ZNF775 (zinc finger protein 775) - Rat Genome Database

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Gene: ZNF775 (zinc finger protein 775) Homo sapiens
Analyze
Symbol: ZNF775
Name: zinc finger protein 775
RGD ID: 1603510
HGNC Page HGNC:28501
Description: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and metal ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. Predicted to be part of PcG protein complex and transcription regulator complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: MGC33584
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
GRCh387150,379,330 - 150,398,630 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7150,368,790 - 150,398,630 (+)EnsemblGRCh38hg38GRCh38
GRCh377150,076,419 - 150,095,718 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367149,707,339 - 149,726,652 (+)NCBINCBI36Build 36hg18NCBI36
Celera7144,633,503 - 144,652,813 (+)NCBICelera
Cytogenetic Map7q36.1NCBI
HuRef7143,892,736 - 143,911,608 (+)NCBIHuRef
CHM1_17150,083,232 - 150,104,110 (+)NCBICHM1_1
T2T-CHM13v2.07151,557,672 - 151,576,951 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27149,414,255 - 149,433,562 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
nucleus  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:15489334   PMID:17081983   PMID:21873635   PMID:21900206   PMID:28514442   PMID:29676528   PMID:30021884   PMID:31391242   PMID:32296183   PMID:33961781   PMID:34673265  
PMID:36949045  


Genomics

Comparative Map Data
ZNF775
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387150,379,330 - 150,398,630 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7150,368,790 - 150,398,630 (+)EnsemblGRCh38hg38GRCh38
GRCh377150,076,419 - 150,095,718 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367149,707,339 - 149,726,652 (+)NCBINCBI36Build 36hg18NCBI36
Celera7144,633,503 - 144,652,813 (+)NCBICelera
Cytogenetic Map7q36.1NCBI
HuRef7143,892,736 - 143,911,608 (+)NCBIHuRef
CHM1_17150,083,232 - 150,104,110 (+)NCBICHM1_1
T2T-CHM13v2.07151,557,672 - 151,576,951 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27149,414,255 - 149,433,562 (+)NCBI
Zfp775
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39648,578,937 - 48,598,482 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl648,578,997 - 48,600,161 (+)EnsemblGRCm39 Ensembl
GRCm38648,602,007 - 48,621,548 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl648,602,063 - 48,623,227 (+)EnsemblGRCm38mm10GRCm38
MGSCv37648,563,179 - 48,573,226 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36648,542,766 - 48,552,813 (+)NCBIMGSCv36mm8
Celera649,124,133 - 49,134,233 (+)NCBICelera
Cytogenetic Map6B2.3NCBI
cM Map623.59NCBI
Zfp775
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8478,887,940 - 78,906,196 (+)NCBIGRCr8
mRatBN7.2477,557,037 - 77,575,296 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl477,548,847 - 77,575,296 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx482,764,568 - 82,782,764 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0478,540,067 - 78,558,275 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0476,980,348 - 76,998,550 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0478,240,326 - 78,258,545 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl478,240,385 - 78,258,545 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04142,904,020 - 142,922,229 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4476,694,083 - 76,723,391 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1476,978,247 - 76,986,903 (+)NCBI
Celera472,494,616 - 72,512,608 (+)NCBICelera
Cytogenetic Map4q24NCBI
Znf775
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554914,980,700 - 4,996,919 (+)NCBIChiLan1.0ChiLan1.0
ZNF775
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26186,826,559 - 186,845,952 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1738,836,743 - 38,856,216 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v07141,995,210 - 142,014,682 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
ZNF775
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11614,694,305 - 14,711,773 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1615,293,488 - 15,321,167 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01616,399,731 - 16,426,867 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1616,425,233 - 16,426,822 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11614,779,800 - 14,807,455 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01615,370,214 - 15,387,791 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01615,411,246 - 15,439,136 (+)NCBIUU_Cfam_GSD_1.0
Znf775
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244051186,902,275 - 6,921,618 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049365275,982,281 - 6,001,154 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF775
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11855,932,337 - 55,954,153 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
ZNF775
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.121118,522,634 - 118,542,687 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366607214,482,875 - 14,502,366 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Znf775
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248006,094,068 - 6,115,215 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZNF775
35 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q35-36.1(chr7:147345844-150426340)x1 copy number loss 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 See cases [RCV000050876] Chr7:129310166..159282390 [GRCh38]
Chr7:128950007..159075079 [GRCh37]
Chr7:128737243..158767840 [NCBI36]
Chr7:7q32.1-36.3		 pathogenic
GRCh38/hg38 7q36.1(chr7:150319864-152674271)x1 copy number loss See cases [RCV000050552] Chr7:150319864..152674271 [GRCh38]
Chr7:150016953..152371356 [GRCh37]
Chr7:149647886..152002289 [NCBI36]
Chr7:7q36.1		 pathogenic
GRCh38/hg38 7q35-36.1(chr7:143884559-152674271)x1 copy number loss 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 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 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 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 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 7q34-36.3(chr7:142358524-159282531)x1 copy number loss See cases [RCV000054177] Chr7:142358524..159282531 [GRCh38]
Chr7:142528609..159075220 [GRCh37]
Chr7:141726947..158767981 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:143884559-159282390)x1 copy number loss 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 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 See cases [RCV000054189] Chr7:148256584..152332535 [GRCh38]
Chr7:147953676..152029620 [GRCh37]
Chr7:147584609..151660553 [NCBI36]
Chr7:7q36.1		 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 See cases [RCV000054176] Chr7:140754198..159307523 [GRCh38]
Chr7:140453998..159100212 [GRCh37]
Chr7:140100467..158792973 [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 7q36.1-36.2(chr7:150113232-154162779)x3 copy number gain See cases [RCV000138566] Chr7:150113232..154162779 [GRCh38]
Chr7:149810321..153859864 [GRCh37]
Chr7:149441254..153490797 [NCBI36]
Chr7:7q36.1-36.2		 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 7q36.1-36.2(chr7:150275734-153342804)x3 copy number gain See cases [RCV000139660] Chr7:150275734..153342804 [GRCh38]
Chr7:149972823..153039889 [GRCh37]
Chr7:149603756..152670822 [NCBI36]
Chr7:7q36.1-36.2		 uncertain significance
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 7q36.1-36.3(chr7:150260297-159325876)x1 copy number loss See cases [RCV000142592] Chr7:150260297..159325876 [GRCh38]
Chr7:149957386..159118566 [GRCh37]
Chr7:149588319..158811327 [NCBI36]
Chr7:7q36.1-36.3		 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 7q32.1-36.3(chr7:128312450-159119220) copy number gain not provided [RCV000767558] Chr7:128312450..159119220 [GRCh37]
Chr7:7q32.1-36.3		 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
GRCh37/hg19 7q35-36.3(chr7:143839360-159138663) copy number loss Abnormal esophagus morphology [RCV000416719] Chr7:143839360..159138663 [GRCh37]
Chr7:7q35-36.3		 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 7q36.1-36.3(chr7:149261179-159075020)x3 copy number gain See cases [RCV000447776] Chr7:149261179..159075020 [GRCh37]
Chr7:7q36.1-36.3		 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
NM_173680.4(ZNF775):c.394G>C (p.Glu132Gln) single nucleotide variant Inborn genetic diseases [RCV003279192] Chr7:150396875 [GRCh38]
Chr7:150093963 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.632G>A (p.Arg211His) single nucleotide variant Inborn genetic diseases [RCV003308565] Chr7:150397113 [GRCh38]
Chr7:150094201 [GRCh37]
Chr7:7q36.1		 uncertain significance
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(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 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 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
NM_173680.4(ZNF775):c.724G>T (p.Gly242Trp) single nucleotide variant Inborn genetic diseases [RCV003267919] Chr7:150397205 [GRCh38]
Chr7:150094293 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q32.3-36.3(chr7:131414604-159126310)x1 copy number loss See cases [RCV001007432] Chr7:131414604..159126310 [GRCh37]
Chr7:7q32.3-36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:149964361-150163624)x3 copy number gain not provided [RCV000849576] Chr7:149964361..150163624 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1(chr7:149968222-152539376)x3 copy number gain not provided [RCV000847582] Chr7:149968222..152539376 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q35-36.3(chr7:145962558-159119707)x1 copy number loss not provided [RCV001006022] Chr7:145962558..159119707 [GRCh37]
Chr7:7q35-36.3		 pathogenic
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
NC_000007.13:g.(?_150066801)_(150759750_?)del deletion Long QT syndrome [RCV001031491] Chr7:150066801..150759750 [GRCh37]
Chr7:7q36.1		 pathogenic
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:143107740-156886246)x3 copy number gain not provided [RCV001249383] Chr7:143107740..156886246 [GRCh37]
Chr7:7q35-36.3		 not provided
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:148695373-159119707)x1 copy number loss not provided [RCV001832910] Chr7:148695373..159119707 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:148153261-157543640)x3 copy number gain not provided [RCV001827941] Chr7:148153261..157543640 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:133851002-159119707)x3 copy number gain not provided [RCV001834520] Chr7:133851002..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
NC_000007.13:g.(?_130781014)_(150301047_?)del deletion not provided [RCV003116360] Chr7:130781014..150301047 [GRCh37]
Chr7:7q32.3-36.1		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:138620939-159233475)x3 copy number gain Neurodevelopmental disorder [RCV003327610] Chr7:138620939..159233475 [GRCh38]
Chr7:7q34-36.3		 likely pathogenic
GRCh37/hg19 7q35-36.3(chr7:146927174-159128556)x3 copy number gain not provided [RCV002279740] Chr7:146927174..159128556 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:149062717-159124131)x1 copy number loss not provided [RCV002279756] Chr7:149062717..159124131 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
NM_173680.4(ZNF775):c.321T>G (p.Phe107Leu) single nucleotide variant Inborn genetic diseases [RCV003297592] Chr7:150396802 [GRCh38]
Chr7:150093890 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1(chr7:150018908-150591382)x1 copy number loss not provided [RCV002474835] Chr7:150018908..150591382 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1(chr7:149332630-151498689)x1 copy number loss not provided [RCV002472413] Chr7:149332630..151498689 [GRCh37]
Chr7:7q36.1		 pathogenic
NM_173680.4(ZNF775):c.218G>A (p.Arg73Lys) single nucleotide variant Inborn genetic diseases [RCV002860582] Chr7:150396699 [GRCh38]
Chr7:150093787 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.160C>T (p.Arg54Cys) single nucleotide variant Inborn genetic diseases [RCV002973589] Chr7:150396641 [GRCh38]
Chr7:150093729 [GRCh37]
Chr7:7q36.1		 likely benign
NM_173680.4(ZNF775):c.1280A>G (p.Asp427Gly) single nucleotide variant Inborn genetic diseases [RCV002883753] Chr7:150397761 [GRCh38]
Chr7:150094849 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1138G>A (p.Ala380Thr) single nucleotide variant Inborn genetic diseases [RCV002884114] Chr7:150397619 [GRCh38]
Chr7:150094707 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1195G>A (p.Glu399Lys) single nucleotide variant Inborn genetic diseases [RCV002973102] Chr7:150397676 [GRCh38]
Chr7:150094764 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1283C>T (p.Thr428Met) single nucleotide variant Inborn genetic diseases [RCV002973900] Chr7:150397764 [GRCh38]
Chr7:150094852 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1100C>G (p.Pro367Arg) single nucleotide variant Inborn genetic diseases [RCV002951239] Chr7:150397581 [GRCh38]
Chr7:150094669 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.854A>C (p.Glu285Ala) single nucleotide variant Inborn genetic diseases [RCV002980680] Chr7:150397335 [GRCh38]
Chr7:150094423 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.557C>G (p.Ser186Cys) single nucleotide variant Inborn genetic diseases [RCV002891455] Chr7:150397038 [GRCh38]
Chr7:150094126 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.826G>T (p.Gly276Cys) single nucleotide variant Inborn genetic diseases [RCV002696680] Chr7:150397307 [GRCh38]
Chr7:150094395 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.557C>A (p.Ser186Tyr) single nucleotide variant Inborn genetic diseases [RCV002712496] Chr7:150397038 [GRCh38]
Chr7:150094126 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.639C>A (p.His213Gln) single nucleotide variant Inborn genetic diseases [RCV002896085] Chr7:150397120 [GRCh38]
Chr7:150094208 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1209G>C (p.Gln403His) single nucleotide variant Inborn genetic diseases [RCV002832520] Chr7:150397690 [GRCh38]
Chr7:150094778 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.818A>C (p.Glu273Ala) single nucleotide variant Inborn genetic diseases [RCV002769265] Chr7:150397299 [GRCh38]
Chr7:150094387 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1301A>G (p.Gln434Arg) single nucleotide variant Inborn genetic diseases [RCV002831485] Chr7:150397782 [GRCh38]
Chr7:150094870 [GRCh37]
Chr7:7q36.1		 likely benign
NM_173680.4(ZNF775):c.1298G>A (p.Gly433Glu) single nucleotide variant Inborn genetic diseases [RCV002965999] Chr7:150397779 [GRCh38]
Chr7:150094867 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1165G>A (p.Ala389Thr) single nucleotide variant Inborn genetic diseases [RCV002965801] Chr7:150397646 [GRCh38]
Chr7:150094734 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1328C>A (p.Pro443Gln) single nucleotide variant Inborn genetic diseases [RCV002831995] Chr7:150397809 [GRCh38]
Chr7:150094897 [GRCh37]
Chr7:7q36.1		 likely benign
NM_173680.4(ZNF775):c.743C>T (p.Pro248Leu) single nucleotide variant Inborn genetic diseases [RCV002677429] Chr7:150397224 [GRCh38]
Chr7:150094312 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.697G>C (p.Ala233Pro) single nucleotide variant Inborn genetic diseases [RCV002679472] Chr7:150397178 [GRCh38]
Chr7:150094266 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh38/hg38 7q33-36.3(chr7:137463392-159345973)x3 copy number gain Neurodevelopmental disorder [RCV003327609] Chr7:137463392..159345973 [GRCh38]
Chr7:7q33-36.3		 pathogenic
NM_173680.4(ZNF775):c.1580C>T (p.Ala527Val) single nucleotide variant Inborn genetic diseases [RCV003206021] Chr7:150398061 [GRCh38]
Chr7:150095149 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.739C>T (p.Arg247Cys) single nucleotide variant Inborn genetic diseases [RCV003218323] Chr7:150397220 [GRCh38]
Chr7:150094308 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.182G>A (p.Arg61Gln) single nucleotide variant Inborn genetic diseases [RCV003208967] Chr7:150396663 [GRCh38]
Chr7:150093751 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.74G>C (p.Arg25Pro) single nucleotide variant Inborn genetic diseases [RCV003181378] Chr7:150396555 [GRCh38]
Chr7:150093643 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1535G>C (p.Ser512Thr) single nucleotide variant Inborn genetic diseases [RCV003193644] Chr7:150398016 [GRCh38]
Chr7:150095104 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1339A>C (p.Ile447Leu) single nucleotide variant Inborn genetic diseases [RCV003263349] Chr7:150397820 [GRCh38]
Chr7:150094908 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1 copy number loss not provided [RCV003334300] Chr7:140154317..152551638 [GRCh37]
Chr7:7q34-36.1		 pathogenic
NM_173680.4(ZNF775):c.430T>A (p.Phe144Ile) single nucleotide variant Inborn genetic diseases [RCV003359592] Chr7:150396911 [GRCh38]
Chr7:150093999 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.1586C>A (p.Ala529Glu) single nucleotide variant Inborn genetic diseases [RCV003369027] Chr7:150398067 [GRCh38]
Chr7:150095155 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q35-36.3(chr7:144940098-159119707)x1 copy number loss not provided [RCV003482991] Chr7:144940098..159119707 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:142099013-159119707)x1 copy number loss not provided [RCV003482989] Chr7:142099013..159119707 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:135639005-159119707)x1 copy number loss not provided [RCV003482988] Chr7:135639005..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:148538593-150967829)x1 copy number loss not provided [RCV003482992] Chr7:148538593..150967829 [GRCh37]
Chr7:7q36.1		 pathogenic
GRCh37/hg19 7q36.1(chr7:148896264-150963866)x1 copy number loss not specified [RCV003986691] Chr7:148896264..150963866 [GRCh37]
Chr7:7q36.1		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:137456457-159119707)x3 copy number gain not specified [RCV003986713] Chr7:137456457..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
NM_173680.4(ZNF775):c.1580C>A (p.Ala527Asp) single nucleotide variant Inborn genetic diseases [RCV003359794] Chr7:150398061 [GRCh38]
Chr7:150095149 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_173680.4(ZNF775):c.454C>T (p.Arg152Cys) single nucleotide variant Inborn genetic diseases [RCV003379498] Chr7:150396935 [GRCh38]
Chr7:150094023 [GRCh37]
Chr7:7q36.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2829
Count of miRNA genes:901
Interacting mature miRNAs:1107
Transcripts:ENST00000329630, ENST00000464630, ENST00000474836, ENST00000476489, ENST00000478789, ENST00000480389, ENST00000481877, ENST00000483664, ENST00000486297, ENST00000490973, ENST00000491664, ENST00000498682
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
RH11671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377150,109,273 - 150,109,477UniSTSGRCh37
Build 367149,740,206 - 149,740,410RGDNCBI36
Celera7144,666,366 - 144,666,570RGD
Cytogenetic Map7q36.1UniSTS
HuRef7143,925,160 - 143,925,364UniSTS
CRA_TCAGchr7v27149,447,115 - 149,447,320UniSTS
GeneMap99-GB4 RH Map7675.52UniSTS
RH47964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377150,082,596 - 150,082,759UniSTSGRCh37
GRCh377150,082,555 - 150,082,759UniSTSGRCh37
Build 367149,713,488 - 149,713,692RGDNCBI36
Celera7144,639,694 - 144,639,857UniSTS
Celera7144,639,653 - 144,639,857RGD
Cytogenetic Map7q36.1UniSTS
HuRef7143,898,950 - 143,899,154UniSTS
HuRef7143,898,991 - 143,899,154UniSTS
CRA_TCAGchr7v27149,420,445 - 149,420,608UniSTS
CRA_TCAGchr7v27149,420,404 - 149,420,608UniSTS
GeneMap99-GB4 RH Map7698.98UniSTS
SHGC-57996  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7q36.1UniSTS
HuRef7143,923,596 - 143,923,775UniSTS
TNG Radiation Hybrid Map768085.0UniSTS


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 1160 36 222 28 511 29 772 571 1166 82 778 128 2 563
Low 1278 2929 1480 571 1425 412 3583 1613 2568 336 682 1485 174 1 1201 2225 5 1
Below cutoff 1 26 24 25 14 24 1 12 1 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_173680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054357930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054357931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054357932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054357933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054357934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC005586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC073111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW402889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC038111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB472309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510991 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000329630   ⟹   ENSP00000330838
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,379,330 - 150,398,630 (+)Ensembl
RefSeq Acc Id: ENST00000478789   ⟹   ENSP00000419336
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,368,790 - 150,396,915 (+)Ensembl
RefSeq Acc Id: ENST00000490973   ⟹   ENSP00000417483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,382,696 - 150,396,979 (+)Ensembl
RefSeq Acc Id: NM_173680   ⟹   NP_775951
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,379,330 - 150,398,630 (+)NCBI
GRCh377150,076,406 - 150,095,719 (+)RGD
Build 367149,707,339 - 149,726,652 (+)NCBI Archive
Celera7144,633,503 - 144,652,813 (+)RGD
HuRef7143,892,736 - 143,911,608 (+)ENTREZGENE
CHM1_17150,083,232 - 150,104,110 (+)NCBI
T2T-CHM13v2.07151,557,672 - 151,576,951 (+)NCBI
CRA_TCAGchr7v27149,414,255 - 149,433,562 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: XM_047420220   ⟹   XP_047276176
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,379,330 - 150,398,630 (+)NCBI
RefSeq Acc Id: XM_047420221   ⟹   XP_047276177
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,379,330 - 150,398,630 (+)NCBI
RefSeq Acc Id: XM_047420222   ⟹   XP_047276178
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,379,330 - 150,398,630 (+)NCBI
RefSeq Acc Id: XM_047420223   ⟹   XP_047276179
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,379,330 - 150,398,630 (+)NCBI
RefSeq Acc Id: XM_047420224   ⟹   XP_047276180
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,379,330 - 150,398,630 (+)NCBI
RefSeq Acc Id: XM_047420225   ⟹   XP_047276181
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,388,426 - 150,398,630 (+)NCBI
RefSeq Acc Id: XM_054357930   ⟹   XP_054213905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07151,557,672 - 151,576,951 (+)NCBI
RefSeq Acc Id: XM_054357931   ⟹   XP_054213906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07151,560,321 - 151,576,951 (+)NCBI
RefSeq Acc Id: XM_054357932   ⟹   XP_054213907
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07151,560,321 - 151,576,951 (+)NCBI
RefSeq Acc Id: XM_054357933   ⟹   XP_054213908
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07151,560,333 - 151,576,951 (+)NCBI
RefSeq Acc Id: XM_054357934   ⟹   XP_054213909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07151,566,769 - 151,576,951 (+)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_775951   ⟸   NM_173680
- UniProtKB: Q8IY24 (UniProtKB/Swiss-Prot),   Q96BV0 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000419336   ⟸   ENST00000478789
RefSeq Acc Id: ENSP00000417483   ⟸   ENST00000490973
RefSeq Acc Id: ENSP00000330838   ⟸   ENST00000329630
RefSeq Acc Id: XP_047276177   ⟸   XM_047420221
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047276180   ⟸   XM_047420224
- Peptide Label: isoform X2
- UniProtKB: Q96BV0 (UniProtKB/Swiss-Prot),   Q8IY24 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047276178   ⟸   XM_047420222
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047276179   ⟸   XM_047420223
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047276176   ⟸   XM_047420220
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047276181   ⟸   XM_047420225
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054213905   ⟸   XM_054357930
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054213906   ⟸   XM_054357931
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054213907   ⟸   XM_054357932
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054213908   ⟸   XM_054357933
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054213909   ⟸   XM_054357934
- Peptide Label: isoform X3
Protein Domains
C2H2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96BV0-F1-model_v2 AlphaFold Q96BV0 1-537 view protein structure

Promoters
RGD ID:6806446
Promoter ID:HG_KWN:60244
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:NM_173680
Position:
Human AssemblyChrPosition (strand)Source
Build 367149,706,421 - 149,707,187 (+)MPROMDB
RGD ID:7212275
Promoter ID:EPDNEW_H11884
Type:initiation region
Name:ZNF775_1
Description:zinc finger protein 775
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11885  EPDNEW_H11886  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,379,361 - 150,379,421EPDNEW
RGD ID:7212277
Promoter ID:EPDNEW_H11885
Type:multiple initiation site
Name:ZNF775_3
Description:zinc finger protein 775
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11884  EPDNEW_H11886  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,385,644 - 150,385,704EPDNEW
RGD ID:7212279
Promoter ID:EPDNEW_H11886
Type:initiation region
Name:ZNF775_2
Description:zinc finger protein 775
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11884  EPDNEW_H11885  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,396,455 - 150,396,515EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28501 AgrOrtholog
COSMIC ZNF775 COSMIC
Ensembl Genes ENSG00000196456 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000329630 ENTREZGENE
  ENST00000329630.10 UniProtKB/Swiss-Prot
  ENST00000478789.5 UniProtKB/TrEMBL
  ENST00000490973.1 UniProtKB/TrEMBL
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000196456 GTEx
HGNC ID HGNC:28501 ENTREZGENE
Human Proteome Map ZNF775 Human Proteome Map
InterPro Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:285971 UniProtKB/Swiss-Prot
NCBI Gene 285971 ENTREZGENE
PANTHER FI01424P-RELATED UniProtKB/TrEMBL
  GASTRULA ZINC FINGER PROTEIN XLCGF49.1-LIKE-RELATED UniProtKB/TrEMBL
  GENE 12845-RELATED UniProtKB/Swiss-Prot
  TRANSCRIPTIONAL REPRESSOR PROTEIN YY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC FINGER AND SCAN DOMAIN-CONTAINING UniProtKB/TrEMBL
Pfam zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162410371 PharmGKB
PROSITE ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt C9JAM7_HUMAN UniProtKB/TrEMBL
  C9JVG2_HUMAN UniProtKB/TrEMBL
  Q8IY24 ENTREZGENE
  Q96BV0 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q8IY24 UniProtKB/Swiss-Prot