KTI12 (KTI12 chromatin associated homolog) - Rat Genome Database

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Gene: KTI12 (KTI12 chromatin associated homolog) Homo sapiens
Analyze
Symbol: KTI12
Name: KTI12 chromatin associated homolog
RGD ID: 1603926
HGNC Page HGNC:25160
Description: Predicted to enable ATP binding activity. Predicted to be involved in tRNA wobble uridine modification.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: KTI12 homolog, chromatin associated; MGC20419; protein KTI12 homolog; RP11-91A18.3; SBBI81; TOT4
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38152,032,103 - 52,033,810 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl152,032,103 - 52,033,810 (-)EnsemblGRCh38hg38GRCh38
GRCh37152,497,775 - 52,499,482 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36152,270,365 - 52,272,060 (-)NCBINCBI36Build 36hg18NCBI36
Celera150,785,258 - 50,786,954 (-)NCBICelera
Cytogenetic Map1p32.3NCBI
HuRef150,615,178 - 50,616,874 (-)NCBIHuRef
CHM1_1152,615,285 - 52,616,980 (-)NCBICHM1_1
T2T-CHM13v2.0151,913,615 - 51,915,323 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:11929532   PMID:12477932   PMID:20467437   PMID:21873635   PMID:25416956   PMID:26186194   PMID:26344197   PMID:28514442   PMID:31091453   PMID:31871319   PMID:33417976   PMID:33961781  
PMID:34373451   PMID:35256949   PMID:35748872   PMID:35831314  


Genomics

Comparative Map Data
KTI12
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38152,032,103 - 52,033,810 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl152,032,103 - 52,033,810 (-)EnsemblGRCh38hg38GRCh38
GRCh37152,497,775 - 52,499,482 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36152,270,365 - 52,272,060 (-)NCBINCBI36Build 36hg18NCBI36
Celera150,785,258 - 50,786,954 (-)NCBICelera
Cytogenetic Map1p32.3NCBI
HuRef150,615,178 - 50,616,874 (-)NCBIHuRef
CHM1_1152,615,285 - 52,616,980 (-)NCBICHM1_1
T2T-CHM13v2.0151,913,615 - 51,915,323 (-)NCBIT2T-CHM13v2.0
Kti12
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394108,705,054 - 108,706,609 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4108,704,982 - 108,706,610 (+)EnsemblGRCm39 Ensembl
GRCm384108,847,857 - 108,849,412 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4108,847,785 - 108,849,413 (+)EnsemblGRCm38mm10GRCm38
MGSCv374108,520,462 - 108,522,017 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364108,345,789 - 108,347,344 (+)NCBIMGSCv36mm8
Celera4107,185,612 - 107,187,167 (+)NCBICelera
Cytogenetic Map4C7NCBI
cM Map450.64NCBI
Kti12
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85128,829,751 - 128,831,273 (+)NCBIGRCr8
mRatBN7.25123,601,059 - 123,602,581 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5123,599,436 - 123,613,964 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5126,223,839 - 126,225,357 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05127,946,945 - 127,948,463 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05127,998,229 - 127,999,747 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05128,464,035 - 128,465,557 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.05132,304,401 - 132,305,923 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.45130,155,806 - 130,157,328 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera5122,335,199 - 122,336,721 (+)NCBICelera
Cytogenetic Map5q34NCBI
Kti12
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554647,082,211 - 7,084,748 (+)NCBIChiLan1.0ChiLan1.0
KTI12
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21174,824,720 - 174,828,214 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11173,965,877 - 173,969,664 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0151,283,145 - 51,285,522 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1152,887,060 - 52,889,068 (-)NCBIpanpan1.1PanPan1.1panPan2
KTI12
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1159,278,351 - 9,280,527 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl159,278,366 - 9,279,770 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha159,430,575 - 9,432,383 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0159,403,076 - 9,404,888 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1159,213,734 - 9,215,542 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0159,303,258 - 9,305,043 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0159,320,643 - 9,322,452 (+)NCBIUU_Cfam_GSD_1.0
Kti12
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505866,523,485 - 66,525,188 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049365228,890,921 - 8,892,809 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
KTI12
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6160,155,842 - 160,157,601 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16160,154,914 - 160,157,600 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.26147,858,180 - 147,860,341 (+)NCBISscrofa10.2Sscrofa10.2susScr3
KTI12
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12080,915,373 - 80,917,901 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366603336,353,680 - 36,356,341 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Kti12
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248591,147,733 - 1,150,376 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in KTI12
21 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p32.3-31.3(chr1:50222546-61618373)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051819]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051819]|See cases [RCV000051819] Chr1:50222546..61618373 [GRCh38]
Chr1:50688218..62084045 [GRCh37]
Chr1:50460805..61856633 [NCBI36]
Chr1:1p32.3-31.3		 pathogenic
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12		 likely benign
GRCh37/hg19 1p32.3(chr1:51729573-55164001)x1 copy number loss See cases [RCV000447334] Chr1:51729573..55164001 [GRCh37]
Chr1:1p32.3		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1		 uncertain significance
GRCh37/hg19 1p33-32.3(chr1:47272184-52505405)x1 copy number loss not provided [RCV001005086] Chr1:47272184..52505405 [GRCh37]
Chr1:1p33-32.3		 pathogenic
GRCh37/hg19 1p32.3-32.2(chr1:51941877-56688514) copy number loss Abnormality of the kidney [RCV001352641] Chr1:51941877..56688514 [GRCh37]
Chr1:1p32.3-32.2		 pathogenic
GRCh37/hg19 1p32.3(chr1:51755130-52521150) copy number gain not specified [RCV002053325] Chr1:51755130..52521150 [GRCh37]
Chr1:1p32.3		 uncertain significance
GRCh38/hg38 1p33-32.3(chr1:50441439-50959811)x2 copy number loss Orofacial cleft 13 [RCV002488680] Chr1:50441439..50959811 [GRCh38]
Chr1:1p33-32.3		 association
NM_138417.3(KTI12):c.103G>A (p.Val35Met) single nucleotide variant not specified [RCV004123274] Chr1:52033659 [GRCh38]
Chr1:52499331 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.497C>T (p.Ala166Val) single nucleotide variant not specified [RCV004132449] Chr1:52033265 [GRCh38]
Chr1:52498937 [GRCh37]
Chr1:1p32.3		 likely benign
NM_138417.3(KTI12):c.50G>A (p.Arg17His) single nucleotide variant not specified [RCV004198102] Chr1:52033712 [GRCh38]
Chr1:52499384 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.1051C>G (p.Gln351Glu) single nucleotide variant not specified [RCV004178928] Chr1:52032711 [GRCh38]
Chr1:52498383 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.1052A>G (p.Gln351Arg) single nucleotide variant not specified [RCV004140216] Chr1:52032710 [GRCh38]
Chr1:52498382 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.680G>A (p.Arg227Gln) single nucleotide variant not specified [RCV004181058] Chr1:52033082 [GRCh38]
Chr1:52498754 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.754C>G (p.Arg252Gly) single nucleotide variant not specified [RCV004110211] Chr1:52033008 [GRCh38]
Chr1:52498680 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.37G>T (p.Gly13Cys) single nucleotide variant not specified [RCV004269113] Chr1:52033725 [GRCh38]
Chr1:52499397 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.819G>T (p.Gln273His) single nucleotide variant not specified [RCV004252778] Chr1:52032943 [GRCh38]
Chr1:52498615 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.254A>G (p.Lys85Arg) single nucleotide variant not specified [RCV004254825] Chr1:52033508 [GRCh38]
Chr1:52499180 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.713C>T (p.Pro238Leu) single nucleotide variant not specified [RCV004270057] Chr1:52033049 [GRCh38]
Chr1:52498721 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.566C>G (p.Thr189Ser) single nucleotide variant not specified [RCV004330148] Chr1:52033196 [GRCh38]
Chr1:52498868 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.814C>T (p.His272Tyr) single nucleotide variant not specified [RCV004363300] Chr1:52032948 [GRCh38]
Chr1:52498620 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.1001A>G (p.Asn334Ser) single nucleotide variant not specified [RCV004352316] Chr1:52032761 [GRCh38]
Chr1:52498433 [GRCh37]
Chr1:1p32.3		 uncertain significance
Single allele inversion Bilateral polymicrogyria [RCV003459046] Chr1:33246132..61045156 [GRCh38]
Chr1:1p35.1-31.3		 likely pathogenic
GRCh37/hg19 1p33-32.2(chr1:47493178-57042671)x3 copy number gain not specified [RCV003986484] Chr1:47493178..57042671 [GRCh37]
Chr1:1p33-32.2		 likely pathogenic
NM_138417.3(KTI12):c.286C>T (p.Arg96Trp) single nucleotide variant not specified [RCV004407019] Chr1:52033476 [GRCh38]
Chr1:52499148 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.307T>G (p.Cys103Gly) single nucleotide variant not specified [RCV004407020] Chr1:52033455 [GRCh38]
Chr1:52499127 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.326G>C (p.Arg109Pro) single nucleotide variant not specified [RCV004407021] Chr1:52033436 [GRCh38]
Chr1:52499108 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.423C>G (p.Asp141Glu) single nucleotide variant not specified [RCV004407022] Chr1:52033339 [GRCh38]
Chr1:52499011 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.454C>T (p.Leu152Phe) single nucleotide variant not specified [RCV004407023] Chr1:52033308 [GRCh38]
Chr1:52498980 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.598T>G (p.Ser200Ala) single nucleotide variant not specified [RCV004407024] Chr1:52033164 [GRCh38]
Chr1:52498836 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.844C>G (p.Leu282Val) single nucleotide variant not specified [RCV004407026] Chr1:52032918 [GRCh38]
Chr1:52498590 [GRCh37]
Chr1:1p32.3		 uncertain significance
NM_138417.3(KTI12):c.601G>A (p.Gly201Ser) single nucleotide variant not specified [RCV004639793] Chr1:52033161 [GRCh38]
Chr1:52498833 [GRCh37]
Chr1:1p32.3		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:223
Count of miRNA genes:206
Interacting mature miRNAs:212
Transcripts:ENST00000371614
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
2314561GLUCO47_HGlucose level QTL 47 (human)1.1Glucose level14477336070773360Human

Markers in Region
G07351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37152,497,831 - 52,498,081UniSTSGRCh37
Build 36152,270,419 - 52,270,669RGDNCBI36
Celera150,785,312 - 50,785,562RGD
Cytogenetic Map1p32.3UniSTS
HuRef150,615,232 - 50,615,482UniSTS
G19690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37152,497,813 - 52,497,930UniSTSGRCh37
Build 36152,270,401 - 52,270,518RGDNCBI36
Celera150,785,294 - 50,785,411RGD
Cytogenetic Map1p32.3UniSTS
HuRef150,615,214 - 50,615,331UniSTS
A001V30  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37152,497,813 - 52,497,930UniSTSGRCh37
Build 36152,270,401 - 52,270,518RGDNCBI36
Celera150,785,294 - 50,785,411RGD
Cytogenetic Map1p32.3UniSTS
HuRef150,615,214 - 50,615,331UniSTS
GeneMap99-GB4 RH Map1151.08UniSTS
NCBI RH Map1312.0UniSTS
A004C17  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37152,498,735 - 52,498,862UniSTSGRCh37
Build 36152,271,323 - 52,271,450RGDNCBI36
Celera150,786,217 - 50,786,344RGD
Cytogenetic Map1p32.3UniSTS
HuRef150,616,137 - 50,616,264UniSTS
GeneMap99-GB4 RH Map1151.6UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2252 4973 1726 2351 6 624 1950 465 2269 7304 6470 53 3734 1 852 1744 1617 174 1

Sequence


Ensembl Acc Id: ENST00000371614   ⟹   ENSP00000360676
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl152,032,103 - 52,033,810 (-)Ensembl
RefSeq Acc Id: NM_138417   ⟹   NP_612426
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38152,032,103 - 52,033,810 (-)NCBI
GRCh37152,497,777 - 52,499,472 (-)RGD
Build 36152,270,365 - 52,272,060 (-)NCBI Archive
Celera150,785,258 - 50,786,954 (-)RGD
HuRef150,615,178 - 50,616,874 (-)ENTREZGENE
CHM1_1152,615,285 - 52,616,980 (-)NCBI
T2T-CHM13v2.0151,913,615 - 51,915,323 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_612426 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH12173 (Get FASTA)   NCBI Sequence Viewer  
  AAL56009 (Get FASTA)   NCBI Sequence Viewer  
  BAG36486 (Get FASTA)   NCBI Sequence Viewer  
  EAX06801 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000360676
  ENSP00000360676.1
GenBank Protein Q96EK9 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_612426   ⟸   NM_138417
- UniProtKB: Q96EK9 (UniProtKB/Swiss-Prot),   B2R9D9 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000360676   ⟸   ENST00000371614

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96EK9-F1-model_v2 AlphaFold Q96EK9 1-354 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25160 AgrOrtholog
COSMIC KTI12 COSMIC
Ensembl Genes ENSG00000198841 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000371614 ENTREZGENE
  ENST00000371614.2 UniProtKB/Swiss-Prot
Gene3D-CATH 3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000198841 GTEx
HGNC ID HGNC:25160 ENTREZGENE
Human Proteome Map KTI12 Human Proteome Map
InterPro KTI12/PSTK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:112970 UniProtKB/Swiss-Prot
NCBI Gene 112970 ENTREZGENE
PANTHER PROTEIN KTI12 HOMOLOG UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR12435 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam KTI12 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142671571 PharmGKB
Superfamily-SCOP P-loop containing nucleoside triphosphate hydrolases UniProtKB/TrEMBL, UniProtKB/Swiss-Prot
UniProt B2R9D9 ENTREZGENE, UniProtKB/TrEMBL
  KTI12_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-07-07 KTI12  KTI12 chromatin associated homolog    KTI12 homolog, chromatin associated (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED