Details for: Mab21l2

Gene ID: 23937

Symbol: Mab21l2

Ensembl ID: ENSMUSG00000057777

Description: mab-21-like 2

Associated with

Other Information

Genular Protein ID: 3791367361

Symbol: MB212_MOUSE

Name: Protein mab-21-like 2

UniProtKB Accession Codes:

Q8BPP1 Q9R1B2 Q9WVF2

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CCDS 1 CTD 1 DNASU 1 EMBL 5 Ensembl 2 GO 7 Gene3D 2 GeneTree 1 Genevisible 1 HOGENOM 1 InParanoid 1 InterPro 3 KEGG 1 MGI 1 MaxQB 1 NCBI Taxonomy 1 OMA 1 OrthoDB 1 PANTHER 2 PRO 1 PaxDb 1 Pfam 2 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 1 RNAct 1 RefSeq 1 SMART 1 SMR 1 STRING 1 TreeFam 1 UCSC 1 UniProtKB 1 VEuPathDB 1 eggNOG 1 iPTMnet 1

Citations:

PubMed ID: 10516425

Title: Genomic cloning and chromosomal localization of the mouse Mab21l2 locus.

PubMed ID: 10516425

DOI: 10.1159/000015421

PubMed ID: 10556287

Title: Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development.

PubMed ID: 10556287

DOI: 10.1093/hmg/8.13.2397

PubMed ID: 10495284

Title: Developmental expression of Mab21l2 during mouse embryogenesis.

PubMed ID: 10495284

DOI: 10.1016/s0925-4773(99)00127-6

PubMed ID: 11857508

Title: Depletion of Mab21l1 and Mab21l2 messages in mouse embryo arrests axial turning, and impairs notochord and neural tube differentiation.

PubMed ID: 11857508

DOI: 10.1002/tera.10018

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 12642482

Title: Cell-autonomous involvement of Mab21l1 is essential for lens placode development.

PubMed ID: 12642482

DOI: 10.1242/dev.00399

PubMed ID: 15385160

Title: Requirement for Mab21l2 during development of murine retina and ventral body wall.

PubMed ID: 15385160

DOI: 10.1016/j.ydbio.2004.07.016

PubMed ID: 24906020

Title: Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.

PubMed ID: 24906020

DOI: 10.1016/j.ajhg.2014.05.005

Sequence Information:

  • Length: 359
  • Mass: 40907
  • Checksum: 24B7A0CF0E78A1AA
  • Sequence:
    • MIAAQAKLVY QLNKYYTERC QARKAAIAKT IREVCKVVSD VLKEVEVQEP RFISSLSEID 
ARYEGLEVIS PTEFEVVLYL NQMGVFNFVD DGSLPGCAVL KLSDGRKRSM SLWVEFITAS 
GYLSARKIRS RFQTLVAQAV DKCSYRDVVK MIADTSEVKL RIRERYVVQI TPAFKCTGIW 
PRSAAQWPMP HIPWPGPNRV AEVKAEGFNL LSKECYSLTG KQSSAESDAW VLQFGEAENR 
LLMGGCRNKC LSVLKTLRDR HLELPGQPLN NYHMKTLLLY ECEKHPRETD WDEACLGDRL 
NGILLQLISC LQCRRCPHYF LPNLDLFQGK PHSALESAAK QTWRLAREIL TNPKSLDKL

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.