ZNF41 (zinc finger protein 41) - Rat Genome Database

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Gene: ZNF41 (zinc finger protein 41) Homo sapiens
Analyze
Symbol: ZNF41
Name: zinc finger protein 41
RGD ID: 1346984
HGNC Page HGNC
Description: Predicted to have DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to localize to nucleus. Implicated in non-syndromic X-linked intellectual disability 89.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: mental retardation, X-linked 89; MGC8941; MRX89
RGD Orthologs
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: AL136981.2   LOC100419707  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX47,445,879 - 47,482,946 (-)EnsemblGRCh38hg38GRCh38
GRCh38.p13 EnsemblX47,445,178 - 47,483,222 (-)EnsemblGRCh38hg38GRCh38
GRCh38X47,444,691 - 47,485,934 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X47,304,577 - 47,342,621 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X47,191,347 - 47,227,289 (-)NCBINCBI36hg18NCBI36
Build 34X47,062,657 - 47,098,599NCBI
CeleraX51,500,825 - 51,537,610 (-)NCBI
Cytogenetic MapXp11.3NCBI
HuRefX45,018,484 - 45,055,126 (-)NCBIHuRef
CHM1_1X47,335,709 - 47,373,791 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Biological Process

Cellular Component
nucleus  (IBA)

References

Additional References at PubMed
PMID:1945843   PMID:2037297   PMID:8088786   PMID:10449920   PMID:12477932   PMID:14628291   PMID:15231748   PMID:15489334   PMID:15772651   PMID:16344560   PMID:20211142   PMID:21873635  
PMID:23871722   PMID:25416956   PMID:25910212   PMID:32296183  


Genomics

Comparative Map Data
ZNF41
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX47,445,879 - 47,482,946 (-)EnsemblGRCh38hg38GRCh38
GRCh38.p13 EnsemblX47,445,178 - 47,483,222 (-)EnsemblGRCh38hg38GRCh38
GRCh38X47,444,691 - 47,485,934 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X47,304,577 - 47,342,621 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X47,191,347 - 47,227,289 (-)NCBINCBI36hg18NCBI36
Build 34X47,062,657 - 47,098,599NCBI
CeleraX51,500,825 - 51,537,610 (-)NCBI
Cytogenetic MapXp11.3NCBI
HuRefX45,018,484 - 45,055,126 (-)NCBIHuRef
CHM1_1X47,335,709 - 47,373,791 (-)NCBICHM1_1
Znf41
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_004955516611,591 - 646,109 (+)NCBIChiLan1.0ChiLan1.0
ZNF41
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1X47,777,784 - 47,820,046 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX47,777,784 - 47,818,791 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0X39,881,999 - 39,922,058 (-)NCBIMhudiblu_PPA_v0panPan3
ZNF41
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X41,031,507 - 41,072,759 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX41,032,742 - 41,071,949 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX15,406,568 - 15,447,850 (-)NCBI
ROS_Cfam_1.0X41,165,779 - 41,207,053 (-)NCBI
UMICH_Zoey_3.1X41,153,327 - 41,194,594 (-)NCBI
UNSW_CanFamBas_1.0X41,141,230 - 41,182,496 (-)NCBI
UU_Cfam_GSD_1.0X41,234,341 - 41,275,611 (-)NCBI
Znf41
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X33,335,385 - 33,386,149 (-)NCBI
SpeTri2.0NW_00493650213,176,781 - 13,226,872 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF41
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 EnsemblX41,934,977 - 41,984,711 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1X41,931,036 - 41,984,439 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
ZNF41
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X44,623,464 - 44,663,024 (-)NCBI
Znf41
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248874,276,293 - 4,292,722 (-)NCBI

Position Markers
DXS1004E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X47,307,895 - 47,307,968UniSTSGRCh37
GRCh37X47,307,912 - 47,308,074UniSTSGRCh37
GRCh37X47,307,879 - 47,307,988UniSTSGRCh37
Build 36X47,192,839 - 47,192,912RGDNCBI36
CeleraX51,503,143 - 51,503,252UniSTS
CeleraX51,503,159 - 51,503,232RGD
CeleraX51,503,176 - 51,503,338UniSTS
Cytogenetic MapXp11.23UniSTS
HuRefX45,020,818 - 45,020,891UniSTS
HuRefX45,020,835 - 45,020,997UniSTS
HuRefX45,020,802 - 45,020,911UniSTS
Stanford-G3 RH MapX1906.0UniSTS
NCBI RH MapX163.9UniSTS
GeneMap99-G3 RH MapX1112.0UniSTS
DXS7585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X47,307,896 - 47,307,968UniSTSGRCh37
Build 36X47,192,840 - 47,192,912RGDNCBI36
CeleraX51,503,160 - 51,503,232RGD
Cytogenetic MapXp11.23UniSTS
HuRefX45,020,819 - 45,020,891UniSTS
DXS1004E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXp11.23UniSTS
Stanford-G3 RH MapX1906.0UniSTS
NCBI RH MapX163.9UniSTS
GeneMap99-G3 RH MapX1112.0UniSTS
DXS1004E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXp11.23UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2007
Count of miRNA genes:712
Interacting mature miRNAs:807
Transcripts:ENST00000313116, ENST00000377065, ENST00000397050, ENST00000432977, ENST00000465311
Prediction methods:Miranda, Pita, Rnahybrid
Result types:miRGate_prediction

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

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


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 89 17 53 10 460 12 67 60 167 86 156 167 4 2 31
Low 2350 2761 1670 610 1289 450 4288 2128 3559 333 1302 1445 170 1 1202 2757 5 1
Below cutoff 210 3 3 201 3 1 9 8 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_008238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324155 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001324157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_007130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_153380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006724550 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006724555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ010017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ010018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ010019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ010020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ010021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ010022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ010023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294858 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL590223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL590283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ053634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471164 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA127531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA567652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA783869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M92443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X60155 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z84466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000313116   ⟹   ENSP00000315173
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX47,445,879 - 47,482,585 (-)Ensembl
RefSeq Acc Id: ENST00000377065   ⟹   ENSP00000366265
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX47,445,879 - 47,482,946 (-)Ensembl
RefSeq Acc Id: ENST00000432977   ⟹   ENSP00000390385
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX47,449,264 - 47,467,548 (-)Ensembl
RefSeq Acc Id: ENST00000465311
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX47,449,264 - 47,467,548 (-)Ensembl
RefSeq Acc Id: ENST00000684689   ⟹   ENSP00000508254
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX47,445,178 - 47,483,222 (-)Ensembl
RefSeq Acc Id: NM_001324139   ⟹   NP_001311068
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324140   ⟹   NP_001311069
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324141   ⟹   NP_001311070
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324142   ⟹   NP_001311071
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324143   ⟹   NP_001311072
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,482,604 (-)NCBI
CHM1_1X47,335,709 - 47,373,468 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324144   ⟹   NP_001311073
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324145   ⟹   NP_001311074
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324147   ⟹   NP_001311076
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324148   ⟹   NP_001311077
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324149   ⟹   NP_001311078
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324150   ⟹   NP_001311079
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324151   ⟹   NP_001311080
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324152   ⟹   NP_001311081
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324153   ⟹   NP_001311082
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,483,222 (-)NCBI
CHM1_1X47,335,709 - 47,373,791 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324154   ⟹   NP_001311083
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,467,670 (-)NCBI
CHM1_1X47,335,709 - 47,358,169 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324155   ⟹   NP_001311084
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,467,670 (-)NCBI
CHM1_1X47,335,709 - 47,358,169 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324156   ⟹   NP_001311085
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,467,669 (-)NCBI
CHM1_1X47,335,709 - 47,358,168 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001324157   ⟹   NP_001311086
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,467,670 (-)NCBI
CHM1_1X47,335,709 - 47,358,169 (-)NCBI
Sequence:
RefSeq Acc Id: NM_007130   ⟹   NP_009061
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,482,604 (-)NCBI
GRCh37X47,305,281 - 47,343,070 (-)NCBI
Build 36X47,191,347 - 47,226,928 (-)NCBI Archive
CeleraX51,500,825 - 51,537,610 (-)RGD
HuRefX45,018,484 - 45,055,126 (-)RGD
CHM1_1X47,335,709 - 47,373,468 (-)NCBI
Sequence:
RefSeq Acc Id: NM_153380   ⟹   NP_700359
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,445,178 - 47,482,946 (-)NCBI
GRCh37X47,305,281 - 47,343,070 (-)NCBI
Build 36X47,191,347 - 47,227,289 (-)NCBI Archive
CeleraX51,500,825 - 51,537,610 (-)RGD
HuRefX45,018,484 - 45,055,126 (-)RGD
CHM1_1X47,335,709 - 47,373,468 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006724550   ⟹   XP_006724613
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,483,206 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006724555   ⟹   XP_006724618
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,482,927 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029810   ⟹   XP_016885299
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,485,934 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029811   ⟹   XP_016885300
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,485,934 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029812   ⟹   XP_016885301
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,482,927 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029813   ⟹   XP_016885302
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,469,762 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029814   ⟹   XP_016885303
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,485,934 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029815   ⟹   XP_016885304
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,483,055 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029816   ⟹   XP_016885305
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,469,842 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029817   ⟹   XP_016885306
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,444,691 - 47,469,842 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001311068 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311069 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311070 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311071 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311072 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311073 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311074 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311076 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311077 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311078 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311079 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311080 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311081 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311082 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311083 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311084 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311085 (Get FASTA)   NCBI Sequence Viewer  
  NP_001311086 (Get FASTA)   NCBI Sequence Viewer  
  NP_009061 (Get FASTA)   NCBI Sequence Viewer  
  NP_700359 (Get FASTA)   NCBI Sequence Viewer  
  XP_006724613 (Get FASTA)   NCBI Sequence Viewer  
  XP_006724618 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885299 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885300 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885301 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885302 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885303 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885304 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885305 (Get FASTA)   NCBI Sequence Viewer  
  XP_016885306 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA61312 (Get FASTA)   NCBI Sequence Viewer  
  AAH15023 (Get FASTA)   NCBI Sequence Viewer  
  BAD92757 (Get FASTA)   NCBI Sequence Viewer  
  BAF82710 (Get FASTA)   NCBI Sequence Viewer  
  BAG57962 (Get FASTA)   NCBI Sequence Viewer  
  CAB51740 (Get FASTA)   NCBI Sequence Viewer  
  CAB53035 (Get FASTA)   NCBI Sequence Viewer  
  CAB53036 (Get FASTA)   NCBI Sequence Viewer  
  CAB53037 (Get FASTA)   NCBI Sequence Viewer  
  CAB53038 (Get FASTA)   NCBI Sequence Viewer  
  CAB53039 (Get FASTA)   NCBI Sequence Viewer  
  CAB53040 (Get FASTA)   NCBI Sequence Viewer  
  CAB53041 (Get FASTA)   NCBI Sequence Viewer  
  EAW59300 (Get FASTA)   NCBI Sequence Viewer  
  EAW59301 (Get FASTA)   NCBI Sequence Viewer  
  EAW59302 (Get FASTA)   NCBI Sequence Viewer  
  EAW59303 (Get FASTA)   NCBI Sequence Viewer  
  EAW59304 (Get FASTA)   NCBI Sequence Viewer  
  EAW59305 (Get FASTA)   NCBI Sequence Viewer  
  EAW59306 (Get FASTA)   NCBI Sequence Viewer  
  EAW59307 (Get FASTA)   NCBI Sequence Viewer  
  EAW59308 (Get FASTA)   NCBI Sequence Viewer  
  P51814 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_009061   ⟸   NM_007130
- Peptide Label: isoform a
- UniProtKB: P51814 (UniProtKB/Swiss-Prot),   A0A024R1C4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_700359   ⟸   NM_153380
- Peptide Label: isoform a
- UniProtKB: P51814 (UniProtKB/Swiss-Prot),   A0A024R1C4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006724613   ⟸   XM_006724550
- Peptide Label: isoform X1
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006724618   ⟸   XM_006724555
- Peptide Label: isoform X2
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311068   ⟸   NM_001324139
- Peptide Label: isoform b
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311076   ⟸   NM_001324147
- Peptide Label: isoform a
- UniProtKB: P51814 (UniProtKB/Swiss-Prot),   A0A024R1C4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001311070   ⟸   NM_001324141
- Peptide Label: isoform b
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311074   ⟸   NM_001324145
- Peptide Label: isoform b
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311078   ⟸   NM_001324149
- Peptide Label: isoform b
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311069   ⟸   NM_001324140
- Peptide Label: isoform a
- UniProtKB: P51814 (UniProtKB/Swiss-Prot),   A0A024R1C4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001311071   ⟸   NM_001324142
- Peptide Label: isoform c
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311082   ⟸   NM_001324153
- Peptide Label: isoform d
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311073   ⟸   NM_001324144
- Peptide Label: isoform a
- UniProtKB: P51814 (UniProtKB/Swiss-Prot),   A0A024R1C4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001311077   ⟸   NM_001324148
- Peptide Label: isoform c
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311080   ⟸   NM_001324151
- Peptide Label: isoform d
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311081   ⟸   NM_001324152
- Peptide Label: isoform b
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311079   ⟸   NM_001324150
- Peptide Label: isoform a
- UniProtKB: P51814 (UniProtKB/Swiss-Prot),   A0A024R1C4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001311072   ⟸   NM_001324143
- Peptide Label: isoform b
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311086   ⟸   NM_001324157
- Peptide Label: isoform h
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311083   ⟸   NM_001324154
- Peptide Label: isoform e
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311084   ⟸   NM_001324155
- Peptide Label: isoform f
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001311085   ⟸   NM_001324156
- Peptide Label: isoform g
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885303   ⟸   XM_017029814
- Peptide Label: isoform X1
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885300   ⟸   XM_017029811
- Peptide Label: isoform X1
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885299   ⟸   XM_017029810
- Peptide Label: isoform X1
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885304   ⟸   XM_017029815
- Peptide Label: isoform X1
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885301   ⟸   XM_017029812
- Peptide Label: isoform X1
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885306   ⟸   XM_017029817
- Peptide Label: isoform X3
- UniProtKB: P51814 (UniProtKB/Swiss-Prot),   A0A024R1C4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016885305   ⟸   XM_017029816
- Peptide Label: isoform X2
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885302   ⟸   XM_017029813
- Peptide Label: isoform X1
- UniProtKB: P51814 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000366265   ⟸   ENST00000377065
RefSeq Acc Id: ENSP00000315173   ⟸   ENST00000313116
RefSeq Acc Id: ENSP00000390385   ⟸   ENST00000432977
RefSeq Acc Id: ENSP00000508254   ⟸   ENST00000684689
Protein Domains
C2H2-type   KRAB

Promoters
RGD ID:6809429
Promoter ID:HG_KWN:66609
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000397050,   OTTHUMT00000056428,   OTTHUMT00000056429
Position:
Human AssemblyChrPosition (strand)Source
Build 36X47,226,951 - 47,227,672 (-)MPROMDB
RGD ID:13605164
Promoter ID:EPDNEW_H28766
Type:initiation region
Name:ZNF41_4
Description:zinc finger protein 41
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28767  EPDNEW_H28768  EPDNEW_H28769  EPDNEW_H28770  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,482,577 - 47,482,637EPDNEW
RGD ID:13605166
Promoter ID:EPDNEW_H28767
Type:initiation region
Name:ZNF41_3
Description:zinc finger protein 41
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28766  EPDNEW_H28768  EPDNEW_H28769  EPDNEW_H28770  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,482,890 - 47,482,950EPDNEW
RGD ID:13605168
Promoter ID:EPDNEW_H28768
Type:initiation region
Name:ZNF41_5
Description:zinc finger protein 41
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28766  EPDNEW_H28767  EPDNEW_H28769  EPDNEW_H28770  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,483,029 - 47,483,089EPDNEW
RGD ID:13605170
Promoter ID:EPDNEW_H28769
Type:initiation region
Name:ZNF41_1
Description:zinc finger protein 41
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28766  EPDNEW_H28767  EPDNEW_H28768  EPDNEW_H28770  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X47,483,209 - 47,483,269EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical 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:10679-156022206)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)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:10679-156013167)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 Xp22.33-11.22(chrX:10679-52809182)x1 copy number loss See cases [RCV000051026] ChrX:10679..52809182 [GRCh38]
ChrX:60679..52838206 [GRCh37]
ChrX:679..52854931 [NCBI36]
ChrX:Xp22.33-11.22
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 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 Xp11.4-11.23(chrX:41434043-47880733)x1 copy number loss See cases [RCV000053088] ChrX:41434043..47880733 [GRCh38]
ChrX:41293296..47619970 [GRCh37]
ChrX:41178240..47625076 [NCBI36]
ChrX:Xp11.4-11.23
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 Xp22.33-11.23(chrX:10679-48344725)x1 copy number loss See cases [RCV000052981] ChrX:10679..48344725 [GRCh38]
ChrX:60679..48204160 [GRCh37]
ChrX:679..48089104 [NCBI36]
ChrX:Xp22.33-11.23
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 Xp22.33-11.21(chrX:2769041-58055036)x1 copy number loss See cases [RCV000053007] ChrX:2769041..58055036 [GRCh38]
ChrX:2687082..58081470 [GRCh37]
ChrX:2697082..58098195 [NCBI36]
ChrX:Xp22.33-11.21
pathogenic
GRCh38/hg38 Xp22.33-11.21(chrX:26102-57302794)x1 copy number loss See cases [RCV000052990] ChrX:26102..57302794 [GRCh38]
ChrX:76102..57329227 [GRCh37]
ChrX:16102..57345952 [NCBI36]
ChrX:Xp22.33-11.21
pathogenic
GRCh38/hg38 Xp22.33-11.1(chrX:253129-58271563)x1 copy number loss See cases [RCV000052994] ChrX:253129..58271563 [GRCh38]
ChrX:169796..58297997 [GRCh37]
ChrX:109796..58314722 [NCBI36]
ChrX:Xp22.33-11.1
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
GRCh38/hg38 Xp22.33-11.21(chrX:10679-55550898)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052971]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052971]|See cases [RCV000052971] ChrX:10679..55550898 [GRCh38]
ChrX:60679..55577331 [GRCh37]
ChrX:679..55594056 [NCBI36]
ChrX:Xp22.33-11.21
pathogenic
GRCh38/hg38 Xp22.33-11.22(chrX:10479-54179172)x3 copy number gain See cases [RCV000053817] ChrX:10479..54179172 [GRCh38]
ChrX:60479..53957191 [GRCh37]
ChrX:479..54222330 [NCBI36]
ChrX:Xp22.33-11.22
pathogenic
NM_007130.3(ZNF41):c.1545A>G (p.Lys515=) single nucleotide variant not provided [RCV000082672] ChrX:47448225 [GRCh38]
ChrX:47307624 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_153380.3(ZNF41):c.945T>G (p.Asp315Glu) single nucleotide variant History of neurodevelopmental disorder [RCV000720970]|not specified [RCV000082673] ChrX:47448825 [GRCh38]
ChrX:47308224 [GRCh37]
ChrX:Xp11.3
benign|likely benign
NM_001324156.1(ZNF41):c.302-72C>T single nucleotide variant not provided [RCV000088660] ChrX:47449438 [GRCh38]
ChrX:47308837 [GRCh37]
ChrX:Xp11.3
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_007130.3(ZNF41):c.73-42A>C single nucleotide variant not provided [RCV000088661] ChrX:47456440 [GRCh38]
ChrX:47315839 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_153380.3(ZNF41):c.374T>G (p.Ile125Arg) single nucleotide variant History of neurodevelopmental disorder [RCV000720964]|not specified [RCV000118944] ChrX:47449396 [GRCh38]
ChrX:47308795 [GRCh37]
ChrX:Xp11.3
benign|likely benign
NM_153380.3(ZNF41):c.660T>G (p.Asn220Lys) single nucleotide variant History of neurodevelopmental disorder [RCV000721016]|not specified [RCV000118945] ChrX:47449110 [GRCh38]
ChrX:47308509 [GRCh37]
ChrX:Xp11.3
benign|likely benign
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 Xp22.33-11.22(chrX:10701-52857805)x1 copy number loss See cases [RCV000133817] ChrX:10701..52857805 [GRCh38]
ChrX:60701..52886834 [GRCh37]
ChrX:701..52903559 [NCBI36]
ChrX:Xp22.33-11.22
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: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: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 Xp22.33-11.23(chrX:10679-50059388)x1 copy number loss See cases [RCV000133745] ChrX:10679..50059388 [GRCh38]
ChrX:60679..49824045 [GRCh37]
ChrX:679..49710785 [NCBI36]
ChrX:Xp22.33-11.23
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 Xp22.33-q11.1(chrX:10701-62712219)x1 copy number loss See cases [RCV000134568] ChrX:10701..62712219 [GRCh38]
ChrX:60701..61931689 [GRCh37]
ChrX:701..61848414 [NCBI36]
ChrX:Xp22.33-q11.1
pathogenic
GRCh38/hg38 Xp22.33-11.21(chrX:10701-58055053)x1 copy number loss See cases [RCV000134026] ChrX:10701..58055053 [GRCh38]
ChrX:60701..58081487 [GRCh37]
ChrX:701..58098212 [NCBI36]
ChrX:Xp22.33-11.21
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 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 Xp11.3(chrX:47470813-47475828)x1 copy number loss See cases [RCV000133987] ChrX:47470813..47475828 [GRCh38]
ChrX:47330212..47335227 [GRCh37]
ChrX:47215156..47220171 [NCBI36]
ChrX:Xp11.3
likely benign
GRCh38/hg38 Xp11.3(chrX:47470813-47475828)x0 copy number loss See cases [RCV000133988] ChrX:47470813..47475828 [GRCh38]
ChrX:47330212..47335227 [GRCh37]
ChrX:47215156..47220171 [NCBI36]
ChrX:Xp11.3
uncertain significance
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 Xp22.31-11.22(chrX:8176030-53962833)x1 copy number loss See cases [RCV000135305] ChrX:8176030..53962833 [GRCh38]
ChrX:8144071..53989266 [GRCh37]
ChrX:8104071..54005991 [NCBI36]
ChrX:Xp22.31-11.22
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 Xp11.3(chrX:47470810-47475689)x1 copy number loss See cases [RCV000134818] ChrX:47470810..47475689 [GRCh38]
ChrX:47330209..47335088 [GRCh37]
ChrX:47215153..47220032 [NCBI36]
ChrX:Xp11.3
conflicting data from submitters
GRCh38/hg38 Xp11.3-11.22(chrX:43361870-50931794)x3 copy number gain See cases [RCV000134956] ChrX:43361870..50931794 [GRCh38]
ChrX:43221119..50674794 [GRCh37]
ChrX:43106063..50691534 [NCBI36]
ChrX:Xp11.3-11.22
pathogenic
GRCh38/hg38 Xp22.33-11.22(chrX:10679-52857805)x3 copy number gain See cases [RCV000134957] ChrX:10679..52857805 [GRCh38]
ChrX:60679..52886834 [GRCh37]
ChrX:679..52903559 [NCBI36]
ChrX:Xp22.33-11.22
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 Xp22.33-11.22(chrX:10679-52213731)x1 copy number loss See cases [RCV000137112] ChrX:10679..52213731 [GRCh38]
ChrX:60679..51948998 [GRCh37]
ChrX:679..51973598 [NCBI36]
ChrX:Xp22.33-11.22
pathogenic|uncertain significance
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 Xp22.33-11.22(chrX:10701-52033734)x1 copy number loss See cases [RCV000137430] ChrX:10701..52033734 [GRCh38]
ChrX:60701..51776830 [GRCh37]
ChrX:701..51793570 [NCBI36]
ChrX:Xp22.33-11.22
pathogenic
GRCh38/hg38 Xp22.33-11.21(chrX:10701-58055036)x1 copy number loss See cases [RCV000137552] ChrX:10701..58055036 [GRCh38]
ChrX:60701..58081470 [GRCh37]
ChrX:701..58098195 [NCBI36]
ChrX:Xp22.33-11.21
pathogenic
GRCh38/hg38 Xp22.33-11.23(chrX:10679-49157514)x1 copy number loss See cases [RCV000137166] ChrX:10679..49157514 [GRCh38]
ChrX:60679..49016667 [GRCh37]
ChrX:679..48903611 [NCBI36]
ChrX:Xp22.33-11.23
pathogenic
GRCh38/hg38 Xp22.33-11.23(chrX:10701-49071220)x1 copy number loss See cases [RCV000137413] ChrX:10701..49071220 [GRCh38]
ChrX:60701..48928877 [GRCh37]
ChrX:701..48815821 [NCBI36]
ChrX:Xp22.33-11.23
pathogenic
GRCh38/hg38 Xp11.3-11.23(chrX:44765664-49343053)x3 copy number gain See cases [RCV000137271] ChrX:44765664..49343053 [GRCh38]
ChrX:44624910..49218180 [GRCh37]
ChrX:44509854..49105124 [NCBI36]
ChrX:Xp11.3-11.23
likely pathogenic
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 Xp22.33-11.1(chrX:10701-58517661)x1 copy number loss See cases [RCV000139343] ChrX:10701..58517661 [GRCh38]
ChrX:60701..58544094 [GRCh37]
ChrX:701..58560819 [NCBI36]
ChrX:Xp22.33-11.1
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 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 Xp22.33-11.22(chrX:10701-53750424)x1 copy number loss See cases [RCV000140711] ChrX:10701..53750424 [GRCh38]
ChrX:60701..53776922 [GRCh37]
ChrX:701..53793647 [NCBI36]
ChrX:Xp22.33-11.22
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 Xp11.3(chrX:47458962-47567078)x2 copy number gain See cases [RCV000141919] ChrX:47458962..47567078 [GRCh38]
ChrX:47318361..47426477 [GRCh37]
ChrX:47203305..47311421 [NCBI36]
ChrX:Xp11.3
uncertain significance
GRCh38/hg38 Xp22.33-11.22(chrX:251879-50289363)x1 copy number loss See cases [RCV000141741] ChrX:251879..50289363 [GRCh38]
ChrX:168546..50032363 [GRCh37]
ChrX:108546..50049103 [NCBI36]
ChrX:Xp22.33-11.22
pathogenic
GRCh38/hg38 Xp11.3-11.22(chrX:46971389-54130971)x3 copy number gain See cases [RCV000141567] ChrX:46971389..54130971 [GRCh38]
ChrX:46818746..53957191 [GRCh37]
ChrX:46703690..54174129 [NCBI36]
ChrX:Xp11.3-11.22
pathogenic
GRCh38/hg38 Xp22.33-q12(chrX:251880-66445845)x1 copy number loss See cases [RCV000142334] ChrX:251880..66445845 [GRCh38]
ChrX:168547..65665687 [GRCh37]
ChrX:108547..65582412 [NCBI36]
ChrX:Xp22.33-q12
pathogenic
GRCh38/hg38 Xp22.33-11.22(chrX:251880-51643625)x1 copy number loss See cases [RCV000142035] ChrX:251880..51643625 [GRCh38]
ChrX:168547..51386559 [GRCh37]
ChrX:108547..51403299 [NCBI36]
ChrX:Xp22.33-11.22
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 Xp11.3-11.23(chrX:47437831-47845763)x2 copy number gain See cases [RCV000143111] ChrX:47437831..47845763 [GRCh38]
ChrX:47297230..47705162 [GRCh37]
ChrX:47182174..47590106 [NCBI36]
ChrX:Xp11.3-11.23
uncertain significance
GRCh38/hg38 Xp11.3-11.23(chrX:44632305-47607180)x2 copy number gain See cases [RCV000143089] ChrX:44632305..47607180 [GRCh38]
ChrX:44491551..47466579 [GRCh37]
ChrX:44376495..47351523 [NCBI36]
ChrX:Xp11.3-11.23
likely 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 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 Xp22.33-11.22(chrX:10701-53131191)x1 copy number loss See cases [RCV000143348] ChrX:10701..53131191 [GRCh38]
ChrX:60701..53047381 [GRCh37]
ChrX:701..53177098 [NCBI36]
ChrX:Xp22.33-11.22
pathogenic
GRCh38/hg38 Xp22.33-11.21(chrX:251879-56428859)x1 copy number loss See cases [RCV000143130] ChrX:251879..56428859 [GRCh38]
ChrX:168546..56455292 [GRCh37]
ChrX:108546..56472017 [NCBI36]
ChrX:Xp22.33-11.21
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 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_001324156.1(ZNF41):c.302-103G>A single nucleotide variant not provided [RCV000179023] ChrX:47449469 [GRCh38]
ChrX:47308868 [GRCh37]
ChrX:Xp11.3
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
NM_007130.3(ZNF41):c.677A>T (p.His226Leu) single nucleotide variant Abnormality of neuronal migration [RCV000201376] ChrX:47449093 [GRCh38]
ChrX:47308492 [GRCh37]
ChrX:Xp11.3
benign
GRCh37/hg19 Xp22.33-11.21(chrX:70297-58066465)x3 copy number gain See cases [RCV000239834] ChrX:70297..58066465 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
GRCh37/hg19 Xp22.33-11.21(chrX:70297-58066465)x1 copy number loss See cases [RCV000239814] ChrX:70297..58066465 [GRCh37]
ChrX:Xp22.33-11.21
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
GRCh37/hg19 Xp11.3-11.23(chrX:43507300-48929622) copy number gain not provided [RCV000767648] ChrX:43507300..48929622 [GRCh37]
ChrX:Xp11.3-11.23
pathogenic
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 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 Xp22.33-q28(chrX:2707626-155250222)x2 copy number gain See cases [RCV000240541] ChrX:2707626..155250222 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
NM_007130.3(ZNF41):c.*49T>C single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000285961] ChrX:47447381 [GRCh38]
ChrX:47306780 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.746A>C (p.Glu249Ala) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000269166] ChrX:47449024 [GRCh38]
ChrX:47308423 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.73-7G>A single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000293548] ChrX:47456405 [GRCh38]
ChrX:47315804 [GRCh37]
ChrX:Xp11.3
likely benign
NM_153380.3(ZNF41):c.786G>A (p.Gln262=) single nucleotide variant History of neurodevelopmental disorder [RCV000721074] ChrX:47448984 [GRCh38]
ChrX:47308383 [GRCh37]
ChrX:Xp11.3
benign|likely benign
NM_007130.3(ZNF41):c.1398G>A (p.Pro466=) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000391717] ChrX:47448372 [GRCh38]
ChrX:47307771 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.-224G>A single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000306307] ChrX:47467705 [GRCh38]
ChrX:47327104 [GRCh37]
ChrX:Xp11.3
likely benign
NM_153380.3(ZNF41):c.901T>C (p.Cys301Arg) single nucleotide variant History of neurodevelopmental disorder [RCV000721010] ChrX:47448869 [GRCh38]
ChrX:47308268 [GRCh37]
ChrX:Xp11.3
benign
NM_007130.3(ZNF41):c.*469C>T single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000272945] ChrX:47446961 [GRCh38]
ChrX:47306360 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.-514C>T single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000358570] ChrX:47482693 [GRCh38]
ChrX:47342092 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.*1033A>G single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000274033] ChrX:47446397 [GRCh38]
ChrX:47305796 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.-231A>G single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000363361] ChrX:47467712 [GRCh38]
ChrX:47327111 [GRCh37]
ChrX:Xp11.3
benign
NM_007130.3(ZNF41):c.1323C>T (p.Cys441=) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000314900] ChrX:47448447 [GRCh38]
ChrX:47307846 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.1275A>T (p.Ala425=) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000367191] ChrX:47448495 [GRCh38]
ChrX:47307894 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.-547C>G single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000319036] ChrX:47482726 [GRCh38]
ChrX:47342125 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.348C>T (p.Phe116=) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000373302] ChrX:47449422 [GRCh38]
ChrX:47308821 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_153380.3(ZNF41):c.387A>G (p.Ser129=) single nucleotide variant History of neurodevelopmental disorder [RCV000721014] ChrX:47449383 [GRCh38]
ChrX:47308782 [GRCh37]
ChrX:Xp11.3
benign
NM_007130.3(ZNF41):c.627T>C (p.Ser209=) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000322145] ChrX:47449143 [GRCh38]
ChrX:47308542 [GRCh37]
ChrX:Xp11.3
likely benign
NM_153380.3(ZNF41):c.590A>G (p.Lys197Arg) single nucleotide variant History of neurodevelopmental disorder [RCV000721054]|not specified [RCV000593276] ChrX:47449180 [GRCh38]
ChrX:47308579 [GRCh37]
ChrX:Xp11.3
benign|likely benign
NM_007130.3(ZNF41):c.2116C>T (p.Leu706Phe) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000284079] ChrX:47447654 [GRCh38]
ChrX:47307053 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.*416A>T single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000325624] ChrX:47447014 [GRCh38]
ChrX:47306413 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.2309G>C (p.Ser770Thr) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000376399] ChrX:47447461 [GRCh38]
ChrX:47306860 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.281A>G (p.His94Arg) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000352555] ChrX:47455935 [GRCh38]
ChrX:47315334 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.743A>G (p.Tyr248Cys) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000326565] ChrX:47449027 [GRCh38]
ChrX:47308426 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.*407A>G single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000382697] ChrX:47447023 [GRCh38]
ChrX:47306422 [GRCh37]
ChrX:Xp11.3
benign
NM_007130.3(ZNF41):c.664A>G (p.Asn222Asp) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000378805] ChrX:47449106 [GRCh38]
ChrX:47308505 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.*982A>C single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000331354] ChrX:47446448 [GRCh38]
ChrX:47305847 [GRCh37]
ChrX:Xp11.3
likely benign
NM_153380.3(ZNF41):c.1578T>A (p.Ala526=) single nucleotide variant History of neurodevelopmental disorder [RCV000720982] ChrX:47448192 [GRCh38]
ChrX:47307591 [GRCh37]
ChrX:Xp11.3
benign|likely benign
NM_153380.3(ZNF41):c.2114G>A (p.Arg705His) single nucleotide variant History of neurodevelopmental disorder [RCV000721077] ChrX:47447656 [GRCh38]
ChrX:47307055 [GRCh37]
ChrX:Xp11.3
likely benign|uncertain significance
NM_153380.3(ZNF41):c.1997C>T (p.Ala666Val) single nucleotide variant History of neurodevelopmental disorder [RCV000720986] ChrX:47447773 [GRCh38]
ChrX:47307172 [GRCh37]
ChrX:Xp11.3
benign|likely benign
NM_007130.3(ZNF41):c.160G>C (p.Asp54His) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000393141] ChrX:47456311 [GRCh38]
ChrX:47315710 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.-42G>A single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000393146] ChrX:47467523 [GRCh38]
ChrX:47326922 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.*957A>G single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000383612] ChrX:47446473 [GRCh38]
ChrX:47305872 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.1700A>G (p.Lys567Arg) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000296952] ChrX:47448070 [GRCh38]
ChrX:47307469 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.2310T>C (p.Ser770=) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000342720] ChrX:47447460 [GRCh38]
ChrX:47306859 [GRCh37]
ChrX:Xp11.3
likely benign
NM_007130.3(ZNF41):c.65C>T (p.Ser22Leu) single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000346077] ChrX:47467417 [GRCh38]
ChrX:47326816 [GRCh37]
ChrX:Xp11.3
benign
NM_007130.3(ZNF41):c.-433_-428GCACGC[3] microsatellite Non-syndromic X-linked intellectual disability [RCV000403527] ChrX:47482600..47482601 [GRCh38]
ChrX:47341999..47342000 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_007130.3(ZNF41):c.-530G>T single nucleotide variant Non-syndromic X-linked intellectual disability [RCV000266202] ChrX:47482709 [GRCh38]
ChrX:47342108 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_153380.3(ZNF41):c.-295_-294insGCGCGCACGC insertion Non-syndromic X-linked intellectual disability [RCV000305148] ChrX:47482600..47482601 [GRCh38]
ChrX:47341999..47342000 [GRCh37]
ChrX:Xp11.3
uncertain significance
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 Xp22.33-11.23(chrX:60814-48317386)x1 copy number loss not provided [RCV000753273] ChrX:60814..48317386 [GRCh37]
ChrX:Xp22.33-11.23
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 Xp22.33-11.21(chrX:168546-55529093)x1 copy number loss See cases [RCV000446584] ChrX:168546..55529093 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
GRCh37/hg19 Xp22.33-11.21(chrX:168546-56684082)x1 copy number loss See cases [RCV000447092] ChrX:168546..56684082 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
GRCh37/hg19 Xp22.33-11.22(chrX:168546-52573789)x1 copy number loss See cases [RCV000447470] ChrX:168546..52573789 [GRCh37]
ChrX:Xp22.33-11.22
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:71267-155255792)x1 copy number loss See cases [RCV000446197] ChrX:71267..155255792 [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 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
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 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss See cases [RCV000448393] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-11.1(chrX:168546-58140271)x1 copy number loss See cases [RCV000447773] ChrX:168546..58140271 [GRCh37]
ChrX:Xp22.33-11.1
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 Xp22.33-11.21(chrX:168546-55240087)x1 copy number loss See cases [RCV000512136] ChrX:168546..55240087 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
GRCh37/hg19 Xp22.33-11.1(chrX:168546-58527164)x1 copy number loss See cases [RCV000510437] ChrX:168546..58527164 [GRCh37]
ChrX:Xp22.33-11.1
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 Xp22.33-11.21(chrX:168546-57504183)x1 copy number loss See cases [RCV000511615] ChrX:168546..57504183 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
GRCh37/hg19 Xp22.33-11.21(chrX:168546-57683964)x1 copy number loss See cases [RCV000512022] ChrX:168546..57683964 [GRCh37]
ChrX:Xp22.33-11.21
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 Xp11.3-11.23(chrX:46326268-48801984)x2 copy number gain See cases [RCV000511234] ChrX:46326268..48801984 [GRCh37]
ChrX:Xp11.3-11.23
likely pathogenic
GRCh37/hg19 Xp22.33-11.21(chrX:168546-54996659)x1 copy number loss See cases [RCV000510822] ChrX:168546..54996659 [GRCh37]
ChrX:Xp22.33-11.21
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 Xp22.33-11.21(chrX:168564-57413442)x1 copy number loss See cases [RCV000512339] ChrX:168564..57413442 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
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
GRCh37/hg19 Xp11.23(chrX:46647617-47413846)x2 copy number gain not provided [RCV000684329] ChrX:46647617..47413846 [GRCh37]
ChrX:Xp11.23
uncertain significance
GRCh37/hg19 Xp22.33-11.21(chrX:60814-55476165)x1 copy number loss not provided [RCV000753275] ChrX:60814..55476165 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
NM_153380.3(ZNF41):c.2215A>T (p.Ile739Leu) single nucleotide variant History of neurodevelopmental disorder [RCV000720960] ChrX:47447555 [GRCh38]
ChrX:47306954 [GRCh37]
ChrX:Xp11.3
uncertain significance
NM_153380.3(ZNF41):c.1694G>A (p.Arg565His) single nucleotide variant History of neurodevelopmental disorder [RCV000721034] ChrX:47448076 [GRCh38]
ChrX:47307475 [GRCh37]
ChrX:Xp11.3
likely benign
NC_000023.10:g.36649710_136649711del100000002insG indel Heterotaxy, visceral, 1, X-linked [RCV000754886] ChrX:36649710..136649711 [GRCh37]
ChrX:Xp21.1-q26.3
pathogenic
GRCh37/hg19 Xp22.33-11.22(chrX:60814-51821765)x1 copy number loss not provided [RCV000753274] ChrX:60814..51821765 [GRCh37]
ChrX:Xp22.33-11.22
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
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 Xp22.33-11.21(chrX:539722-55509385)x1 copy number loss not provided [RCV001007224] ChrX:539722..55509385 [GRCh37]
ChrX:Xp22.33-11.21
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
GRCh37/hg19 Xp22.33-11.22(chrX:60814-50519984)x1 copy number loss See cases [RCV000790583] ChrX:60814..50519984 [GRCh37]
ChrX:Xp22.33-11.22
pathogenic
GRCh37/hg19 Xp22.33-q11.1(chrX:168546-61877279)x1 copy number loss not provided [RCV000846273] ChrX:168546..61877279 [GRCh37]
ChrX:Xp22.33-q11.1
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 Xp11.23(chrX:47191508-47362805)x3 copy number gain not provided [RCV000846257] ChrX:47191508..47362805 [GRCh37]
ChrX:Xp11.23
uncertain significance
GRCh37/hg19 Xp11.23(chrX:46942052-47379255)x3 copy number gain not provided [RCV001258952] ChrX:46942052..47379255 [GRCh37]
ChrX:Xp11.23
uncertain significance
GRCh37/hg19 Xp22.33-11.21(chrX:219609-55466476)x1 copy number loss See cases [RCV001263061] ChrX:219609..55466476 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
GRCh37/hg19 Xp22.33-11.21(chrX:168546-56457794)x1 copy number loss not provided [RCV001281358] ChrX:168546..56457794 [GRCh37]
ChrX:Xp22.33-11.21
pathogenic
NC_000023.10:g.(?_46696536)_(47436910_?)dup duplication Epilepsy, X-linked, with variable learning disabilities and behavior disorders [RCV001309817] ChrX:46696536..47436910 [GRCh37]
ChrX:Xp11.23
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13107 AgrOrtholog
COSMIC ZNF41 COSMIC
Ensembl Genes ENSG00000147124 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000315173 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000366265 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000390385 UniProtKB/TrEMBL
Ensembl Transcript ENST00000313116 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000377065 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000432977 UniProtKB/TrEMBL
GTEx ENSG00000147124 GTEx
HGNC ID HGNC:13107 ENTREZGENE
Human Proteome Map ZNF41 Human Proteome Map
InterPro KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KRAB_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:7592 UniProtKB/Swiss-Prot
NCBI Gene 7592 ENTREZGENE
OMIM 300848 OMIM
  314995 OMIM
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37682 PharmGKB
PROSITE KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF109640 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R1C4 ENTREZGENE, UniProtKB/TrEMBL
  B1AQ29_HUMAN UniProtKB/TrEMBL
  P51814 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A8K1V6 UniProtKB/Swiss-Prot
  B4DH01 UniProtKB/Swiss-Prot
  Q96LE8 UniProtKB/Swiss-Prot
  Q9UMC4 UniProtKB/Swiss-Prot
  Q9UMV5 UniProtKB/Swiss-Prot
  Q9UMV6 UniProtKB/Swiss-Prot
  Q9UMV7 UniProtKB/Swiss-Prot
  Q9UMV8 UniProtKB/Swiss-Prot
  Q9UMV9 UniProtKB/Swiss-Prot
  Q9UMW0 UniProtKB/Swiss-Prot
  Q9UMW1 UniProtKB/Swiss-Prot