LHX8 - LIM homeobox 8 Gene

Also Known as LHX7

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 431707

About LHX8

Cytogenetic location: 1p31.1 Genomic coordinates (GRCh38): 1:75,128,434-75,199,454 (from NCBI)

This gene has 4 transcripts (splice variants), 268 orthologues and 20 paralogues. Low expression observed in reference dataset.

Summary

The protein encoded by this gene is a member of the LIM homeobox family of proteins, which are involved in patterning and differentiation of various tissue types. These proteins contain two tandemly repeated cysteine-rich double-zinc finger motifs known as LIM domains, in addition to a DNA-binding homeodomain. This family member is a transcription factor that plays a role in tooth morphogenesis. It is also involved in oogenesis and in neuronal differentiation. This gene is a candidate gene for cleft palate, and it is also associated with odontoma formation. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]

LHX8 Products (2)

mRNA Protein Name
NM_001001933.1 NP_001001933.1 LIM/homeobox protein Lhx8 isoform 1
NM_001256114.2 NP_001243043.1 LIM/homeobox protein Lhx8 isoform 2
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 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

LHX8 Protein Structure

LIM

LIM: LIM domain (75 - 131)

LIM

LIM: LIM domain (136 - 190)

Homeobox

Homeobox: Homeobox domain (226 - 282)

  • 0
  • 100
  • 200
  • 300
  • 356 a.a.
Protein Preferred Names Protein Names

LIM/homeobox protein Lhx8

  • LIM-homeodomain protein Lhx8

LHX8 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LHX8 Q68G74 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
LHX8 Q68G74 NUTM1 Homo sapiens Q86Y26 25416956
Intra
LHX8 Q68G74 KIF1B Homo sapiens O60333-2 32814053
Intra
LHX8 Q68G74 KIF1B Homo sapiens O60333-2 32814053
Intra
LHX8 Q68G74 KIF1B Homo sapiens O60333-2 32814053
Intra
LHX8 Q68G74 DMWD Homo sapiens G5E9A7 32814053
Intra
LHX8 Q68G74 DMWD Homo sapiens G5E9A7 32814053
Intra
LHX8 Q68G74 DMWD Homo sapiens G5E9A7 32814053
Intra
LHX8 Q68G74 ABI2 Homo sapiens Q9NYB9-2 32296183
Intra
LHX8 Q68G74 FOXN1 Homo sapiens O15353 32296183
Intra
LHX8 Q68G74 FOXN1 Homo sapiens O15353 32296183
Intra
LHX8 Q68G74 BANP Homo sapiens Q8N9N5-2 32296183
Intra
LHX8 Q68G74 EFS Homo sapiens O43281-2 32296183
Intra
LHX8 Q68G74 EFS Homo sapiens O43281-2 32296183
Intra
LHX8 Q68G74 FIGLA Homo sapiens Q6QHK4 32296183
Intra
LHX8 Q68G74 FIGLA Homo sapiens Q6QHK4 32296183
Intra
LHX8 Q68G74 LDB1 Homo sapiens Q86U70-2 32296183
Intra
LHX8 Q68G74 LDB1 Homo sapiens Q86U70-2 32296183
Intra
LHX8 Q68G74 LDB1 Homo sapiens Q86U70-2 32296183
Intra
LHX8 Q68G74 ATF6B Homo sapiens Q96QL7 32296183
Intra
LHX8 Q68G74 ATF6B Homo sapiens Q96QL7 32296183
Intra
LHX8 Q68G74 ATF6B Homo sapiens Q96QL7 32296183
Intra
LHX8 Q68G74 TSC1 Homo sapiens Q86WV8 32814053
Intra
LHX8 Q68G74 TSC1 Homo sapiens Q86WV8 32814053
Intra
LHX8 Q68G74 TSC1 Homo sapiens Q86WV8 32814053
Intra
LHX8 Q68G74 SCYL3 Homo sapiens Q8IZE3 25416956
Intra
LHX8 Q68G74 SCYL3 Homo sapiens Q8IZE3 25416956
Intra
LHX8 Q68G74 SCYL3 Homo sapiens Q8IZE3 25416956
Intra
LHX8 Q68G74 PRPF31 Homo sapiens Q8WWY3 32296183
Intra
LHX8 Q68G74 TBC1D1 Homo sapiens Q86TI0 32296183
Intra
LHX8 Q68G74 TBC1D1 Homo sapiens Q86TI0 32296183
Intra
LHX8 Q68G74 TBC1D1 Homo sapiens Q86TI0 32296183
Intra
LHX8 Q68G74 GLE1 Homo sapiens Q53GS7 32814053
Intra
LHX8 Q68G74 GLE1 Homo sapiens Q53GS7 32814053
Intra
LHX8 Q68G74 GLE1 Homo sapiens Q53GS7 32814053
Intra
LHX8 Q68G74 LDB2 Homo sapiens O43679 32296183
Intra
LHX8 Q68G74 LDB2 Homo sapiens O43679 32296183
Intra
LHX8 Q68G74 FGFR3 Homo sapiens P22607 32814053
Intra
LHX8 Q68G74 FGFR3 Homo sapiens P22607 32814053
Intra
LHX8 Q68G74 FGFR3 Homo sapiens P22607 32814053
Intra
LHX8 Q68G74 CCT5 Homo sapiens P48643 32814053
Intra
LHX8 Q68G74 CCT5 Homo sapiens P48643 32814053
Intra
LHX8 Q68G74 CCT5 Homo sapiens P48643 32814053
Intra
LHX8 Q68G74 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
LHX8 Q68G74 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
LHX8 Q68G74 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
LHX8 Q68G74 SPRED1 Homo sapiens Q7Z699 32814053
Intra
LHX8 Q68G74 SPRED1 Homo sapiens Q7Z699 32814053
Intra
LHX8 Q68G74 SPRED1 Homo sapiens Q7Z699 32814053
Intra
LHX8 Q68G74 LDB1 Homo sapiens Q86U70 25416956
Intra
LHX8 Q68G74 LDB1 Homo sapiens Q86U70 35140242
Intra
LHX8 Q68G74 LDB1 Homo sapiens Q86U70 35140242
Intra
LHX8 Q68G74 WFS1 Homo sapiens O76024 32814053
Intra
LHX8 Q68G74 WFS1 Homo sapiens O76024 32814053
Intra
LHX8 Q68G74 WFS1 Homo sapiens O76024 32814053
Intra
LHX8 Q68G74 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
LHX8 Q68G74 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
LHX8 Q68G74 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
LHX8 Q68G74 GINS4 Homo sapiens Q9BRT9 32296183
Intra
LHX8 Q68G74 GRN Homo sapiens P28799 32814053
Intra
LHX8 Q68G74 GRN Homo sapiens P28799 32814053
Intra
LHX8 Q68G74 GRN Homo sapiens P28799 32814053
Intra
LHX8 Q68G74 KLF3 Homo sapiens P57682 25416956
Intra
LHX8 Q68G74 KLF3 Homo sapiens P57682 25416956
Intra
LHX8 Q68G74 TBC1D22B Homo sapiens Q9NU19 32296183
Intra
LHX8 Q68G74 PEX1 Homo sapiens O43933 32814053
Intra
LHX8 Q68G74 PEX1 Homo sapiens O43933 32814053
Intra
LHX8 Q68G74 PEX1 Homo sapiens O43933 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Odontoma
Neuropathy, Hereditary Sensory And Autonomic, Type Iia
  • Hereditary Sensory And Autonomic Neuropathy Type 2

  • Hsan2

  • HSAN2A

  • Morvan Disease

  • Hereditary Sensory And Autonomic Neuropathy Type Ii

  • Neurogenic Acroosteolysis

  • Hsan Iia

  • Hsn2a

  • Hsn Iia

  • Neuropathy, Progressive Sensory, Of Children

  • Neuropathy, Congenital Sensory

  • Neuropathy, Hereditary Sensory And Autonomic, Type Ii

  • Hereditary Sensory And Autonomic Neuropathy Type 2a

  • Hereditary Sensory And Autonomic Neuropathy Type Iia

  • Hsanii

  • Congenital Sensory Neuropathy

  • Hsan Type Ii

  • Morvan Syndrome

  • Neuropathy, Hereditary Sensory And Autonomic, Type 2a

  • Morvan'S Disease

  • Neuropathy, Hereditary Sensory, Type Iia

  • Acroosteolysis, Neurogenic

  • Acroosteolysis, Giaccai Type

  • Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive

  • Hereditary Sensory Autonomic Neuropathy Type 2

  • Giaccai Type Acroosteolysis

  • Hereditary Sensory Neuropathy Type 2

  • Hereditary Sensory Radicular Neuropathy, Recessive Form

  • Hsan2b

  • Hsan2c

  • Hsan2d

  • Hsn Type Ii

  • Autosomal Recessive Sensory Radicular Neuropathy

  • Limbic Encephalitis-Neuromyotonia-Hyperhidrosis-Polyneuropathy Syndrome

  • Morvan Fibrillary Chorea

  • Neuropathy, Hereditary Sensory And Autonomic, 2a

  • Acroosteolysis Giaccai Type

  • Hereditary Sensory Neuropathy Type Iia

  • Hereditary Sensory Radicular Neuropathy Autosomal Recessive

  • Progressive Sensory Neuropathy Of Children

  • Neuropathy Congenital Sensory

  • Charcot-Marie-Tooth Disease

  • Neuropathy, Sensory And Autonomic, Hereditary, Type Iia

  • Hereditary Sensory Autonomic Neuropathy, Type 2

  • Hereditary Motor And Sensory-Neuropathy Type Ii

  • Sensory Neuropathy, Hereditary

  • Neuropathy, Hereditary Sensory And Autonomic, Type Iib

Geotrichosis
Cerebral Hemisphere Lipoma
  • Lipoma Of The Cerebral Hemisphere

Corpus Callosum Lipoma
  • Lipoma Of The Corpus Callosum

  • Lipoma Of Corpus Callosum

Cleft Lip
  • Cheiloschisis

  • Labium Leporinum

  • Cleft Lip, Unilateral, Complete

  • Complete Unilateral Cleft Lip

  • Hare Lip

  • Congenital Fissure Of Lip

  • Isolated Cleft Lip

  • Cleft Lip Without Cleft Palate

  • Cleft Lip Without Cleft Palate, Unilateral

  • Isolated Cleft Lip, Unilateral

  • Cleft Lip Without Cleft Palate, Bilateral

  • Isolated Cleft Lip, Bilateral

Cleft Palate, Isolated
  • Cleft Palate

  • Isolated Cleft Palate

  • CPI

  • Cp

  • Palatoschisis

  • Cleft Palate Isolated

  • Uranostaphyloschisis

  • Congenital Fissure Of Palate

  • Cleft Of Secondary Palate

Central Nervous System Lipoma
  • Lipoma Of The Cns

Premature Menopause
  • Primary Ovarian Insufficiency

  • Premature Ovarian Failure

  • Hypergonadotropic Hypogonadism

  • Premature Ovarian Insufficiency

  • Menopause - Premature

  • Menopause Praecox

  • Menopause Premature

  • Menopause, Premature

  • Female Hypergonadotropic Hypogonadism

  • Hypergonadotrophic Ovarian Failure

  • Primary Female Hypogonadism

  • Pof - [Premature Ovarian Failure]

  • Ovarian Failure

  • Ovarian Secretion Suppression

  • Ovary Hyposecretion

  • Ovary Secretion Deficiency

  • Premature Menopause Nos

Van Der Woude Syndrome
  • Lip-Pit Syndrome

  • Vws

  • Cleft Lip And/Or Palate With Mucous Cysts Of Lower Lip

  • Vdws

  • Lps

  • Lip Pit Syndrome

  • Cleft Lip/Palate With Mucous Cysts Of Lower Lip

  • Myopathy, Actin, Congenital, With Excess Of Thin Myofilaments

Orofacial Cleft
  • Cleft, Orofacial

Tooth Agenesis
  • Oligodontia

  • Hypodontia

  • Selective Tooth Agenesis

  • Tooth Agenesis, Selective

  • Familial Tooth Agenesis

  • Anodontia

  • Congenital Absence Of One Tooth

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
Mus musculus LHX8 MGD MGI:1096343
Canis familiaris LHX8 VGNC VGNC:42668
Rattus norvegicus LHX8 RGD RGD:1308749
Bos taurus LHX8 VGNC VGNC:30877
Felis catus LHX8 VGNC VGNC:63225
Macaca mulatta LHX8 VGNC VGNC:74144
Others LHX8 NCBI