TDRD9 - tudor domain containing 9 Gene

Also Known as HLS; SPNE; HIG-1; NET54; SPGF30; C14orf75

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 122402

About TDRD9

Cytogenetic location: 14q32.33 Genomic coordinates (GRCh38): 14:103,928,456-104,052,667 (from NCBI)

This gene has 7 transcripts (splice variants), 196 orthologues, 18 paralogues and is associated with 2 phenotypes. Biased expression in testis (RPKM 26.4) and thyroid (RPKM 5.7).

Summary

Predicted to enable RNA binding activity. Involved in spermatogenesis. Located in cytoplasm and nucleus. Implicated in spermatogenic failure 30. [provided by Alliance of Genome Resources, Apr 2022]

TDRD9 Products (1)

mRNA Protein Name
NM_153046.3 NP_694591.2 ATP-dependent RNA helicase TDRD9
Biological Process GO Annotation Evidence References Source
involved in spermatogenesis IMP
IMP: Inferred from mutant phenotype
28536242 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
28536242 GOA
located in nucleus IDA
IDA: Inferred from direct assay
28536242 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TDRD9 Protein Structure

DEAD

DEAD: DEAD/DEAH box helicase (138 - 294)

Helicase_C

Helicase_C: Helicase conserved C-terminal domain (409 - 500)

HA2

HA2: Helicase associated domain (HA2) (566 - 664)

TUDOR

TUDOR: Tudor domain (904 - 1013)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1382 a.a.
Protein Preferred Names Protein Names

ATP-dependent RNA helicase TDRD9

  • hypoxia-inducible HIG-1

Related Diseases

Diseases Alias
Spermatogenic Failure 30
  • SPGF30

Spermatogenic Failure
  • Azoospermia

  • Spgf

  • Spermatogenic Failure, Susceptibility To

  • Absent Sperm

  • Aspermatogenesis

  • Infertility Due To Azoospermia

  • Hypospermatogenesis

  • Azoospermatism

Male Infertility With Azoospermia Or Oligozoospermia Due To Single Gene Mutation
Spermatogenic Failure, Y-Linked, 2
  • SPGFY2

  • Spermatogenic Failure, Nonobstructive, Y-Linked

  • Y-Linked Spermatogenic Failure 2

  • Azoospermia, Nonobstructive, Y-Linked

  • Oligozoospermia, Nonobstructive, Y-Linked

  • Oligospermia, Nonobstructive, Y-Linked

  • Spermatogenic Arrest, Y-Linked

  • Nonobstructive Y-Linked Spermatogenic Failure

  • Spermatogenic Failure Y-Linked 2

  • Azoospermia Non-Obstructive Y-Linked

  • Non-Obstructive Azoospermia And Infertility

  • Oligospermia Non-Obstructive Y-Linked

  • Oligozoospermia Non-Obstructive Y-Linked

  • Spermatogenic Arrest Y-Linked

  • Spermatogenic Failure Nonobstructive Y-Linked

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta TDRD9 VGNC VGNC:99264
Felis catus TDRD9 VGNC VGNC:66051
Rattus norvegicus TDRD9 RGD RGD:1306942
Bos taurus TDRD9 VGNC VGNC:35722
Canis familiaris TDRD9 VGNC VGNC:47226
Mus musculus TDRD9 MGD MGI:1921941