ABI3 (ABI family member 3) - Rat Genome Database

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Gene: ABI3 (ABI family member 3) Homo sapiens
Analyze
Symbol: ABI3
Name: ABI family member 3
RGD ID: 1323432
HGNC Page HGNC
Description: Enables identical protein binding activity. Involved in defense response to tumor cell and positive regulation of cellular senescence. Acts upstream of or within regulation of cell migration. Located in cytoplasm and lamellipodium. Part of SCAR complex.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ABI family, member 3; ABI gene family member 3; ABI gene family, member 3; NESH; new molecule including SH3; SSH3BP3
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 Ensembl1749,210,411 - 49,223,225 (+)EnsemblGRCh38hg38GRCh38
GRCh381749,210,582 - 49,223,225 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371747,288,069 - 47,300,587 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361744,642,588 - 44,655,586 (+)NCBINCBI36hg18NCBI36
Build 341744,642,587 - 44,655,586NCBI
Celera1743,742,068 - 43,755,066 (+)NCBI
Cytogenetic Map17q21.32NCBI
HuRef1742,653,954 - 42,666,932 (+)NCBIHuRef
CHM1_11747,352,844 - 47,365,842 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

References

Additional References at PubMed
PMID:10978530   PMID:11076863   PMID:11230166   PMID:11256614   PMID:11501947   PMID:11956071   PMID:12011975   PMID:12477932   PMID:15489334   PMID:15489336   PMID:16189514   PMID:16381901  
PMID:17101133   PMID:18480067   PMID:19060904   PMID:19946888   PMID:21223585   PMID:21516116   PMID:21873635   PMID:23382691   PMID:23535732   PMID:25416956   PMID:26428302   PMID:27036019  
PMID:27107014   PMID:28298427   PMID:28714976   PMID:29892012   PMID:30326945   PMID:30585266   PMID:30705288   PMID:31127786   PMID:31540324   PMID:32296183   PMID:32894242  


Genomics

Comparative Map Data
ABI3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1749,210,411 - 49,223,225 (+)EnsemblGRCh38hg38GRCh38
GRCh381749,210,582 - 49,223,225 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371747,288,069 - 47,300,587 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361744,642,588 - 44,655,586 (+)NCBINCBI36hg18NCBI36
Build 341744,642,587 - 44,655,586NCBI
Celera1743,742,068 - 43,755,066 (+)NCBI
Cytogenetic Map17q21.32NCBI
HuRef1742,653,954 - 42,666,932 (+)NCBIHuRef
CHM1_11747,352,844 - 47,365,842 (+)NCBICHM1_1
Abi3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391195,720,898 - 95,733,302 (-)NCBIGRCm39mm39
GRCm39 Ensembl1195,720,900 - 95,733,302 (-)Ensembl
GRCm381195,830,072 - 95,842,476 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1195,830,074 - 95,842,476 (-)EnsemblGRCm38mm10GRCm38
MGSCv371195,691,386 - 95,703,790 (-)NCBIGRCm37mm9NCBIm37
MGSCv361195,648,481 - 95,658,250 (-)NCBImm8
Celera11105,472,261 - 105,484,667 (-)NCBICelera
Cytogenetic Map11DNCBI
Abi3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21080,769,819 - 80,780,816 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl1080,769,822 - 80,780,816 (-)Ensembl
Rnor_6.01083,644,086 - 83,655,182 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1083,644,086 - 83,655,182 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01083,448,188 - 83,459,284 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41084,542,949 - 84,554,040 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11084,557,318 - 84,568,410 (-)NCBI
Celera1079,537,629 - 79,548,619 (-)NCBICelera
Cytogenetic Map10q26NCBI
Abi3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495545112,241,084 - 12,248,857 (-)NCBIChiLan1.0ChiLan1.0
ABI3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1178,364,561 - 8,376,930 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl178,364,561 - 8,376,930 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0178,381,551 - 8,394,537 (-)NCBIMhudiblu_PPA_v0panPan3
ABI3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1925,374,823 - 25,385,016 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl925,374,525 - 25,385,003 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha924,834,241 - 24,844,759 (+)NCBI
ROS_Cfam_1.0926,170,737 - 26,181,212 (+)NCBI
UMICH_Zoey_3.1924,938,804 - 24,949,363 (+)NCBI
UNSW_CanFamBas_1.0925,197,882 - 25,208,480 (+)NCBI
UU_Cfam_GSD_1.0925,326,932 - 25,337,496 (+)NCBI
Abi3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560224,770,374 - 24,794,548 (+)NCBI
SpeTri2.0NW_00493649012,280,717 - 12,290,602 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LOC100621521
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11225,426,116 - 25,441,309 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21225,368,386 - 25,383,802 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ABI3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11669,613,308 - 69,625,887 (+)NCBIChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366607740,718,582 - 40,731,186 (+)NCBIVero_WHO_p1.0
Abi3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247955,448,375 - 5,455,784 (+)NCBIHetGla_female_1.0hetGla2

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1346
Count of miRNA genes:527
Interacting mature miRNAs:596
Transcripts:ENST00000225941, ENST00000419580, ENST00000571035, ENST00000573347
Prediction methods:Microtar, Miranda, 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 451 930 703 45 1619 39 902 128 631 163 444 1203 7 709 507 1
Low 1864 2044 991 557 278 399 3349 2019 2862 219 923 206 158 1 495 2251 1 2
Below cutoff 30 14 16 10 37 11 54 41 209 20 46 60 4 30 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000225941   ⟹   ENSP00000225941
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1749,210,707 - 49,223,225 (+)Ensembl
RefSeq Acc Id: ENST00000419580   ⟹   ENSP00000406651
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1749,210,411 - 49,223,036 (+)Ensembl
RefSeq Acc Id: ENST00000571035   ⟹   ENSP00000459171
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1749,219,858 - 49,223,007 (+)Ensembl
RefSeq Acc Id: ENST00000573347   ⟹   ENSP00000460776
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1749,219,563 - 49,222,562 (+)Ensembl
RefSeq Acc Id: NM_001135186   ⟹   NP_001128658
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381749,210,707 - 49,223,225 (+)NCBI
GRCh371747,287,589 - 47,300,587 (+)RGD
Celera1743,742,068 - 43,755,066 (+)RGD
HuRef1742,653,954 - 42,666,932 (+)RGD
CHM1_11747,352,844 - 47,365,842 (+)NCBI
Sequence:
RefSeq Acc Id: NM_016428   ⟹   NP_057512
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381749,210,707 - 49,223,225 (+)NCBI
GRCh371747,287,589 - 47,300,587 (+)RGD
Build 361744,642,588 - 44,655,586 (+)NCBI Archive
Celera1743,742,068 - 43,755,066 (+)RGD
HuRef1742,653,954 - 42,666,932 (+)RGD
CHM1_11747,352,844 - 47,365,842 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005257429   ⟹   XP_005257486
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381749,210,582 - 49,223,225 (+)NCBI
GRCh371747,287,589 - 47,300,587 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011524873   ⟹   XP_011523175
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381749,210,582 - 49,223,225 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017024721   ⟹   XP_016880210
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381749,210,582 - 49,223,225 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_057512   ⟸   NM_016428
- Peptide Label: isoform 1
- Sequence:
RefSeq Acc Id: NP_001128658   ⟸   NM_001135186
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: XP_005257486   ⟸   XM_005257429
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011523175   ⟸   XM_011524873
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016880210   ⟸   XM_017024721
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000459171   ⟸   ENST00000571035
RefSeq Acc Id: ENSP00000460776   ⟸   ENST00000573347
RefSeq Acc Id: ENSP00000406651   ⟸   ENST00000419580
RefSeq Acc Id: ENSP00000225941   ⟸   ENST00000225941
Protein Domains
SH3

Promoters
RGD ID:6793659
Promoter ID:HG_KWN:26527
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001135186,   NM_016428
Position:
Human AssemblyChrPosition (strand)Source
Build 361744,641,926 - 44,643,122 (+)MPROMDB
RGD ID:6811115
Promoter ID:HG_ACW:35156
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ABI3.DAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361744,651,821 - 44,652,321 (+)MPROMDB
RGD ID:7235569
Promoter ID:EPDNEW_H23531
Type:initiation region
Name:ABI3_2
Description:ABI family member 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23533  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381749,210,155 - 49,210,215EPDNEW
RGD ID:7235575
Promoter ID:EPDNEW_H23533
Type:initiation region
Name:ABI3_1
Description:ABI family member 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23531  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381749,210,707 - 49,210,767EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2
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 17q21.31-21.33(chr17:44955325-49381173)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|See cases [RCV000052480] Chr17:44955325..49381173 [GRCh38]
Chr17:43032693..47458535 [GRCh37]
Chr17:40388219..44813534 [NCBI36]
Chr17:17q21.31-21.33
pathogenic
GRCh38/hg38 17q21.32-21.33(chr17:48520885-49511208)x1 copy number loss See cases [RCV000053431] Chr17:48520885..49511208 [GRCh38]
Chr17:46598247..47588570 [GRCh37]
Chr17:43953246..44943569 [NCBI36]
Chr17:17q21.32-21.33
pathogenic
GRCh38/hg38 17q21.32-22(chr17:49137864-52147810)x1 copy number loss See cases [RCV000053432] Chr17:49137864..52147810 [GRCh38]
Chr17:47215226..50225170 [GRCh37]
Chr17:44570225..47580169 [NCBI36]
Chr17:17q21.32-22
pathogenic
NM_001143804.1(PHOSPHO1):c.872C>T (p.Ser291Leu) single nucleotide variant Malignant melanoma [RCV000071548] Chr17:49224253 [GRCh38]
Chr17:47301615 [GRCh37]
Chr17:44656614 [NCBI36]
Chr17:17q21.32
not provided
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1
pathogenic
GRCh38/hg38 17q21.32-21.33(chr17:47986886-49329397)x1 copy number loss See cases [RCV000142900] Chr17:47986886..49329397 [GRCh38]
Chr17:46064252..47406759 [GRCh37]
Chr17:43419251..44761758 [NCBI36]
Chr17:17q21.32-21.33
pathogenic
GRCh38/hg38 17q21.32-21.33(chr17:48450628-49552921)x3 copy number gain See cases [RCV000143451] Chr17:48450628..49552921 [GRCh38]
Chr17:46527990..47630283 [GRCh37]
Chr17:43882989..44985282 [NCBI36]
Chr17:17q21.32-21.33
uncertain significance
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
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 17q21.32-22(chr17:46481089-51396368)x1 copy number loss not provided [RCV000513510] Chr17:46481089..51396368 [GRCh37]
Chr17:17q21.32-22
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
NM_016428.3(ABI3):c.285+9C>T single nucleotide variant not provided [RCV000947834] Chr17:49216707 [GRCh38]
Chr17:47294069 [GRCh37]
Chr17:17q21.32
benign
GRCh37/hg19 17q21.32-21.33(chr17:46899690-47540874)x3 copy number gain not provided [RCV000849505] Chr17:46899690..47540874 [GRCh37]
Chr17:17q21.32-21.33
uncertain significance
NM_016428.3(ABI3):c.261A>G (p.Glu87=) single nucleotide variant not provided [RCV000889143] Chr17:49216674 [GRCh38]
Chr17:47294036 [GRCh37]
Chr17:17q21.32
benign
NM_016428.3(ABI3):c.522T>C (p.Pro174=) single nucleotide variant not provided [RCV000947835] Chr17:49219599 [GRCh38]
Chr17:47296961 [GRCh37]
Chr17:17q21.32
benign
NM_016428.3(ABI3):c.290T>A (p.Val97Glu) single nucleotide variant Early-onset dementia of unclear type [RCV001090103] Chr17:49217743 [GRCh38]
Chr17:47295105 [GRCh37]
Chr17:17q21.32
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:29859 AgrOrtholog
COSMIC ABI3 COSMIC
Ensembl Genes ENSG00000108798 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000225941 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000406651 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000459171 UniProtKB/TrEMBL
  ENSP00000460776 UniProtKB/TrEMBL
Ensembl Transcript ENST00000225941 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000419580 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000571035 UniProtKB/TrEMBL
  ENST00000573347 UniProtKB/TrEMBL
GTEx ENSG00000108798 GTEx
HGNC ID HGNC:29859 ENTREZGENE
Human Proteome Map ABI3 Human Proteome Map
InterPro ABI UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ABI3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Abl-interactor_HHR_dom UniProtKB/Swiss-Prot
  SH3-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:51225 UniProtKB/Swiss-Prot
NCBI Gene 51225 ENTREZGENE
OMIM 606363 OMIM
PANTHER PTHR10460 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10460:SF7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Abi_HHR UniProtKB/Swiss-Prot
  SH3_9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134951642 PharmGKB
PRINTS SH3DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50044 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt ABI3_HUMAN UniProtKB/Swiss-Prot
  I3L1X2_HUMAN UniProtKB/TrEMBL
  I3L3W4_HUMAN UniProtKB/TrEMBL
  L8ECG8_HUMAN UniProtKB/TrEMBL
  Q9P2A4 ENTREZGENE
UniProt Secondary C9IZN8 UniProtKB/Swiss-Prot
  Q9H0P6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 ABI3  ABI family member 3    ABI family, member 3  Symbol and/or name change 5135510 APPROVED
2011-09-01 ABI3  ABI family, member 3  ABI3  ABI family, member 3  Symbol and/or name change 5135510 APPROVED