SLC44A4

solute carrier family 44 member 4
OMIM: 606107, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC44A4 in Mendeliome


Version 1.4516

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
Phenotypes
  • nonsyndromic genetic hearing loss MONDO:0019497

Red SLC44A4 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.332

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Literature
Phenotypes
  • nonsyndromic genetic hearing loss MONDO:0019497