Changes between Version 165 and Version 166 of OrthologTableUpdates


Ignore:
Timestamp:
Mar 9, 2021, 2:11:21 PM (3 months ago)
Author:
vw253
Comment:

--

Legend:

Unmodified
Added
Removed
Modified
  • OrthologTableUpdates

    v165 v166  
    11
    2 SPBC83.04       ANAPC15 PF05841 needs to merge with PF15243
    3 SPBC651.10      SLF1    PMID:32389690   PF08691
    4 SPAC11E3.08c    SLF2    PMID:32389690   PF08691
    5 SPAC1952.14     GADD45GIP1  (using Pfam out group, sea anemone) (PubMed:28892042, PubMed:25838379, PubMed:25278503).
    6 SPBC887.07      MRPL14  Phylome
    7 SPBC56F2.14     MRPL53  Pfam & jackhammer)
    8 SPAC24C9.13c    CHCH1 
    9 SPMIT.08        MRPS24 
    10 
    11 SPAC25B8.04c    MSS51   
    12 SPCC285.10      SPRYD3  Panther,Roundup
    13 SPAC5D6.07c     SNX14   Orthofinder Added autosomal recessive spinocerebellar ataxia 20  MONDO:0014601
    14 SPAPB17E12.10c  MRM2    Panther,phylum (divergent copy in fission yeast) Added mitochondrial DNA depletion syndrome 17 MONDO:0032815
    15 SPBC31F10.10    ZMYND19 Orthofinder
    16 SPAC23A1.18c    MRPL43  (Found with jackhammer software, submitted merge to Pfam & Panther)
    17 SPBC947.14c     UQCC2   (Found with jackhammer software, submitted merge to Pfam & Panther) ADD mitochondrial complex III deficiency nuclear type 7 MONDO:0014356
    18 SPCC1795.08c    EP400,EP400P1 (Panther)
    19 SPAC637.09      REXO1,REXO1L1P,REXO5 Orthofinder,Roundup,Treefam
    20 SPAC2F3.14c     FNBP4   (Found with jackhammer software) This prediction might be controversial based on available functional data in human, but is strongly supported by human interactions.
     2 * SPBC83.04    ANAPC15 PF05841 needs to merge with PF15243
     3 * SSPBC651.10  SLF1    PMID:32389690   PF08691
     4 * SSPAC11E3.08c        SLF2    PMID:32389690   PF08691
     5 * SSPAC1952.14 GADD45GIP1  (using Pfam out group, sea anemone) (PubMed:28892042, PubMed:25838379, PubMed:25278503).
     6 * SSPBC887.07  MRPL14  Phylome
     7 * SSPBC56F2.14 MRPL53  Pfam & jackhammer)
     8 * SSPAC24C9.13c        CHCH1 
     9 * SSPMIT.08    MRPS24 
     10
     11 * SSPAC25B8.04c        MSS51   
     12 * SSPCC285.10  SPRYD3  Panther,Roundup
     13 * SSPAC5D6.07c SNX14   Orthofinder Added autosomal recessive spinocerebellar ataxia 20  MONDO:0014601
     14 * SSPAPB17E12.10c      MRM2    Panther,phylum (divergent copy in fission yeast) Added mitochondrial DNA depletion syndrome 17 MONDO:0032815
     15 * SSPBC31F10.10        ZMYND19 Orthofinder
     16 * SSPAC23A1.18c        MRPL43  (Found with jackhammer software, submitted merge to Pfam & Panther)
     17 * SSPBC947.14c UQCC2   (Found with jackhammer software, submitted merge to Pfam & Panther) ADD mitochondrial complex III deficiency nuclear type 7 MONDO:0014356
     18 * SSPCC1795.08c        EP400,EP400P1 (Panther)
     19 * SSPAC637.09  REXO1,REXO1L1P,REXO5 Orthofinder,Roundup,Treefam
     20 * SSPAC2F3.14c FNBP4   (Found with jackhammer software) This prediction might be controversial based on available functional data in human, but is strongly supported by human interactions.
    2121
    2222