ZMYM3 (zinc finger MYM-type containing 3) - Rat Genome Database

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Gene: ZMYM3 (zinc finger MYM-type containing 3) Homo sapiens
Analyze
Symbol: ZMYM3
Name: zinc finger MYM-type containing 3
RGD ID: 1350026
HGNC Page HGNC
Description: Predicted to have DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. Localizes to nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: DXS6673E; KIAA0385; MYM; XFIM; zinc finger MYM-type protein 3; zinc finger protein 261; zinc finger, MYM-type 3; ZNF198L2; ZNF261
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
GRCh38.p13 EnsemblX71,239,624 - 71,255,146 (-)EnsemblGRCh38hg38GRCh38
GRCh38X71,239,624 - 71,255,197 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X70,459,474 - 70,475,047 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X70,376,199 - 70,391,148 (-)NCBINCBI36hg18NCBI36
Build 34X70,242,494 - 70,256,967NCBI
CeleraX70,813,352 - 70,828,925 (-)NCBI
Cytogenetic MapXq13.1NCBI
HuRefX64,255,232 - 64,292,202 (-)NCBIHuRef
CHM1_1X70,352,552 - 70,368,124 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
nucleoplasm  (IDA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:8817323   PMID:8889548   PMID:9205841   PMID:10486218   PMID:10662551   PMID:12477932   PMID:12493763   PMID:12838571   PMID:15302935   PMID:15489334   PMID:15790807   PMID:16079794  
PMID:16344560   PMID:17081983   PMID:18029348   PMID:20360068   PMID:20562864   PMID:21258344   PMID:21832049   PMID:21834987   PMID:21873635   PMID:22094256   PMID:22586326   PMID:22658674  
PMID:22939629   PMID:23752268   PMID:24457600   PMID:24722188   PMID:25133527   PMID:25609649   PMID:26186194   PMID:26275350   PMID:26344197   PMID:26496610   PMID:26760575   PMID:27248496  
PMID:27705803   PMID:28242625   PMID:28514442   PMID:29180619   PMID:29332164   PMID:29467282   PMID:29509190   PMID:30021884   PMID:30425250   PMID:30804502   PMID:30889214   PMID:30909162  
PMID:31073040   PMID:31091453   PMID:31527615   PMID:31753913   PMID:32786267   PMID:32814053   PMID:33173136  


Genomics

Comparative Map Data
ZMYM3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX71,239,624 - 71,255,146 (-)EnsemblGRCh38hg38GRCh38
GRCh38X71,239,624 - 71,255,197 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X70,459,474 - 70,475,047 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X70,376,199 - 70,391,148 (-)NCBINCBI36hg18NCBI36
Build 34X70,242,494 - 70,256,967NCBI
CeleraX70,813,352 - 70,828,925 (-)NCBI
Cytogenetic MapXq13.1NCBI
HuRefX64,255,232 - 64,292,202 (-)NCBIHuRef
CHM1_1X70,352,552 - 70,368,124 (-)NCBICHM1_1
Zmym3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X100,447,990 - 100,464,986 (-)NCBIGRCm39mm39
GRCm39 EnsemblX100,447,990 - 100,464,455 (-)Ensembl
GRCm38X101,404,384 - 101,421,385 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX101,404,384 - 101,420,849 (-)EnsemblGRCm38mm10GRCm38
MGSCv37X98,599,723 - 98,616,024 (-)NCBIGRCm37mm9NCBIm37
MGSCv36X97,607,104 - 97,623,568 (-)NCBImm8
CeleraX88,321,182 - 88,337,387 (-)NCBICelera
Cytogenetic MapXDNCBI
cM MapX44.1NCBI
Zmym3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2X66,528,585 - 66,544,234 (-)NCBI
Rnor_6.0 EnsemblX71,299,662 - 71,313,542 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0X71,298,737 - 71,313,529 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0X72,150,498 - 72,165,290 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4X89,476,632 - 89,491,430 (-)NCBIRGSC3.4rn4RGSC3.4
CeleraX66,884,238 - 66,900,192 (-)NCBICelera
Cytogenetic MapXq22NCBI
Zmym3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495547510,801,255 - 10,818,375 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495547510,801,637 - 10,818,123 (-)NCBIChiLan1.0ChiLan1.0
ZMYM3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1X70,559,268 - 70,574,360 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX70,559,268 - 70,573,852 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0X60,503,245 - 60,518,830 (-)NCBIMhudiblu_PPA_v0panPan3
ZMYM3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X55,588,739 - 55,604,157 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX55,590,006 - 55,603,487 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX46,415,595 - 46,431,036 (-)NCBI
ROS_Cfam_1.0X56,557,450 - 56,572,898 (-)NCBI
UMICH_Zoey_3.1X54,525,342 - 54,540,780 (-)NCBI
UNSW_CanFamBas_1.0X55,857,003 - 55,872,441 (-)NCBI
UU_Cfam_GSD_1.0X55,783,973 - 55,799,421 (-)NCBI
Zmym3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X46,597,823 - 46,614,335 (+)NCBI
SpeTri2.0NW_004936762360,581 - 376,509 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZMYM3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1X57,261,923 - 57,279,427 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X64,829,886 - 64,832,212 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZMYM3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X61,035,332 - 61,050,757 (-)NCBI
ChlSab1.1 EnsemblX61,035,325 - 61,050,172 (-)Ensembl
Vero_WHO_p1.0NW_0236660652,900,606 - 2,916,059 (-)NCBI
Zmym3
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046249031,532,324 - 1,548,784 (-)NCBI

Position Markers
RH79687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,459,497 - 70,459,759UniSTSGRCh37
Build 36X70,376,222 - 70,376,484RGDNCBI36
CeleraX70,813,375 - 70,813,637RGD
Cytogenetic MapXq13.1UniSTS
HuRefX64,276,665 - 64,276,927UniSTS
GeneMap99-GB4 RH MapX238.28UniSTS
RH98882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,459,813 - 70,459,992UniSTSGRCh37
Build 36X70,376,538 - 70,376,717RGDNCBI36
CeleraX70,813,691 - 70,813,870RGD
Cytogenetic MapXq13.1UniSTS
HuRefX64,276,981 - 64,277,160UniSTS
GeneMap99-GB4 RH MapX231.7UniSTS
DXS7119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,454,189 - 70,454,597UniSTSGRCh37
Build 36X70,370,914 - 70,371,322RGDNCBI36
CeleraX70,808,070 - 70,808,475RGD
CeleraX70,808,092 - 70,808,475UniSTS
Cytogenetic MapXq13.1UniSTS
HuRefX64,271,111 - 64,271,511UniSTS
WI-20232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,459,544 - 70,459,809UniSTSGRCh37
Build 36X70,376,269 - 70,376,534RGDNCBI36
CeleraX70,813,422 - 70,813,687RGD
Cytogenetic MapXq13.1UniSTS
HuRefX64,276,712 - 64,276,977UniSTS
GeneMap99-GB4 RH MapX241.0UniSTS
Whitehead-RH MapX163.6UniSTS
NCBI RH MapX474.9UniSTS
PMC22091P4  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,474,908 - 70,475,046UniSTSGRCh37
Build 36X70,391,633 - 70,391,771RGDNCBI36
CeleraX70,828,786 - 70,828,924RGD
Cytogenetic MapXq13.1UniSTS
PMC22091P5  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,469,419 - 70,470,352UniSTSGRCh37
Build 36X70,386,144 - 70,387,077RGDNCBI36
CeleraX70,823,297 - 70,824,230RGD
Cytogenetic MapXq13.1UniSTS
HuRefX64,286,445 - 64,287,378UniSTS
RH1704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,444,159 - 70,444,310UniSTSGRCh37
Build 36X70,360,884 - 70,361,035RGDNCBI36
CeleraX70,798,040 - 70,798,191RGD
Cytogenetic MapXq13.1UniSTS
HuRefX64,261,498 - 64,261,649UniSTS
GeneMap99-GB4 RH MapX236.53UniSTS
NCBI RH MapX372.9UniSTS
STS-X95808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,460,525 - 70,460,764UniSTSGRCh37
Build 36X70,377,250 - 70,377,489RGDNCBI36
CeleraX70,814,403 - 70,814,642RGD
Cytogenetic MapXq13.1UniSTS
HuRefX64,277,693 - 64,277,932UniSTS
GeneMap99-GB4 RH MapX238.71UniSTS
NCBI RH MapX376.1UniSTS
MARC_17083-17084:1023819377:2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X70,464,692 - 70,465,245UniSTSGRCh37
Build 36X70,381,417 - 70,381,970RGDNCBI36
CeleraX70,818,570 - 70,819,123RGD
HuRefX64,281,859 - 64,282,412UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:9506
Count of miRNA genes:1026
Interacting mature miRNAs:1225
Transcripts:ENST00000314425, ENST00000353904, ENST00000373978, ENST00000373981, ENST00000373982, ENST00000373984, ENST00000373988, ENST00000373998, ENST00000470832, ENST00000489332
Prediction methods:Microtar, Miranda, Pita, Pita,Microtar, 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.


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 2023 1391 1405 299 1144 166 3196 898 2843 293 1422 1541 147 1 850 1869 3
Low 416 1570 320 324 782 298 1161 1295 891 126 38 72 27 354 919 3 2
Below cutoff 29 1 1 25 1 4

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_016407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001171162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001171163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_201599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005262309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005262310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB002383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL590762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY927528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013009 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB305871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA331402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA539831 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X95808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000314425   ⟹   ENSP00000322845
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,239,624 - 71,254,140 (-)Ensembl
RefSeq Acc Id: ENST00000373978   ⟹   ENSP00000363090
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,249,209 - 71,254,539 (-)Ensembl
RefSeq Acc Id: ENST00000373981   ⟹   ENSP00000363093
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,249,204 - 71,254,575 (-)Ensembl
RefSeq Acc Id: ENST00000373982   ⟹   ENSP00000363094
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,249,201 - 71,254,140 (-)Ensembl
RefSeq Acc Id: ENST00000373984   ⟹   ENSP00000363096
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,239,626 - 71,254,129 (-)Ensembl
RefSeq Acc Id: ENST00000373988   ⟹   ENSP00000363100
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,239,626 - 71,255,060 (-)Ensembl
RefSeq Acc Id: ENST00000373998   ⟹   ENSP00000363110
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,239,624 - 71,255,146 (-)Ensembl
RefSeq Acc Id: ENST00000470832
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,243,617 - 71,244,470 (-)Ensembl
RefSeq Acc Id: ENST00000489332
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX71,239,626 - 71,254,127 (-)Ensembl
RefSeq Acc Id: NM_001171162   ⟹   NP_001164633
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,239,624 - 71,255,197 (-)NCBI
GRCh37X70,459,474 - 70,475,047 (-)RGD
CeleraX70,813,352 - 70,828,925 (-)RGD
HuRefX64,255,232 - 64,292,202 (-)RGD
CHM1_1X70,352,552 - 70,368,124 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001171163   ⟹   NP_001164634
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,249,204 - 71,254,649 (-)NCBI
GRCh37X70,459,474 - 70,475,047 (-)NCBI
CeleraX70,813,352 - 70,828,925 (-)RGD
HuRefX64,255,232 - 64,292,202 (-)RGD
CHM1_1X70,362,131 - 70,367,576 (-)NCBI
Sequence:
RefSeq Acc Id: NM_005096   ⟹   NP_005087
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,239,624 - 71,254,649 (-)NCBI
GRCh37X70,459,474 - 70,475,047 (-)RGD
GRCh37X70,459,474 - 70,475,047 (-)NCBI
Build 36X70,376,199 - 70,391,148 (-)NCBI Archive
CeleraX70,813,352 - 70,828,925 (-)RGD
HuRefX64,255,232 - 64,292,202 (-)RGD
CHM1_1X70,352,552 - 70,367,576 (-)NCBI
Sequence:
RefSeq Acc Id: NM_201599   ⟹   NP_963893
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,239,624 - 71,254,140 (-)NCBI
GRCh37X70,459,474 - 70,475,047 (-)NCBI
Build 36X70,376,199 - 70,390,671 (-)NCBI Archive
CeleraX70,813,352 - 70,828,925 (-)RGD
HuRefX64,255,232 - 64,292,202 (-)RGD
CHM1_1X70,352,552 - 70,367,115 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005262309   ⟹   XP_005262366
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,239,626 - 71,254,689 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005262310   ⟹   XP_005262367
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,239,626 - 71,254,145 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011531062   ⟹   XP_011529364
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,239,626 - 71,254,537 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_005087   ⟸   NM_005096
- Peptide Label: isoform 1
- UniProtKB: Q14202 (UniProtKB/Swiss-Prot),   A8K3Z7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_963893   ⟸   NM_201599
- Peptide Label: isoform 1
- UniProtKB: Q14202 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001164634   ⟸   NM_001171163
- Peptide Label: isoform 3
- UniProtKB: Q14202 (UniProtKB/Swiss-Prot),   A8K3Z7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001164633   ⟸   NM_001171162
- Peptide Label: isoform 2
- UniProtKB: Q14202 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005262366   ⟸   XM_005262309
- Peptide Label: isoform X1
- UniProtKB: Q14202 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005262367   ⟸   XM_005262310
- Peptide Label: isoform X2
- UniProtKB: Q14202 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011529364   ⟸   XM_011531062
- Peptide Label: isoform X1
- UniProtKB: Q14202 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000363110   ⟸   ENST00000373998
RefSeq Acc Id: ENSP00000363090   ⟸   ENST00000373978
RefSeq Acc Id: ENSP00000363093   ⟸   ENST00000373981
RefSeq Acc Id: ENSP00000363094   ⟸   ENST00000373982
RefSeq Acc Id: ENSP00000363096   ⟸   ENST00000373984
RefSeq Acc Id: ENSP00000363100   ⟸   ENST00000373988
RefSeq Acc Id: ENSP00000322845   ⟸   ENST00000314425
Protein Domains
TRASH

Promoters
RGD ID:6813859
Promoter ID:HG_ACW:84218
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:ZMYM3.FAPR07,   ZMYM3.JAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 36X70,388,806 - 70,389,306 (-)MPROMDB
RGD ID:6809423
Promoter ID:HG_KWN:67173
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000373978,   ENST00000373982,   ENST00000373984,   ENST00000373988,   NM_201599,   OTTHUMT00000057160,   OTTHUMT00000057161,   UC004DZK.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36X70,390,711 - 70,392,127 (-)MPROMDB
RGD ID:6809422
Promoter ID:HG_KWN:67174
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   NB4
Transcripts:ENST00000373981,   NM_001171162,   NM_005096,   UC004DZM.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36X70,391,496 - 70,391,996 (-)MPROMDB
RGD ID:13627410
Promoter ID:EPDNEW_H28980
Type:initiation region
Name:ZMYM3_1
Description:zinc finger MYM-type containing 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28981  EPDNEW_H28982  EPDNEW_H28983  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,254,140 - 71,254,200EPDNEW
RGD ID:13627412
Promoter ID:EPDNEW_H28981
Type:initiation region
Name:ZMYM3_4
Description:zinc finger MYM-type containing 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28980  EPDNEW_H28982  EPDNEW_H28983  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,254,540 - 71,254,600EPDNEW
RGD ID:13627414
Promoter ID:EPDNEW_H28982
Type:initiation region
Name:ZMYM3_3
Description:zinc finger MYM-type containing 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28980  EPDNEW_H28981  EPDNEW_H28983  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,254,689 - 71,254,749EPDNEW
RGD ID:13627416
Promoter ID:EPDNEW_H28983
Type:initiation region
Name:ZMYM3_2
Description:zinc finger MYM-type containing 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28980  EPDNEW_H28981  EPDNEW_H28982  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X71,255,263 - 71,255,323EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_005096.3(ZMYM3):c.-618C>T single nucleotide variant Lung cancer [RCV000102744] ChrX:71255079 [GRCh38]
ChrX:70474929 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh38/hg38 Xp22.33-q28(chrX:3092486-155699618)x2 copy number gain See cases [RCV000050889] ChrX:3092486..155699618 [GRCh38]
ChrX:3010527..154929279 [GRCh37]
ChrX:3020527..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x3 copy number gain See cases [RCV000050810] ChrX:20140..155699618 [GRCh38]
ChrX:70140..154929279 [GRCh37]
ChrX:10140..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x1 copy number loss See cases [RCV000050811] ChrX:20140..155699618 [GRCh38]
ChrX:70140..154929279 [GRCh37]
ChrX:10140..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]|See cases [RCV000050385] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1 copy number loss See cases [RCV000050699] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1 copy number loss Global developmental delay [RCV000050386]|See cases [RCV000050386] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3 copy number gain See cases [RCV000050697] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xp11.21-q28(chrX:57372584-155996431)x1 copy number loss See cases [RCV000051665] ChrX:57372584..155996431 [GRCh38]
ChrX:57399017..155226096 [GRCh37]
ChrX:57415742..154879290 [NCBI36]
ChrX:Xp11.21-q28
pathogenic
GRCh38/hg38 Xq11.1-28(chrX:63279794-155939524)x1 copy number loss See cases [RCV000051666] ChrX:63279794..155939524 [GRCh38]
ChrX:62499671..155169188 [GRCh37]
ChrX:62416396..154822382 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26101-155999293)x3 copy number gain See cases [RCV000052322] ChrX:26101..155999293 [GRCh38]
ChrX:76101..155228958 [GRCh37]
ChrX:16101..154882152 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2790845-155699618)x3 copy number gain See cases [RCV000052359] ChrX:2790845..155699618 [GRCh38]
ChrX:2708886..154929279 [GRCh37]
ChrX:2718886..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:237659-156022362)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]|See cases [RCV000052327] ChrX:237659..156022362 [GRCh38]
ChrX:154326..155252027 [GRCh37]
ChrX:94326..154905221 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:27245-155996431)x3 copy number gain See cases [RCV000052324] ChrX:27245..155996431 [GRCh38]
ChrX:77245..155226096 [GRCh37]
ChrX:17245..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq12-21.1(chrX:67621041-76868590)x2 copy number gain See cases [RCV000052416] ChrX:67621041..76868590 [GRCh38]
ChrX:66840883..76009501 [GRCh37]
ChrX:66757608..76005403 [NCBI36]
ChrX:Xq12-21.1
pathogenic
GRCh38/hg38 Xq12-13.3(chrX:68382004-75243150)x2 copy number gain See cases [RCV000052417] ChrX:68382004..75243150 [GRCh38]
ChrX:67601846..74462985 [GRCh37]
ChrX:67518571..74379710 [NCBI36]
ChrX:Xq12-13.3
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40704-156022362)x3 copy number gain See cases [RCV000052325] ChrX:40704..156022362 [GRCh38]
ChrX:90704..155252027 [GRCh37]
ChrX:30704..154905221 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1 copy number loss Global developmental delay [RCV000052986]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]|Intellectual functioning disability [RCV000052988]|Global developmental delay [RCV000052989]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]|See cases [RCV000052986] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q22.1(chrX:675360-100368517)x1 copy number loss See cases [RCV000053005] ChrX:675360..100368517 [GRCh38]
ChrX:636095..99623515 [GRCh37]
ChrX:556095..99510171 [NCBI36]
ChrX:Xp22.33-q22.1
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1 copy number loss Hypoplastic left heart [RCV000052982]|See cases [RCV000052982] ChrX:14245..155999293 [GRCh38]
ChrX:64245..155228958 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3 copy number gain Global developmental delay [RCV000052984]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]|See cases [RCV000052984] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
NM_005096.3(ZMYM3):c.2415C>T (p.Ile805=) single nucleotide variant Malignant melanoma [RCV000073242] ChrX:71246510 [GRCh38]
ChrX:70466360 [GRCh37]
ChrX:70383085 [NCBI36]
ChrX:Xq13.1
not provided
NM_201599.3(ZMYM3):c.1008G>A (p.Ser336=) single nucleotide variant not specified [RCV000082824] ChrX:71250497 [GRCh38]
ChrX:70470347 [GRCh37]
ChrX:Xq13.1
benign
NM_201599.3(ZMYM3):c.4065C>T (p.Arg1355=) single nucleotide variant not provided [RCV000082825] ChrX:71240964 [GRCh38]
ChrX:70460814 [GRCh37]
ChrX:Xq13.1
conflicting interpretations of pathogenicity|uncertain significance
NM_201599.3(ZMYM3):c.1321C>T (p.Arg441Trp) single nucleotide variant not provided [RCV000115021] ChrX:71249610 [GRCh38]
ChrX:70469460 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022826)x4 copy number gain See cases [RCV000133654] ChrX:10679..156022826 [GRCh38]
ChrX:60679..155252491 [GRCh37]
ChrX:679..154905685 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-155978689)x1 copy number loss See cases [RCV000133792] ChrX:10701..155978689 [GRCh38]
ChrX:60701..155208354 [GRCh37]
ChrX:701..154861548 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1 copy number loss See cases [RCV000050386] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3 copy number gain See cases [RCV000050385] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3 copy number gain See cases [RCV000052984] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1 copy number loss See cases [RCV000052986] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1 copy number loss See cases [RCV000052982] ChrX:14245..155999293 [GRCh38]
ChrX:64245..155228958 [GRCh37]
ChrX:4245..154882152 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-155999253)x3 copy number gain See cases [RCV000134564] ChrX:20297..155999253 [GRCh38]
ChrX:70297..155228918 [GRCh37]
ChrX:10297..154882112 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq11.1-21.1(chrX:62712219-78605009)x3 copy number gain See cases [RCV000134569] ChrX:62712219..78605009 [GRCh38]
ChrX:61931689..77860506 [GRCh37]
ChrX:61848414..77747162 [NCBI36]
ChrX:Xq11.1-21.1
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x1 copy number loss See cases [RCV000133947] ChrX:10701..156003242 [GRCh38]
ChrX:60701..155232907 [GRCh37]
ChrX:701..154886101 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xq11.1-28(chrX:62712230-155978888)x3 copy number gain See cases [RCV000134025] ChrX:62712230..155978888 [GRCh38]
ChrX:61931700..155208553 [GRCh37]
ChrX:61848425..154861747 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x3 copy number gain See cases [RCV000133911] ChrX:10701..156003242 [GRCh38]
ChrX:60701..155232907 [GRCh37]
ChrX:701..154886101 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|likely pathogenic|conflicting data from submitters
GRCh38/hg38 Xp21.1-q28(chrX:37076284-156016920)x1 copy number loss See cases [RCV000135300] ChrX:37076284..156016920 [GRCh38]
ChrX:37094357..155246585 [GRCh37]
ChrX:37004278..154899779 [NCBI36]
ChrX:Xp21.1-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156026127)x1 copy number loss See cases [RCV000135321] ChrX:20297..156026127 [GRCh38]
ChrX:70297..155255792 [GRCh37]
ChrX:10297..154908986 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp11.22-q21.31(chrX:53985575-92203108)x1 copy number loss See cases [RCV000135306] ChrX:53985575..92203108 [GRCh38]
ChrX:54012008..91458107 [GRCh37]
ChrX:54028733..91344763 [NCBI36]
ChrX:Xp11.22-q21.31
pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:36237706-156022206)x1 copy number loss See cases [RCV000135552] ChrX:36237706..156022206 [GRCh38]
ChrX:36255823..155251871 [GRCh37]
ChrX:36165744..154905065 [NCBI36]
ChrX:Xp21.1-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x1 copy number loss See cases [RCV000136097] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40904-155998166)x1 copy number loss See cases [RCV000136478] ChrX:40904..155998166 [GRCh38]
ChrX:90904..155227831 [GRCh37]
ChrX:30904..154881025 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q25(chrX:10701-128393708) copy number loss See cases [RCV000136094] ChrX:10701..128393708 [GRCh38]
ChrX:60701..127527686 [GRCh37]
ChrX:701..127355367 [NCBI36]
ChrX:Xp22.33-q25
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10001-156030895)x1 copy number loss See cases [RCV000136005] ChrX:10001..156030895 [GRCh38]
ChrX:60001..155260560 [GRCh37]
ChrX:1..154913754 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q13.3(chrX:10679-76420505)x3 copy number gain See cases [RCV000137137] ChrX:10679..76420505 [GRCh38]
ChrX:60679..75640898 [GRCh37]
ChrX:679..75557302 [NCBI36]
ChrX:Xp22.33-q13.3
pathogenic|likely benign
GRCh38/hg38 Xp22.33-q28(chrX:2765636-155522304)x3 copy number gain See cases [RCV000136791] ChrX:2765636..155522304 [GRCh38]
ChrX:2683677..154751965 [GRCh37]
ChrX:2693677..154405159 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2782275-155611794)x2 copy number gain See cases [RCV000136841] ChrX:2782275..155611794 [GRCh38]
ChrX:2700316..154785891 [GRCh37]
ChrX:2710316..154494649 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq11.1-28(chrX:62561604-156003242)x3 copy number gain See cases [RCV000137553] ChrX:62561604..156003242 [GRCh38]
ChrX:61781074..155232907 [GRCh37]
ChrX:61697799..154886101 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xp11.23-q22.1(chrX:49100536-102174742)x1 copy number loss See cases [RCV000137414] ChrX:49100536..102174742 [GRCh38]
ChrX:48957474..101429714 [GRCh37]
ChrX:48844418..101316370 [NCBI36]
ChrX:Xp11.23-q22.1
pathogenic|likely benign
GRCh38/hg38 Xp22.33-q22.3(chrX:10701-106113403)x1 copy number loss See cases [RCV000137886] ChrX:10701..106113403 [GRCh38]
ChrX:60701..105357395 [GRCh37]
ChrX:701..105244051 [NCBI36]
ChrX:Xp22.33-q22.3
pathogenic
GRCh38/hg38 Xp22.2-q27.3(chrX:13020141-143473520)x1 copy number loss See cases [RCV000138678] ChrX:13020141..143473520 [GRCh38]
ChrX:13038260..142561303 [GRCh37]
ChrX:12948181..142388969 [NCBI36]
ChrX:Xp22.2-q27.3
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:1085618-155699644)x1 copy number loss See cases [RCV000139278] ChrX:1085618..155699644 [GRCh38]
ChrX:1118268..154929305 [GRCh37]
ChrX:1038268..154582499 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq11.1-28(chrX:62712219-156003242)x3 copy number gain See cases [RCV000139416] ChrX:62712219..156003242 [GRCh38]
ChrX:61931689..155232907 [GRCh37]
ChrX:61848414..154886101 [NCBI36]
ChrX:Xq11.1-28
pathogenic|likely benign
GRCh38/hg38 Xp22.33-q21.31(chrX:10701-88318651)x1 copy number loss See cases [RCV000139352] ChrX:10701..88318651 [GRCh38]
ChrX:60701..87573652 [GRCh37]
ChrX:701..87460308 [NCBI36]
ChrX:Xp22.33-q21.31
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004181)x3 copy number gain See cases [RCV000139888] ChrX:251880..156004181 [GRCh38]
ChrX:168547..155233846 [GRCh37]
ChrX:108547..154887040 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2299223-155992188)x3 copy number gain See cases [RCV000141400] ChrX:2299223..155992188 [GRCh38]
ChrX:2217264..155221853 [GRCh37]
ChrX:2227264..154875047 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156016920)x3 copy number gain See cases [RCV000141401] ChrX:20297..156016920 [GRCh38]
ChrX:70297..155246585 [GRCh37]
ChrX:10297..154899779 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x4 copy number gain See cases [RCV000140786] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x1 copy number loss See cases [RCV000140787] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic|conflicting data from submitters
GRCh38/hg38 Xp11.22-q24(chrX:50289384-119297604) copy number loss See cases [RCV000141742] ChrX:50289384..119297604 [GRCh38]
ChrX:50032384..118431567 [GRCh37]
ChrX:50049124..118315595 [NCBI36]
ChrX:Xp11.22-q24
pathogenic
GRCh38/hg38 Xq12-21.1(chrX:66445907-78172208)x3 copy number gain See cases [RCV000142336] ChrX:66445907..78172208 [GRCh38]
ChrX:65665749..77427705 [GRCh37]
ChrX:65582474..77314361 [NCBI36]
ChrX:Xq12-21.1
pathogenic
GRCh38/hg38 Xp22.33-q24(chrX:251879-118847157)x3 copy number gain See cases [RCV000142134] ChrX:251879..118847157 [GRCh38]
ChrX:168546..117981120 [GRCh37]
ChrX:108546..117865148 [NCBI36]
ChrX:Xp22.33-q24
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x3 copy number gain See cases [RCV000142625] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp11.22-q28(chrX:53144751-156003242)x1 copy number loss See cases [RCV000143349] ChrX:53144751..156003242 [GRCh38]
ChrX:53321095..155232907 [GRCh37]
ChrX:53190658..154886101 [NCBI36]
ChrX:Xp11.22-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x1 copy number loss See cases [RCV000143441] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:108546..154886925 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x3 copy number gain See cases [RCV000143433] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x3 copy number gain See cases [RCV000143219] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:108547..154886925 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp11.21-q13.3(chrX:56431359-76557419)x1 copy number loss See cases [RCV000143131] ChrX:56431359..76557419 [GRCh38]
ChrX:56457792..75777827 [GRCh37]
ChrX:56474517..75694231 [NCBI36]
ChrX:Xp11.21-q13.3
pathogenic
GRCh38/hg38 Xq13.1(chrX:71071787-71777197)x2 copy number gain See cases [RCV000143302] ChrX:71071787..71777197 [GRCh38]
ChrX:70291637..70997047 [GRCh37]
ChrX:70208362..70913772 [NCBI36]
ChrX:Xq13.1
uncertain significance
GRCh38/hg38 Xq13.1(chrX:71022322-71682982)x2 copy number gain See cases [RCV000143525] ChrX:71022322..71682982 [GRCh38]
ChrX:70242172..70902832 [GRCh37]
ChrX:70158897..70819557 [NCBI36]
ChrX:Xq13.1
uncertain significance
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3 copy number gain See cases [RCV000148141] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1 copy number loss See cases [RCV000148135] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
NM_201599.3(ZMYM3):c.3552G>A (p.Thr1184=) single nucleotide variant not provided [RCV000154162] ChrX:71242420 [GRCh38]
ChrX:70462270 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.195C>G (p.Gly65=) single nucleotide variant not provided [RCV000154163] ChrX:71253061 [GRCh38]
ChrX:70472911 [GRCh37]
ChrX:Xq13.1
conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x2 copy number gain See cases [RCV000240106] ChrX:150002..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155246643)x3 copy number gain See cases [RCV000240122] ChrX:71267..155246643 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155246643)x3 copy number gain See cases [RCV000240143] ChrX:62063537..155246643 [GRCh37]
ChrX:Xq11.1-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255839)x1 copy number loss See cases [RCV000239832] ChrX:71267..155255839 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.2-q28(chrX:13147668-155250222)x3 copy number gain See cases [RCV000239798] ChrX:13147668..155250222 [GRCh37]
ChrX:Xp22.2-q28
pathogenic
NM_201599.3(ZMYM3):c.3880C>T (p.Arg1294Cys) single nucleotide variant not specified [RCV000238617] ChrX:71241267 [GRCh38]
ChrX:70461117 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh37/hg19 Xp22.33-q28(chrX:176426-155250222)x3 copy number gain See cases [RCV000239843] ChrX:176426..155250222 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255839)x3 copy number gain See cases [RCV000239934] ChrX:70297..155255839 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155234036)x2 copy number gain See cases [RCV000239874] ChrX:71267..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp11.21-q21.1(chrX:55240087-78225374)x1 copy number loss See cases [RCV000511311] ChrX:55240087..78225374 [GRCh37]
ChrX:Xp11.21-q21.1
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:56457791-155233731)x3 copy number gain See cases [RCV000511307] ChrX:56457791..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155224766)x1 copy number loss See cases [RCV000239902] ChrX:71267..155224766 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246271)x3 copy number gain See cases [RCV000239989] ChrX:60701..155246271 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:553069-155233731)x1 copy number loss See cases [RCV000446026] ChrX:553069..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp11.3-q21.1(chrX:44734936-79676121)x3 copy number gain See cases [RCV000240019] ChrX:44734936..79676121 [GRCh37]
ChrX:Xp11.3-q21.1
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:176426-155236656)x3 copy number gain See cases [RCV000240552] ChrX:176426..155236656 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:225816-155234036)x2 copy number gain See cases [RCV000240464] ChrX:225816..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x3 copy number gain See cases [RCV000240314] ChrX:150002..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155250222)x3 copy number gain See cases [RCV000240148] ChrX:62063537..155250222 [GRCh37]
ChrX:Xq11.1-28
pathogenic
GRCh37/hg19 Xq13.1(chrX:70459474-70654410)x2 copy number gain See cases [RCV000240450] ChrX:70459474..70654410 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh37/hg19 Xp22.33-q28(chrX:2707626-155250222)x2 copy number gain See cases [RCV000240541] ChrX:2707626..155250222 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2 copy number gain not provided [RCV000488046] ChrX:11692290..121187337 [GRCh37]
ChrX:Xp22.2-q25
uncertain significance
Single allele duplication Syndromic X-linked intellectual disability Lubs type [RCV000768455] ChrX:15323210..153542100 [GRCh37]
ChrX:Xp22.2-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-154930047)x3 copy number gain See cases [RCV000449437] ChrX:168546..154930047 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3 copy number gain See cases [RCV000449330] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792) copy number loss See cases [RCV000449461] ChrX:70297..155255792 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155081533)x3 copy number gain See cases [RCV000447253] ChrX:168546..155081533 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq13.1-28(chrX:68701338-155233731)x3 copy number gain See cases [RCV000446471] ChrX:68701338..155233731 [GRCh37]
ChrX:Xq13.1-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255792)x1 copy number loss See cases [RCV000446197] ChrX:71267..155255792 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:2703632-155233731)x1 copy number loss See cases [RCV000446712] ChrX:2703632..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246225)x3 copy number gain See cases [RCV000446270] ChrX:60701..155246225 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:318707-155224707)x1 copy number loss See cases [RCV000446667] ChrX:318707..155224707 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp11.1-q28(chrX:58140271-155046703)x3 copy number gain See cases [RCV000446151] ChrX:58140271..155046703 [GRCh37]
ChrX:Xp11.1-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4 copy number gain See cases [RCV000446932] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155196888)x3 copy number gain See cases [RCV000446310] ChrX:168546..155196888 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
NM_201599.3(ZMYM3):c.4056G>A (p.Leu1352=) single nucleotide variant not specified [RCV000423835] ChrX:71240973 [GRCh38]
ChrX:70460823 [GRCh37]
ChrX:Xq13.1
likely benign
GRCh37/hg19 Xp22.33-q28(chrX:168566-155233731)x1 copy number loss See cases [RCV000445720] ChrX:168566..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55532799-150239235)x1 copy number loss See cases [RCV000448870] ChrX:55532799..150239235 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss See cases [RCV000448393] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)x4 copy number gain See cases [RCV000448034] ChrX:70297..155255792 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155246585)x1 copy number loss See cases [RCV000448652] ChrX:70297..155246585 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168547-151304063)x1 copy number loss See cases [RCV000510382] ChrX:168547..151304063 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q23(chrX:168547-112474026)x1 copy number loss See cases [RCV000510419] ChrX:168547..112474026 [GRCh37]
ChrX:Xp22.33-q23
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731) copy number gain See cases [RCV000512020] ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55000501-155230750)x3 copy number gain See cases [RCV000511787] ChrX:55000501..155230750 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp21.1-q22.1(chrX:37521774-98488534)x1 copy number loss See cases [RCV000512026] ChrX:37521774..98488534 [GRCh37]
ChrX:Xp21.1-q22.1
pathogenic
GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1 copy number loss See cases [RCV000511413] ChrX:31088082..155233731 [GRCh37]
ChrX:Xp21.2-q28
pathogenic
GRCh37/hg19 Xq13.1(chrX:70287671-70997047)x3 copy number gain See cases [RCV000511625] ChrX:70287671..70997047 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh37/hg19 Xp11.21-q28(chrX:57511767-155233731)x3 copy number gain See cases [RCV000510826] ChrX:57511767..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:57415659-155233731)x3 copy number gain See cases [RCV000512173] ChrX:57415659..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp22.33-q13.3(chrX:168546-74549686) copy number loss See cases [RCV000512142] ChrX:168546..74549686 [GRCh37]
ChrX:Xp22.33-q13.3
pathogenic
GRCh37/hg19 Xq13.1(chrX:70287671-70997047)x2 copy number gain See cases [RCV000512522] ChrX:70287671..70997047 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.1111A>G (p.Thr371Ala) single nucleotide variant Inborn genetic diseases [RCV000622843] ChrX:71250166 [GRCh38]
ChrX:70470016 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh37/hg19 Xp22.31-q21.31(chrX:7841947-90815333)x1,2 copy number gain not provided [RCV000684261] ChrX:7841947..90815333 [GRCh37]
ChrX:Xp22.31-q21.31
pathogenic
NM_201599.3(ZMYM3):c.1470+6G>C single nucleotide variant not provided [RCV000678361] ChrX:71249455 [GRCh38]
ChrX:70469305 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh37/hg19 Xp11.23-q13.2(chrX:48115450-73424191)x1 copy number loss not provided [RCV000753535] ChrX:48115450..73424191 [GRCh37]
ChrX:Xp11.23-q13.2
pathogenic
GRCh37/hg19 Xq13.1(chrX:70313664-70568458)x2 copy number gain not provided [RCV000753588] ChrX:70313664..70568458 [GRCh37]
ChrX:Xq13.1
benign
GRCh37/hg19 Xq11.1-28(chrX:61694576-155254881)x1 copy number loss not provided [RCV000753556] ChrX:61694576..155254881 [GRCh37]
ChrX:Xq11.1-28
pathogenic
Single allele duplication Autistic disorder of childhood onset [RCV000754365] ChrX:1..156040895 [GRCh38]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155254881)x2 copy number gain not provided [RCV000753277] ChrX:60814..155254881 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x1 copy number loss not provided [RCV000753271] ChrX:60262..155245765 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x3 copy number gain not provided [RCV000753272] ChrX:60262..155245765 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:181779-155171702)x1 copy number loss not provided [RCV000753278] ChrX:181779..155171702 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155236712)x2 copy number gain not provided [RCV000753276] ChrX:60814..155236712 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
NC_000023.10:g.36649710_136649711del100000002insG indel Heterotaxy, visceral, 1, X-linked [RCV000754886] ChrX:36649710..136649711 [GRCh37]
ChrX:Xp21.1-q26.3
pathogenic
NM_201599.3(ZMYM3):c.2055C>A (p.Thr685=) single nucleotide variant not provided [RCV000927105] ChrX:71247827 [GRCh38]
ChrX:70467677 [GRCh37]
ChrX:Xq13.1
likely benign
NM_201599.3(ZMYM3):c.921C>A (p.Thr307=) single nucleotide variant not provided [RCV000904761] ChrX:71250584 [GRCh38]
ChrX:70470434 [GRCh37]
ChrX:Xq13.1
benign
NM_201599.3(ZMYM3):c.3800G>A (p.Arg1267Gln) single nucleotide variant Intellectual disability [RCV001260796]|not provided [RCV000995949] ChrX:71242172 [GRCh38]
ChrX:70462022 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.3774T>C (p.Tyr1258=) single nucleotide variant not provided [RCV000995950] ChrX:71242198 [GRCh38]
ChrX:70462048 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.990G>A (p.Leu330=) single nucleotide variant not provided [RCV000995952] ChrX:71250515 [GRCh38]
ChrX:70470365 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.683C>T (p.Ala228Val) single nucleotide variant not provided [RCV000995953] ChrX:71251586 [GRCh38]
ChrX:70471436 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.2367C>G (p.Asn789Lys) single nucleotide variant not provided [RCV000954794] ChrX:71246640 [GRCh38]
ChrX:70466490 [GRCh37]
ChrX:Xq13.1
benign
NM_201599.3(ZMYM3):c.3813T>C (p.Pro1271=) single nucleotide variant not provided [RCV000896208] ChrX:71241334 [GRCh38]
ChrX:70461184 [GRCh37]
ChrX:Xq13.1
likely benign
NM_201599.3(ZMYM3):c.3945C>T (p.Asn1315=) single nucleotide variant not provided [RCV000964230] ChrX:71241084 [GRCh38]
ChrX:70460934 [GRCh37]
ChrX:Xq13.1
benign
NM_201599.3(ZMYM3):c.1061C>T (p.Thr354Ile) single nucleotide variant not provided [RCV000902206] ChrX:71250444 [GRCh38]
ChrX:70470294 [GRCh37]
ChrX:Xq13.1
benign
46,Y,inv(X)(p21.1q13.3) inversion Elevated serum creatine phosphokinase [RCV000856573] ChrX:32196272..75245806 [GRCh37]
ChrX:Xp21.1-q13.3
likely pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4 copy number gain not provided [RCV000846039] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
NM_201599.3(ZMYM3):c.1745G>A (p.Ser582Asn) single nucleotide variant not provided [RCV001090310] ChrX:71248517 [GRCh38]
ChrX:70468367 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.3371G>A (p.Arg1124Gln) single nucleotide variant not provided [RCV000851322] ChrX:71243890 [GRCh38]
ChrX:70463740 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh37/hg19 Xp11.1-q28(chrX:58455352-155233731)x1 copy number loss not provided [RCV000846274] ChrX:58455352..155233731 [GRCh37]
ChrX:Xp11.1-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss not provided [RCV000848828] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp11.4-q21.32(chrX:40572613-92796528)x1 copy number loss not provided [RCV000845670] ChrX:40572613..92796528 [GRCh37]
ChrX:Xp11.4-q21.32
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:54941868-155233731)x1 copy number loss not provided [RCV000848218] ChrX:54941868..155233731 [GRCh37]
ChrX:Xp11.21-q28
uncertain significance
NM_201599.3(ZMYM3):c.3451C>T (p.Arg1151Trp) single nucleotide variant not provided [RCV000995951] ChrX:71243066 [GRCh38]
ChrX:70462916 [GRCh37]
ChrX:Xq13.1
uncertain significance
NM_201599.3(ZMYM3):c.1056C>A (p.Thr352=) single nucleotide variant not provided [RCV000929632] ChrX:71250449 [GRCh38]
ChrX:70470299 [GRCh37]
ChrX:Xq13.1
likely benign
NM_201599.3(ZMYM3):c.3803-4A>G single nucleotide variant not provided [RCV000882851] ChrX:71241348 [GRCh38]
ChrX:70461198 [GRCh37]
ChrX:Xq13.1
benign
NM_201599.3(ZMYM3):c.1212C>T (p.Ala404=) single nucleotide variant not provided [RCV000891185] ChrX:71250065 [GRCh38]
ChrX:70469915 [GRCh37]
ChrX:Xq13.1
likely benign
GRCh37/hg19 Xq13.1(chrX:70386654-70743623)x0 copy number gain See cases [RCV001263049] ChrX:70386654..70743623 [GRCh37]
ChrX:Xq13.1
uncertain significance
GRCh37/hg19 Xp11.21-q28(chrX:55507789-155198481)x3 copy number gain See cases [RCV001263024] ChrX:55507789..155198481 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:56469080-155233731)x3 copy number gain not provided [RCV001281359] ChrX:56469080..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13054 AgrOrtholog
COSMIC ZMYM3 COSMIC
Ensembl Genes ENSG00000147130 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000322845 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000363090 UniProtKB/TrEMBL
  ENSP00000363093 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000363094 UniProtKB/TrEMBL
  ENSP00000363096 UniProtKB/TrEMBL
  ENSP00000363100 UniProtKB/TrEMBL
  ENSP00000363110 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000314425 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000373978 UniProtKB/TrEMBL
  ENST00000373981 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000373982 UniProtKB/TrEMBL
  ENST00000373984 UniProtKB/TrEMBL
  ENST00000373988 UniProtKB/TrEMBL
  ENST00000373998 ENTREZGENE, UniProtKB/Swiss-Prot
GTEx ENSG00000147130 GTEx
HGNC ID HGNC:13054 ENTREZGENE
Human Proteome Map ZMYM3 Human Proteome Map
InterPro DUF3504 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRASH_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_MYM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9203 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 9203 ENTREZGENE
OMIM 300061 OMIM
Pfam DUF3504 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-FCS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37632 PharmGKB
SMART TRASH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6NC58_HUMAN UniProtKB/TrEMBL
  A6NHB5_HUMAN UniProtKB/TrEMBL
  A6NHN7_HUMAN UniProtKB/TrEMBL
  A6NL54_HUMAN UniProtKB/TrEMBL
  A8K3Z7 ENTREZGENE, UniProtKB/TrEMBL
  L8E7R4_HUMAN UniProtKB/TrEMBL
  L8E863_HUMAN UniProtKB/TrEMBL
  Q14202 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary D3DVV3 UniProtKB/Swiss-Prot
  O15089 UniProtKB/Swiss-Prot
  Q96E26 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-18 ZMYM3  zinc finger MYM-type containing 3    zinc finger, MYM-type 3  Symbol and/or name change 5135510 APPROVED