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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
Term:abnormal vitelline vein topology
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Accession:MP:0013986 term browser browse the term
Definition:abnormal position of the paired veins that carry blood from the yolk sac back to the embryo


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abnormal vitelline vein topology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G 1700067K01Rik RIKEN cDNA 1700067K01 gene IEA MGI NCBI chr 8:84,727,145...84,731,399
Ensembl chr 8:84,728,131...84,731,399 		JBrowse link
G Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 IEA MGI NCBI chr 5:89,821,700...90,031,521
Ensembl chr 5:89,824,946...90,031,193 		JBrowse link
G Atg16l1 autophagy related 16 like 1 IEA MGI NCBI chr 1:87,683,730...87,720,150
Ensembl chr 1:87,683,592...87,720,150 		JBrowse link
G Atp11a ATPase, class VI, type 11A IEA MGI NCBI chr 8:12,807,016...12,918,728
Ensembl chr 8:12,807,014...12,918,728 		JBrowse link
G B9d2 B9 protein domain 2 IEA MGI NCBI chr 7:25,380,205...25,385,987
Ensembl chr 7:25,380,205...25,385,983 		JBrowse link
G Cbx6 chromobox 6 IEA MGI NCBI chr15:79,708,099...79,718,534
Ensembl chr15:79,708,097...79,718,889 		JBrowse link
G Celf4 CUGBP, Elav-like family member 4 IEA MGI NCBI chr18:25,610,677...25,887,577
Ensembl chr18:25,610,689...25,887,214 		JBrowse link
G Chst11 carbohydrate sulfotransferase 11 IEA MGI NCBI chr10:82,820,274...83,031,738
Ensembl chr10:82,821,332...83,031,734 		JBrowse link
G Chtop chromatin target of PRMT1 IEA MGI NCBI chr 3:90,405,846...90,417,400
Ensembl chr 3:90,406,263...90,416,805 		JBrowse link
G Cmip c-Maf inducing protein IEA MGI NCBI chr 8:117,983,758...118,188,245
Ensembl chr 8:117,983,803...118,186,169 		JBrowse link
G Crim1 cysteine rich transmembrane BMP regulator 1 IEA MGI NCBI chr17:78,507,602...78,684,021
Ensembl chr17:78,507,677...78,684,021 		JBrowse link
G H13 histocompatibility 13 IEA MGI NCBI chr 2:152,511,292...152,550,590
Ensembl chr 2:152,511,381...152,550,590 		JBrowse link
G Nxn nucleoredoxin IEA MGI NCBI chr11:76,148,052...76,289,967
Ensembl chr11:76,148,024...76,289,966 		JBrowse link
G Prmt7 protein arginine N-methyltransferase 7 IEA MGI NCBI chr 8:106,937,686...106,978,326
Ensembl chr 8:106,937,568...106,979,426 		JBrowse link
G Prrc2b proline-rich coiled-coil 2B IEA MGI NCBI chr 2:32,041,002...32,124,549
Ensembl chr 2:32,041,094...32,124,549 		JBrowse link
G Rala v-ral simian leukemia viral oncogene A (ras related) IEA MGI NCBI chr13:18,055,160...18,118,802
Ensembl chr13:18,055,156...18,118,824 		JBrowse link
G Setd5 SET domain containing 5 IEA MGI NCBI chr 6:113,054,326...113,130,393
Ensembl chr 6:113,054,326...113,130,396 		JBrowse link
G Sh3pxd2a SH3 and PX domains 2A IEA MGI NCBI chr19:47,248,613...47,453,053
Ensembl chr19:47,248,613...47,452,840 		JBrowse link
G Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 IEA MGI NCBI chr 9:108,539,335...108,561,841
Ensembl chr 9:108,539,287...108,561,840 		JBrowse link
G Traf6 TNF receptor-associated factor 6 IEA MGI NCBI chr 2:101,508,765...101,532,013
Ensembl chr 2:101,508,774...101,532,014 		JBrowse link
G Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble IEA MGI NCBI chr19:52,919,710...53,027,093
Ensembl chr19:52,920,357...53,028,645 		JBrowse link
G Zmynd11 zinc finger, MYND domain containing 11 IEA MGI NCBI chr13:9,734,872...9,816,050
Ensembl chr13:9,734,869...9,815,366 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 17090
    embryo phenotype 2533
      abnormal extraembryonic tissue morphology 1004
        abnormal vitelline vasculature morphology 279
          abnormal vitelline vein morphology 34
            abnormal vitelline vein topology 22
Path 2
Term Annotations click to browse term
  mammalian phenotype 17090
    cardiovascular system phenotype 4121
      abnormal cardiovascular system morphology 3210
        abnormal blood vessel morphology 1783
          abnormal vascular development 666
            abnormal angiogenesis 475
              abnormal vein development 80
                abnormal vitelline vein morphology 34
                  abnormal vitelline vein topology 22
paths to the root