TOMM20L (translocase of outer mitochondrial membrane 20 like) - Rat Genome Database

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Gene: TOMM20L (translocase of outer mitochondrial membrane 20 like) Homo sapiens
Analyze
Symbol: TOMM20L
Name: translocase of outer mitochondrial membrane 20 like
RGD ID: 1602627
HGNC Page HGNC:33752
Description: Predicted to enable mitochondrion targeting sequence binding activity. Predicted to contribute to protein transmembrane transporter activity. Predicted to be involved in protein import into mitochondrial matrix and tRNA import into mitochondrion. Predicted to be located in mitochondrial outer membrane. Predicted to be part of mitochondrial outer membrane translocase complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: TOMM20-like protein 1; translocase of outer mitochondrial membrane 20 homolog (yeast)-like; translocase of outer mitochondrial membrane 20 homolog type I; translocase of outer mitochondrial membrane 20 homolog-like; UNQ9438
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Note: July 18, 2008: Although this gene has been referred to as TIMM9, TIMM9 is a distinct locus, located in a head-head orientation to UNQ9438. [18 Jul 2008]
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381458,395,930 - 58,417,080 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1458,395,928 - 58,408,702 (+)EnsemblGRCh38hg38GRCh38
GRCh371458,862,648 - 58,875,420 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361457,932,385 - 57,945,172 (+)NCBINCBI36Build 36hg18NCBI36
Celera1438,912,616 - 38,925,391 (+)NCBICelera
Cytogenetic Map14q23.1NCBI
HuRef1439,027,270 - 39,040,037 (+)NCBIHuRef
CHM1_11458,801,207 - 58,813,988 (+)NCBICHM1_1
T2T-CHM13v2.01452,602,950 - 52,624,123 (+)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

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:12975309   PMID:15733919   PMID:21873635   PMID:26186194   PMID:28514442   PMID:29987050   PMID:32296183   PMID:33961781  


Genomics

Comparative Map Data
TOMM20L
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381458,395,930 - 58,417,080 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1458,395,928 - 58,408,702 (+)EnsemblGRCh38hg38GRCh38
GRCh371458,862,648 - 58,875,420 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361457,932,385 - 57,945,172 (+)NCBINCBI36Build 36hg18NCBI36
Celera1438,912,616 - 38,925,391 (+)NCBICelera
Cytogenetic Map14q23.1NCBI
HuRef1439,027,270 - 39,040,037 (+)NCBIHuRef
CHM1_11458,801,207 - 58,813,988 (+)NCBICHM1_1
T2T-CHM13v2.01452,602,950 - 52,624,123 (+)NCBIT2T-CHM13v2.0
Tomm20l
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391271,158,202 - 71,169,996 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1271,158,202 - 71,169,995 (+)EnsemblGRCm39 Ensembl
GRCm381271,111,428 - 71,123,222 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1271,111,428 - 71,123,221 (+)EnsemblGRCm38mm10GRCm38
MGSCv371272,212,415 - 72,224,209 (+)NCBIGRCm37MGSCv37mm9NCBIm37
Celera1272,211,475 - 72,223,254 (+)NCBICelera
Cytogenetic Map12C2NCBI
cM Map1229.39NCBI
Tomm20l
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8695,335,681 - 95,346,116 (+)NCBIGRCr8
mRatBN7.2689,594,016 - 89,612,070 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl689,599,873 - 89,610,147 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.0693,538,377 - 93,549,533 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl693,539,271 - 93,651,154 (+)NCBIRnor6.0rn6Rnor6.0
Rnor_5.06103,004,605 - 103,015,121 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4693,208,302 - 93,218,521 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera688,083,111 - 88,094,268 (+)NCBICelera
Cytogenetic Map6q24NCBI
TOMM20L
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21559,517,614 - 59,531,404 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11458,728,289 - 58,748,838 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01438,987,239 - 39,001,441 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11457,255,851 - 57,268,343 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1457,255,851 - 57,268,343 (+)Ensemblpanpan1.1panPan2
TOMM20L
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1833,747,643 - 33,761,655 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl833,747,284 - 33,755,880 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha833,508,932 - 33,517,299 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0833,989,091 - 33,997,455 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl833,989,091 - 33,997,435 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1833,601,633 - 33,609,978 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0833,669,762 - 33,678,101 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0834,044,093 - 34,052,460 (+)NCBIUU_Cfam_GSD_1.0
Tomm20l
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864071,392,612 - 71,412,432 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049364952,779,851 - 2,786,233 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TOMM20L
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1187,475,006 - 187,486,729 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11187,474,745 - 187,496,040 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21208,367,169 - 208,408,948 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TOMM20L
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12435,578,996 - 35,591,613 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2435,579,540 - 35,591,495 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605323,859,161 - 23,881,058 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in TOMM20L
9 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q22.3-23.3(chr14:57041036-67208231)x1 copy number loss See cases [RCV000051521] Chr14:57041036..67208231 [GRCh38]
Chr14:57507754..67674948 [GRCh37]
Chr14:56577507..66744701 [NCBI36]
Chr14:14q22.3-23.3		 pathogenic
GRCh38/hg38 14q23.1(chr14:58146022-61273619)x1 copy number loss See cases [RCV000051522] Chr14:58146022..61273619 [GRCh38]
Chr14:58612740..61740337 [GRCh37]
Chr14:57682493..60810090 [NCBI36]
Chr14:14q23.1		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q23.1-23.2(chr14:57653413-64093528)x1 copy number loss See cases [RCV000138348] Chr14:57653413..64093528 [GRCh38]
Chr14:58120131..64560246 [GRCh37]
Chr14:57189884..63629999 [NCBI36]
Chr14:14q23.1-23.2		 pathogenic
GRCh38/hg38 14q23.1(chr14:58288658-58509423)x1 copy number loss See cases [RCV000143427] Chr14:58288658..58509423 [GRCh38]
Chr14:58755376..58976141 [GRCh37]
Chr14:57825129..58045894 [NCBI36]
Chr14:14q23.1		 uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.1(chr14:58737402-58884615)x1 copy number loss Thyroid hemiagenesis [RCV000488902] Chr14:58737402..58884615 [GRCh37]
Chr14:14q23.1		 pathogenic|likely pathogenic
GRCh37/hg19 14q23.1(chr14:58737402-58891576)x1 copy number loss Thyroid hemiagenesis [RCV000488884] Chr14:58737402..58891576 [GRCh37]
Chr14:14q23.1		 likely pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
NM_207377.3(TOMM20L):c.196A>G (p.Lys66Glu) single nucleotide variant not specified [RCV004303364] Chr14:58402695 [GRCh38]
Chr14:58869413 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.1(chr14:58666970-59006831)x3 copy number gain not provided [RCV000738498] Chr14:58666970..59006831 [GRCh37]
Chr14:14q23.1		 benign
GRCh37/hg19 14q23.1(chr14:58668869-58927173)x3 copy number gain not provided [RCV000738500] Chr14:58668869..58927173 [GRCh37]
Chr14:14q23.1		 benign
GRCh37/hg19 14q23.1(chr14:58669403-59014522)x3 copy number gain not provided [RCV000738501] Chr14:58669403..59014522 [GRCh37]
Chr14:14q23.1		 benign
GRCh37/hg19 14q22.3-23.1(chr14:56605398-59404256)x1 copy number loss not provided [RCV001006637] Chr14:56605398..59404256 [GRCh37]
Chr14:14q22.3-23.1		 pathogenic
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3 copy number gain 14q22.2q24.3 duplication [RCV001506967] Chr14:54654001..75828024 [GRCh37]
Chr14:14q22.2-24.3		 likely pathogenic
NC_000014.8:g.(?_58711639)_(59014694_?)del deletion Joubert syndrome 23 [RCV001949574] Chr14:58711639..59014694 [GRCh37]
Chr14:14q23.1		 pathogenic
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
GRCh37/hg19 14q23.1(chr14:58833909-59109480)x3 copy number gain not provided [RCV002474852] Chr14:58833909..59109480 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q22.3-23.2(chr14:57804997-63590203)x1 copy number loss not provided [RCV002472446] Chr14:57804997..63590203 [GRCh37]
Chr14:14q22.3-23.2		 likely pathogenic
NM_207377.3(TOMM20L):c.104G>A (p.Gly35Glu) single nucleotide variant not specified [RCV004207051] Chr14:58396061 [GRCh38]
Chr14:58862779 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.280A>T (p.Ile94Phe) single nucleotide variant not specified [RCV004110175] Chr14:58407343 [GRCh38]
Chr14:58874061 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.143G>A (p.Arg48Lys) single nucleotide variant not specified [RCV004133334] Chr14:58396304 [GRCh38]
Chr14:58863022 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.25C>G (p.Arg9Gly) single nucleotide variant not specified [RCV004131544] Chr14:58395982 [GRCh38]
Chr14:58862700 [GRCh37]
Chr14:14q23.1		 likely benign
NM_207377.3(TOMM20L):c.235C>T (p.Arg79Trp) single nucleotide variant not specified [RCV004215812] Chr14:58402734 [GRCh38]
Chr14:58869452 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.313G>A (p.Glu105Lys) single nucleotide variant not specified [RCV004183231] Chr14:58407376 [GRCh38]
Chr14:58874094 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.100C>G (p.Arg34Gly) single nucleotide variant not specified [RCV004122012] Chr14:58396057 [GRCh38]
Chr14:58862775 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q22.3-23.1(chr14:57675327-59806898)x1 copy number loss not provided [RCV003326901] Chr14:57675327..59806898 [GRCh37]
Chr14:14q22.3-23.1		 uncertain significance
NM_207377.3(TOMM20L):c.451C>A (p.Pro151Thr) single nucleotide variant not specified [RCV004346650] Chr14:58408574 [GRCh38]
Chr14:58875292 [GRCh37]
Chr14:14q23.1		 uncertain significance
GRCh37/hg19 14q22.3-23.2(chr14:55667390-64447598)x1 copy number loss not provided [RCV003483204] Chr14:55667390..64447598 [GRCh37]
Chr14:14q22.3-23.2		 pathogenic
GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3 copy number gain not provided [RCV003485022] Chr14:20511673..61826023 [GRCh37]
Chr14:14q11.2-23.1		 pathogenic
GRCh37/hg19 14q22.3-24.1(chr14:57588965-68334517)x3 copy number gain not provided [RCV003485034] Chr14:57588965..68334517 [GRCh37]
Chr14:14q22.3-24.1		 likely pathogenic
NM_012460.4(TIMM9):c.200T>G (p.Phe67Cys) single nucleotide variant not specified [RCV004469886] Chr14:58409104 [GRCh38]
Chr14:58875822 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.66C>G (p.Phe22Leu) single nucleotide variant not specified [RCV004467995] Chr14:58396023 [GRCh38]
Chr14:58862741 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.288C>A (p.His96Gln) single nucleotide variant not specified [RCV004687563] Chr14:58407351 [GRCh38]
Chr14:58874069 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.88A>G (p.Asn30Asp) single nucleotide variant not specified [RCV004682566] Chr14:58396045 [GRCh38]
Chr14:58862763 [GRCh37]
Chr14:14q23.1		 likely benign
NM_207377.3(TOMM20L):c.266A>C (p.Glu89Ala) single nucleotide variant not specified [RCV004682567] Chr14:58407329 [GRCh38]
Chr14:58874047 [GRCh37]
Chr14:14q23.1		 uncertain significance
NM_207377.3(TOMM20L):c.387A>T (p.Lys129Asn) single nucleotide variant not specified [RCV004682568] Chr14:58407450 [GRCh38]
Chr14:58874168 [GRCh37]
Chr14:14q23.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:249
Count of miRNA genes:202
Interacting mature miRNAs:205
Transcripts:ENST00000360945, ENST00000557754
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.

Markers in Region
RH46962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371458,875,500 - 58,875,635UniSTSGRCh37
Build 361457,945,253 - 57,945,388RGDNCBI36
Celera1438,925,472 - 38,925,607RGD
Cytogenetic Map14q21UniSTS
Cytogenetic Map14q23.1UniSTS
HuRef1439,040,118 - 39,040,253UniSTS
GeneMap99-GB4 RH Map14134.21UniSTS
NCBI RH Map14593.7UniSTS
RH44925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371458,875,500 - 58,875,611UniSTSGRCh37
Build 361457,945,253 - 57,945,364RGDNCBI36
Celera1438,925,472 - 38,925,583RGD
Cytogenetic Map14q21UniSTS
Cytogenetic Map14q23.1UniSTS
HuRef1439,040,118 - 39,040,229UniSTS
GeneMap99-GB4 RH Map14134.11UniSTS
NCBI RH Map14626.5UniSTS
RH78893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371458,874,320 - 58,874,440UniSTSGRCh37
Build 361457,944,073 - 57,944,193RGDNCBI36
Celera1438,924,292 - 38,924,412RGD
Cytogenetic Map14q23.1UniSTS
HuRef1439,038,938 - 39,039,058UniSTS
GeneMap99-GB4 RH Map14134.11UniSTS
RH66721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371458,869,570 - 58,869,707UniSTSGRCh37
Build 361457,939,323 - 57,939,460RGDNCBI36
Celera1438,919,542 - 38,919,679RGD
Cytogenetic Map14q23.1UniSTS
HuRef1439,034,197 - 39,034,334UniSTS
GeneMap99-GB4 RH Map14137.13UniSTS
NCBI RH Map14627.8UniSTS


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
1126 2286 2336 1768 4208 1576 2097 4 504 1502 353 2148 5816 5381 49 3045 1 799 1657 1483 164

Sequence


Ensembl Acc Id: ENST00000360945   ⟹   ENSP00000354204
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1458,395,930 - 58,408,702 (+)Ensembl
Ensembl Acc Id: ENST00000557754   ⟹   ENSP00000451683
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1458,395,928 - 58,408,613 (+)Ensembl
RefSeq Acc Id: NM_207377   ⟹   NP_997260
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381458,395,930 - 58,408,702 (+)NCBI
GRCh371458,862,644 - 58,875,419 (+)RGD
Build 361457,932,385 - 57,945,172 (+)NCBI Archive
Celera1438,912,616 - 38,925,391 (+)RGD
HuRef1439,027,270 - 39,040,037 (+)RGD
CHM1_11458,801,207 - 58,813,988 (+)NCBI
T2T-CHM13v2.01452,602,950 - 52,615,753 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011536742   ⟹   XP_011535044
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381458,395,930 - 58,408,702 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011536743   ⟹   XP_011535045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381458,395,930 - 58,417,080 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011536744   ⟹   XP_011535046
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381458,395,930 - 58,408,702 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054376021   ⟹   XP_054231996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01452,602,950 - 52,615,753 (+)NCBI
RefSeq Acc Id: XM_054376022   ⟹   XP_054231997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01452,602,950 - 52,624,123 (+)NCBI
RefSeq Acc Id: XM_054376023   ⟹   XP_054231998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01452,602,950 - 52,615,753 (+)NCBI
RefSeq Acc Id: NP_997260   ⟸   NM_207377
- UniProtKB: B2RPR0 (UniProtKB/Swiss-Prot),   Q6UXN7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011535045   ⟸   XM_011536743
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011535044   ⟸   XM_011536742
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011535046   ⟸   XM_011536744
- Peptide Label: isoform X3
- Sequence:
Ensembl Acc Id: ENSP00000451683   ⟸   ENST00000557754
Ensembl Acc Id: ENSP00000354204   ⟸   ENST00000360945
RefSeq Acc Id: XP_054231997   ⟸   XM_054376022
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054231996   ⟸   XM_054376021
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054231998   ⟸   XM_054376023
- Peptide Label: isoform X3

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q6UXN7-F1-model_v2 AlphaFold Q6UXN7 1-152 view protein structure

Promoters
RGD ID:6791961
Promoter ID:HG_KWN:19479
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000360945
Position:
Human AssemblyChrPosition (strand)Source
Build 361457,932,246 - 57,932,862 (+)MPROMDB
RGD ID:7227735
Promoter ID:EPDNEW_H19614
Type:initiation region
Name:TOMM20L_1
Description:translocase of outer mitochondrial membrane 20 like
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
GRCh381458,395,985 - 58,396,045EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:33752 AgrOrtholog
COSMIC TOMM20L COSMIC
Ensembl Genes ENSG00000196860 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000360945 ENTREZGENE
  ENST00000360945.7 UniProtKB/Swiss-Prot
  ENST00000557754.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.960.10 UniProtKB/Swiss-Prot
GTEx ENSG00000196860 GTEx
HGNC ID HGNC:33752 ENTREZGENE
Human Proteome Map TOMM20L Human Proteome Map
InterPro MAS20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MAS20_rcpt_metazoan UniProtKB/Swiss-Prot
  Tom20_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:387990 UniProtKB/Swiss-Prot
NCBI Gene 387990 ENTREZGENE
PANTHER PTHR12430 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TOMM20-LIKE PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MAS20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162406689 PharmGKB
PIRSF MAS20_rcpt UniProtKB/Swiss-Prot
PRINTS EUOM20RECPTR UniProtKB/Swiss-Prot
  OM20RECEPTOR UniProtKB/Swiss-Prot
Superfamily-SCOP SSF47157 UniProtKB/Swiss-Prot
UniProt B2RPR0 ENTREZGENE
  G3V4A4_HUMAN UniProtKB/TrEMBL
  Q6UXN7 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B2RPR0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-29 TOMM20L  translocase of outer mitochondrial membrane 20 like    translocase of outer mitochondrial membrane 20 homolog (yeast)-like  Symbol and/or name change 5135510 APPROVED