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Search references for FAM136A. Phrases containing FAM136A
See searches and references containing FAM136A!FAM136A
Protein-coding gene in the species Homo sapiens
Protein FAM136A is a protein that in humans is encoded by the FAM136A gene. Mutations in FAM136A are associated to Ménière's disease. GRCh38: Ensembl release
FAM136A
Human chromosome
similarity 49 member A FAM98A: Family with sequence similarity 98 member A FAM136A: Family with sequence similarity 136 member A FBXO11: F-box protein 11
Chromosome_2
Q5BKY9 5361 FAM135A HGNC:21084; Q9P2D6 5362 FAM135B HGNC:28029; Q49AJ0 5363 FAM136A HGNC:25911; Q96C01 5364 FAM149A HGNC:24527; A5PLN7 5365 FAM149B1 HGNC:29162;
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
Mammalian protein found in Homo sapiens
with liability to pressure palsies) deletion. This protein interacts with FAM136A. GRCh38: Ensembl release 89: ENSG00000006695 – Ensembl, May 2017 GRCm38:
COX10
Protein found in humans
A, Lopez-Escamez JA (2014). "Identification of two novel mutations in FAM136A and DTNA genes in autosomal dominant familial Meniere's disease". Human
Dystrobrevin_alpha
FAM136A
FAM136A
FAM136A
FAM136A
Girl/Female
Hindu
Comfortable, Happy
Boy/Male
Hindu
Enter, Admission
Girl/Female
Arabic, Muslim
Highly Skilled; Expert
Girl/Female
Bengali, Indian
Fraction of Time
Surname or Lastname
English
English : unexplained.Norwegian : habitational name from a farmstead in Agder named Strai, of uncertain derivation.
Girl/Female
Indian, Telugu
Happiness Like Goddess Lakshmi
Boy/Male
Arabic, Muslim
Virtuous of the Religion
Girl/Female
Welsh
Legendary daughter of KyvwIch.
Boy/Male
Indian
A Part of God Ram
Girl/Female
Hindu, Indian, Malayalam, Marathi
Moon Rays
FAM136A
FAM136A
FAM136A
FAM136A
FAM136A