MITD1 (microtubule interacting and trafficking domain containing 1) - Rat Genome Database

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Gene: MITD1 (microtubule interacting and trafficking domain containing 1) Homo sapiens
Analyze
Symbol: MITD1
Name: microtubule interacting and trafficking domain containing 1
RGD ID: 1602187
HGNC Page HGNC:25207
Description: Enables identical protein binding activity; phosphatidylinositol binding activity; and protein domain specific binding activity. Involved in midbody abscission. Located in intracellular membrane-bounded organelle; membrane; and midbody.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: MIT domain-containing protein 1; MIT, microtubule interacting and transport, domain containing 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38299,161,427 - 99,181,058 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl299,161,427 - 99,181,058 (-)EnsemblGRCh38hg38GRCh38
GRCh37299,785,726 - 99,797,521 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36299,152,158 - 99,163,924 (-)NCBINCBI36Build 36hg18NCBI36
Celera293,990,319 - 94,002,087 (-)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef293,551,497 - 93,563,265 (-)NCBIHuRef
CHM1_1299,790,624 - 99,802,390 (-)NCBICHM1_1
T2T-CHM13v2.0299,620,306 - 99,639,936 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:15489334   PMID:15815621   PMID:16344560   PMID:16730941   PMID:17207965   PMID:18029348   PMID:19056867   PMID:20195357   PMID:21674799   PMID:21873635   PMID:21926972  
PMID:22190034   PMID:23015756   PMID:23045692   PMID:23376485   PMID:23533145   PMID:25416956   PMID:26344197   PMID:26496610   PMID:27107014   PMID:28007894   PMID:29053956   PMID:29150431  
PMID:30021884   PMID:30442762   PMID:31091453   PMID:32296183   PMID:32780723   PMID:33200223   PMID:33961781   PMID:34346239   PMID:34599178   PMID:34732716   PMID:35271311   PMID:35914814  
PMID:36046690   PMID:36291174   PMID:36732658  


Genomics

Comparative Map Data
MITD1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38299,161,427 - 99,181,058 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl299,161,427 - 99,181,058 (-)EnsemblGRCh38hg38GRCh38
GRCh37299,785,726 - 99,797,521 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36299,152,158 - 99,163,924 (-)NCBINCBI36Build 36hg18NCBI36
Celera293,990,319 - 94,002,087 (-)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef293,551,497 - 93,563,265 (-)NCBIHuRef
CHM1_1299,790,624 - 99,802,390 (-)NCBICHM1_1
T2T-CHM13v2.0299,620,306 - 99,639,936 (-)NCBIT2T-CHM13v2.0
Mitd1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39137,913,882 - 37,929,530 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl137,913,882 - 37,929,492 (-)EnsemblGRCm39 Ensembl
GRCm38137,874,801 - 37,890,449 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl137,874,801 - 37,890,411 (-)EnsemblGRCm38mm10GRCm38
MGSCv37137,935,735 - 37,947,256 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36137,823,275 - 37,834,979 (-)NCBIMGSCv36mm8
Celera137,659,809 - 37,671,331 (-)NCBICelera
Cytogenetic Map1BNCBI
cM Map116.13NCBI
Mitd1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8947,609,743 - 47,621,033 (-)NCBIGRCr8
mRatBN7.2940,113,943 - 40,125,280 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl940,113,946 - 40,125,289 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx948,609,792 - 48,621,053 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0953,732,547 - 53,743,808 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0952,014,641 - 52,025,935 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0944,472,364 - 44,483,723 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl944,472,365 - 44,560,837 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0944,169,744 - 44,181,102 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4936,827,857 - 36,839,148 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1936,829,271 - 36,840,562 (-)NCBI
Celera937,868,172 - 37,879,466 (-)NCBICelera
Cytogenetic Map9q21NCBI
Mitd1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554705,493,144 - 5,509,437 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554705,493,361 - 5,509,437 (-)NCBIChiLan1.0ChiLan1.0
MITD1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21229,248,958 - 29,263,284 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A29,251,722 - 29,266,044 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A100,116,263 - 100,130,580 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A100,097,758 - 100,111,589 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A100,097,758 - 100,111,589 (-)Ensemblpanpan1.1panPan2
MITD1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11043,513,240 - 43,525,543 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1043,513,277 - 43,523,883 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1043,436,787 - 43,456,434 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01044,385,417 - 44,405,067 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1044,385,431 - 44,398,060 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11044,095,468 - 44,115,110 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01044,378,979 - 44,391,206 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01044,563,444 - 44,583,084 (+)NCBIUU_Cfam_GSD_1.0
Mitd1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629284,937,949 - 84,949,823 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366611,618,975 - 1,633,278 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366611,619,703 - 1,632,558 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MITD1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl355,054,517 - 55,069,866 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1355,054,475 - 55,078,180 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2357,688,426 - 57,703,819 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MITD1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1142,894,096 - 2,902,790 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666041170,496,653 - 170,506,461 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Mitd1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247494,172,007 - 4,185,890 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247494,166,358 - 4,185,980 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MITD1
88 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_145199.3(LIPT1):c.635T>G (p.Val212Gly) single nucleotide variant not provided [RCV000519561] Chr2:99162592 [GRCh38]
Chr2:99779055 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.292C>G (p.Arg98Gly) single nucleotide variant Lipoyl transferase 1 deficiency [RCV000170327]|not provided [RCV001560053] Chr2:99162249 [GRCh38]
Chr2:99778712 [GRCh37]
Chr2:2q11.2		 pathogenic|conflicting interpretations of pathogenicity|not provided
GRCh38/hg38 2q11.1-12.1(chr2:94817406-103252396)x3 copy number gain See cases [RCV000052946] Chr2:94817406..103252396 [GRCh38]
Chr2:95618109..103868854 [GRCh37]
Chr2:94846878..103235286 [NCBI36]
Chr2:2q11.1-12.1		 pathogenic
GRCh38/hg38 2q11.2-13(chr2:97672522-110211318)x3 copy number gain See cases [RCV000052947] Chr2:97672522..110211318 [GRCh38]
Chr2:98288985..110968895 [GRCh37]
Chr2:97655417..110326184 [NCBI36]
Chr2:2q11.2-13		 pathogenic
GRCh38/hg38 2p11.2-q11.2(chr2:91443218-102334856)x3 copy number gain See cases [RCV000052945] Chr2:91443218..102334856 [GRCh38]
Chr2:91617683..102951316 [GRCh37]
Chr2:90981410..102317748 [NCBI36]
Chr2:2p11.2-q11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:98787057-100785053)x1 copy number loss See cases [RCV000054057] Chr2:98787057..100785053 [GRCh38]
Chr2:99403520..101401515 [GRCh37]
Chr2:98769952..100767947 [NCBI36]
Chr2:2q11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:98411773-101636907)x1 copy number loss See cases [RCV000139206] Chr2:98411773..101636907 [GRCh38]
Chr2:99028236..102253369 [GRCh37]
Chr2:98394668..101619801 [NCBI36]
Chr2:2q11.2		 likely pathogenic
GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3 copy number gain See cases [RCV000141075] Chr2:94678532..110602409 [GRCh38]
Chr2:95344257..111359986 [GRCh37]
Chr2:94707984..111076455 [NCBI36]
Chr2:2q11.1-13		 pathogenic
NM_145199.3(LIPT1):c.535A>G (p.Thr179Ala) single nucleotide variant Lipoyl transferase 1 deficiency [RCV000170325] Chr2:99162492 [GRCh38]
Chr2:99778955 [GRCh37]
Chr2:2q11.2		 pathogenic|not provided
NM_145199.3(LIPT1):c.212C>T (p.Ser71Phe) single nucleotide variant Lipoyl transferase 1 deficiency [RCV000170326]|not provided [RCV001551057] Chr2:99162169 [GRCh38]
Chr2:99778632 [GRCh37]
Chr2:2q11.2		 pathogenic|likely pathogenic|not provided
NM_145199.3(LIPT1):c.875C>G (p.Ser292Ter) single nucleotide variant Lipoyl transferase 1 deficiency [RCV000351422]|not provided [RCV000725739] Chr2:99162832 [GRCh38]
Chr2:99779295 [GRCh37]
Chr2:2q11.2		 pathogenic|likely pathogenic
NM_145199.3(LIPT1):c.293G>A (p.Arg98Gln) single nucleotide variant not provided [RCV000523319] Chr2:99162250 [GRCh38]
Chr2:99778713 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_145199.3(LIPT1):c.79dup (p.Thr27fs) duplication not provided [RCV000522755] Chr2:99162029..99162030 [GRCh38]
Chr2:99778492..99778493 [GRCh37]
Chr2:2q11.2		 likely pathogenic|conflicting interpretations of pathogenicity
GRCh37/hg19 2q11.1-12.3(chr2:95529039-108518266) copy number gain See cases [RCV000449270] Chr2:95529039..108518266 [GRCh37]
Chr2:2q11.1-12.3		 pathogenic
GRCh37/hg19 2q11.1-13(chr2:95327499-111370025)x4 copy number gain See cases [RCV000446842] Chr2:95327499..111370025 [GRCh37]
Chr2:2q11.1-13		 pathogenic
NM_145199.3(LIPT1):c.315A>G (p.Thr105=) single nucleotide variant not provided [RCV001520901]|not specified [RCV000417504] Chr2:99162272 [GRCh38]
Chr2:99778735 [GRCh37]
Chr2:2q11.2		 benign
NM_145199.3(LIPT1):c.753G>A (p.Thr251=) single nucleotide variant not specified [RCV000424859] Chr2:99162710 [GRCh38]
Chr2:99779173 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.*15C>T single nucleotide variant not specified [RCV000424959] Chr2:99163094 [GRCh38]
Chr2:99779557 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.565T>C (p.Leu189=) single nucleotide variant Lipoyl transferase 1 deficiency [RCV001730678]|not provided [RCV001521777]|not specified [RCV000419186] Chr2:99162522 [GRCh38]
Chr2:99778985 [GRCh37]
Chr2:2q11.2		 benign
NM_145199.3(LIPT1):c.613A>G (p.Thr205Ala) single nucleotide variant LIPT1-related condition [RCV003912713]|not provided [RCV000889918]|not specified [RCV000442901] Chr2:99162570 [GRCh38]
Chr2:99779033 [GRCh37]
Chr2:2q11.2		 benign
NM_145199.3(LIPT1):c.131A>G (p.Asn44Ser) single nucleotide variant Inborn genetic diseases [RCV002527168]|Lipoyl transferase 1 deficiency [RCV000680033]|not provided [RCV003126760] Chr2:99162088 [GRCh38]
Chr2:99778551 [GRCh37]
Chr2:2q11.2		 likely pathogenic|uncertain significance
NM_145199.3(LIPT1):c.1053A>G (p.Thr351=) single nucleotide variant not provided [RCV001698371] Chr2:99163010 [GRCh38]
Chr2:99779473 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.508G>A (p.Gly170Ser) single nucleotide variant not provided [RCV000422364] Chr2:99162465 [GRCh38]
Chr2:99778928 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.711T>C (p.Ala237=) single nucleotide variant Lipoyl transferase 1 deficiency [RCV001730679]|not provided [RCV001521778]|not specified [RCV000429922] Chr2:99162668 [GRCh38]
Chr2:99779131 [GRCh37]
Chr2:2q11.2		 benign
GRCh37/hg19 2q11.2(chr2:99688765-99797625)x3 copy number gain See cases [RCV000448873] Chr2:99688765..99797625 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:95691600-100587394) copy number gain See cases [RCV000447723] Chr2:95691600..100587394 [GRCh37]
Chr2:2q11.1-11.2		 pathogenic
NM_145199.3(LIPT1):c.369del (p.Lys123fs) deletion Abnormal cardiovascular system morphology [RCV001270041]|Lipoyl transferase 1 deficiency [RCV001782966]|not provided [RCV000483728]|not specified [RCV002298615] Chr2:99162326 [GRCh38]
Chr2:99778789 [GRCh37]
Chr2:2q11.2		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q11.1-12.2(chr2:95518497-107186127) copy number gain See cases [RCV000511158] Chr2:95518497..107186127 [GRCh37]
Chr2:2q11.1-12.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_138798.3(MITD1):c.16C>A (p.Leu6Met) single nucleotide variant Inborn genetic diseases [RCV003251663] Chr2:99180966 [GRCh38]
Chr2:99797429 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.1107T>A (p.Ile369=) single nucleotide variant LIPT1-related condition [RCV003900371]|not provided [RCV000929113] Chr2:99163064 [GRCh38]
Chr2:99779527 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.488C>T (p.Ser163Leu) single nucleotide variant not provided [RCV000657854] Chr2:99162445 [GRCh38]
Chr2:99778908 [GRCh37]
Chr2:2q11.2		 likely pathogenic|conflicting interpretations of pathogenicity
Single allele deletion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3		 likely pathogenic
GRCh37/hg19 2q11.1-13(chr2:96353030-114045463)x3 copy number gain not provided [RCV000682168] Chr2:96353030..114045463 [GRCh37]
Chr2:2q11.1-13		 pathogenic
NM_145199.3(LIPT1):c.713A>G (p.Tyr238Cys) single nucleotide variant not provided [RCV000709787] Chr2:99162670 [GRCh38]
Chr2:99779133 [GRCh37]
Chr2:2q11.2		 not provided
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q11.2(chr2:99778872-99924918)x3 copy number gain not provided [RCV000740534] Chr2:99778872..99924918 [GRCh37]
Chr2:2q11.2		 benign
NM_145199.3(LIPT1):c.906A>T (p.Ile302=) single nucleotide variant not provided [RCV001907803] Chr2:99162863 [GRCh38]
Chr2:99779326 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.-1-270del deletion not provided [RCV001534400] Chr2:99161678 [GRCh38]
Chr2:99778141 [GRCh37]
Chr2:2q11.2		 benign
NM_145199.3(LIPT1):c.726T>C (p.Asp242=) single nucleotide variant not provided [RCV000923864] Chr2:99162683 [GRCh38]
Chr2:99779146 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.57C>T (p.Val19=) single nucleotide variant not provided [RCV000892264] Chr2:99162014 [GRCh38]
Chr2:99778477 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.452G>A (p.Arg151Lys) single nucleotide variant LIPT1-related condition [RCV003958145]|not provided [RCV000901357] Chr2:99162409 [GRCh38]
Chr2:99778872 [GRCh37]
Chr2:2q11.2		 likely benign|conflicting interpretations of pathogenicity
NM_145199.3(LIPT1):c.681A>G (p.Leu227=) single nucleotide variant not provided [RCV000941093] Chr2:99162638 [GRCh38]
Chr2:99779101 [GRCh37]
Chr2:2q11.2		 likely benign
GRCh37/hg19 2q11.2(chr2:99785140-99817216)x1 copy number loss not provided [RCV000846899] Chr2:99785140..99817216 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.2(chr2:99542665-100190293)x1 copy number loss not provided [RCV000849567] Chr2:99542665..100190293 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.539T>C (p.Leu180Ser) single nucleotide variant Lipoyl transferase 1 deficiency [RCV001250060] Chr2:99162496 [GRCh38]
Chr2:99778959 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.302G>A (p.Ser101Asn) single nucleotide variant See cases [RCV003232625] Chr2:99162259 [GRCh38]
Chr2:99778722 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.578T>C (p.Leu193Pro) single nucleotide variant Lipoyl transferase 1 deficiency [RCV003126310] Chr2:99162535 [GRCh38]
Chr2:99778998 [GRCh37]
Chr2:2q11.2		 uncertain significance
NC_000002.12:g.99163192C>A single nucleotide variant not provided [RCV001637793] Chr2:99163192 [GRCh38]
Chr2:99779655 [GRCh37]
Chr2:2q11.2		 benign
NC_000002.12:g.99163192del deletion not provided [RCV001555759] Chr2:99163192 [GRCh38]
Chr2:99779655 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.1026C>A (p.Thr342=) single nucleotide variant LIPT1-related condition [RCV003950758]|not provided [RCV000912173] Chr2:99162983 [GRCh38]
Chr2:99779446 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.2T>C (p.Met1Thr) single nucleotide variant not provided [RCV001577022] Chr2:99161959 [GRCh38]
Chr2:99778422 [GRCh37]
Chr2:2q11.2		 likely pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:95341388-100340514)x3 copy number gain not provided [RCV002473932] Chr2:95341388..100340514 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
NC_000002.12:g.99163191dup duplication not provided [RCV001672076] Chr2:99163179..99163180 [GRCh38]
Chr2:99779642..99779643 [GRCh37]
Chr2:2q11.2		 benign
GRCh37/hg19 2q11.2(chr2:99356669-99984607)x3 copy number gain not provided [RCV001259644] Chr2:99356669..99984607 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_145199.3(LIPT1):c.1A>T (p.Met1Leu) single nucleotide variant not provided [RCV002087190] Chr2:99161958 [GRCh38]
Chr2:99778421 [GRCh37]
Chr2:2q11.2		 pathogenic|benign|likely benign
NM_145199.3(LIPT1):c.972del (p.Asp325fs) deletion Lipoyltransferase 1 deficiency [RCV001333559] Chr2:99162929 [GRCh38]
Chr2:99779392 [GRCh37]
Chr2:2q11.2		 pathogenic
NM_145199.3(LIPT1):c.858_861delinsGTATTA (p.His286fs) indel not provided [RCV001756733] Chr2:99162815..99162818 [GRCh38]
Chr2:99779278..99779281 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.808G>T (p.Glu270Ter) single nucleotide variant not provided [RCV001964286] Chr2:99162765 [GRCh38]
Chr2:99779228 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.967A>G (p.Ile323Val) single nucleotide variant not provided [RCV002025646] Chr2:99162924 [GRCh38]
Chr2:99779387 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.808G>A (p.Glu270Lys) single nucleotide variant not provided [RCV001926526] Chr2:99162765 [GRCh38]
Chr2:99779228 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.184A>G (p.Ile62Val) single nucleotide variant not provided [RCV001946545] Chr2:99162141 [GRCh38]
Chr2:99778604 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.765_766del (p.Phe256fs) deletion Lipoyl transferase 1 deficiency [RCV001782386] Chr2:99162721..99162722 [GRCh38]
Chr2:99779184..99779185 [GRCh37]
Chr2:2q11.2		 likely pathogenic
NM_145199.3(LIPT1):c.396_399del (p.Leu132_Ile133insTer) microsatellite Lipoyl transferase 1 deficiency [RCV001782385] Chr2:99162349..99162352 [GRCh38]
Chr2:99778812..99778815 [GRCh37]
Chr2:2q11.2		 likely pathogenic
GRCh37/hg19 2q11.2(chr2:99725222-99846305) copy number loss not specified [RCV002053217] Chr2:99725222..99846305 [GRCh37]
Chr2:2q11.2		 uncertain significance
NC_000002.12:g.99163178_99163179insA insertion not provided [RCV001786018] Chr2:99163178..99163179 [GRCh38]
Chr2:99779641..99779642 [GRCh37]
Chr2:2q11.2		 benign
NM_145199.3(LIPT1):c.643C>A (p.Leu215Ile) single nucleotide variant not provided [RCV002036947] Chr2:99162600 [GRCh38]
Chr2:99779063 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.121G>A (p.Val41Ile) single nucleotide variant not provided [RCV002000726] Chr2:99162078 [GRCh38]
Chr2:99778541 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.975C>A (p.Asp325Glu) single nucleotide variant not provided [RCV001921276] Chr2:99162932 [GRCh38]
Chr2:99779395 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.885A>C (p.Glu295Asp) single nucleotide variant not provided [RCV001904442] Chr2:99162842 [GRCh38]
Chr2:99779305 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.807G>C (p.Trp269Cys) single nucleotide variant not provided [RCV001864766] Chr2:99162764 [GRCh38]
Chr2:99779227 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.784A>G (p.Lys262Glu) single nucleotide variant not provided [RCV001978756] Chr2:99162741 [GRCh38]
Chr2:99779204 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.949C>G (p.His317Asp) single nucleotide variant not provided [RCV001899683] Chr2:99162906 [GRCh38]
Chr2:99779369 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.587C>T (p.Pro196Leu) single nucleotide variant Lipoyl transferase 1 deficiency [RCV003483853]|not provided [RCV001922739] Chr2:99162544 [GRCh38]
Chr2:99779007 [GRCh37]
Chr2:2q11.2		 uncertain significance|not provided
NM_145199.3(LIPT1):c.406G>T (p.Ala136Ser) single nucleotide variant not provided [RCV001885585] Chr2:99162363 [GRCh38]
Chr2:99778826 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.752_801del (p.Thr251fs) deletion not provided [RCV001951810] Chr2:99162706..99162755 [GRCh38]
Chr2:99779169..99779218 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.824A>G (p.Lys275Arg) single nucleotide variant not provided [RCV001940582] Chr2:99162781 [GRCh38]
Chr2:99779244 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.546T>C (p.Cys182=) single nucleotide variant not provided [RCV002162130] Chr2:99162503 [GRCh38]
Chr2:99778966 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.594A>G (p.Gln198=) single nucleotide variant LIPT1-related condition [RCV003958718]|not provided [RCV002120037] Chr2:99162551 [GRCh38]
Chr2:99779014 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.522C>G (p.Ala174=) single nucleotide variant not provided [RCV002154515] Chr2:99162479 [GRCh38]
Chr2:99778942 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.861G>A (p.Val287=) single nucleotide variant not provided [RCV003110545] Chr2:99162818 [GRCh38]
Chr2:99779281 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.316G>A (p.Val106Ile) single nucleotide variant Lipoyl transferase 1 deficiency [RCV003389350]|See cases [RCV003233013] Chr2:99162273 [GRCh38]
Chr2:99778736 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 copy number loss See cases [RCV002287563] Chr2:11504318..111365996 [GRCh37]
Chr2:2p25.1-q13		 pathogenic
NM_138798.3(MITD1):c.506G>A (p.Gly169Asp) single nucleotide variant Inborn genetic diseases [RCV003285935] Chr2:99170624 [GRCh38]
Chr2:99787087 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_138798.3(MITD1):c.730A>C (p.Lys244Gln) single nucleotide variant Inborn genetic diseases [RCV003283063] Chr2:99169395 [GRCh38]
Chr2:99785858 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.1051A>C (p.Thr351Pro) single nucleotide variant not provided [RCV002296278] Chr2:99163008 [GRCh38]
Chr2:99779471 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.553G>A (p.Asp185Asn) single nucleotide variant not provided [RCV002614558] Chr2:99162510 [GRCh38]
Chr2:99778973 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.965A>G (p.Glu322Gly) single nucleotide variant not provided [RCV003012115] Chr2:99162922 [GRCh38]
Chr2:99779385 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.655G>T (p.Asp219Tyr) single nucleotide variant Inborn genetic diseases [RCV002685131] Chr2:99162612 [GRCh38]
Chr2:99779075 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.109A>T (p.Ile37Phe) single nucleotide variant Inborn genetic diseases [RCV002905462] Chr2:99162066 [GRCh38]
Chr2:99778529 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.736C>G (p.His246Asp) single nucleotide variant Inborn genetic diseases [RCV002883484] Chr2:99162693 [GRCh38]
Chr2:99779156 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.140T>C (p.Val47Ala) single nucleotide variant not provided [RCV002616660] Chr2:99162097 [GRCh38]
Chr2:99778560 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.892G>C (p.Val298Leu) single nucleotide variant not provided [RCV002819516] Chr2:99162849 [GRCh38]
Chr2:99779312 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.941C>T (p.Ala314Val) single nucleotide variant Inborn genetic diseases [RCV002845606] Chr2:99162898 [GRCh38]
Chr2:99779361 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_138798.3(MITD1):c.410T>G (p.Phe137Cys) single nucleotide variant Inborn genetic diseases [RCV002781962] Chr2:99171410 [GRCh38]
Chr2:99787873 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.551C>G (p.Thr184Ser) single nucleotide variant Inborn genetic diseases [RCV003000804] Chr2:99162508 [GRCh38]
Chr2:99778971 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.654G>C (p.Lys218Asn) single nucleotide variant not provided [RCV002800080] Chr2:99162611 [GRCh38]
Chr2:99779074 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_138798.3(MITD1):c.626G>A (p.Arg209Lys) single nucleotide variant Inborn genetic diseases [RCV002924956] Chr2:99169578 [GRCh38]
Chr2:99786041 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_138798.3(MITD1):c.371A>G (p.Tyr124Cys) single nucleotide variant Inborn genetic diseases [RCV002704172] Chr2:99171529 [GRCh38]
Chr2:99787992 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.576G>A (p.Leu192=) single nucleotide variant not provided [RCV002889233] Chr2:99162533 [GRCh38]
Chr2:99778996 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.1062A>G (p.Gln354=) single nucleotide variant not provided [RCV002801174] Chr2:99163019 [GRCh38]
Chr2:99779482 [GRCh37]
Chr2:2q11.2		 likely benign
NM_138798.3(MITD1):c.323G>A (p.Arg108His) single nucleotide variant Inborn genetic diseases [RCV002956405] Chr2:99171577 [GRCh38]
Chr2:99788040 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.212C>G (p.Ser71Cys) single nucleotide variant Inborn genetic diseases [RCV002804500] Chr2:99162169 [GRCh38]
Chr2:99778632 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_138798.3(MITD1):c.175T>C (p.Cys59Arg) single nucleotide variant Inborn genetic diseases [RCV002940777] Chr2:99173993 [GRCh38]
Chr2:99790456 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.754G>T (p.Asp252Tyr) single nucleotide variant not provided [RCV003031417] Chr2:99162711 [GRCh38]
Chr2:99779174 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.441G>T (p.Gln147His) single nucleotide variant not provided [RCV002833193] Chr2:99162398 [GRCh38]
Chr2:99778861 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.1013C>T (p.Pro338Leu) single nucleotide variant Inborn genetic diseases [RCV002831547] Chr2:99162970 [GRCh38]
Chr2:99779433 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.319dup (p.Tyr107fs) duplication not provided [RCV002810191] Chr2:99162275..99162276 [GRCh38]
Chr2:99778738..99778739 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.970C>T (p.Arg324Cys) single nucleotide variant not provided [RCV003090341] Chr2:99162927 [GRCh38]
Chr2:99779390 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.879C>T (p.His293=) single nucleotide variant not provided [RCV002670978] Chr2:99162836 [GRCh38]
Chr2:99779299 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.152T>C (p.Ile51Thr) single nucleotide variant not provided [RCV002583804] Chr2:99162109 [GRCh38]
Chr2:99778572 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.935T>C (p.Ile312Thr) single nucleotide variant not provided [RCV002607622] Chr2:99162892 [GRCh38]
Chr2:99779355 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.560C>T (p.Thr187Met) single nucleotide variant not provided [RCV003071843] Chr2:99162517 [GRCh38]
Chr2:99778980 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.495A>G (p.Thr165=) single nucleotide variant not provided [RCV002590204] Chr2:99162452 [GRCh38]
Chr2:99778915 [GRCh37]
Chr2:2q11.2		 likely benign
NM_138798.3(MITD1):c.193A>G (p.Ile65Val) single nucleotide variant Inborn genetic diseases [RCV003299890] Chr2:99173975 [GRCh38]
Chr2:99790438 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.995T>C (p.Ile332Thr) single nucleotide variant Inborn genetic diseases [RCV003366439] Chr2:99162952 [GRCh38]
Chr2:99779415 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:95773428-102550061)x3 copy number gain not provided [RCV003484069] Chr2:95773428..102550061 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
NM_145199.3(LIPT1):c.806G>A (p.Trp269Ter) single nucleotide variant Lipoyl transferase 1 deficiency [RCV003389324] Chr2:99162763 [GRCh38]
Chr2:99779226 [GRCh37]
Chr2:2q11.2		 likely pathogenic
NM_145199.3(LIPT1):c.150G>T (p.Trp50Cys) single nucleotide variant not provided [RCV003739395] Chr2:99162107 [GRCh38]
Chr2:99778570 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.561G>A (p.Thr187=) single nucleotide variant not provided [RCV003727541] Chr2:99162518 [GRCh38]
Chr2:99778981 [GRCh37]
Chr2:2q11.2		 benign
NM_145199.3(LIPT1):c.109A>G (p.Ile37Val) single nucleotide variant not provided [RCV003551461] Chr2:99162066 [GRCh38]
Chr2:99778529 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.507C>T (p.Ile169=) single nucleotide variant not provided [RCV003706639] Chr2:99162464 [GRCh38]
Chr2:99778927 [GRCh37]
Chr2:2q11.2		 likely benign
NM_145199.3(LIPT1):c.368del (p.Lys123fs) deletion not specified [RCV003988268] Chr2:99162318 [GRCh38]
Chr2:99778781 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_145199.3(LIPT1):c.1074A>G (p.Leu358=) single nucleotide variant LIPT1-related condition [RCV003907234] Chr2:99163031 [GRCh38]
Chr2:99779494 [GRCh37]
Chr2:2q11.2		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1026
Count of miRNA genes:616
Interacting mature miRNAs:671
Transcripts:ENST00000289359, ENST00000409107, ENST00000413710, ENST00000422537, ENST00000438121, ENST00000464685, ENST00000466880, ENST00000483721, ENST00000487588
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
GDB:434012  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map10p11.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map14q31UniSTS
L18506  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map19p13UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2253 1501 1302 231 1287 99 3305 937 1860 230 1219 1486 149 1 1116 1892 5 1
Low 186 1488 424 393 662 366 1052 1260 1874 189 241 127 26 88 896 1 1
Below cutoff 2 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001320417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001320418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001320419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_138798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047443276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047443277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001738611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001738612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC092587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311658 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL161992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC018453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG504564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU507044 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ859758 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA109248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA987247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000289359   ⟹   ENSP00000289359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,169,263 - 99,181,058 (-)Ensembl
RefSeq Acc Id: ENST00000409107   ⟹   ENSP00000387316
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,169,445 - 99,181,050 (-)Ensembl
RefSeq Acc Id: ENST00000413710   ⟹   ENSP00000491218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,169,263 - 99,181,034 (-)Ensembl
RefSeq Acc Id: ENST00000422537   ⟹   ENSP00000413371
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,161,947 - 99,180,927 (-)Ensembl
RefSeq Acc Id: ENST00000438121   ⟹   ENSP00000408117
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,173,347 - 99,181,035 (-)Ensembl
RefSeq Acc Id: ENST00000464685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,169,263 - 99,180,962 (-)Ensembl
RefSeq Acc Id: ENST00000466880
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,170,535 - 99,178,335 (-)Ensembl
RefSeq Acc Id: ENST00000483721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,169,266 - 99,170,905 (-)Ensembl
RefSeq Acc Id: ENST00000487588
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl299,161,427 - 99,171,405 (-)Ensembl
RefSeq Acc Id: NM_001320417   ⟹   NP_001307346
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,169,263 - 99,181,058 (-)NCBI
CHM1_1299,790,624 - 99,802,422 (-)NCBI
T2T-CHM13v2.0299,628,141 - 99,639,936 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001320418   ⟹   NP_001307347
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,169,263 - 99,181,058 (-)NCBI
CHM1_1299,790,624 - 99,802,422 (-)NCBI
T2T-CHM13v2.0299,628,141 - 99,639,936 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001320419   ⟹   NP_001307348
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,169,263 - 99,181,058 (-)NCBI
CHM1_1299,790,624 - 99,802,422 (-)NCBI
T2T-CHM13v2.0299,628,141 - 99,639,936 (-)NCBI
Sequence:
RefSeq Acc Id: NM_138798   ⟹   NP_620153
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,169,263 - 99,181,058 (-)NCBI
GRCh37299,785,726 - 99,797,524 (-)NCBI
Build 36299,152,158 - 99,163,924 (-)NCBI Archive
Celera293,990,319 - 94,002,087 (-)RGD
HuRef293,551,497 - 93,563,265 (-)ENTREZGENE
CHM1_1299,790,624 - 99,802,422 (-)NCBI
T2T-CHM13v2.0299,628,141 - 99,639,936 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011510581   ⟹   XP_011508883
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,161,427 - 99,181,058 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017003314   ⟹   XP_016858803
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,161,427 - 99,181,058 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017003315   ⟹   XP_016858804
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,167,776 - 99,181,058 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047443276   ⟹   XP_047299232
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,167,635 - 99,181,058 (-)NCBI
RefSeq Acc Id: XM_047443277   ⟹   XP_047299233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,170,533 - 99,181,058 (-)NCBI
RefSeq Acc Id: XM_054340480   ⟹   XP_054196455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0299,620,306 - 99,639,936 (-)NCBI
RefSeq Acc Id: XM_054340481   ⟹   XP_054196456
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0299,626,511 - 99,639,936 (-)NCBI
RefSeq Acc Id: XM_054340482   ⟹   XP_054196457
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0299,620,306 - 99,639,936 (-)NCBI
RefSeq Acc Id: XM_054340483   ⟹   XP_054196458
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0299,626,652 - 99,639,936 (-)NCBI
RefSeq Acc Id: XM_054340484   ⟹   XP_054196459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0299,629,411 - 99,639,936 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_620153   ⟸   NM_138798
- Peptide Label: isoform 1
- UniProtKB: Q69YV0 (UniProtKB/Swiss-Prot),   Q8WV92 (UniProtKB/Swiss-Prot),   H7C3Q6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011508883   ⟸   XM_011510581
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001307348   ⟸   NM_001320419
- Peptide Label: isoform 4
- UniProtKB: B8ZZL5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001307347   ⟸   NM_001320418
- Peptide Label: isoform 3
- UniProtKB: B8ZZL5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001307346   ⟸   NM_001320417
- Peptide Label: isoform 2
- UniProtKB: Q8WV92 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016858803   ⟸   XM_017003314
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016858804   ⟸   XM_017003315
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: ENSP00000408117   ⟸   ENST00000438121
RefSeq Acc Id: ENSP00000491218   ⟸   ENST00000413710
RefSeq Acc Id: ENSP00000289359   ⟸   ENST00000289359
RefSeq Acc Id: ENSP00000387316   ⟸   ENST00000409107
RefSeq Acc Id: ENSP00000413371   ⟸   ENST00000422537
RefSeq Acc Id: XP_047299232   ⟸   XM_047443276
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047299233   ⟸   XM_047443277
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054196457   ⟸   XM_054340482
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054196455   ⟸   XM_054340480
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054196456   ⟸   XM_054340481
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054196458   ⟸   XM_054340483
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054196459   ⟸   XM_054340484
- Peptide Label: isoform X5
Protein Domains
MIT

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8WV92-F1-model_v2 AlphaFold Q8WV92 1-249 view protein structure

Promoters
RGD ID:6797809
Promoter ID:HG_KWN:34088
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000329956
Position:
Human AssemblyChrPosition (strand)Source
Build 36299,161,859 - 99,162,359 (-)MPROMDB
RGD ID:6797808
Promoter ID:HG_KWN:34089
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000308656,   ENST00000409107,   ENST00000409145,   OTTHUMT00000253126,   OTTHUMT00000253130,   OTTHUMT00000329952,   OTTHUMT00000329953,   OTTHUMT00000329955,   OTTHUMT00000330291,   OTTHUMT00000330294,   UC002SZT.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36299,163,776 - 99,164,276 (-)MPROMDB
RGD ID:6861184
Promoter ID:EPDNEW_H3741
Type:initiation region
Name:MITD1_1
Description:microtubule interacting and trafficking domain containing 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38299,180,987 - 99,181,047EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25207 AgrOrtholog
COSMIC MITD1 COSMIC
Ensembl Genes ENSG00000158411 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000289359 ENTREZGENE
  ENST00000289359.6 UniProtKB/Swiss-Prot
  ENST00000409107 ENTREZGENE
  ENST00000409107.1 UniProtKB/TrEMBL
  ENST00000413710.2 UniProtKB/TrEMBL
  ENST00000422537.6 UniProtKB/TrEMBL
  ENST00000438121.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.870.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Phosphotransferase system, lactose/cellobiose-type IIA subunit UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000158411 GTEx
HGNC ID HGNC:25207 ENTREZGENE
Human Proteome Map MITD1 Human Proteome Map
InterPro MIT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIT_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIT_C_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIT_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MITD1_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:129531 UniProtKB/Swiss-Prot
NCBI Gene 129531 ENTREZGENE
PANTHER MIT DOMAIN-CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UNCHARACTERIZED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MIT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIT_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA147357601 PharmGKB
SMART MIT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF116846 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1W2PP14_HUMAN UniProtKB/TrEMBL
  B8ZZL5 ENTREZGENE, UniProtKB/TrEMBL
  F8WED5_HUMAN UniProtKB/TrEMBL
  H7C3Q6 ENTREZGENE, UniProtKB/TrEMBL
  MITD1_HUMAN UniProtKB/Swiss-Prot
  Q69YV0 ENTREZGENE
  Q8WV92 ENTREZGENE
UniProt Secondary Q69YV0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-10 MITD1  microtubule interacting and trafficking domain containing 1    MIT, microtubule interacting and transport, domain containing 1  Symbol and/or name change 5135510 APPROVED