H-InvDB_9.0 released on May 27, 2015.
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Keyword
H-Inv ID (HIT)
H-Inv cluster ID (HIX)
H-Inv protein ID (HIP)
H-Inv gene family/group (HIF)
Accession number
Chromosome number
Chromosome band
Definition*
Data source ID
---
CCDS ID
dbSNP ID (rs number)
EC number
Ensembl ID
EntrezGene ID
FR ID
FR Accession number
GO ID
GO name*
HGNC gene symbol
HGNC gene name*
InterPro ID
InterPro name*
OMIM ID
OMIM title*
Pathway ID
Pathway name*
RefSeq (gene) ID
RefSeq (protein) ID
SCOP ID
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H-Inv cluster ID:
HIX0011883
Created date:
26-Mar-2013
Last modified:
27-May-2015
Definition:
Calmodulin; CaM;
Select format
Flat file
XML file
Gene structure
H-Inv cluster ID
HIX0011883
Genomic location
Chromosome
14
Location
14q32.11
Position
90862846- 90874618
Strand
+
Antisense cluster ID(s)
HIX0038045
overlap at CDSs (all)
HIX0221642
overlap at CDSs (all)
Database links
RefSeq
NA
Ensembl
NA
Entrez Gene
Entrez Gene ID:801
;
KEGG GENES
KEGG GENES(801)
;
GeneCard
NA
*GeneCards is provided free to academic non-profit institutions.
etc
Human-Gene diversity Of Life-style related Diseases
;
Cluster member H-Inv ID(s)
HIT000053157
;
HIT000035481
;
HIT000029639
;
HIT000033853
;
HIT000033560
;
HIT000054462
;
HIT000056870
;
HIT000195117
;
HIT000099738
;
HIT000422734
;
HIT000250944
;
HIT000097366
;
HIT000218356
;
Additional cluster member candidate(s)
NA
Related H-InvDB links
H-DBAS
;
G-integra
;
cDNA-genome multiple alignment
;
ORF multiple alignment
;
TOP
1-10
11-13
LAST
Cluster member (s)
Locus member number
1
H-Inv ID
HIT000053157
Accession number
BC047523.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Calmodulin; CaM;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P62158
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
Representative transcript;
Splicing isoform
Genomic location
Chromosome
14
Location
14q32.11
Position
90863377- 90874396
Strand
+
Gene structure
7 exons
TOP
1-10
11-13
LAST
Locus member number
2
H-Inv ID
HIT000035481
Accession number
BC011834.2
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Calmodulin; CaM;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P62158
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90863376- 90871952
Strand
+
Gene structure
6 exons
TOP
1-10
11-13
LAST
Locus member number
3
H-Inv ID
HIT000029639
Accession number
BC000454.2
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Calmodulin; CaM;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P62158
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
Splicing isoform
Genomic location
Chromosome
14
Location
14q32.11
Position
90863393- 90871451
Strand
+
Gene structure
6 exons
TOP
1-10
11-13
LAST
Locus member number
4
H-Inv ID
HIT000033853
Accession number
BC008597.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Calmodulin; CaM;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P62158
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90863393- 90871451
Strand
+
Gene structure
6 exons
TOP
1-10
11-13
LAST
Locus member number
5
H-Inv ID
HIT000033560
Accession number
BC007965.2
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Similar to Calmodulin.
Similarity category
Category: Similar to known protein(Category II).
Similar to known protein (
NP_001734
) [Identity/coverage = 100.0%/99.33%] to Homo sapiens protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
Splicing isoform
Genomic location
Chromosome
14
Location
14q32.11
Position
90864606- 90871451
Strand
+
Gene structure
6 exons
TOP
1-10
11-13
LAST
Locus member number
6
H-Inv ID
HIT000054462
Accession number
BX537677.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Hypothetical short protein.
Similarity category
Category: Hypothetical short protein(Category VI).
Hypothetical short protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90871276- 90874605
Strand
+
Gene structure
1 exons
TOP
1-10
11-13
LAST
Locus member number
7
H-Inv ID
HIT000056870
Accession number
BX648223.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Hypothetical short protein.
Similarity category
Category: Hypothetical short protein(Category VI).
Hypothetical short protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90871727- 90874605
Strand
+
Gene structure
1 exons
TOP
1-10
11-13
LAST
Locus member number
8
H-Inv ID
HIT000195117
Accession number
M27319.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Calmodulin; CaM;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P62158
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90863490- 90871323
Strand
+
Gene structure
6 exons
TOP
1-10
11-13
LAST
Locus member number
9
H-Inv ID
HIT000099738
Accession number
BT006818.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Calmodulin; CaM;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P62158
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90866408- 90871059
Strand
+
Gene structure
5 exons
TOP
1-10
11-13
LAST
Locus member number
10
H-Inv ID
HIT000422734
Accession number
AK289937.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Similar to Calmodulin.
Similarity category
Category: Similar to known protein(Category II).
Similar to known protein (
NP_001734
) [Identity/coverage = 99.324%/99.33%] to Homo sapiens protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
Splicing isoform
Genomic location
Chromosome
14
Location
14q32.11
Position
90863477- 90871416
Strand
+
Gene structure
7 exons
TOP
1-10
11-13
LAST
Locus member number
11
H-Inv ID
HIT000250944
Accession number
AY189287.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Similar to Calmodulin.
Similarity category
Category: Similar to known protein(Category II).
Similar to known protein (
NP_005175
) [Identity/coverage = 100.0%/99.33%] to Homo sapiens protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90864276- 90871129
Strand
+
Gene structure
5 exons
TOP
1-10
11-13
LAST
Locus member number
12
H-Inv ID
HIT000097366
Accession number
BC042831.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Hypothetical short protein.
Similarity category
Category: Hypothetical short protein(Category VI).
Hypothetical short protein.
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90873689- 90874609
Strand
+
Gene structure
1 exons
TOP
1-10
11-13
LAST
Locus member number
13
H-Inv ID
HIT000218356
Accession number
U16851.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Non-protein-coding;
Definition
Non-protein-coding transcript, unclassifiable transcript.
Similarity category
Category: Non-protein coding transcript.
NA
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Transcript feature
NA
Genomic location
Chromosome
14
Location
14q32.11
Position
90863382- 90863487
Strand
+
Gene structure
1 exons
Alternative splicing (AS) information
Pattern of alternative splicing isoforms
5' terminal AS; 3' terminal AS; Internal AS;
Position of alternative splicing isoforms
Cassette; Retained intron;
Alternative splicing isoform H-Inv ID(s)
HIT000422734
;
HIT000053157
;
HIT000033560
;
HIT000029639
;
Related H-InvDB links
H-DBAS
;
G-integra
;
cDNA-genome multiple alignment
;
ORF multiple alignment
;
Gene function information
H-Inv cluster ID
HIX0011883
Representative H-Inv ID
HIT000053157
Accession number
BC047523.1
CAGE tag ID
NA
EST ID
NA
Coding potential
Protein coding;
Definition
Calmodulin; CaM;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P62158
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Gene family/group
H-Inv gene family/group ID
NA
Gene family/group name
NA
Evidence motif (InterPro) ID
NA
Gene symbol/name
HGNC symbol
NA
HGNC aliases
NA
HGNC name
NA
Protein-protein interaction (PPI)
H-Inv protein ID
HIP000024994
No. of interaction
151
Interaction partner(s)
HIP000021606
;
HIP000021999
;
HIP000022920
;
HIP000023827
;
HIP000024080
;
HIP000024373
;
HIP000024429
;
HIP000024433
;
HIP000024603
;
HIP000024723
;
HIP000025001
;
HIP000025001
;
HIP000025184
;
HIP000025256
;
HIP000025619
;
HIP000025619
;
HIP000025817
;
HIP000026231
;
HIP000026561
;
HIP000026650
;
HIP000027004
;
HIP000028648
;
HIP000028806
;
HIP000028948
;
HIP000029106
;
HIP000029669
;
HIP000029733
;
HIP000029919
;
HIP000030386
;
HIP000030765
;
HIP000032098
;
HIP000032397
;
HIP000032749
;
HIP000032846
;
HIP000032870
;
HIP000033674
;
HIP000034651
;
HIP000036736
;
HIP000036736
;
HIP000037607
;
HIP000039461
;
HIP000040522
;
HIP000040680
;
HIP000041107
;
HIP000041308
;
HIP000041429
;
HIP000042652
;
HIP000044043
;
HIP000046719
;
HIP000046896
;
HIP000047664
;
HIP000048107
;
HIP000048801
;
HIP000049174
;
HIP000049915
;
HIP000049997
;
HIP000050005
;
HIP000051355
;
HIP000052086
;
HIP000052329
;
HIP000052586
;
HIP000053726
;
HIP000054580
;
HIP000057472
;
HIP000057536
;
HIP000058633
;
HIP000059613
;
HIP000060603
;
HIP000060858
;
HIP000063272
;
HIP000063383
;
HIP000064456
;
HIP000065273
;
HIP000065299
;
HIP000067584
;
HIP000067617
;
HIP000069367
;
HIP000069837
;
HIP000069887
;
HIP000071741
;
HIP000072281
;
HIP000074095
;
HIP000074116
;
HIP000074361
;
HIP000075478
;
HIP000075551
;
HIP000075910
;
HIP000076060
;
HIP000077638
;
HIP000079704
;
HIP000080465
;
HIP000080779
;
HIP000082634
;
HIP000082747
;
HIP000083424
;
HIP000084122
;
HIP000084148
;
HIP000085076
;
HIP000085708
;
HIP000086514
;
HIP000086839
;
HIP000086928
;
HIP000088283
;
HIP000088399
;
HIP000091330
;
HIP000091500
;
HIP000093491
;
HIP000094907
;
HIP000095322
;
HIP000096838
;
HIP000096868
;
HIP000097117
;
HIP000097471
;
HIP000098226
;
HIP000099275
;
HIP000101550
;
HIP000101991
;
HIP000101991
;
HIP000102217
;
HIP000102293
;
HIP000102581
;
HIP000102898
;
HIP000104180
;
HIP000104327
;
HIP000104847
;
HIP000105099
;
HIP000106041
;
HIP000106185
;
HIP000107233
;
HIP000107622
;
HIP000109499
;
HIP000110634
;
HIP000113005
;
HIP000113507
;
HIP000116213
;
HIP000116715
;
HIP000117036
;
HIP000128485
;
HIP000129551
;
HIP000131477
;
HIP000136079
;
HIP000145170
;
HIP000146754
;
HIP000148595
;
HIP000176829
;
HIP000177086
;
HIP000200174
;
HIP000246810
;
HIP000254467
;
HIP000254467
;
HIP000359409
;
BIND
19092; 200006; 200007; 200008; 200009; 200010; 200012; 200013; 300817; 301726; 58062;
DIP
102879E; 103745E; 104171E; 112446E; 112851E; 113176E; 114308E; 114414E; 114783E; 114827E; 115144E; 115983E; 116983E; 117513E; 175832E; 177437E; 185610E; 31E; 489E;
MINT
MINT-15764; MINT-15765; MINT-15766; MINT-16955; MINT-16956; MINT-16957; MINT-17793; MINT-17795; MINT-3295975; MINT-48052; MINT-48084; MINT-48113; MINT-48186; MINT-48261; MINT-48323; MINT-48456; MINT-48550; MINT-48603; MINT-48670; MINT-48738; MINT-48841; MINT-48939; MINT-49007; MINT-49067; MINT-49123; MINT-49173; MINT-49204; MINT-49236; MINT-49274; MINT-49341; MINT-49428; MINT-49484; MINT-49550; MINT-49596; MINT-5114545; MINT-5114562; MINT-51633; MINT-51634; MINT-51635; MINT-51636; MINT-51637; MINT-51638; MINT-51639; MINT-51640; MINT-51641; MINT-51642; MINT-58231; MINT-58232; MINT-58233; MINT-58242; MINT-58244; MINT-6175484; MINT-63955; MINT-63956; MINT-6595938; MINT-6596013; MINT-67316; MINT-7148437; MINT-7297878; MINT-7899812; MINT-7988100; MINT-7988123; MINT-8200174; MINT-8200205;
HPRD
00017; 00019; 00032; 00043; 00045; 00051; 00146; 00239; 00251; 00277; 00279; 00352; 00455; 00559; 00579; 00589; 00592; 00656; 00677; 00679; 00777; 00800; 00828; 00918; 00941; 00942; 00975; 01028; 01038; 01061; 01098; 01142; 01166; 01167; 01168; 01169; 01198; 01203; 01224; 01227; 01235; 01238; 01239; 01241; 01281; 01286; 01346; 01347; 01387; 01404; 01422; 01442; 01476; 01491; 01498; 01535; 01536; 01540; 01549; 01550; 01585; 01615; 01618; 01628; 01684; 01710; 01787; 01790; 01817; 01818; 01843; 01852; 01855; 01861; 01862; 01863; 01890; 02043; 02177; 02274; 02367; 02429; 02437; 02484; 02524; 02543; 02577; 02795; 02811; 02884; 02917; 02963; 02985; 03007; 03009; 03015; 03070; 03072; 03183; 03195; 03276; 03283; 03311; 03378; 03390; 03428; 03465; 03533; 03538; 03648; 03677; 03757; 03771; 03780; 03828; 03833; 03914; 03929; 03947; 03965; 04009; 04043; 04045; 04130; 04172; 04235; 04274; 04300; 04462; 04541; 04585; 04713; 04728; 04921; 04978; 04979; 04980; 05059; 05125; 05230; 05255; 05270; 05322; 05327; 05353; 05412; 05442; 05457; 05667; 05803; 05804; 05890; 05934; 05982; 06060; 06120; 06467; 06532; 06692; 06763; 06886; 07505; 07519; 08014; 08356; 08555; 08599; 08830; 08922; 08946; 09073; 09077; 09235; 09253; 09315; 09323; 10040; 10369; 10406; 10515; 10551; 10848; 11049; 11366; 11474; 11476; 11613; 11792; 11871; 13000; 13882; 14727; 14746; 15253; 15302; 15926; 15999; 16241; 17279; 17627; 18124; 18125; 18206; 19599;
IntAct
NA
Database links
RefSeq
NA
Ensembl
NA
Entrez Gene
Entrez Gene ID:801
;
KEGG GENES
KEGG GENES(801)
;
GeneCard
NA
*GeneCards is provided free to academic non-profit institutions.
etc
Human-Gene diversity Of Life-style related Diseases
;
Related H-InvDB links
G-integra
;
PPI view
;
H-DBAS
;
Gene family;
Similarity search tool
;
TACT
;
Gene expression information
Last modified:27-May-2015
Tissue-specific expression
NA
Probe
information
AceGene
NA
Affymetrix
GeneChip
HG-Focus
200655_s_at;
HG-U133
200653_s_at; 200655_s_at; 209563_x_at; 213688_at;
HG-U133A
200653_s_at; 200655_s_at; 209563_x_at; 213688_at;
HG-U133A_2
200653_s_at; 200655_s_at; 209563_x_at; 213688_at;
HG-U133B
NA
HG-U133_Plus_2
200653_s_at; 200655_s_at; 209563_x_at; 213688_at;
HG-U95
41143_at; 955_at;
HG-U95A
41143_at;
HG-U95B
NA
HG-U95C
NA
HG-U95D
NA
HG-U95E
NA
HG-U95Av2
NA
HuEx-1_0
3051591; 3548351; 3548352; 3548360; 3548362; 3548363; 3548366; 3548368; 3548371; 3548372; 3548374; 3548375; 3576080; 3576081; 3576083; 3576084; 3576085; 3983844; 3983845;
HuGeneFL
NA
Agilent
Human 1A Oligo Microarray:PGID215
A_23_P163179;
Whole Human Genome Oligo Microarray:PGID247
A_23_P163178;
Related H-InvDB links
H-ANGEL
;
DNAProbeLocator
;