MARCHF7 (membrane associated ring-CH-type finger 7) - Rat Genome Database

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Gene: MARCHF7 (membrane associated ring-CH-type finger 7) Homo sapiens
Analyze
Symbol: MARCHF7
Name: membrane associated ring-CH-type finger 7
RGD ID: 1603971
HGNC Page HGNC:17393
Description: Enables MDM2/MDM4 family protein binding activity; ubiquitin conjugating enzyme binding activity; and ubiquitin protein ligase activity. Involved in several processes, including negative regulation of signal transduction by p53 class mediator; protein monoubiquitination; and regulation of protein metabolic process. Located in nucleus. Is active in centrosome.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: AXO; AXOT; axotrophin; DKFZp586F1122; E3 ubiquitin-protein ligase MARCH7; E3 ubiquitin-protein ligase MARCHF7; MARCH-VII; MARCH7; membrane associated ring finger 7; membrane-associated ring finger (C3HC4) 7, E3 ubiquitin protein ligase; membrane-associated RING finger protein 7; membrane-associated RING-CH protein VII; RING finger protein 177; RING-type E3 ubiquitin transferase MARCH7; RING-type E3 ubiquitin transferase MARCHF7; RNF177
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382159,712,506 - 159,771,027 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2159,712,457 - 159,771,027 (+)EnsemblGRCh38hg38GRCh38
GRCh372160,569,017 - 160,627,538 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362160,277,256 - 160,333,330 (+)NCBINCBI36Build 36hg18NCBI36
Celera2154,180,871 - 154,236,930 (+)NCBICelera
Cytogenetic Map2q24.2NCBI
HuRef2152,452,965 - 152,508,987 (+)NCBIHuRef
CHM1_12160,575,406 - 160,631,457 (+)NCBICHM1_1
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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:8125298   PMID:12477932   PMID:14702039   PMID:14722266   PMID:15489334   PMID:15670816   PMID:15815621   PMID:16344560   PMID:16713569   PMID:16868077   PMID:17161353   PMID:18410486  
PMID:18654987   PMID:19549727   PMID:19901269   PMID:21873635   PMID:22493164   PMID:22544753   PMID:23105109   PMID:24905733   PMID:25552655   PMID:25594175   PMID:26186194   PMID:26673895  
PMID:26972000   PMID:27302477   PMID:28498859   PMID:28514442   PMID:29295817   PMID:30008934   PMID:31006800   PMID:31073040   PMID:32296183   PMID:32694731   PMID:33729124   PMID:33729478  
PMID:33961781   PMID:34611473   PMID:35271311   PMID:36538041   PMID:36583798   PMID:37314216   PMID:37317656   PMID:37337032   PMID:37915253  


Genomics

Comparative Map Data
MARCHF7
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382159,712,506 - 159,771,027 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2159,712,457 - 159,771,027 (+)EnsemblGRCh38hg38GRCh38
GRCh372160,569,017 - 160,627,538 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362160,277,256 - 160,333,330 (+)NCBINCBI36Build 36hg18NCBI36
Celera2154,180,871 - 154,236,930 (+)NCBICelera
Cytogenetic Map2q24.2NCBI
HuRef2152,452,965 - 152,508,987 (+)NCBIHuRef
CHM1_12160,575,406 - 160,631,457 (+)NCBICHM1_1
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBIT2T-CHM13v2.0
Marchf7
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39260,040,086 - 60,079,555 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl260,040,231 - 60,081,020 (+)EnsemblGRCm39 Ensembl
GRCm38260,209,936 - 60,248,385 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl260,209,887 - 60,250,676 (+)EnsemblGRCm38mm10GRCm38
MGSCv37260,047,993 - 60,086,442 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36260,010,775 - 60,049,224 (+)NCBIMGSCv36mm8
Celera261,923,924 - 61,943,391 (+)NCBICelera
Cytogenetic Map2C1.1NCBI
cM Map234.46NCBI
Marchf7
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8365,090,640 - 65,128,768 (+)NCBIGRCr8
mRatBN7.2344,680,229 - 44,720,172 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl344,681,632 - 44,720,168 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx348,047,948 - 48,080,007 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0356,631,520 - 56,663,579 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0354,396,643 - 54,428,707 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0346,284,961 - 46,325,230 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl346,286,712 - 46,324,057 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0351,392,847 - 51,433,354 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4341,922,568 - 41,954,630 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1341,818,939 - 41,851,002 (+)NCBI
Celera342,729,497 - 42,761,557 (+)NCBICelera
Cytogenetic Map3q21NCBI
Marchf7
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544913,835,811 - 13,859,699 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495544913,834,561 - 13,875,864 (-)NCBIChiLan1.0ChiLan1.0
MARCHF7
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21362,403,498 - 62,459,350 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12B62,418,484 - 62,474,327 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02B47,004,211 - 47,059,901 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12B164,377,538 - 164,432,907 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2B164,377,605 - 164,432,907 (+)Ensemblpanpan1.1panPan2
MARCHF7
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1365,481,449 - 5,533,139 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl365,481,456 - 5,531,957 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha365,619,700 - 5,671,174 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0365,603,860 - 5,655,631 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl365,603,884 - 5,657,936 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1365,621,952 - 5,673,466 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0365,664,667 - 5,716,347 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0365,707,592 - 5,759,332 (+)NCBIUU_Cfam_GSD_1.0
Marchf7
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303122,600,884 - 122,651,472 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493646918,962,655 - 19,017,100 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493646918,966,239 - 19,016,829 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MARCHF7
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1566,649,049 - 66,699,950 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11566,649,363 - 66,699,647 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21573,887,325 - 73,935,314 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MARCHF7
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11045,121,817 - 45,178,547 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1045,121,538 - 45,177,271 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666040154,403,774 - 154,459,270 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Marchf7
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247325,889,181 - 5,928,471 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MARCHF7
51 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q24.1-24.3(chr2:158382388-166605758)x1 copy number loss See cases [RCV000051003] Chr2:158382388..166605758 [GRCh38]
Chr2:159238900..167462268 [GRCh37]
Chr2:158947146..167170514 [NCBI36]
Chr2:2q24.1-24.3
pathogenic
GRCh38/hg38 2q24.1-24.3(chr2:154366788-167048902)x3 copy number gain See cases [RCV000052950] Chr2:154366788..167048902 [GRCh38]
Chr2:155223300..167905412 [GRCh37]
Chr2:154931546..167613658 [NCBI36]
Chr2:2q24.1-24.3
pathogenic
GRCh38/hg38 2q23.1-24.3(chr2:148917286-163204623)x1 copy number loss See cases [RCV000054093] Chr2:148917286..163204623 [GRCh38]
Chr2:149674855..164061133 [GRCh37]
Chr2:149391325..163769379 [NCBI36]
Chr2:2q23.1-24.3
pathogenic
GRCh38/hg38 2q24.1-31.1(chr2:154294042-175989372)x3 copy number gain See cases [RCV000142286] Chr2:154294042..175989372 [GRCh38]
Chr2:155150555..176854100 [GRCh37]
Chr2:154858801..176562346 [NCBI36]
Chr2:2q24.1-31.1
pathogenic
GRCh37/hg19 2q24.1-31.3(chr2:156489430-182921298)x3 copy number gain See cases [RCV000239848] Chr2:156489430..182921298 [GRCh37]
Chr2:2q24.1-31.3
pathogenic
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
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 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626436] Chr2:104172062..168223828 [GRCh37]
Chr2:2q12.1-24.3
drug response
NM_001282805.2(MARCHF7):c.757A>G (p.Ile253Val) single nucleotide variant not specified [RCV004309478] Chr2:159748047 [GRCh38]
Chr2:160604558 [GRCh37]
Chr2:2q24.2
uncertain significance
GRCh37/hg19 2q24.1-24.3(chr2:157970774-169270675)x1 copy number loss See cases [RCV000512264] Chr2:157970774..169270675 [GRCh37]
Chr2:2q24.1-24.3
pathogenic
Single allele deletion Autistic behavior [RCV000627115] Chr2:160075929..164666149 [GRCh37]
Chr2:2q24.2-24.3
likely pathogenic
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 2q23.3-31.2(chr2:152409978-179325736)x3 copy number gain not provided [RCV000740654] Chr2:152409978..179325736 [GRCh37]
Chr2:2q23.3-31.2
pathogenic
NM_001282805.2(MARCHF7):c.1492G>A (p.Asp498Asn) single nucleotide variant not specified [RCV004313113] Chr2:159748782 [GRCh38]
Chr2:160605293 [GRCh37]
Chr2:2q24.2
uncertain significance
GRCh37/hg19 2q24.1-24.2(chr2:158925958-162489191)x1 copy number loss not provided [RCV001005346] Chr2:158925958..162489191 [GRCh37]
Chr2:2q24.1-24.2
pathogenic
NM_001282805.2(MARCHF7):c.968C>T (p.Ala323Val) single nucleotide variant not specified [RCV004305500] Chr2:159748258 [GRCh38]
Chr2:160604769 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.176C>T (p.Ala59Val) single nucleotide variant not specified [RCV004293278] Chr2:159743083 [GRCh38]
Chr2:160599594 [GRCh37]
Chr2:2q24.2
uncertain significance
GRCh37/hg19 2q24.2-24.3(chr2:160075929-164666149) copy number loss Autistic behavior [RCV001200909] Chr2:160075929..164666149 [GRCh37]
Chr2:2q24.2-24.3
likely pathogenic
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
GRCh37/hg19 2q24.2-31.1(chr2:160347642-174075851)x1 copy number loss 2q24 microdeletion syndrome [RCV002271993] Chr2:160347642..174075851 [GRCh37]
Chr2:2q24.2-31.1
pathogenic
GRCh37/hg19 2q24.1-24.3(chr2:158950827-164456735) copy number loss not specified [RCV002053256] Chr2:158950827..164456735 [GRCh37]
Chr2:2q24.1-24.3
pathogenic
GRCh37/hg19 2q24.2(chr2:159844069-161073462) copy number loss BAZ2B-related disorder [RCV003234630] Chr2:159844069..161073462 [GRCh37]
Chr2:2q24.2
pathogenic
NM_001282805.2(MARCHF7):c.1178G>T (p.Arg393Ile) single nucleotide variant not specified [RCV004316972] Chr2:159748468 [GRCh38]
Chr2:160604979 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1851T>G (p.Asp617Glu) single nucleotide variant not specified [RCV004259888] Chr2:159759293 [GRCh38]
Chr2:160615804 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1846G>A (p.Glu616Lys) single nucleotide variant not specified [RCV004273159] Chr2:159759288 [GRCh38]
Chr2:160615799 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.910T>G (p.Leu304Val) single nucleotide variant not specified [RCV004274585] Chr2:159748200 [GRCh38]
Chr2:160604711 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.84C>A (p.Ser28Arg) single nucleotide variant not specified [RCV004248821] Chr2:159729106 [GRCh38]
Chr2:160585617 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.460A>C (p.Ile154Leu) single nucleotide variant not specified [RCV004365900] Chr2:159745883 [GRCh38]
Chr2:160602394 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1622T>C (p.Leu541Ser) single nucleotide variant not specified [RCV004360005] Chr2:159752410 [GRCh38]
Chr2:160608921 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1106A>C (p.Asp369Ala) single nucleotide variant not specified [RCV004347720] Chr2:159748396 [GRCh38]
Chr2:160604907 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1088A>G (p.Asn363Ser) single nucleotide variant not specified [RCV004343082] Chr2:159748378 [GRCh38]
Chr2:160604889 [GRCh37]
Chr2:2q24.2
uncertain significance
GRCh37/hg19 2q24.1-24.3(chr2:157718631-165360287)x1 copy number loss not specified [RCV003986232] Chr2:157718631..165360287 [GRCh37]
Chr2:2q24.1-24.3
pathogenic
NM_001282805.2(MARCHF7):c.229C>T (p.Arg77Cys) single nucleotide variant not specified [RCV004411378] Chr2:159743136 [GRCh38]
Chr2:160599647 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.230G>A (p.Arg77His) single nucleotide variant not specified [RCV004411379] Chr2:159743137 [GRCh38]
Chr2:160599648 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.307G>T (p.Ala103Ser) single nucleotide variant not specified [RCV004411380] Chr2:159743214 [GRCh38]
Chr2:160599725 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.315A>C (p.Arg105Ser) single nucleotide variant not specified [RCV004411381] Chr2:159743222 [GRCh38]
Chr2:160599733 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.329G>A (p.Gly110Asp) single nucleotide variant not specified [RCV004411382] Chr2:159743236 [GRCh38]
Chr2:160599747 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.488G>A (p.Arg163Gln) single nucleotide variant not specified [RCV004411383] Chr2:159745911 [GRCh38]
Chr2:160602422 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.488G>C (p.Arg163Pro) single nucleotide variant not specified [RCV004411384] Chr2:159745911 [GRCh38]
Chr2:160602422 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.575G>A (p.Ser192Asn) single nucleotide variant not specified [RCV004411386] Chr2:159747865 [GRCh38]
Chr2:160604376 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.590A>G (p.Asn197Ser) single nucleotide variant not specified [RCV004411387] Chr2:159747880 [GRCh38]
Chr2:160604391 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.669A>T (p.Arg223Ser) single nucleotide variant not specified [RCV004411388] Chr2:159747959 [GRCh38]
Chr2:160604470 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.795A>C (p.Arg265Ser) single nucleotide variant not specified [RCV004411389] Chr2:159748085 [GRCh38]
Chr2:160604596 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.940T>G (p.Ser314Ala) single nucleotide variant not specified [RCV004411390] Chr2:159748230 [GRCh38]
Chr2:160604741 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.979C>T (p.Arg327Cys) single nucleotide variant not specified [RCV004411391] Chr2:159748269 [GRCh38]
Chr2:160604780 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.2038C>T (p.His680Tyr) single nucleotide variant not specified [RCV004411377] Chr2:159764656 [GRCh38]
Chr2:160621167 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.2005C>G (p.Arg669Gly) single nucleotide variant not specified [RCV004411376] Chr2:159762991 [GRCh38]
Chr2:160619502 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1921C>G (p.Leu641Val) single nucleotide variant not specified [RCV004411374] Chr2:159762907 [GRCh38]
Chr2:160619418 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1570G>C (p.Ala524Pro) single nucleotide variant not specified [RCV004411373] Chr2:159748860 [GRCh38]
Chr2:160605371 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1513G>C (p.Asp505His) single nucleotide variant not specified [RCV004411372] Chr2:159748803 [GRCh38]
Chr2:160605314 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1445C>G (p.Ser482Cys) single nucleotide variant not specified [RCV004411371] Chr2:159748735 [GRCh38]
Chr2:160605246 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1400C>T (p.Ala467Val) single nucleotide variant not specified [RCV004411370] Chr2:159748690 [GRCh38]
Chr2:160605201 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1399G>T (p.Ala467Ser) single nucleotide variant not specified [RCV004411369] Chr2:159748689 [GRCh38]
Chr2:160605200 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1312A>G (p.Asn438Asp) single nucleotide variant not specified [RCV004411368] Chr2:159748602 [GRCh38]
Chr2:160605113 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1268T>C (p.Ile423Thr) single nucleotide variant not specified [RCV004411367] Chr2:159748558 [GRCh38]
Chr2:160605069 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1208G>C (p.Arg403Pro) single nucleotide variant not specified [RCV004411366] Chr2:159748498 [GRCh38]
Chr2:160605009 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1208G>A (p.Arg403Gln) single nucleotide variant not specified [RCV004411365] Chr2:159748498 [GRCh38]
Chr2:160605009 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1150C>T (p.Pro384Ser) single nucleotide variant not specified [RCV004411364] Chr2:159748440 [GRCh38]
Chr2:160604951 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1142A>G (p.Asn381Ser) single nucleotide variant not specified [RCV004411363] Chr2:159748432 [GRCh38]
Chr2:160604943 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.1127A>G (p.Glu376Gly) single nucleotide variant not specified [RCV004411362] Chr2:159748417 [GRCh38]
Chr2:160604928 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.110A>G (p.Tyr37Cys) single nucleotide variant not specified [RCV004411361] Chr2:159729132 [GRCh38]
Chr2:160585643 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.367C>G (p.Gln123Glu) single nucleotide variant not specified [RCV004636553] Chr2:159745790 [GRCh38]
Chr2:160602301 [GRCh37]
Chr2:2q24.2
uncertain significance
NM_001282805.2(MARCHF7):c.214A>G (p.Ile72Val) single nucleotide variant not specified [RCV004643061] Chr2:159743121 [GRCh38]
Chr2:160599632 [GRCh37]
Chr2:2q24.2
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1730
Count of miRNA genes:700
Interacting mature miRNAs:819
Transcripts:ENST00000259050, ENST00000409175, ENST00000409591, ENST00000420397, ENST00000421037, ENST00000461582, ENST00000473749, ENST00000478396, ENST00000539065
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
406977121GWAS626097_Hneutrophil count, basophil count QTL GWAS626097 (human)1e-12basophil quantity (VT:0002607)blood basophil count (CMO:0000034)2159712765159712766Human
407256934GWAS905910_Hblood protein measurement QTL GWAS905910 (human)5e-23blood protein measurementblood protein measurement (CMO:0000028)2159745359159745360Human
407006691GWAS655667_Hmean corpuscular hemoglobin QTL GWAS655667 (human)2e-09mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)2159736378159736379Human
407337957GWAS986933_Hinsomnia QTL GWAS986933 (human)1e-10insomnia2159760715159760716Human
407106791GWAS755767_Hplatelet crit QTL GWAS755767 (human)5e-50platelet critplateletcrit (CMO:0001349)2159748003159748004Human
407394444GWAS1043420_Hurate measurement, bone density QTL GWAS1043420 (human)9e-12bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)2159720129159720130Human
407406848GWAS1055824_Hurate measurement, bone density QTL GWAS1055824 (human)2e-08bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)2159715343159715344Human
406998317GWAS647293_Hbirth weight QTL GWAS647293 (human)1e-08birth weightneonatal body weight (CMO:0002079)2159712765159712766Human
406951665GWAS600641_Hplatelet count QTL GWAS600641 (human)2e-16platelet quantity (VT:0003179)platelet count (CMO:0000029)2159748030159748031Human
407101939GWAS750915_Hleukocyte count QTL GWAS750915 (human)1e-11leukocyte quantity (VT:0000217)white blood cell count (CMO:0000027)2159748003159748004Human
406973141GWAS622117_Hprotein measurement QTL GWAS622117 (human)1e-70protein measurement2159745420159745421Human
407231825GWAS880801_Hchildhood trauma measurement, alcohol consumption measurement QTL GWAS880801 (human)2e-08childhood trauma measurement, alcohol consumption measurementethanol drink intake rate (CMO:0001407)2159723067159723068Human
406963639GWAS612615_Hneutrophil count, eosinophil count QTL GWAS612615 (human)9e-12eosinophil quantity (VT:0002602)blood eosinophil count (CMO:0000033)2159712765159712766Human
407106613GWAS755589_Hplatelet count QTL GWAS755589 (human)5e-46platelet quantity (VT:0003179)platelet count (CMO:0000029)2159736378159736379Human
407259120GWAS908096_Haspartate aminotransferase measurement QTL GWAS908096 (human)8e-10aspartate aminotransferase measurementblood aspartate aminotransferase activity level (CMO:0000580)2159744239159744240Human
406942582GWAS591558_Hinsomnia measurement QTL GWAS591558 (human)5e-09insomnia measurement2159713522159713523Human
406973142GWAS622118_Hprotein measurement QTL GWAS622118 (human)7e-31protein measurement2159713180159713181Human
407223282GWAS872258_Hinsomnia QTL GWAS872258 (human)8e-09insomnia2159765413159765414Human
407270012GWAS918988_Hplatelet count QTL GWAS918988 (human)3e-20platelet quantity (VT:0003179)platelet count (CMO:0000029)2159736378159736379Human
406960762GWAS609738_Hgranulocyte count QTL GWAS609738 (human)8e-12granulocyte countblood granulocyte count (CMO:0000111)2159712765159712766Human
407187224GWAS836200_Haspartate aminotransferase measurement QTL GWAS836200 (human)2e-09aspartate aminotransferase measurementblood aspartate aminotransferase activity level (CMO:0000580)2159744239159744240Human
406974430GWAS623406_Hneutrophil count QTL GWAS623406 (human)2e-12neutrophil quantity (VT:0000222)blood neutrophil count (CMO:0000030)2159712765159712766Human

Markers in Region
D2S1731E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,622,976 - 160,623,191UniSTSGRCh37
Build 362160,331,222 - 160,331,437RGDNCBI36
Celera2154,234,822 - 154,235,037RGD
Cytogenetic Map2q24.2UniSTS
HuRef2152,506,879 - 152,507,094UniSTS
AXOT_710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,624,371 - 160,625,143UniSTSGRCh37
Build 362160,332,617 - 160,333,389RGDNCBI36
Celera2154,236,217 - 154,236,989RGD
HuRef2152,508,274 - 152,509,046UniSTS
RH77955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,570,991 - 160,571,141UniSTSGRCh37
Build 362160,279,237 - 160,279,387RGDNCBI36
Celera2154,182,852 - 154,183,002RGD
Cytogenetic Map2q24.2UniSTS
HuRef2152,454,946 - 152,455,096UniSTS
NCBI RH Map21124.7UniSTS
RH70502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,625,222 - 160,625,377UniSTSGRCh37
Build 362160,333,468 - 160,333,623RGDNCBI36
Celera2154,237,068 - 154,237,223RGD
Cytogenetic Map2qUniSTS
Cytogenetic Map2q24.2UniSTS
HuRef2152,509,125 - 152,509,280UniSTS
GeneMap99-GB4 RH Map2529.49UniSTS
G20298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,622,997 - 160,623,150UniSTSGRCh37
Build 362160,331,243 - 160,331,396RGDNCBI36
Celera2154,234,843 - 154,234,996RGD
Cytogenetic Map2q24.2UniSTS
HuRef2152,506,900 - 152,507,053UniSTS
A005L03  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,622,997 - 160,623,150UniSTSGRCh37
Build 362160,331,243 - 160,331,396RGDNCBI36
Celera2154,234,843 - 154,234,996RGD
Cytogenetic Map2q24.2UniSTS
HuRef2152,506,900 - 152,507,053UniSTS
GeneMap99-GB4 RH Map2529.49UniSTS
RH69485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,592,006 - 160,592,128UniSTSGRCh37
Build 362160,300,252 - 160,300,374RGDNCBI36
Celera2154,203,853 - 154,203,975RGD
Cytogenetic Map2q24.2UniSTS
HuRef2152,475,934 - 152,476,056UniSTS
GeneMap99-GB4 RH Map2529.49UniSTS
A007L02  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372160,625,397 - 160,625,561UniSTSGRCh37
Build 362160,333,643 - 160,333,807RGDNCBI36
Celera2154,237,243 - 154,237,407RGD
Cytogenetic Map2qUniSTS
Cytogenetic Map2q24.2UniSTS
HuRef2152,509,300 - 152,509,464UniSTS
GeneMap99-GB4 RH Map2527.62UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001282805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376249 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376252 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_022826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164794 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004721 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343405 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343406 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343415 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC009961 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI863394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022973 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK124225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK222880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292836 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL050171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL597638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX882469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI462287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR627026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA825046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000259050   ⟹   ENSP00000259050
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,712,499 - 159,771,027 (+)Ensembl
Ensembl Acc Id: ENST00000409175   ⟹   ENSP00000386830
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,712,506 - 159,771,027 (+)Ensembl
Ensembl Acc Id: ENST00000409591   ⟹   ENSP00000387238
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,733,965 - 159,767,409 (+)Ensembl
Ensembl Acc Id: ENST00000420397   ⟹   ENSP00000391493
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,752,490 - 159,767,960 (+)Ensembl
Ensembl Acc Id: ENST00000421037   ⟹   ENSP00000392862
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,712,507 - 159,743,211 (+)Ensembl
Ensembl Acc Id: ENST00000461582
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,745,770 - 159,752,525 (+)Ensembl
Ensembl Acc Id: ENST00000473749
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,712,523 - 159,748,126 (+)Ensembl
Ensembl Acc Id: ENST00000478396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,759,292 - 159,767,850 (+)Ensembl
Ensembl Acc Id: ENST00000539065   ⟹   ENSP00000442992
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2159,712,457 - 159,768,583 (+)Ensembl
RefSeq Acc Id: NM_001282805   ⟹   NP_001269734
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
HuRef2152,452,923 - 152,508,997 (+)NCBI
CHM1_12160,575,364 - 160,631,467 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001282806   ⟹   NP_001269735
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,583 (+)NCBI
HuRef2152,452,923 - 152,508,997 (+)NCBI
CHM1_12160,575,364 - 160,631,467 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,951 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001282807   ⟹   NP_001269736
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,733,964 - 159,771,027 (+)NCBI
HuRef2152,452,923 - 152,508,997 (+)NCBI
CHM1_12160,596,799 - 160,631,467 (+)NCBI
T2T-CHM13v2.02160,191,320 - 160,228,395 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376234   ⟹   NP_001363163
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376235   ⟹   NP_001363164
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376236   ⟹   NP_001363165
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376237   ⟹   NP_001363166
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376238   ⟹   NP_001363167
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376239   ⟹   NP_001363168
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376240   ⟹   NP_001363169
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376241   ⟹   NP_001363170
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376242   ⟹   NP_001363171
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376243   ⟹   NP_001363172
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376244   ⟹   NP_001363173
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376245   ⟹   NP_001363174
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376246   ⟹   NP_001363175
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376247   ⟹   NP_001363176
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376248   ⟹   NP_001363177
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376249   ⟹   NP_001363178
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376250   ⟹   NP_001363179
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376251   ⟹   NP_001363180
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376252   ⟹   NP_001363181
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376253   ⟹   NP_001363182
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376254   ⟹   NP_001363183
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001376255   ⟹   NP_001363184
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NM_022826   ⟹   NP_073737
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
GRCh372160,568,980 - 160,625,084 (+)NCBI
Build 362160,277,256 - 160,333,330 (+)NCBI Archive
Celera2154,180,871 - 154,236,930 (+)RGD
HuRef2152,452,923 - 152,508,997 (+)NCBI
CHM1_12160,575,364 - 160,631,467 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
Sequence:
RefSeq Acc Id: NR_164789
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NR_164790
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NR_164791
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NR_164792
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NR_164793
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NR_164794
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: NR_164795
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,768,573 (+)NCBI
T2T-CHM13v2.02160,169,869 - 160,225,941 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017004721   ⟹   XP_016860210
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047445508   ⟹   XP_047301464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445511   ⟹   XP_047301467
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445513   ⟹   XP_047301469
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445514   ⟹   XP_047301470
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,713,050 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445515   ⟹   XP_047301471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,713,050 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445516   ⟹   XP_047301472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445517   ⟹   XP_047301473
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445518   ⟹   XP_047301474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445519   ⟹   XP_047301475
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445520   ⟹   XP_047301476
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445521   ⟹   XP_047301477
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445523   ⟹   XP_047301479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,713,050 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445524   ⟹   XP_047301480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445525   ⟹   XP_047301481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445526   ⟹   XP_047301482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445527   ⟹   XP_047301483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445528   ⟹   XP_047301484
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445529   ⟹   XP_047301485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_047445530   ⟹   XP_047301486
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,771,027 (+)NCBI
RefSeq Acc Id: XM_054343403   ⟹   XP_054199378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343404   ⟹   XP_054199379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343405   ⟹   XP_054199380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343406   ⟹   XP_054199381
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,170,482 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343407   ⟹   XP_054199382
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343408   ⟹   XP_054199383
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343409   ⟹   XP_054199384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343410   ⟹   XP_054199385
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343411   ⟹   XP_054199386
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343412   ⟹   XP_054199387
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343413   ⟹   XP_054199388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,170,135 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343414   ⟹   XP_054199389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343415   ⟹   XP_054199390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343416   ⟹   XP_054199391
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343417   ⟹   XP_054199392
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343418   ⟹   XP_054199393
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343419   ⟹   XP_054199394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343420   ⟹   XP_054199395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
RefSeq Acc Id: XM_054343421   ⟹   XP_054199396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02160,169,869 - 160,228,395 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001269734 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269735 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269736 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363163 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363164 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363165 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363166 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363167 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363168 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363169 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363170 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363171 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363172 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363173 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363174 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363175 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363176 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363177 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363178 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363179 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363180 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363181 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363182 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363183 (Get FASTA)   NCBI Sequence Viewer  
  NP_001363184 (Get FASTA)   NCBI Sequence Viewer  
  NP_073737 (Get FASTA)   NCBI Sequence Viewer  
  XP_016860210 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301464 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301467 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301469 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301470 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301471 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301472 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301473 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301474 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301475 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301476 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301477 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301479 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301480 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301481 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301482 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301483 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301484 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301485 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301486 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199378 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199379 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199380 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199381 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199382 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199383 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199384 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199385 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199386 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199387 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199388 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199389 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199390 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199391 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199392 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199393 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199394 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199395 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199396 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH03404 (Get FASTA)   NCBI Sequence Viewer  
  AAH65014 (Get FASTA)   NCBI Sequence Viewer  
  AAY14941 (Get FASTA)   NCBI Sequence Viewer  
  BAB14340 (Get FASTA)   NCBI Sequence Viewer  
  BAD96600 (Get FASTA)   NCBI Sequence Viewer  
  BAF85525 (Get FASTA)   NCBI Sequence Viewer  
  BAH12936 (Get FASTA)   NCBI Sequence Viewer  
  BAH13681 (Get FASTA)   NCBI Sequence Viewer  
  BAH14753 (Get FASTA)   NCBI Sequence Viewer  
  CAE91593 (Get FASTA)   NCBI Sequence Viewer  
  EAX11401 (Get FASTA)   NCBI Sequence Viewer  
  EAX11402 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000259050
  ENSP00000259050.3
  ENSP00000386830
  ENSP00000386830.1
  ENSP00000387238
  ENSP00000387238.1
  ENSP00000391493.1
  ENSP00000392862.1
  ENSP00000442992
  ENSP00000442992.1
GenBank Protein Q9H992 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_073737   ⟸   NM_022826
- Peptide Label: isoform a
- UniProtKB: Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   Q9H992 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269734   ⟸   NM_001282805
- Peptide Label: isoform a
- UniProtKB: Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   Q9H992 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269735   ⟸   NM_001282806
- Peptide Label: isoform b
- UniProtKB: B7Z5K0 (UniProtKB/TrEMBL),   F5H6W4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269736   ⟸   NM_001282807
- Peptide Label: isoform c
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016860210   ⟸   XM_017004721
- Peptide Label: isoform X4
- UniProtKB: F5H6W4 (UniProtKB/TrEMBL),   B7Z5K0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001363170   ⟸   NM_001376241
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363171   ⟸   NM_001376242
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363165   ⟸   NM_001376236
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363164   ⟸   NM_001376235
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363163   ⟸   NM_001376234
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363168   ⟸   NM_001376239
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363172   ⟸   NM_001376243
- Peptide Label: isoform d
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363169   ⟸   NM_001376240
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363173   ⟸   NM_001376244
- Peptide Label: isoform e
- UniProtKB: B7Z5K0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363177   ⟸   NM_001376248
- Peptide Label: isoform g
- UniProtKB: B7Z5K0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363181   ⟸   NM_001376252
- Peptide Label: isoform h
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363184   ⟸   NM_001376255
- Peptide Label: isoform j
RefSeq Acc Id: NP_001363179   ⟸   NM_001376250
- Peptide Label: isoform h
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363182   ⟸   NM_001376253
- Peptide Label: isoform i
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363180   ⟸   NM_001376251
- Peptide Label: isoform h
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363183   ⟸   NM_001376254
- Peptide Label: isoform i
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363167   ⟸   NM_001376238
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363166   ⟸   NM_001376237
- Peptide Label: isoform a
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot),   B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363174   ⟸   NM_001376245
- Peptide Label: isoform e
- UniProtKB: B7Z5K0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363176   ⟸   NM_001376247
- Peptide Label: isoform g
- UniProtKB: B7Z5K0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363178   ⟸   NM_001376249
- Peptide Label: isoform h
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001363175   ⟸   NM_001376246
- Peptide Label: isoform f
- UniProtKB: B7ZAR7 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000259050   ⟸   ENST00000259050
Ensembl Acc Id: ENSP00000442992   ⟸   ENST00000539065
Ensembl Acc Id: ENSP00000387238   ⟸   ENST00000409591
Ensembl Acc Id: ENSP00000391493   ⟸   ENST00000420397
Ensembl Acc Id: ENSP00000386830   ⟸   ENST00000409175
Ensembl Acc Id: ENSP00000392862   ⟸   ENST00000421037
RefSeq Acc Id: XP_047301469   ⟸   XM_047445513
- Peptide Label: isoform X1
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047301474   ⟸   XM_047445518
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301483   ⟸   XM_047445527
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047301472   ⟸   XM_047445516
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301480   ⟸   XM_047445524
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047301473   ⟸   XM_047445517
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301481   ⟸   XM_047445525
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047301486   ⟸   XM_047445530
- Peptide Label: isoform X4
- UniProtKB: F5H6W4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047301482   ⟸   XM_047445526
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047301464   ⟸   XM_047445508
- Peptide Label: isoform X1
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047301477   ⟸   XM_047445521
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301485   ⟸   XM_047445529
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047301475   ⟸   XM_047445519
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301476   ⟸   XM_047445520
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301484   ⟸   XM_047445528
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047301467   ⟸   XM_047445511
- Peptide Label: isoform X1
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047301470   ⟸   XM_047445514
- Peptide Label: isoform X1
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047301479   ⟸   XM_047445523
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301471   ⟸   XM_047445515
- Peptide Label: isoform X1
- UniProtKB: Q9H992 (UniProtKB/Swiss-Prot),   Q53GQ1 (UniProtKB/Swiss-Prot),   D3DPB0 (UniProtKB/Swiss-Prot),   B7Z7P5 (UniProtKB/Swiss-Prot),   A8K9X1 (UniProtKB/Swiss-Prot),   Q9BTR9 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054199380   ⟸   XM_054343405
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054199384   ⟸   XM_054343409
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199392   ⟸   XM_054343417
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054199382   ⟸   XM_054343407
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199389   ⟸   XM_054343414
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054199383   ⟸   XM_054343408
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199390   ⟸   XM_054343415
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054199396   ⟸   XM_054343421
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054199391   ⟸   XM_054343416
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054199395   ⟸   XM_054343420
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054199378   ⟸   XM_054343403
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054199387   ⟸   XM_054343412
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199394   ⟸   XM_054343419
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054199385   ⟸   XM_054343410
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199386   ⟸   XM_054343411
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199393   ⟸   XM_054343418
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054199379   ⟸   XM_054343404
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054199388   ⟸   XM_054343413
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199381   ⟸   XM_054343406
- Peptide Label: isoform X1
Protein Domains
RING-CH-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H992-F1-model_v2 AlphaFold Q9H992 1-704 view protein structure

Promoters
RGD ID:6861832
Promoter ID:EPDNEW_H4080
Type:initiation region
Name:MARCH7_3
Description:membrane associated ring-CH-type finger 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4074  EPDNEW_H4082  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,261 - 159,712,321EPDNEW
RGD ID:6861836
Promoter ID:EPDNEW_H4082
Type:initiation region
Name:MARCH7_1
Description:membrane associated ring-CH-type finger 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4074  EPDNEW_H4080  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382159,712,506 - 159,712,566EPDNEW
RGD ID:6797124
Promoter ID:HG_KWN:35578
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:OTTHUMT00000255040,   OTTHUMT00000333703,   OTTHUMT00000333704,   OTTHUMT00000333764,   OTTHUMT00000333765,   UC002UAU.1,   UC002UAW.1,   UC010FOQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362160,277,161 - 160,277,917 (-)MPROMDB
RGD ID:6797782
Promoter ID:HG_KWN:35579
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000409591,   UC010FOR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362160,298,066 - 160,298,566 (+)MPROMDB
RGD ID:6797778
Promoter ID:HG_KWN:35581
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC002UAY.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362160,312,676 - 160,313,176 (+)MPROMDB
RGD ID:6797779
Promoter ID:HG_KWN:35582
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000333762
Position:
Human AssemblyChrPosition (strand)Source
Build 362160,317,099 - 160,317,599 (+)MPROMDB
RGD ID:6797780
Promoter ID:HG_KWN:35583
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000333763,   UC002UAZ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362160,323,436 - 160,323,936 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17393 AgrOrtholog
COSMIC MARCHF7 COSMIC
Ensembl Genes ENSG00000136536 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000259050 ENTREZGENE
  ENST00000259050.8 UniProtKB/Swiss-Prot
  ENST00000409175 ENTREZGENE
  ENST00000409175.6 UniProtKB/Swiss-Prot
  ENST00000409591 ENTREZGENE
  ENST00000409591.5 UniProtKB/Swiss-Prot
  ENST00000420397.1 UniProtKB/TrEMBL
  ENST00000421037.1 UniProtKB/TrEMBL
  ENST00000539065 ENTREZGENE
  ENST00000539065.5 UniProtKB/TrEMBL
Gene3D-CATH 3.30.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000136536 GTEx
HGNC ID HGNC:17393 ENTREZGENE
Human Proteome Map MARCHF7 Human Proteome Map
InterPro RING-CH-type_E3_ubiq-ligase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING-CH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING/FYVE/PHD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:64844 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 64844 ENTREZGENE
OMIM 613334 OMIM
PANTHER E3 UBIQUITIN-PROTEIN LIGASE MARCHF7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MARCH7/10 E3 UBIQUITIN PROTEIN LIGASE FAMILY MEMBER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam RINGv UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA166351954 PharmGKB
PROSITE ZF_RING_CH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART RINGv UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP RING/U-box UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K9X1 ENTREZGENE
  B7Z5K0 ENTREZGENE, UniProtKB/TrEMBL
  B7Z7P5 ENTREZGENE
  B7ZAR7 ENTREZGENE, UniProtKB/TrEMBL
  C9J159_HUMAN UniProtKB/TrEMBL
  D3DPB0 ENTREZGENE
  F5H6W4 ENTREZGENE, UniProtKB/TrEMBL
  H7BZU7_HUMAN UniProtKB/TrEMBL
  MARH7_HUMAN UniProtKB/Swiss-Prot
  Q53GQ1 ENTREZGENE
  Q9BTR9 ENTREZGENE
  Q9H992 ENTREZGENE
UniProt Secondary A8K9X1 UniProtKB/Swiss-Prot
  B7Z7P5 UniProtKB/Swiss-Prot
  D3DPB0 UniProtKB/Swiss-Prot
  Q53GQ1 UniProtKB/Swiss-Prot
  Q9BTR9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-07-16 MARCHF7  membrane associated ring-CH-type finger 7  MARCH7  membrane associated ring-CH-type finger 7  Symbol and/or name change 5135510 APPROVED
2015-12-01 MARCH7  membrane associated ring-CH-type finger 7  MARCH7  membrane-associated ring finger (C3HC4) 7, E3 ubiquitin protein ligase  Symbol and/or name change 5135510 APPROVED
2012-03-01 MARCH7  membrane-associated ring finger (C3HC4) 7, E3 ubiquitin protein ligase  MARCH7  membrane-associated ring finger (C3HC4) 7  Symbol and/or name change 5135510 APPROVED