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Cellular Component
Molecular Function
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![]() Biological Process Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | regulation of transcription, DNA-templated | | NAS | | 2290271 | (PMID:7633419) | UniProtKB | PMID:7633419 | regulation of transcription, DNA-templated | | IEA | InterPro:IPR001909, InterPro:IPR036051 | 2290271 | | InterPro | GO_REF:0000002 | |
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1. | GOA_HUMAN data from the GO Consortium |
2. | RGD automated import pipeline for gene-chemical interactions |
PubMed | 7633419 9169157 9847074 12477932 12690205 12853948 15489334 18255255 20211142 23455924 25315684 25416956 27107014 28514442 |
ZNF212 (Homo sapiens - human) |
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Zfp212 (Mus musculus - house mouse) |
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Zfp212 (Rattus norvegicus - Norway rat) |
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Znf212 (Chinchilla lanigera - long-tailed chinchilla) |
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ZNF212 (Pan paniscus - bonobo/pygmy chimpanzee) |
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ZNF212 (Canis lupus familiaris - dog) |
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Znf212 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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ZNF212 (Sus scrofa - pig) |
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GDB:4585595 |
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D7S2048E |
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ZNF212_8773 |
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SGC31646 |
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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. |
RefSeq Transcripts | NM_012256 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
GenBank Nucleotide | AACC02000041 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC004890 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AI242662 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK074821 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK315086 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC022785 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471146 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KT584591 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U38864 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_012256 ⟹ NP_036388 | |||||||||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | |||||||||||||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
AGAATGCACCTGGCATCAACACGGCGGCGGCGGCGGCGGCTTCCAACAGGCTCTGGGGCGCCGAhide sequence |
Protein RefSeqs | NP_036388 | (Get FASTA) | NCBI Sequence Viewer |
GenBank Protein | AAC51296 | (Get FASTA) | NCBI Sequence Viewer |
AAD45826 | (Get FASTA) | NCBI Sequence Viewer | |
AAH22785 | (Get FASTA) | NCBI Sequence Viewer | |
BAG37551 | (Get FASTA) | NCBI Sequence Viewer | |
BAG52008 | (Get FASTA) | NCBI Sequence Viewer | |
EAL24431 | (Get FASTA) | NCBI Sequence Viewer | |
EAW80053 | (Get FASTA) | NCBI Sequence Viewer | |
EAW80054 | (Get FASTA) | NCBI Sequence Viewer | |
Q9UDV6 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_036388 ⟸ NM_012256 |
- UniProtKB: | Q9UDV6 (UniProtKB/Swiss-Prot), A0A090N8N3 (UniProtKB/TrEMBL), B3KQE6 (UniProtKB/TrEMBL) |
- Sequence: |
MAESAPARHRRKRRSTPLTSSTLPSQATEKSSYFQTTEISLWTVVAAIQAVEKKMESQAARLQShide sequence |
RGD ID: | 6806433 | |||||||||
Promoter ID: | HG_KWN:60209 | |||||||||
Type: | CpG-Island | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | MPROMDB | |||||||||
Tissues & Cell Lines: | CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, K562, Lymphoblastoid, NB4 | |||||||||
Transcripts: | ENST00000335870 | |||||||||
Position: |
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RGD ID: | 7212239 | |||||||||
Promoter ID: | EPDNEW_H11863 | |||||||||
Type: | multiple initiation site | |||||||||
Name: | ZNF212_1 | |||||||||
Description: | zinc finger protein 212 | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing. | |||||||||
Position: |
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Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 7q35-36.1(chr7:147345844-150426340)x1 | copy number loss | Abnormality of the nervous system [RCV000050838]|See cases [RCV000050838] | Chr7:147345844..150426340 [GRCh38] Chr7:147042936..150123428 [GRCh37] Chr7:146673869..149754361 [NCBI36] Chr7:7q35-36.1 |
pathogenic |
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 | copy number gain | Cleft palate, isolated [RCV000050876]|See cases [RCV000050876] | Chr7:129310166..159282390 [GRCh38] Chr7:128950007..159075079 [GRCh37] Chr7:128737243..158767840 [NCBI36] Chr7:7q32.1-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.1(chr7:143884559-152674271)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050750]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050750]|See cases [RCV000050750] | Chr7:143884559..152674271 [GRCh38] Chr7:143581652..152371356 [GRCh37] Chr7:143212585..152002289 [NCBI36] Chr7:7q35-36.1 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|See cases [RCV000051101] | Chr7:132850196..159325876 [GRCh38] Chr7:132534956..159118566 [GRCh37] Chr7:132185496..158811327 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.3(chr7:147250465-159325876)x1 | copy number loss | Abnormality of the kidney [RCV000051108]|See cases [RCV000051108] | Chr7:147250465..159325876 [GRCh38] Chr7:146947557..159118566 [GRCh37] Chr7:146578490..158811327 [NCBI36] Chr7:7q35-36.3 |
pathogenic |
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 | copy number loss | Ambiguous genitalia [RCV000052250]|See cases [RCV000052250] | Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 | copy number gain | Global developmental delay [RCV000053576]|See cases [RCV000053576] | Chr7:136309982..159307523 [GRCh38] Chr7:135994730..159100212 [GRCh37] Chr7:135645270..158792973 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:142021716-159325876)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|See cases [RCV000053577] | Chr7:142021716..159325876 [GRCh38] Chr7:142528609..159118566 [GRCh37] Chr7:141367985..158811327 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.3(chr7:143884559-159282390)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054178]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054178]|See cases [RCV000054178] | Chr7:143884559..159282390 [GRCh38] Chr7:143581652..159075079 [GRCh37] Chr7:143212585..158767840 [NCBI36] Chr7:7q35-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.3(chr7:145699944-159296617)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054188]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054188]|See cases [RCV000054188] | Chr7:145699944..159296617 [GRCh38] Chr7:145397037..159089306 [GRCh37] Chr7:145027970..158782067 [NCBI36] Chr7:7q35-36.3 |
pathogenic |
GRCh38/hg38 7q36.1(chr7:148256584-152332535)x1 | copy number loss | Attention deficit-hyperactivity disorder [RCV000054189]|See cases [RCV000054189] | Chr7:148256584..152332535 [GRCh38] Chr7:147953676..152029620 [GRCh37] Chr7:147584609..151660553 [NCBI36] Chr7:7q36.1 |
pathogenic |
GRCh38/hg38 7q32.3-36.1(chr7:132023155-149309794)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|See cases [RCV000054172] | Chr7:132023155..149309794 [GRCh38] Chr7:131707914..149006885 [GRCh37] Chr7:131358454..148637818 [NCBI36] Chr7:7q32.3-36.1 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:139365967-159282531)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|See cases [RCV000054175] | Chr7:139365967..159282531 [GRCh38] Chr7:139050713..159075220 [GRCh37] Chr7:138701253..158767981 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:140754198-159307523)x1 | copy number loss | Corpus callosum agenesis [RCV000054176]|See cases [RCV000054176] | Chr7:140754198..159307523 [GRCh38] Chr7:140453998..159100212 [GRCh37] Chr7:140100467..158792973 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:142358524-159282531)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054177]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054177]|See cases [RCV000054177] | Chr7:142358524..159282531 [GRCh38] Chr7:142528609..159075220 [GRCh37] Chr7:141726947..158767981 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 | copy number loss | See cases [RCV000135401] | Chr7:54185..159282390 [GRCh38] Chr7:54185..159075079 [GRCh37] Chr7:149268..158767840 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh38/hg38 7q35-36.2(chr7:147345844-153833351)x3 | copy number gain | See cases [RCV000135825] | Chr7:147345844..153833351 [GRCh38] Chr7:147042936..153530436 [GRCh37] Chr7:146673869..153161369 [NCBI36] Chr7:7q35-36.2 |
pathogenic |
GRCh38/hg38 7q33-36.2(chr7:137751200-154815582)x3 | copy number gain | See cases [RCV000136592] | Chr7:137751200..154815582 [GRCh38] Chr7:137435946..154607292 [GRCh37] Chr7:137086486..154238225 [NCBI36] Chr7:7q33-36.2 |
pathogenic |
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 | copy number gain | See cases [RCV000136717] | Chr7:97419852..158923762 [GRCh38] Chr7:97049164..158716453 [GRCh37] Chr7:96887100..158409214 [NCBI36] Chr7:7q21.3-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:141960861-159335866)x1 | copy number loss | See cases [RCV000137256] | Chr7:141960861..159335866 [GRCh38] Chr7:142528609..159128556 [GRCh37] Chr7:141307130..158821317 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.3(chr7:145436544-159331441)x1 | copy number loss | See cases [RCV000137338] | Chr7:145436544..159331441 [GRCh38] Chr7:145133637..159124131 [GRCh37] Chr7:144764570..158816892 [NCBI36] Chr7:7q35-36.3 |
pathogenic|likely pathogenic |
GRCh38/hg38 7q35-36.3(chr7:145250254-159335866)x1 | copy number loss | See cases [RCV000138005] | Chr7:145250254..159335866 [GRCh38] Chr7:144947347..159128556 [GRCh37] Chr7:144578280..158821317 [NCBI36] Chr7:7q35-36.3 |
pathogenic |
GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 | copy number loss | See cases [RCV000138120] | Chr7:134666829..158591882 [GRCh38] Chr7:134351581..158384574 [GRCh37] Chr7:134002121..158077335 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.3(chr7:146047157-157522158)x1 | copy number loss | See cases [RCV000137781] | Chr7:146047157..157522158 [GRCh38] Chr7:145744250..157314852 [GRCh37] Chr7:145375183..157007613 [NCBI36] Chr7:7q35-36.3 |
pathogenic |
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 | copy number gain | See cases [RCV000138847] | Chr7:121863759..159335865 [GRCh38] Chr7:121503813..159128555 [GRCh37] Chr7:121291049..158821316 [NCBI36] Chr7:7q31.32-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.1(chr7:143596735-150089125)x4 | copy number gain | See cases [RCV000138555] | Chr7:143596735..150089125 [GRCh38] Chr7:143293828..149786214 [GRCh37] Chr7:143003950..149417147 [NCBI36] Chr7:7q35-36.1 |
likely pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 | copy number gain | See cases [RCV000139654] | Chr7:132444095..159335866 [GRCh38] Chr7:132128854..159128556 [GRCh37] Chr7:131779394..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 | copy number gain | See cases [RCV000141413] | Chr7:115459015..159325817 [GRCh38] Chr7:115099069..159118507 [GRCh37] Chr7:114886305..158811268 [NCBI36] Chr7:7q31.2-36.3 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 | copy number gain | See cases [RCV000142802] | Chr7:131228764..159335866 [GRCh38] Chr7:130913523..159128556 [GRCh37] Chr7:130564063..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 | copy number gain | See cases [RCV000143754] | Chr7:131171478..159327017 [GRCh38] Chr7:130856237..159119707 [GRCh37] Chr7:130506777..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 | copy number gain | See cases [RCV000143707] | Chr7:132438072..159327017 [GRCh38] Chr7:132122831..159119707 [GRCh37] Chr7:131773371..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.3(chr7:147144002-159327017)x1 | copy number loss | See cases [RCV000143503] | Chr7:147144002..159327017 [GRCh38] Chr7:146841094..159119707 [GRCh37] Chr7:146472027..158812468 [NCBI36] Chr7:7q35-36.3 |
pathogenic |
GRCh37/hg19 7q33-36.3(chr7:137589621-159119707)x3 | copy number gain | See cases [RCV000449264] | Chr7:137589621..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 | copy number loss | See cases [RCV000446044] | Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
Single allele | copy number loss | Abnormality of esophagus morphology [RCV000416719]|Abnormality of the esophagus [RCV000416719] | Chr7:143839360..159138663 [GRCh37] | pathogenic |
GRCh37/hg19 7q33-36.3(chr7:133799185-159119707)x1 | copy number loss | See cases [RCV000448836] | Chr7:133799185..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 | copy number gain | See cases [RCV000447709] | Chr7:98969247..159119707 [GRCh37] Chr7:7q22.1-36.3 |
pathogenic |
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 | copy number gain | See cases [RCV000447956] | Chr7:128276078..159119707 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:140636858-159119707)x1 | copy number loss | See cases [RCV000510250] | Chr7:140636858..159119707 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) | copy number gain | See cases [RCV000510686] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q33-36.3(chr7:136758593-159119707)x3 | copy number gain | See cases [RCV000510490] | Chr7:136758593..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 | copy number gain | See cases [RCV000511549] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q36.1(chr7:148189771-150867270)x4 | copy number gain | See cases [RCV000511618] | Chr7:148189771..150867270 [GRCh37] Chr7:7q36.1 |
uncertain significance |
GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1 | copy number loss | See cases [RCV000511889] | Chr7:137917376..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:140133025-158982771)x1 | copy number loss | not provided [RCV000682910] | Chr7:140133025..158982771 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 | copy number gain | not provided [RCV000682911] | Chr7:98693388..159119707 [GRCh37] Chr7:7q22.1-36.3 |
pathogenic |
GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3 | copy number gain | not provided [RCV000849569] | Chr7:130592554..159119707 [GRCh37] Chr7:7q32.3-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 | copy number gain | not provided [RCV000746280] | Chr7:44935..159126310 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 | copy number gain | not provided [RCV000746278] | Chr7:10704..159122532 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:139623170-158329903)x3 | copy number gain | not provided [RCV000747070] | Chr7:139623170..158329903 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:141938235-159126310)x1 | copy number loss | not provided [RCV000747083] | Chr7:141938235..159126310 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q35-36.1(chr7:143711059-152573935)x3 | copy number gain | not provided [RCV000747094] | Chr7:143711059..152573935 [GRCh37] Chr7:7q35-36.1 |
benign |
GRCh37/hg19 7q36.1-36.3(chr7:148238976-159126310)x1 | copy number loss | not provided [RCV000747115] | Chr7:148238976..159126310 [GRCh37] Chr7:7q36.1-36.3 |
pathogenic |
GRCh37/hg19 7q36.1(chr7:148693072-148976137)x1 | copy number loss | not provided [RCV000747124] | Chr7:148693072..148976137 [GRCh37] Chr7:7q36.1 |
benign |
GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220) | copy number gain | not provided [RCV000767558] | Chr7:128312450..159119220 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
Single allele | duplication | not provided [RCV000844986] | Chr7:147897705..149874566 [GRCh37] Chr7:7q35-36.1 |
not provided |
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 | copy number gain | not provided [RCV000848126] | Chr7:10365..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:13004 | AgrOrtholog |
COSMIC | ZNF212 | COSMIC |
Ensembl Genes | ENSG00000170260 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSP00000338572 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSP00000418167 | UniProtKB/TrEMBL | |
ENSP00000418281 | UniProtKB/TrEMBL | |
ENSP00000419261 | UniProtKB/TrEMBL | |
ENSP00000419419 | UniProtKB/TrEMBL | |
Ensembl Transcript | ENST00000335870 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENST00000462724 | UniProtKB/TrEMBL | |
ENST00000481584 | UniProtKB/TrEMBL | |
ENST00000486371 | UniProtKB/TrEMBL | |
ENST00000488917 | UniProtKB/TrEMBL | |
GTEx | ENSG00000170260 | GTEx |
HGNC ID | HGNC:13004 | ENTREZGENE |
Human Proteome Map | ZNF212 | Human Proteome Map |
InterPro | DUF3669_Znf | UniProtKB/Swiss-Prot |
KRAB | UniProtKB/Swiss-Prot | |
KRAB_dom_sf | UniProtKB/Swiss-Prot | |
Znf_C2H2_sf | UniProtKB/Swiss-Prot | |
Znf_C2H2_type | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:7988 | UniProtKB/Swiss-Prot |
NCBI Gene | 7988 | ENTREZGENE |
OMIM | 602386 | OMIM |
Pfam | DUF3669 | UniProtKB/Swiss-Prot |
KRAB | UniProtKB/Swiss-Prot | |
zf-C2H2 | UniProtKB/Swiss-Prot | |
PharmGKB | PA37583 | PharmGKB |
PROSITE | KRAB | UniProtKB/Swiss-Prot |
ZINC_FINGER_C2H2_1 | UniProtKB/Swiss-Prot | |
ZINC_FINGER_C2H2_2 | UniProtKB/Swiss-Prot | |
SMART | KRAB | UniProtKB/Swiss-Prot |
ZnF_C2H2 | UniProtKB/Swiss-Prot | |
Superfamily-SCOP | SSF109640 | UniProtKB/Swiss-Prot |
SSF57667 | UniProtKB/Swiss-Prot | |
UniGene | Hs.490510 | ENTREZGENE |
UniProt | A0A090N8N3 | ENTREZGENE, UniProtKB/TrEMBL |
B3KQE6 | ENTREZGENE, UniProtKB/TrEMBL | |
F2Z3G9_HUMAN | UniProtKB/TrEMBL | |
H7C589_HUMAN | UniProtKB/TrEMBL | |
H7C5A9_HUMAN | UniProtKB/TrEMBL | |
Q9UDV6 | ENTREZGENE, UniProtKB/Swiss-Prot | |
UniProt Secondary | B2RCF4 | UniProtKB/Swiss-Prot |
Q13396 | UniProtKB/Swiss-Prot | |
Q8N664 | UniProtKB/Swiss-Prot |
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More on ZNF212 | |
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Alliance Gene |
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NCBI Gene |
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Ensembl Gene |
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JBrowse: hg19 hg38 |
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HGNC Report |
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NCBI Genome Data Viewer |
CRRD Object Information | |
CRRD ID: | 1317263 |
Created: | 2005-01-12 |
Species: | Homo sapiens |
Last Modified: | 2019-11-26 |
Status: | ACTIVE |
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.