TTLL3 (tubulin tyrosine ligase like 3) - Rat Genome Database

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Gene: TTLL3 (tubulin tyrosine ligase like 3) Homo sapiens
Analyze
Symbol: TTLL3
Name: tubulin tyrosine ligase like 3
RGD ID: 1322614
HGNC Page HGNC:24483
Description: Enables protein-glycine ligase activity. Predicted to be involved in axoneme assembly; flagellated sperm motility; and protein polyglycylation. Predicted to be located in sperm flagellum. Predicted to be active in axoneme and microtubule cytoskeleton.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp434B103; DKFZp686D076; FLJ13898; HOTTL; MGC120529; MGC120530; MGC120532; tubulin monoglycylase TTLL3; tubulin tyrosine ligase-like family member 3; tubulin tyrosine ligase-like family, member 3; tubulin--tyrosine ligase-like protein 3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Pig
Green Monkey
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
GRCh3839,809,727 - 9,836,365 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl39,808,086 - 9,855,138 (+)EnsemblGRCh38hg38GRCh38
GRCh3739,851,411 - 9,878,049 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3639,826,405 - 9,853,040 (+)NCBINCBI36Build 36hg18NCBI36
Build 3439,835,060 - 9,852,083NCBI
Celera39,786,607 - 9,813,341 (+)NCBICelera
Cytogenetic Map3p25.3NCBI
HuRef39,787,987 - 9,814,322 (+)NCBIHuRef
CHM1_139,801,835 - 9,828,234 (+)NCBICHM1_1
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
axoneme  (IBA,ISS)
cilium  (IEA,ISS)
cytoplasm  (IEA)
cytoskeleton  (IEA)
cytosol  (TAS)
microtubule  (IEA)
microtubule cytoskeleton  (IBA,ISS)
motile cilium  (IEA)
sperm flagellum  (IBA,ISS)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:11054573   PMID:12477932   PMID:14702039   PMID:15342556   PMID:16344560   PMID:19524510   PMID:21873635   PMID:21988832   PMID:25852190   PMID:26186194   PMID:28514442  
PMID:28611215   PMID:33961781  


Genomics

Comparative Map Data
TTLL3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3839,809,727 - 9,836,365 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl39,808,086 - 9,855,138 (+)EnsemblGRCh38hg38GRCh38
GRCh3739,851,411 - 9,878,049 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3639,826,405 - 9,853,040 (+)NCBINCBI36Build 36hg18NCBI36
Build 3439,835,060 - 9,852,083NCBI
Celera39,786,607 - 9,813,341 (+)NCBICelera
Cytogenetic Map3p25.3NCBI
HuRef39,787,987 - 9,814,322 (+)NCBIHuRef
CHM1_139,801,835 - 9,828,234 (+)NCBICHM1_1
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBIT2T-CHM13v2.0
Ttll3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm396113,366,221 - 113,391,553 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl6113,366,221 - 113,391,548 (+)EnsemblGRCm39 Ensembl
GRCm386113,389,260 - 113,414,592 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl6113,389,260 - 113,414,587 (+)EnsemblGRCm38mm10GRCm38
MGSCv376113,339,254 - 113,364,577 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv366113,363,535 - 113,380,341 (+)NCBIMGSCv36mm8
Celera6115,216,098 - 115,241,496 (+)NCBICelera
Cytogenetic Map6E3NCBI
cM Map652.76NCBI
Ttll3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr84148,088,575 - 148,113,526 (+)NCBIGRCr8
mRatBN7.24146,532,958 - 146,558,425 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl4146,533,953 - 146,557,889 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx4151,918,070 - 151,941,859 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.04147,698,921 - 147,722,704 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.04146,320,479 - 146,344,323 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.04145,341,059 - 145,366,614 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4145,342,193 - 145,365,496 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04208,639,199 - 208,663,129 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44149,280,690 - 149,282,413 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.14149,518,583 - 149,541,367 (+)NCBI
Celera4135,091,168 - 135,114,283 (+)NCBICelera
Cytogenetic Map4q42NCBI
Ttll3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049555611,330,378 - 1,353,217 (+)NCBIChiLan1.0ChiLan1.0
TTLL3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v229,818,264 - 9,860,776 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan139,823,029 - 9,853,120 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v039,759,871 - 9,786,690 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.139,999,039 - 10,023,520 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl39,999,144 - 10,035,633 (+)Ensemblpanpan1.1panPan2
TTLL3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1208,414,289 - 8,439,071 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl208,415,723 - 8,439,056 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha208,448,436 - 8,473,969 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0208,444,532 - 8,470,192 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl208,444,532 - 8,468,370 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1208,166,994 - 8,192,655 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0208,511,679 - 8,537,126 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0208,485,119 - 8,510,785 (-)NCBIUU_Cfam_GSD_1.0
TTLL3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1366,056,890 - 66,123,977 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11366,094,069 - 66,123,984 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21373,170,509 - 73,203,964 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TTLL3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12245,817,048 - 45,843,878 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666041120,717,115 - 120,749,917 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in TTLL3
88 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3p25.3-25.2(chr3:8581778-12015238)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051480]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051480]|See cases [RCV000051480] Chr3:8581778..12015238 [GRCh38]
Chr3:8623464..12056738 [GRCh37]
Chr3:8598464..12031738 [NCBI36]
Chr3:3p25.3-25.2		 pathogenic
GRCh38/hg38 3p25.3(chr3:9393349-9956171)x1 copy number loss See cases [RCV000051481] Chr3:9393349..9956171 [GRCh38]
Chr3:9435033..9997855 [GRCh37]
Chr3:9410033..9972855 [NCBI36]
Chr3:3p25.3		 pathogenic
GRCh38/hg38 3p25.3(chr3:9654297-10228687)x1 copy number loss See cases [RCV000051482] Chr3:9654297..10228687 [GRCh38]
Chr3:9695981..10270371 [GRCh37]
Chr3:9670981..10245371 [NCBI36]
Chr3:3p25.3		 pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:52266-11089569)x1 copy number loss See cases [RCV000051447] Chr3:52266..11089569 [GRCh38]
Chr3:93949..11131255 [GRCh37]
Chr3:68949..11106255 [NCBI36]
Chr3:3p26.3-25.3		 pathogenic
GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3 copy number gain See cases [RCV000051097] Chr3:52266..37148076 [GRCh38]
Chr3:93949..37189567 [GRCh37]
Chr3:68949..37164571 [NCBI36]
Chr3:3p26.3-22.2		 pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:52066-20280127)x3 copy number gain See cases [RCV000051690] Chr3:52066..20280127 [GRCh38]
Chr3:93749..20321619 [GRCh37]
Chr3:68749..20296623 [NCBI36]
Chr3:3p26.3-24.3		 pathogenic
GRCh38/hg38 3p26.3-24.1(chr3:52266-29248782)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051718]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051718]|See cases [RCV000051718] Chr3:52266..29248782 [GRCh38]
Chr3:93949..29290273 [GRCh37]
Chr3:68949..29265277 [NCBI36]
Chr3:3p26.3-24.1		 pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:63843-19510600)x3 copy number gain See cases [RCV000051719] Chr3:63843..19510600 [GRCh38]
Chr3:105526..19552092 [GRCh37]
Chr3:80526..19527096 [NCBI36]
Chr3:3p26.3-24.3		 pathogenic
GRCh38/hg38 3p25.3(chr3:9624696-10039318)x1 copy number loss See cases [RCV000133641] Chr3:9624696..10039318 [GRCh38]
Chr3:9666380..10081002 [GRCh37]
Chr3:9641380..10056002 [NCBI36]
Chr3:3p25.3		 uncertain significance
GRCh38/hg38 3p26.1-25.3(chr3:8038727-11240931)x4 copy number gain See cases [RCV000135641] Chr3:8038727..11240931 [GRCh38]
Chr3:8080414..11282617 [GRCh37]
Chr3:8055414..11257617 [NCBI36]
Chr3:3p26.1-25.3		 likely pathogenic
GRCh38/hg38 3p25.3-25.2(chr3:9394874-11690612)x1 copy number loss See cases [RCV000137433] Chr3:9394874..11690612 [GRCh38]
Chr3:9436558..11732086 [GRCh37]
Chr3:9411558..11707086 [NCBI36]
Chr3:3p25.3-25.2		 pathogenic
GRCh38/hg38 3p26.1-25.2(chr3:7975734-12636917)x3 copy number gain See cases [RCV000137309] Chr3:7975734..12636917 [GRCh38]
Chr3:8017421..12678416 [GRCh37]
Chr3:7992421..12653416 [NCBI36]
Chr3:3p26.1-25.2		 likely pathogenic
GRCh38/hg38 3p25.3(chr3:8812036-9953438)x3 copy number gain See cases [RCV000137329] Chr3:8812036..9953438 [GRCh38]
Chr3:8853722..9995122 [GRCh37]
Chr3:8828722..9970122 [NCBI36]
Chr3:3p25.3		 uncertain significance
GRCh38/hg38 3p26.3-25.2(chr3:32241-12681483)x1 copy number loss See cases [RCV000138143] Chr3:32241..12681483 [GRCh38]
Chr3:73914..12722982 [GRCh37]
Chr3:48914..12697982 [NCBI36]
Chr3:3p26.3-25.2		 pathogenic
GRCh38/hg38 3p26.3-24.1(chr3:32241-30064208)x3 copy number gain See cases [RCV000138004] Chr3:32241..30064208 [GRCh38]
Chr3:73914..30105699 [GRCh37]
Chr3:48914..30080703 [NCBI36]
Chr3:3p26.3-24.1		 pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:32241-20334387)x3 copy number gain See cases [RCV000137941] Chr3:32241..20334387 [GRCh38]
Chr3:73914..20375879 [GRCh37]
Chr3:48914..20350883 [NCBI36]
Chr3:3p26.3-24.3		 pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:32241-11379835)x1 copy number loss See cases [RCV000138376] Chr3:32241..11379835 [GRCh38]
Chr3:73914..11421309 [GRCh37]
Chr3:48914..11396309 [NCBI36]
Chr3:3p26.3-25.3		 pathogenic|likely benign
GRCh38/hg38 3p25.3(chr3:8941623-10151752)x3 copy number gain See cases [RCV000138535] Chr3:8941623..10151752 [GRCh38]
Chr3:8983307..10193436 [GRCh37]
Chr3:8958307..10168436 [NCBI36]
Chr3:3p25.3		 likely benign|uncertain significance
GRCh38/hg38 3p26.3-25.1(chr3:32241-13613818)x3 copy number gain See cases [RCV000138946] Chr3:32241..13613818 [GRCh38]
Chr3:73914..13655318 [GRCh37]
Chr3:48914..13630319 [NCBI36]
Chr3:3p26.3-25.1		 pathogenic
GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3 copy number gain See cases [RCV000141810] Chr3:53308..41381521 [GRCh38]
Chr3:94991..41423012 [GRCh37]
Chr3:69991..41398016 [NCBI36]
Chr3:3p26.3-22.1		 pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:20213-11221602)x1 copy number loss See cases [RCV000141731] Chr3:20213..11221602 [GRCh38]
Chr3:61891..11263288 [GRCh37]
Chr3:36891..11238288 [NCBI36]
Chr3:3p26.3-25.3		 pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:32241-10323124)x1 copy number loss See cases [RCV000143325] Chr3:32241..10323124 [GRCh38]
Chr3:73914..10364808 [GRCh37]
Chr3:48914..10339808 [NCBI36]
Chr3:3p26.3-25.3		 pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:32241-10631310)x1 copy number loss See cases [RCV000143173] Chr3:32241..10631310 [GRCh38]
Chr3:73914..10672995 [GRCh37]
Chr3:48914..10647995 [NCBI36]
Chr3:3p26.3-25.3		 pathogenic
GRCh38/hg38 3p26.1-25.1(chr3:7356110-14360442)x3 copy number gain See cases [RCV000143766] Chr3:7356110..14360442 [GRCh38]
Chr3:7397797..14401942 [GRCh37]
Chr3:7372797..14376946 [NCBI36]
Chr3:3p26.1-25.1		 pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:688897-11051142)x1 copy number loss See cases [RCV000143706] Chr3:688897..11051142 [GRCh38]
Chr3:730581..11092828 [GRCh37]
Chr3:705581..11067828 [NCBI36]
Chr3:3p26.3-25.3		 pathogenic
GRCh37/hg19 3p25.3(chr3:9405337-10168892)x3 copy number gain See cases [RCV000240180] Chr3:9405337..10168892 [GRCh37]
Chr3:3p25.3		 likely pathogenic
GRCh37/hg19 3p25.3-25.2(chr3:8922160-12338637)x1 copy number loss See cases [RCV000240139] Chr3:8922160..12338637 [GRCh37]
Chr3:3p25.3-25.2		 pathogenic
NM_001387446.1(TTLL3):c.-20G>A single nucleotide variant not specified [RCV004318588] Chr3:9810642 [GRCh38]
Chr3:9852326 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p25.3(chr3:9666380-10028247)x1 copy number loss See cases [RCV000446848] Chr3:9666380..10028247 [GRCh37]
Chr3:3p25.3		 pathogenic
GRCh37/hg19 3p26.3-24.2(chr3:61891-24432821)x3 copy number gain See cases [RCV000447247] Chr3:61891..24432821 [GRCh37]
Chr3:3p26.3-24.2		 pathogenic
GRCh37/hg19 3p26.3-22.2(chr3:61891-36710181)x3 copy number gain See cases [RCV000448528] Chr3:61891..36710181 [GRCh37]
Chr3:3p26.3-22.2		 pathogenic
GRCh37/hg19 3p26.1-25.3(chr3:6842555-10153209)x1 copy number loss See cases [RCV000448839] Chr3:6842555..10153209 [GRCh37]
Chr3:3p26.1-25.3		 pathogenic
GRCh37/hg19 3p26.3-22.3(chr3:61891-33958201)x3 copy number gain See cases [RCV000510429] Chr3:61891..33958201 [GRCh37]
Chr3:3p26.3-22.3		 pathogenic
GRCh37/hg19 3p26.3-22.2(chr3:61891-37459464)x3 copy number gain See cases [RCV000511463] Chr3:61891..37459464 [GRCh37]
Chr3:3p26.3-22.2		 pathogenic
GRCh37/hg19 3p26.3-25.2(chr3:61891-12575409)x1 copy number loss See cases [RCV000511155] Chr3:61891..12575409 [GRCh37]
Chr3:3p26.3-25.2		 pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
NM_001025930.5(TTLL3):c.130G>A (p.Glu44Lys) single nucleotide variant not specified [RCV004292969] Chr3:9810136 [GRCh38]
Chr3:9851820 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2306G>A (p.Arg769Gln) single nucleotide variant not specified [RCV004332062] Chr3:9835347 [GRCh38]
Chr3:9877031 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
GRCh37/hg19 3p25.3(chr3:9600759-10000398)x3 copy number gain See cases [RCV000512318] Chr3:9600759..10000398 [GRCh37]
Chr3:3p25.3		 likely benign
GRCh37/hg19 3p26.3-25.3(chr3:61891-10104842)x1 copy number loss not provided [RCV000682180] Chr3:61891..10104842 [GRCh37]
Chr3:3p26.3-25.3		 pathogenic
GRCh37/hg19 3p26.3-24.3(chr3:1897972-19519085)x3 copy number gain not provided [RCV000682215] Chr3:1897972..19519085 [GRCh37]
Chr3:3p26.3-24.3		 pathogenic
GRCh37/hg19 3p26.1-24.3(chr3:5173870-16760262)x3 copy number gain not provided [RCV000682233] Chr3:5173870..16760262 [GRCh37]
Chr3:3p26.1-24.3		 pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
GRCh37/hg19 3p25.3(chr3:9547959-9898582)x1 copy number loss not provided [RCV000742227] Chr3:9547959..9898582 [GRCh37]
Chr3:3p25.3		 benign
NM_001387446.1(TTLL3):c.1004-4G>A single nucleotide variant not provided [RCV000961432] Chr3:9826993 [GRCh38]
Chr3:9868677 [GRCh37]
Chr3:3p25.3		 benign
NM_001387446.1(TTLL3):c.2311C>T (p.Pro771Ser) single nucleotide variant not specified [RCV004302191] Chr3:9835352 [GRCh38]
Chr3:9877036 [GRCh37]
Chr3:3p25.3		 uncertain significance
Single allele duplication Neurodevelopmental disorder [RCV000787461] Chr3:9453917..12015126 [GRCh37]
Chr3:3p25.3-25.2		 uncertain significance
GRCh37/hg19 3p25.3(chr3:8883205-9954034)x3 copy number gain not provided [RCV000848799] Chr3:8883205..9954034 [GRCh37]
Chr3:3p25.3		 uncertain significance
NC_000003.12:g.(?_9701780)_(9944589_?)dup duplication Atrioventricular septal defect, susceptibility to, 2 [RCV001031368] Chr3:9743464..9986273 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.3-25.3(chr3:61891-10287825)x1 copy number loss not provided [RCV001007530] Chr3:61891..10287825 [GRCh37]
Chr3:3p26.3-25.3		 pathogenic
NM_001387446.1(TTLL3):c.2027C>T (p.Ala676Val) single nucleotide variant not specified [RCV004319116] Chr3:9834882 [GRCh38]
Chr3:9876566 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.855C>T (p.His285=) single nucleotide variant not provided [RCV000957834] Chr3:9825800 [GRCh38]
Chr3:9867484 [GRCh37]
Chr3:3p25.3		 benign
GRCh37/hg19 3p26.3-25.3(chr3:61892-11679509)x1 copy number loss not provided [RCV002473616] Chr3:61892..11679509 [GRCh37]
Chr3:3p26.3-25.3		 pathogenic
NM_001025930.5(TTLL3):c.173G>T (p.Arg58Leu) single nucleotide variant not specified [RCV004682787] Chr3:9810179 [GRCh38]
Chr3:9851863 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p25.3(chr3:9870413-9930906)x1 copy number loss not provided [RCV001259808] Chr3:9870413..9930906 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p25.3(chr3:9501646-9991928)x4 copy number gain not provided [RCV001795849] Chr3:9501646..9991928 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.3-22.2(chr3:61891-36710181) copy number gain not specified [RCV002053300] Chr3:61891..36710181 [GRCh37]
Chr3:3p26.3-22.2		 pathogenic
GRCh37/hg19 3p26.1-25.3(chr3:6842555-10153209) copy number loss not specified [RCV002053327] Chr3:6842555..10153209 [GRCh37]
Chr3:3p26.1-25.3		 pathogenic
GRCh37/hg19 3p25.3(chr3:9754611-10295828) copy number gain not specified [RCV002053329] Chr3:9754611..10295828 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.3-24.2(chr3:61891-24432821) copy number gain not specified [RCV002053299] Chr3:61891..24432821 [GRCh37]
Chr3:3p26.3-24.2		 pathogenic
NC_000003.11:g.(?_8775563)_(9986075_?)dup duplication Long QT syndrome [RCV001923348] Chr3:8775563..9986075 [GRCh37]
Chr3:3p25.3		 uncertain significance
NC_000003.11:g.(?_7782024)_(11078652_?)dup duplication Atrioventricular septal defect, susceptibility to, 2 [RCV001875165] Chr3:7782024..11078652 [GRCh37]
Chr3:3p26.1-25.3		 uncertain significance
NM_001025930.5(TTLL3):c.137G>A (p.Arg46His) single nucleotide variant not specified [RCV004682791] Chr3:9810143 [GRCh38]
Chr3:9851827 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.3-25.3(chr3:60931-10687964)x3 copy number gain not provided [RCV002468435] Chr3:60931..10687964 [GRCh37]
Chr3:3p26.3-25.3		 pathogenic
GRCh37/hg19 3p26.3-25.3(chr3:61892-9899605)x1 copy number loss not provided [RCV002472571] Chr3:61892..9899605 [GRCh37]
Chr3:3p26.3-25.3		 pathogenic
GRCh37/hg19 3p25.3(chr3:9754612-10295828)x3 copy number gain not provided [RCV002472444] Chr3:9754612..10295828 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1906A>G (p.Arg636Gly) single nucleotide variant not specified [RCV004190403] Chr3:9834761 [GRCh38]
Chr3:9876445 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1035G>A (p.Met345Ile) single nucleotide variant not specified [RCV004237210] Chr3:9827028 [GRCh38]
Chr3:9868712 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1862C>G (p.Pro621Arg) single nucleotide variant not specified [RCV004139464] Chr3:9834805 [GRCh38]
Chr3:9876489 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2368G>T (p.Gly790Trp) single nucleotide variant not specified [RCV004087485] Chr3:9835409 [GRCh38]
Chr3:9877093 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001025930.5(TTLL3):c.119C>A (p.Pro40Gln) single nucleotide variant not specified [RCV004082801] Chr3:9810125 [GRCh38]
Chr3:9851809 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1999C>T (p.Leu667Phe) single nucleotide variant not specified [RCV004113365] Chr3:9834854 [GRCh38]
Chr3:9876538 [GRCh37]
Chr3:3p25.3		 likely benign
NM_001387446.1(TTLL3):c.-77C>T single nucleotide variant not specified [RCV004201013] Chr3:9810359 [GRCh38]
Chr3:9852043 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2317G>A (p.Ala773Thr) single nucleotide variant not specified [RCV004198528] Chr3:9835358 [GRCh38]
Chr3:9877042 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.619C>T (p.Arg207Trp) single nucleotide variant not specified [RCV004147646] Chr3:9817666 [GRCh38]
Chr3:9859350 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2426C>T (p.Pro809Leu) single nucleotide variant not specified [RCV004096474] Chr3:9835467 [GRCh38]
Chr3:9877151 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001025930.5(TTLL3):c.71C>A (p.Ser24Tyr) single nucleotide variant not specified [RCV004180622] Chr3:9810077 [GRCh38]
Chr3:9851761 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2417C>T (p.Pro806Leu) single nucleotide variant not specified [RCV004191663] Chr3:9835458 [GRCh38]
Chr3:9877142 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1973T>C (p.Leu658Pro) single nucleotide variant not specified [RCV004087700] Chr3:9834828 [GRCh38]
Chr3:9876512 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001025930.5(TTLL3):c.118C>G (p.Pro40Ala) single nucleotide variant not specified [RCV004082800] Chr3:9810124 [GRCh38]
Chr3:9851808 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1763C>T (p.Thr588Ile) single nucleotide variant not specified [RCV004107906] Chr3:9834706 [GRCh38]
Chr3:9876390 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.-134C>T single nucleotide variant not specified [RCV004199000] Chr3:9810302 [GRCh38]
Chr3:9851986 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.584G>T (p.Arg195Leu) single nucleotide variant not specified [RCV004101259] Chr3:9818846 [GRCh38]
Chr3:9860530 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2069G>C (p.Cys690Ser) single nucleotide variant not specified [RCV004176689] Chr3:9835110 [GRCh38]
Chr3:9876794 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.-153C>T single nucleotide variant not specified [RCV004107279] Chr3:9810283 [GRCh38]
Chr3:9851967 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1784G>A (p.Arg595His) single nucleotide variant not specified [RCV004210070] Chr3:9833204 [GRCh38]
Chr3:9874888 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2172G>T (p.Arg724Ser) single nucleotide variant not specified [RCV004165915] Chr3:9835213 [GRCh38]
Chr3:9876897 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1690G>A (p.Val564Met) single nucleotide variant not specified [RCV004174273] Chr3:9833110 [GRCh38]
Chr3:9874794 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.-168G>A single nucleotide variant not specified [RCV004175373] Chr3:9810268 [GRCh38]
Chr3:9851952 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001025930.5(TTLL3):c.238G>A (p.Gly80Ser) single nucleotide variant not specified [RCV004079651] Chr3:9810244 [GRCh38]
Chr3:9851928 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.-87C>T single nucleotide variant not specified [RCV004297346] Chr3:9810349 [GRCh38]
Chr3:9852033 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1828C>T (p.Arg610Cys) single nucleotide variant not specified [RCV004266556] Chr3:9834683 [GRCh38]
Chr3:9876367 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.2-25.3(chr3:3691505-9917651)x1 copy number loss 3p- syndrome [RCV003330127] Chr3:3691505..9917651 [GRCh37]
Chr3:3p26.2-25.3		 pathogenic
NM_001198793.1(ARPC4-TTLL3):c.1703G>C (p.Cys568Ser) single nucleotide variant not specified [RCV004339994] Chr3:9829361 [GRCh38]
Chr3:9871045 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1546G>A (p.Ala516Thr) single nucleotide variant not specified [RCV004350133] Chr3:9829204 [GRCh38]
Chr3:9870888 [GRCh37]
Chr3:3p25.3		 uncertain significance
Single allele deletion not provided [RCV003448703] Chr3:61435..9944653 [GRCh37]
Chr3:3p26.3-25.3		 pathogenic
GRCh37/hg19 3p26.3-24.1(chr3:310747-28297447)x3 copy number gain not provided [RCV003484107] Chr3:310747..28297447 [GRCh37]
Chr3:3p26.3-24.1		 pathogenic
GRCh37/hg19 3p25.3(chr3:9655252-10332544)x3 copy number gain not provided [RCV003484118] Chr3:9655252..10332544 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.1-25.3(chr3:6306331-11468530)x1 copy number loss not specified [RCV003986402] Chr3:6306331..11468530 [GRCh37]
Chr3:3p26.1-25.3		 pathogenic
GRCh37/hg19 3p26.3-22.3(chr3:61891-33946644)x3 copy number gain not specified [RCV003986437] Chr3:61891..33946644 [GRCh37]
Chr3:3p26.3-22.3		 pathogenic
NM_001198793.1(ARPC4-TTLL3):c.1651G>A (p.Val551Met) single nucleotide variant not specified [RCV004418127] Chr3:9829309 [GRCh38]
Chr3:9870993 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1669C>T (p.Arg557Cys) single nucleotide variant not specified [RCV004418128] Chr3:9829327 [GRCh38]
Chr3:9871011 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1726A>G (p.Ile576Val) single nucleotide variant not specified [RCV004418133] Chr3:9829384 [GRCh38]
Chr3:9871068 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.580G>A (p.Gly194Arg) single nucleotide variant not specified [RCV004418140] Chr3:9813328 [GRCh38]
Chr3:9855012 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.584C>T (p.Thr195Ile) single nucleotide variant not specified [RCV004418141] Chr3:9813332 [GRCh38]
Chr3:9855016 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.829G>A (p.Asp277Asn) single nucleotide variant not specified [RCV004418144] Chr3:9820662 [GRCh38]
Chr3:9862346 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1249G>A (p.Asp417Asn) single nucleotide variant not specified [RCV004418110] Chr3:9827188 [GRCh38]
Chr3:9868872 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1247G>A (p.Arg416His) single nucleotide variant not specified [RCV004418109] Chr3:9827186 [GRCh38]
Chr3:9868870 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1066T>C (p.Cys356Arg) single nucleotide variant not specified [RCV004418103] Chr3:9827005 [GRCh38]
Chr3:9868689 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1649G>C (p.Gly550Ala) single nucleotide variant not specified [RCV004418125] Chr3:9829307 [GRCh38]
Chr3:9870991 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1696C>T (p.Arg566Cys) single nucleotide variant not specified [RCV004418129] Chr3:9829354 [GRCh38]
Chr3:9871038 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1712G>C (p.Gly571Ala) single nucleotide variant not specified [RCV004418132] Chr3:9829370 [GRCh38]
Chr3:9871054 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.373C>T (p.Arg125Trp) single nucleotide variant not specified [RCV004418135] Chr3:9812985 [GRCh38]
Chr3:9854669 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.845C>T (p.Ala282Val) single nucleotide variant not specified [RCV004418145] Chr3:9820678 [GRCh38]
Chr3:9862362 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1088T>C (p.Met363Thr) single nucleotide variant not specified [RCV004418104] Chr3:9827027 [GRCh38]
Chr3:9868711 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1160G>A (p.Arg387Gln) single nucleotide variant not specified [RCV004418106] Chr3:9827099 [GRCh38]
Chr3:9868783 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1010A>G (p.Asp337Gly) single nucleotide variant not specified [RCV004418101] Chr3:9825901 [GRCh38]
Chr3:9867585 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1342G>C (p.Glu448Gln) single nucleotide variant not specified [RCV004418115] Chr3:9829000 [GRCh38]
Chr3:9870684 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1363C>T (p.Pro455Ser) single nucleotide variant not specified [RCV004418118] Chr3:9829021 [GRCh38]
Chr3:9870705 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1385T>C (p.Met462Thr) single nucleotide variant not specified [RCV004418119] Chr3:9829043 [GRCh38]
Chr3:9870727 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1445C>A (p.Ser482Tyr) single nucleotide variant not specified [RCV004418120] Chr3:9829103 [GRCh38]
Chr3:9870787 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1597G>A (p.Ala533Thr) single nucleotide variant not specified [RCV004418122] Chr3:9829255 [GRCh38]
Chr3:9870939 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1602C>A (p.Ser534Arg) single nucleotide variant not specified [RCV004418123] Chr3:9829260 [GRCh38]
Chr3:9870944 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.371T>C (p.Ile124Thr) single nucleotide variant not specified [RCV004418134] Chr3:9812983 [GRCh38]
Chr3:9854667 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.629C>T (p.Pro210Leu) single nucleotide variant not specified [RCV004418142] Chr3:9817676 [GRCh38]
Chr3:9859360 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.814G>C (p.Ala272Pro) single nucleotide variant not specified [RCV004418143] Chr3:9820647 [GRCh38]
Chr3:9862331 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1358G>A (p.Arg453Gln) single nucleotide variant not specified [RCV004418117] Chr3:9829016 [GRCh38]
Chr3:9870700 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1697G>C (p.Arg566Pro) single nucleotide variant not specified [RCV004418131] Chr3:9829355 [GRCh38]
Chr3:9871039 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1225C>G (p.Pro409Ala) single nucleotide variant not specified [RCV004418107] Chr3:9827164 [GRCh38]
Chr3:9868848 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1246C>T (p.Arg416Cys) single nucleotide variant not specified [RCV004418108] Chr3:9827185 [GRCh38]
Chr3:9868869 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1110C>A (p.Asn370Lys) single nucleotide variant not specified [RCV004418105] Chr3:9827049 [GRCh38]
Chr3:9868733 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.386G>A (p.Arg129His) single nucleotide variant not specified [RCV004418136] Chr3:9812998 [GRCh38]
Chr3:9854682 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1315T>C (p.Cys439Arg) single nucleotide variant not specified [RCV004418114] Chr3:9828973 [GRCh38]
Chr3:9870657 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1631C>A (p.Thr544Asn) single nucleotide variant not specified [RCV004418124] Chr3:9829289 [GRCh38]
Chr3:9870973 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1697G>A (p.Arg566His) single nucleotide variant not specified [RCV004418130] Chr3:9829355 [GRCh38]
Chr3:9871039 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1262G>A (p.Arg421His) single nucleotide variant not specified [RCV004418112] Chr3:9827201 [GRCh38]
Chr3:9868885 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1271C>T (p.Thr424Met) single nucleotide variant not specified [RCV004418113] Chr3:9827210 [GRCh38]
Chr3:9868894 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.482G>A (p.Ser161Asn) single nucleotide variant not specified [RCV004418138] Chr3:9813094 [GRCh38]
Chr3:9854778 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.519G>C (p.Glu173Asp) single nucleotide variant not specified [RCV004418139] Chr3:9813267 [GRCh38]
Chr3:9854951 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.899A>G (p.Gln300Arg) single nucleotide variant not specified [RCV004418146] Chr3:9820732 [GRCh38]
Chr3:9862416 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1555G>A (p.Val519Met) single nucleotide variant not specified [RCV004418121] Chr3:9829213 [GRCh38]
Chr3:9870897 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.479A>G (p.Asp160Gly) single nucleotide variant not specified [RCV004418137] Chr3:9813091 [GRCh38]
Chr3:9854775 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1261C>T (p.Arg421Cys) single nucleotide variant not specified [RCV004418111] Chr3:9827200 [GRCh38]
Chr3:9868884 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001198793.1(ARPC4-TTLL3):c.1051G>A (p.Gly351Arg) single nucleotide variant not specified [RCV004418102] Chr3:9825942 [GRCh38]
Chr3:9867626 [GRCh37]
Chr3:3p25.3		 uncertain significance
GRCh37/hg19 3p26.3-22.3(chr3:60000-34461438)x3 copy number gain not provided [RCV004577500] Chr3:60000..34461438 [GRCh37]
Chr3:3p26.3-22.3		 pathogenic
NM_001025930.5(TTLL3):c.104A>C (p.Asn35Thr) single nucleotide variant not specified [RCV004481456] Chr3:9810110 [GRCh38]
Chr3:9851794 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001025930.5(TTLL3):c.185G>A (p.Arg62Lys) single nucleotide variant not specified [RCV004481458] Chr3:9810191 [GRCh38]
Chr3:9851875 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1717C>T (p.Arg573Trp) single nucleotide variant not specified [RCV004481459] Chr3:9833137 [GRCh38]
Chr3:9874821 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.1772G>A (p.Arg591Gln) single nucleotide variant not specified [RCV004481460] Chr3:9833192 [GRCh38]
Chr3:9874876 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001025930.5(TTLL3):c.239G>T (p.Gly80Val) single nucleotide variant not specified [RCV004481461] Chr3:9810245 [GRCh38]
Chr3:9851929 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2264G>A (p.Arg755His) single nucleotide variant not specified [RCV004481462] Chr3:9835305 [GRCh38]
Chr3:9876989 [GRCh37]
Chr3:3p25.3		 likely benign
NM_001387446.1(TTLL3):c.-89C>T single nucleotide variant not specified [RCV004481463] Chr3:9810347 [GRCh38]
Chr3:9852031 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.-84G>A single nucleotide variant not specified [RCV004481464] Chr3:9810352 [GRCh38]
Chr3:9852036 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.40G>A (p.Ala14Thr) single nucleotide variant not specified [RCV004481465] Chr3:9810701 [GRCh38]
Chr3:9852385 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.-105G>A single nucleotide variant not specified [RCV004682790] Chr3:9810331 [GRCh38]
Chr3:9852015 [GRCh37]
Chr3:3p25.3		 uncertain significance
NC_000003.11:g.(?_9703931)_(11078652_?)del deletion Myoclonic-atonic epilepsy [RCV004582222] Chr3:9703931..11078652 [GRCh37]
Chr3:3p25.3		 pathogenic
NC_000003.11:g.(?_9470623)_(11078652_?)dup duplication not provided [RCV004582249] Chr3:9470623..11078652 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.583C>T (p.Arg195Cys) single nucleotide variant not specified [RCV004682786] Chr3:9818845 [GRCh38]
Chr3:9860529 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.584G>A (p.Arg195His) single nucleotide variant not specified [RCV004682789] Chr3:9818846 [GRCh38]
Chr3:9860530 [GRCh37]
Chr3:3p25.3		 uncertain significance
NM_001387446.1(TTLL3):c.2176G>C (p.Asp726His) single nucleotide variant not specified [RCV004682788] Chr3:9835217 [GRCh38]
Chr3:9876901 [GRCh37]
Chr3:3p25.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:12927
Count of miRNA genes:1258
Interacting mature miRNAs:1671
Transcripts:ENST00000310252, ENST00000383827, ENST00000397241, ENST00000414814, ENST00000417065, ENST00000418745, ENST00000419081, ENST00000422738, ENST00000426827, ENST00000426895, ENST00000427220, ENST00000427853, ENST00000430390, ENST00000430718, ENST00000430793, ENST00000431204, ENST00000438141, ENST00000438596, ENST00000439814, ENST00000443148, ENST00000452597, ENST00000452823, ENST00000455274, ENST00000459758, ENST00000466245, ENST00000471058, ENST00000473661, ENST00000474948, ENST00000482269, ENST00000483051, ENST00000492440, ENST00000493241, ENST00000496246, ENST00000496526, ENST00000547186, ENST00000602338
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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
2316345GLUCO224_HGlucose level QTL 224 (human)1.270.008Glucose level3121543441Human

Markers in Region
RH17932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3739,876,887 - 9,877,024UniSTSGRCh37
Build 3639,851,887 - 9,852,024RGDNCBI36
Celera39,812,188 - 9,812,325RGD
Cytogenetic Map3pUniSTS
Cytogenetic Map3p25.3UniSTS
HuRef39,813,169 - 9,813,306UniSTS
GeneMap99-GB4 RH Map344.58UniSTS
NCBI RH Map3132.9UniSTS
SHGC-33325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3739,876,941 - 9,877,068UniSTSGRCh37
Build 3639,851,941 - 9,852,068RGDNCBI36
Celera39,812,242 - 9,812,369RGD
Cytogenetic Map3pUniSTS
Cytogenetic Map3p25.3UniSTS
HuRef39,813,223 - 9,813,350UniSTS
TNG Radiation Hybrid Map36201.0UniSTS
GeneMap99-GB4 RH Map346.91UniSTS
Whitehead-RH Map351.3UniSTS
GeneMap99-G3 RH Map3346.0UniSTS
TTLL3_9463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3739,876,406 - 9,877,233UniSTSGRCh37
Build 3639,851,406 - 9,852,233RGDNCBI36
Celera39,811,707 - 9,812,534RGD
HuRef39,812,688 - 9,813,515UniSTS
RH47393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3739,876,893 - 9,877,018UniSTSGRCh37
Build 3639,851,893 - 9,852,018RGDNCBI36
Celera39,812,194 - 9,812,319RGD
Cytogenetic Map3pUniSTS
Cytogenetic Map3p25.3UniSTS
HuRef39,813,175 - 9,813,300UniSTS
GeneMap99-GB4 RH Map346.91UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
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Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


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
1204 2439 2788 2250 4972 1726 2351 5 624 1951 465 2269 7301 6467 53 3733 1 852 1744 1617 172

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001025930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387457 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_037162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170661 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA742169 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC018809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC022382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF078842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023960 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125875 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL096725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009479 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028169 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC098298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC098361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC099735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC105638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM674442 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM717061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP357921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX440835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB854808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA267460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000310252   ⟹   ENSP00000312148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,813,294 - 9,834,821 (+)Ensembl
Ensembl Acc Id: ENST00000383827   ⟹   ENSP00000373338
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,818,372 - 9,836,315 (+)Ensembl
Ensembl Acc Id: ENST00000414814   ⟹   ENSP00000399930
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,808,086 - 9,816,094 (+)Ensembl
Ensembl Acc Id: ENST00000417065   ⟹   ENSP00000408128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,721 - 9,818,871 (+)Ensembl
Ensembl Acc Id: ENST00000418745   ⟹   ENSP00000400462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,740 - 9,816,125 (+)Ensembl
Ensembl Acc Id: ENST00000419081   ⟹   ENSP00000401686
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,700 - 9,817,656 (+)Ensembl
Ensembl Acc Id: ENST00000422738   ⟹   ENSP00000412915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,810,602 - 9,818,921 (+)Ensembl
Ensembl Acc Id: ENST00000426827   ⟹   ENSP00000389904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,810,247 - 9,817,767 (+)Ensembl
Ensembl Acc Id: ENST00000426895   ⟹   ENSP00000392549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,988 - 9,836,354 (+)Ensembl
Ensembl Acc Id: ENST00000427220   ⟹   ENSP00000395912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,935 - 9,835,404 (+)Ensembl
Ensembl Acc Id: ENST00000430390   ⟹   ENSP00000396606
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,810,670 - 9,835,404 (+)Ensembl
Ensembl Acc Id: ENST00000430718   ⟹   ENSP00000402197
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,874 - 9,816,204 (+)Ensembl
Ensembl Acc Id: ENST00000430793   ⟹   ENSP00000403874
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,820,294 - 9,835,358 (+)Ensembl
Ensembl Acc Id: ENST00000431204   ⟹   ENSP00000398996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,810,247 - 9,829,252 (+)Ensembl
Ensembl Acc Id: ENST00000438141   ⟹   ENSP00000409246
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,820,294 - 9,835,332 (+)Ensembl
Ensembl Acc Id: ENST00000438596   ⟹   ENSP00000414965
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,721 - 9,817,658 (+)Ensembl
Ensembl Acc Id: ENST00000439814   ⟹   ENSP00000394481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,740 - 9,816,105 (+)Ensembl
Ensembl Acc Id: ENST00000443148   ⟹   ENSP00000398097
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,816,074 - 9,835,096 (+)Ensembl
Ensembl Acc Id: ENST00000452597   ⟹   ENSP00000399782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,808,517 - 9,816,179 (+)Ensembl
Ensembl Acc Id: ENST00000452823   ⟹   ENSP00000399191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,813,309 - 9,825,901 (+)Ensembl
Ensembl Acc Id: ENST00000455274   ⟹   ENSP00000409632
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,819,303 - 9,855,138 (+)Ensembl
Ensembl Acc Id: ENST00000459758
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,721 - 9,817,799 (+)Ensembl
Ensembl Acc Id: ENST00000466245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,825,861 - 9,829,335 (+)Ensembl
Ensembl Acc Id: ENST00000471058   ⟹   ENSP00000473314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,829,163 - 9,835,403 (+)Ensembl
Ensembl Acc Id: ENST00000473661   ⟹   ENSP00000430051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,818,561 - 9,835,404 (+)Ensembl
Ensembl Acc Id: ENST00000474948   ⟹   ENSP00000473376
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,813,309 - 9,820,616 (+)Ensembl
Ensembl Acc Id: ENST00000482269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,825,406 - 9,829,054 (+)Ensembl
Ensembl Acc Id: ENST00000483051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,813,248 - 9,836,315 (+)Ensembl
Ensembl Acc Id: ENST00000492440
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,825,566 - 9,828,162 (+)Ensembl
Ensembl Acc Id: ENST00000493241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,834,084 - 9,835,208 (+)Ensembl
Ensembl Acc Id: ENST00000496246   ⟹   ENSP00000473440
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,813,307 - 9,820,647 (+)Ensembl
Ensembl Acc Id: ENST00000496526
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,813,303 - 9,835,403 (+)Ensembl
Ensembl Acc Id: ENST00000602338
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,820,349 - 9,821,041 (+)Ensembl
Ensembl Acc Id: ENST00000685419   ⟹   ENSP00000510679
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,810,262 - 9,836,365 (+)Ensembl
Ensembl Acc Id: ENST00000703870   ⟹   ENSP00000515513
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,809,891 - 9,835,328 (+)Ensembl
Ensembl Acc Id: ENST00000715597   ⟹   ENSP00000520491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl39,810,402 - 9,835,362 (+)Ensembl
RefSeq Acc Id: NM_001025930   ⟹   NP_001021100
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,915 - 9,836,365 (+)NCBI
GRCh3739,851,632 - 9,878,040 (+)NCBI
Build 3639,826,904 - 9,853,040 (+)NCBI Archive
Celera39,786,607 - 9,813,341 (+)RGD
HuRef39,787,987 - 9,814,322 (+)ENTREZGENE
CHM1_139,801,835 - 9,828,234 (+)NCBI
T2T-CHM13v2.039,801,867 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001366051   ⟹   NP_001352980
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387446   ⟹   NP_001374375
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387447   ⟹   NP_001374376
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387448   ⟹   NP_001374377
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387449   ⟹   NP_001374378
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387450   ⟹   NP_001374379
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387451   ⟹   NP_001374380
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387452   ⟹   NP_001374381
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387453   ⟹   NP_001374382
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387454   ⟹   NP_001374383
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387455   ⟹   NP_001374384
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387456   ⟹   NP_001374385
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387457   ⟹   NP_001374386
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387458   ⟹   NP_001374387
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387459   ⟹   NP_001374388
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387460   ⟹   NP_001374389
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387461   ⟹   NP_001374390
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387462   ⟹   NP_001374391
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387463   ⟹   NP_001374392
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387464   ⟹   NP_001374393
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387465   ⟹   NP_001374394
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387466   ⟹   NP_001374395
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387467   ⟹   NP_001374396
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NR_037162
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
GRCh3739,851,632 - 9,878,040 (+)NCBI
HuRef39,787,987 - 9,814,322 (+)ENTREZGENE
CHM1_139,801,835 - 9,828,234 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170661
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,727 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,801,679 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170662
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170663
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170664
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170665
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,262 - 9,836,365 (+)NCBI
T2T-CHM13v2.039,802,243 - 9,828,366 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001021100 (Get FASTA)   NCBI Sequence Viewer  
  NP_001352980 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374375 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374376 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374377 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374378 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374379 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374380 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374381 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374382 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374383 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374384 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374385 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374386 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374387 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374388 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374389 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374390 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374391 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374392 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374393 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374394 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374395 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374396 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF23353 (Get FASTA)   NCBI Sequence Viewer  
  AAH98298 (Get FASTA)   NCBI Sequence Viewer  
  AAH98361 (Get FASTA)   NCBI Sequence Viewer  
  AAH99735 (Get FASTA)   NCBI Sequence Viewer  
  AAI05639 (Get FASTA)   NCBI Sequence Viewer  
  BAB14741 (Get FASTA)   NCBI Sequence Viewer  
  BAG37589 (Get FASTA)   NCBI Sequence Viewer  
  BAG59759 (Get FASTA)   NCBI Sequence Viewer  
  CAB46375 (Get FASTA)   NCBI Sequence Viewer  
  CAD38794 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000312148
  ENSP00000312148.7
  ENSP00000373338.1
  ENSP00000389904.1
  ENSP00000392549
  ENSP00000392549.5
  ENSP00000394481.1
  ENSP00000395912.1
  ENSP00000396606.1
  ENSP00000398097.1
  ENSP00000398996.1
  ENSP00000399191.1
  ENSP00000399782.1
  ENSP00000399930.1
  ENSP00000400462.1
  ENSP00000401686.1
  ENSP00000402197.1
  ENSP00000403874
  ENSP00000403874.1
  ENSP00000408128.1
  ENSP00000409246.1
  ENSP00000409632.1
  ENSP00000412915.1
  ENSP00000414965.1
  ENSP00000430051.1
  ENSP00000473314.1
  ENSP00000473376.1
  ENSP00000473440.1
  ENSP00000510679
  ENSP00000510679.1
  ENSP00000515513
  ENSP00000515513.1
  ENSP00000520491
  ENSP00000520491.1
GenBank Protein Q9Y4R7 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001021100   ⟸   NM_001025930
- Peptide Label: isoform 1
- UniProtKB: J3KQB2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001352980   ⟸   NM_001366051
- Peptide Label: isoform 2
- UniProtKB: Q9Y4R7 (UniProtKB/Swiss-Prot),   Q9H876 (UniProtKB/Swiss-Prot),   Q96GG8 (UniProtKB/Swiss-Prot),   Q8NDN8 (UniProtKB/Swiss-Prot),   Q6ZU95 (UniProtKB/Swiss-Prot),   Q6AWA3 (UniProtKB/Swiss-Prot),   Q4KMS8 (UniProtKB/Swiss-Prot),   Q9UI99 (UniProtKB/Swiss-Prot)
Ensembl Acc Id: ENSP00000409246   ⟸   ENST00000438141
Ensembl Acc Id: ENSP00000414965   ⟸   ENST00000438596
Ensembl Acc Id: ENSP00000394481   ⟸   ENST00000439814
Ensembl Acc Id: ENSP00000392549   ⟸   ENST00000426895
Ensembl Acc Id: ENSP00000389904   ⟸   ENST00000426827
Ensembl Acc Id: ENSP00000399782   ⟸   ENST00000452597
Ensembl Acc Id: ENSP00000399191   ⟸   ENST00000452823
Ensembl Acc Id: ENSP00000395912   ⟸   ENST00000427220
Ensembl Acc Id: ENSP00000399930   ⟸   ENST00000414814
Ensembl Acc Id: ENSP00000409632   ⟸   ENST00000455274
Ensembl Acc Id: ENSP00000312148   ⟸   ENST00000310252
Ensembl Acc Id: ENSP00000408128   ⟸   ENST00000417065
Ensembl Acc Id: ENSP00000398097   ⟸   ENST00000443148
Ensembl Acc Id: ENSP00000473440   ⟸   ENST00000496246
Ensembl Acc Id: ENSP00000400462   ⟸   ENST00000418745
Ensembl Acc Id: ENSP00000401686   ⟸   ENST00000419081
Ensembl Acc Id: ENSP00000396606   ⟸   ENST00000430390
Ensembl Acc Id: ENSP00000402197   ⟸   ENST00000430718
Ensembl Acc Id: ENSP00000403874   ⟸   ENST00000430793
Ensembl Acc Id: ENSP00000398996   ⟸   ENST00000431204
Ensembl Acc Id: ENSP00000473314   ⟸   ENST00000471058
Ensembl Acc Id: ENSP00000430051   ⟸   ENST00000473661
Ensembl Acc Id: ENSP00000473376   ⟸   ENST00000474948
Ensembl Acc Id: ENSP00000412915   ⟸   ENST00000422738
Ensembl Acc Id: ENSP00000373338   ⟸   ENST00000383827
RefSeq Acc Id: NP_001374383   ⟸   NM_001387454
- Peptide Label: isoform 11
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374389   ⟸   NM_001387460
- Peptide Label: isoform 14
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374394   ⟸   NM_001387465
- Peptide Label: isoform 18
- UniProtKB: H3BLT7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374377   ⟸   NM_001387448
- Peptide Label: isoform 5
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374384   ⟸   NM_001387455
- Peptide Label: isoform 11
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374388   ⟸   NM_001387459
- Peptide Label: isoform 14
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374393   ⟸   NM_001387464
- Peptide Label: isoform 18
- UniProtKB: H3BLT7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374396   ⟸   NM_001387467
- Peptide Label: isoform 20
- UniProtKB: B2RCJ2 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374379   ⟸   NM_001387450
- Peptide Label: isoform 7
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374375   ⟸   NM_001387446
- Peptide Label: isoform 3
- UniProtKB: A0A8I5KXU2 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374385   ⟸   NM_001387456
- Peptide Label: isoform 11
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374376   ⟸   NM_001387447
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001374386   ⟸   NM_001387457
- Peptide Label: isoform 12
- UniProtKB: A0AAQ5BIG3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374380   ⟸   NM_001387451
- Peptide Label: isoform 8
- UniProtKB: A0AAQ5BIG3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374378   ⟸   NM_001387449
- Peptide Label: isoform 6
- UniProtKB: A0AAQ5BIG3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374390   ⟸   NM_001387461
- Peptide Label: isoform 15
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374387   ⟸   NM_001387458
- Peptide Label: isoform 13
- UniProtKB: A0AAQ5BIG3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374382   ⟸   NM_001387453
- Peptide Label: isoform 10
- UniProtKB: A0AAQ5BIG3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374392   ⟸   NM_001387463
- Peptide Label: isoform 17
- UniProtKB: H3BLT7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374381   ⟸   NM_001387452
- Peptide Label: isoform 9
RefSeq Acc Id: NP_001374395   ⟸   NM_001387466
- Peptide Label: isoform 19
RefSeq Acc Id: NP_001374391   ⟸   NM_001387462
- Peptide Label: isoform 16
- UniProtKB: A0A994J3Y4 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000510679   ⟸   ENST00000685419
Ensembl Acc Id: ENSP00000515513   ⟸   ENST00000703870
Ensembl Acc Id: ENSP00000520491   ⟸   ENST00000715597
Protein Domains
TTL

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y4R7-F1-model_v2 AlphaFold Q9Y4R7 1-772 view protein structure

Promoters
RGD ID:6863492
Promoter ID:EPDNEW_H4911
Type:initiation region
Name:TTLL3_6
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,808,544 - 9,808,604EPDNEW
RGD ID:6863494
Promoter ID:EPDNEW_H4912
Type:initiation region
Name:TTLL3_1
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,725 - 9,809,785EPDNEW
RGD ID:6863500
Promoter ID:EPDNEW_H4913
Type:initiation region
Name:TTLL3_2
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,809,915 - 9,809,975EPDNEW
RGD ID:6863498
Promoter ID:EPDNEW_H4914
Type:initiation region
Name:TTLL3_3
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,283 - 9,810,343EPDNEW
RGD ID:6863522
Promoter ID:EPDNEW_H4915
Type:initiation region
Name:TTLL3_11
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,602 - 9,810,662EPDNEW
RGD ID:6863502
Promoter ID:EPDNEW_H4916
Type:multiple initiation site
Name:TTLL3_10
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,810,753 - 9,810,813EPDNEW
RGD ID:6863504
Promoter ID:EPDNEW_H4917
Type:initiation region
Name:TTLL3_9
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,813,008 - 9,813,068EPDNEW
RGD ID:6863506
Promoter ID:EPDNEW_H4918
Type:initiation region
Name:TTLL3_5
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,818,366 - 9,818,426EPDNEW
RGD ID:6863508
Promoter ID:EPDNEW_H4919
Type:initiation region
Name:TTLL3_4
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4920  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,818,791 - 9,818,851EPDNEW
RGD ID:6863510
Promoter ID:EPDNEW_H4920
Type:initiation region
Name:TTLL3_7
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4921  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,818,934 - 9,818,994EPDNEW
RGD ID:6801842
Promoter ID:HG_KWN:43642
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:OTTHUMT00000338966,   OTTHUMT00000338967
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,824,251 - 9,825,327 (+)MPROMDB
RGD ID:6801007
Promoter ID:HG_KWN:43643
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000310252,   ENST00000397241,   OTTHUMT00000258267,   OTTHUMT00000258268,   OTTHUMT00000258269,   OTTHUMT00000308972,   OTTHUMT00000308973,   OTTHUMT00000308974,   OTTHUMT00000308975,   OTTHUMT00000308976,   OTTHUMT00000338965,   OTTHUMT00000338972,   OTTHUMT00000338973,   OTTHUMT00000338974,   OTTHUMT00000338975,   OTTHUMT00000338976
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,825,446 - 9,827,162 (+)MPROMDB
RGD ID:6801847
Promoter ID:HG_KWN:43644
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000258270,   OTTHUMT00000258271,   OTTHUMT00000338986,   OTTHUMT00000338987,   OTTHUMT00000338988,   UC010HCO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,829,614 - 9,830,114 (+)MPROMDB
RGD ID:6801843
Promoter ID:HG_KWN:43645
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000338969
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,832,234 - 9,832,734 (+)MPROMDB
RGD ID:6863512
Promoter ID:EPDNEW_H4921
Type:initiation region
Name:TTLL3_8
Description:tubulin tyrosine ligase like 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4911  EPDNEW_H4912  EPDNEW_H4914  EPDNEW_H4913  EPDNEW_H4916  EPDNEW_H4917  EPDNEW_H4918  EPDNEW_H4919  EPDNEW_H4920  EPDNEW_H4915  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3839,835,372 - 9,835,432EPDNEW
RGD ID:6801846
Promoter ID:HG_KWN:43646
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000258273,   OTTHUMT00000308977,   OTTHUMT00000338971,   OTTHUMT00000338992,   UC003BTI.2,   UC003BTJ.2
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,835,601 - 9,837,372 (+)MPROMDB
RGD ID:6801841
Promoter ID:HG_KWN:43647
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000258272,   OTTHUMT00000258274,   OTTHUMT00000338989
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,842,326 - 9,842,826 (+)MPROMDB
RGD ID:6801005
Promoter ID:HG_KWN:43648
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562
Transcripts:ENST00000287619,   OTTHUMT00000338990
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,845,414 - 9,845,914 (+)MPROMDB
RGD ID:6801844
Promoter ID:HG_KWN:43650
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000338991
Position:
Human AssemblyChrPosition (strand)Source
Build 3639,850,746 - 9,851,246 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24483 AgrOrtholog
COSMIC TTLL3 COSMIC
Ensembl Genes ENSG00000214021 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000310252 ENTREZGENE
  ENST00000310252.11 UniProtKB/TrEMBL
  ENST00000383827.5 UniProtKB/Swiss-Prot
  ENST00000414814.5 UniProtKB/TrEMBL
  ENST00000417065.5 UniProtKB/TrEMBL
  ENST00000418745.5 UniProtKB/TrEMBL
  ENST00000419081.5 UniProtKB/TrEMBL
  ENST00000422738.5 UniProtKB/TrEMBL
  ENST00000426827.5 UniProtKB/TrEMBL
  ENST00000426895 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000426895.10 UniProtKB/Swiss-Prot
  ENST00000427220.5 UniProtKB/TrEMBL
  ENST00000430390.5 UniProtKB/TrEMBL
  ENST00000430718.5 UniProtKB/TrEMBL
  ENST00000430793 ENTREZGENE
  ENST00000430793.1 UniProtKB/Swiss-Prot
  ENST00000431204.5 UniProtKB/TrEMBL
  ENST00000438141.5 UniProtKB/Swiss-Prot
  ENST00000438596.5 UniProtKB/TrEMBL
  ENST00000439814.5 UniProtKB/TrEMBL
  ENST00000443148.5 UniProtKB/TrEMBL
  ENST00000452597.5 UniProtKB/TrEMBL
  ENST00000452823.5 UniProtKB/TrEMBL
  ENST00000455274.5 UniProtKB/TrEMBL
  ENST00000471058.1 UniProtKB/TrEMBL
  ENST00000473661.5 UniProtKB/TrEMBL
  ENST00000474948.5 UniProtKB/TrEMBL
  ENST00000496246.5 UniProtKB/TrEMBL
  ENST00000685419 ENTREZGENE
  ENST00000685419.1 UniProtKB/TrEMBL
  ENST00000703870 ENTREZGENE
  ENST00000703870.1 UniProtKB/TrEMBL
  ENST00000715597 ENTREZGENE
  ENST00000715597.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.1490.20 UniProtKB/TrEMBL
  ATP-grasp fold, B domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000214021 GTEx
HGNC ID HGNC:24483 ENTREZGENE
Human Proteome Map TTLL3 Human Proteome Map
InterPro ATP_grasp_subdomain_1 UniProtKB/TrEMBL
  TTL/TTLL_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TTLL_monoglycylase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:26140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 26140 ENTREZGENE
OMIM 619195 OMIM
PANTHER PTHR45870:SF1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TUBULIN MONOGLYCYLASE TTLL3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam TTL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134942870 PharmGKB
PROSITE TTL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Glutathione synthetase ATP-binding domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A8I5KXU2 ENTREZGENE, UniProtKB/TrEMBL
  A0A994J3Y4 ENTREZGENE, UniProtKB/TrEMBL
  A0AAQ5BIG3 ENTREZGENE, UniProtKB/TrEMBL
  B2RCJ2 ENTREZGENE, UniProtKB/TrEMBL
  C9IZU0_HUMAN UniProtKB/TrEMBL
  C9JKU2_HUMAN UniProtKB/TrEMBL
  C9JNK2_HUMAN UniProtKB/TrEMBL
  C9JNK7_HUMAN UniProtKB/TrEMBL
  C9JQ30_HUMAN UniProtKB/TrEMBL
  C9JRM2_HUMAN UniProtKB/TrEMBL
  C9JSD3_HUMAN UniProtKB/TrEMBL
  C9JUK0_HUMAN UniProtKB/TrEMBL
  C9JW59_HUMAN UniProtKB/TrEMBL
  C9JWZ9_HUMAN UniProtKB/TrEMBL
  C9JZ73_HUMAN UniProtKB/TrEMBL
  E5RGZ6_HUMAN UniProtKB/TrEMBL
  F8WBP6_HUMAN UniProtKB/TrEMBL
  F8WD18_HUMAN UniProtKB/TrEMBL
  H0Y5E3_HUMAN UniProtKB/TrEMBL
  H3BLT7 ENTREZGENE, UniProtKB/TrEMBL
  H7C0T5_HUMAN UniProtKB/TrEMBL
  H7C197_HUMAN UniProtKB/TrEMBL
  J3KQB2 ENTREZGENE, UniProtKB/TrEMBL
  Q4KMS8 ENTREZGENE
  Q6AWA3 ENTREZGENE
  Q6ZU95 ENTREZGENE
  Q8NDN8 ENTREZGENE
  Q96GG8 ENTREZGENE
  Q9H876 ENTREZGENE
  Q9UI99 ENTREZGENE
  Q9Y4R7 ENTREZGENE
  R4GMR7_HUMAN UniProtKB/TrEMBL
  R4GMW2_HUMAN UniProtKB/TrEMBL
  R4GN12_HUMAN UniProtKB/TrEMBL
  TTLL3_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q4KMS8 UniProtKB/Swiss-Prot
  Q6AWA3 UniProtKB/Swiss-Prot
  Q6ZU95 UniProtKB/Swiss-Prot
  Q8NDN8 UniProtKB/Swiss-Prot
  Q96GG8 UniProtKB/Swiss-Prot
  Q9H876 UniProtKB/Swiss-Prot
  Q9UI99 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 TTLL3  tubulin tyrosine ligase like 3    tubulin tyrosine ligase-like family member 3  Symbol and/or name change 5135510 APPROVED
2015-01-20 TTLL3  tubulin tyrosine ligase-like family member 3    tubulin tyrosine ligase-like family, member 3  Symbol and/or name change 5135510 APPROVED