P-POD: Princeton Protein Orthology Database: GO3/OrthoMCL1958

This family has 13 members: 1 Caenorhabditis elegans, 3 Danio rerio, 1 Drosophila melanogaster, 2 Gallus gallus, 2 Homo sapiens, 2 Mus musculus, 2 Rattus norvegicus.

Interactive Java Applets: Notung Tree Analysis · Jalview Alignment

GO3/OrthoMCL1958
13 members.
OrganismProtein (Synonyms)DescriptionAmiGO
C. elegansUniProtKB:Q09488 · WB:WBGene00004860 (C32D5.2 · sma-6)⌘
D. rerioUniProtKB:Q66HY1 · ZFIN:ZDB-GENE-040912-150 (bmpr1ab)bone morphogenetic protein receptor, type IA,b⌘
D. rerioUniProtKB:Q1RLX1 · ZFIN:ZDB-GENE-000502-1 (bmpr1a)bone morphogenetic protein receptor, type 1a⌘
D. rerioUniProtKB:Q9W629 · ZFIN:ZDB-GENE-991208-8 (bmpr1b)bone morphogenetic protein receptor, type 1b⌘
D. melanogasterUniProtKB:Q9VMT1 · FB:FBgn0003716 (Brk25D · Activin-A-receptor-25D · Brk25D2 · thickvein · Tkv · Dtfr · Atr25D · Thickveins · Thickvein · str · tkv · dtfr · STK-A · l(2)04415 · l(2)25Da · tkv1 · slater · TKV · CG14026 · thickveins · Brk25D1 · Atkv)DPP receptor · thick veins · BMP receptor kinase 25D · Thick veins⌘
G. gallusENTREZ:396030 · UniProtKB:Q05438 (IPI00583739 · Q05438 · BMR1B_CHICK · BMPR1B)Bone morphogenetic protein receptor type-1B⌘
G. gallusUniProtKB:Q90754 (BRK-1 · IPI00588411 · Q90754) · ENTREZ:396308⌘
H. sapiensENSEMBL:ENSG00000107779 · UniProtKB:P36894 (BMR1A_HUMAN · IPI00005731 · BMPR1A · ALK3 · ACVRLK3 · P36894)Bone morphogenetic protein receptor type-1A⌘
H. sapiensENSEMBL:ENSG00000138696 · UniProtKB:O00238 (O00238 · BMR1B_HUMAN · IPI00010862 · BMPR1B)Bone morphogenetic protein receptor type-1B⌘
M. musculusUniProtKB:P36895 · MGI:MGI:1338938 (Bmpr · BMPR-IA · ALK3 · Bmpr1a)bone morphogenetic protein receptor, type 1A⌘
M. musculusUniProtKB:P36898 · MGI:MGI:107191 (Alk6 · BMPR-IB · BMR1B_MOUSE · CFK-43a · IPI00128197 · Acvrlk6 · Bmpr1b)bone morphogenetic protein receptor, type 1B⌘
R. norvegicusNCBI:XP_213162 · RGD:1560624
R. norvegicusUniProtKB:Q78EA7 · RGD:70989 (Bmpr1a)bone morphogenetic protein receptor, type IA⌘

No functional conservation results.

DescriptionSuffix
Sequences in this family.fasta
mafft aligned Fasta file.afasta
phyml newick file.newick
Notung rooted & rearranged newick file.newick.rooting.0.rearrange.0
Notung Homolog Table.newick.rooting.0.rearrange.0.homologs.csv
OMIM (6)
ENSEMBL:ENSG00000107779 · UniProtKB:P36894#158350 COWDEN DISEASE; CD;;COWDEN SYNDROME; CS;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED
ENSEMBL:ENSG00000138696 · UniProtKB:O00238#612242 CHROMOSOME 10q23 DELETION SYNDROMEJUVENILE POLYPOSIS OF INFANCY, INCLUDED;;JUVENILE POLYPOSIS, INFANTILE, INCLUDED
#610069 POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2
#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED
ENSEMBL:ENSG00000138696 · UniProtKB:O00238#609441 CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES
#112600 BRACHYDACTYLY, TYPE A2; BDA2;;BRACHYMESOPHALANGY II;;MOHR-WRIEDT TYPE BRACHYDACTYLY
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