WNK2 (WNK lysine deficient protein kinase 2) - Rat Genome Database

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Gene: WNK2 (WNK lysine deficient protein kinase 2) Homo sapiens
Analyze
Symbol: WNK2
Name: WNK lysine deficient protein kinase 2
RGD ID: 1349205
HGNC Page HGNC:14542
Description: Predicted to enable ATP binding activity and protein serine/threonine kinase activity. Involved in monoatomic ion homeostasis; negative regulation of cell population proliferation; and regulation of signal transduction. Located in cytosol.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: antigen NY-CO-43; KIAA1760; mitogen-activated protein kinase kinase kinase; NY-CO-43; P/OKcl.13; PRKWNK2; protein kinase lysine-deficient 2; protein kinase with no lysine 2; protein kinase, lysine deficient 2; SDCCAG43; serine/threonine-protein kinase WNK2; serologically defined colon cancer antigen 43
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38993,184,139 - 93,320,569 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl993,184,122 - 93,320,572 (+)EnsemblGRCh38hg38GRCh38
GRCh37995,946,421 - 96,082,851 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36994,987,033 - 95,122,675 (+)NCBINCBI36Build 36hg18NCBI36
Build 34993,026,766 - 93,162,409NCBI
Celera966,388,916 - 66,525,074 (+)NCBICelera
Cytogenetic Map9q22.31NCBI
HuRef965,623,639 - 65,760,276 (+)NCBIHuRef
CHM1_1996,093,815 - 96,229,891 (+)NCBICHM1_1
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBIT2T-CHM13v2.0
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

Cellular Component
cytoplasm  (IBA,IDA,IEA)
cytosol  (IDA)
plasma membrane  (IEA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. WNK-Cab39-NKCC1 signaling increases the susceptibility to ischemic brain damage in hypertensive rats. Bhuiyan MIH, etal., J Cereb Blood Flow Metab. 2017 Aug;37(8):2780-2794. doi: 10.1177/0271678X16675368. Epub 2016 Jan 1.
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9610721   PMID:11214970   PMID:11280764   PMID:11498583   PMID:11571656   PMID:12477932   PMID:14702039   PMID:15489334   PMID:16713569   PMID:17474147   PMID:17578925   PMID:17667937  
PMID:18593598   PMID:18768590   PMID:19001526   PMID:19724895   PMID:19851296   PMID:20198315   PMID:20379614   PMID:20525693   PMID:20936779   PMID:21733846   PMID:21873635   PMID:21988832  
PMID:22199357   PMID:23035050   PMID:23387299   PMID:23797875   PMID:23838290   PMID:23912455   PMID:25596741   PMID:26186194   PMID:28514442   PMID:28611215   PMID:29117863   PMID:29507755  
PMID:30021884   PMID:30258100   PMID:31009242   PMID:31349001   PMID:31884577   PMID:32093151   PMID:32447640   PMID:32707033   PMID:32768499   PMID:33001583   PMID:33961781   PMID:34061329  
PMID:34079125   PMID:34349018   PMID:34857952   PMID:35044719   PMID:35271311   PMID:35439318   PMID:35748872   PMID:35849656   PMID:36168627   PMID:36270769   PMID:37689310   PMID:37704626  
PMID:38091885  


Genomics

Comparative Map Data
WNK2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38993,184,139 - 93,320,569 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl993,184,122 - 93,320,572 (+)EnsemblGRCh38hg38GRCh38
GRCh37995,946,421 - 96,082,851 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36994,987,033 - 95,122,675 (+)NCBINCBI36Build 36hg18NCBI36
Build 34993,026,766 - 93,162,409NCBI
Celera966,388,916 - 66,525,074 (+)NCBICelera
Cytogenetic Map9q22.31NCBI
HuRef965,623,639 - 65,760,276 (+)NCBIHuRef
CHM1_1996,093,815 - 96,229,891 (+)NCBICHM1_1
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBIT2T-CHM13v2.0
Wnk2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391349,189,778 - 49,302,110 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1349,189,779 - 49,301,490 (-)EnsemblGRCm39 Ensembl
GRCm381349,036,302 - 49,148,574 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1349,036,303 - 49,148,014 (-)EnsemblGRCm38mm10GRCm38
MGSCv371349,131,671 - 49,243,383 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361349,048,239 - 49,160,516 (-)NCBIMGSCv36mm8
Celera1350,126,696 - 50,238,177 (-)NCBICelera
Cytogenetic Map13A5NCBI
cM Map1325.07NCBI
Wnk2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81715,709,648 - 15,818,874 (+)NCBIGRCr8
mRatBN7.21715,503,672 - 15,612,479 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1715,504,261 - 15,612,479 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1715,390,684 - 15,499,052 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01716,995,723 - 17,104,089 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01715,317,444 - 15,425,805 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01715,923,508 - 16,032,271 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1715,924,048 - 16,032,420 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01717,986,985 - 18,095,251 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41721,461,980 - 21,600,361 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11721,462,134 - 21,600,354 (+)NCBI
Celera1715,234,024 - 15,342,287 (+)NCBICelera
Cytogenetic Map17p14NCBI
Wnk2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555154,729,347 - 4,852,920 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555154,730,647 - 4,852,920 (-)NCBIChiLan1.0ChiLan1.0
WNK2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21146,102,884 - 46,243,805 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1946,109,305 - 46,246,187 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0964,307,620 - 64,444,141 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1992,372,410 - 92,506,734 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl992,372,410 - 92,507,916 (+)Ensemblpanpan1.1panPan2
WNK2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1198,433,897 - 98,533,427 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl198,454,799 - 98,493,085 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha198,827,313 - 98,927,715 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0199,049,650 - 99,150,488 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl199,049,659 - 99,151,162 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1198,663,461 - 98,763,845 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0198,398,830 - 98,499,197 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0199,154,381 - 99,254,788 (-)NCBIUU_Cfam_GSD_1.0
Wnk2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049448,321,159 - 8,440,700 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364872,537,630 - 2,657,173 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364872,537,630 - 2,657,172 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
WNK2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl342,711,444 - 42,834,753 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1342,711,388 - 42,837,650 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2344,130,013 - 44,136,442 (-)NCBISscrofa10.2Sscrofa10.2susScr3
WNK2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.112103,574,377 - 103,713,502 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl12103,592,147 - 103,713,321 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603891,848,638 - 92,010,722 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Wnk2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248683,261,766 - 3,387,585 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248683,261,569 - 3,388,273 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in WNK2
115 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000050348] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.31-22.33(chr9:91596533-97018746)x1 copy number loss See cases [RCV000052916] Chr9:91596533..97018746 [GRCh38]
Chr9:94358815..99781028 [GRCh37]
Chr9:93398636..98820849 [NCBI36]
Chr9:9q22.31-22.33		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 copy number gain See cases [RCV000053746] Chr9:193412..138114463 [GRCh38]
Chr9:214367..141008915 [GRCh37]
Chr9:204367..140128736 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] Chr9:193412..138179445 [GRCh38]
Chr9:266045..141073897 [GRCh37]
Chr9:256045..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.31-22.33(chr9:92561720-98122580)x3 copy number gain See cases [RCV000053773] Chr9:92561720..98122580 [GRCh38]
Chr9:95324002..100884862 [GRCh37]
Chr9:94363823..99924683 [NCBI36]
Chr9:9q22.31-22.33		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 copy number gain See cases [RCV000053745] Chr9:193412..138124532 [GRCh38]
Chr9:204193..141018984 [GRCh37]
Chr9:194193..140138805 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3 copy number gain See cases [RCV000053752] Chr9:88522292..113687796 [GRCh38]
Chr9:91137207..116450076 [GRCh37]
Chr9:90327027..115489897 [NCBI36]
Chr9:9q22.1-32		 pathogenic
NM_006648.3(WNK2):c.1581C>T (p.Ile527=) single nucleotide variant Malignant melanoma [RCV000068749] Chr9:93247581 [GRCh38]
Chr9:96009863 [GRCh37]
Chr9:95049684 [NCBI36]
Chr9:9q22.31		 not provided
NM_006648.4(WNK2):c.6089G>A (p.Ser2030Asn) single nucleotide variant not specified [RCV004483065] Chr9:93299235 [GRCh38]
Chr9:96061517 [GRCh37]
Chr9:95101338 [NCBI36]
Chr9:9q22.31		 uncertain significance|not provided
NM_001282394.1(WNK2):c.5819+32G>T single nucleotide variant Lung cancer [RCV000108494] Chr9:93293205 [GRCh38]
Chr9:96055487 [GRCh37]
Chr9:9q22.31		 uncertain significance
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) copy number gain See cases [RCV000133791] Chr9:204193..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3 copy number gain See cases [RCV000136788] Chr9:68420430..106579493 [GRCh38]
Chr9:71130848..109341774 [GRCh37]
Chr9:70225166..108381595 [NCBI36]
Chr9:9q21.11-31.2		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 copy number gain See cases [RCV000138783] Chr9:193412..138124524 [GRCh38]
Chr9:204090..141018976 [GRCh37]
Chr9:194090..140138797 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000139207] Chr9:193412..138159073 [GRCh38]
Chr9:68420641..141053525 [GRCh37]
Chr9:67910461..140173346 [NCBI36]
Chr9:9p11.2-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000138962] Chr9:193412..138159073 [GRCh38]
Chr9:204104..141053525 [GRCh37]
Chr9:194104..140173346 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic|conflicting data from submitters
GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3 copy number gain See cases [RCV000139789] Chr9:69627642..111454304 [GRCh38]
Chr9:72242558..114216584 [GRCh37]
Chr9:71432378..113256405 [NCBI36]
Chr9:9q21.12-31.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 copy number gain See cases [RCV000141876] Chr9:203861..138125937 [GRCh38]
Chr9:203861..141020389 [GRCh37]
Chr9:193861..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 copy number gain See cases [RCV000143476] Chr9:203862..138125937 [GRCh38]
Chr9:203862..141020389 [GRCh37]
Chr9:193862..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000148113] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 copy number gain See cases [RCV000240081] Chr9:163131..141122114 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_006648.4(WNK2):c.2018A>G (p.Gln673Arg) single nucleotide variant not specified [RCV004318433] Chr9:93253066 [GRCh38]
Chr9:96015348 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4801dup (p.Asp1601fs) duplication Inborn genetic diseases [RCV000623597] Chr9:93289548..93289549 [GRCh38]
Chr9:96051830..96051831 [GRCh37]
Chr9:9q22.31		 likely pathogenic
NM_006648.4(WNK2):c.3983A>C (p.Glu1328Ala) single nucleotide variant not specified [RCV004282409] Chr9:93268696 [GRCh38]
Chr9:96030978 [GRCh37]
Chr9:9q22.31		 uncertain significance
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) copy number gain Global developmental delay [RCV000626548] Chr9:71069743..140999928 [GRCh37]
Chr9:9q21.11-34.3		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) copy number gain See cases [RCV000449375] Chr9:62525..141006407 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 copy number gain not specified [RCV003986800] Chr9:203861..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 copy number gain See cases [RCV000448978] Chr9:203864..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_006648.4(WNK2):c.3313G>A (p.Ala1105Thr) single nucleotide variant not specified [RCV004308174] Chr9:93262060 [GRCh38]
Chr9:96024342 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5114C>T (p.Pro1705Leu) single nucleotide variant not specified [RCV004328727] Chr9:93292579 [GRCh38]
Chr9:96054861 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1790A>G (p.His597Arg) single nucleotide variant not specified [RCV004316134] Chr9:93247790 [GRCh38]
Chr9:96010072 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.407C>T (p.Ala136Val) single nucleotide variant not specified [RCV004308935] Chr9:93185336 [GRCh38]
Chr9:95947618 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3635A>G (p.Lys1212Arg) single nucleotide variant not specified [RCV004311913] Chr9:93263972 [GRCh38]
Chr9:96026254 [GRCh37]
Chr9:9q22.31		 uncertain significance
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) copy number gain See cases [RCV000512392] Chr9:203862..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q22.31(chr9:94907633-96493970)x1 copy number loss not provided [RCV000683156] Chr9:94907633..96493970 [GRCh37]
Chr9:9q22.31		 uncertain significance
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 copy number gain not provided [RCV000748053] Chr9:10590..141107672 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 copy number gain not provided [RCV000748063] Chr9:46587..141066491 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 copy number gain not provided [RCV000748054] Chr9:10590..141114095 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_006648.4(WNK2):c.1076-9C>T single nucleotide variant not provided [RCV000961955] Chr9:93234799 [GRCh38]
Chr9:95997081 [GRCh37]
Chr9:9q22.31		 benign
NM_006648.4(WNK2):c.4230G>A (p.Ala1410=) single nucleotide variant not provided [RCV000967134] Chr9:93288984 [GRCh38]
Chr9:96051266 [GRCh37]
Chr9:9q22.31		 benign
NM_006648.4(WNK2):c.6327G>A (p.Ala2109=) single nucleotide variant not provided [RCV000968150] Chr9:93308395 [GRCh38]
Chr9:96070677 [GRCh37]
Chr9:9q22.31		 benign
NM_006648.4(WNK2):c.3966C>T (p.Pro1322=) single nucleotide variant not provided [RCV000967133] Chr9:93268679 [GRCh38]
Chr9:96030961 [GRCh37]
Chr9:9q22.31		 benign
GRCh37/hg19 9q21.2-22.32(chr9:79520825-97201274) copy number gain not provided [RCV000767645] Chr9:79520825..97201274 [GRCh37]
Chr9:9q21.2-22.32		 pathogenic
NM_006648.4(WNK2):c.531G>C (p.Glu177Asp) single nucleotide variant not specified [RCV004302232] Chr9:93185460 [GRCh38]
Chr9:95947742 [GRCh37]
Chr9:9q22.31		 uncertain significance
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 copy number gain not provided [RCV000845900] Chr9:203861..141020388 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 copy number gain not provided [RCV000847808] Chr9:71416475..141020389 [GRCh37]
Chr9:9q21.11-34.3		 pathogenic
NM_006648.4(WNK2):c.4277T>C (p.Leu1426Pro) single nucleotide variant not specified [RCV004332780] Chr9:93289031 [GRCh38]
Chr9:96051313 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.2112G>C (p.Met704Ile) single nucleotide variant not specified [RCV004292292] Chr9:93256376 [GRCh38]
Chr9:96018658 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.349G>A (p.Glu117Lys) single nucleotide variant not specified [RCV004284350] Chr9:93185278 [GRCh38]
Chr9:95947560 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1999C>G (p.Pro667Ala) single nucleotide variant not specified [RCV004296110] Chr9:93253047 [GRCh38]
Chr9:96015329 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5545C>T (p.Arg1849Trp) single nucleotide variant not provided [RCV000883513] Chr9:93293010 [GRCh38]
Chr9:96055292 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.2190+7G>A single nucleotide variant not provided [RCV000959075] Chr9:93256461 [GRCh38]
Chr9:96018743 [GRCh37]
Chr9:9q22.31		 benign
NM_006648.4(WNK2):c.2272C>A (p.His758Asn) single nucleotide variant not provided [RCV000951100] Chr9:93257029 [GRCh38]
Chr9:96019311 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.2723G>C (p.Gly908Ala) single nucleotide variant not provided [RCV000956732] Chr9:93259271 [GRCh38]
Chr9:96021553 [GRCh37]
Chr9:9q22.31		 benign
NM_006648.4(WNK2):c.4549C>T (p.Pro1517Ser) single nucleotide variant not specified [RCV004313601] Chr9:93289303 [GRCh38]
Chr9:96051585 [GRCh37]
Chr9:9q22.31		 uncertain significance
NC_000009.11:g.12246100_101559378inv inversion Recurrent spontaneous abortion [RCV000999471] Chr9:12246100..101559378 [GRCh37]
Chr9:9p23-q22.33		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) copy number gain not specified [RCV002053823] Chr9:353349..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410) copy number gain not specified [RCV002053853] Chr9:71349994..122603410 [GRCh37]
Chr9:9q21.11-33.2		 likely pathogenic
GRCh37/hg19 9q22.2-31.1(chr9:93864974-106661581)x1 copy number loss Gorlin syndrome [RCV002279743] Chr9:93864974..106661581 [GRCh37]
Chr9:9q22.2-31.1		 pathogenic
GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311) copy number loss Distal tetrasomy 15q [RCV002280776] Chr9:19356861..119513311 [GRCh37]
Chr9:9p22.1-q33.1		 uncertain significance
GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3 copy number gain See cases [RCV002292402] Chr9:203861..131603223 [GRCh37]
Chr9:9p24.3-q34.11		 pathogenic
NM_006648.4(WNK2):c.3757G>A (p.Val1253Ile) single nucleotide variant not specified [RCV004321111] Chr9:93267806 [GRCh38]
Chr9:96030088 [GRCh37]
Chr9:9q22.31		 uncertain significance
GRCh37/hg19 9q22.31-22.32(chr9:95711603-98469214)x1 copy number loss not provided [RCV002474678] Chr9:95711603..98469214 [GRCh37]
Chr9:9q22.31-22.32		 pathogenic
NM_006648.4(WNK2):c.6563C>T (p.Ala2188Val) single nucleotide variant not specified [RCV004195802] Chr9:93317566 [GRCh38]
Chr9:96079848 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4660G>A (p.Glu1554Lys) single nucleotide variant not specified [RCV004158277] Chr9:93289414 [GRCh38]
Chr9:96051696 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1430G>A (p.Arg477Lys) single nucleotide variant not specified [RCV004126487] Chr9:93239864 [GRCh38]
Chr9:96002146 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4496T>A (p.Leu1499Gln) single nucleotide variant not specified [RCV004217699] Chr9:93289250 [GRCh38]
Chr9:96051532 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4832C>T (p.Ala1611Val) single nucleotide variant not specified [RCV004135639] Chr9:93289586 [GRCh38]
Chr9:96051868 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2105C>T (p.Pro702Leu) single nucleotide variant not specified [RCV004218508] Chr9:93256369 [GRCh38]
Chr9:96018651 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1963C>G (p.Pro655Ala) single nucleotide variant not specified [RCV004188960] Chr9:93253011 [GRCh38]
Chr9:96015293 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2558C>T (p.Ala853Val) single nucleotide variant not specified [RCV004121244] Chr9:93259106 [GRCh38]
Chr9:96021388 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2602C>T (p.Pro868Ser) single nucleotide variant not specified [RCV004223666] Chr9:93259150 [GRCh38]
Chr9:96021432 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5444G>A (p.Arg1815Gln) single nucleotide variant not specified [RCV004095164] Chr9:93292909 [GRCh38]
Chr9:96055191 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5094A>T (p.Glu1698Asp) single nucleotide variant not specified [RCV004233063] Chr9:93292559 [GRCh38]
Chr9:96054841 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4348G>A (p.Val1450Met) single nucleotide variant not specified [RCV004138335] Chr9:93289102 [GRCh38]
Chr9:96051384 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5042T>C (p.Val1681Ala) single nucleotide variant not specified [RCV004080603] Chr9:93292507 [GRCh38]
Chr9:96054789 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.3014T>C (p.Leu1005Pro) single nucleotide variant not specified [RCV004225873] Chr9:93259562 [GRCh38]
Chr9:96021844 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3363G>T (p.Glu1121Asp) single nucleotide variant not specified [RCV004160734] Chr9:93262672 [GRCh38]
Chr9:96024954 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2990C>T (p.Ala997Val) single nucleotide variant not specified [RCV004196818] Chr9:93259538 [GRCh38]
Chr9:96021820 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4291G>C (p.Glu1431Gln) single nucleotide variant not specified [RCV004234474] Chr9:93289045 [GRCh38]
Chr9:96051327 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3124G>A (p.Val1042Met) single nucleotide variant not specified [RCV004186667] Chr9:93261871 [GRCh38]
Chr9:96024153 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5606G>A (p.Ser1869Asn) single nucleotide variant not specified [RCV004140804] Chr9:93293071 [GRCh38]
Chr9:96055353 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2680G>A (p.Val894Met) single nucleotide variant not specified [RCV004236603] Chr9:93259228 [GRCh38]
Chr9:96021510 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1532C>T (p.Ala511Val) single nucleotide variant not specified [RCV004145639] Chr9:93239966 [GRCh38]
Chr9:96002248 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5029G>A (p.Val1677Ile) single nucleotide variant not specified [RCV004160710] Chr9:93292494 [GRCh38]
Chr9:96054776 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.6623C>T (p.Thr2208Ile) single nucleotide variant not specified [RCV004132498] Chr9:93317626 [GRCh38]
Chr9:96079908 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2996C>T (p.Pro999Leu) single nucleotide variant not specified [RCV004134989] Chr9:93259544 [GRCh38]
Chr9:96021826 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.6601G>A (p.Ala2201Thr) single nucleotide variant not specified [RCV004093345] Chr9:93317604 [GRCh38]
Chr9:96079886 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.2836C>T (p.Pro946Ser) single nucleotide variant not specified [RCV004148362] Chr9:93259384 [GRCh38]
Chr9:96021666 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2562G>C (p.Leu854Phe) single nucleotide variant not specified [RCV004186556] Chr9:93259110 [GRCh38]
Chr9:96021392 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4403C>T (p.Ala1468Val) single nucleotide variant not specified [RCV004117404] Chr9:93289157 [GRCh38]
Chr9:96051439 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2488C>A (p.Pro830Thr) single nucleotide variant not specified [RCV004227448] Chr9:93259036 [GRCh38]
Chr9:96021318 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5347G>A (p.Asp1783Asn) single nucleotide variant not specified [RCV004229118] Chr9:93292812 [GRCh38]
Chr9:96055094 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4273G>A (p.Gly1425Arg) single nucleotide variant not specified [RCV004147673] Chr9:93289027 [GRCh38]
Chr9:96051309 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4438C>T (p.Pro1480Ser) single nucleotide variant not specified [RCV004208245] Chr9:93289192 [GRCh38]
Chr9:96051474 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3245G>A (p.Ser1082Asn) single nucleotide variant not specified [RCV004121573] Chr9:93261992 [GRCh38]
Chr9:96024274 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.412G>A (p.Ala138Thr) single nucleotide variant not specified [RCV004101963] Chr9:93185341 [GRCh38]
Chr9:95947623 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5537G>A (p.Arg1846Lys) single nucleotide variant not specified [RCV004245177] Chr9:93293002 [GRCh38]
Chr9:96055284 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4319A>T (p.His1440Leu) single nucleotide variant not specified [RCV004078718] Chr9:93289073 [GRCh38]
Chr9:96051355 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4433C>G (p.Pro1478Arg) single nucleotide variant not specified [RCV004212660] Chr9:93289187 [GRCh38]
Chr9:96051469 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.6605C>T (p.Pro2202Leu) single nucleotide variant not specified [RCV004176555] Chr9:93317608 [GRCh38]
Chr9:96079890 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4888C>T (p.Pro1630Ser) single nucleotide variant not specified [RCV004210911] Chr9:93289999 [GRCh38]
Chr9:96052281 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.260A>G (p.Glu87Gly) single nucleotide variant not specified [RCV004204630] Chr9:93185189 [GRCh38]
Chr9:95947471 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5099C>T (p.Ser1700Leu) single nucleotide variant not specified [RCV004185628] Chr9:93292564 [GRCh38]
Chr9:96054846 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.1913G>A (p.Gly638Asp) single nucleotide variant not specified [RCV004201976] Chr9:93252961 [GRCh38]
Chr9:96015243 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3289C>T (p.Pro1097Ser) single nucleotide variant not specified [RCV004074794] Chr9:93262036 [GRCh38]
Chr9:96024318 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2473G>C (p.Val825Leu) single nucleotide variant not specified [RCV004115068] Chr9:93259021 [GRCh38]
Chr9:96021303 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5090G>C (p.Gly1697Ala) single nucleotide variant not specified [RCV004108725] Chr9:93292555 [GRCh38]
Chr9:96054837 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.232C>T (p.Leu78Phe) single nucleotide variant not specified [RCV004080701] Chr9:93185161 [GRCh38]
Chr9:95947443 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4831G>A (p.Ala1611Thr) single nucleotide variant not specified [RCV004172410] Chr9:93289585 [GRCh38]
Chr9:96051867 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4625T>G (p.Val1542Gly) single nucleotide variant not specified [RCV004132168] Chr9:93289379 [GRCh38]
Chr9:96051661 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2593C>G (p.Pro865Ala) single nucleotide variant not specified [RCV004141043] Chr9:93259141 [GRCh38]
Chr9:96021423 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.6616G>A (p.Val2206Met) single nucleotide variant not specified [RCV004138503] Chr9:93317619 [GRCh38]
Chr9:96079901 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.707G>A (p.Arg236Gln) single nucleotide variant not specified [RCV004145181] Chr9:93229721 [GRCh38]
Chr9:95992003 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2707G>A (p.Val903Met) single nucleotide variant not specified [RCV004102141] Chr9:93259255 [GRCh38]
Chr9:96021537 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4454A>G (p.His1485Arg) single nucleotide variant not specified [RCV004213664] Chr9:93289208 [GRCh38]
Chr9:96051490 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5456C>T (p.Pro1819Leu) single nucleotide variant not specified [RCV004203955] Chr9:93292921 [GRCh38]
Chr9:96055203 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2030C>T (p.Ala677Val) single nucleotide variant not specified [RCV004129636] Chr9:93253078 [GRCh38]
Chr9:96015360 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2444C>T (p.Pro815Leu) single nucleotide variant not specified [RCV004089310] Chr9:93258992 [GRCh38]
Chr9:96021274 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.380A>C (p.Asp127Ala) single nucleotide variant not specified [RCV004093865] Chr9:93185309 [GRCh38]
Chr9:95947591 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2162C>T (p.Pro721Leu) single nucleotide variant not specified [RCV004098693] Chr9:93256426 [GRCh38]
Chr9:96018708 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1931C>T (p.Ala644Val) single nucleotide variant not specified [RCV004223068] Chr9:93252979 [GRCh38]
Chr9:96015261 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2068G>C (p.Ala690Pro) single nucleotide variant not specified [RCV004330023] Chr9:93256332 [GRCh38]
Chr9:96018614 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.6106C>T (p.Arg2036Cys) single nucleotide variant not specified [RCV004253902] Chr9:93299252 [GRCh38]
Chr9:96061534 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2337G>T (p.Gln779His) single nucleotide variant not specified [RCV004255208] Chr9:93257094 [GRCh38]
Chr9:96019376 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.6523G>A (p.Ala2175Thr) single nucleotide variant not specified [RCV004276797] Chr9:93317526 [GRCh38]
Chr9:96079808 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.2208G>T (p.Gln736His) single nucleotide variant not specified [RCV004277189] Chr9:93256965 [GRCh38]
Chr9:96019247 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.509G>C (p.Arg170Pro) single nucleotide variant not specified [RCV004251384] Chr9:93185438 [GRCh38]
Chr9:95947720 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3890A>G (p.Asn1297Ser) single nucleotide variant not specified [RCV004278424] Chr9:93268042 [GRCh38]
Chr9:96030324 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.263G>T (p.Arg88Leu) single nucleotide variant not specified [RCV004250816] Chr9:93185192 [GRCh38]
Chr9:95947474 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2251C>G (p.Pro751Ala) single nucleotide variant not specified [RCV004272036] Chr9:93257008 [GRCh38]
Chr9:96019290 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3862G>A (p.Gly1288Arg) single nucleotide variant not specified [RCV004259018] Chr9:93267911 [GRCh38]
Chr9:96030193 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.6031C>A (p.Gln2011Lys) single nucleotide variant not specified [RCV004267732] Chr9:93299177 [GRCh38]
Chr9:96061459 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5702G>A (p.Arg1901Gln) single nucleotide variant not specified [RCV004335272] Chr9:93293167 [GRCh38]
Chr9:96055449 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2060C>T (p.Pro687Leu) single nucleotide variant not specified [RCV004337656] Chr9:93256324 [GRCh38]
Chr9:96018606 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2050G>A (p.Gly684Ser) single nucleotide variant not specified [RCV004359694] Chr9:93256314 [GRCh38]
Chr9:96018596 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4931T>C (p.Met1644Thr) single nucleotide variant not specified [RCV004341421] Chr9:93290042 [GRCh38]
Chr9:96052324 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2924C>T (p.Pro975Leu) single nucleotide variant not specified [RCV004357530] Chr9:93259472 [GRCh38]
Chr9:96021754 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1573G>A (p.Val525Ile) single nucleotide variant not specified [RCV004350103] Chr9:93247573 [GRCh38]
Chr9:96009855 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1610C>G (p.Ala537Gly) single nucleotide variant not specified [RCV004354639] Chr9:93247610 [GRCh38]
Chr9:96009892 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4295C>T (p.Thr1432Met) single nucleotide variant not specified [RCV004343072] Chr9:93289049 [GRCh38]
Chr9:96051331 [GRCh37]
Chr9:9q22.31		 uncertain significance
Single allele deletion not provided [RCV003448676] Chr9:92679543..109378847 [GRCh37]
Chr9:9q22.2-31.2		 pathogenic
NM_006648.4(WNK2):c.3138G>C (p.Pro1046=) single nucleotide variant not provided [RCV003425710] Chr9:93261885 [GRCh38]
Chr9:96024167 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.3924C>T (p.Thr1308=) single nucleotide variant not provided [RCV003425711] Chr9:93268637 [GRCh38]
Chr9:96030919 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.3971C>T (p.Pro1324Leu) single nucleotide variant not specified [RCV004483043] Chr9:93268684 [GRCh38]
Chr9:96030966 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.40C>G (p.Leu14Val) single nucleotide variant not specified [RCV004483044] Chr9:93184969 [GRCh38]
Chr9:95947251 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4333G>T (p.Ala1445Ser) single nucleotide variant not specified [RCV004483045] Chr9:93289087 [GRCh38]
Chr9:96051369 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4379C>T (p.Pro1460Leu) single nucleotide variant not specified [RCV004483046] Chr9:93289133 [GRCh38]
Chr9:96051415 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.4490C>T (p.Ala1497Val) single nucleotide variant not specified [RCV004483047] Chr9:93289244 [GRCh38]
Chr9:96051526 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.451G>C (p.Val151Leu) single nucleotide variant not specified [RCV004483048] Chr9:93185380 [GRCh38]
Chr9:95947662 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4780C>T (p.Arg1594Cys) single nucleotide variant not specified [RCV004483049] Chr9:93289534 [GRCh38]
Chr9:96051816 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.487C>T (p.Pro163Ser) single nucleotide variant not specified [RCV004483050] Chr9:93185416 [GRCh38]
Chr9:95947698 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.4880A>T (p.Glu1627Val) single nucleotide variant not specified [RCV004483051] Chr9:93289991 [GRCh38]
Chr9:96052273 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5054G>A (p.Arg1685His) single nucleotide variant not specified [RCV004483052] Chr9:93292519 [GRCh38]
Chr9:96054801 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.5075A>T (p.Asp1692Val) single nucleotide variant not specified [RCV004483053] Chr9:93292540 [GRCh38]
Chr9:96054822 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5123T>C (p.Met1708Thr) single nucleotide variant not specified [RCV004483054] Chr9:93292588 [GRCh38]
Chr9:96054870 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.512A>C (p.Asp171Ala) single nucleotide variant not specified [RCV004483055] Chr9:93185441 [GRCh38]
Chr9:95947723 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5221C>T (p.Pro1741Ser) single nucleotide variant not specified [RCV004483056] Chr9:93292686 [GRCh38]
Chr9:96054968 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5257A>C (p.Thr1753Pro) single nucleotide variant not specified [RCV004483057] Chr9:93292722 [GRCh38]
Chr9:96055004 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5317G>A (p.Val1773Ile) single nucleotide variant not specified [RCV004483058] Chr9:93292782 [GRCh38]
Chr9:96055064 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5333C>A (p.Ala1778Asp) single nucleotide variant not specified [RCV004483059] Chr9:93292798 [GRCh38]
Chr9:96055080 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5413G>A (p.Val1805Met) single nucleotide variant not specified [RCV004483060] Chr9:93292878 [GRCh38]
Chr9:96055160 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5462A>G (p.Gln1821Arg) single nucleotide variant not specified [RCV004483061] Chr9:93292927 [GRCh38]
Chr9:96055209 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5474C>T (p.Ser1825Phe) single nucleotide variant not specified [RCV004483062] Chr9:93292939 [GRCh38]
Chr9:96055221 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5513A>G (p.Lys1838Arg) single nucleotide variant not specified [RCV004483063] Chr9:93292978 [GRCh38]
Chr9:96055260 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.5908G>A (p.Val1970Met) single nucleotide variant not specified [RCV004483064] Chr9:93298052 [GRCh38]
Chr9:96060334 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.6584C>T (p.Thr2195Met) single nucleotide variant not specified [RCV004483066] Chr9:93317587 [GRCh38]
Chr9:96079869 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.872A>G (p.Lys291Arg) single nucleotide variant not specified [RCV004483067] Chr9:93230905 [GRCh38]
Chr9:95993187 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1720C>A (p.Gln574Lys) single nucleotide variant not specified [RCV004483025] Chr9:93247720 [GRCh38]
Chr9:96010002 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1910T>C (p.Leu637Pro) single nucleotide variant not specified [RCV004483026] Chr9:93252958 [GRCh38]
Chr9:96015240 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.1922C>A (p.Ala641Asp) single nucleotide variant not specified [RCV004483027] Chr9:93252970 [GRCh38]
Chr9:96015252 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2078C>T (p.Pro693Leu) single nucleotide variant not specified [RCV004483028] Chr9:93256342 [GRCh38]
Chr9:96018624 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2270C>T (p.Pro757Leu) single nucleotide variant not specified [RCV004483029] Chr9:93257027 [GRCh38]
Chr9:96019309 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2282C>T (p.Pro761Leu) single nucleotide variant not specified [RCV004483030] Chr9:93257039 [GRCh38]
Chr9:96019321 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2305G>A (p.Val769Met) single nucleotide variant not specified [RCV004483031] Chr9:93257062 [GRCh38]
Chr9:96019344 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2360C>A (p.Pro787Gln) single nucleotide variant not specified [RCV004483032] Chr9:93257117 [GRCh38]
Chr9:96019399 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2434G>A (p.Gly812Ser) single nucleotide variant not specified [RCV004483033] Chr9:93258982 [GRCh38]
Chr9:96021264 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.2624C>T (p.Thr875Ile) single nucleotide variant not specified [RCV004483035] Chr9:93259172 [GRCh38]
Chr9:96021454 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2642C>T (p.Pro881Leu) single nucleotide variant not specified [RCV004483036] Chr9:93259190 [GRCh38]
Chr9:96021472 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.2989G>A (p.Ala997Thr) single nucleotide variant not specified [RCV004483037] Chr9:93259537 [GRCh38]
Chr9:96021819 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3365A>G (p.Gln1122Arg) single nucleotide variant not specified [RCV004483039] Chr9:93262674 [GRCh38]
Chr9:96024956 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3466G>A (p.Ala1156Thr) single nucleotide variant not specified [RCV004483040] Chr9:93263621 [GRCh38]
Chr9:96025903 [GRCh37]
Chr9:9q22.31		 likely benign
NM_006648.4(WNK2):c.3530C>T (p.Ala1177Val) single nucleotide variant not specified [RCV004483041] Chr9:93263685 [GRCh38]
Chr9:96025967 [GRCh37]
Chr9:9q22.31		 uncertain significance
NM_006648.4(WNK2):c.3721G>A (p.Ala1241Thr) single nucleotide variant not specified [RCV004483042] Chr9:93267770 [GRCh38]
Chr9:96030052 [GRCh37]
Chr9:9q22.31		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:8930
Count of miRNA genes:1290
Interacting mature miRNAs:1664
Transcripts:ENST00000297954, ENST00000349097, ENST00000356055, ENST00000395475, ENST00000395477, ENST00000411624, ENST00000427277, ENST00000432730, ENST00000448039, ENST00000448251, ENST00000453718, ENST00000460335, ENST00000462595, ENST00000464625, ENST00000467401, ENST00000471076, ENST00000474009, ENST00000478583, ENST00000479696
Prediction methods:Microtar, 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
D9S1803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37996,073,834 - 96,073,985UniSTSGRCh37
Build 36995,113,655 - 95,113,806RGDNCBI36
Celera966,516,050 - 66,516,215RGD
Cytogenetic Map9q22UniSTS
HuRef965,751,250 - 65,751,415UniSTS
HuRef342,683,108 - 42,683,577UniSTS
Marshfield Genetic Map9100.74RGD
Marshfield Genetic Map9100.74UniSTS
Genethon Genetic Map9100.4UniSTS
TNG Radiation Hybrid Map934752.0UniSTS
deCODE Assembly Map996.58UniSTS
SGC30759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37996,075,528 - 96,075,657UniSTSGRCh37
Build 36995,115,349 - 95,115,478RGDNCBI36
Celera966,517,758 - 66,517,887RGD
Cytogenetic Map9q22.3UniSTS
HuRef965,752,958 - 65,753,087UniSTS
GeneMap99-GB4 RH Map9305.32UniSTS
Whitehead-RH Map9347.7UniSTS
NCBI RH Map9793.7UniSTS
SHGC-58613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37996,046,942 - 96,047,058UniSTSGRCh37
Build 36995,086,763 - 95,086,879RGDNCBI36
Celera966,489,158 - 66,489,274RGD
Cytogenetic Map9q22.3UniSTS
HuRef965,724,407 - 65,724,523UniSTS
RH66306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37996,081,299 - 96,081,424UniSTSGRCh37
Build 36995,121,120 - 95,121,245RGDNCBI36
Celera966,523,519 - 66,523,644RGD
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9q22.3UniSTS
HuRef965,758,721 - 65,758,846UniSTS
GeneMap99-GB4 RH Map9305.42UniSTS
IB543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37996,081,302 - 96,081,429UniSTSGRCh37
Build 36995,121,123 - 95,121,250RGDNCBI36
Celera966,523,522 - 66,523,649RGD
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9q22.3UniSTS
HuRef965,758,724 - 65,758,851UniSTS
GeneMap99-GB4 RH Map9305.42UniSTS
Whitehead-RH Map9346.2UniSTS
WI-15809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37996,080,507 - 96,080,631UniSTSGRCh37
Build 36995,120,328 - 95,120,452RGDNCBI36
Celera966,522,727 - 66,522,851RGD
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9q22.3UniSTS
HuRef965,757,929 - 65,758,053UniSTS
GeneMap99-GB4 RH Map9305.39UniSTS
Whitehead-RH Map9347.7UniSTS
NCBI RH Map9793.7UniSTS


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
High
Medium 2005 902 312 174 196 32 2018 1851 1825 27 495 101 144 19 1369
Low 412 1061 1203 268 398 255 2030 316 1832 145 906 1257 21 782 1402 4
Below cutoff 9 1010 175 157 811 154 280 14 20 183 38 226 6 1 403 17

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001282394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005252137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005252140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005252144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518928 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015045 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015047 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015048 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015049 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423744 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423748 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423752 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423753 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423758 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423759 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423765 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423767 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423775 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423778 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363595 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363596 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363597 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363600 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363601 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363602 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB044546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB051547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839164 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF039702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ242724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK124314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL354991 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL390760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL583839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC037965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY151846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000297954   ⟹   ENSP00000297954
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,184,122 - 93,319,205 (+)Ensembl
RefSeq Acc Id: ENST00000395477   ⟹   ENSP00000378860
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,184,930 - 93,320,572 (+)Ensembl
RefSeq Acc Id: ENST00000411624   ⟹   ENSP00000414622
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,234,923 - 93,319,208 (+)Ensembl
RefSeq Acc Id: ENST00000427277   ⟹   ENSP00000411181
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,184,139 - 93,320,569 (+)Ensembl
RefSeq Acc Id: ENST00000432730   ⟹   ENSP00000415038
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,184,930 - 93,319,204 (+)Ensembl
RefSeq Acc Id: ENST00000448039   ⟹   ENSP00000412465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,184,930 - 93,259,075 (+)Ensembl
RefSeq Acc Id: ENST00000448251   ⟹   ENSP00000390441
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,263,948 - 93,320,572 (+)Ensembl
RefSeq Acc Id: ENST00000453718   ⟹   ENSP00000413325
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,289,187 - 93,308,584 (+)Ensembl
RefSeq Acc Id: ENST00000460335
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,308,501 - 93,309,195 (+)Ensembl
RefSeq Acc Id: ENST00000462595
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,267,020 - 93,267,815 (+)Ensembl
RefSeq Acc Id: ENST00000464625
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,256,726 - 93,259,251 (+)Ensembl
RefSeq Acc Id: ENST00000467401
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,306,637 - 93,320,564 (+)Ensembl
RefSeq Acc Id: ENST00000471076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,315,488 - 93,320,566 (+)Ensembl
RefSeq Acc Id: ENST00000474009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,293,089 - 93,308,588 (+)Ensembl
RefSeq Acc Id: ENST00000478583
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,263,266 - 93,268,040 (+)Ensembl
RefSeq Acc Id: ENST00000479696
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,293,133 - 93,300,326 (+)Ensembl
RefSeq Acc Id: ENST00000693671
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl993,204,975 - 93,247,571 (+)Ensembl
RefSeq Acc Id: NM_001282394   ⟹   NP_001269323
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
HuRef965,623,639 - 65,760,276 (+)NCBI
CHM1_1996,093,815 - 96,228,692 (+)NCBI
T2T-CHM13v2.09105,350,754 - 105,486,591 (+)NCBI
Sequence:
RefSeq Acc Id: NM_006648   ⟹   NP_006639
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
GRCh37995,946,437 - 96,082,854 (+)NCBI
Build 36994,987,033 - 95,122,675 (+)NCBI Archive
Celera966,388,916 - 66,525,074 (+)RGD
HuRef965,623,639 - 65,760,276 (+)RGD
CHM1_1996,093,815 - 96,229,891 (+)NCBI
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005252137   ⟹   XP_005252194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
GRCh37995,946,437 - 96,082,854 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005252140   ⟹   XP_005252197
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
GRCh37995,946,437 - 96,082,854 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005252144   ⟹   XP_005252201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,309,196 (+)NCBI
GRCh37995,946,437 - 96,082,854 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015045   ⟹   XP_016870534
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015047   ⟹   XP_016870536
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015048   ⟹   XP_016870537
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015049   ⟹   XP_016870538
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015050   ⟹   XP_016870539
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015051   ⟹   XP_016870540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015052   ⟹   XP_016870541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015053   ⟹   XP_016870542
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015054   ⟹   XP_016870543
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015055   ⟹   XP_016870544
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047423741   ⟹   XP_047279697
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423742   ⟹   XP_047279698
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423743   ⟹   XP_047279699
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423744   ⟹   XP_047279700
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423745   ⟹   XP_047279701
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423746   ⟹   XP_047279702
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_047423747   ⟹   XP_047279703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423748   ⟹   XP_047279704
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423749   ⟹   XP_047279705
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423750   ⟹   XP_047279706
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423751   ⟹   XP_047279707
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423752   ⟹   XP_047279708
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423753   ⟹   XP_047279709
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423754   ⟹   XP_047279710
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423756   ⟹   XP_047279712
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423757   ⟹   XP_047279713
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423758   ⟹   XP_047279714
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423759   ⟹   XP_047279715
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_047423760   ⟹   XP_047279716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_047423761   ⟹   XP_047279717
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423762   ⟹   XP_047279718
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423763   ⟹   XP_047279719
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_047423764   ⟹   XP_047279720
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423765   ⟹   XP_047279721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423767   ⟹   XP_047279723
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423768   ⟹   XP_047279724
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423769   ⟹   XP_047279725
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_047423770   ⟹   XP_047279726
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423771   ⟹   XP_047279727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,139 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423772   ⟹   XP_047279728
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,201,922 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_047423773   ⟹   XP_047279729
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,201,922 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423774   ⟹   XP_047279730
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,201,922 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423775   ⟹   XP_047279731
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,201,922 - 93,319,208 (+)NCBI
RefSeq Acc Id: XM_047423776   ⟹   XP_047279732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,201,922 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_047423778   ⟹   XP_047279734
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,201,922 - 93,320,569 (+)NCBI
RefSeq Acc Id: XM_047423779   ⟹   XP_047279735
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,201,922 - 93,309,196 (+)NCBI
RefSeq Acc Id: XM_054363573   ⟹   XP_054219548
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363574   ⟹   XP_054219549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363575   ⟹   XP_054219550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363576   ⟹   XP_054219551
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363577   ⟹   XP_054219552
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363578   ⟹   XP_054219553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363579   ⟹   XP_054219554
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363580   ⟹   XP_054219555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363581   ⟹   XP_054219556
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363582   ⟹   XP_054219557
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363583   ⟹   XP_054219558
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363584   ⟹   XP_054219559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363585   ⟹   XP_054219560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363586   ⟹   XP_054219561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363587   ⟹   XP_054219562
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363588   ⟹   XP_054219563
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363589   ⟹   XP_054219564
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363590   ⟹   XP_054219565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363591   ⟹   XP_054219566
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363592   ⟹   XP_054219567
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363593   ⟹   XP_054219568
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363594   ⟹   XP_054219569
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363595   ⟹   XP_054219570
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363596   ⟹   XP_054219571
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363597   ⟹   XP_054219572
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363598   ⟹   XP_054219573
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363599   ⟹   XP_054219574
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363600   ⟹   XP_054219575
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363601   ⟹   XP_054219576
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363602   ⟹   XP_054219577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363603   ⟹   XP_054219578
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363604   ⟹   XP_054219579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363605   ⟹   XP_054219580
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363606   ⟹   XP_054219581
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363607   ⟹   XP_054219582
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363608   ⟹   XP_054219583
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363609   ⟹   XP_054219584
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363610   ⟹   XP_054219585
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363611   ⟹   XP_054219586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363612   ⟹   XP_054219587
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363613   ⟹   XP_054219588
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363614   ⟹   XP_054219589
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,350,754 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363615   ⟹   XP_054219590
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,368,455 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363616   ⟹   XP_054219591
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,368,455 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363617   ⟹   XP_054219592
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,368,455 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363618   ⟹   XP_054219593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,368,455 - 105,486,593 (+)NCBI
RefSeq Acc Id: XM_054363619   ⟹   XP_054219594
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,368,455 - 105,476,573 (+)NCBI
RefSeq Acc Id: XM_054363620   ⟹   XP_054219595
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,368,455 - 105,487,952 (+)NCBI
RefSeq Acc Id: XM_054363621   ⟹   XP_054219596
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09105,368,455 - 105,476,573 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001269323 (Get FASTA)   NCBI Sequence Viewer  
  NP_006639 (Get FASTA)   NCBI Sequence Viewer  
  XP_005252194 (Get FASTA)   NCBI Sequence Viewer  
  XP_005252197 (Get FASTA)   NCBI Sequence Viewer  
  XP_005252201 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870534 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870536 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870537 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870538 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870539 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870540 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870541 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870542 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870543 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870544 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279697 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279698 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279699 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279700 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279701 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279702 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279703 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279704 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279705 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279706 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279707 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279708 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279709 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279710 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279712 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279713 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279714 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279715 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279716 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279717 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279718 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279719 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279720 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279721 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279723 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279724 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279725 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279726 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279727 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279728 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279729 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279730 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279731 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279732 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279734 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279735 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219548 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219549 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219550 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219551 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219552 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219553 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219554 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219555 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219556 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219557 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219558 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219559 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219560 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219561 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219562 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219563 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219564 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219565 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219566 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219567 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219568 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219569 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219570 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219571 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219572 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219573 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219574 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219575 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219576 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219577 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219578 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219579 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219580 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219581 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219582 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219583 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219584 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219585 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219586 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219587 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219588 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219589 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219590 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219591 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219592 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219593 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219594 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219595 (Get FASTA)   NCBI Sequence Viewer  
  XP_054219596 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC18051 (Get FASTA)   NCBI Sequence Viewer  
  AAH37965 (Get FASTA)   NCBI Sequence Viewer  
  BAB18648 (Get FASTA)   NCBI Sequence Viewer  
  BAB21851 (Get FASTA)   NCBI Sequence Viewer  
  CAB44308 (Get FASTA)   NCBI Sequence Viewer  
  EAW62857 (Get FASTA)   NCBI Sequence Viewer  
  EAW62858 (Get FASTA)   NCBI Sequence Viewer  
  EAW62859 (Get FASTA)   NCBI Sequence Viewer  
  EAW62860 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000297954
  ENSP00000297954.4
  ENSP00000378860.2
  ENSP00000411181
  ENSP00000411181.4
  ENSP00000412465.1
  ENSP00000413325.1
  ENSP00000414622
  ENSP00000414622.1
  ENSP00000415038
  ENSP00000415038.2
GenBank Protein Q9Y3S1 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_006639   ⟸   NM_006648
- Peptide Label: isoform 2
- UniProtKB: F8W9F9 (UniProtKB/TrEMBL),   E9PCD1 (UniProtKB/TrEMBL),   H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005252197   ⟸   XM_005252140
- Peptide Label: isoform X7
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005252194   ⟸   XM_005252137
- Peptide Label: isoform X1
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005252201   ⟸   XM_005252144
- Peptide Label: isoform X15
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269323   ⟸   NM_001282394
- Peptide Label: isoform 1
- UniProtKB: Q9C0A3 (UniProtKB/Swiss-Prot),   Q8IY36 (UniProtKB/Swiss-Prot),   Q5VWF2 (UniProtKB/Swiss-Prot),   Q5VWF1 (UniProtKB/Swiss-Prot),   Q9H3P4 (UniProtKB/Swiss-Prot),   Q9Y3S1 (UniProtKB/Swiss-Prot),   H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870538   ⟸   XM_017015049
- Peptide Label: isoform X5
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870543   ⟸   XM_017015054
- Peptide Label: isoform X25
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870536   ⟸   XM_017015047
- Peptide Label: isoform X3
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870541   ⟸   XM_017015052
- Peptide Label: isoform X12
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870534   ⟸   XM_017015045
- Peptide Label: isoform X2
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870539   ⟸   XM_017015050
- Peptide Label: isoform X6
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870544   ⟸   XM_017015055
- Peptide Label: isoform X26
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870537   ⟸   XM_017015048
- Peptide Label: isoform X4
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870542   ⟸   XM_017015053
- Peptide Label: isoform X13
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016870540   ⟸   XM_017015051
- Peptide Label: isoform X9
- UniProtKB: H0Y7T5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000414622   ⟸   ENST00000411624
RefSeq Acc Id: ENSP00000411181   ⟸   ENST00000427277
RefSeq Acc Id: ENSP00000413325   ⟸   ENST00000453718
RefSeq Acc Id: ENSP00000297954   ⟸   ENST00000297954
RefSeq Acc Id: ENSP00000415038   ⟸   ENST00000432730
RefSeq Acc Id: ENSP00000390441   ⟸   ENST00000448251
RefSeq Acc Id: ENSP00000412465   ⟸   ENST00000448039
RefSeq Acc Id: ENSP00000378860   ⟸   ENST00000395477
RefSeq Acc Id: XP_047279701   ⟸   XM_047423745
- Peptide Label: isoform X16
RefSeq Acc Id: XP_047279707   ⟸   XM_047423751
- Peptide Label: isoform X22
RefSeq Acc Id: XP_047279717   ⟸   XM_047423761
- Peptide Label: isoform X33
RefSeq Acc Id: XP_047279723   ⟸   XM_047423767
- Peptide Label: isoform X38
RefSeq Acc Id: XP_047279710   ⟸   XM_047423754
- Peptide Label: isoform X27
RefSeq Acc Id: XP_047279697   ⟸   XM_047423741
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047279703   ⟸   XM_047423747
- Peptide Label: isoform X18
RefSeq Acc Id: XP_047279708   ⟸   XM_047423752
- Peptide Label: isoform X23
RefSeq Acc Id: XP_047279718   ⟸   XM_047423762
- Peptide Label: isoform X34
RefSeq Acc Id: XP_047279724   ⟸   XM_047423768
- Peptide Label: isoform X39
RefSeq Acc Id: XP_047279709   ⟸   XM_047423753
- Peptide Label: isoform X24
RefSeq Acc Id: XP_047279712   ⟸   XM_047423756
- Peptide Label: isoform X28
RefSeq Acc Id: XP_047279726   ⟸   XM_047423770
- Peptide Label: isoform X41
RefSeq Acc Id: XP_047279727   ⟸   XM_047423771
- Peptide Label: isoform X42
RefSeq Acc Id: XP_047279698   ⟸   XM_047423742
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047279705   ⟸   XM_047423749
- Peptide Label: isoform X20
RefSeq Acc Id: XP_047279713   ⟸   XM_047423757
- Peptide Label: isoform X29
RefSeq Acc Id: XP_047279720   ⟸   XM_047423764
- Peptide Label: isoform X36
RefSeq Acc Id: XP_047279700   ⟸   XM_047423744
- Peptide Label: isoform X14
RefSeq Acc Id: XP_047279699   ⟸   XM_047423743
- Peptide Label: isoform X11
RefSeq Acc Id: XP_047279706   ⟸   XM_047423750
- Peptide Label: isoform X21
RefSeq Acc Id: XP_047279714   ⟸   XM_047423758
- Peptide Label: isoform X30
RefSeq Acc Id: XP_047279721   ⟸   XM_047423765
- Peptide Label: isoform X37
RefSeq Acc Id: XP_047279704   ⟸   XM_047423748
- Peptide Label: isoform X19
RefSeq Acc Id: XP_047279715   ⟸   XM_047423759
- Peptide Label: isoform X31
RefSeq Acc Id: XP_047279725   ⟸   XM_047423769
- Peptide Label: isoform X40
RefSeq Acc Id: XP_047279719   ⟸   XM_047423763
- Peptide Label: isoform X35
RefSeq Acc Id: XP_047279702   ⟸   XM_047423746
- Peptide Label: isoform X17
RefSeq Acc Id: XP_047279716   ⟸   XM_047423760
- Peptide Label: isoform X32
RefSeq Acc Id: XP_047279729   ⟸   XM_047423773
- Peptide Label: isoform X44
RefSeq Acc Id: XP_047279734   ⟸   XM_047423778
- Peptide Label: isoform X48
RefSeq Acc Id: XP_047279730   ⟸   XM_047423774
- Peptide Label: isoform X45
RefSeq Acc Id: XP_047279731   ⟸   XM_047423775
- Peptide Label: isoform X46
RefSeq Acc Id: XP_047279728   ⟸   XM_047423772
- Peptide Label: isoform X43
RefSeq Acc Id: XP_047279732   ⟸   XM_047423776
- Peptide Label: isoform X47
RefSeq Acc Id: XP_047279735   ⟸   XM_047423779
- Peptide Label: isoform X49
RefSeq Acc Id: XP_054219563   ⟸   XM_054363588
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054219569   ⟸   XM_054363594
- Peptide Label: isoform X22
RefSeq Acc Id: XP_054219580   ⟸   XM_054363605
- Peptide Label: isoform X33
RefSeq Acc Id: XP_054219585   ⟸   XM_054363610
- Peptide Label: isoform X38
RefSeq Acc Id: XP_054219574   ⟸   XM_054363599
- Peptide Label: isoform X27
RefSeq Acc Id: XP_054219555   ⟸   XM_054363580
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054219565   ⟸   XM_054363590
- Peptide Label: isoform X18
RefSeq Acc Id: XP_054219570   ⟸   XM_054363595
- Peptide Label: isoform X23
RefSeq Acc Id: XP_054219581   ⟸   XM_054363606
- Peptide Label: isoform X34
RefSeq Acc Id: XP_054219586   ⟸   XM_054363611
- Peptide Label: isoform X39
RefSeq Acc Id: XP_054219571   ⟸   XM_054363596
- Peptide Label: isoform X24
RefSeq Acc Id: XP_054219575   ⟸   XM_054363600
- Peptide Label: isoform X28
RefSeq Acc Id: XP_054219588   ⟸   XM_054363613
- Peptide Label: isoform X41
RefSeq Acc Id: XP_054219589   ⟸   XM_054363614
- Peptide Label: isoform X42
RefSeq Acc Id: XP_054219548   ⟸   XM_054363573
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054219554   ⟸   XM_054363579
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054219552   ⟸   XM_054363577
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054219557   ⟸   XM_054363582
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054219567   ⟸   XM_054363592
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054219572   ⟸   XM_054363597
- Peptide Label: isoform X25
RefSeq Acc Id: XP_054219576   ⟸   XM_054363601
- Peptide Label: isoform X29
RefSeq Acc Id: XP_054219583   ⟸   XM_054363608
- Peptide Label: isoform X36
RefSeq Acc Id: XP_054219550   ⟸   XM_054363575
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054219559   ⟸   XM_054363584
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054219561   ⟸   XM_054363586
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054219549   ⟸   XM_054363574
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054219553   ⟸   XM_054363578
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054219558   ⟸   XM_054363583
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054219568   ⟸   XM_054363593
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054219573   ⟸   XM_054363598
- Peptide Label: isoform X26
RefSeq Acc Id: XP_054219577   ⟸   XM_054363602
- Peptide Label: isoform X30
RefSeq Acc Id: XP_054219584   ⟸   XM_054363609
- Peptide Label: isoform X37
RefSeq Acc Id: XP_054219551   ⟸   XM_054363576
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054219560   ⟸   XM_054363585
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054219556   ⟸   XM_054363581
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054219566   ⟸   XM_054363591
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054219562   ⟸   XM_054363587
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054219578   ⟸   XM_054363603
- Peptide Label: isoform X31
RefSeq Acc Id: XP_054219587   ⟸   XM_054363612
- Peptide Label: isoform X40
RefSeq Acc Id: XP_054219582   ⟸   XM_054363607
- Peptide Label: isoform X35
RefSeq Acc Id: XP_054219564   ⟸   XM_054363589
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054219579   ⟸   XM_054363604
- Peptide Label: isoform X32
RefSeq Acc Id: XP_054219591   ⟸   XM_054363616
- Peptide Label: isoform X44
RefSeq Acc Id: XP_054219595   ⟸   XM_054363620
- Peptide Label: isoform X48
RefSeq Acc Id: XP_054219592   ⟸   XM_054363617
- Peptide Label: isoform X45
RefSeq Acc Id: XP_054219593   ⟸   XM_054363618
- Peptide Label: isoform X46
RefSeq Acc Id: XP_054219590   ⟸   XM_054363615
- Peptide Label: isoform X43
RefSeq Acc Id: XP_054219594   ⟸   XM_054363619
- Peptide Label: isoform X47
RefSeq Acc Id: XP_054219596   ⟸   XM_054363621
- Peptide Label: isoform X49
Protein Domains
Protein kinase   Serine/threonine-protein kinase OSR1/WNK CCT

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y3S1-F1-model_v2 AlphaFold Q9Y3S1 1-2297 view protein structure

Promoters
RGD ID:7215509
Promoter ID:EPDNEW_H13501
Type:initiation region
Name:WNK2_1
Description:WNK lysine deficient protein kinase 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38993,184,926 - 93,184,986EPDNEW
RGD ID:6807589
Promoter ID:HG_KWN:64081
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562
Transcripts:ENST00000297954,   ENST00000349097,   ENST00000395475,   ENST00000395477,   NM_006648,   UC010MRC.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36994,986,016 - 94,986,516 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14542 AgrOrtholog
COSMIC WNK2 COSMIC
Ensembl Genes ENSG00000165238 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000297954 ENTREZGENE
  ENST00000297954.9 UniProtKB/Swiss-Prot
  ENST00000395477.6 UniProtKB/TrEMBL
  ENST00000411624 ENTREZGENE
  ENST00000411624.5 UniProtKB/TrEMBL
  ENST00000427277 ENTREZGENE
  ENST00000427277.7 UniProtKB/TrEMBL
  ENST00000432730 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000432730.6 UniProtKB/Swiss-Prot
  ENST00000448039.6 UniProtKB/TrEMBL
  ENST00000453718.2 UniProtKB/TrEMBL
Gene3D-CATH Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000165238 GTEx
HGNC ID HGNC:14542 ENTREZGENE
Human Proteome Map WNK2 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinase_OSR1/WNK_CCT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:65268 UniProtKB/Swiss-Prot
NCBI Gene 65268 ENTREZGENE
OMIM 606249 OMIM
PANTHER SERINE/THREONINE-PROTEIN KINASE WNK WITH NO LYSINE -RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SERINE/THREONINE-PROTEIN KINASE WNK2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam OSR1_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33783 PharmGKB
PROSITE PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6PVV2_HUMAN UniProtKB/TrEMBL
  E9PCD1 ENTREZGENE, UniProtKB/TrEMBL
  F8W9F9 ENTREZGENE
  H0Y7J9_HUMAN UniProtKB/TrEMBL
  H0Y7R3_HUMAN UniProtKB/TrEMBL
  H0Y7T5 ENTREZGENE, UniProtKB/TrEMBL
  Q5VWF1 ENTREZGENE
  Q5VWF2 ENTREZGENE
  Q8IY36 ENTREZGENE
  Q9C0A3 ENTREZGENE
  Q9H3P4 ENTREZGENE
  Q9Y3S1 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary F8W9F9 UniProtKB/TrEMBL
  Q5VWF1 UniProtKB/Swiss-Prot
  Q5VWF2 UniProtKB/Swiss-Prot
  Q8IY36 UniProtKB/Swiss-Prot
  Q9C0A3 UniProtKB/Swiss-Prot
  Q9H3P4 UniProtKB/Swiss-Prot