Y46E12BL.8

Caenorhabditis elegans

Enriched in I4 neuron; I5 neuron; M3L; M5 neuron; and MI neuron based on single-cell RNA-seq studies.

T14G11.6

Caenorhabditis elegans

Enriched in MI neuron based on single-cell RNA-seq studies. Is affected by prg-1 based on RNA-seq studies.

T14G11.5

Caenorhabditis elegans

Enriched in MI neuron based on single-cell RNA-seq studies. Is affected by nfki-1 based on RNA-seq studies.

K03A1.8

Caenorhabditis elegans

Enriched in MI neuron and neurons based on RNA-seq and single-cell RNA-seq studies. Is affected by etr-1 and ogt-1 based on RNA-seq studies.

T14G11.4

Caenorhabditis elegans

Enriched in M2 neuron; M2L; M5 neuron; MI neuron; and neurons based on RNA-seq and single-cell RNA-seq studies. Is affected by cep-1 and ogt-1 based on RNA-seq studies.

LINC01412

Homo sapiens

ASSOCIATED WITH Mowat-Wilson syndrome

LINC02993

Homo sapiens

ASSOCIATED WITH Mowat-Wilson syndrome

Y6B3B.9

Caenorhabditis elegans

Predicted to enable endonuclease activity. Predicted to be involved in maturation of 5.8S rRNA and maturation of LSU-rRNA. Predicted to be located in nucleus. Predicted to be part of Las1 complex. Human ortholog(s) of this gene implicated in Wilson-Turner syndrome. Is an ortholog of human LAS1L (LAS1 like ribosome biogenesis factor).

sams-5

Caenorhabditis elegans

Predicted to enable methionine adenosyltransferase activity. Predicted to be involved in S-adenosylmethionine biosynthetic process. Predicted to be located in cytosol. Expressed in MI neuron. Human ortholog(s) of this gene implicated in hypermethioninemia and lung cancer. Is an ortholog of human MAT1A (methionine adenosyltransferase 1A) and MAT2A (methionine adenosyltransferase 2A).

ATXN7L3-AS1

Homo sapiens

ASSOCIATED WITH childhood-onset neurodegeneration with brain atrophy; genetic disease; Wilson disease