Protein Gli3

URN urn:agi-llid:2737
Connectivity 117
Name Gli3
Description GLI family zinc finger 3
Notes This gene encodes a protein which belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription factors and are mediators of Sonic hedgehog (Shh) signaling. The protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. Mutations in this gene have been associated with several diseases, including Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B. [provided by RefSeq]

Pathway pancreatic cancer pathway

GO Molecular Function chromatin binding
nucleic acid binding
transcription repressor activity
transcription factor activity
beta-catenin binding
transcription repressor binding
DNA binding
histone acetyltransferase binding
histone deacetylase binding
sequence-specific DNA binding
metal ion binding
zinc ion binding

GO Cellular Component intracellular
cilium
cytoplasm
cytosol
nucleolus
mediator complex
transcriptional repressor complex
nucleus

GO Biological Process negative regulation of cell proliferation
pattern specification process
developmental growth
anatomical structure development
anatomical structure formation involved in morphogenesis
telencephalon development
forebrain development
inner ear development
neural tube development
tube development
pallium development
regulation of cell differentiation
hindgut morphogenesis
embryonic morphogenesis
negative regulation of cell differentiation
mammary gland specification
anterior-posterior pattern formation
proximal-distal pattern formation
dorsal-ventral pattern formation
spinal cord dorsal-ventral patterning
forebrain dorsal-ventral pattern formation
central nervous system development
embryonic digestive tract development
anterior semicircular canal development
lateral semicircular canal development
brain development
kidney development
lung development
heart development
artery development
metanephros development
mammary gland development
camera-type eye development
positive regulation of chondrocyte differentiation
neuron fate commitment
embryonic digestive tract morphogenesis
embryonic digit morphogenesis
branching morphogenesis of a tube
limb morphogenesis
optic nerve morphogenesis
branching involved in ureteric bud morphogenesis
embryonic skeletal system morphogenesis
embryonic limb morphogenesis
camera-type eye morphogenesis
odontogenesis of dentine-containing tooth
in utero embryonic development
axon guidance
negative regulation of Wnt receptor signaling pathway through beta-catenin
regulation of transcription
negative regulation of transcription
negative regulation of transcription from RNA polymerase II promoter
positive regulation of transcription
positive regulation of transcription from RNA polymerase II promoter
positive regulation of gene-specific transcription from RNA polymerase II promoter
regulation of gene-specific transcription
positive regulation of protein import into nucleus
regulation of apoptosis
transcription
regulation of gene expression
protein processing
smoothened signaling pathway
smoothened signaling pathway involved in dorsal-ventral neural tube patterning
smoothened signaling pathway involved in ventral spinal cord interneuron specification
smoothened signaling pathway involved in spinal cord motor neuron cell fate specification

Ariadne Ontology GLI-like
Oncogenes

Group GLI-like
Oncogenes
negative regulation of cell proliferation
pattern specification process
developmental growth
anatomical structure development
anatomical structure formation involved in morphogenesis
telencephalon development
forebrain development
inner ear development
neural tube development
tube development
pallium development
regulation of cell differentiation
hindgut morphogenesis
embryonic morphogenesis
negative regulation of cell differentiation
mammary gland specification
anterior-posterior pattern formation
proximal-distal pattern formation
dorsal-ventral pattern formation
spinal cord dorsal-ventral patterning
forebrain dorsal-ventral pattern formation
central nervous system development
embryonic digestive tract development
anterior semicircular canal development
lateral semicircular canal development
brain development
kidney development
lung development
heart development
artery development
metanephros development
mammary gland development
camera-type eye development
positive regulation of chondrocyte differentiation
neuron fate commitment
embryonic digestive tract morphogenesis
embryonic digit morphogenesis
branching morphogenesis of a tube
limb morphogenesis
optic nerve morphogenesis
branching involved in ureteric bud morphogenesis
embryonic skeletal system morphogenesis
embryonic limb morphogenesis
camera-type eye morphogenesis
odontogenesis of dentine-containing tooth
in utero embryonic development
axon guidance
negative regulation of Wnt receptor signaling pathway through beta-catenin
regulation of transcription
negative regulation of transcription
negative regulation of transcription from RNA polymerase II promoter
positive regulation of transcription
positive regulation of transcription from RNA polymerase II promoter
positive regulation of gene-specific transcription from RNA polymerase II promoter
regulation of gene-specific transcription
positive regulation of protein import into nucleus
regulation of apoptosis
transcription
regulation of gene expression
protein processing
smoothened signaling pathway
smoothened signaling pathway involved in dorsal-ventral neural tube patterning
smoothened signaling pathway involved in ventral spinal cord interneuron specification
smoothened signaling pathway involved in spinal cord motor neuron cell fate specification
chromatin binding
nucleic acid binding
transcription repressor activity
transcription factor activity
beta-catenin binding
transcription repressor binding
DNA binding
histone acetyltransferase binding
histone deacetylase binding
sequence-specific DNA binding
metal ion binding
zinc ion binding
intracellular
cilium
cytoplasm
cytosol
nucleolus
mediator complex
transcriptional repressor complex
nucleus

MedScan ID 2737

Hugo ID 4319

Human chromosome position 7p13

LocusLink ID 2737
14634

Alias PHS
ACLS
GCPS
PAPA
PAPB
PAP-A
PAPA1
PPDIV
zinc finger protein GLI3
oncogene GLI3
OTTHUMP00000159085
DNA-binding protein
GLI-Kruppel family member GLI3
glioma-associated oncogene family zinc finger 3
Xt
Bph
Pdn
add
AI854843
AU023367
extra toes
brachyphalangy
OTTMUSP00000029127
OTTMUSP00000029128
polydactyly Nagoya
anterior digit pattern deformity
anterior digit pattern deformity mutant
DNA-binding GLI3
extra toes mutant
GLI family zinc finger 3
GLI3
GLI-Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome)
OTTHUMP00000025248
PPD IV

Organism Homo sapiens
Mus musculus

GenBank ID NC_000007
NM_000168
NP_000159
NT_007819
NT_079592
NW_001839004
NW_923240
NG_008434
AC_000139
AC_000068
AC_000050
AC005026
AAP21869
AC005028
AAS01998
AC005158
AAS02015
AC073852
AJ250408
CAB59315
CH236951
EAL24002
CH471073
EAW94144
EAW94145
M20674
AA330409
AI863961
AK299299
BAG61313
AK308429
BC113616
AAI13617
BC117168
AAI17169
BF194991
BI497308
DA713549
M57609
AAA52564
P10071
NC_000079
NM_008130
NP_032156
NT_039578
NW_001030513
AC_000035
AC163610
AC173115
AC173210
AF418601
CH466561
EDL32734
AK037232
AK045960
AK048009
AK053922
AK144851
BAE26100
AK158261
BAE34433
BC141135
AAI41136
BC145445
AAI45446
CA752350
X95255
CAA64543
Q3TYX7
Q3UMJ8
Q61602

OMIM ID 165240
200990
175700
241800
146510
174200
174700

Mouse chromosome position 13 14.0 cM

GO ID 0008013
0003682
0035035
0042826
0046872
0043565
0003700
0016564
0008270
0048646
0060873
0009952
0060840
0007411
0001658
0048593
0048589
0048566
0042733
0048704
0021798
0007507
0007442
0001701
0048839
0060875
0035108
0030324
0030879
0001656
0090090
0045596
0008285
0000122
0021915
0048663
0042475
0021631
0021543
0007389
0032332
0010552
0042307
0045941
0045944
0016485
0009954
0042981
0060831
0021776
0021775
0021513
0035295
0005929
0005737
0005829
0005622
0016592
0005634
0017053
0003677
0003676
0048856
0007420
0048754
0043010
0007417
0009953
0048557
0030326
0048598
0030900
0001822
0060594
0016481
0045595
0010468
0032583
0045449
0007224
0021537
0006350
0048558
0005730
0070491

Swiss-Prot Accession P10071
B2RUG4
Q3TYX7
Q61602
Q3UMJ8
A4D1W1
O75219
Q17RW4
Q75MT0
Q75MU9
Q9UDT5
Q9UJ39

PIR ID A35927

Unigene ID Hs.21509
Mm.5098

KEGG ID hsa:2737
mmu:14634

Swiss-Prot ID GLI3_MOUSE
GLI3_HUMAN
B2RUG4_MOUSE
Q3TYX7_MOUSE

Cell Localization Nucleus

IPI ID IPI00123429
IPI00018889
IPI00651982
IPI00857095

Homologene ID 139

MGI ID 95729