STK25 (serine/threonine kinase 25) - Rat Genome Database

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Pathways
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Gene: STK25 (serine/threonine kinase 25) Homo sapiens
Analyze
Symbol: STK25
Name: serine/threonine kinase 25
RGD ID: 1342524
HGNC Page HGNC:11404
Description: Enables protein homodimerization activity. Involved in several processes, including Golgi reassembly; establishment of Golgi localization; and intrinsic apoptotic signaling pathway in response to hydrogen peroxide. Located in cytoplasm. Colocalizes with Golgi apparatus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp686J1430; serine/threonine kinase 25 (STE20 homolog, yeast); serine/threonine kinase 25 (Ste20, yeast homolog); serine/threonine-protein kinase 25; SOK-1; SOK1; Ste20, yeast homolog; ste20-like kinase; ste20/oxidant stress response kinase 1; sterile 20 (oxidant stress response kinase 1); sterile 20/oxidant stress-response kinase 1; yeast Sps1/Ste20-related kinase 1; YSK1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: STK25P1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382241,492,670 - 241,509,572 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl2241,492,670 - 241,509,730 (-)EnsemblGRCh38hg38GRCh38
GRCh372242,432,085 - 242,448,987 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362242,083,105 - 242,096,707 (-)NCBINCBI36Build 36hg18NCBI36
Build 342242,154,422 - 242,168,024NCBI
Celera2236,104,013 - 236,117,625 (-)NCBICelera
Cytogenetic Map2q37.3NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBIHuRef
CHM1_12242,440,093 - 242,454,954 (-)NCBICHM1_1
T2T-CHM13v2.02241,992,007 - 242,008,899 (-)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)
extracellular exosome  (HDA)
Golgi apparatus  (IDA,IEA)
Golgi membrane  (ISO)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. YSK1, a novel mammalian protein kinase structurally related to Ste20 and SPS1, but is not involved in the known MAPK pathways. Osada S, etal., Oncogene 1997 May 1;14(17):2047-57.
3. Activation of a human Ste20-like kinase by oxidant stress defines a novel stress response pathway. Pombo CM, etal., EMBO J 1996 Sep 2;15(17):4537-46.
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:12477932   PMID:14702039   PMID:15037601   PMID:15489334   PMID:15815621   PMID:16189514   PMID:16344560   PMID:17253963   PMID:17353931   PMID:17657516   PMID:18364353  
PMID:18782753   PMID:19615732   PMID:19953087   PMID:20098747   PMID:20332113   PMID:20360068   PMID:20592472   PMID:20949042   PMID:21396913   PMID:21423148   PMID:21516116   PMID:21561863  
PMID:21832049   PMID:21873635   PMID:21900206   PMID:22199357   PMID:22291017   PMID:22391949   PMID:22652780   PMID:22782892   PMID:22939629   PMID:23455922   PMID:23533145   PMID:23535732  
PMID:23665169   PMID:23889253   PMID:24705354   PMID:25416956   PMID:25550858   PMID:26186194   PMID:26344197   PMID:26553096   PMID:26871637   PMID:27107012   PMID:28380382   PMID:28514442  
PMID:29513927   PMID:29996891   PMID:30646538   PMID:30948712   PMID:31091453   PMID:31515488   PMID:31586073   PMID:32292165   PMID:32296183   PMID:32707033   PMID:32994395   PMID:33170807  
PMID:33545068   PMID:33961781   PMID:34079125   PMID:34624527   PMID:35217361   PMID:35271311   PMID:35349179   PMID:35977512  


Genomics

Comparative Map Data
STK25
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382241,492,670 - 241,509,572 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl2241,492,670 - 241,509,730 (-)EnsemblGRCh38hg38GRCh38
GRCh372242,432,085 - 242,448,987 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362242,083,105 - 242,096,707 (-)NCBINCBI36Build 36hg18NCBI36
Build 342242,154,422 - 242,168,024NCBI
Celera2236,104,013 - 236,117,625 (-)NCBICelera
Cytogenetic Map2q37.3NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBIHuRef
CHM1_12242,440,093 - 242,454,954 (-)NCBICHM1_1
T2T-CHM13v2.02241,992,007 - 242,008,899 (-)NCBIT2T-CHM13v2.0
Stk25
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39193,548,473 - 93,581,937 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl193,547,473 - 93,586,381 (-)EnsemblGRCm39 Ensembl
GRCm38193,620,751 - 93,654,216 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl193,619,751 - 93,658,659 (-)EnsemblGRCm38mm10GRCm38
MGSCv37195,517,328 - 95,532,304 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36195,452,310 - 95,466,056 (-)NCBIMGSCv36mm8
Celera196,566,463 - 96,582,514 (-)NCBICelera
Cytogenetic Map1DNCBI
cM Map147.25NCBI
Stk25
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2994,161,834 - 94,174,095 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl994,161,836 - 94,174,244 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx9102,597,351 - 102,609,489 (-)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.09107,733,180 - 107,745,363 (-)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.09106,089,281 - 106,101,464 (-)NCBIRnor_WKY
Rnor_6.09100,767,578 - 100,779,715 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl9100,767,579 - 100,779,715 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.09100,420,925 - 100,433,656 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4992,907,764 - 92,919,903 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1993,112,533 - 93,124,672 (-)NCBI
Celera991,695,836 - 91,707,760 (-)NCBICelera
Cytogenetic Map9q36NCBI
Stk25
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955542272,715 - 280,110 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955542268,406 - 279,323 (+)NCBIChiLan1.0ChiLan1.0
STK25
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan12B144,213,015 - 144,226,459 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02B128,766,408 - 128,779,939 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12B247,560,624 - 247,574,249 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2B247,560,624 - 247,574,249 (-)Ensemblpanpan1.1panPan2
STK25
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12551,425,597 - 51,434,479 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2551,425,597 - 51,434,479 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2551,637,993 - 51,646,876 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02551,612,976 - 51,626,491 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2551,617,610 - 51,626,491 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12551,467,502 - 51,476,383 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02551,207,431 - 51,216,291 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02551,483,680 - 51,492,565 (-)NCBIUU_Cfam_GSD_1.0
Stk25
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303192,792,530 - 192,798,829 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936745420,073 - 426,393 (+)EnsemblSpeTri2.0
SpeTri2.0NW_004936745420,591 - 426,890 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
STK25
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl15140,144,336 - 140,154,366 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.115140,144,334 - 140,154,361 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.215154,683,027 - 154,693,144 (-)NCBISscrofa10.2Sscrofa10.2susScr3
STK25
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.110127,571,024 - 127,580,628 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl10127,571,665 - 127,580,071 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604071,742,570 - 71,772,625 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Stk25
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248475,511,007 - 5,530,764 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248475,511,590 - 5,530,773 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in STK25
25 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
Single allele deletion Intellectual disability [RCV001293367] Chr2:237201756..243048760 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1 copy number loss See cases [RCV000050304] Chr2:231770279..242126245 [GRCh38]
Chr2:232634989..243059659 [GRCh37]
Chr2:232343233..242717069 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:236555233-242126245)x1 copy number loss See cases [RCV000051120] Chr2:236555233..242126245 [GRCh38]
Chr2:237463876..243059659 [GRCh37]
Chr2:237128615..242717069 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:237643996-242126245)x1 copy number loss See cases [RCV000051133] Chr2:237643996..242126245 [GRCh38]
Chr2:238552639..243059659 [GRCh37]
Chr2:238217378..242717069 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234345842-242126245)x1 copy number loss See cases [RCV000051163] Chr2:234345842..242126245 [GRCh38]
Chr2:235254486..243059659 [GRCh37]
Chr2:234919225..242717069 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235741079-242032456)x1 copy number loss See cases [RCV000052673] Chr2:235741079..242032456 [GRCh38]
Chr2:236649723..242974607 [GRCh37]
Chr2:236314462..242623280 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:236775572-242065349)x1 copy number loss See cases [RCV000052674] Chr2:236775572..242065349 [GRCh38]
Chr2:237684215..243007500 [GRCh37]
Chr2:237348954..242656173 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:237526184-241996090)x1 copy number loss See cases [RCV000052675] Chr2:237526184..241996090 [GRCh38]
Chr2:238434827..242938241 [GRCh37]
Chr2:238099566..242586914 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:237643996-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052700]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052700]|See cases [RCV000052700] Chr2:237643996..242065208 [GRCh38]
Chr2:238552639..243007359 [GRCh37]
Chr2:238217378..242656032 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:238939181-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052701]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052701]|See cases [RCV000052701] Chr2:238939181..242065208 [GRCh38]
Chr2:239860877..243007359 [GRCh37]
Chr2:239525814..242656032 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:240067206-242086301)x1 copy number loss See cases [RCV000052702] Chr2:240067206..242086301 [GRCh38]
Chr2:241006623..243028452 [GRCh37]
Chr2:240655296..242677125 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:240444819-242086301)x1 copy number loss See cases [RCV000052703] Chr2:240444819..242086301 [GRCh38]
Chr2:241384236..243028452 [GRCh37]
Chr2:241032909..242677125 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:240506951-242065349)x1 copy number loss See cases [RCV000052704] Chr2:240506951..242065349 [GRCh38]
Chr2:241446368..243007500 [GRCh37]
Chr2:241095041..242656173 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:241179464-242065349)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052705]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052705]|See cases [RCV000052705] Chr2:241179464..242065349 [GRCh38]
Chr2:242118879..243007500 [GRCh37]
Chr2:241767552..242656173 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:241249295-242086301)x1 copy number loss See cases [RCV000052706] Chr2:241249295..242086301 [GRCh38]
Chr2:242188710..243028452 [GRCh37]
Chr2:241837383..242677125 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:241179664-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052707]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052707]|See cases [RCV000052707] Chr2:241179664..242065208 [GRCh38]
Chr2:242119079..243007359 [GRCh37]
Chr2:241767752..242656032 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234172536-242086301)x1 copy number loss See cases [RCV000052669] Chr2:234172536..242086301 [GRCh38]
Chr2:235081180..243028452 [GRCh37]
Chr2:234745919..242677125 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234668159-242126245)x1 copy number loss See cases [RCV000052670] Chr2:234668159..242126245 [GRCh38]
Chr2:235576803..243059659 [GRCh37]
Chr2:235241542..242717069 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:234906462-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052671]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052671]|See cases [RCV000052671] Chr2:234906462..242065208 [GRCh38]
Chr2:235815106..243007359 [GRCh37]
Chr2:235479845..242656032 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235268768-242065208)x1 copy number loss See cases [RCV000052672] Chr2:235268768..242065208 [GRCh38]
Chr2:236177412..243007359 [GRCh37]
Chr2:235842151..242656032 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:231375505-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052639]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052639]|See cases [RCV000052639] Chr2:231375505..242065208 [GRCh38]
Chr2:232240216..243007359 [GRCh37]
Chr2:231948460..242656032 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:232857728-242065349)x1 copy number loss See cases [RCV000052640] Chr2:232857728..242065349 [GRCh38]
Chr2:233722438..243007500 [GRCh37]
Chr2:233430682..242656173 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:233420162-242086301)x1 copy number loss See cases [RCV000052641] Chr2:233420162..242086301 [GRCh38]
Chr2:233995840..243028452 [GRCh37]
Chr2:233704084..242677125 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:233453611-242099155)x1 copy number loss See cases [RCV000052642] Chr2:233453611..242099155 [GRCh38]
Chr2:234362257..243041306 [GRCh37]
Chr2:234026996..242689979 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234225537-241565907)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052975]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052975]|See cases [RCV000052975] Chr2:234225537..241565907 [GRCh38]
Chr2:235134181..242505322 [GRCh37]
Chr2:234798920..242153995 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235268768-242126245)x3 copy number gain See cases [RCV000052976] Chr2:235268768..242126245 [GRCh38]
Chr2:236177412..243059659 [GRCh37]
Chr2:235842151..242717069 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235563664-242086301)x3 copy number gain See cases [RCV000052977] Chr2:235563664..242086301 [GRCh38]
Chr2:236472308..243028452 [GRCh37]
Chr2:236137047..242677125 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:240910571-242126392)x3 copy number gain See cases [RCV000052980] Chr2:240910571..242126392 [GRCh38]
Chr2:241849988..243059659 [GRCh37]
Chr2:241498661..242717216 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3 copy number gain See cases [RCV000052958] Chr2:188818195..242065208 [GRCh38]
Chr2:189682921..243007359 [GRCh37]
Chr2:189391166..242656032 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3 copy number gain See cases [RCV000052959] Chr2:190310736..241892770 [GRCh38]
Chr2:191175462..242834921 [GRCh37]
Chr2:190883707..242483594 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q36.1-37.3(chr2:223992431-242126245)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|See cases [RCV000052972] Chr2:223992431..242126245 [GRCh38]
Chr2:224857148..243059659 [GRCh37]
Chr2:224565392..242717069 [NCBI36]
Chr2:2q36.1-37.3		 pathogenic
GRCh38/hg38 2q36.3-37.3(chr2:227803148-242086301)x3 copy number gain See cases [RCV000052973] Chr2:227803148..242086301 [GRCh38]
Chr2:228667864..243028452 [GRCh37]
Chr2:228376108..242677125 [NCBI36]
Chr2:2q36.3-37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:238756369-241771051)x3 copy number gain See cases [RCV000133659] Chr2:238756369..241771051 [GRCh38]
Chr2:239665010..242710466 [GRCh37]
Chr2:239329749..242359139 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:241481406-242126245)x1 copy number loss See cases [RCV000134170] Chr2:241481406..242126245 [GRCh38]
Chr2:242420821..243059659 [GRCh37]
Chr2:242069494..242717069 [NCBI36]
Chr2:2q37.3		 uncertain significance
GRCh38/hg38 2q37.3(chr2:240171137-242065208)x1 copy number loss See cases [RCV000135842] Chr2:240171137..242065208 [GRCh38]
Chr2:241110554..243007359 [GRCh37]
Chr2:240759227..242656032 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:237034476-242065208)x1 copy number loss See cases [RCV000135864] Chr2:237034476..242065208 [GRCh38]
Chr2:237943119..243007359 [GRCh37]
Chr2:237607858..242656032 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:236966763-242065208)x1 copy number loss See cases [RCV000135570] Chr2:236966763..242065208 [GRCh38]
Chr2:237875406..243007359 [GRCh37]
Chr2:237540145..242656032 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:240507151-242065208)x1 copy number loss See cases [RCV000135545] Chr2:240507151..242065208 [GRCh38]
Chr2:241446568..243007359 [GRCh37]
Chr2:241095241..242656032 [NCBI36]
Chr2:2q37.3		 likely pathogenic
GRCh38/hg38 2q37.3(chr2:237232204-242065208)x1 copy number loss See cases [RCV000136566] Chr2:237232204..242065208 [GRCh38]
Chr2:238140847..243007359 [GRCh37]
Chr2:237805586..242656032 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3 copy number gain See cases [RCV000135934] Chr2:210579676..242126245 [GRCh38]
Chr2:211444400..243059659 [GRCh37]
Chr2:211152645..242717069 [NCBI36]
Chr2:2q34-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235028429-242066108)x1 copy number loss See cases [RCV000136968] Chr2:235028429..242066108 [GRCh38]
Chr2:235937073..243008259 [GRCh37]
Chr2:235601812..242656932 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:234835780-242065208)x1 copy number loss See cases [RCV000137069] Chr2:234835780..242065208 [GRCh38]
Chr2:235744424..243007359 [GRCh37]
Chr2:235409163..242656032 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235603604-241771051)x1 copy number loss See cases [RCV000136648] Chr2:235603604..241771051 [GRCh38]
Chr2:236512248..242710466 [GRCh37]
Chr2:236176987..242359139 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic|uncertain significance
GRCh38/hg38 2q37.3(chr2:240067206-242126245)x1 copy number loss See cases [RCV000136686] Chr2:240067206..242126245 [GRCh38]
Chr2:241006623..243059659 [GRCh37]
Chr2:240655296..242717069 [NCBI36]
Chr2:2q37.3		 pathogenic|uncertain significance
GRCh38/hg38 2q37.3(chr2:238833519-242126245)x1 copy number loss See cases [RCV000138117] Chr2:238833519..242126245 [GRCh38]
Chr2:239742160..243059659 [GRCh37]
Chr2:239406907..242717069 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:240187901-242126245)x1 copy number loss See cases [RCV000138565] Chr2:240187901..242126245 [GRCh38]
Chr2:241127318..243059659 [GRCh37]
Chr2:240775991..242717069 [NCBI36]
Chr2:2q37.3		 likely pathogenic
GRCh38/hg38 2q37.3(chr2:237902870-242126251)x1 copy number loss See cases [RCV000139808] Chr2:237902870..242126251 [GRCh38]
Chr2:238811512..243059659 [GRCh37]
Chr2:238476251..242717075 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:236775762-242126251)x1 copy number loss See cases [RCV000139527] Chr2:236775762..242126251 [GRCh38]
Chr2:237684405..243059659 [GRCh37]
Chr2:237349144..242717075 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:236413722-242126251)x1 copy number loss See cases [RCV000139805] Chr2:236413722..242126251 [GRCh38]
Chr2:237322365..243059659 [GRCh37]
Chr2:236987104..242717075 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:240228628-242126245)x1 copy number loss See cases [RCV000140648] Chr2:240228628..242126245 [GRCh38]
Chr2:241168045..243059659 [GRCh37]
Chr2:240816718..242717069 [NCBI36]
Chr2:2q37.3		 uncertain significance
GRCh38/hg38 2q37.3(chr2:240671231-242092126)x1 copy number loss See cases [RCV000141077] Chr2:240671231..242092126 [GRCh38]
Chr2:241610648..243034277 [GRCh37]
Chr2:241259321..242682950 [NCBI36]
Chr2:2q37.3		 likely pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235846916-241841232)x1 copy number loss See cases [RCV000141661] Chr2:235846916..241841232 [GRCh38]
Chr2:236755560..242783384 [GRCh37]
Chr2:236420299..242432057 [NCBI36]
Chr2:2q37.2-37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:239507342-241841232)x1 copy number loss See cases [RCV000141691] Chr2:239507342..241841232 [GRCh38]
Chr2:240429036..242783384 [GRCh37]
Chr2:240093973..242432057 [NCBI36]
Chr2:2q37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234159653-241841232)x1 copy number loss See cases [RCV000142291] Chr2:234159653..241841232 [GRCh38]
Chr2:235068297..242783384 [GRCh37]
Chr2:234733036..242432057 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3 copy number gain See cases [RCV000142307] Chr2:189436149..241841232 [GRCh38]
Chr2:190300875..242783384 [GRCh37]
Chr2:190009120..242432057 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q37.3(chr2:239642965-241841232)x1 copy number loss See cases [RCV000143423] Chr2:239642965..241841232 [GRCh38]
Chr2:240564659..242783384 [GRCh37]
Chr2:240229596..242432057 [NCBI36]
Chr2:2q37.3		 likely pathogenic
GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3 copy number gain See cases [RCV000143216] Chr2:218101759..242126245 [GRCh38]
Chr2:218966482..243059659 [GRCh37]
Chr2:218674727..242717069 [NCBI36]
Chr2:2q35-37.3		 pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1 copy number loss See cases [RCV000148260] Chr2:231770279..242126245 [GRCh38]
Chr2:232634989..243059659 [GRCh37]
Chr2:232343233..242717069 [NCBI36]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:239873381-243006013)x3 copy number gain See cases [RCV000167564] Chr2:239873381..243006013 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:237816758-242783384)x1 copy number loss See cases [RCV000449023] Chr2:237816758..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:233784243-243040217)x1 copy number loss See cases [RCV000446034] Chr2:233784243..243040217 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:242416476-242783384)x1 copy number loss See cases [RCV000446678] Chr2:242416476..242783384 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q37.3(chr2:237938270-242783384)x1 copy number loss See cases [RCV000446532] Chr2:237938270..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234495262-242783384)x1 copy number loss See cases [RCV000446061] Chr2:234495262..242783384 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236285213-242783384)x1 copy number loss See cases [RCV000445750] Chr2:236285213..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:242045569-243040217)x1 copy number loss See cases [RCV000448540] Chr2:242045569..243040217 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.3(chr2:238072533-242783384)x1 copy number loss See cases [RCV000447929] Chr2:238072533..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236911223-242783384)x1 copy number loss See cases [RCV000447965] Chr2:236911223..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236577291-242783384)x1 copy number loss See cases [RCV000448691] Chr2:236577291..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234495262-242783384)x1 copy number loss See cases [RCV000512077] Chr2:234495262..242783384 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:240541136-242783384)x1 copy number loss See cases [RCV000510186] Chr2:240541136..242783384 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.3(chr2:239748306-242783384)x1 copy number loss See cases [RCV000510310] Chr2:239748306..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:242305098-242783384)x3 copy number gain See cases [RCV000510462] Chr2:242305098..242783384 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q34-37.3(chr2:213518431-242783384)x3 copy number gain See cases [RCV000512009] Chr2:213518431..242783384 [GRCh37]
Chr2:2q34-37.3		 pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:235539337-242783384)x1 copy number loss See cases [RCV000511491] Chr2:235539337..242783384 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:240630455-242783384)x1 copy number loss See cases [RCV000511956] Chr2:240630455..242783384 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.3(chr2:240161377-242783384)x1 copy number loss See cases [RCV000511227] Chr2:240161377..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:240141439-242783384)x3 copy number gain See cases [RCV000512298] Chr2:240141439..242783384 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.3(chr2:237545100-242783384)x1 copy number loss See cases [RCV000512231] Chr2:237545100..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:241997911-242783384)x3 copy number gain See cases [RCV000512463] Chr2:241997911..242783384 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q37.3(chr2:242016876-242783384)x1 copy number loss not provided [RCV000682102] Chr2:242016876..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:241810311-242783384)x1 copy number loss not provided [RCV000682110] Chr2:241810311..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:240457943-242783384)x1 copy number loss not provided [RCV000682145] Chr2:240457943..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:240076138-242783384)x1 copy number loss not provided [RCV000682146] Chr2:240076138..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:239884390-242783384)x1 copy number loss not provided [RCV000682148] Chr2:239884390..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:235790256-242783384)x1 copy number loss not provided [RCV000682160] Chr2:235790256..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234716425-242783384)x3 copy number gain not provided [RCV000682161] Chr2:234716425..242783384 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:238037759-243101834)x1 copy number loss not provided [RCV000740979] Chr2:238037759..243101834 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:241847589-243101834)x1 copy number loss not provided [RCV000741039] Chr2:241847589..243101834 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:239894072-243048760)x1 copy number loss See cases [RCV000790569] Chr2:239894072..243048760 [GRCh37]
Chr2:2q37.3		 pathogenic
NM_014808.4(FARP2):c.3027G>A (p.Glu1009=) single nucleotide variant not provided [RCV000966844] Chr2:241493424 [GRCh38]
Chr2:242432839 [GRCh37]
Chr2:2q37.3		 likely benign
NM_014808.4(FARP2):c.3138G>A (p.Glu1046=) single nucleotide variant not provided [RCV000895982] Chr2:241494098 [GRCh38]
Chr2:242433513 [GRCh37]
Chr2:2q37.3		 likely benign
GRCh37/hg19 2q37.3(chr2:242177268-242478356)x1 copy number loss not provided [RCV001005389] Chr2:242177268..242478356 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:237028693-242708080) copy number loss Chromosome 2q37 deletion syndrome [RCV000767787] Chr2:237028693..242708080 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:238795602-242918203) copy number loss Chromosome 2q37 deletion syndrome [RCV000767788] Chr2:238795602..242918203 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.3(chr2:239071623-243048760) copy number loss Chromosome 2q37 deletion syndrome [RCV000767789] Chr2:239071623..243048760 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:240112450-242783384)x1 copy number loss not provided [RCV001005385] Chr2:240112450..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:241404033-242684292)x1 copy number loss not provided [RCV000997728] Chr2:241404033..242684292 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q37.3(chr2:241810850-243048760)x3 copy number gain See cases [RCV001194552] Chr2:241810850..243048760 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q36.3-37.3(chr2:230814690-242783384)x3 copy number gain not provided [RCV001007519] Chr2:230814690..242783384 [GRCh37]
Chr2:2q36.3-37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:237265271-242783384)x3 copy number gain not provided [RCV001005380] Chr2:237265271..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:235942616-242783384)x1 copy number loss not provided [RCV002472625] Chr2:235942616..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:242379032-242783384)x1 copy number loss not provided [RCV002473812] Chr2:242379032..242783384 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q37.3(chr2:242011633-243199373)x1 copy number loss not provided [RCV001005388] Chr2:242011633..243199373 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.3(chr2:242340265-242783384)x1 copy number loss not provided [RCV001005390] Chr2:242340265..242783384 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:233110452-243028452)x1 copy number loss Chromosome 2q37 deletion syndrome [RCV001263221] Chr2:233110452..243028452 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234791927-242783384)x1 copy number loss not provided [RCV001007522] Chr2:234791927..242783384 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:239914717-242783384)x1 copy number loss not provided [RCV001005384] Chr2:239914717..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:238863455-243048760)x3 copy number gain See cases [RCV001194532] Chr2:238863455..243048760 [GRCh37]
Chr2:2q37.3		 uncertain significance
NC_000002.11:g.(?_241808273)_(242708241_?)del deletion not provided [RCV001031165] Chr2:241808273..242708241 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:241791028-242842568)x3 copy number gain See cases [RCV001194599] Chr2:241791028..242842568 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q37.3(chr2:241880799-242783384)x1 copy number loss not provided [RCV001005387] Chr2:241880799..242783384 [GRCh37]
Chr2:2q37.3		 likely pathogenic
GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3 copy number gain See cases [RCV001263052] Chr2:178397959..243007457 [GRCh37]
Chr2:2q31.2-37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236472789-242783384) copy number loss Chromosome 2q37 deletion syndrome [RCV002280740] Chr2:236472789..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:240208466-243199373)x3 copy number gain not provided [RCV001827620] Chr2:240208466..243199373 [GRCh37]
Chr2:2q37.3		 uncertain significance
GRCh37/hg19 2q37.3(chr2:239436367-242783384)x1 copy number loss not provided [RCV001834263] Chr2:239436367..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:237499041-242783384)x1 copy number loss not provided [RCV001827851] Chr2:237499041..242783384 [GRCh37]
Chr2:2q37.3		 pathogenic
NC_000002.11:g.(?_238233417)_(242801596_?)del deletion D-2-hydroxyglutaric aciduria 1 [RCV003120750]|Hereditary spastic paraplegia 30 [RCV001920651]|not provided [RCV001920650] Chr2:238233417..242801596 [GRCh37]
Chr2:2q37.3		 pathogenic|uncertain significance
NC_000002.11:g.(?_236403331)_(242801596_?)dup duplication not provided [RCV001879163] Chr2:236403331..242801596 [GRCh37]
Chr2:2q37.2-37.3		 uncertain significance
NC_000002.11:g.(?_236877086)_(242801596_?)del deletion not provided [RCV001956380] Chr2:236877086..242801596 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
NC_000002.11:g.(?_238233417)_(242800990_?)dup duplication D-2-hydroxyglutaric aciduria 1 [RCV001918744]|Hereditary spastic paraplegia 30 [RCV001942893] Chr2:238233417..242800990 [GRCh37]
Chr2:2q37.3		 uncertain significance
Single allele deletion Chromosome 2q37 deletion syndrome [RCV002247720] Chr2:236710422..242106504 [GRCh38]
Chr2:2q37.3		 pathogenic
NC_000002.11:g.(?_236403331)_(242801596_?)del deletion Bethlem myopathy 1 [RCV003113452] Chr2:236403331..242801596 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
GRCh37/hg19 2q37.3(chr2:239229304-243199373)x1 copy number loss not provided [RCV002293050] Chr2:239229304..243199373 [GRCh37]
Chr2:2q37.3		 pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:233227837-242783384) copy number loss Chromosome 2q37 deletion syndrome [RCV002280739] Chr2:233227837..242783384 [GRCh37]
Chr2:2q37.1-37.3		 pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236878509-242783384)x1 copy number loss not provided [RCV002473939] Chr2:236878509..242783384 [GRCh37]
Chr2:2q37.2-37.3		 pathogenic
NM_001271977.2(STK25):c.1021A>G (p.Ser341Gly) single nucleotide variant Inborn genetic diseases [RCV002772509] Chr2:241498246 [GRCh38]
Chr2:242437661 [GRCh37]
Chr2:2q37.3		 likely benign
NM_001271977.2(STK25):c.1276C>T (p.Arg426Cys) single nucleotide variant Inborn genetic diseases [RCV002689753] Chr2:241495667 [GRCh38]
Chr2:242435082 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.764C>T (p.Pro255Leu) single nucleotide variant Inborn genetic diseases [RCV002883490] Chr2:241498996 [GRCh38]
Chr2:242438411 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.2930G>A (p.Gly977Asp) single nucleotide variant Inborn genetic diseases [RCV002924542] Chr2:241493327 [GRCh38]
Chr2:242432742 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.2882A>G (p.Tyr961Cys) single nucleotide variant Inborn genetic diseases [RCV002884254] Chr2:241493023 [GRCh38]
Chr2:242432438 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.1093G>A (p.Val365Ile) single nucleotide variant Inborn genetic diseases [RCV002854660] Chr2:241497627 [GRCh38]
Chr2:242437042 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.3044A>G (p.Glu1015Gly) single nucleotide variant Inborn genetic diseases [RCV002919448] Chr2:241493441 [GRCh38]
Chr2:242432856 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.2968C>A (p.His990Asn) single nucleotide variant Inborn genetic diseases [RCV002874429] Chr2:241493365 [GRCh38]
Chr2:242432780 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.301G>A (p.Gly101Ser) single nucleotide variant Inborn genetic diseases [RCV002853610] Chr2:241500757 [GRCh38]
Chr2:242440172 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.3097A>G (p.Ser1033Gly) single nucleotide variant Inborn genetic diseases [RCV002965385] Chr2:241494057 [GRCh38]
Chr2:242433472 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.1034C>T (p.Pro345Leu) single nucleotide variant Inborn genetic diseases [RCV002835857] Chr2:241497686 [GRCh38]
Chr2:242437101 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.1277G>A (p.Arg426His) single nucleotide variant Inborn genetic diseases [RCV002680439] Chr2:241495666 [GRCh38]
Chr2:242435081 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.1087C>T (p.Arg363Trp) single nucleotide variant Inborn genetic diseases [RCV003180624] Chr2:241497633 [GRCh38]
Chr2:242437048 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.976C>T (p.Arg326Trp) single nucleotide variant Inborn genetic diseases [RCV003194674] Chr2:241498291 [GRCh38]
Chr2:242437706 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.2854G>A (p.Val952Ile) single nucleotide variant Inborn genetic diseases [RCV003221013] Chr2:241492995 [GRCh38]
Chr2:242432410 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.2956G>A (p.Ala986Thr) single nucleotide variant Inborn genetic diseases [RCV003188562] Chr2:241493353 [GRCh38]
Chr2:242432768 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.953T>G (p.Ile318Ser) single nucleotide variant Inborn genetic diseases [RCV003208449] Chr2:241498314 [GRCh38]
Chr2:242437729 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.386A>G (p.Asp129Gly) single nucleotide variant Inborn genetic diseases [RCV003198684] Chr2:241500214 [GRCh38]
Chr2:242439629 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.23C>T (p.Ala8Val) single nucleotide variant Inborn genetic diseases [RCV003209302] Chr2:241508013 [GRCh38]
Chr2:242447428 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_001271977.2(STK25):c.1230G>T (p.Glu410Asp) single nucleotide variant Inborn genetic diseases [RCV003201318] Chr2:241496409 [GRCh38]
Chr2:242435824 [GRCh37]
Chr2:2q37.3		 uncertain significance
NM_014808.4(FARP2):c.3070G>A (p.Ala1024Thr) single nucleotide variant Inborn genetic diseases [RCV003216990] Chr2:241494030 [GRCh38]
Chr2:242433445 [GRCh37]
Chr2:2q37.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:13225
Count of miRNA genes:1352
Interacting mature miRNAs:1817
Transcripts:ENST00000316586, ENST00000401869, ENST00000403346, ENST00000405585, ENST00000405883, ENST00000413760, ENST00000420551, ENST00000423004, ENST00000424537, ENST00000426941, ENST00000429279, ENST00000435225, ENST00000436402, ENST00000436917, ENST00000439101, ENST00000440109, ENST00000442307, ENST00000450497, ENST00000452891, ENST00000461760, ENST00000462953, ENST00000465009, ENST00000470438, ENST00000472181, ENST00000478403, ENST00000479442, ENST00000483603, ENST00000487962, ENST00000492127, ENST00000494699, ENST00000495143, ENST00000495372, ENST00000496159, ENST00000535007, ENST00000543554
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
WI-15981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372242,434,106 - 242,434,232UniSTSGRCh37
Build 362242,082,779 - 242,082,905RGDNCBI36
Celera2236,103,687 - 236,103,813RGD
Cytogenetic Map2q37.3UniSTS
HuRef2234,189,611 - 234,189,737UniSTS
GeneMap99-GB4 RH Map2741.5UniSTS
Whitehead-RH Map21079.8UniSTS
NCBI RH Map21915.5UniSTS
WI-19287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372242,434,449 - 242,434,737UniSTSGRCh37
Build 362242,083,122 - 242,083,410RGDNCBI36
Celera2236,104,030 - 236,104,318RGD
Cytogenetic Map2q37.3UniSTS
HuRef2234,189,954 - 234,190,242UniSTS
GeneMap99-GB4 RH Map2741.4UniSTS
Whitehead-RH Map21076.6UniSTS
NCBI RH Map21915.5UniSTS
STK25_9122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372242,434,506 - 242,435,042UniSTSGRCh37
Build 362242,083,179 - 242,083,715RGDNCBI36
Celera2236,104,087 - 236,104,623RGD
HuRef2234,190,011 - 234,190,547UniSTS
RH47049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372242,434,651 - 242,434,783UniSTSGRCh37
Build 362242,083,324 - 242,083,456RGDNCBI36
Celera2236,104,232 - 236,104,364RGD
Cytogenetic Map2q37.3UniSTS
HuRef2234,190,156 - 234,190,288UniSTS
GeneMap99-GB4 RH Map2741.5UniSTS
NCBI RH Map21915.5UniSTS
D15S1477  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q32-q35UniSTS
Cytogenetic Map5q11UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map2q31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q11.21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map1q31.3UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map3p25-p24UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map3p12UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map14q11.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p22.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map15q21-q23UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map17qUniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map6p24.2UniSTS
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2438 2649 1672 572 1669 413 4355 2128 3677 411 1457 1611 175 1 1204 2788 5 2
Low 1 342 54 52 282 52 2 69 57 8 3 2 1
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001271977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001271978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001271979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001271980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282307 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510493 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003169 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047442924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047442925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC110299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC091505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT019961 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU541010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB250694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR936874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D63780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA624380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC353271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ093965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY052981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY315908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X99325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000316586   ⟹   ENSP00000325748
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,492,670 - 241,508,584 (-)Ensembl
RefSeq Acc Id: ENST00000401869   ⟹   ENSP00000385687
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,019 - 241,508,362 (-)Ensembl
RefSeq Acc Id: ENST00000403346   ⟹   ENSP00000384162
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,017 - 241,508,688 (-)Ensembl
RefSeq Acc Id: ENST00000405585   ⟹   ENSP00000385541
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,249 - 241,508,584 (-)Ensembl
RefSeq Acc Id: ENST00000405883   ⟹   ENSP00000384444
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,022 - 241,508,556 (-)Ensembl
RefSeq Acc Id: ENST00000413760   ⟹   ENSP00000395104
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,499,033 - 241,509,326 (-)Ensembl
RefSeq Acc Id: ENST00000420551   ⟹   ENSP00000404552
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,501,517 - 241,508,586 (-)Ensembl
RefSeq Acc Id: ENST00000423004   ⟹   ENSP00000404469
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,496,396 - 241,500,244 (-)Ensembl
RefSeq Acc Id: ENST00000424537   ⟹   ENSP00000417020
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,498,989 - 241,508,333 (-)Ensembl
RefSeq Acc Id: ENST00000426941   ⟹   ENSP00000414191
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,501,393 - 241,508,571 (-)Ensembl
RefSeq Acc Id: ENST00000429279   ⟹   ENSP00000404960
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,499,323 - 241,508,595 (-)Ensembl
RefSeq Acc Id: ENST00000435225   ⟹   ENSP00000401114
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,500,172 - 241,502,003 (-)Ensembl
RefSeq Acc Id: ENST00000436402   ⟹   ENSP00000412617
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,499,387 - 241,508,362 (-)Ensembl
RefSeq Acc Id: ENST00000436917
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,500,860 - 241,508,582 (-)Ensembl
RefSeq Acc Id: ENST00000439101   ⟹   ENSP00000406208
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,500,260 - 241,508,332 (-)Ensembl
RefSeq Acc Id: ENST00000440109   ⟹   ENSP00000403866
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,500,143 - 241,509,730 (-)Ensembl
RefSeq Acc Id: ENST00000442307   ⟹   ENSP00000403607
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,498,989 - 241,508,624 (-)Ensembl
RefSeq Acc Id: ENST00000450497   ⟹   ENSP00000399212
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,498,743 - 241,501,526 (-)Ensembl
RefSeq Acc Id: ENST00000452891
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,500,763 - 241,508,571 (-)Ensembl
RefSeq Acc Id: ENST00000461760
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,498,670 - 241,509,298 (-)Ensembl
RefSeq Acc Id: ENST00000462953
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,497,333 - 241,498,332 (-)Ensembl
RefSeq Acc Id: ENST00000465009
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,538 - 241,498,732 (-)Ensembl
RefSeq Acc Id: ENST00000470438
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,490 - 241,498,249 (-)Ensembl
RefSeq Acc Id: ENST00000472181
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,493,388 - 241,495,153 (-)Ensembl
RefSeq Acc Id: ENST00000478403
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,448 - 241,499,190 (-)Ensembl
RefSeq Acc Id: ENST00000479442
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,499,903 - 241,500,871 (-)Ensembl
RefSeq Acc Id: ENST00000483603
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,500,780 - 241,508,607 (-)Ensembl
RefSeq Acc Id: ENST00000487962
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,050 - 241,499,972 (-)Ensembl
RefSeq Acc Id: ENST00000492127
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,499,407 - 241,501,698 (-)Ensembl
RefSeq Acc Id: ENST00000494699
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,495,046 - 241,496,538 (-)Ensembl
RefSeq Acc Id: ENST00000495143
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,498,510 - 241,499,320 (-)Ensembl
RefSeq Acc Id: ENST00000495372
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,501,357 - 241,508,583 (-)Ensembl
RefSeq Acc Id: ENST00000496159
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,500,047 - 241,501,698 (-)Ensembl
RefSeq Acc Id: ENST00000535007   ⟹   ENSP00000446008
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,494,707 - 241,508,695 (-)Ensembl
RefSeq Acc Id: ENST00000543554   ⟹   ENSP00000444886
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2241,494,707 - 241,509,572 (-)Ensembl
RefSeq Acc Id: NM_001271977   ⟹   NP_001258906
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
GRCh372242,434,122 - 242,449,145 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,077 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001271978   ⟹   NP_001258907
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,345 (-)NCBI
GRCh372242,434,122 - 242,449,145 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,453,742 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,672 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001271979   ⟹   NP_001258908
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
GRCh372242,434,122 - 242,449,145 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,077 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001271980   ⟹   NP_001258909
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
GRCh372242,434,122 - 242,449,145 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,077 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282305   ⟹   NP_001269234
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,494,707 - 241,509,572 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,954 (-)NCBI
T2T-CHM13v2.02241,994,044 - 242,008,899 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282306   ⟹   NP_001269235
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,077 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282307   ⟹   NP_001269236
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,077 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282308   ⟹   NP_001269237
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,077 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
Sequence:
RefSeq Acc Id: NM_006374   ⟹   NP_006365
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
GRCh372242,434,122 - 242,449,145 (-)NCBI
Build 362242,083,105 - 242,096,707 (-)NCBI Archive
Celera2236,104,013 - 236,117,625 (-)RGD
HuRef2234,189,627 - 234,204,482 (-)NCBI
CHM1_12242,440,093 - 242,454,077 (-)NCBI
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011510493   ⟹   XP_011508795
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,496,565 - 241,508,345 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011510494   ⟹   XP_011508796
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011510495   ⟹   XP_011508797
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,509,572 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011510496   ⟹   XP_011508798
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,496,561 - 241,508,345 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017003170   ⟹   XP_016858659
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047442924   ⟹   XP_047298880
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,496,398 - 241,508,345 (-)NCBI
RefSeq Acc Id: XM_047442925   ⟹   XP_047298881
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,492,670 - 241,508,584 (-)NCBI
RefSeq Acc Id: XM_054340182   ⟹   XP_054196157
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02241,995,902 - 242,007,672 (-)NCBI
RefSeq Acc Id: XM_054340183   ⟹   XP_054196158
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02241,995,735 - 242,007,672 (-)NCBI
RefSeq Acc Id: XM_054340184   ⟹   XP_054196159
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
RefSeq Acc Id: XM_054340185   ⟹   XP_054196160
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
RefSeq Acc Id: XM_054340186   ⟹   XP_054196161
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02241,992,007 - 242,007,911 (-)NCBI
RefSeq Acc Id: XM_054340187   ⟹   XP_054196162
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02241,995,898 - 242,007,672 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001258906 (Get FASTA)   NCBI Sequence Viewer  
  NP_001258907 (Get FASTA)   NCBI Sequence Viewer  
  NP_001258908 (Get FASTA)   NCBI Sequence Viewer  
  NP_001258909 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269234 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269235 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269236 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269237 (Get FASTA)   NCBI Sequence Viewer  
  NP_006365 (Get FASTA)   NCBI Sequence Viewer  
  XP_011508795 (Get FASTA)   NCBI Sequence Viewer  
  XP_011508796 (Get FASTA)   NCBI Sequence Viewer  
  XP_011508797 (Get FASTA)   NCBI Sequence Viewer  
  XP_011508798 (Get FASTA)   NCBI Sequence Viewer  
  XP_016858659 (Get FASTA)   NCBI Sequence Viewer  
  XP_047298880 (Get FASTA)   NCBI Sequence Viewer  
  XP_047298881 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196157 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196158 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196159 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196160 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196161 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196162 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH07852 (Get FASTA)   NCBI Sequence Viewer  
  AAH15793 (Get FASTA)   NCBI Sequence Viewer  
  AAH91505 (Get FASTA)   NCBI Sequence Viewer  
  AAV38764 (Get FASTA)   NCBI Sequence Viewer  
  AAY14683 (Get FASTA)   NCBI Sequence Viewer  
  AAY88740 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33986 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33987 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33988 (Get FASTA)   NCBI Sequence Viewer  
  BAA20420 (Get FASTA)   NCBI Sequence Viewer  
  BAF84497 (Get FASTA)   NCBI Sequence Viewer  
  BAF84636 (Get FASTA)   NCBI Sequence Viewer  
  BAG52488 (Get FASTA)   NCBI Sequence Viewer  
  BAG59817 (Get FASTA)   NCBI Sequence Viewer  
  BAG62789 (Get FASTA)   NCBI Sequence Viewer  
  BAG63964 (Get FASTA)   NCBI Sequence Viewer  
  BAG64697 (Get FASTA)   NCBI Sequence Viewer  
  BAH14337 (Get FASTA)   NCBI Sequence Viewer  
  CAA67700 (Get FASTA)   NCBI Sequence Viewer  
  CAI59786 (Get FASTA)   NCBI Sequence Viewer  
  EAW71265 (Get FASTA)   NCBI Sequence Viewer  
  EAW71266 (Get FASTA)   NCBI Sequence Viewer  
  O00506 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_006365   ⟸   NM_006374
- Peptide Label: isoform 1
- UniProtKB: Q5BJF1 (UniProtKB/Swiss-Prot),   O00506 (UniProtKB/Swiss-Prot),   A0A024R4B2 (UniProtKB/TrEMBL),   A0A0S2Z4Y9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001258909   ⟸   NM_001271980
- Peptide Label: isoform 2
- UniProtKB: O00506 (UniProtKB/Swiss-Prot),   A0A0S2Z4Y2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001258908   ⟸   NM_001271979
- Peptide Label: isoform 2
- UniProtKB: O00506 (UniProtKB/Swiss-Prot),   B3KRS6 (UniProtKB/TrEMBL),   A0A0S2Z4Y2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001258906   ⟸   NM_001271977
- Peptide Label: isoform 1
- UniProtKB: Q5BJF1 (UniProtKB/Swiss-Prot),   O00506 (UniProtKB/Swiss-Prot),   A0A024R4B2 (UniProtKB/TrEMBL),   A0A0S2Z4Y9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001258907   ⟸   NM_001271978
- Peptide Label: isoform 1
- UniProtKB: Q5BJF1 (UniProtKB/Swiss-Prot),   O00506 (UniProtKB/Swiss-Prot),   A0A024R4B2 (UniProtKB/TrEMBL),   Q96BA2 (UniProtKB/TrEMBL),   A0A0S2Z4Y9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269234   ⟸   NM_001282305
- Peptide Label: isoform 3
- UniProtKB: O00506 (UniProtKB/Swiss-Prot),   B4E185 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269237   ⟸   NM_001282308
- Peptide Label: isoform 3
- UniProtKB: O00506 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001269236   ⟸   NM_001282307
- Peptide Label: isoform 3
- UniProtKB: O00506 (UniProtKB/Swiss-Prot),   B4DMA5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269235   ⟸   NM_001282306
- Peptide Label: isoform 4
- UniProtKB: B4DVS7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011508797   ⟸   XM_011510495
- Peptide Label: isoform X3
- UniProtKB: B4DVS7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011508796   ⟸   XM_011510494
- Peptide Label: isoform X3
- UniProtKB: B4DVS7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011508798   ⟸   XM_011510496
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011508795   ⟸   XM_011510493
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016858659   ⟸   XM_017003170
- Peptide Label: isoform X3
- UniProtKB: B4DVS7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000404469   ⟸   ENST00000423004
RefSeq Acc Id: ENSP00000417020   ⟸   ENST00000424537
RefSeq Acc Id: ENSP00000399212   ⟸   ENST00000450497
RefSeq Acc Id: ENSP00000406208   ⟸   ENST00000439101
RefSeq Acc Id: ENSP00000444886   ⟸   ENST00000543554
RefSeq Acc Id: ENSP00000414191   ⟸   ENST00000426941
RefSeq Acc Id: ENSP00000395104   ⟸   ENST00000413760
RefSeq Acc Id: ENSP00000404960   ⟸   ENST00000429279
RefSeq Acc Id: ENSP00000403866   ⟸   ENST00000440109
RefSeq Acc Id: ENSP00000385687   ⟸   ENST00000401869
RefSeq Acc Id: ENSP00000403607   ⟸   ENST00000442307
RefSeq Acc Id: ENSP00000384162   ⟸   ENST00000403346
RefSeq Acc Id: ENSP00000446008   ⟸   ENST00000535007
RefSeq Acc Id: ENSP00000385541   ⟸   ENST00000405585
RefSeq Acc Id: ENSP00000384444   ⟸   ENST00000405883
RefSeq Acc Id: ENSP00000404552   ⟸   ENST00000420551
RefSeq Acc Id: ENSP00000325748   ⟸   ENST00000316586
RefSeq Acc Id: ENSP00000401114   ⟸   ENST00000435225
RefSeq Acc Id: ENSP00000412617   ⟸   ENST00000436402
RefSeq Acc Id: XP_047298881   ⟸   XM_047442925
- Peptide Label: isoform X3
- UniProtKB: B4DVS7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047298880   ⟸   XM_047442924
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054196161   ⟸   XM_054340186
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054196159   ⟸   XM_054340184
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054196160   ⟸   XM_054340185
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054196158   ⟸   XM_054340183
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054196162   ⟸   XM_054340187
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054196157   ⟸   XM_054340182
- Peptide Label: isoform X1
Protein Domains
Protein kinase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O00506-F1-model_v2 AlphaFold O00506 1-426 view protein structure

Promoters
RGD ID:6863356
Promoter ID:EPDNEW_H4843
Type:initiation region
Name:STK25_2
Description:serine/threonine kinase 25
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4844  EPDNEW_H4845  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,508,343 - 241,508,403EPDNEW
RGD ID:6863358
Promoter ID:EPDNEW_H4844
Type:initiation region
Name:STK25_1
Description:serine/threonine kinase 25
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4843  EPDNEW_H4845  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,508,584 - 241,508,644EPDNEW
RGD ID:6863360
Promoter ID:EPDNEW_H4845
Type:initiation region
Name:STK25_3
Description:serine/threonine kinase 25
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4843  EPDNEW_H4844  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382241,508,787 - 241,508,847EPDNEW
RGD ID:6798288
Promoter ID:HG_KWN:38216
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000323152
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,083,639 - 242,084,139 (-)MPROMDB
RGD ID:6798286
Promoter ID:HG_KWN:38217
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000323133
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,084,451 - 242,085,552 (-)MPROMDB
RGD ID:6798291
Promoter ID:HG_KWN:38218
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000323125,   OTTHUMT00000323127,   OTTHUMT00000323128,   OTTHUMT00000323129,   OTTHUMT00000323130,   OTTHUMT00000323131,   OTTHUMT00000323132,   UC002WBK.1,   UC002WBL.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,086,381 - 242,089,467 (-)MPROMDB
RGD ID:6798290
Promoter ID:HG_KWN:38220
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000403346,   OTTHUMT00000257265,   OTTHUMT00000323103,   OTTHUMT00000323104,   OTTHUMT00000323105,   OTTHUMT00000323106,   OTTHUMT00000323107,   OTTHUMT00000323108,   OTTHUMT00000323110,   OTTHUMT00000323111,   OTTHUMT00000323117,   OTTHUMT00000323118,   OTTHUMT00000323151,   UC002WBM.1,   UC002WBO.1,   UC010FZO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,096,131 - 242,097,262 (-)MPROMDB
RGD ID:6852388
Promoter ID:EP74002
Type:initiation region
Name:HS_STK25_3
Description:Serine/threonine kinase 25 (STE20 homolog, yeast).
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:alternative promoter #3 of 3; 5' exon 1; site 3; major promoter.; see alsoEP73999  EP74001  
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,096,385 - 242,096,445EPD
RGD ID:6852386
Promoter ID:EP74001
Type:initiation region
Name:HS_STK25_2
Description:Serine/threonine kinase 25 (STE20 homolog, yeast).
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:alternative promoter #2 of 3; 5' exon 1; site 2.; see alsoEP73999  EP74002  
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,096,629 - 242,096,689EPD
RGD ID:6852384
Promoter ID:EP73999
Type:initiation region
Name:HS_STK25_1
Description:Serine/threonine kinase 25 (STE20 homolog, yeast).
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:alternative promoter #1 of 3; 5' exon 1; site 1.; see alsoEP74001  EP74002  
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,096,683 - 242,096,743EPD
RGD ID:6798287
Promoter ID:HG_KWN:38221
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000323119,   OTTHUMT00000323121,   OTTHUMT00000323126
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,097,346 - 242,097,846 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11404 AgrOrtholog
COSMIC STK25 COSMIC
Ensembl Genes ENSG00000115694 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000325748 ENTREZGENE
  ENSP00000325748.4 UniProtKB/Swiss-Prot
  ENSP00000384162 ENTREZGENE
  ENSP00000384162.3 UniProtKB/Swiss-Prot
  ENSP00000384444 ENTREZGENE
  ENSP00000384444.3 UniProtKB/Swiss-Prot
  ENSP00000385541 ENTREZGENE
  ENSP00000385541.1 UniProtKB/Swiss-Prot
  ENSP00000385687 ENTREZGENE
  ENSP00000385687.1 UniProtKB/Swiss-Prot
  ENSP00000395104.1 UniProtKB/TrEMBL
  ENSP00000399212.1 UniProtKB/TrEMBL
  ENSP00000401114.1 UniProtKB/TrEMBL
  ENSP00000403607.1 UniProtKB/TrEMBL
  ENSP00000403866.1 UniProtKB/TrEMBL
  ENSP00000404469.1 UniProtKB/TrEMBL
  ENSP00000404552.1 UniProtKB/TrEMBL
  ENSP00000404960.1 UniProtKB/TrEMBL
  ENSP00000406208.1 UniProtKB/TrEMBL
  ENSP00000412617.1 UniProtKB/TrEMBL
  ENSP00000414191.1 UniProtKB/TrEMBL
  ENSP00000417020.1 UniProtKB/TrEMBL
  ENSP00000444886 ENTREZGENE
  ENSP00000444886.1 UniProtKB/Swiss-Prot
  ENSP00000446008 ENTREZGENE
  ENSP00000446008.1 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000316586 ENTREZGENE
  ENST00000316586.9 UniProtKB/Swiss-Prot
  ENST00000401869 ENTREZGENE
  ENST00000401869.5 UniProtKB/Swiss-Prot
  ENST00000403346 ENTREZGENE
  ENST00000403346.7 UniProtKB/Swiss-Prot
  ENST00000405585 ENTREZGENE
  ENST00000405585.5 UniProtKB/Swiss-Prot
  ENST00000405883 ENTREZGENE
  ENST00000405883.7 UniProtKB/Swiss-Prot
  ENST00000413760.5 UniProtKB/TrEMBL
  ENST00000420551.1 UniProtKB/TrEMBL
  ENST00000423004.5 UniProtKB/TrEMBL
  ENST00000424537.5 UniProtKB/TrEMBL
  ENST00000426941.1 UniProtKB/TrEMBL
  ENST00000429279.5 UniProtKB/TrEMBL
  ENST00000435225.5 UniProtKB/TrEMBL
  ENST00000436402.5 UniProtKB/TrEMBL
  ENST00000439101.5 UniProtKB/TrEMBL
  ENST00000440109.5 UniProtKB/TrEMBL
  ENST00000442307.5 UniProtKB/TrEMBL
  ENST00000450497.5 UniProtKB/TrEMBL
  ENST00000535007 ENTREZGENE
  ENST00000535007.5 UniProtKB/Swiss-Prot
  ENST00000543554 ENTREZGENE
  ENST00000543554.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.12.70 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000115694 GTEx
HGNC ID HGNC:11404 ENTREZGENE
Human Proteome Map STK25 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDC10_dimerisation_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kinase_ATP_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser-Thr/Tyr_kinase_cat_dom UniProtKB/TrEMBL
  STK_STK25 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10494 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 10494 ENTREZGENE
OMIM 602255 OMIM
PANTHER SERINE/THREONINE-PROTEIN KINASE 25 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STERILE20-LIKE KINASE, ISOFORM B-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36211 PharmGKB
PRINTS TYRKINASE UniProtKB/TrEMBL
PROSITE PROTEIN_KINASE_ATP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R4B2 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z4Y2 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z4Y9 ENTREZGENE
  A0A0S2Z503_HUMAN UniProtKB/TrEMBL
  B3KRS6 ENTREZGENE, UniProtKB/TrEMBL
  B4DMA5 ENTREZGENE, UniProtKB/TrEMBL
  B4DVS7 ENTREZGENE, UniProtKB/TrEMBL
  B4E185 ENTREZGENE, UniProtKB/TrEMBL
  C9J232_HUMAN UniProtKB/TrEMBL
  C9J6L2_HUMAN UniProtKB/TrEMBL
  C9J8E8_HUMAN UniProtKB/TrEMBL
  C9JCC0_HUMAN UniProtKB/TrEMBL
  C9JDH9_HUMAN UniProtKB/TrEMBL
  C9JFA1_HUMAN UniProtKB/TrEMBL
  C9JIH8_HUMAN UniProtKB/TrEMBL
  C9JJV0_HUMAN UniProtKB/TrEMBL
  C9JN58_HUMAN UniProtKB/TrEMBL
  C9K0M6_HUMAN UniProtKB/TrEMBL
  E7EM58_HUMAN UniProtKB/TrEMBL
  H7C279_HUMAN UniProtKB/TrEMBL
  O00506 ENTREZGENE
  Q5BJF1 ENTREZGENE
  Q96BA2 ENTREZGENE, UniProtKB/TrEMBL
  STK25_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A0A0S2Z4Y9 UniProtKB/TrEMBL
  A8K6Z3 UniProtKB/Swiss-Prot
  A8K7D2 UniProtKB/Swiss-Prot
  B7Z9K1 UniProtKB/Swiss-Prot
  Q15522 UniProtKB/Swiss-Prot
  Q5BJF1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-07-27 STK25  serine/threonine kinase 25  STK25  serine/threonine kinase 25 (STE20 homolog, yeast)  Symbol and/or name change 5135510 APPROVED