtccgtcttgccctgtggctcctctggggactcctcctgcaccagggc
cagagcctcagccatagtcacagtgagaaggcgacaggaaccagctcgggggccaactct
gaggagtccactgcagcagagttttgccgaattgacaagcccctgtgtcacagtgaggat
gagaaactcagcttcgaggcagtccgtaacatccacaaactgatggacgatgatgccaat
ggtgatgtggatgtggaagaaagtgatgagttcctgagggaagacctcaattaccatgac
ccaacagtgaaacacagcaccttccatggtgaggataagctcatcagcgtggaggacctg
tggaaggcatggaagtcatcagaagtatacaattggaccgtggatgaggtggtacagtgg
ctgatcacatatgtggagctgcctcagtatgaggagaccttccggaagctgcagctcagt
ggccatgccatgccaaggctggctgtcaccaacaccaccatgacagggactgtgctgaag
atgacagaccggagtcatcggcagaagctgcagctgaaggctctggatacagtgctcttt
gggcctcctctcttgactcgccataatcacctcaaggacttcatgctggtggtgtctatc
gttattggtgtgggcggctgctggtttgcctatatccagaaccgttactccaaggagcac
atgaagaagatgatgaaggacttggaggggttacaccgagctgagcagagtctgcatgac
cttcaggaaaggctgcacaaggcccaggaggagcaccgcacagtggaggtggagaaggtc
catctggaaaagaagctgcgcgatgagatcaaccttgctaagcaggaagcccagcggctg
aaggagctgcgggagggtactgagaatgagcggagccgccaaaaatatgctgaggaggag
ttggagcaggttcgggaggccttgaggaaagcagagaaggagctagaatctcacagctca
tggtatgctccagaggcccttcagaagtggctgcagctgacacatgaggtggaggtgcaa
tattacaacatcaagaagcaaaatgctgagaagcagctgctggtggccaaggagggggct
gagaagataaaaaagaagagaaacacactctttggcaccttccacgtggcccacagctct
tccctggatgatgtagatcataaaattctaacagctaagcaagcactgagcgaggtgaca
gcagcattgcgggagcgcctgcaccgctggcaacagatcgagatcctctgtggcttccag
attgtcaacaaccctggcatccactcactggtggctgccctcaacatagaccccagctgg
atgggcagtacacgccccaaccctgctcacttcatcatgactgacgacgtggatgacatg
gatgaggagattgtgtctcccttgtccatgcagtcccctagcctgcagagcagtgttcgg
cagcgcctgacggagccacagcatggcctgggatctcagagggatttgacccattccgat
tcggagtcctccctccacatgagtgaccgccagcgtgtggcccccaaacctcctcagatg
agccgtgctgcagacgaggctctcaatgccatgacttccaatggcagccaccggctgatc
gagggggtccacccagggtctctggtggagaaactgcctgacagccctgccctggccaag
aaggcattactggcgctgaaccatgggctggacaaggcccacagcctgatggagctgagc
ccctcagccccacctggtggctctccacatttggattcttcccgttctcacagccccagc
tccccagacccagacacaccatctccagttggggacagccgagccctgcaagccagccga
aacacacgcattccccacctggctggcaagaaggctgtggctgaggaggataatggctct
attggcgaggaaacagactccagcccaggccggaagaagtttcccctcaaaatctttaag
aagcctcttaagaagtag
DBGET
integrated database retrieval system
