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2025-05-09 16:43:42, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_017449 4866 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens EPH receptor B2 (EPHB2), transcript variant 1, mRNA.
ACCESSION NM_017449
VERSION NM_017449.3 GI:111118977
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 4866)
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 4866)
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 4866)
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 4866)
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 4866)
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 4866)
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 4866)
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 4866)
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 4866)
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 4866)
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 AF025304.1.
On Aug 2, 2006 this sequence version replaced gi:56119210.
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 (1) encodes the shorter isoform
(1).
CCDS Note: The coding region has been updated to represent an
alternative 3' splice pattern, resulting in a shorter and distinct
C-terminus that is better supported by available transcript and
homology data.
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 :: AB210018.1 [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 AF025304.1 1454-1616
1737-1845 AL035704.9 15359-15467
1846-1910 AL035704.9 16301-16365
1911-2033 AL035704.9 25874-25996
2034-2281 AL035704.9 26597-26844
2282-2497 AL035704.9 27840-28055
2498-2647 AL035704.9 28909-29058
2648-2841 AL035704.9 30269-30462
2842-2997 AL035704.9 32331-32486
2998-4866 AL035704.9 33349-35217
FEATURES Location/Qualifiers
source 1..4866
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1p36.1-p35"
gene 1..4866
/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="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..3106
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/EC_number="2.7.10.1"
/note="isoform 1 precursor is encoded by transcript
variant 1; 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 1 precursor"
/protein_id="NP_059145.2"
/db_xref="GI:111118978"
/db_xref="CCDS:CCDS229.2"
/db_xref="GeneID:2048"
/db_xref="HGNC:3393"
/db_xref="MIM:600997"
/translation="
MALRRLGAALLLLPLLAAVEETLMDSTTATAELGWMVHPPSGWEEVSGYDENMNTIRTYQVCNVFESSQNNWLRTKFIRRRGAHRIHVEMKFSVRDCSSIPSVPGSCKETFNLYYYEADFDSATKTFPNWMENPWVKVDTIAADESFSQVDLGGRVMKINTEVRSFGPVSRSGFYLAFQDYGGCMSLIAVRVFYRKCPRIIQNGAIFQETLSGAESTSLVAARGSCIANAEEVDVPIKLYCNGDGEWLVPIGRCMCKAGFEAVENGTVCRGCPSGTFKANQGDEACTHCPINSRTTSEGATNCVCRNGYYRADLDPLDMPCTTIPSAPQAVISSVNETSLMLEWTPPRDSGGREDLVYNIICKSCGSGRGACTRCGDNVQYAPRQLGLTEPRIYISDLLAHTQYTFEIQAVNGVTDQSPFSPQFASVNITTNQAAPSAVSIMHQVSRTVDSITLSWSQPDQPNGVILDYELQYYEKELSEYNATAIKSPTNTVTVQGLKAGAIYVFQVRARTVAGYGRYSGKMYFQTMTEAEYQTSIQEKLPLIIGSSAAGLVFLIAVVVIAIVCNRRGFERADSEYTDKLQHYTSGHMTPGMKIYIDPFTYEDPNEAVREFAKEIDISCVKIEQVIGAGEFGEVCSGHLKLPGKREIFVAIKTLKSGYTEKQRRDFLSEASIMGQFDHPNVIHLEGVVTKSTPVMIITEFMENGSLDSFLRQNDGQFTVIQLVGMLRGIAAGMKYLADMNYVHRDLAARNILVNSNLVCKVSDFGLSRFLEDDTSDPTYTSALGGKIPIRWTAPEAIQYRKFTSASDVWSYGIVMWEVMSYGERPYWDMTNQDVINAIEQDYRLPPPMDCPSALHQLMLDCWQKDRNHRPKFGQIVNTLDKMIRNPNSLKAMAPLSSGINLPLLDRTIPDYTSFNTVDEWLEAIKMGQYKESFANAGFTSFDVVSQMMMEDILRVGVTLAGHQKKILNSIQVMRAQMNQIQSVEV
"
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..3103
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/product="ephrin type-B receptor 2 isoform 1"
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 1775..1837
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P29323.5);
transmembrane region"
misc_feature 1874..1876
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1895..1897
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1931..1933
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1949..1951
/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 1991..2797
/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 2006..2785
/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(2024..2038,2048..2050,2096..2098,2102..2104,
2240..2245,2249..2251,2261..2263,2381..2383,2393..2398,
2402..2404,2435..2437,2498..2512,2537..2539,2639..2641)
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/note="active site"
/db_xref="CDD:173638"
misc_feature order(2024..2032,2036..2038,2048..2050,2096..2098,
2102..2104,2240..2245,2249..2251,2261..2263,2396..2398,
2402..2404,2435..2437)
/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 2120..2122
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2351..2353
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2369..2371
/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(2381..2383,2393..2395,2498..2512,2537..2539,
2639..2641)
/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 2432..2518
/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 2468..2470
/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 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 2483..2485
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2543..2545
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2873..3085
/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 2873..3076
/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(2879..2884,2888..2890,2954..2956,2972..2977,
2999..3001,3023..3034,3038..3043,3065..3067,3077..3079)
/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(2879..2881,2888..2890,2906..2908,2969..2971,
3053..3055,3062..3067)
/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(2933..2935,3032..3034)
/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 2933..2935
/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(2981..2998,3005..3007,3059..3061,3068..3070,
3077..3082)
/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..1910
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1847
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200219468"
variation 1849
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:376417187"
variation 1867
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:56264796"
variation 1869
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146071874"
variation 1870
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200494586"
variation 1878
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375717760"
variation 1897
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200015506"
variation 1903
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200099574"
exon 1911..2033
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 1921
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:56108846"
variation 1933
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142696573"
variation 1963
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:137975389"
variation 1998
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:200952273"
variation 2002
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376597441"
variation 2003
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149475426"
variation 2026
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371734479"
exon 2034..2281
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2039
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:112384431"
variation 2041..2042
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace=""
/replace="g"
/db_xref="dbSNP:35262576"
variation 2042
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:201626283"
variation 2094
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142173175"
variation 2101
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:55927202"
variation 2115
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:202216139"
variation 2116
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:199972358"
variation 2125
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375552698"
variation 2177
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:28936395"
variation 2209
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369642059"
variation 2210
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372886782"
variation 2279
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375886598"
variation 2280
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150002185"
exon 2282..2497
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2305
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201544391"
variation 2309
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:121912582"
variation 2311
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370900320"
variation 2332
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375579646"
variation 2335
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375588609"
variation 2336
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142161660"
variation 2371
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149590849"
variation 2404
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:368213597"
variation 2405
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201892962"
variation 2410
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141476431"
variation 2420
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201156841"
variation 2434
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147014777"
variation 2450
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:367548936"
variation 2464
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141632768"
exon 2498..2647
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2500
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376647308"
variation 2501
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138551214"
variation 2516
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369660719"
variation 2529
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372696024"
variation 2547
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376209284"
variation 2554
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201751121"
variation 2557
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370226176"
variation 2560
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373295870"
variation 2570
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376515026"
STS 2585..2794
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="MARC_17495-17496:1030378704:1"
/db_xref="UniSTS:268320"
exon 2648..2841
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2673
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140172215"
variation 2675
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:55826626"
variation 2688
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:376945636"
variation 2755
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:199695952"
variation 2762
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:201327859"
variation 2769
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143865228"
variation 2770
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:55993650"
variation 2782
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:142464595"
variation 2785
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147815673"
variation 2792
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372653137"
variation 2803
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199868010"
exon 2842..2997
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 2854
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201578620"
variation 2868
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370710705"
variation 2896
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138093963"
variation 2902
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375575103"
variation 2905
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368101425"
variation 2912
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054792"
variation 2916
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace=""
/replace="c"
/db_xref="dbSNP:66534620"
variation 2920
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149030035"
variation 2927
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141672966"
variation 2947
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138938253"
variation 2956
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201185822"
variation 2975
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:78707665"
exon 2998..4866
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/inference="alignment:Splign:1.39.8"
variation 3009
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200208409"
variation 3061
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:369377482"
variation 3068
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:372681830"
variation 3069
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142146570"
STS 3121..3236
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="GDB:593997"
/db_xref="UniSTS:157983"
variation 3121
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:202088860"
variation 3127
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2229871"
variation 3155
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373982551"
variation 3157
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:140655693"
variation 3166
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371418612"
STS 3173..3268
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="D1S3214"
/db_xref="UniSTS:39105"
variation 3177
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:111422315"
variation 3206
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368971406"
variation 3251
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375096051"
variation 3284
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377206396"
variation 3287
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:188399389"
variation 3293
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="t"
/db_xref="dbSNP:76826147"
variation 3297
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace=""
/replace="a"
/db_xref="dbSNP:56871920"
variation 3319
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377584109"
variation 3336
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369027672"
variation 3383
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:180810246"
variation 3390
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372635662"
variation 3430
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:185077182"
STS 3488..3632
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/standard_name="GDB:636068"
/db_xref="UniSTS:158519"
variation 3506
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:79966863"
variation 3731
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:189454653"
variation 3867
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:138319537"
variation 3883
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:77863597"
variation 3908
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:149199458"
variation 3980
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="c"
/db_xref="dbSNP:368495544"
variation 4020
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:181945619"
polyA_site 4127
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
variation 4155
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:187028066"
variation 4180
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370791639"
polyA_site 4209
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
variation 4236
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:41266949"
variation 4357
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146762731"
variation 4364
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:139185835"
variation 4382
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:143121637"
variation 4504
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191464781"
variation 4595
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147471914"
variation 4644
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295022"
variation 4645
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="g"
/replace="t"
/db_xref="dbSNP:181505314"
variation 4663
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2675498"
variation 4711
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="g"
/db_xref="dbSNP:113699887"
variation 4767
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:77096904"
variation 4811
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="a"
/replace="g"
/db_xref="dbSNP:185396266"
polyA_signal 4842..4847
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
variation 4848
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
/replace="c"
/replace="t"
/db_xref="dbSNP:189865592"
polyA_site 4866
/gene="EPHB2"
/gene_synonym="CAPB; DRT; EK5; EPHT3; ERK; Hek5; PCBC;
Tyro5"
ORIGIN
cattctgctggctgcgcggtggcggcggctgtgtgtgcgccgcgccttgccgccccccctggccccccgagcccggggcgcgcgctcccgcccgggccgtccgggccccgcggcgccgcggcccgaggccccgggaagcgcagccatggctctgcggaggctgggggccgcgctgctgctgctgccgctgctcgccgccgtggaagaaacgctaatggactccactacagcgactgctgagctgggctggatggtgcatcctccatcagggtgggaagaggtgagtggctacgatgagaacatgaacacgatccgcacgtaccaggtgtgcaacgtgtttgagtcaagccagaacaactggctacggaccaagtttatccggcgccgtggcgcccaccgcatccacgtggagatgaagttttcggtgcgtgactgcagcagcatccccagcgtgcctggctcctgcaaggagaccttcaacctctattactatgaggctgactttgactcggccaccaagaccttccccaactggatggagaatccatgggtgaaggtggataccattgcagccgacgagagcttctcccaggtggacctgggtggccgcgtcatgaaaatcaacaccgaggtgcggagcttcggacctgtgtcccgcagcggcttctacctggccttccaggactatggcggctgcatgtccctcatcgccgtgcgtgtcttctaccgcaagtgcccccgcatcatccagaatggcgccatcttccaggaaaccctgtcgggggctgagagcacatcgctggtggctgcccggggcagctgcatcgccaatgcggaagaggtggatgtacccatcaagctctactgtaacggggacggcgagtggctggtgcccatcgggcgctgcatgtgcaaagcaggcttcgaggccgttgagaatggcaccgtctgccgaggttgtccatctgggactttcaaggccaaccaaggggatgaggcctgtacccactgtcccatcaacagccggaccacttctgaaggggccaccaactgtgtctgccgcaatggctactacagagcagacctggaccccctggacatgccctgcacaaccatcccctccgcgccccaggctgtgatttccagtgtcaatgagacctccctcatgctggagtggacccctccccgcgactccggaggccgagaggacctcgtctacaacatcatctgcaagagctgtggctcgggccggggtgcctgcacccgctgcggggacaatgtacagtacgcaccacgccagctaggcctgaccgagccacgcatttacatcagtgacctgctggcccacacccagtacaccttcgagatccaggctgtgaacggcgttactgaccagagccccttctcgcctcagttcgcctctgtgaacatcaccaccaaccaggcagctccatcggcagtgtccatcatgcatcaggtgagccgcaccgtggacagcattaccctgtcgtggtcccagccggaccagcccaatggcgtgatcctggactatgagctgcagtactatgagaaggagctcagtgagtacaacgccacagccataaaaagccccaccaacacggtcaccgtgcagggcctcaaagccggcgccatctatgtcttccaggtgcgggcacgcaccgtggcaggctacgggcgctacagcggcaagatgtacttccagaccatgacagaagccgagtaccagacaagcatccaggagaagttgccactcatcatcggctcctcggccgctggcctggtcttcctcattgctgtggttgtcatcgccatcgtgtgtaacagacgggggtttgagcgtgctgactcggagtacacggacaagctgcaacactacaccagtggccacatgaccccaggcatgaagatctacatcgatcctttcacctacgaggaccccaacgaggcagtgcgggagtttgccaaggaaattgacatctcctgtgtcaaaattgagcaggtgatcggagcaggggagtttggcgaggtctgcagtggccacctgaagctgccaggcaagagagagatctttgtggccatcaagacgctcaagtcgggctacacggagaagcagcgccgggacttcctgagcgaagcctccatcatgggccagttcgaccatcccaacgtcatccacctggagggtgtcgtgaccaagagcacacctgtgatgatcatcaccgagttcatggagaatggctccctggactcctttctccggcaaaacgatgggcagttcacagtcatccagctggtgggcatgcttcggggcatcgcagctggcatgaagtacctggcagacatgaactatgttcaccgtgacctggctgcccgcaacatcctcgtcaacagcaacctggtctgcaaggtgtcggactttgggctctcacgctttctagaggacgatacctcagaccccacctacaccagtgccctgggcggaaagatccccatccgctggacagccccggaagccatccagtaccggaagttcacctcggccagtgatgtgtggagctacggcattgtcatgtgggaggtgatgtcctatggggagcggccctactgggacatgaccaaccaggatgtaatcaatgccattgagcaggactatcggctgccaccgcccatggactgcccgagcgccctgcaccaactcatgctggactgttggcagaaggaccgcaaccaccggcccaagttcggccaaattgtcaacacgctagacaagatgatccgcaatcccaacagcctcaaagccatggcgcccctctcctctggcatcaacctgccgctgctggaccgcacgatccccgactacaccagctttaacacggtggacgagtggctggaggccatcaagatggggcagtacaaggagagcttcgccaatgccggcttcacctcctttgacgtcgtgtctcagatgatgatggaggacattctccgggttggggtcactttggctggccaccagaaaaaaatcctgaacagtatccaggtgatgcgggcgcagatgaaccagattcagtctgtggaggtttgacattcacctgcctcggctcacctcttcctccaagccccgccccctctgccccacgtgccggccctcctggtgctctatccactgcagggccagccactcgccaggaggccacgggccacgggaagaaccaagcggtgccagccacgagacgtcaccaagaaaacatgcaactcaaacgacggaaaaaaaaagggaatgggaaaaaagaaaacagatcctgggagggggcgggaaatacaaggaatattttttaaagaggattctcataaggaaagcaatgactgttcttgcgggggataaaaaagggcttgggagattcatgcgatgtgtccaatcggagacaaaagcagtttctctccaactccctctgggaaggtgacctggccagagccaagaaacactttcagaaaaacaaatgtgaaggggagagacaggggccgcccttggctcctgtccctgctgctcctctaggcctcactcaacaaccaagcgcctggaggacgggacagatggacagacagccaccctgagaacccctctgggaaaatctattcctgccaccactgggcaaacagaagaatttttctgtctttggagagtattttagaaactccaatgaaagacactgtttctcctgttggctcacagggctgaaaggggcttttgtcctcctgggtcagggagaacgcggggaccccagaaaggtcagccttcctgaggatgggcaacccccaggtctgcagctccaggtacatatcacgcgcacagcctggcagcctggccctcctggtgcccactcccgccagcccctgcctcgaggactgatactgcagtgactgccgtcagctccgactgccgctgagaagggttgatcctgcatctgggtttgtttacagcaattcctggactcgggggtattttggtcacagggtggttttggtttagggggtttgtttgttgggttgttttttgttttttggttttttttaatgacaatgaagtgacactttgacatttcctaccttttgaggacttgatccttctccaggaagaaggtgctttctgcttactgacttaggcaatacaccaagggcgagattttatatgcacatttctggatttttttatacggttttcattgacactcttccctcctcccacctgccaccaggcctcaccaaagcccactgccatggggccatctgggccattcagagactggagtgagatttgggtgtggagggggaggcgccaaggtggaggagcttcccactccaggactgttgatgaaagggacagattgaggaggaagtgggctctgaggctgcagggctggaagtccttgcccacttcccactctcctgccccaatctatctagtacttcccaggcaaataggcccctttgaggctcctgagtgccctcagatggtcaaaacccagttttccctctgggagcctaaaccaggctgcatcggaggccaggacccggatcattcactgtgataccctgccctccagagggtgcgctcagagacacgggcaagcatgcctcttcccttccctggagagaaagtgtgtgatttctctcccacctccttccccccaccagacctttgctgggcctaaaggtcttggccatggggacgccctcagtctagggatctggccacagactccctcctgtgaaccaacacagacacccaagcagagcaatcagttagtgaattgaatggaaataaacgctttagttataatatga
//
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_059145 -> EC 2.7.10.1
by
@meso_cacase at
DBCLS
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