GGA3 (golgi associated, gamma adaptin ear containing, ARF binding protein 3) - Rat Genome Database

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Gene: GGA3 (golgi associated, gamma adaptin ear containing, ARF binding protein 3) Homo sapiens
Analyze
Symbol: GGA3
Name: golgi associated, gamma adaptin ear containing, ARF binding protein 3
RGD ID: 1319955
HGNC Page HGNC
Description: Enables small GTPase binding activity and ubiquitin binding activity. Involved in several processes, including negative regulation of amyloid-beta formation; protein destabilization; and protein transport. Located in lysosome and trans-Golgi network. Part of protein-containing complex.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ADP-ribosylation factor-binding protein GGA3; golgi-associated, gamma adaptin ear containing, ARF binding protein 3; Golgi-localized, gamma ear-containing, ARF-binding protein 3; KIAA0154
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1775,236,599 - 75,262,363 (-)EnsemblGRCh38hg38GRCh38
GRCh381775,225,464 - 75,262,363 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371773,232,694 - 73,258,444 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361770,744,290 - 70,769,272 (-)NCBINCBI36hg18NCBI36
Build 341770,744,289 - 70,769,272NCBI
Celera1769,825,023 - 69,850,791 (-)NCBI
Cytogenetic Map17q25.1NCBI
HuRef1768,642,387 - 68,668,634 (-)NCBIHuRef
CHM1_11773,297,254 - 73,323,022 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:8590280   PMID:8889548   PMID:10747088   PMID:10747089   PMID:10749927   PMID:10814529   PMID:11301005   PMID:11387475   PMID:11390366   PMID:11859375   PMID:11950392   PMID:12032548  
PMID:12060753   PMID:12213833   PMID:12215646   PMID:12221117   PMID:12477932   PMID:12505986   PMID:12810073   PMID:12858162   PMID:14567678   PMID:14638859   PMID:14660606   PMID:14665628  
PMID:14702039   PMID:15039775   PMID:15039776   PMID:15047686   PMID:15143060   PMID:15231748   PMID:15345724   PMID:15489334   PMID:15494413   PMID:15615712   PMID:15701688   PMID:15966896  
PMID:16135791   PMID:16344560   PMID:16473621   PMID:16977309   PMID:16996030   PMID:17116753   PMID:17314030   PMID:17494868   PMID:17553422   PMID:17804820   PMID:18162163   PMID:18199687  
PMID:18418388   PMID:18439901   PMID:18638397   PMID:19327867   PMID:19788741   PMID:19815556   PMID:20012524   PMID:20150893   PMID:20484053   PMID:20848231   PMID:21440067   PMID:21517092  
PMID:21664574   PMID:22658674   PMID:22836275   PMID:23143332   PMID:23970038   PMID:24056087   PMID:24407285   PMID:25195858   PMID:25468996   PMID:26053850   PMID:26344197   PMID:26446845  
PMID:26638075   PMID:26811329   PMID:26935970   PMID:27901063   PMID:28100775   PMID:28190767   PMID:28581508   PMID:28700943   PMID:28718761   PMID:29273463   PMID:29358589   PMID:29395067  
PMID:29467281   PMID:29568061   PMID:31076515   PMID:31732153   PMID:32296183   PMID:32334026   PMID:32513696   PMID:34079125  


Genomics

Comparative Map Data
GGA3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1775,236,599 - 75,262,363 (-)EnsemblGRCh38hg38GRCh38
GRCh381775,225,464 - 75,262,363 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371773,232,694 - 73,258,444 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361770,744,290 - 70,769,272 (-)NCBINCBI36hg18NCBI36
Build 341770,744,289 - 70,769,272NCBI
Celera1769,825,023 - 69,850,791 (-)NCBI
Cytogenetic Map17q25.1NCBI
HuRef1768,642,387 - 68,668,634 (-)NCBIHuRef
CHM1_11773,297,254 - 73,323,022 (-)NCBICHM1_1
Gga3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3911115,475,081 - 115,495,501 (-)NCBIGRCm39mm39
GRCm39 Ensembl11115,475,081 - 115,494,877 (-)Ensembl
GRCm3811115,584,255 - 115,604,517 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11115,584,255 - 115,604,051 (-)EnsemblGRCm38mm10GRCm38
MGSCv3711115,445,569 - 115,465,220 (-)NCBIGRCm37mm9NCBIm37
MGSCv3611115,400,801 - 115,419,975 (-)NCBImm8
Celera11127,352,022 - 127,371,680 (-)NCBICelera
Cytogenetic Map11E2NCBI
Gga3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.210100,825,426 - 100,844,462 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl10100,825,426 - 100,844,462 (-)Ensembl
Rnor_6.010104,137,655 - 104,156,576 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl10104,137,655 - 104,156,576 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.010104,124,628 - 104,143,981 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.410105,665,476 - 105,684,513 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.110105,680,483 - 105,698,186 (-)NCBI
Celera1099,399,869 - 99,418,903 (-)NCBICelera
Cytogenetic Map10q32.1NCBI
Gga3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555532,108,379 - 2,124,748 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555532,103,694 - 2,124,748 (-)NCBIChiLan1.0ChiLan1.0
GGA3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11774,737,164 - 74,762,039 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1774,737,164 - 74,762,039 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01769,185,045 - 69,208,766 (-)NCBIMhudiblu_PPA_v0panPan3
GGA3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.195,235,377 - 5,250,982 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl95,235,025 - 5,249,361 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha95,913,638 - 5,929,958 (+)NCBI
ROS_Cfam_1.095,904,719 - 5,921,031 (+)NCBI
UMICH_Zoey_3.195,943,474 - 5,959,763 (+)NCBI
UNSW_CanFamBas_1.096,053,691 - 6,070,007 (+)NCBI
UU_Cfam_GSD_1.096,113,427 - 6,130,011 (+)NCBI
Gga3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244056025,863,468 - 5,886,500 (+)NCBI
SpeTri2.0NW_004936594531,844 - 548,487 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
GGA3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl126,047,340 - 6,074,478 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1126,051,854 - 6,072,424 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2126,023,618 - 6,034,858 (+)NCBISscrofa10.2Sscrofa10.2susScr3
GGA3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11646,410,941 - 46,432,560 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl1646,411,391 - 46,432,991 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366607717,181,468 - 17,202,614 (+)NCBIVero_WHO_p1.0
Gga3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248015,057,611 - 5,073,276 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
RH98808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371773,232,750 - 73,232,985UniSTSGRCh37
Build 361770,744,345 - 70,744,580RGDNCBI36
Celera1769,825,079 - 69,825,314RGD
Cytogenetic Map17q25.1UniSTS
HuRef1768,642,443 - 68,642,678UniSTS
GeneMap99-GB4 RH Map17474.99UniSTS
RH25373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371773,233,092 - 73,233,203UniSTSGRCh37
Build 361770,744,687 - 70,744,798RGDNCBI36
Celera1769,825,421 - 69,825,532RGD
Cytogenetic Map17q25.1UniSTS
HuRef1768,642,785 - 68,642,896UniSTS
UniSTS:146574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371773,233,279 - 73,233,553UniSTSGRCh37
Build 361770,744,874 - 70,745,148RGDNCBI36
Celera1769,825,608 - 69,825,882RGD
HuRef1768,642,972 - 68,643,246UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:11600
Count of miRNA genes:1295
Interacting mature miRNAs:1697
Transcripts:ENST00000245541, ENST00000351904, ENST00000537584, ENST00000537686, ENST00000538886, ENST00000577435, ENST00000578208, ENST00000578275, ENST00000578348, ENST00000578773, ENST00000578896, ENST00000579743, ENST00000580646, ENST00000580799, ENST00000582200, ENST00000582232, ENST00000582376, ENST00000582486, ENST00000582717, ENST00000582821, ENST00000583282, ENST00000583667, ENST00000584243, ENST00000584550, ENST00000584978
Prediction methods:Microtar, Miranda, Pita, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2429 2649 1542 448 1871 289 4297 1923 2982 289 1445 1598 175 1 1203 2734 4 2
Low 10 342 184 176 80 176 59 274 752 130 15 15 1 54 2
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001172703 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001172704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001291641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001291642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_138619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024388 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC022211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AEKP01093165 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF190864 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF219138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF219139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK124541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051732 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC063285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC070044 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM981305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB240770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D63876 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA312660 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY030361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000537686   ⟹   ENSP00000438085
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,236,599 - 75,261,606 (-)Ensembl
RefSeq Acc Id: ENST00000538886   ⟹   ENSP00000446421
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,236,599 - 75,261,600 (-)Ensembl
RefSeq Acc Id: ENST00000577435   ⟹   ENSP00000461963
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,242,889 - 75,261,617 (-)Ensembl
RefSeq Acc Id: ENST00000578208
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,238,357 - 75,238,985 (-)Ensembl
RefSeq Acc Id: ENST00000578348   ⟹   ENSP00000463288
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,237,284 - 75,262,361 (-)Ensembl
RefSeq Acc Id: ENST00000578773   ⟹   ENSP00000464268
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,238,246 - 75,239,551 (-)Ensembl
RefSeq Acc Id: ENST00000578896
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,240,949 - 75,242,368 (-)Ensembl
RefSeq Acc Id: ENST00000579743   ⟹   ENSP00000481953
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,243,517 - 75,262,358 (-)Ensembl
RefSeq Acc Id: ENST00000580646   ⟹   ENSP00000464574
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,237,522 - 75,239,538 (-)Ensembl
RefSeq Acc Id: ENST00000580799   ⟹   ENSP00000462473
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,241,669 - 75,261,593 (-)Ensembl
RefSeq Acc Id: ENST00000582232
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,240,794 - 75,241,733 (-)Ensembl
RefSeq Acc Id: ENST00000582376   ⟹   ENSP00000464365
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,243,135 - 75,261,593 (-)Ensembl
RefSeq Acc Id: ENST00000582486   ⟹   ENSP00000462629
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,237,427 - 75,262,361 (-)Ensembl
RefSeq Acc Id: ENST00000582717   ⟹   ENSP00000462081
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,238,238 - 75,262,363 (-)Ensembl
RefSeq Acc Id: ENST00000582821
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,241,865 - 75,261,590 (-)Ensembl
RefSeq Acc Id: ENST00000583282   ⟹   ENSP00000463115
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,237,526 - 75,239,081 (-)Ensembl
RefSeq Acc Id: ENST00000583667
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,238,965 - 75,240,437 (-)Ensembl
RefSeq Acc Id: ENST00000584243   ⟹   ENSP00000464318
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,242,884 - 75,261,585 (-)Ensembl
RefSeq Acc Id: ENST00000584550   ⟹   ENSP00000462279
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,238,179 - 75,239,545 (-)Ensembl
RefSeq Acc Id: ENST00000613421
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,236,602 - 75,261,623 (-)Ensembl
RefSeq Acc Id: ENST00000614198
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,236,600 - 75,240,450 (-)Ensembl
RefSeq Acc Id: ENST00000621217   ⟹   ENSP00000484733
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,236,599 - 75,261,621 (-)Ensembl
RefSeq Acc Id: ENST00000621870   ⟹   ENSP00000479464
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,236,599 - 75,261,600 (-)Ensembl
RefSeq Acc Id: ENST00000649398   ⟹   ENSP00000496890
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1775,236,621 - 75,261,631 (-)Ensembl
RefSeq Acc Id: NM_001172703   ⟹   NP_001166174
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,262,363 (-)NCBI
GRCh371773,232,694 - 73,258,444 (-)ENTREZGENE
HuRef1768,642,387 - 68,668,634 (-)ENTREZGENE
CHM1_11773,297,247 - 73,323,052 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001172704   ⟹   NP_001166175
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,262,363 (-)NCBI
GRCh371773,232,694 - 73,258,444 (-)ENTREZGENE
HuRef1768,642,387 - 68,668,634 (-)ENTREZGENE
CHM1_11773,297,247 - 73,323,052 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001291641   ⟹   NP_001278570
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,606 (-)NCBI
CHM1_11773,297,247 - 73,322,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001291642   ⟹   NP_001278571
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,606 (-)NCBI
CHM1_11773,297,247 - 73,322,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014001   ⟹   NP_054720
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,606 (-)NCBI
GRCh371773,232,694 - 73,258,444 (-)ENTREZGENE
Build 361770,744,290 - 70,769,272 (-)NCBI Archive
HuRef1768,642,387 - 68,668,634 (-)ENTREZGENE
CHM1_11773,297,247 - 73,322,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_138619   ⟹   NP_619525
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,606 (-)NCBI
GRCh371773,232,694 - 73,258,444 (-)ENTREZGENE
Build 361770,744,290 - 70,769,272 (-)NCBI Archive
HuRef1768,642,387 - 68,668,634 (-)ENTREZGENE
CHM1_11773,297,247 - 73,322,322 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011524563   ⟹   XP_011522865
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,225,464 - 75,261,623 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024385   ⟹   XP_016879874
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,623 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024386   ⟹   XP_016879875
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,623 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024387   ⟹   XP_016879876
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,620 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024388   ⟹   XP_016879877
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,262,361 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024389   ⟹   XP_016879878
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,262,363 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024390   ⟹   XP_016879879
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,262,361 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024392   ⟹   XP_016879881
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,617 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024450665   ⟹   XP_024306433
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,236,599 - 75,261,630 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001166174 (Get FASTA)   NCBI Sequence Viewer  
  NP_001166175 (Get FASTA)   NCBI Sequence Viewer  
  NP_001278570 (Get FASTA)   NCBI Sequence Viewer  
  NP_001278571 (Get FASTA)   NCBI Sequence Viewer  
  NP_054720 (Get FASTA)   NCBI Sequence Viewer  
  NP_619525 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522865 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879874 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879875 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879876 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879877 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879878 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879879 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879881 (Get FASTA)   NCBI Sequence Viewer  
  XP_024306433 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF05709 (Get FASTA)   NCBI Sequence Viewer  
  AAF42848 (Get FASTA)   NCBI Sequence Viewer  
  AAF42849 (Get FASTA)   NCBI Sequence Viewer  
  AAH70044 (Get FASTA)   NCBI Sequence Viewer  
  BAA09926 (Get FASTA)   NCBI Sequence Viewer  
  BAF84340 (Get FASTA)   NCBI Sequence Viewer  
  BAF84374 (Get FASTA)   NCBI Sequence Viewer  
  BAH11485 (Get FASTA)   NCBI Sequence Viewer  
  BAH12442 (Get FASTA)   NCBI Sequence Viewer  
  BAH13578 (Get FASTA)   NCBI Sequence Viewer  
  BAH13665 (Get FASTA)   NCBI Sequence Viewer  
  BAH13705 (Get FASTA)   NCBI Sequence Viewer  
  BAH14238 (Get FASTA)   NCBI Sequence Viewer  
  EAW89252 (Get FASTA)   NCBI Sequence Viewer  
  EAW89253 (Get FASTA)   NCBI Sequence Viewer  
  EAW89254 (Get FASTA)   NCBI Sequence Viewer  
  EAW89255 (Get FASTA)   NCBI Sequence Viewer  
  EAW89256 (Get FASTA)   NCBI Sequence Viewer  
  EAW89257 (Get FASTA)   NCBI Sequence Viewer  
  EAW89258 (Get FASTA)   NCBI Sequence Viewer  
  EAW89259 (Get FASTA)   NCBI Sequence Viewer  
  EAW89260 (Get FASTA)   NCBI Sequence Viewer  
  Q9NZ52 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001166175   ⟸   NM_001172704
- Peptide Label: isoform 2
- UniProtKB: Q9NZ52 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001166174   ⟸   NM_001172703
- Peptide Label: isoform 1
- UniProtKB: Q9NZ52 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_054720   ⟸   NM_014001
- Peptide Label: isoform short
- UniProtKB: Q9NZ52 (UniProtKB/Swiss-Prot),   A8K6M0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_619525   ⟸   NM_138619
- Peptide Label: isoform long
- UniProtKB: Q9NZ52 (UniProtKB/Swiss-Prot),   A8K6M0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001278571   ⟸   NM_001291642
- Peptide Label: isoform 3
- UniProtKB: Q9NZ52 (UniProtKB/Swiss-Prot),   A8K6M0 (UniProtKB/TrEMBL),   B7Z456 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001278570   ⟸   NM_001291641
- Peptide Label: isoform 1
- UniProtKB: Q9NZ52 (UniProtKB/Swiss-Prot),   A8K6M0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522865   ⟸   XM_011524563
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016879878   ⟸   XM_017024389
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016879879   ⟸   XM_017024390
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016879877   ⟸   XM_017024388
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016879874   ⟸   XM_017024385
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016879875   ⟸   XM_017024386
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016879881   ⟸   XM_017024392
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016879876   ⟸   XM_017024387
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_024306433   ⟸   XM_024450665
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: ENSP00000462473   ⟸   ENST00000580799
RefSeq Acc Id: ENSP00000464574   ⟸   ENST00000580646
RefSeq Acc Id: ENSP00000496890   ⟸   ENST00000649398
RefSeq Acc Id: ENSP00000479464   ⟸   ENST00000621870
RefSeq Acc Id: ENSP00000464365   ⟸   ENST00000582376
RefSeq Acc Id: ENSP00000484733   ⟸   ENST00000621217
RefSeq Acc Id: ENSP00000462081   ⟸   ENST00000582717
RefSeq Acc Id: ENSP00000462629   ⟸   ENST00000582486
RefSeq Acc Id: ENSP00000463115   ⟸   ENST00000583282
RefSeq Acc Id: ENSP00000462279   ⟸   ENST00000584550
RefSeq Acc Id: ENSP00000464318   ⟸   ENST00000584243
RefSeq Acc Id: ENSP00000438085   ⟸   ENST00000537686
RefSeq Acc Id: ENSP00000461963   ⟸   ENST00000577435
RefSeq Acc Id: ENSP00000446421   ⟸   ENST00000538886
RefSeq Acc Id: ENSP00000463288   ⟸   ENST00000578348
RefSeq Acc Id: ENSP00000464268   ⟸   ENST00000578773
RefSeq Acc Id: ENSP00000481953   ⟸   ENST00000579743
Protein Domains
GAE   GAT   VHS

Promoters
RGD ID:6811183
Promoter ID:HG_ACW:36308
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:GGA3.GAPR07,   GGA3.JAPR07,   GGA3.LAPR07,   GGA3.RAPR07,   GGA3.TAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361770,748,041 - 70,748,541 (-)MPROMDB
RGD ID:6794347
Promoter ID:HG_KWN:27089
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_014001,   NM_015971,   NM_138619,   NR_033345,   UC002JNI.1,   UC002JNJ.1,   UC002JNL.2,   UC002JNN.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361770,768,586 - 70,769,527 (+)MPROMDB
RGD ID:7236283
Promoter ID:EPDNEW_H23888
Type:initiation region
Name:GGA3_1
Description:golgi associated, gamma adaptin ear containing, ARF binding protein3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381775,261,603 - 75,261,663EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3 copy number gain See cases [RCV000052486] Chr17:69209079..83086677 [GRCh38]
Chr17:67205220..81044553 [GRCh37]
Chr17:64716815..78637842 [NCBI36]
Chr17:17q24.3-25.3
pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3
pathogenic
GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3 copy number gain See cases [RCV000143342] Chr17:69916435..83102552 [GRCh38]
Chr17:67912576..81048189 [GRCh37]
Chr17:65424171..78653717 [NCBI36]
Chr17:17q24.3-25.3
pathogenic
GRCh37/hg19 17q25.1(chr17:72901452-73518861)x3 copy number gain not provided [RCV000585184] Chr17:72901452..73518861 [GRCh37]
Chr17:17q25.1
uncertain significance
GRCh37/hg19 17q24.2-25.3(chr17:64241326-81041938)x3 copy number gain See cases [RCV000447577] Chr17:64241326..81041938 [GRCh37]
Chr17:17q24.2-25.3
pathogenic
NM_000169.3(GLA):c.48T>G (p.Leu16=) single nucleotide variant not provided [RCV001703605] Chr17:75261947 [GRCh38]
Chr17:73258028 [GRCh37]
Chr17:17q25.1
benign|likely benign
NM_015971.4(MRPS7):c.27C>T (p.Ala9=) single nucleotide variant not specified [RCV000438455] Chr17:75261927 [GRCh38]
Chr17:73258008 [GRCh37]
Chr17:17q25.1
likely benign
NM_015971.4(MRPS7):c.5C>T (p.Ala2Val) single nucleotide variant not specified [RCV000421254] Chr17:75261905 [GRCh38]
Chr17:73257986 [GRCh37]
Chr17:17q25.1
benign
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NM_015971.4(MRPS7):c.66T>C (p.Ala22=) single nucleotide variant not specified [RCV000602192] Chr17:75261966 [GRCh38]
Chr17:73258047 [GRCh37]
Chr17:17q25.1
likely benign
NM_001172703.3(GGA3):c.-177+431C>T single nucleotide variant not specified [RCV000611884] Chr17:75261851 [GRCh38]
Chr17:73257932 [GRCh37]
Chr17:17q25.1
likely benign
GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3 copy number gain See cases [RCV000512573] Chr17:67002415..81041938 [GRCh37]
Chr17:17q24.2-25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q25.1(chr17:72962625-73281784)x3 copy number gain not provided [RCV000683960] Chr17:72962625..73281784 [GRCh37]
Chr17:17q25.1
uncertain significance
GRCh37/hg19 17q25.1(chr17:73057756-73429731)x3 copy number gain not provided [RCV000683961] Chr17:73057756..73429731 [GRCh37]
Chr17:17q25.1
uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3 copy number gain not provided [RCV000683952] Chr17:63689671..81041938 [GRCh37]
Chr17:17q24.1-25.3
pathogenic
NM_024844.5(NUP85):c.1430C>T (p.Ala477Val) single nucleotide variant Nephrotic syndrome, type 17 [RCV000721154] Chr17:75232884 [GRCh38]
Chr17:73228979 [GRCh37]
Chr17:17q25.1
pathogenic|uncertain significance
NM_024844.5(NUP85):c.1933C>T (p.Arg645Trp) single nucleotide variant Nephrotic syndrome, type 17 [RCV000721155] Chr17:75235641 [GRCh38]
Chr17:73231736 [GRCh37]
Chr17:17q25.1
pathogenic|likely pathogenic
NM_024844.5(NUP85):c.1741G>C (p.Ala581Pro) single nucleotide variant Nephrotic syndrome, type 17 [RCV000721157] Chr17:75234762 [GRCh38]
Chr17:73230857 [GRCh37]
Chr17:17q25.1
pathogenic|likely pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q25.1(chr17:73230856-73323772)x3 copy number gain not provided [RCV000739670] Chr17:73230856..73323772 [GRCh37]
Chr17:17q25.1
benign
GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3 copy number gain not provided [RCV000762750] Chr17:64159738..74891024 [GRCh37]
Chr17:17q24.1-25.2
likely pathogenic
null deletion not provided [RCV001610165] Chr17:75262006 [GRCh38]
Chr17:73258087 [GRCh37]
Chr17:17q25.1
benign
NM_138619.4(GGA3):c.105G>A (p.Gln35=) single nucleotide variant not provided [RCV000884757] Chr17:75246732 [GRCh38]
Chr17:73242813 [GRCh37]
Chr17:17q25.1
benign
NM_015971.4(MRPS7):c.83+245T>G single nucleotide variant not provided [RCV000830550] Chr17:75262228 [GRCh38]
Chr17:73258309 [GRCh37]
Chr17:17q25.1
benign
NM_015971.4(MRPS7):c.83+22G>C single nucleotide variant not provided [RCV000835553] Chr17:75262005 [GRCh38]
Chr17:73258086 [GRCh37]
Chr17:17q25.1
benign
NM_015971.4(MRPS7):c.83+23C>G single nucleotide variant not provided [RCV000835554] Chr17:75262006 [GRCh38]
Chr17:73258087 [GRCh37]
Chr17:17q25.1
benign
GRCh37/hg19 17q25.1(chr17:72945415-73414786)x3 copy number gain not provided [RCV001006917] Chr17:72945415..73414786 [GRCh37]
Chr17:17q25.1
uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3 copy number gain not provided [RCV000849900] Chr17:62778720..81041938 [GRCh37]
Chr17:17q24.1-25.3
pathogenic
NM_138619.4(GGA3):c.1966T>C (p.Leu656=) single nucleotide variant not provided [RCV000955529] Chr17:75238747 [GRCh38]
Chr17:73234828 [GRCh37]
Chr17:17q25.1
benign
NM_014362.4(HIBCH):c.438+9A>T single nucleotide variant not provided [RCV001720805] Chr17:75262012 [GRCh38]
Chr17:73258093 [GRCh37]
benign
NM_002055.5(GFAP):c.469G>A (p.Asp157Asn) deletion not provided [RCV001657665] Chr17:75262004..75262005 [GRCh38]
Chr17:73258085..73258086 [GRCh37]
Chr17:17q25.1
benign
null single nucleotide variant not provided [RCV001669061] Chr17:75262120 [GRCh38]
Chr17:73258201 [GRCh37]
Chr17:17q25.1
benign
null single nucleotide variant not provided [RCV001614050] Chr17:75261732 [GRCh38]
Chr17:73257813 [GRCh37]
Chr17:17q25.1
benign
GRCh37/hg19 17q25.1(chr17:73218219-73443987)x3 copy number gain not provided [RCV001006918] Chr17:73218219..73443987 [GRCh37]
Chr17:17q25.1
uncertain significance
NM_024844.5(NUP85):c.1465T>C (p.Trp489Arg) single nucleotide variant Nephrotic syndrome, type 17 [RCV001332564] Chr17:75232919 [GRCh38]
Chr17:73229014 [GRCh37]
Chr17:17q25.1
uncertain significance
null deletion not provided [RCV001674993] Chr17:75262005..75262006 [GRCh38]
Chr17:73258086..73258087 [GRCh37]
Chr17:17q25.1
benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17079 AgrOrtholog
COSMIC GGA3 COSMIC
Ensembl Genes ENSG00000125447 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000438085 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000446421 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000461963 UniProtKB/TrEMBL
  ENSP00000462081 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000462279 UniProtKB/TrEMBL
  ENSP00000462473 UniProtKB/TrEMBL
  ENSP00000462629 UniProtKB/TrEMBL
  ENSP00000463115 UniProtKB/TrEMBL
  ENSP00000463288 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000464268 UniProtKB/TrEMBL
  ENSP00000464318 UniProtKB/TrEMBL
  ENSP00000464365 UniProtKB/TrEMBL
  ENSP00000464574 UniProtKB/TrEMBL
  ENSP00000479464 UniProtKB/TrEMBL
  ENSP00000481953 UniProtKB/TrEMBL
  ENSP00000484733 UniProtKB/TrEMBL
  ENSP00000496890 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000537686 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000538886 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000577435 UniProtKB/TrEMBL
  ENST00000578348 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000578773 UniProtKB/TrEMBL
  ENST00000579743 UniProtKB/TrEMBL
  ENST00000580646 UniProtKB/TrEMBL
  ENST00000580799 UniProtKB/TrEMBL
  ENST00000582376 UniProtKB/TrEMBL
  ENST00000582486 UniProtKB/TrEMBL
  ENST00000582717 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000583282 UniProtKB/TrEMBL
  ENST00000584243 UniProtKB/TrEMBL
  ENST00000584550 UniProtKB/TrEMBL
  ENST00000621217 UniProtKB/TrEMBL
  ENST00000621870 UniProtKB/TrEMBL
  ENST00000649398 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.58.160 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.25.40.90 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000125447 GTEx
HGNC ID HGNC:17079 ENTREZGENE
Human Proteome Map GGA3 Human Proteome Map
InterPro Clathrin_a/b/g-adaptin_app_Ig UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Clathrin_app_Ig-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENTH_VHS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAE_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAT_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAT_GGA3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAT_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GGA3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GGA_N-GAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VHS_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23163 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 23163 ENTREZGENE
OMIM 606006 OMIM
PANTHER PTHR45905:SF3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Alpha_adaptinC2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GGA_N-GAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VHS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA28659 PharmGKB
PROSITE GAE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VHS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Alpha_adaptinC2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VHS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48464 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49348 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WYN2_HUMAN UniProtKB/TrEMBL
  A8K6M0 ENTREZGENE, UniProtKB/TrEMBL
  B7Z1E9_HUMAN UniProtKB/TrEMBL
  B7Z456 ENTREZGENE, UniProtKB/TrEMBL
  G3V1K5_HUMAN UniProtKB/TrEMBL
  GGA3_HUMAN UniProtKB/Swiss-Prot
  J3KS27_HUMAN UniProtKB/TrEMBL
  J3KSG3_HUMAN UniProtKB/TrEMBL
  J3KSS7_HUMAN UniProtKB/TrEMBL
  J3KTR5_HUMAN UniProtKB/TrEMBL
  J3QRK7_HUMAN UniProtKB/TrEMBL
  J3QRP3_HUMAN UniProtKB/TrEMBL
  J3QRS8_HUMAN UniProtKB/TrEMBL
  J3QS87_HUMAN UniProtKB/TrEMBL
  Q9NZ52 ENTREZGENE
UniProt Secondary B7Z7E2 UniProtKB/Swiss-Prot
  B7Z7M9 UniProtKB/Swiss-Prot
  J3KRN0 UniProtKB/Swiss-Prot
  Q15017 UniProtKB/Swiss-Prot
  Q6IS16 UniProtKB/Swiss-Prot
  Q9UJY3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-05-10 GGA3  golgi associated, gamma adaptin ear containing, ARF binding protein 3  GGA3  golgi-associated, gamma adaptin ear containing, ARF binding protein 3  Symbol and/or name change 5135510 APPROVED
2011-07-27 GGA3  golgi-associated, gamma adaptin ear containing, ARF binding protein 3  GGA3  golgi associated, gamma adaptin ear containing, ARF binding protein 3  Symbol and/or name change 5135510 APPROVED