PKHD1L1 - PKHD1 like 1 Gene

Also Known as PKHDL1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 93035

About PKHD1L1

Cytogenetic location: 8q23.1-q23.2 Genomic coordinates (GRCh38): 8:109,362,461-109,537,207 (from NCBI)

This gene has 4 transcripts (splice variants), 154 orthologues and 36 paralogues. Biased expression in thyroid (RPKM 10.5) and lymph node (RPKM 0.8).

Summary

Predicted to act upstream of or within sensory perception of sound. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

PKHD1L1 Products (1)

mRNA Protein Name
NM_177531.6 NP_803875.2 fibrocystin-L precursor

PKHD1L1 Protein Structure

TIG

TIG: IPT/TIG domain (31 - 118)

TIG

TIG: IPT/TIG domain (146 - 255)

TIG

TIG: IPT/TIG domain (271 - 337)

PA14

PA14: PA14 domain (364 - 466)

TIG

TIG: IPT/TIG domain (1067 - 1138)

TIG

TIG: IPT/TIG domain (1156 - 1234)

TIG

TIG: IPT/TIG domain (1240 - 1313)

TIG

TIG: IPT/TIG domain (1331 - 1386)

TIG

TIG: IPT/TIG domain (1566 - 1641)

TIG

TIG: IPT/TIG domain (1659 - 1743)

TIG

TIG: IPT/TIG domain (1749 - 1823)

TIG

TIG: IPT/TIG domain (1833 - 1910)

TIG

TIG: IPT/TIG domain (1916 - 1997)

TIG

TIG: IPT/TIG domain (2000 - 2085)

TIG

TIG: IPT/TIG domain (2091 - 2165)

G8

G8: G8 domain (2185 - 2303)

G8

G8: G8 domain (3036 - 3173)

Beta_helix

Beta_helix: Right handed beta helix region (3409 - 3539)

  • 0
  • 700
  • 1400
  • 2100
  • 2800
  • 3500
  • 4243 a.a.
Protein Preferred Names Protein Names

fibrocystin-L

  • PKHD1-like protein 1

Related Diseases

Diseases Alias
Ciliary Dyskinesia, Primary, 5

  • Primary Ciliary Dyskinesia 5

  • CILD5

  • Ciliary Dyskinesia, Primary, 5, Without Situs Inversus

  • Primary Ciliary Dyskinesia 5 Without Situs Inversus

  • Ics5

  • Immotile Cilia Syndrome 5

  • Primary Ciliary Dyskinesia 5 With Or Without Situs Inversus

  • Dyskinesia, Ciliary, Primary, Type 5
Polycystic Kidney Disease

  • Polycystic Kidney Diseases

  • Pkd

  • Polycystic Renal Disease

  • Kidney Disease, Polycystic

  • Polycystic Kidney, Autosomal Dominant
Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease

  • Autosomal Recessive Polycystic Kidney Disease

  • Arpkd

  • Polycystic Kidney Disease, Autosomal Recessive

  • Polycystic Kidney And Hepatic Disease 1

  • Pkhd1

  • PKD4

  • Polycystic Kidney Disease 4 With Or Without Hepatic Disease

  • Polycystic Kidney Disease, Infantile, Type I

  • Polycystic Kidney Disease, Infantile Type

  • Polycystic Kidney, Autosomal Recessive

  • Pkd3, Formerly

  • Polycystic Kidney Disease 4, With Or Without Hepatic Disease

  • Arpkd/Chf

  • Ar-Pkd

  • Polycystic Kidney Disease 4, With Or Without Polycystic Liver Disease

  • Infantile Polycystic Kidney Disease Type I

  • Pkd3

  • Kidney, Polycystic, Disease, Type 4, With/Without Hepatic Disease

  • Polycystic Kidney Disease 3, Autosomal Dominant
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS10597 PKHD1L1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus PKHD1L1 VGNC VGNC:109395
Felis catus PKHD1L1 VGNC VGNC:64193
Mus musculus PKHD1L1 MGD MGI:2183153
Macaca mulatta PKHD1L1 VGNC VGNC:75834
Rattus norvegicus PKHD1L1 RGD RGD:1310406
Canis familiaris PKHD1L1 VGNC VGNC:44606
Others PKHD1L1 NCBI