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2025-05-09 16:41:06, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_004442 4869 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens EPH receptor B2 (EPHB2), transcript variant 2, mRNA.
ACCESSION NM_004442
VERSION NM_004442.6 GI:111118979
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 4869)
AUTHORS Wang,S.D., Rath,P., Lal,B., Richard,J.P., Li,Y., Goodwin,C.R.,
Laterra,J. and Xia,S.
TITLE EphB2 receptor controls proliferation/migration dichotomy of
glioblastoma by interacting with focal adhesion kinase
JOURNAL Oncogene 31 (50), 5132-5143 (2012)
PUBMED 22310282
REMARK GeneRIF: EphB2 silencing increased tumor cell proliferation.
REFERENCE 2 (bases 1 to 4869)
AUTHORS Sikkema,A.H., den Dunnen,W.F., Hulleman,E., van Vuurden,D.G.,
Garcia-Manero,G., Yang,H., Scherpen,F.J., Kampen,K.R., Hoving,E.W.,
Kamps,W.A., Diks,S.H., Peppelenbosch,M.P. and de Bont,E.S.
TITLE EphB2 activity plays a pivotal role in pediatric medulloblastoma
cell adhesion and invasion
JOURNAL Neuro-oncology 14 (9), 1125-1135 (2012)
PUBMED 22723427
REMARK GeneRIF: High ephrin-B1 expression is associated with
medulloblastoma.
REFERENCE 3 (bases 1 to 4869)
AUTHORS Tu,Y., He,S., Fu,J., Li,G., Xu,R., Lu,H. and Deng,J.
TITLE Expression of EphrinB2 and EphB4 in glioma tissues correlated to
the progression of glioma and the prognosis of glioblastoma
patients
JOURNAL Clin Transl Oncol 14 (3), 214-220 (2012)
PUBMED 22374425
REMARK GeneRIF: Data indicated for the first time that EphrinB2 and EphB4
expressions increase according to the histopathological grade and
KPS score of glioma, and their expression levels are related to the
progression-free survival of glioblastoma patients.
REFERENCE 4 (bases 1 to 4869)
AUTHORS Azab,F., Azab,A.K., Maiso,P., Calimeri,T., Flores,L., Liu,Y.,
Quang,P., Roccaro,A.M., Sacco,A., Ngo,H.T., Zhang,Y., Morgan,B.L.,
Carrasco,R.D. and Ghobrial,I.M.
TITLE Eph-B2/ephrin-B2 interaction plays a major role in the adhesion and
proliferation of Waldenstrom's macroglobulinemia
JOURNAL Clin. Cancer Res. 18 (1), 91-104 (2012)
PUBMED 22010211
REMARK GeneRIF: High Eph-B2 is associated with Waldenstrom's
macroglobulinemia.
REFERENCE 5 (bases 1 to 4869)
AUTHORS Benzinou,M., Clermont,F.F., Letteboer,T.G., Kim,J.H., Espejel,S.,
Harradine,K.A., Arbelaez,J., Luu,M.T., Roy,R., Quigley,D.,
Higgins,M.N., Zaid,M., Aouizerat,B.E., van Amstel,J.K., Giraud,S.,
Dupuis-Girod,S., Lesca,G., Plauchu,H., Hughes,C.C., Westermann,C.J.
and Akhurst,R.J.
TITLE Mouse and human strategies identify PTPN14 as a modifier of
angiogenesis and hereditary haemorrhagic telangiectasia
JOURNAL Nat Commun 3, 616 (2012)
PUBMED 22233626
REMARK GeneRIF: PTPN14 has a role in angiogenesis and/or arteriovenous
fate, acting via EphrinB2 and ACVRL1/activin receptor-like kinase 1
Erratum:[Nat Commun. 2012;3:1148]
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 4869)
AUTHORS Saito,T., Seki,N., Matsuda,Y., Kitahara,M., Murata,M., Kanda,N.,
Nomura,N., Yamamoto,T. and Hori,T.A.
TITLE Identification of the human ERK gene as a putative receptor
tyrosine kinase and its chromosomal localization to 1p36.1: a
comparative mapping of human, mouse, and rat chromosomes
JOURNAL Genomics 26 (2), 382-384 (1995)
PUBMED 7601466
REFERENCE 7 (bases 1 to 4869)
AUTHORS Fox,G.M., Holst,P.L., Chute,H.T., Lindberg,R.A., Janssen,A.M.,
Basu,R. and Welcher,A.A.
TITLE cDNA cloning and tissue distribution of five human EPH-like
receptor protein-tyrosine kinases
JOURNAL Oncogene 10 (5), 897-905 (1995)
PUBMED 7898931
REFERENCE 8 (bases 1 to 4869)
AUTHORS Bannister,A.J., Brown,H.J., Sutherland,J.A. and Kouzarides,T.
TITLE Phosphorylation of the c-Fos and c-Jun HOB1 motif stimulates its
activation capacity
JOURNAL Nucleic Acids Res. 22 (24), 5173-5176 (1994)
PUBMED 7816602
REFERENCE 9 (bases 1 to 4869)
AUTHORS Iwase,T., Tanaka,M., Suzuki,M., Naito,Y., Sugimura,H. and Kino,I.
TITLE Identification of protein-tyrosine kinase genes preferentially
expressed in embryo stomach and gastric cancer
JOURNAL Biochem. Biophys. Res. Commun. 194 (2), 698-705 (1993)
PUBMED 7688222
REFERENCE 10 (bases 1 to 4869)
AUTHORS Chan,J. and Watt,V.M.
TITLE eek and erk, new members of the eph subclass of receptor
protein-tyrosine kinases
JOURNAL Oncogene 6 (6), 1057-1061 (1991)
PUBMED 1648701
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL158086.32, AL512444.20,
AL035704.9 and L41939.1.
This sequence is a reference standard in the RefSeqGene project.
On Aug 2, 2006 this sequence version replaced gi:55774977.
Summary: Ephrin receptors and their ligands, the ephrins, mediate
numerous developmental processes, particularly in the nervous
system. Based on their structures and sequence relationships,
ephrins are divided into the ephrin-A (EFNA) class, which are
anchored to the membrane by a glycosylphosphatidylinositol linkage,
and the ephrin-B (EFNB) class, which are transmembrane proteins.
The Eph family of receptors are divided into 2 groups based on the
similarity of their extracellular domain sequences and their
affinities for binding ephrin-A and ephrin-B ligands. Ephrin
receptors make up the largest subgroup of the receptor tyrosine
kinase (RTK) family. The protein encoded by this gene is a receptor
for ephrin-B family members. [provided by RefSeq, Jul 2008].
Transcript Variant: This variant (2) uses an alternate in-frame
splice site in the 3' coding region, compared to variant 1,
resulting in a longer protein (isoform 2).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: L41939.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025086 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-206 AL158086.32 83555-83760
207-271 AL512444.20 25897-25961
272-956 AL512444.20 28868-29552
957-1112 AL512444.20 107513-107668
1113-1448 AL512444.20 109353-109688
1449-1573 AL035704.9 2246-2370
1574-1736 L41939.1 1533-1695
1737-1845 AL035704.9 15359-15467
1846-1913 AL035704.9 16298-16365
1914-2036 AL035704.9 25874-25996
2037-2284 AL035704.9 26597-26844
2285-2500 AL035704.9 27840-28055
2501-2650 AL035704.9 28909-29058
2651-2844 AL035704.9 30269-30462
2845-3000 AL035704.9 32331-32486
3001-4869 AL035704.9 33349-35217
FEATURES Location/Qualifiers
source 1..4869
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1p36.1-p35"
gene 1..4869
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="EPH receptor B2"
/db_xref="GeneID:2048"
/db_xref="HGNC:3393"
/db_xref="HPRD:02997"
/db_xref="MIM:600997"
exon 1..206
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
CDS 146..3109
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/EC_number="2.7.10.1"
/note="isoform 2 precursor is encoded by transcript
variant 2; elk-related tyrosine kinase; ephrin type-B
receptor 2; protein-tyrosine kinase HEK5; eph tyrosine
kinase 3; EPH-like kinase 5; tyrosine-protein kinase
TYRO5; renal carcinoma antigen NY-REN-47; tyrosine-protein
kinase receptor EPH-3; developmentally-regulated
Eph-related tyrosine kinase"
/codon_start=1
/product="ephrin type-B receptor 2 isoform 2 precursor"
/protein_id="NP_004433.2"
/db_xref="GI:21396504"
/db_xref="CCDS:CCDS230.1"
/db_xref="GeneID:2048"
/db_xref="HGNC:3393"
/db_xref="HPRD:02997"
/db_xref="MIM:600997"
/translation="
MALRRLGAALLLLPLLAAVEETLMDSTTATAELGWMVHPPSGWEEVSGYDENMNTIRTYQVCNVFESSQNNWLRTKFIRRRGAHRIHVEMKFSVRDCSSIPSVPGSCKETFNLYYYEADFDSATKTFPNWMENPWVKVDTIAADESFSQVDLGGRVMKINTEVRSFGPVSRSGFYLAFQDYGGCMSLIAVRVFYRKCPRIIQNGAIFQETLSGAESTSLVAARGSCIANAEEVDVPIKLYCNGDGEWLVPIGRCMCKAGFEAVENGTVCRGCPSGTFKANQGDEACTHCPINSRTTSEGATNCVCRNGYYRADLDPLDMPCTTIPSAPQAVISSVNETSLMLEWTPPRDSGGREDLVYNIICKSCGSGRGACTRCGDNVQYAPRQLGLTEPRIYISDLLAHTQYTFEIQAVNGVTDQSPFSPQFASVNITTNQAAPSAVSIMHQVSRTVDSITLSWSQPDQPNGVILDYELQYYEKELSEYNATAIKSPTNTVTVQGLKAGAIYVFQVRARTVAGYGRYSGKMYFQTMTEAEYQTSIQEKLPLIIGSSAAGLVFLIAVVVIAIVCNRRRGFERADSEYTDKLQHYTSGHMTPGMKIYIDPFTYEDPNEAVREFAKEIDISCVKIEQVIGAGEFGEVCSGHLKLPGKREIFVAIKTLKSGYTEKQRRDFLSEASIMGQFDHPNVIHLEGVVTKSTPVMIITEFMENGSLDSFLRQNDGQFTVIQLVGMLRGIAAGMKYLADMNYVHRDLAARNILVNSNLVCKVSDFGLSRFLEDDTSDPTYTSALGGKIPIRWTAPEAIQYRKFTSASDVWSYGIVMWEVMSYGERPYWDMTNQDVINAIEQDYRLPPPMDCPSALHQLMLDCWQKDRNHRPKFGQIVNTLDKMIRNPNSLKAMAPLSSGINLPLLDRTIPDYTSFNTVDEWLEAIKMGQYKESFANAGFTSFDVVSQMMMEDILRVGVTLAGHQKKILNSIQVMRAQMNQIQSVEV
"
sig_peptide 146..199
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 200..3106
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/product="ephrin type-B receptor 2 isoform 2"
misc_feature 200..733
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Ligand Binding Domain of Ephrin type-B Receptor 2;
Region: EphR_LBD_B2; cd10477"
/db_xref="CDD:198445"
misc_feature order(227..235,239..241,275..286,290..292,302..304,
308..310,314..316,323..325,422..430,440..442,446..448,
584..586,590..613,617..622,695..697,701..703,707..709)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="ephrin binding site [polypeptide binding]; other
site"
/db_xref="CDD:198445"
misc_feature 938..1051
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="GCC2 and GCC3; Region: GCC2_GCC3; pfam07699"
/db_xref="CDD:148998"
misc_feature 1118..1438
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cd00063"
/db_xref="CDD:28945"
misc_feature order(1118..1120,1343..1345,1388..1390)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Interdomain contacts; other site"
/db_xref="CDD:28945"
misc_feature order(1391..1393,1397..1399,1403..1408)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Cytokine receptor motif; other site"
/db_xref="CDD:28945"
misc_feature 1451..1726
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cd00063"
/db_xref="CDD:28945"
misc_feature order(1451..1453,1643..1645,1688..1690)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Interdomain contacts; other site"
/db_xref="CDD:28945"
misc_feature order(1691..1696,1700..1705)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Cytokine receptor motif; other site"
/db_xref="CDD:28945"
misc_feature 1877..1879
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1898..1900
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1934..1936
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1952..1954
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:02997"
misc_feature 1994..2800
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Catalytic domain of the Protein Tyrosine Kinases,
Class EphB Ephrin Receptors; Region: PTKc_EphR_B; cd05065"
/db_xref="CDD:173638"
misc_feature 2009..2788
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Protein tyrosine kinase; Region: Pkinase_Tyr;
pfam07714"
/db_xref="CDD:203736"
misc_feature order(2027..2041,2051..2053,2099..2101,2105..2107,
2243..2248,2252..2254,2264..2266,2384..2386,2396..2401,
2405..2407,2438..2440,2501..2515,2540..2542,2642..2644)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="active site"
/db_xref="CDD:173638"
misc_feature order(2027..2035,2039..2041,2051..2053,2099..2101,
2105..2107,2243..2248,2252..2254,2264..2266,2399..2401,
2405..2407,2438..2440)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="ATP binding site [chemical binding]; other site"
/db_xref="CDD:173638"
misc_feature 2123..2125
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2354..2356
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2372..2374
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature order(2384..2386,2396..2398,2501..2515,2540..2542,
2642..2644)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="substrate binding site [chemical binding]; other
site"
/db_xref="CDD:173638"
misc_feature 2435..2521
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="activation loop (A-loop); other site"
/db_xref="CDD:173638"
misc_feature 2471..2473
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:02997"
misc_feature 2474..2476
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:02997"
misc_feature 2486..2488
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2546..2548
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2876..3088
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="SAM domain of EPH-B2 subfamily of tyrosine kinase
receptors; Region: SAM_EPH-B2; cd09552"
/db_xref="CDD:188951"
misc_feature 2876..3079
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="Sterile alpha motif; Region: SAM; smart00454"
/db_xref="CDD:197735"
misc_feature order(2882..2887,2891..2893,2957..2959,2975..2980,
3002..3004,3026..3037,3041..3046,3068..3070,3080..3082)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="homooligomer interface [polypeptide binding]; other
site"
/db_xref="CDD:188951"
misc_feature order(2882..2884,2891..2893,2909..2911,2972..2974,
3056..3058,3065..3070)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="putative homodimer interface (head-to-head)
[polypeptide binding]; other site"
/db_xref="CDD:188951"
misc_feature order(2936..2938,3035..3037)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="putative phosphorylation site [posttranslational
modification]; other site"
/db_xref="CDD:188951"
misc_feature 2936..2938
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature order(2984..3001,3008..3010,3062..3064,3071..3073,
3080..3085)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="homodimer interface (tail-to-tail) [polypeptide
binding]; other site"
/db_xref="CDD:188951"
exon 207..271
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 210
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201121087"
variation 223
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144258519"
variation 225
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372861666"
variation 236
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141486320"
variation 255
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:113343034"
exon 272..956
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 309
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:202156735"
variation 310
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201427890"
variation 335
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:72653677"
variation 365
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372282301"
variation 380
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:139122679"
variation 384
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:181872637"
variation 387
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368075671"
variation 391
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146514629"
variation 392
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201337795"
variation 424
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371651342"
variation 437
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200905937"
variation 451
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375951467"
variation 459
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:113970284"
variation 460
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:369585313"
variation 498
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:200904787"
variation 592
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:372861886"
variation 609
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:185887197"
variation 610
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:145478829"
variation 611
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376990288"
variation 628
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144238498"
variation 652
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:199957897"
variation 655
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:61732489"
variation 691
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377706540"
variation 709
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373502541"
variation 712
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:150957873"
variation 715
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:147098147"
variation 729
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370909083"
variation 741
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201754821"
variation 769
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141122680"
variation 780
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:202146067"
variation 799
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149351655"
variation 802
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1371869"
variation 817
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:368738883"
variation 831
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200990235"
variation 835
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:374426229"
variation 853
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146009391"
variation 891
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:202178471"
variation 895
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:113102633"
variation 898
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:368639670"
variation 902
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200565776"
variation 932
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150803261"
variation 938
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:202059800"
variation 947
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369702152"
exon 957..1112
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 964
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372620832"
variation 980
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:35882952"
variation 992
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:142113032"
variation 1026
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147727992"
variation 1069
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:12083517"
variation 1075
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:75882465"
variation 1094
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:150415344"
exon 1113..1448
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1124
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200298851"
variation 1126
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:199559345"
variation 1133
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142890560"
variation 1190
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368529651"
variation 1192
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370793503"
variation 1226
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:56180036"
variation 1245
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199648689"
variation 1251
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141626076"
variation 1256
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200609603"
variation 1273
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:200412547"
variation 1279
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:147147271"
variation 1288
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375578940"
variation 1289
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368104279"
variation 1306
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:147798911"
variation 1381
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:139840326"
variation 1385
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149014913"
exon 1449..1573
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1456
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375004699"
variation 1484
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199940448"
variation 1490
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369350136"
variation 1510
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200120268"
variation 1522
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2229872"
variation 1533
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377028693"
variation 1538
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371215652"
variation 1566
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138869509"
exon 1574..1736
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1574
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138075206"
variation 1576
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200298496"
variation 1595..1596
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace=""
/replace="cccccc"
/db_xref="dbSNP:138296617"
variation 1595
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:116848191"
variation 1621
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370664820"
variation 1628
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201691912"
variation 1646
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373865135"
variation 1648
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:147223001"
variation 1681
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142703174"
variation 1687
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:367743248"
variation 1690
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:309472"
variation 1693
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:34273063"
variation 1697
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369387828"
exon 1737..1845
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1744
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370702549"
variation 1793
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:144480560"
variation 1816
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141173528"
variation 1829
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:199607174"
variation 1834
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:35847739"
exon 1846..1913
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1850
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200219468"
variation 1852
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:376417187"
variation 1870
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:56264796"
variation 1872
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146071874"
variation 1873
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200494586"
variation 1881
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375717760"
variation 1900
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200015506"
variation 1906
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200099574"
exon 1914..2036
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1924
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:56108846"
variation 1936
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142696573"
variation 1966
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:137975389"
variation 2001
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:200952273"
variation 2005
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376597441"
variation 2006
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149475426"
variation 2029
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371734479"
exon 2037..2284
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2042
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:112384431"
variation 2044..2045
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace=""
/replace="g"
/db_xref="dbSNP:35262576"
variation 2045
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:201626283"
variation 2097
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142173175"
variation 2104
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:55927202"
variation 2118
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:202216139"
variation 2119
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:199972358"
variation 2128
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375552698"
variation 2180
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:28936395"
variation 2212
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369642059"
variation 2213
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372886782"
variation 2282
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375886598"
variation 2283
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150002185"
exon 2285..2500
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2308
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201544391"
variation 2312
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:121912582"
variation 2314
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370900320"
variation 2335
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375579646"
variation 2338
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375588609"
variation 2339
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142161660"
variation 2374
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149590849"
variation 2407
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:368213597"
variation 2408
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201892962"
variation 2413
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141476431"
variation 2423
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201156841"
variation 2437
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147014777"
variation 2453
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:367548936"
variation 2467
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141632768"
exon 2501..2650
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2503
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376647308"
variation 2504
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138551214"
variation 2519
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369660719"
variation 2532
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372696024"
variation 2550
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376209284"
variation 2557
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201751121"
variation 2560
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370226176"
variation 2563
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373295870"
variation 2573
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376515026"
STS 2588..2797
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="MARC_17495-17496:1030378704:1"
/db_xref="UniSTS:268320"
exon 2651..2844
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2676
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140172215"
variation 2678
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:55826626"
variation 2691
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:376945636"
variation 2758
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:199695952"
variation 2765
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:201327859"
variation 2772
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143865228"
variation 2773
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:55993650"
variation 2785
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:142464595"
variation 2788
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147815673"
variation 2795
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372653137"
variation 2806
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199868010"
exon 2845..3000
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2857
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201578620"
variation 2871
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370710705"
variation 2899
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138093963"
variation 2905
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375575103"
variation 2908
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368101425"
variation 2915
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054792"
variation 2919
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace=""
/replace="c"
/db_xref="dbSNP:66534620"
variation 2923
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149030035"
variation 2930
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141672966"
variation 2950
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138938253"
variation 2959
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201185822"
variation 2978
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:78707665"
exon 3001..4869
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 3012
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200208409"
variation 3064
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:369377482"
variation 3071
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:372681830"
variation 3072
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142146570"
STS 3124..3239
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="GDB:593997"
/db_xref="UniSTS:157983"
variation 3124
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:202088860"
variation 3130
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2229871"
variation 3158
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373982551"
variation 3160
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:140655693"
variation 3169
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371418612"
STS 3176..3271
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="D1S3214"
/db_xref="UniSTS:39105"
variation 3180
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:111422315"
variation 3209
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368971406"
variation 3254
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375096051"
variation 3287
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377206396"
variation 3290
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:188399389"
variation 3296
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:76826147"
variation 3300
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace=""
/replace="a"
/db_xref="dbSNP:56871920"
variation 3322
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377584109"
variation 3339
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369027672"
variation 3386
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:180810246"
variation 3393
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372635662"
variation 3433
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:185077182"
STS 3491..3635
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="GDB:636068"
/db_xref="UniSTS:158519"
variation 3509
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:79966863"
variation 3734
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:189454653"
variation 3870
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138319537"
variation 3886
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:77863597"
variation 3911
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:149199458"
variation 3983
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:368495544"
variation 4023
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:181945619"
polyA_site 4130
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
variation 4158
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:187028066"
variation 4183
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370791639"
polyA_site 4212
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
variation 4239
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:41266949"
variation 4360
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146762731"
variation 4367
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:139185835"
variation 4385
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:143121637"
variation 4507
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191464781"
variation 4598
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147471914"
variation 4647
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295022"
variation 4648
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:181505314"
variation 4666
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2675498"
variation 4714
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:113699887"
variation 4770
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:77096904"
variation 4814
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:185396266"
polyA_signal 4845..4850
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
variation 4851
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:189865592"
polyA_site 4869
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
ORIGIN
cattctgctggctgcgcggtggcggcggctgtgtgtgcgccgcgccttgccgccccccctggccccccgagcccggggcgcgcgctcccgcccgggccgtccgggccccgcggcgccgcggcccgaggccccgggaagcgcagccatggctctgcggaggctgggggccgcgctgctgctgctgccgctgctcgccgccgtggaagaaacgctaatggactccactacagcgactgctgagctgggctggatggtgcatcctccatcagggtgggaagaggtgagtggctacgatgagaacatgaacacgatccgcacgtaccaggtgtgcaacgtgtttgagtcaagccagaacaactggctacggaccaagtttatccggcgccgtggcgcccaccgcatccacgtggagatgaagttttcggtgcgtgactgcagcagcatccccagcgtgcctggctcctgcaaggagaccttcaacctctattactatgaggctgactttgactcggccaccaagaccttccccaactggatggagaatccatgggtgaaggtggataccattgcagccgacgagagcttctcccaggtggacctgggtggccgcgtcatgaaaatcaacaccgaggtgcggagcttcggacctgtgtcccgcagcggcttctacctggccttccaggactatggcggctgcatgtccctcatcgccgtgcgtgtcttctaccgcaagtgcccccgcatcatccagaatggcgccatcttccaggaaaccctgtcgggggctgagagcacatcgctggtggctgcccggggcagctgcatcgccaatgcggaagaggtggatgtacccatcaagctctactgtaacggggacggcgagtggctggtgcccatcgggcgctgcatgtgcaaagcaggcttcgaggccgttgagaatggcaccgtctgccgaggttgtccatctgggactttcaaggccaaccaaggggatgaggcctgtacccactgtcccatcaacagccggaccacttctgaaggggccaccaactgtgtctgccgcaatggctactacagagcagacctggaccccctggacatgccctgcacaaccatcccctccgcgccccaggctgtgatttccagtgtcaatgagacctccctcatgctggagtggacccctccccgcgactccggaggccgagaggacctcgtctacaacatcatctgcaagagctgtggctcgggccggggtgcctgcacccgctgcggggacaatgtacagtacgcaccacgccagctaggcctgaccgagccacgcatttacatcagtgacctgctggcccacacccagtacaccttcgagatccaggctgtgaacggcgttactgaccagagccccttctcgcctcagttcgcctctgtgaacatcaccaccaaccaggcagctccatcggcagtgtccatcatgcatcaggtgagccgcaccgtggacagcattaccctgtcgtggtcccagccggaccagcccaatggcgtgatcctggactatgagctgcagtactatgagaaggagctcagtgagtacaacgccacagccataaaaagccccaccaacacggtcaccgtgcagggcctcaaagccggcgccatctatgtcttccaggtgcgggcacgcaccgtggcaggctacgggcgctacagcggcaagatgtacttccagaccatgacagaagccgagtaccagacaagcatccaggagaagttgccactcatcatcggctcctcggccgctggcctggtcttcctcattgctgtggttgtcatcgccatcgtgtgtaacagaagacgggggtttgagcgtgctgactcggagtacacggacaagctgcaacactacaccagtggccacatgaccccaggcatgaagatctacatcgatcctttcacctacgaggaccccaacgaggcagtgcgggagtttgccaaggaaattgacatctcctgtgtcaaaattgagcaggtgatcggagcaggggagtttggcgaggtctgcagtggccacctgaagctgccaggcaagagagagatctttgtggccatcaagacgctcaagtcgggctacacggagaagcagcgccgggacttcctgagcgaagcctccatcatgggccagttcgaccatcccaacgtcatccacctggagggtgtcgtgaccaagagcacacctgtgatgatcatcaccgagttcatggagaatggctccctggactcctttctccggcaaaacgatgggcagttcacagtcatccagctggtgggcatgcttcggggcatcgcagctggcatgaagtacctggcagacatgaactatgttcaccgtgacctggctgcccgcaacatcctcgtcaacagcaacctggtctgcaaggtgtcggactttgggctctcacgctttctagaggacgatacctcagaccccacctacaccagtgccctgggcggaaagatccccatccgctggacagccccggaagccatccagtaccggaagttcacctcggccagtgatgtgtggagctacggcattgtcatgtgggaggtgatgtcctatggggagcggccctactgggacatgaccaaccaggatgtaatcaatgccattgagcaggactatcggctgccaccgcccatggactgcccgagcgccctgcaccaactcatgctggactgttggcagaaggaccgcaaccaccggcccaagttcggccaaattgtcaacacgctagacaagatgatccgcaatcccaacagcctcaaagccatggcgcccctctcctctggcatcaacctgccgctgctggaccgcacgatccccgactacaccagctttaacacggtggacgagtggctggaggccatcaagatggggcagtacaaggagagcttcgccaatgccggcttcacctcctttgacgtcgtgtctcagatgatgatggaggacattctccgggttggggtcactttggctggccaccagaaaaaaatcctgaacagtatccaggtgatgcgggcgcagatgaaccagattcagtctgtggaggtttgacattcacctgcctcggctcacctcttcctccaagccccgccccctctgccccacgtgccggccctcctggtgctctatccactgcagggccagccactcgccaggaggccacgggccacgggaagaaccaagcggtgccagccacgagacgtcaccaagaaaacatgcaactcaaacgacggaaaaaaaaagggaatgggaaaaaagaaaacagatcctgggagggggcgggaaatacaaggaatattttttaaagaggattctcataaggaaagcaatgactgttcttgcgggggataaaaaagggcttgggagattcatgcgatgtgtccaatcggagacaaaagcagtttctctccaactccctctgggaaggtgacctggccagagccaagaaacactttcagaaaaacaaatgtgaaggggagagacaggggccgcccttggctcctgtccctgctgctcctctaggcctcactcaacaaccaagcgcctggaggacgggacagatggacagacagccaccctgagaacccctctgggaaaatctattcctgccaccactgggcaaacagaagaatttttctgtctttggagagtattttagaaactccaatgaaagacactgtttctcctgttggctcacagggctgaaaggggcttttgtcctcctgggtcagggagaacgcggggaccccagaaaggtcagccttcctgaggatgggcaacccccaggtctgcagctccaggtacatatcacgcgcacagcctggcagcctggccctcctggtgcccactcccgccagcccctgcctcgaggactgatactgcagtgactgccgtcagctccgactgccgctgagaagggttgatcctgcatctgggtttgtttacagcaattcctggactcgggggtattttggtcacagggtggttttggtttagggggtttgtttgttgggttgttttttgttttttggttttttttaatgacaatgaagtgacactttgacatttcctaccttttgaggacttgatccttctccaggaagaaggtgctttctgcttactgacttaggcaatacaccaagggcgagattttatatgcacatttctggatttttttatacggttttcattgacactcttccctcctcccacctgccaccaggcctcaccaaagcccactgccatggggccatctgggccattcagagactggagtgagatttgggtgtggagggggaggcgccaaggtggaggagcttcccactccaggactgttgatgaaagggacagattgaggaggaagtgggctctgaggctgcagggctggaagtccttgcccacttcccactctcctgccccaatctatctagtacttcccaggcaaataggcccctttgaggctcctgagtgccctcagatggtcaaaacccagttttccctctgggagcctaaaccaggctgcatcggaggccaggacccggatcattcactgtgataccctgccctccagagggtgcgctcagagacacgggcaagcatgcctcttcccttccctggagagaaagtgtgtgatttctctcccacctccttccccccaccagacctttgctgggcctaaaggtcttggccatggggacgccctcagtctagggatctggccacagactccctcctgtgaaccaacacagacacccaagcagagcaatcagttagtgaattgaatggaaataaacgctttagttataatatga
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:2048 -> Molecular function: GO:0004713 [protein tyrosine kinase activity] evidence: ISS
GeneID:2048 -> Molecular function: GO:0005005 [transmembrane-ephrin receptor activity] evidence: ISS
GeneID:2048 -> Molecular function: GO:0005005 [transmembrane-ephrin receptor activity] evidence: TAS
GeneID:2048 -> Molecular function: GO:0005102 [receptor binding] evidence: IEA
GeneID:2048 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
GeneID:2048 -> Molecular function: GO:0008046 [axon guidance receptor activity] evidence: IEA
GeneID:2048 -> Biological process: GO:0001525 [angiogenesis] evidence: ISS
GeneID:2048 -> Biological process: GO:0001655 [urogenital system development] evidence: ISS
GeneID:2048 -> Biological process: GO:0006468 [protein phosphorylation] evidence: TAS
GeneID:2048 -> Biological process: GO:0007399 [nervous system development] evidence: TAS
GeneID:2048 -> Biological process: GO:0007411 [axon guidance] evidence: ISS
GeneID:2048 -> Biological process: GO:0007411 [axon guidance] evidence: TAS
GeneID:2048 -> Biological process: GO:0007413 [axonal fasciculation] evidence: ISS
GeneID:2048 -> Biological process: GO:0007612 [learning] evidence: IEA
GeneID:2048 -> Biological process: GO:0016310 [phosphorylation] evidence: ISS
GeneID:2048 -> Biological process: GO:0018108 [peptidyl-tyrosine phosphorylation] evidence: ISS
GeneID:2048 -> Biological process: GO:0021631 [optic nerve morphogenesis] evidence: IEA
GeneID:2048 -> Biological process: GO:0021952 [central nervous system projection neuron axonogenesis] evidence: IEA
GeneID:2048 -> Biological process: GO:0022038 [corpus callosum development] evidence: ISS
GeneID:2048 -> Biological process: GO:0031290 [retinal ganglion cell axon guidance] evidence: IEA
GeneID:2048 -> Biological process: GO:0042472 [inner ear morphogenesis] evidence: ISS
GeneID:2048 -> Biological process: GO:0048013 [ephrin receptor signaling pathway] evidence: ISS
GeneID:2048 -> Biological process: GO:0048170 [positive regulation of long-term neuronal synaptic plasticity] evidence: IEA
GeneID:2048 -> Biological process: GO:0048593 [camera-type eye morphogenesis] evidence: IEA
GeneID:2048 -> Biological process: GO:0050771 [negative regulation of axonogenesis] evidence: IEA
GeneID:2048 -> Biological process: GO:0050878 [regulation of body fluid levels] evidence: ISS
GeneID:2048 -> Biological process: GO:0051965 [positive regulation of synapse assembly] evidence: ISS
GeneID:2048 -> Biological process: GO:0060021 [palate development] evidence: ISS
GeneID:2048 -> Biological process: GO:0060996 [dendritic spine development] evidence: ISS
GeneID:2048 -> Biological process: GO:0060997 [dendritic spine morphogenesis] evidence: ISS
GeneID:2048 -> Biological process: GO:0071679 [commissural neuron axon guidance] evidence: ISS
GeneID:2048 -> Cellular component: GO:0005887 [integral to plasma membrane] evidence: ISS
GeneID:2048 -> Cellular component: GO:0030424 [axon] evidence: ISS
GeneID:2048 -> Cellular component: GO:0030425 [dendrite] evidence: ISS
GeneID:2048 -> Cellular component: GO:0043025 [neuronal cell body] evidence: IEA
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_004433 -> EC 2.7.10.1
by
@meso_cacase at
DBCLS
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