ZMAT2 (zinc finger matrin-type 2) - Rat Genome Database

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Gene: ZMAT2 (zinc finger matrin-type 2) Homo sapiens
Analyze
Symbol: ZMAT2
Name: zinc finger matrin-type 2
RGD ID: 1353598
HGNC Page HGNC:26433
Description: Predicted to enable DNA binding activity and zinc ion binding activity. Involved in mRNA splicing, via spliceosome. Located in nucleus. Part of U2-type precatalytic spliceosome.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ31121; hSNU23; Ptg-12; Snu23; zinc finger matrin-type protein 2; zinc finger, matrin type 2; zinc finger, matrin-type 2
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
GRCh385140,700,447 - 140,706,686 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5140,698,680 - 140,706,686 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,080,032 - 140,086,271 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,060,216 - 140,066,423 (+)NCBINCBI36Build 36hg18NCBI36
Build 345140,060,215 - 140,066,423NCBI
Celera5136,156,780 - 136,162,987 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,225,283 - 135,231,489 (+)NCBIHuRef
CHM1_15139,513,287 - 139,519,494 (+)NCBICHM1_1
T2T-CHM13v2.05141,225,840 - 141,232,080 (+)NCBIT2T-CHM13v2.0
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

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:8889549   PMID:14702039   PMID:15342556   PMID:15489334   PMID:15635413   PMID:17207965   PMID:20195357   PMID:21145461   PMID:21873635   PMID:21988832   PMID:22379092   PMID:23275563  
PMID:25281560   PMID:25416956   PMID:26344197   PMID:26638075   PMID:27634302   PMID:28514442   PMID:28781166   PMID:29117863   PMID:29298432   PMID:29395067   PMID:29568061   PMID:29778605  
PMID:30380419   PMID:30415952   PMID:30862715   PMID:30890647   PMID:31515488   PMID:31980649   PMID:32005145   PMID:32296183   PMID:32538781   PMID:32814053   PMID:33916271   PMID:33961781  
PMID:34079125   PMID:34597346   PMID:34780483   PMID:35013218   PMID:35271311   PMID:35439318   PMID:35831314   PMID:35944360   PMID:36232890   PMID:36273042   PMID:36373674   PMID:38113892  


Genomics

Comparative Map Data
ZMAT2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385140,700,447 - 140,706,686 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5140,698,680 - 140,706,686 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,080,032 - 140,086,271 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,060,216 - 140,066,423 (+)NCBINCBI36Build 36hg18NCBI36
Build 345140,060,215 - 140,066,423NCBI
Celera5136,156,780 - 136,162,987 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,225,283 - 135,231,489 (+)NCBIHuRef
CHM1_15139,513,287 - 139,519,494 (+)NCBICHM1_1
T2T-CHM13v2.05141,225,840 - 141,232,080 (+)NCBIT2T-CHM13v2.0
Zmat2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391836,926,976 - 36,932,713 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1836,926,929 - 36,932,719 (+)EnsemblGRCm39 Ensembl
GRCm381836,793,923 - 36,799,660 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1836,793,876 - 36,799,666 (+)EnsemblGRCm38mm10GRCm38
MGSCv371836,953,577 - 36,959,314 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361836,919,897 - 36,925,634 (+)NCBIMGSCv36mm8
Celera1837,245,957 - 37,251,695 (+)NCBICelera
Cytogenetic Map18B2NCBI
cM Map1819.46NCBI
Zmat2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81828,683,617 - 28,688,252 (+)NCBIGRCr8
mRatBN7.21828,409,606 - 28,414,241 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1828,398,795 - 28,414,747 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1828,536,739 - 28,541,374 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01829,298,815 - 29,303,450 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01828,634,043 - 28,638,678 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01829,639,991 - 29,644,626 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1829,639,872 - 29,644,652 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01829,343,457 - 29,348,092 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41829,493,269 - 29,497,904 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1828,130,152 - 28,134,786 (+)NCBICelera
Cytogenetic Map18p11NCBI
Zmat2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554181,633 - 10,844 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554184,335 - 10,844 (-)NCBIChiLan1.0ChiLan1.0
ZMAT2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24135,958,207 - 135,964,505 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15134,097,839 - 134,104,056 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05136,065,016 - 136,071,333 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15142,180,981 - 142,187,294 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5142,180,981 - 142,187,292 (+)Ensemblpanpan1.1panPan2
ZMAT2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1235,851,972 - 35,860,818 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl235,852,109 - 35,858,065 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha232,891,058 - 32,899,813 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0236,307,705 - 36,316,471 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl236,307,742 - 36,316,471 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1233,359,792 - 33,368,549 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0234,227,918 - 34,236,665 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0234,980,511 - 34,989,269 (+)NCBIUU_Cfam_GSD_1.0
Zmat2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213151,971,143 - 151,978,212 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365319,630,958 - 9,641,948 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365319,633,460 - 9,640,366 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZMAT2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl2142,411,089 - 142,419,137 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.12142,410,970 - 142,417,012 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.22148,355,582 - 148,361,604 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZMAT2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12343,333,078 - 43,340,082 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2343,333,164 - 43,339,163 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603434,516,814 - 34,523,942 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Zmat2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474333,444,432 - 33,451,490 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZMAT2
1 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 copy number gain See cases [RCV000051193] Chr5:130860928..155321811 [GRCh38]
Chr5:130196621..154701371 [GRCh37]
Chr5:130224520..154681564 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-32(chr5:138871137-145812309)x1 copy number loss See cases [RCV000052142] Chr5:138871137..145812309 [GRCh38]
Chr5:138206826..145191872 [GRCh37]
Chr5:138234725..145172065 [NCBI36]
Chr5:5q31.2-32
pathogenic
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 copy number loss See cases [RCV000053524] Chr5:106619588..156124387 [GRCh38]
Chr5:105955289..155551397 [GRCh37]
Chr5:105983188..155483975 [NCBI36]
Chr5:5q21.3-33.2
pathogenic
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 copy number gain See cases [RCV000138808] Chr5:129847794..153353546 [GRCh38]
Chr5:129183487..152733106 [GRCh37]
Chr5:129211386..152713299 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-31.3(chr5:138942857-144605017)x3 copy number gain See cases [RCV000142806] Chr5:138942857..144605017 [GRCh38]
Chr5:138278546..143984580 [GRCh37]
Chr5:138306445..143964773 [NCBI36]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3
likely benign
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3
pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NC_000005.9:g.(?_86400000)_(154000000_?)del deletion Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] Chr5:86400000..154000000 [GRCh37]
Chr5:5q14.3-33.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5q31.2-31.3(chr5:139147238-141540491)x1 copy number loss not provided [RCV000682600] Chr5:139147238..141540491 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32
uncertain significance
NC_000005.9:g.(?_136633338)_(140998481_?)dup duplication PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] Chr5:136633338..140998481 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q31.2-31.3(chr5:139493717-140517454)x1 copy number loss PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001801202] Chr5:139493717..140517454 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) copy number gain not specified [RCV002053526] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
NM_144723.3(ZMAT2):c.271G>A (p.Asp91Asn) single nucleotide variant Inborn genetic diseases [RCV003282316] Chr5:140703952 [GRCh38]
Chr5:140083537 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q31.3(chr5:140082762-140773954)x3 copy number gain not provided [RCV002474614] Chr5:140082762..140773954 [GRCh37]
Chr5:5q31.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:729
Count of miRNA genes:395
Interacting mature miRNAs:429
Transcripts:ENST00000274712, ENST00000506644, ENST00000519913
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
D5S2381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,078,636 - 140,078,731UniSTSGRCh37
Build 365140,058,820 - 140,058,915RGDNCBI36
Celera5136,155,384 - 136,155,479RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,223,887 - 135,223,982UniSTS
TNG Radiation Hybrid Map564277.0UniSTS
Stanford-G3 RH Map55256.0UniSTS
Whitehead-YAC Contig Map5 UniSTS
GeneMap99-G3 RH Map55344.0UniSTS
D5S2600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,086,033 - 140,086,126UniSTSGRCh37
Build 365140,066,217 - 140,066,310RGDNCBI36
Celera5136,162,781 - 136,162,874RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,231,283 - 135,231,376UniSTS
GeneMap99-G3 RH Map55344.0UniSTS
G20504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,078,624 - 140,078,761UniSTSGRCh37
Build 365140,058,808 - 140,058,945RGDNCBI36
Celera5136,155,372 - 136,155,509RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,223,875 - 135,224,012UniSTS
A005U15  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,078,624 - 140,078,761UniSTSGRCh37
Build 365140,058,808 - 140,058,945RGDNCBI36
Celera5136,155,372 - 136,155,509RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,223,875 - 135,224,012UniSTS
GeneMap99-GB4 RH Map5529.31UniSTS
NCBI RH Map5889.1UniSTS
RH12406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,085,966 - 140,086,223UniSTSGRCh37
Build 365140,066,150 - 140,066,407RGDNCBI36
Celera5136,162,714 - 136,162,971RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,231,216 - 135,231,473UniSTS
GeneMap99-GB4 RH Map5529.31UniSTS
NCBI RH Map5889.1UniSTS


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 adipose tissue appendage entire extraembryonic component
High 5
Medium 2432 2923 1721 620 1947 462 4355 2135 3706 417 1443 1608 171 1204 2788 4
Low 61 2 2 1 2 58 2 1
Below cutoff

Sequence


RefSeq Acc Id: ENST00000274712   ⟹   ENSP00000274712
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,700,447 - 140,706,686 (+)Ensembl
RefSeq Acc Id: ENST00000506644   ⟹   ENSP00000473644
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,700,464 - 140,705,881 (+)Ensembl
RefSeq Acc Id: ENST00000519913   ⟹   ENSP00000473397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,698,680 - 140,704,502 (+)Ensembl
RefSeq Acc Id: NM_144723   ⟹   NP_653324
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,700,447 - 140,706,686 (+)NCBI
GRCh375140,078,265 - 140,086,248 (+)NCBI
Build 365140,060,216 - 140,066,423 (+)NCBI Archive
Celera5136,156,780 - 136,162,987 (+)RGD
HuRef5135,225,283 - 135,231,489 (+)ENTREZGENE
CHM1_15139,513,200 - 139,519,521 (+)NCBI
T2T-CHM13v2.05141,225,840 - 141,232,080 (+)NCBI
Sequence:
RefSeq Acc Id: NP_653324   ⟸   NM_144723
- UniProtKB: Q96NC0 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000473397   ⟸   ENST00000519913
RefSeq Acc Id: ENSP00000473644   ⟸   ENST00000506644
RefSeq Acc Id: ENSP00000274712   ⟸   ENST00000274712
Protein Domains
U1-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96NC0-F1-model_v2 AlphaFold Q96NC0 1-199 view protein structure

Promoters
RGD ID:6803717
Promoter ID:HG_KWN:51297
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000251674
Position:
Human AssemblyChrPosition (strand)Source
Build 365140,059,984 - 140,060,484 (+)MPROMDB
RGD ID:6870852
Promoter ID:EPDNEW_H8591
Type:initiation region
Name:ZMAT2_2
Description:zinc finger matrin-type 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8592  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,691,614 - 140,691,674EPDNEW
RGD ID:6870854
Promoter ID:EPDNEW_H8592
Type:multiple initiation site
Name:ZMAT2_1
Description:zinc finger matrin-type 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8591  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,700,448 - 140,700,508EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26433 AgrOrtholog
COSMIC ZMAT2 COSMIC
Ensembl Genes ENSG00000146007 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000274712 ENTREZGENE
  ENST00000274712.8 UniProtKB/Swiss-Prot
  ENST00000506644.3 UniProtKB/TrEMBL
  ENST00000519913.6 UniProtKB/TrEMBL
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000146007 GTEx
HGNC ID HGNC:26433 ENTREZGENE
Human Proteome Map ZMAT2 Human Proteome Map
InterPro Matrin/U1-like-C_Znf_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Snu23 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_jaz UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/TrEMBL
KEGG Report hsa:153527 UniProtKB/Swiss-Prot
NCBI Gene 153527 ENTREZGENE
OMIM 619930 OMIM
PANTHER PTHR45986 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC FINGER MATRIN-TYPE PROTEIN 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam zf-C2H2_jaz UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-met UniProtKB/TrEMBL
PharmGKB PA134931664 PharmGKB
SMART ZnF_U1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt Q96NC0 ENTREZGENE
  R4GMX9_HUMAN UniProtKB/TrEMBL
  R4GNG8_HUMAN UniProtKB/TrEMBL
  ZMAT2_HUMAN UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-16 ZMAT2  zinc finger matrin-type 2    zinc finger, matrin-type 2  Symbol and/or name change 5135510 APPROVED
2011-07-27 ZMAT2  zinc finger, matrin-type 2  ZMAT2  zinc finger, matrin type 2  Symbol and/or name change 5135510 APPROVED