SH3RF3 (SH3 domain containing ring finger 3) - Rat Genome Database
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Gene: SH3RF3 (SH3 domain containing ring finger 3) Homo sapiens
Analyze
Symbol: SH3RF3
Name: SH3 domain containing ring finger 3
RGD ID: 1344960
HGNC Page HGNC
Description: Exhibits ubiquitin protein ligase activity. Involved in positive regulation of JNK cascade and protein autoubiquitination; INTERACTS WITH 17beta-estradiol; aflatoxin B1; aflatoxin B2.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: E3 ubiquitin-protein ligase SH3RF3; FLJ00204; plenty of SH3s 2; plenty of SH3s-2; POSH2; SH3 domain-containing RING finger protein 3; SH3 multiple domains 4; SH3 multiple domains protein 4; SH3MD4
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 Ensembl2109,129,205 - 109,504,634 (+)EnsemblGRCh38hg38GRCh38
GRCh382109,129,205 - 109,504,635 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372110,259,067 - 110,262,207 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh372109,745,997 - 110,107,395 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362109,112,429 - 109,432,377 (+)NCBINCBI36hg18NCBI36
Build 362109,616,360 - 109,619,489 (+)NCBINCBI36hg18NCBI36
Celera2104,055,768 - 104,430,967 (+)NCBI
Cytogenetic Map2q13NCBI
HuRef2103,343,871 - 103,705,816 (+)NCBIHuRef
HuRef2103,707,988 - 103,718,182 (+)NCBIHuRef
CHM1_12109,750,291 - 110,266,409 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Molecular Function

References

Additional References at PubMed
PMID:14702039   PMID:16374509   PMID:20379614   PMID:20696164   PMID:24255178   PMID:27173435   PMID:28611215   PMID:29117863   PMID:30021884   PMID:32427938  


Genomics

Comparative Map Data
SH3RF3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2109,129,205 - 109,504,634 (+)EnsemblGRCh38hg38GRCh38
GRCh382109,129,205 - 109,504,635 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372110,259,067 - 110,262,207 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh372109,745,997 - 110,107,395 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362109,112,429 - 109,432,377 (+)NCBINCBI36hg18NCBI36
Build 362109,616,360 - 109,619,489 (+)NCBINCBI36hg18NCBI36
Celera2104,055,768 - 104,430,967 (+)NCBI
Cytogenetic Map2q13NCBI
HuRef2103,343,871 - 103,705,816 (+)NCBIHuRef
HuRef2103,707,988 - 103,718,182 (+)NCBIHuRef
CHM1_12109,750,291 - 110,266,409 (+)NCBICHM1_1
Sh3rf3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391058,649,181 - 58,974,738 (+)NCBIGRCm39mm39
GRCm381058,811,908 - 59,138,916 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1058,813,359 - 59,138,916 (+)EnsemblGRCm38mm10GRCm38
MGSCv371058,276,107 - 58,601,664 (+)NCBIGRCm37mm9NCBIm37
MGSCv361058,379,278 - 58,534,271 (+)NCBImm8
Celera1059,913,446 - 60,238,898 (+)NCBICelera
Cytogenetic Map10B4NCBI
Sh3rf3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.02028,355,671 - 28,720,020 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2028,572,242 - 28,717,243 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02030,292,511 - 30,527,551 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera2028,211,679 - 28,542,578 (+)NCBICelera
Cytogenetic Map20q11NCBI
Sh3rf3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495547012,539,851 - 12,614,804 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495547012,446,604 - 12,615,689 (+)NCBIChiLan1.0ChiLan1.0
SH3RF3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12A111,066,794 - 111,222,876 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A110,848,452 - 111,219,915 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v02A92,137,951 - 92,519,627 (-)NCBIMhudiblu_PPA_v0panPan3
SH3RF3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl1034,376,326 - 34,730,657 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.11034,374,376 - 34,730,548 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Sh3rf3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_004936829714,518 - 914,894 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SH3RF3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl347,133,532 - 47,339,541 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1347,128,448 - 47,339,569 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2349,215,802 - 49,373,969 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SH3RF3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11412,657,402 - 13,030,467 (+)NCBI
ChlSab1.1 Ensembl1412,871,670 - 13,030,464 (+)Ensembl
Sh3rf3
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474912,109,084 - 12,319,732 (+)NCBI

Position Markers
D2S1891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372110,093,954 - 110,094,213UniSTSGRCh37
Build 362109,460,386 - 109,460,645RGDNCBI36
Celera2104,403,380 - 104,403,639RGD
Cytogenetic Map2q13UniSTS
HuRef2103,692,382 - 103,692,641UniSTS
Marshfield Genetic Map2120.29RGD
Marshfield Genetic Map2120.29UniSTS
Genethon Genetic Map2124.6UniSTS
D2S1893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372109,854,718 - 109,854,981UniSTSGRCh37
Build 362109,221,150 - 109,221,413RGDNCBI36
Celera2104,163,985 - 104,164,248RGD
Cytogenetic Map2q13UniSTS
HuRef2103,452,015 - 103,452,276UniSTS
Marshfield Genetic Map2120.29RGD
Marshfield Genetic Map2120.29UniSTS
Genethon Genetic Map2124.6UniSTS
Whitehead-YAC Contig Map2 UniSTS
HSC16A112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372110,262,017 - 110,262,191UniSTSGRCh37
Build 362109,619,299 - 109,619,473RGDNCBI36
Celera2104,430,777 - 104,430,951RGD
Cytogenetic Map2q13UniSTS
HuRef2103,717,992 - 103,718,166UniSTS
GeneMap99-GB4 RH Map2388.63UniSTS
Whitehead-RH Map2623.2UniSTS
RH103435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372109,745,021 - 109,745,149UniSTSGRCh37
Build 362109,111,453 - 109,111,581RGDNCBI36
Celera2104,054,811 - 104,054,939RGD
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map2q13UniSTS
HuRef2103,342,914 - 103,343,042UniSTS
GeneMap99-GB4 RH Map2387.9UniSTS
RH120416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372109,788,007 - 109,788,344UniSTSGRCh37
Build 362109,154,439 - 109,154,776RGDNCBI36
Celera2104,097,754 - 104,098,091RGD
Cytogenetic Map2q13UniSTS
HuRef2103,385,765 - 103,386,102UniSTS
D2S199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372110,014,919 - 110,015,317UniSTSGRCh37
Build 362109,381,351 - 109,381,749RGDNCBI36
Celera2104,324,345 - 104,324,743RGD
Cytogenetic Map2q13UniSTS
HuRef2103,612,995 - 103,613,393UniSTS
SHGC-153258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372109,854,729 - 109,854,851UniSTSGRCh37
Build 362109,221,161 - 109,221,283RGDNCBI36
Celera2104,163,996 - 104,164,118RGD
Cytogenetic Map2q13UniSTS
HuRef2103,452,026 - 103,452,148UniSTS
TNG Radiation Hybrid Map1162163.0UniSTS
SHGC-152525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372109,854,729 - 109,854,954UniSTSGRCh37
GRCh372109,854,729 - 109,854,932UniSTSGRCh37
GRCh372109,854,729 - 109,854,928UniSTSGRCh37
Build 362109,221,161 - 109,221,364RGDNCBI36
Celera2104,163,996 - 104,164,199RGD
Celera2104,163,996 - 104,164,221UniSTS
Celera2104,163,996 - 104,164,195UniSTS
Cytogenetic Map2q13UniSTS
HuRef2103,452,026 - 103,452,227UniSTS
HuRef2103,452,026 - 103,452,225UniSTS
HuRef2103,452,026 - 103,452,249UniSTS
TNG Radiation Hybrid Map142708.0UniSTS
IB846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372110,253,153 - 110,253,415UniSTSGRCh37
Celera2104,421,853 - 104,422,115RGD
Cytogenetic Map2q13UniSTS
HuRef2103,709,128 - 103,709,390UniSTS
GeneMap99-GB4 RH Map2389.85UniSTS
Whitehead-RH Map2613.2UniSTS
RH65580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372109,875,439 - 109,875,617UniSTSGRCh37
Build 362109,241,871 - 109,242,049RGDNCBI36
Celera2104,184,691 - 104,184,869RGD
Cytogenetic Map2q13UniSTS
HuRef2103,472,827 - 103,473,005UniSTS
GeneMap99-GB4 RH Map2388.63UniSTS
RH11810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372110,262,015 - 110,262,144UniSTSGRCh37
Build 362109,619,297 - 109,619,426RGDNCBI36
Celera2104,430,775 - 104,430,904RGD
Cytogenetic Map2q13UniSTS
HuRef2103,717,990 - 103,718,119UniSTS
GeneMap99-GB4 RH Map2390.14UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1955
Count of miRNA genes:974
Interacting mature miRNAs:1176
Transcripts:ENST00000309415, ENST00000418513, ENST00000444352
Prediction methods:Microtar, Miranda, Rnahybrid
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 adipose tissue appendage entire extraembryonic component
High
Medium 569 1312 184 11 168 12 1231 348 197 70 471 521 1 603 812 1
Low 1806 1566 1426 501 1461 339 3086 1820 3229 316 954 1024 168 601 1976 1
Below cutoff 25 104 106 104 172 106 25 21 274 22 17 38 1 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001099289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011511109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011511110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA916456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC109344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC133109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC139850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC140485 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC153804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC233025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AEKP01200292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL831825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ307286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DV080665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY224642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000309415   ⟹   ENSP00000309186
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2109,129,205 - 109,504,634 (+)Ensembl
RefSeq Acc Id: NM_001099289   ⟹   NP_001092759
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382109,129,205 - 109,504,634 (+)NCBI
GRCh372110,259,067 - 110,262,207 (+)NCBI
GRCh372109,745,997 - 110,107,395 (+)RGD
Build 362109,616,360 - 109,619,489 (+)NCBI Archive
Celera2104,055,768 - 104,430,967 (+)RGD
HuRef2103,707,988 - 103,718,182 (+)NCBI
HuRef2103,343,871 - 103,705,816 (+)RGD
CHM1_12109,750,291 - 110,266,409 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011511109   ⟹   XP_011509411
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382109,129,439 - 109,484,065 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011511110   ⟹   XP_011509412
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382109,392,779 - 109,504,635 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001092759   ⟸   NM_001099289
- Peptide Label: precursor
- UniProtKB: Q8TEJ3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011509411   ⟸   XM_011511109
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011509412   ⟸   XM_011511110
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000309186   ⟸   ENST00000309415
Protein Domains
SH3


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001099289.2(SH3RF3):c.573+102779T>A single nucleotide variant Lung cancer [RCV000091140] Chr2:109232892 [GRCh38]
Chr2:109849348 [GRCh37]
Chr2:2q13
uncertain significance
NM_001099289.2(SH3RF3):c.574-83585G>T single nucleotide variant Lung cancer [RCV000091141] Chr2:109264089 [GRCh38]
Chr2:109880545 [GRCh37]
Chr2:2q13
uncertain significance
GRCh38/hg38 2q12.3-13(chr2:108593876-109700179)x3 copy number gain See cases [RCV000053142] Chr2:108593876..109700179 [GRCh38]
Chr2:109210332..110457756 [GRCh37]
Chr2:108576764..109815045 [NCBI36]
Chr2:2q12.3-13
uncertain significance
GRCh38/hg38 2q12.3-13(chr2:107962353-109700179)x1 copy number loss See cases [RCV000134167] Chr2:107962353..109700179 [GRCh38]
Chr2:108578809..110457756 [GRCh37]
Chr2:107945241..109815045 [NCBI36]
Chr2:2q12.3-13
pathogenic|uncertain significance
GRCh38/hg38 2q12.3-13(chr2:108593876-109700179)x1 copy number loss See cases [RCV000135738] Chr2:108593876..109700179 [GRCh38]
Chr2:109210332..110457756 [GRCh37]
Chr2:108576764..109815045 [NCBI36]
Chr2:2q12.3-13
uncertain significance
GRCh38/hg38 2q12.3-13(chr2:108681906-109700179)x3 copy number gain See cases [RCV000136575] Chr2:108681906..109700179 [GRCh38]
Chr2:109298362..110457756 [GRCh37]
Chr2:108664794..109815045 [NCBI36]
Chr2:2q12.3-13
likely benign|uncertain significance
GRCh38/hg38 2q13(chr2:108719125-110611314)x3 copy number gain See cases [RCV000137361] Chr2:108719125..110611314 [GRCh38]
Chr2:109335581..111368891 [GRCh37]
Chr2:108702013..111085360 [NCBI36]
Chr2:2q13
uncertain significance
GRCh38/hg38 2q11.2-13(chr2:101710825-110791418)x3 copy number gain See cases [RCV000138645] Chr2:101710825..110791418 [GRCh38]
Chr2:102327287..111548995 [GRCh37]
Chr2:101693719..111265466 [NCBI36]
Chr2:2q11.2-13
pathogenic
GRCh38/hg38 2q12.2-13(chr2:106516472-110576905)x3 copy number gain See cases [RCV000139569] Chr2:106516472..110576905 [GRCh38]
Chr2:107132928..111334482 [GRCh37]
Chr2:106499360..110857227 [NCBI36]
Chr2:2q12.2-13
uncertain significance
GRCh38/hg38 2q12.2-14.1(chr2:106428663-112379067)x3 copy number gain See cases [RCV000140834] Chr2:106428663..112379067 [GRCh38]
Chr2:107045119..113136644 [GRCh37]
Chr2:106411551..112853115 [NCBI36]
Chr2:2q12.2-14.1
uncertain significance
GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3 copy number gain See cases [RCV000141075] Chr2:94678532..110602409 [GRCh38]
Chr2:95344257..111359986 [GRCh37]
Chr2:94707984..111076455 [NCBI36]
Chr2:2q11.1-13
pathogenic
GRCh38/hg38 2q12.3-13(chr2:108660713-109735214)x1 copy number loss See cases [RCV000141950] Chr2:108660713..109735214 [GRCh38]
Chr2:109277169..110492791 [GRCh37]
Chr2:108643601..109850080 [NCBI36]
Chr2:2q12.3-13
uncertain significance
GRCh38/hg38 2q12.3-13(chr2:108526866-109746741)x1 copy number loss See cases [RCV000142089] Chr2:108526866..109746741 [GRCh38]
Chr2:109143322..110504318 [GRCh37]
Chr2:108509754..109861607 [NCBI36]
Chr2:2q12.3-13
uncertain significance
GRCh38/hg38 2q12.3-13(chr2:108579001-109736559)x1 copy number loss See cases [RCV000051261] Chr2:108579001..109736559 [GRCh38]
Chr2:109195457..110494136 [GRCh37]
Chr2:108561889..109851425 [NCBI36]
Chr2:2q12.3-13
pathogenic
GRCh38/hg38 2q11.2-13(chr2:97672522-110211318)x3 copy number gain See cases [RCV000052947] Chr2:97672522..110211318 [GRCh38]
Chr2:98288985..110968895 [GRCh37]
Chr2:97655417..110326184 [NCBI36]
Chr2:2q11.2-13
pathogenic
GRCh38/hg38 2q12.2-13(chr2:106696282-110223328)x3 copy number gain See cases [RCV000053141] Chr2:106696282..110223328 [GRCh38]
Chr2:107312738..110980905 [GRCh37]
Chr2:106679170..110338194 [NCBI36]
Chr2:2q12.2-13
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24699 AgrOrtholog
COSMIC SH3RF3 COSMIC
Ensembl Genes ENSG00000172985 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000309186 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000309415 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 3.30.40.10 UniProtKB/Swiss-Prot
GTEx ENSG00000172985 GTEx
HGNC ID HGNC:24699 ENTREZGENE
Human Proteome Map SH3RF3 Human Proteome Map
InterPro SH3-like_dom_sf UniProtKB/Swiss-Prot
  SH3_domain UniProtKB/Swiss-Prot
  SH3RF1/SH3RF3 UniProtKB/Swiss-Prot
  SH3RF1/SH3RF3_SH3_4 UniProtKB/Swiss-Prot
  SH3RF3_SH3_3 UniProtKB/Swiss-Prot
  Znf_C3HC4_RING-type UniProtKB/Swiss-Prot
  Znf_RING UniProtKB/Swiss-Prot
  Znf_RING/FYVE/PHD UniProtKB/Swiss-Prot
  Znf_RING_CS UniProtKB/Swiss-Prot
KEGG Report hsa:344558 UniProtKB/Swiss-Prot
NCBI Gene 344558 ENTREZGENE
OMIM 618933 OMIM
PANTHER PTHR14167:SF62 UniProtKB/Swiss-Prot
Pfam SH3_1 UniProtKB/Swiss-Prot
  SH3_9 UniProtKB/Swiss-Prot
  zf-C3HC4 UniProtKB/Swiss-Prot
PharmGKB PA162403291 PharmGKB
PROSITE SH3 UniProtKB/Swiss-Prot
  ZF_RING_1 UniProtKB/Swiss-Prot
  ZF_RING_2 UniProtKB/Swiss-Prot
SMART RING UniProtKB/Swiss-Prot
  SH3 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF50044 UniProtKB/Swiss-Prot
UniGene Hs.171244 ENTREZGENE
  Hs.535157 ENTREZGENE
  Hs.712087 ENTREZGENE
UniProt Q8TEJ3 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A0SDZ7 UniProtKB/Swiss-Prot
  A8MPR1 UniProtKB/Swiss-Prot
  Q8NDU1 UniProtKB/Swiss-Prot