HSFY2 (heat shock transcription factor Y-linked 2) - Rat Genome Database

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Gene: HSFY2 (heat shock transcription factor Y-linked 2) Homo sapiens
Analyze
Symbol: HSFY2 (Ensembl: HSFY1)
Name: heat shock transcription factor Y-linked 2 (Ensembl:heat shock transcription factor Y-linked 1)
RGD ID: 1348679
HGNC Page HGNC:23950
Description: Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ25453; heat shock transcription factor 2-like protein; heat shock transcription factor, Y-linked; heat shock transcription factor, Y-linked 2; HSF2-like; HSF2L; HSFY; HSFY1
RGD Orthologs
Mouse
Rat
Dog
Alliance Genes
More Info more info ...
Related Pseudogenes: HSFY1P1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38Y18,731,440 - 18,790,764 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 EnsemblY18,731,440 - 18,773,735 (-)EnsemblGRCh38hg38GRCh38
GRCh38.p14 EnsemblY18,546,691 - 18,588,963 (+)EnsemblGRCh38hg38GRCh38
GRCh37Y20,893,326 - 20,935,621 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36Y19,352,714 - 19,395,009 (-)NCBINCBI36Build 36hg18NCBI36
Build 34Y19,321,825 - 19,323,746NCBI
CeleraY6,839,462 - 6,881,754 (+)NCBICelera
Cytogenetic MapYq11.222NCBI
HuRefY14,604,979 - 14,647,513 (-)NCBIHuRef
T2T-CHM13v2.0Y19,637,916 - 19,697,230 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

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

Biological Process

Cellular Component
chromatin  (ISA)
cytoplasm  (IEA)
cytosol  (IDA)
nucleoplasm  (IDA)
nucleus  (IBA,IEA)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Autism  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
2. 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:12815422   PMID:14702039   PMID:14985478   PMID:15044259   PMID:15489334   PMID:19274049   PMID:21873635   PMID:24722188   PMID:25036637   PMID:25416956   PMID:25910212   PMID:26871637  
PMID:28473536   PMID:29892012   PMID:31515488   PMID:32296183   PMID:32814053  


Genomics

Comparative Map Data
HSFY2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38Y18,731,440 - 18,790,764 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 EnsemblY18,731,440 - 18,773,735 (-)EnsemblGRCh38hg38GRCh38
GRCh38.p14 EnsemblY18,546,691 - 18,588,963 (+)EnsemblGRCh38hg38GRCh38
GRCh37Y20,893,326 - 20,935,621 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36Y19,352,714 - 19,395,009 (-)NCBINCBI36Build 36hg18NCBI36
Build 34Y19,321,825 - 19,323,746NCBI
CeleraY6,839,462 - 6,881,754 (+)NCBICelera
Cytogenetic MapYq11.222NCBI
HuRefY14,604,979 - 14,647,513 (-)NCBIHuRef
T2T-CHM13v2.0Y19,637,916 - 19,697,230 (-)NCBIT2T-CHM13v2.0
Hsfy2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39156,675,203 - 56,676,610 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl156,675,203 - 56,676,594 (-)EnsemblGRCm39 Ensembl
GRCm38156,636,044 - 56,637,451 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl156,636,044 - 56,637,435 (-)EnsemblGRCm38mm10GRCm38
MGSCv37156,692,888 - 56,694,295 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36156,580,600 - 56,581,988 (-)NCBIMGSCv36mm8
Celera157,150,974 - 57,152,382 (-)NCBICelera
Cytogenetic Map1C1.3NCBI
cM Map128.72NCBI
Hsfy2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8965,676,744 - 65,678,157 (-)NCBIGRCr8
mRatBN7.2958,182,415 - 58,183,828 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl958,182,253 - 58,184,500 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx966,682,537 - 66,683,950 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0971,798,442 - 71,799,855 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0970,116,517 - 70,117,930 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0963,289,937 - 63,291,350 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl963,289,944 - 63,291,350 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0963,097,408 - 63,098,821 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4955,495,514 - 55,496,927 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1955,642,502 - 55,643,909 (-)NCBI
Celera955,646,697 - 55,648,110 (-)NCBICelera
Cytogenetic Map9q31NCBI
LOC119868754
(Canis lupus familiaris - dog)		 No map positions available.


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 Yp11.2-q12(chrY:2786811-56885333)x2 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050325]|Global developmental delay [RCV000050326]|Abnormality of the heart [RCV000050327]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050325]|See cases [RCV000050325] ChrY:2786811..56885333 [GRCh38]
ChrY:2654852..59031480 [GRCh37]
ChrY:Yp11.2-q12		 pathogenic
GRCh38/hg38 Yp11.2-q11.223(chrY:2788370-20525326)x2 copy number gain See cases [RCV000050823] ChrY:2788370..20525326 [GRCh38]
ChrY:2656411..22687212 [GRCh37]
ChrY:2716411..21096600 [NCBI36]
ChrY:Yp11.2-q11.223		 pathogenic
GRCh38/hg38 Yp11.2-q11.223(chrY:2786811-22358529)x2 copy number gain See cases [RCV000050942] ChrY:2786811..22358529 [GRCh38]
ChrY:2654852..24504676 [GRCh37]
ChrY:2714852..22914064 [NCBI36]
ChrY:Yp11.2-q11.223		 pathogenic
GRCh37/hg19 Yq11.21-12(chrY:14698756-59031480)x0 copy number loss See cases [RCV000050825] ChrY:14698756..59031480 [GRCh37]
ChrY:13208776..57440868 [NCBI36]
ChrY:Yq11.21-12		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:13404515-57208726)x0 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051778]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051778]|See cases [RCV000051778] ChrY:13404515..57208726 [GRCh38]
ChrY:15516395..59354877 [GRCh37]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:12586822-57208726)x0 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051768]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051768]|See cases [RCV000051768] ChrY:12586822..57208726 [GRCh38]
ChrY:14698756..59354877 [GRCh37]
ChrY:13208776..57764265 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:2786811-26389995)x0 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051767]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051767]|See cases [RCV000051767] ChrY:2786811..26389995 [GRCh38]
ChrY:2654852..28536142 [GRCh37]
ChrY:2714852..26945530 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh37/hg19 Yp11.3-q12(chrY:2651665-59031480)x2 copy number gain See cases [RCV000052585] ChrY:2651665..59031480 [GRCh37]
ChrY:2711665..57440868 [NCBI36]
ChrY:Yp11.3-q12		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:2786611-26409996)x2 copy number gain See cases [RCV000052586] ChrY:2786611..26409996 [GRCh38]
ChrY:2654652..28556143 [GRCh37]
ChrY:2714652..26965531 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:2786811-26463830)x2 copy number gain See cases [RCV000052587] ChrY:2786811..26463830 [GRCh38]
ChrY:2654852..28609977 [GRCh37]
ChrY:2714852..27019365 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:2786811-26483746)x2 copy number gain See cases [RCV000052588] ChrY:2786811..26483746 [GRCh38]
ChrY:2654852..28629893 [GRCh37]
ChrY:2714852..27039281 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh38/hg38 Yp11.2-q12(chrY:2783624-26637948)x2 copy number gain See cases [RCV000052551] ChrY:2783624..26637948 [GRCh38]
ChrY:2651665..28784095 [GRCh37]
ChrY:2711665..27193483 [NCBI36]
ChrY:Yp11.2-q12		 pathogenic
GRCh38/hg38 Yp11.2-q11.223(chrY:2787210-22302412)x2 copy number gain See cases [RCV000054342] ChrY:2787210..22302412 [GRCh38]
ChrY:2655251..24448559 [GRCh37]
ChrY:2715251..22857947 [NCBI36]
ChrY:Yp11.2-q11.223		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:6478684-26574618)x2 copy number gain See cases [RCV000054344] ChrY:6478684..26574618 [GRCh38]
ChrY:6346725..28720765 [GRCh37]
ChrY:6406725..27130153 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh38/hg38 Yq11.222(chrY:17251556-19150076)x2 copy number gain See cases [RCV000054352] ChrY:17251556..19150076 [GRCh38]
ChrY:19363436..21311962 [GRCh37]
ChrY:17872830..19771350 [NCBI36]
ChrY:Yq11.222		 uncertain significance
GRCh38/hg38 Yq11.221-12(chrY:14076802-57165209)x0 copy number loss See cases [RCV000133870] ChrY:14076802..57165209 [GRCh38]
ChrY:16188682..59311360 [GRCh37]
ChrY:14698076..57720748 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yq11.222(chrY:17307218-18891526)x2 copy number gain See cases [RCV000133844] ChrY:17307218..18891526 [GRCh38]
ChrY:19419098..21053412 [GRCh37]
ChrY:17928492..19512800 [NCBI36]
ChrY:Yq11.222		 uncertain significance
GRCh38/hg38 Yq11.221-12(chrY:13404515-57208726)x0 copy number loss See cases [RCV000051778] ChrY:13404515..57208726 [GRCh38]
ChrY:15516395..59354877 [GRCh37]
ChrY:14025789..57764265 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh37/hg19 Yp11.31-q12(chrY:2654852-59031480)x0 copy number loss See cases [RCV000133673] ChrY:2654852..59031480 [GRCh37]
ChrY:2714852..57440868 [NCBI36]
ChrY:Yp11.31-q12		 pathogenic
GRCh37/hg19 Yp11.31-q12(chrY:2654852-59031480)x3 copy number gain See cases [RCV000133672] ChrY:2654852..59031480 [GRCh37]
ChrY:2714852..57440868 [NCBI36]
ChrY:Yp11.31-q12		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:12965721-57212647)x0 copy number loss See cases [RCV000135325] ChrY:12965721..57212647 [GRCh38]
ChrY:15077631..59358798 [GRCh37]
ChrY:13587025..57768186 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:6270281-26463761)x0 copy number loss See cases [RCV000134844] ChrY:6270281..26463761 [GRCh38]
ChrY:6138322..28609908 [GRCh37]
ChrY:6198322..27019296 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh38/hg38 Yq11.222(chrY:17251756-19149935)x2 copy number gain See cases [RCV000135753] ChrY:17251756..19149935 [GRCh38]
ChrY:19363636..21311821 [GRCh37]
ChrY:17873030..19771209 [NCBI36]
ChrY:Yq11.222		 benign|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh37/hg19 Yq11.221-12(chrY:16183453-59011762)x2 copy number gain See cases [RCV000135766] ChrY:16183453..59011762 [GRCh37]
ChrY:14692847..57421150 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yq11.222-12(chrY:18664321-26637948)x2 copy number gain See cases [RCV000135767] ChrY:18664321..26637948 [GRCh38]
ChrY:20826207..28784095 [GRCh37]
ChrY:19285595..27193483 [NCBI36]
ChrY:Yq11.222-12		 pathogenic
GRCh38/hg38 Yp11.32-q12(chrY:10701-57189762) copy number loss See cases [RCV000135689] ChrY:10701..57189762 [GRCh38]
ChrY:10701..59335913 [GRCh37]
ChrY:701..57745301 [NCBI36]
ChrY:Yp11.32-q12		 pathogenic
GRCh38/hg38 Yp11.32-q12(chrY:10701-57189762)x0 copy number loss See cases [RCV000135690] ChrY:10701..57189762 [GRCh38]
ChrY:10701..59335913 [GRCh37]
ChrY:701..57745301 [NCBI36]
ChrY:Yp11.32-q12		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:13948013-57208726)x0 copy number loss See cases [RCV000135529] ChrY:13948013..57208726 [GRCh38]
ChrY:16059893..59354877 [GRCh37]
ChrY:14569287..57764265 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:2786596-26575961)x0 copy number loss See cases [RCV000136110] ChrY:2786596..26575961 [GRCh38]
ChrY:2654637..28722108 [GRCh37]
ChrY:2714637..27131496 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh38/hg38 Yq11.221-11.223(chrY:13908860-22358529)x1 copy number gain See cases [RCV000136525] ChrY:13908860..22358529 [GRCh38]
ChrY:16020740..24504676 [GRCh37]
ChrY:14530134..22914064 [NCBI36]
ChrY:Yq11.221-11.223		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:15631816-57211010)x0 copy number loss See cases [RCV000135882] ChrY:15631816..57211010 [GRCh38]
ChrY:17743696..59357161 [GRCh37]
ChrY:16253090..57766549 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yp11.2-q11.23(chrY:2855704-24288951)x2 copy number gain See cases [RCV000136851] ChrY:2855704..24288951 [GRCh38]
ChrY:2723745..26435098 [GRCh37]
ChrY:2783745..24844486 [NCBI36]
ChrY:Yp11.2-q11.23		 pathogenic
GRCh38/hg38 Yq11.222(chrY:18664321-19478314)x2 copy number gain See cases [RCV000136631] ChrY:18664321..19478314 [GRCh38]
ChrY:20826207..21640200 [GRCh37]
ChrY:19285595..20099588 [NCBI36]
ChrY:Yq11.222		 uncertain significance
GRCh38/hg38 Yq11.222-12(chrY:18545732-57189762)x0 copy number loss See cases [RCV000137556] ChrY:18545732..57189762 [GRCh38]
ChrY:20707618..59335913 [GRCh37]
ChrY:19167006..57745301 [NCBI36]
ChrY:Yq11.222-12		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:14062885-57189762)x0 copy number loss See cases [RCV000138875] ChrY:14062885..57189762 [GRCh38]
ChrY:16174765..59335913 [GRCh37]
ChrY:14684159..57745301 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yq11.222(chrY:18545732-19487468)x2 copy number gain See cases [RCV000138359] ChrY:18545732..19487468 [GRCh38]
ChrY:20707618..21649354 [GRCh37]
ChrY:19167006..20108742 [NCBI36]
ChrY:Yq11.222		 likely benign
GRCh38/hg38 Yq11.222(chrY:17951462-18799924)x2 copy number gain See cases [RCV000138267] ChrY:17951462..18799924 [GRCh38]
ChrY:20063342..20961810 [GRCh37]
ChrY:18572736..19421198 [NCBI36]
ChrY:Yq11.222		 likely benign
GRCh37/hg19 Yp11.31-q12(chrY:2650559-59032389)x2 copy number gain See cases [RCV000138422] ChrY:2650559..59032389 [GRCh37]
ChrY:2710559..57441777 [NCBI36]
ChrY:Yp11.31-q12		 pathogenic
GRCh38/hg38 Yp11.2-q12(chrY:2133003-56884424)x0 copy number loss See cases [RCV000139324] ChrY:2133003..56884424 [GRCh38]
ChrY:1167123..59030571 [GRCh37]
ChrY:1137123..57439959 [NCBI36]
ChrY:Yp11.2-q12		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:16311571-57190586)x0 copy number loss See cases [RCV000139941] ChrY:16311571..57190586 [GRCh38]
ChrY:18423451..59336737 [GRCh37]
ChrY:16932845..57746125 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yp11.31-q12(chrY:378139-57181562)x1 copy number loss See cases [RCV000141411] ChrY:378139..57181562 [GRCh38]
ChrY:288874..59327713 [GRCh37]
ChrY:258874..57737101 [NCBI36]
ChrY:Yp11.31-q12		 pathogenic
GRCh38/hg38 Yq11.222(chrY:17461577-18864368)x4 copy number gain See cases [RCV000140572] ChrY:17461577..18864368 [GRCh38]
ChrY:19573457..21026254 [GRCh37]
ChrY:18082851..19485642 [NCBI36]
ChrY:Yq11.222		 likely benign
GRCh38/hg38 Yq11.21-12(chrY:10624004-57190586)x0 copy number loss See cases [RCV000141809] ChrY:10624004..57190586 [GRCh38]
ChrY:13134518..59336737 [GRCh37]
ChrY:11244518..57746125 [NCBI36]
ChrY:Yq11.21-12		 pathogenic
GRCh38/hg38 Yq11.222(chrY:18664296-19478351)x2 copy number gain See cases [RCV000142479] ChrY:18664296..19478351 [GRCh38]
ChrY:20826182..21640237 [GRCh37]
ChrY:19285570..20099625 [NCBI36]
ChrY:Yq11.222		 likely benign
GRCh38/hg38 Yq11.221-12(chrY:12702930-26653790)x1 copy number gain See cases [RCV000142197] ChrY:12702930..26653790 [GRCh38]
ChrY:14814859..28799937 [GRCh37]
ChrY:13324253..27209325 [NCBI36]
ChrY:Yq11.221-12		 pathogenic
GRCh38/hg38 Yq11.221-12(chrY:12881571-26653790)x1 copy number gain See cases [RCV000142059] ChrY:12881571..26653790 [GRCh38]
ChrY:14993486..28799937 [GRCh37]
ChrY:13502880..27209325 [NCBI36]
ChrY:Yq11.221-12		 likely benign
GRCh38/hg38 Yq11.222-11.223(chrY:18664321-22358529)x2 copy number gain See cases [RCV000142769] ChrY:18664321..22358529 [GRCh38]
ChrY:20826207..24504676 [GRCh37]
ChrY:19285595..22914064 [NCBI36]
ChrY:Yq11.222-11.223		 uncertain significance
GRCh38/hg38 Yq11.21-12(chrY:11680193-26653790)x4 copy number gain See cases [RCV000143421] ChrY:11680193..26653790 [GRCh38]
ChrY:13800899..28799937 [GRCh37]
ChrY:12310899..27209325 [NCBI36]
ChrY:Yq11.21-12		 likely pathogenic
GRCh37/hg19 Yp11.31-q12(chrY:2654852-59031480)x2 copy number gain See cases [RCV000148271] ChrY:2654852..59031480 [GRCh37]
ChrY:2714852..57440868 [NCBI36]
ChrY:Yp11.31-q12		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:20297-59358845)x2 copy number gain See cases [RCV000240246] ChrY:20297..59358845 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:10701-59349277)x1 copy number loss See cases [RCV000240213] ChrY:10701..59349277 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:100002-59353228)x2 copy number gain See cases [RCV000239812] ChrY:100002..59353228 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:21267-59349649)x2 copy number gain See cases [RCV000239787] ChrY:21267..59349649 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yq11.221-11.222(chrY:19320885-21332123)x2 copy number gain See cases [RCV000515571] ChrY:19320885..21332123 [GRCh37]
ChrY:Yq11.221-11.222		 uncertain significance
GRCh38/hg38 Yq11.222(chrY:18782131-18855730)x3 copy number gain See cases [RCV000135062] ChrY:18782131..18855730 [GRCh38]
ChrY:20944017..21017616 [GRCh37]
ChrY:19403405..19477004 [NCBI36]
ChrY:Yq11.222		 benign
GRCh38/hg38 Yq11.222(chrY:18774616-19429188)x2 copy number gain See cases [RCV000138049] ChrY:18774616..19429188 [GRCh38]
ChrY:20936502..21591074 [GRCh37]
ChrY:19395890..20050462 [NCBI36]
ChrY:Yq11.222		 likely benign
GRCh37/hg19 Yp11.32-q12(chrY:21267-59337042)x2 copy number gain See cases [RCV000239958] ChrY:21267..59337042 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yq11.221-12(chrY:16188682-59349649)x0 copy number loss See cases [RCV000240102] ChrY:16188682..59349649 [GRCh37]
ChrY:Yq11.221-12		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:126426-59349649)x2 copy number gain See cases [RCV000240301] ChrY:126426..59349649 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:126426-59353228)x2 copy number gain See cases [RCV000240305] ChrY:126426..59353228 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yq11.221-12(chrY:15415024-59349591)x0 copy number loss See cases [RCV000446382] ChrY:15415024..59349591 [GRCh37]
ChrY:Yq11.221-12		 pathogenic
GRCh37/hg19 Yq11.222-12(chrY:20805226-59336998)x0 copy number loss See cases [RCV000447602] ChrY:20805226..59336998 [GRCh37]
ChrY:Yq11.222-12		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:20297-59356174) copy number loss See cases [RCV000448395] ChrY:20297..59356174 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yq11.221-11.222(chrY:19419098-21251249)x2 copy number gain See cases [RCV000448564] ChrY:19419098..21251249 [GRCh37]
ChrY:Yq11.221-11.222		 benign
GRCh37/hg19 Yq11.222-11.23(chrY:20359545-27839018)x2 copy number gain See cases [RCV000448226] ChrY:20359545..27839018 [GRCh37]
ChrY:Yq11.222-11.23		 likely benign
GRCh37/hg19 Yp11.32-q12(chrY:1684070-36905226)x3 copy number gain See cases [RCV000510438] ChrY:1684070..36905226 [GRCh37]
ChrY:Yp11.32-q12		 uncertain significance
GRCh37/hg19 Yq11.21-12(chrY:13871147-59336737)x0 copy number loss See cases [RCV000510252] ChrY:13871147..59336737 [GRCh37]
ChrY:Yq11.21-12		 pathogenic
GRCh37/hg19 Yp11.31-q11.23(chrY:2650141-28799937)x2 copy number gain See cases [RCV000510700] ChrY:2650141..28799937 [GRCh37]
ChrY:Yp11.31-q11.23		 uncertain significance
GRCh37/hg19 Yp11.31-q11.23(chrY:2650141-28799937)x0 copy number loss See cases [RCV000511418] ChrY:2650141..28799937 [GRCh37]
ChrY:Yp11.31-q11.23		 pathogenic
GRCh37/hg19 Yp11.32-q11.23(chrY:168546-28451874)x1 copy number loss See cases [RCV000511281] ChrY:168546..28451874 [GRCh37]
ChrY:Yp11.32-q11.23		 pathogenic
GRCh37/hg19 Yq11.221-11.222(chrY:19574920-21155525)x2 copy number gain not provided [RCV000684430] ChrY:19574920..21155525 [GRCh37]
ChrY:Yq11.221-11.222		 likely benign
GRCh37/hg19 Yq11.221-11.23(chrY:19574920-28423925)x2 copy number gain not provided [RCV000684441] ChrY:19574920..28423925 [GRCh37]
ChrY:Yq11.221-11.23		 likely benign
GRCh37/hg19 Yp11.31-q11.223(chrY:2650140-24070172)x2 copy number gain not provided [RCV000684444] ChrY:2650140..24070172 [GRCh37]
ChrY:Yp11.31-q11.223		 pathogenic
GRCh37/hg19 Yq11.21-12(chrY:13410538-59032808)x0 copy number loss not provided [RCV000684445] ChrY:13410538..59032808 [GRCh37]
ChrY:Yq11.21-12		 pathogenic
GRCh37/hg19 Yq11.222-11.223(chrY:20618887-24820716)x0 copy number loss not provided [RCV000684439] ChrY:20618887..24820716 [GRCh37]
ChrY:Yq11.222-11.223		 likely benign
GRCh37/hg19 Yp11.31-q11.23(chrY:2655180-28727063)x0 copy number gain not provided [RCV000753972] ChrY:2655180..28727063 [GRCh37]
ChrY:Yp11.31-q11.23		 pathogenic
GRCh37/hg19 Yq11.1-12(chrY:13132024-28817458)x0 copy number loss not provided [RCV000754010] ChrY:13132024..28817458 [GRCh37]
ChrY:Yq11.1-12		 pathogenic
Single allele duplication Autism [RCV000754378] ChrY:1..57227415 [GRCh38]
ChrY:Yp11.32-q12		 likely pathogenic
GRCh37/hg19 Yp11.31-q12(chrY:2655180-58883690)x2 copy number gain not provided [RCV000753973] ChrY:2655180..58883690 [GRCh37]
ChrY:Yp11.31-q12		 pathogenic
GRCh37/hg19 Yq11.222(chrY:20354974-20969451)x3 copy number gain not provided [RCV000754025] ChrY:20354974..20969451 [GRCh37]
ChrY:Yq11.222		 benign
GRCh37/hg19 Yq11.222(chrY:20836567-21121563)x0 copy number loss not provided [RCV000754033] ChrY:20836567..21121563 [GRCh37]
ChrY:Yq11.222		 benign
GRCh37/hg19 Yq11.222-11.23(chrY:20111978-28423925)x0 copy number loss Male infertility [RCV001090077] ChrY:20111978..28423925 [GRCh37]
ChrY:Yq11.222-11.23		 pathogenic
GRCh37/hg19 Yp11.31-q11.223(chrY:2650278-24445033) copy number gain not provided [RCV000767654] ChrY:2650278..24445033 [GRCh37]
ChrY:Yp11.31-q11.223		 pathogenic
GRCh37/hg19 Yq11.222-11.23(chrY:20608554-28799937)x0 copy number loss Male infertility [RCV001090069] ChrY:20608554..28799937 [GRCh37]
ChrY:Yq11.222-11.23		 pathogenic
GRCh37/hg19 Yq11.221-12(chrY:16053146-59343488)x2 copy number gain not provided [RCV000848067] ChrY:16053146..59343488 [GRCh37]
ChrY:Yq11.221-12		 pathogenic
GRCh37/hg19 Yq11.221-12(chrY:15190336-59343488)x0 copy number loss not provided [RCV000847612] ChrY:15190336..59343488 [GRCh37]
ChrY:Yq11.221-12		 pathogenic
GRCh37/hg19 Yq11.221-11.23(chrY:15427283-28799937)x0 copy number loss Male infertility [RCV001090085] ChrY:15427283..28799937 [GRCh37]
ChrY:Yq11.221-11.23		 pathogenic
GRCh37/hg19 Yq11.221-11.23(chrY:19567361-28458663)x2 copy number gain not provided [RCV001007396] ChrY:19567361..28458663 [GRCh37]
ChrY:Yq11.221-11.23		 likely benign
GRCh37/hg19 Yq11.221-11.23(chrY:18546605-28799937)x0 copy number loss Male infertility [RCV001090076] ChrY:18546605..28799937 [GRCh37]
ChrY:Yq11.221-11.23		 pathogenic
GRCh37/hg19 Yq11.21-11.223(chrY:14495040-24070172)x0 copy number loss Male infertility [RCV001090078] ChrY:14495040..24070172 [GRCh37]
ChrY:Yq11.21-11.223		 pathogenic
GRCh37/hg19 Yp11.32-q11.23(chrY:168546-28799937)x2 copy number gain not provided [RCV001007377] ChrY:168546..28799937 [GRCh37]
ChrY:Yp11.32-q11.23		 pathogenic
GRCh37/hg19 Yq11.222(chrY:20563480-21028944)x2 copy number gain not provided [RCV001007397] ChrY:20563480..21028944 [GRCh37]
ChrY:Yq11.222		 likely benign
GRCh37/hg19 Yq11.21-11.23(chrY:13800703-28799937)x0 copy number loss Male infertility [RCV001090084] ChrY:13800703..28799937 [GRCh37]
ChrY:Yq11.21-11.23		 pathogenic
GRCh37/hg19 Yp11.32-q12(chrY:1-59373566) copy number gain Global developmental delay [RCV002280747] ChrY:1..59373566 [GRCh37]
ChrY:Yp11.32-q12		 pathogenic
GRCh37/hg19 Yp11.31-q11.23(chrY:2650424-28799654) copy number loss not provided [RCV002221453] ChrY:2650424..28799654 [GRCh37]
ChrY:Yp11.31-q11.23		 pathogenic
GRCh37/hg19 Yq11.21-11.23(chrY:13905421-28799654) copy number loss not provided [RCV002221454] ChrY:13905421..28799654 [GRCh37]
ChrY:Yq11.21-11.23		 pathogenic
GRCh37/hg19 Yq11.221-12(chrY:16203971-59336737)x0 copy number loss not provided [RCV002474928] ChrY:16203971..59336737 [GRCh37]
ChrY:Yq11.221-12		 uncertain significance
GRCh37/hg19 Yq11.21-12(chrY:14370813-59373566)x0 copy number loss not provided [RCV002473934] ChrY:14370813..59373566 [GRCh37]
ChrY:Yq11.21-12		 pathogenic
GRCh37/hg19 Yq11.222(chrY:20618888-21621968)x2 copy number gain not provided [RCV003483995] ChrY:20618888..21621968 [GRCh37]
ChrY:Yq11.222		 uncertain significance
GRCh37/hg19 Yq11.222(chrY:20609790-21376079)x2 copy number gain not provided [RCV003483994] ChrY:20609790..21376079 [GRCh37]
ChrY:Yq11.222		 uncertain significance
GRCh37/hg19 Yq11.221-11.23(chrY:18921311-28799937)x0 copy number loss not provided [RCV003482939] ChrY:18921311..28799937 [GRCh37]
ChrY:Yq11.221-11.23		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:917
Count of miRNA genes:709
Interacting mature miRNAs:789
Transcripts:ENST00000304790, ENST00000344884, ENST00000382852, ENST00000491902
Prediction methods:Microtar, 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.

Markers in Region
DYS208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,927,033 - 20,927,180UniSTSGRCh37
GRCh37Y20,716,994 - 20,717,141UniSTSGRCh37
CeleraY6,847,899 - 6,848,046RGD
Cytogenetic MapYq11.222UniSTS
HuRefY14,638,685 - 14,638,832UniSTS
TNG Radiation Hybrid MapY3843.0UniSTS
RH93149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,933,863 - 20,933,997UniSTSGRCh37
GRCh37Y20,710,181 - 20,710,315UniSTSGRCh37
CeleraY6,841,086 - 6,841,220RGD
Cytogenetic MapYq11.222UniSTS
HuRefY14,645,755 - 14,645,889UniSTS
sY1237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,934,230 - 20,934,379UniSTSGRCh37
GRCh37Y20,709,799 - 20,709,948UniSTSGRCh37
CeleraY6,840,704 - 6,840,853RGD
Cytogenetic MapYq11.222UniSTS
HuRefY14,646,122 - 14,646,271UniSTS
DYS209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,932,050 - 20,932,311UniSTSGRCh37
GRCh37Y20,711,867 - 20,712,128UniSTSGRCh37
CeleraY6,842,772 - 6,843,033RGD
Cytogenetic MapYq11.222UniSTS
HuRefY14,643,942 - 14,644,203UniSTS
TNG Radiation Hybrid MapY3843.0UniSTS
Stanford-G3 RH MapY957.0UniSTS
G66365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,933,010 - 20,933,259UniSTSGRCh37
GRCh37Y20,710,919 - 20,711,168UniSTSGRCh37
CeleraY6,841,824 - 6,842,073RGD
Cytogenetic MapYq11.222UniSTS
HuRefY14,644,902 - 14,645,151UniSTS
sY1119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,931,735 - 20,932,012UniSTSGRCh37
GRCh37Y20,712,166 - 20,712,439UniSTSGRCh37
CeleraY6,843,071 - 6,843,344UniSTS
HuRefY14,643,387 - 14,643,904UniSTS
sY1946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,906,367 - 20,906,655UniSTSGRCh37
GRCh37Y20,737,520 - 20,737,808UniSTSGRCh37
CeleraY6,868,425 - 6,868,713UniSTS
HuRefY14,618,020 - 14,618,308UniSTS
sY1947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,916,452 - 20,916,742UniSTSGRCh37
GRCh37Y20,727,433 - 20,727,723UniSTSGRCh37
CeleraY6,858,338 - 6,858,628UniSTS
HuRefY14,628,105 - 14,628,395UniSTS
sY1949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37Y20,901,473 - 20,901,726UniSTSGRCh37
GRCh37Y20,742,449 - 20,742,702UniSTSGRCh37
CeleraY6,873,354 - 6,873,607UniSTS
HuRefY14,613,126 - 14,613,379UniSTS


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

endocrine system exocrine system hemolymphoid system hepatobiliary system musculoskeletal system nervous system renal system reproductive system respiratory system
High
Medium
Low
Below cutoff 2 2 1 2 1 13 2 8 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000304790   ⟹   ENSP00000306549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,771,814 - 18,773,735 (-)Ensembl
RefSeq Acc Id: ENST00000307393   ⟹   ENSP00000303599
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,546,720 - 18,548,592 (+)Ensembl
RefSeq Acc Id: ENST00000309834   ⟹   ENSP00000311166
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,546,691 - 18,588,963 (+)Ensembl
RefSeq Acc Id: ENST00000338876   ⟹   ENSP00000342302
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,546,691 - 18,588,963 (+)Ensembl
RefSeq Acc Id: ENST00000344884   ⟹   ENSP00000340971
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,731,440 - 18,773,715 (-)Ensembl
RefSeq Acc Id: ENST00000382852   ⟹   ENSP00000372303
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,768,921 - 18,773,686 (-)Ensembl
RefSeq Acc Id: ENST00000382856   ⟹   ENSP00000372307
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,546,720 - 18,551,465 (+)Ensembl
RefSeq Acc Id: ENST00000491902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblY18,731,440 - 18,773,715 (-)Ensembl
RefSeq Acc Id: NM_001001877   ⟹   NP_001001877
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38Y18,731,440 - 18,773,735 (-)NCBI
GRCh37Y20,893,326 - 20,935,621 (-)RGD
Build 36Y19,352,714 - 19,394,989 (-)NCBI Archive
HuRefY14,604,979 - 14,647,513 (-)ENTREZGENE
T2T-CHM13v2.0Y19,637,916 - 19,680,200 (-)NCBI
Sequence:
RefSeq Acc Id: NM_153716   ⟹   NP_714927
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38Y18,771,814 - 18,773,735 (-)NCBI
GRCh37Y20,893,326 - 20,935,621 (-)RGD
Build 36Y19,393,089 - 19,395,009 (-)NCBI Archive
HuRefY14,604,979 - 14,647,513 (-)ENTREZGENE
T2T-CHM13v2.0Y19,678,279 - 19,680,200 (-)NCBI
Sequence:
RefSeq Acc Id: NR_003509
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38Y18,731,440 - 18,773,735 (-)NCBI
GRCh37Y20,893,326 - 20,935,621 (-)RGD
Build 36Y19,352,714 - 19,395,009 (-)NCBI Archive
HuRefY14,604,979 - 14,647,513 (-)ENTREZGENE
T2T-CHM13v2.0Y19,637,916 - 19,680,200 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005262508   ⟹   XP_005262565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38Y18,771,814 - 18,773,726 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017030030   ⟹   XP_016885519
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38Y18,771,814 - 18,790,764 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017030031   ⟹   XP_016885520
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38Y18,769,508 - 18,773,735 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054328252   ⟹   XP_054184227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0Y19,678,279 - 19,697,230 (-)NCBI
RefSeq Acc Id: XM_054328253   ⟹   XP_054184228
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0Y19,678,279 - 19,680,191 (-)NCBI
RefSeq Acc Id: XM_054328254   ⟹   XP_054184229
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0Y19,675,975 - 19,680,200 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_001001877   ⟸   NM_001001877
- Peptide Label: isoform 2
- UniProtKB: Q96LI6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_714927   ⟸   NM_153716
- Peptide Label: isoform 1
- UniProtKB: Q9BZA2 (UniProtKB/Swiss-Prot),   Q7Z4L8 (UniProtKB/Swiss-Prot),   Q17RC0 (UniProtKB/Swiss-Prot),   Q9BZA3 (UniProtKB/Swiss-Prot),   Q96LI6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005262565   ⟸   XM_005262508
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016885520   ⟸   XM_017030031
- Peptide Label: isoform X3
- UniProtKB: Q96LI6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016885519   ⟸   XM_017030030
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000303599   ⟸   ENST00000307393
RefSeq Acc Id: ENSP00000311166   ⟸   ENST00000309834
RefSeq Acc Id: ENSP00000342302   ⟸   ENST00000338876
RefSeq Acc Id: ENSP00000372303   ⟸   ENST00000382852
RefSeq Acc Id: ENSP00000372307   ⟸   ENST00000382856
RefSeq Acc Id: ENSP00000306549   ⟸   ENST00000304790
RefSeq Acc Id: ENSP00000340971   ⟸   ENST00000344884
RefSeq Acc Id: XP_054184229   ⟸   XM_054328254
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054184227   ⟸   XM_054328252
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054184228   ⟸   XM_054328253
- Peptide Label: isoform X2

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96LI6-F1-model_v2 AlphaFold Q96LI6 1-401 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23950 AgrOrtholog
COSMIC HSFY2 COSMIC
Ensembl Genes ENSG00000169953 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000172468 Ensembl, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000304790 ENTREZGENE
  ENST00000304790.3 UniProtKB/Swiss-Prot
  ENST00000307393.3 UniProtKB/Swiss-Prot
  ENST00000309834.8 UniProtKB/Swiss-Prot
  ENST00000338876.8 UniProtKB/Swiss-Prot
  ENST00000344884 ENTREZGENE
  ENST00000344884.4 UniProtKB/Swiss-Prot
  ENST00000382852 ENTREZGENE
  ENST00000382852.1 UniProtKB/Swiss-Prot
  ENST00000382856.2 UniProtKB/Swiss-Prot
  ENST00000491902 ENTREZGENE
Gene3D-CATH 1.10.10.10 UniProtKB/Swiss-Prot
GTEx ENSG00000169953 GTEx
  ENSG00000172468 GTEx
HGNC ID HGNC:23950 ENTREZGENE
Human Proteome Map HSFY2 Human Proteome Map
InterPro HSF_DNA-bd UniProtKB/Swiss-Prot
  HSF_fam UniProtKB/Swiss-Prot
  WH-like_DNA-bd_sf UniProtKB/Swiss-Prot
  WH_DNA-bd_sf UniProtKB/Swiss-Prot
KEGG Report hsa:159119 UniProtKB/Swiss-Prot
  hsa:86614 UniProtKB/Swiss-Prot
NCBI Gene 159119 ENTREZGENE
PANTHER PTHR10015 UniProtKB/Swiss-Prot
  PTHR10015:SF336 UniProtKB/Swiss-Prot
Pfam HSF_DNA-bind UniProtKB/Swiss-Prot
PharmGKB PA134894795 PharmGKB
SMART HSF UniProtKB/Swiss-Prot
Superfamily-SCOP SSF46785 UniProtKB/Swiss-Prot
UniProt HSFY1_HUMAN UniProtKB/Swiss-Prot
  Q17RC0 ENTREZGENE
  Q7Z4L8 ENTREZGENE
  Q96LI6 ENTREZGENE
  Q9BZA2 ENTREZGENE
  Q9BZA3 ENTREZGENE
UniProt Secondary Q17RC0 UniProtKB/Swiss-Prot
  Q7Z4L8 UniProtKB/Swiss-Prot
  Q9BZA2 UniProtKB/Swiss-Prot
  Q9BZA3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-05-01 HSFY2  heat shock transcription factor Y-linked 2  HSFY2  heat shock transcription factor, Y-linked 2  Symbol and/or name change 5135510 APPROVED
2015-10-06 HSFY2  heat shock transcription factor, Y-linked 2  HSFY2  heat shock transcription factor, Y linked 2  Symbol and/or name change 5135510 APPROVED