ARBA annotations in gene reviews: failure breakdown
Generated by gene_side_failures.py; do not edit by hand. Per-row detail is in
gene_side_rows.tsv; per-rule counts in gene_side_rules.tsv.
- ARBA annotations in reviewed genes: 6051 from 2305 rules
- review actions: ACCEPT 2592, KEEP_AS_NON_CORE 1951, MARK_AS_OVER_ANNOTATED 658, MODIFY 603, REMOVE 133, UNDECIDED 110, PENDING 3, NEW 1
Outcome by how general the ARBA term is
| term generality |
rows |
kept |
modify |
over-annotated |
remove |
| very general (>200 descendants) |
1347 |
55% |
15% |
25% |
3% |
| general (21-200) |
1642 |
75% |
11% |
12% |
2% |
| specific (1-20) |
1984 |
83% |
8% |
4% |
2% |
| leaf (0) |
1078 |
86% |
5% |
4% |
3% |
What went wrong (1394 rows not kept)
| kind of failure |
rows |
share |
| true but uninformative |
867 |
62% |
| overreach |
179 |
13% |
| wrong |
125 |
9% |
| unclassified |
118 |
8% |
| different term needed |
105 |
8% |
Annotations judged wrong (133 REMOVE rows, classified by hand)
| failure mode |
rows |
meaning |
| WRONG_LOCATION |
15 |
The location is contradicted by the protein's topology or experiments. |
| WRONG_ACTIVITY |
15 |
The protein does not have this activity (wrong reaction, wrong substrate, or wrong enzyme class). |
| WRONG_PROCESS |
14 |
The protein's real activity is used in a different process. |
| WRONG_TAXON |
13 |
The process does not exist in the organism's lineage. |
| ROLE_CONFUSION |
13 |
The protein binds, makes, regulates or is acted on by the molecule or activity, and is annotated as performing the step itself. |
| TOO_GENERAL |
11 |
Removed as uninformative rather than wrong. |
| WRONG_PARALOG |
11 |
The function belongs to a paralog or a different subfamily. |
| UNSUPPORTED |
10 |
No evidence for the organism, or experiments argue against it. |
| TERM_MISREAD |
8 |
The term's definition does not mean what the rule assumed (e.g. visual perception for an eye-development factor). |
| INDIRECT |
8 |
The protein affects the process only indirectly. |
| NONCATALYTIC_HOMOLOG |
7 |
The family has the activity but this member has lost it. |
| WRONG_DIRECTION |
3 |
The regulation sign is opposite to the evidence. |
| OBSOLETE_OR_PSEUDOGENE |
2 |
The term is obsolete or the gene is a pseudogene. |
| SPURIOUS_SIGNATURE |
2 |
The annotation comes from a false domain prediction or a rule artefact. |
| TOO_SPECIFIC |
1 |
Claims more than computational inference can support. |
Failure categories, all rows not kept
REMOVE rows use the hand classification; other rows use the keyword heuristic.
| category |
rows |
REMOVE |
over-annotated |
MODIFY |
| NEEDS_MORE_SPECIFIC (true but uninformative) |
468 |
0 |
0 |
468 |
| TOO_GENERAL (true but uninformative) |
399 |
11 |
387 |
1 |
| INDIRECT_EFFECT (overreach) |
118 |
0 |
118 |
0 |
| UNCLASSIFIED (unclassified) |
118 |
0 |
117 |
1 |
| OTHER_TERM (different term needed) |
105 |
0 |
0 |
105 |
| TOO_SPECIFIC (overreach) |
29 |
1 |
0 |
28 |
| WRONG_PARALOG (wrong) |
23 |
11 |
12 |
0 |
| WRONG_TAXON (wrong) |
20 |
13 |
7 |
0 |
| WRONG_LOCATION (wrong) |
16 |
15 |
1 |
0 |
| WRONG_ACTIVITY (wrong) |
15 |
15 |
0 |
0 |
| NO_EVIDENCE (overreach) |
14 |
0 |
14 |
0 |
| WRONG_PROCESS (wrong) |
14 |
14 |
0 |
0 |
| ROLE_CONFUSION (wrong) |
13 |
13 |
0 |
0 |
| UNSUPPORTED (overreach) |
10 |
10 |
0 |
0 |
| TERM_MISREAD (wrong) |
8 |
8 |
0 |
0 |
| INDIRECT (overreach) |
8 |
8 |
0 |
0 |
| NONCATALYTIC_HOMOLOG (wrong) |
7 |
7 |
0 |
0 |
| WRONG_DIRECTION (wrong) |
3 |
3 |
0 |
0 |
| OBSOLETE_OR_PSEUDOGENE (wrong) |
2 |
2 |
0 |
0 |
| SPURIOUS_SIGNATURE (wrong) |
2 |
2 |
0 |
0 |
| NONCATALYTIC (wrong) |
1 |
0 |
1 |
0 |
| SUBSTRATE_OR_CARGO (wrong) |
1 |
0 |
1 |
0 |
Examples per category
NEEDS_MORE_SPECIFIC
- ARATH/AGO1 · defense response to virus (MODIFY): The electronic defense annotation is supported by ago1 virus hypersensitivity and AGO1 loading of viral siRNAs in PMID:11910010 and PMID:17158744. The RNAi-specific antiviral term captures the demonstrated mechanism more
- ARATH/AP2 · DNA binding (MODIFY): Replace generic DNA binding with AP2's more informative transcription factor and promoter/cis-regulatory binding activities.
- ARATH/CLV1 · developmental process (MODIFY): Replace the broad ARBA developmental annotation with the existing meristem-specific process.
- ARATH/CLV1 · regulation of developmental process (MODIFY): Use the more precise meristem process for the core developmental role of CLV1.
TOO_GENERAL
- 9CAUD/g022 · DNA metabolic process (REMOVE): Appropriately identified as too general. DNA metabolic process encompasses many different processes including repair, recombination, and degradation. The viral-specific replication terms are more informative and accurate
- 9CAUD/g022 · catalytic activity, acting on a nucleic acid (REMOVE): Adds no information beyond GO:0003887; treated the same way as the other generic MF rows here (transferase activity, nucleotidyltransferase activity).
- AILME/A0A7N5KEZ3_AILME · cytosol (MARK_AS_OVER_ANNOTATED): Biologically the relevant location of a KAP is the cross-linked keratin matrix of the cornified hair/claw, captured by the keratin-filament term, not free cytosol. The cytosol annotation is a broad ARBA rule-based assign
- ARAHY/A0A444Z7V7 · cytoplasm (MARK_AS_OVER_ANNOTATED): ARBA-derived annotation. While the catalytic domain is cytoplasm-facing, the protein is an integral membrane glycosyltransferase with 7 predicted transmembrane helices. Calling it cytoplasmic is uninformative given that
INDIRECT_EFFECT
- ARAHY/A0A444Z7V7 · response to cold (MARK_AS_OVER_ANNOTATED): ARBA-derived annotation. Cold-responsive transcriptional changes in cell wall genes are a secondary consequence of stress-induced growth adjustments, not a direct molecular function of this glycosyltransferase. No specif
- ARATH/ABI5 · signal transduction (MARK_AS_OVER_ANNOTATED): ABI5 is a downstream transcriptional effector of ABA signaling rather than a general signal transducer. The generic parent over-annotates; the more specific abscisic acid-activated signaling pathway (a UniProt keyword an
- ARATH/AHP1 · plant gross anatomical part developmental process (MARK_AS_OVER_ANNOTATED): Too general to be informative; AHP1 affects development indirectly via cytokinin and CKI1 phosphorelay signaling.
- ARATH/ARR5 · regulation of DNA-templated transcription (MARK_AS_OVER_ANNOTATED): ARR5 lacks a DNA-binding domain; it dampens cytokinin-induced transcription indirectly by negative feedback on the phosphorelay (e.g. at the level of AHPs), which is better captured by negative regulation of cytokinin-ac
UNCLASSIFIED
- ARATH/ARR12 · response to wounding (MARK_AS_OVER_ANNOTATED): Type-B ARR signaling contributes to wound-induced callus formation via cytokinin, but ARR12 is not established as part of the wound response itself.
- ARATH/CRY2 · system development (MARK_AS_OVER_ANNOTATED): System development does not capture the CRY2 mechanism and should not be used when specific light signaling and flowering annotations are available.
- DANRE/smad3a · BMP signaling pathway (MARK_AS_OVER_ANNOTATED): SMAD3 is the receptor-regulated SMAD of the TGF-beta/activin/nodal branch; its C-terminal SSVS motif is phosphorylated by TGF-beta type I receptors, and in zebrafish the Smad3 reporter is blocked by ALK4/ALK5 inhibitors.
- DANRE/smad3b · dorsal/ventral pattern formation (MARK_AS_OVER_ANNOTATED): Dorsal/ventral patterning in zebrafish is driven mainly by BMP-SMAD1/5. Smad3b activates goosecoid when overexpressed, but no smad3b loss-of-function evidence shows a dorsal/ventral patterning defect. Treated identically
OTHER_TERM
- ARATH/CRY1 · regulation of post-embryonic development (MODIFY): The evidence supports CRY1 regulation of photomorphogenesis and light-dependent growth, not a generic role in overall development.
- ARATH/CRY1 · system development (MODIFY): The evidence supports CRY1 regulation of photomorphogenesis and light-dependent growth, not a generic role in overall development.
- ARATH/CRY1 · flavin adenine dinucleotide metabolic process (MODIFY): CRY1 binds FAD and undergoes flavin photoreduction during blue-light signaling, but there is no evidence that CRY1 is part of FAD biosynthesis, degradation, or cofactor metabolism as a biological process.
- ARATH/CRY2 · flavin adenine dinucleotide metabolic process (MODIFY): The evidence concerns FAD redox photochemistry and light sensitivity, not FAD biosynthesis, catabolism, or metabolism. Replace with FAD binding and blue-light photoreceptor activity.
TOO_SPECIFIC
- ARATH/ARR12 · regulation of cytokinin-activated signaling pathway (MODIFY): ARR12 is an integral component of the cytokinin-activated signaling pathway (its terminal transcription factor), not a separate regulator of it; the pathway term is more accurate.
- DORPE/P21613 · anterograde axonal transport of mitochondrion (MODIFY): While kinesin-1-dependent anterograde mitochondrial transport is well established in mammals, the specific cargo (mitochondria) has not been demonstrated for squid kinesin. The squid giant axon studies focus on general o
- DROME/Lis-1 · dynein complex (MODIFY): LIS1 is a transiently associated regulator rather than a dynein subunit; microtubule associated complex (the parent, and the term used for the human ortholog) plus dynein complex binding better represent this.
- SOLLC/PG2 · cell wall modification involved in abscission (MODIFY): PG2 does modify/disassemble the cell wall, but it does so during fruit RIPENING, not in abscission. The annotation is a family-level ARBA over-generalization: the GH28 polygalacturonase family includes abscission-zone PG
WRONG_PARALOG
- ARATH/CYCD6-1 · stomatal lineage progression (REMOVE): No evidence links CYCD6;1 to the stomatal lineage; its expression and function are confined to root ground-tissue formative divisions and lateral root primordia. This appears to be an over-propagation of a D-type cyclin
- DANRE/fgf8b · mesoderm development (MARK_AS_OVER_ANNOTATED): The fgf8a evidence behind this kind of rule is gastrula-stage mesoderm formation (ace;oep interactions). fgf8b is not expressed during gastrulation and has no loss-of-function data; its somite expression begins at the 8-
- DANRE/fgf8b · anterior/posterior pattern specification (MARK_AS_OVER_ANNOTATED): No fgf8b-specific evidence. The fgf8a data for this term are from gastrula and early neural plate patterning, before fgf8b is expressed.
- DANRE/fgf8b · negative regulation of endodermal cell fate specification (REMOVE): This is a blastula/gastrula process: FGF/ERK signalling limits Nodal-induced endoderm progenitors (PMID:16672336), a role of fgf8a. fgf8b is not expressed during gastrulation and there is no evidence that it acts in endo
WRONG_TAXON
- DROME/AMPKalpha · nematode pharyngeal pumping (REMOVE): Nematode-specific process with no counterpart in Drosophila; taxonomically inappropriate electronic annotation.
- EMENI/flbD · post-embryonic development (MARK_AS_OVER_ANNOTATED): ARBA propagation from multicellular animal/plant Myb orthologs; not applicable to fungal conidiation.
- EMENI/flbD · tissue development (MARK_AS_OVER_ANNOTATED): Filamentous fungi do not form tissues in this sense; ARBA over-propagation.
- EMENI/flbD · positive regulation of post-embryonic development (MARK_AS_OVER_ANNOTATED): ARBA propagation from multicellular orthologs; inapplicable to fungi.
WRONG_LOCATION
- CANAL/BCY1 · membrane (REMOVE): Bcy1 is not a generic membrane protein; it is soluble and mainly cytosolic. A conditional subpopulation is enriched around the vacuolar membrane during growth on glycerol, but that specific location is already covered by
- DANRE/cryabb · plasma membrane (REMOVE): Nothing supports this location for cryabb: the protein is a soluble cytosolic sHSP recovered from the soluble lens proteome (PMID:16420472), and the ARBA rule that generated the row is a co-occurrence prediction rather t
- DANRE/dla · cytoplasm (REMOVE): Dla immunolocalisation found punctate membrane/cortical staining and explicitly did not support broad cytoplasmic localisation; cytoplasm is not an appropriate location for this transmembrane ligand.
- DROME/rdgBbeta · nucleus (REMOVE): No published evidence supports nuclear localization for rdgBbeta or PITPNC1. The human ortholog was localized to the cytoplasm by immunofluorescence (PMID:10531358). The protein lacks nuclear localization signals. This A
WRONG_ACTIVITY
- DORPE/P21613 · polypeptide conformation or assembly isomerase activity (REMOVE): Kinesin-1 is a microtubule motor protein. It does not have any known chaperone, foldase, or isomerase activity. This annotation is likely a false positive from the ARBA automated annotation pipeline and should be removed
- DROME/ci · DNA-binding transcription factor binding (REMOVE): Removed. No characterised Drosophila Ci partner is a DNA-binding transcription factor: the documented partners are Costal-2 (a kinesin-related protein), Fused (a kinase), Suppressor of fused, Slimb and Roadkill/HIB (ubiq
- PSEPK/PP_2320 · carboxypeptidase activity (REMOVE): The closely matched ErfK/LdtPae2 subfamily resolves the YkuD reaction as lipoprotein-acceptor L,D-transpeptidation.
- PSEPK/hisI · phosphoribosyl-ATP diphosphatase activity (REMOVE): This ARBA assignment appears to have propagated across a family that also contains bifunctional HisIE proteins. Q88D15 is a 130-residue standalone phosphoribosyl-AMP cyclohydrolase, whereas adjacent Q88D14 is the reviewe
NO_EVIDENCE
- DANRE/dla · stem cell differentiation (MARK_AS_OVER_ANNOTATED): Dla is expressed in adult proliferative zones, but there is no direct evidence that it regulates stem cell differentiation.
- DORPE/P21613 · female gamete generation (MARK_AS_OVER_ANNOTATED): There is no published evidence linking squid kinesin heavy chain P21613 to female gamete generation. The annotation likely derives from ARBA rules built on kinesin-1 function in Drosophila oogenesis. While plausible, it
- DORPE/P21613 · establishment or maintenance of microtubule cytoskeleton polarity (MARK_AS_OVER_ANNOTATED): This annotation confuses kinesin's dependence on microtubule polarity for directional transport with a role in establishing or maintaining that polarity. Kinesin-1 reads microtubule polarity but does not set it. There is
- DROME/wry · cell morphogenesis (MARK_AS_OVER_ANNOTATED): ARBA rules transferred from canonical Notch-pathway proteins; there is no evidence that Wry acts in neural or glial development or cell morphogenesis, and wry deficiencies lack the sensory-organ and wing defects typical
WRONG_PROCESS
- DORPE/AP180 · locomotion (REMOVE): This annotation is inappropriate for a clathrin assembly protein. AP180 functions in clathrin coat assembly and synaptic vesicle endocytosis. Any connection to locomotion would be extremely indirect (via synaptic transmi
- DROME/CG6051 · glycerophospholipid biosynthetic process (REMOVE): This annotation is incorrect. CG6051/LST2 does not participate in glycerophospholipid biosynthesis. The protein binds to phosphatidylinositol-3-phosphate (a phospholipid) via its FYVE domain but has no biosynthetic activ
- PSEAI/merA · response to oxidative stress (REMOVE): MerA is specifically induced by mercury via MerR, not by oxidative stress signals
- PSEPK/catB · peptide metabolic process (REMOVE): CatB is a muconate cycloisomerase in aromatic compound catabolism, not a peptide metabolic enzyme.
ROLE_CONFUSION
- DROME/CG6051 · phosphatidylinositol-3-phosphate phosphatase activity (REMOVE): This annotation is fundamentally incorrect. CG6051 contains a FYVE domain that BINDS phosphatidylinositol-3-phosphate (PI3P) but does not possess phosphatase activity. The protein lacks any phosphatase catalytic domains.
- DROME/CG6051 · phosphoprotein phosphatase activity (REMOVE): This annotation is incorrect. CG6051/LST2 does not have phosphatase activity. Instead, it is a SUBSTRATE of phosphorylation - the protein is phosphorylated by mTORC1 kinase at multiple serine residues (S549, S550, S810 i
- DROME/CG6051 · phosphatidylinositol dephosphorylation (REMOVE): This annotation is incorrect. CG6051/LST2 does not catalyze phosphatidylinositol dephosphorylation. The protein binds PI3P through its FYVE domain but has no phosphatase activity. This is another instance of automated pr
- DROME/CG6051 · phosphatidylinositol-3,5-bisphosphate 3-phosphatase activity (REMOVE): This annotation is completely incorrect. CG6051/LST2 has no phosphatase activity whatsoever. The protein contains only a FYVE zinc finger domain for PI3P binding and lacks any phosphatase catalytic domains. This specific
UNSUPPORTED
- CANAL/BCY1 · cellular response to starvation (REMOVE): Bcy1 controls PKA in nutrient and stress signaling, but this broad starvation response row is not supported by a specific Candida assay and does not capture Bcy1's direct work in the PKA holoenzyme.
- DANRE/dla · mesenchyme development (REMOVE): Transferred from mammalian Delta-like biology; in zebrafish, fin mesenchyme is present in deltaA mutants, and no evidence links Dla to mesenchyme development.
- DICDI/phg2 · anatomical structure morphogenesis (REMOVE): Phg2 has no demonstrated role in morphogenesis of a multicellular structure; once development starts, phg2 mutants develop with wild-type morphology. Cell-level shape effects are already covered by cell morphogenesis.
- DROME/CG6051 · midbody abscission (REMOVE): This annotation lacks supporting evidence. While some FYVE domain proteins participate in cytokinesis and midbody abscission through endosomal trafficking roles, there is no specific evidence that CG6051/LST2 is involved
TERM_MISREAD
- DESVH/Q72F05 · metal ion transport (REMOVE): This annotation represents a mapping error or overly broad inference. In GO usage and biological convention, K+ is classified under "monoatomic cation" and "potassium ion" terms rather than "metal ion" terms. The term GO
- PSEPK/pvdD · monocarboxylic acid biosynthetic process (REMOVE): The focused structural accounting found that native KT2440 pyoverdine variants carry two or three free carboxylic acid groups. GO:0072330 is therefore chemically inapt, because it describes formation of acids with one ca
- SCHPO/vas2 · intercellular transport (REMOVE): GO:0010496 means movement between cells, as verified in QuickGO. The experimentally established Vas2/AP-1 pathway sorts cargo between compartments inside a cell. This ARBA assertion conflates intercellular and intracellu
- human/AP3D1 · intercellular transport (REMOVE): GO:0010496 is defined as the movement of substances between cells. Nothing in the AP-3 literature has AP3D1 transferring material from one cell to another; every characterised cargo (LAMP1/LAMP2, CD63, tyrosinase, VAMP7,
INDIRECT
- human/BAK1 · regulation of transport (REMOVE): The annotation is a stress, development, transport, or signaling-level projection from ortholog or ARBA/Ensembl data and is too far from BAK's direct MOMP effector activity to retain for human BAK1.
- human/BAK1 · regulation of protein metabolic process (REMOVE): The annotation is a stress, development, transport, or signaling-level projection from ortholog or ARBA/Ensembl data and is too far from BAK's direct MOMP effector activity to retain for human BAK1.
- human/BAK1 · regulation of intracellular signal transduction (REMOVE): The annotation is a stress, development, transport, or signaling-level projection from ortholog or ARBA/Ensembl data and is too far from BAK's direct MOMP effector activity to retain for human BAK1.
- human/BAX · cellular response to stress (REMOVE): Many stresses can signal upstream to BAX, but that does not make BAX a direct executor of a generic cellular response to stress.
NONCATALYTIC_HOMOLOG
- PSEPK/pyrC' · hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides (REMOVE): The direct genetic and sequence evidence establishes loss of dihydroorotase catalysis.
- PSEPK/recC · catalytic activity, acting on DNA (REMOVE): RecC recognizes DNA and stimulates RecB helicase processivity, whereas RecB and RecD supply motor activity and RecB supplies nuclease catalysis. A generic catalytic-DNA term therefore misrepresents RecC's direct role.
- human/ASAH2B · sphingosine biosynthetic process (REMOVE): [file:human/ASAH2B/ASAH2B-bioinformatics/RESULTS.md "Active site ASAH2 S354 (Nucleophile): outside aligned region"] [file:human/ASAH2B/ASAH2B-uniprot.txt "DE RecName: Full=Putative inactive neutral ceramidase B {ECO:0000
- human/ASAH2B · ceramide biosynthetic process (REMOVE): [file:human/ASAH2B/ASAH2B-bioinformatics/RESULTS.md "Active site ASAH2 S354 (Nucleophile): outside aligned region"] [file:human/ASAH2B/ASAH2B-uniprot.txt "DE RecName: Full=Putative inactive neutral ceramidase B {ECO:0000
WRONG_DIRECTION
- human/PTEN · positive regulation of macromolecule metabolic process (REMOVE): This annotation is too vague and potentially misleading. PTEN generally suppresses anabolic metabolism through mTOR inhibition rather than promoting macromolecule metabolism.
- mouse/Dll3 · negative regulation of neurogenesis (REMOVE): Rule-based transfer from activating Delta ligands; for Dll3, overexpression data point in the opposite direction (promotion of neurogenesis as a Notch antagonist) and there is no loss-of-function support.
- yeast/HDA1 · positive regulation of macromolecule biosynthetic process (REMOVE): This annotation is mechanistically inconsistent with HDA1's documented function. HDA1 catalyzes histone deacetylation that typically promotes gene silencing and heterochromatin formation, resulting in negative regulation
OBSOLETE_OR_PSEUDOGENE
- human/MTRR · obsolete L-amino acid metabolic process (REMOVE): The term is obsolete and uninformatively broad; the specific L-methionine biosynthetic process (GO:0071265) and homocysteine annotations already capture the relevant biology. This over-propagated electronic annotation sh
- human/SNRPGP15 · small nuclear ribonucleoprotein complex (REMOVE): SNRPGP15 is an HGNC pseudogene locus (Ensembl biotype processed_pseudogene) and A8MWD9 is PE5 with a UniProt pseudogene CAUTION. The GRCh38 locus and the UniProt-cited clone AC012318 both carry TGA at codon 75 (Arg75 in
SPURIOUS_SIGNATURE
- worm/lrx-1 · vesicle-mediated transport (REMOVE): Based on false LDL receptor domain predictions; no evidence for cargo receptor function. Falcon deep research explicitly states there is no evidence base to claim lrx-1 mediates endocytosis or binds lipoprotein ligands.
- yeast/DNM1 · metal ion transport (REMOVE): No evidence that Dnm1 transports metal ions; an ARBA rule artefact with no biological basis for this GTPase.
NONCATALYTIC
- human/PDHX · dihydrolipoyllysine-residue acetyltransferase activity (MARK_AS_OVER_ANNOTATED): PDHX retains the E2-like inner-core fold (hence the ARBA family mapping) but lacks the catalytic histidine required for transacetylase activity; it is a structural/E3-anchoring subunit, not a catalytic acyltransferase. T
SUBSTRATE_OR_CARGO
- human/SIAH1 · amyloid fibril formation (MARK_AS_OVER_ANNOTATED): SIAH1 monoubiquitylates alpha-synuclein and ubiquitinates synphilin-1 and influences inclusion formation, but amyloid fibril formation is the substrate's property; assigning it as a SIAH1 process is an over-annotation.
Rules with the most rows not kept
| rule |
rows |
kept |
modify |
rejected |
| ARBA00026971 |
155 |
112 |
19 |
23 |
| ARBA00027533 |
39 |
5 |
21 |
13 |
| ARBA00028902 |
35 |
9 |
13 |
11 |
| ARBA00028763 |
46 |
25 |
6 |
15 |
| ARBA00027702 |
29 |
10 |
5 |
14 |
| ARBA00028334 |
38 |
21 |
9 |
8 |
| ARBA00029247 |
32 |
15 |
3 |
14 |
| ARBA00098139 |
29 |
13 |
0 |
15 |
| ARBA00027557 |
15 |
0 |
14 |
1 |
| ARBA00029050 |
29 |
16 |
9 |
4 |
| ARBA00026300 |
33 |
20 |
3 |
9 |
| ARBA00028953 |
30 |
19 |
5 |
6 |
| ARBA00026583 |
29 |
18 |
1 |
10 |
| ARBA00028747 |
15 |
4 |
2 |
9 |
| ARBA00027126 |
13 |
3 |
3 |
7 |
| ARBA00028689 |
24 |
15 |
3 |
6 |
| ARBA00027316 |
11 |
3 |
8 |
0 |
| ARBA00027930 |
43 |
34 |
3 |
5 |
| ARBA00027200 |
17 |
9 |
7 |
1 |
| ARBA00028665 |
14 |
6 |
0 |
8 |
| ARBA00028859 |
14 |
6 |
0 |
8 |
| ARBA00027483 |
11 |
3 |
0 |
7 |
| ARBA00027429 |
26 |
18 |
3 |
4 |
| ARBA00028065 |
13 |
6 |
3 |
4 |
| ARBA00027236 |
9 |
2 |
2 |
5 |