hu.MAP 3.0: Complex View
Human Protein Complex Map
Search for a protein
Complex: huMAP3_15301.1
Confidence: Medium
Proteins| Genename | Protein Name | Uniprot Annotation Score | Links |
|---|---|---|---|
| FANCB | Fanconi anemia group B protein (Protein FACB) (Fanconi anemia-associated polypeptide of 95 kDa) (FAAP95) | 5 | UniProt NCBI |
| FANCL | E3 ubiquitin-protein ligase FANCL (EC 2.3.2.27) (Fanconi anemia group L protein) (Fanconi anemia-associated polypeptide of 43 kDa) (FAAP43) (RING-type E3 ubiquitin transferase FANCL) | 5 | UniProt NCBI |
| FANCC | Fanconi anemia group C protein (Protein FACC) | 5 | UniProt NCBI |
Enrichments
| Term ID | Corrected Pval | Fraction Complex Coverage | Proteins | Term Name |
|---|---|---|---|---|
| CORUM:1152 | 8.18540495785e-09 | 1.0 | FANCB FANCC FANCL | FA complex (Fanconi anemia complex) |
| CORUM:245 | 1.30966479326e-08 | 1.0 | FANCB FANCC FANCL | FA core complex (Fanconi anemia core complex) |
| CORUM:1624 | 1.30966479326e-08 | 1.0 | FANCB FANCC FANCL | FA core complex (Fanconi anemia core complex) |
| CORUM:6884 | 1.96449718988e-08 | 1.0 | FANCB FANCC FANCL | Fanconi anemia FAAP100 complex |
| CORUM:2739 | 2.80642455698e-08 | 1.0 | FANCB FANCC FANCL | FA complex (Fanconi anemia complex) |
| KEGG:03460 | 9.62454150431e-07 | 1.0 | FANCB FANCC FANCL | Fanconi anemia pathway |
| HP:0005522 | 1.33355732665e-06 | 1.0 | FANCB FANCC FANCL | Pyridoxine-responsive sideroblastic anemia |
| HP:0010469 | 1.53359092564e-06 | 1.0 | FANCB FANCC FANCL | Absent testis |
| HP:0003974 | 1.75267534359e-06 | 1.0 | FANCB FANCC FANCL | Absent radius |
| HP:0009822 | 1.99167652681e-06 | 1.0 | FANCB FANCC FANCL | Aplasia involving forearm bones |
| HP:0003953 | 1.99167652681e-06 | 1.0 | FANCB FANCC FANCL | Absent forearm bone |
| HP:0100867 | 2.53289297431e-06 | 1.0 | FANCB FANCC FANCL | Duodenal stenosis |
| HP:0010293 | 2.53289297431e-06 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia of the uvula |
| HP:0012848 | 2.53289297431e-06 | 1.0 | FANCB FANCC FANCL | Small intestinal stenosis |
| HP:0100760 | 2.83684013123e-06 | 1.0 | FANCB FANCC FANCL | Clubbing of toes |
| HP:0002245 | 2.83684013123e-06 | 1.0 | FANCB FANCC FANCL | Meckel diverticulum |
| REAC:R-HSA-6783310 | 3.05391101381e-06 | 1.0 | FANCB FANCC FANCL | Fanconi Anemia Pathway |
| HP:0100587 | 3.51574204298e-06 | 1.0 | FANCB FANCC FANCL | Abnormal preputium morphology |
| HP:0001924 | 4.29509372738e-06 | 1.0 | FANCB FANCC FANCL | Sideroblastic anemia |
| HP:0001549 | 6.72840287535e-06 | 1.0 | FANCB FANCC FANCL | Abnormal ileum morphology |
| CORUM:6885 | 1.02521027753e-05 | 0.666666666667 | FANCB FANCL | L-B-P100 subcomplex |
| HP:0000813 | 1.22877782241e-05 | 1.0 | FANCB FANCC FANCL | Bicornuate uterus |
| HP:0007874 | 1.49774074816e-05 | 1.0 | FANCB FANCC FANCL | Almond-shaped palpebral fissure |
| HP:0100026 | 1.59541949261e-05 | 1.0 | FANCB FANCC FANCL | Arteriovenous malformation |
| HP:0003022 | 1.80333320308e-05 | 1.0 | FANCB FANCC FANCL | Hypoplasia of the ulna |
| WP:WP4946 | 1.81493241431e-05 | 1.0 | FANCB FANCC FANCL | DNA repair pathways full network |
| HP:0003220 | 1.91374135837e-05 | 1.0 | FANCB FANCC FANCL | Abnormality of chromosome stability |
| HP:0009777 | 2.02856583987e-05 | 1.0 | FANCB FANCC FANCL | Absent thumb |
| HP:0200005 | 2.02856583987e-05 | 1.0 | FANCB FANCC FANCL | Abnormal shape of the palpebral fissure |
| GO:0043240 | 2.11464090368e-05 | 1.0 | FANCB FANCC FANCL | Fanconi anaemia nuclear complex |
| HP:0006495 | 2.27181016004e-05 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia of the ulna |
| HP:0007565 | 2.53375892063e-05 | 1.0 | FANCB FANCC FANCL | Multiple cafe-au-lait spots |
| HP:0001199 | 3.607878731e-05 | 1.0 | FANCB FANCC FANCL | Triphalangeal thumb |
| HP:0000072 | 3.96257034203e-05 | 1.0 | FANCB FANCC FANCL | Hydroureter |
| HP:0009821 | 4.74019013381e-05 | 1.0 | FANCB FANCC FANCL | Forearm undergrowth |
| HP:0006501 | 4.94931616912e-05 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia of the radius |
| CORUM:1625 | 5.12534978153e-05 | 0.666666666667 | FANCB FANCC | FA core complex (Fanconi anemia core complex) |
| HP:0008572 | 5.84730249882e-05 | 1.0 | FANCB FANCC FANCL | External ear malformation |
| HP:0009380 | 6.08760260151e-05 | 1.0 | FANCB FANCC FANCL | Aplasia of the fingers |
| HP:0009824 | 6.84781687233e-05 | 1.0 | FANCB FANCC FANCL | Upper limb undergrowth |
| HP:0002246 | 6.84781687233e-05 | 1.0 | FANCB FANCC FANCL | Abnormal duodenum morphology |
| HP:0005344 | 7.38825396815e-05 | 1.0 | FANCB FANCC FANCL | Abnormal carotid artery morphology |
| HP:0002575 | 8.55295176317e-05 | 1.0 | FANCB FANCC FANCL | Tracheoesophageal fistula |
| HP:0000027 | 9.17859797648e-05 | 1.0 | FANCB FANCC FANCL | Azoospermia |
| HP:0006503 | 9.5025484933e-05 | 1.0 | FANCB FANCC FANCL | Aplasia/hypoplasia involving forearm bones |
| CORUM:248 | 0.000122991556209 | 0.666666666667 | FANCL FANCC | BRAFT complex |
| HP:0012745 | 0.000144309953562 | 1.0 | FANCB FANCC FANCL | Short palpebral fissure |
| HP:0008669 | 0.000167058363283 | 1.0 | FANCB FANCC FANCL | Abnormal spermatogenesis |
| HP:0002863 | 0.000167058363283 | 1.0 | FANCB FANCC FANCL | Myelodysplasia |
| HP:0001053 | 0.000171877354532 | 1.0 | FANCB FANCC FANCL | Hypopigmented skin patches |
| HP:0010161 | 0.000171877354532 | 1.0 | FANCB FANCC FANCL | Abnormal toe phalanx morphology |
| CORUM:244 | 0.000187886616059 | 0.666666666667 | FANCL FANCC | BRAFT complex |
| HP:0000957 | 0.000197366484344 | 1.0 | FANCB FANCC FANCL | Cafe-au-lait spot |
| HP:0008055 | 0.000202749206644 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia affecting the uvea |
| HP:0008053 | 0.000202749206644 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia of the iris |
| HP:0000453 | 0.000202749206644 | 1.0 | FANCB FANCC FANCL | Choanal atresia |
| HP:0002414 | 0.000208228914932 | 1.0 | FANCB FANCC FANCL | Spina bifida |
| HP:0001217 | 0.000213806475153 | 1.0 | FANCB FANCC FANCL | Clubbing |
| HP:0000415 | 0.000249375220083 | 1.0 | FANCB FANCC FANCL | Abnormality of the choanae |
| HP:0008062 | 0.000255661990337 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia affecting the anterior segment of the eye |
| HP:0000324 | 0.000262053540095 | 1.0 | FANCB FANCC FANCL | Facial asymmetry |
| HP:0010301 | 0.000268550735304 | 1.0 | FANCB FANCC FANCL | Spinal dysraphism |
| HP:0009601 | 0.00027515444191 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia of the thumb |
| HP:0002023 | 0.000281865525859 | 1.0 | FANCB FANCC FANCL | Anal atresia |
| HP:0000010 | 0.000324435446754 | 1.0 | FANCB FANCC FANCL | Recurrent urinary tract infections |
| HP:0002251 | 0.000331922418602 | 1.0 | FANCB FANCC FANCL | Aganglionic megacolon |
| HP:0004362 | 0.000331922418602 | 1.0 | FANCB FANCC FANCL | Abnormal enteric ganglion morphology |
| HP:0031105 | 0.000331922418602 | 1.0 | FANCB FANCC FANCL | Abnormal uterus morphology |
| HP:0025028 | 0.000339523695364 | 1.0 | FANCB FANCC FANCL | Abnormal enteric nervous system morphology |
| HP:0025633 | 0.000339523695364 | 1.0 | FANCB FANCC FANCL | Abnormal ureter morphology |
| HP:0012331 | 0.000339523695364 | 1.0 | FANCB FANCC FANCL | Abnormal autonomic nervous system morphology |
| HP:0040071 | 0.000347240142986 | 1.0 | FANCB FANCC FANCL | Abnormal morphology of ulna |
| HP:0001882 | 0.000355072627414 | 1.0 | FANCB FANCC FANCL | Leukopenia |
| HP:0012041 | 0.000363022014595 | 1.0 | FANCB FANCC FANCL | Decreased fertility in males |
| HP:0002778 | 0.000477396204013 | 1.0 | FANCB FANCC FANCL | Abnormal tracheal morphology |
| HP:0001646 | 0.000496879996123 | 1.0 | FANCB FANCC FANCL | Abnormal aortic valve morphology |
| HP:0012145 | 0.000506817596046 | 1.0 | FANCB FANCC FANCL | Abnormality of multiple cell lineages in the bone marrow |
| GO:0036297 | 0.000524430944113 | 1.0 | FANCB FANCC FANCL | interstrand cross-link repair |
| HP:0010468 | 0.000547892893599 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia of the testes |
| HP:0001562 | 0.000591129593157 | 1.0 | FANCB FANCC FANCL | Oligohydramnios |
| HP:0001636 | 0.000625008876824 | 1.0 | FANCB FANCC FANCL | Tetralogy of Fallot |
| HP:0000340 | 0.000660158503737 | 1.0 | FANCB FANCC FANCL | Sloping forehead |
| HP:0010972 | 0.000660158503737 | 1.0 | FANCB FANCC FANCL | Anemia of inadequate production |
| HP:0000172 | 0.000672161385623 | 1.0 | FANCB FANCC FANCL | Abnormal uvula morphology |
| HP:0045058 | 0.000709041173276 | 1.0 | FANCB FANCC FANCL | Abnormality of the testis size |
| HP:0001034 | 0.000734362309502 | 1.0 | FANCB FANCC FANCL | Hypermelanotic macule |
| HP:0009602 | 0.000773463249455 | 1.0 | FANCB FANCC FANCL | Abnormality of thumb phalanx |
| HP:0000268 | 0.000773463249455 | 1.0 | FANCB FANCC FANCL | Dolichocephaly |
| HP:0005561 | 0.000786798822721 | 1.0 | FANCB FANCC FANCL | Abnormal bone marrow cell morphology |
| HP:0000104 | 0.000841673840766 | 1.0 | FANCB FANCC FANCL | Renal agenesis |
| HP:0002818 | 0.000884463712025 | 1.0 | FANCB FANCC FANCL | Abnormal morphology of the radius |
| HP:0034915 | 0.000884463712025 | 1.0 | FANCB FANCC FANCL | Abnormal anus morphology |
| HP:0001010 | 0.000899042784202 | 1.0 | FANCB FANCC FANCL | Hypopigmentation of the skin |
| HP:0006101 | 0.0009137811905 | 1.0 | FANCB FANCC FANCL | Finger syndactyly |
| HP:0009892 | 0.000986522412937 | 0.666666666667 | FANCB FANCL | Anotia |
| HP:0000483 | 0.0010214841295 | 1.0 | FANCB FANCC FANCL | Astigmatism |
| HP:0000025 | 0.00105373976382 | 1.0 | FANCB FANCC FANCL | Functional abnormality of male internal genitalia |
| HP:0040072 | 0.00110338533207 | 1.0 | FANCB FANCC FANCL | Abnormal forearm bone morphology |
| HP:0002973 | 0.00112027388307 | 1.0 | FANCB FANCC FANCL | Abnormal forearm morphology |
| HP:0007400 | 0.00113733389144 | 1.0 | FANCB FANCC FANCL | Irregular hyperpigmentation |
| HP:0004378 | 0.00113733389144 | 1.0 | FANCB FANCC FANCL | Abnormality of the anus |
| HP:0012733 | 0.00118955132024 | 1.0 | FANCB FANCC FANCL | Macule |
| HP:0002031 | 0.00118955132024 | 1.0 | FANCB FANCC FANCL | Abnormal esophagus morphology |
| HP:0003221 | 0.00132788970801 | 0.666666666667 | FANCL FANCC | Chromosomal breakage induced by crosslinking agents |
| GO:0006513 | 0.00136394338287 | 1.0 | FANCB FANCC FANCL | protein monoubiquitination |
| HP:0001770 | 0.00137511062657 | 1.0 | FANCB FANCC FANCL | Toe syndactyly |
| HP:0000130 | 0.00145442611343 | 1.0 | FANCB FANCC FANCL | Abnormality of the uterus |
| HP:0009826 | 0.0014747204313 | 1.0 | FANCB FANCC FANCL | Limb undergrowth |
| HP:0100542 | 0.0014747204313 | 1.0 | FANCB FANCC FANCL | Abnormal localization of kidney |
| HP:0008517 | 0.00151751896202 | 0.666666666667 | FANCB FANCL | Aplasia/Hypoplasia of the sacrum |
| HP:0001710 | 0.00153673431077 | 1.0 | FANCB FANCC FANCL | Conotruncal defect |
| HP:0002827 | 0.00153673431077 | 1.0 | FANCB FANCC FANCL | Hip dislocation |
| HP:0003026 | 0.00166592917139 | 1.0 | FANCB FANCC FANCL | Short long bone |
| HP:0002244 | 0.00166592917139 | 1.0 | FANCB FANCC FANCL | Abnormal small intestine morphology |
| HP:0000520 | 0.00168814156034 | 1.0 | FANCB FANCC FANCL | Proptosis |
| HP:0100736 | 0.00177896547375 | 1.0 | FANCB FANCC FANCL | Abnormal soft palate morphology |
| HP:0011563 | 0.00184918073078 | 1.0 | FANCB FANCC FANCL | Abnormal ventriculoarterial connection |
| HP:0006824 | 0.00187298992474 | 1.0 | FANCB FANCC FANCL | Cranial nerve paralysis |
| HP:0011545 | 0.00192121967075 | 1.0 | FANCB FANCC FANCL | Abnormal connection of the cardiac segments |
| HP:0031910 | 0.00192121967075 | 1.0 | FANCB FANCC FANCL | Abnormal cranial nerve physiology |
| HP:0000144 | 0.00199510567422 | 1.0 | FANCB FANCC FANCL | Decreased fertility |
| HP:0012874 | 0.00207086212173 | 1.0 | FANCB FANCC FANCL | Abnormal male reproductive system physiology |
| HP:0000568 | 0.0021224171016 | 1.0 | FANCB FANCC FANCL | Microphthalmia |
| REAC:R-HSA-73894 | 0.00220643087689 | 1.0 | FANCB FANCC FANCL | DNA Repair |
| HP:0001639 | 0.00230958793402 | 1.0 | FANCB FANCC FANCL | Hypertrophic cardiomyopathy |
| HP:0002270 | 0.00233719257068 | 1.0 | FANCB FANCC FANCL | Abnormality of the autonomic nervous system |
| HP:0002823 | 0.0023930599632 | 1.0 | FANCB FANCC FANCL | Abnormal femur morphology |
| HP:0200007 | 0.00244981062097 | 1.0 | FANCB FANCC FANCL | Abnormal size of the palpebral fissures |
| HP:0045005 | 0.00253660788401 | 1.0 | FANCB FANCC FANCL | Neural tube defect |
| HP:0410043 | 0.00253660788401 | 1.0 | FANCB FANCC FANCL | Abnormal neural tube morphology |
| HP:0002143 | 0.002595597013 | 1.0 | FANCB FANCC FANCL | Abnormal spinal cord morphology |
| HP:0004377 | 0.002595597013 | 1.0 | FANCB FANCC FANCL | Hematological neoplasm |
| HP:0001537 | 0.00262543146143 | 1.0 | FANCB FANCC FANCL | Umbilical hernia |
| HP:0000953 | 0.00271630473377 | 1.0 | FANCB FANCC FANCL | Hyperpigmentation of the skin |
| HP:0001551 | 0.00277803718069 | 1.0 | FANCB FANCC FANCL | Abnormal umbilicus morphology |
| HP:0100887 | 0.00293644474028 | 1.0 | FANCB FANCC FANCL | Abnormality of globe size |
| HP:0030311 | 0.00293644474028 | 1.0 | FANCB FANCC FANCL | Lower extremity joint dislocation |
| HP:0007700 | 0.00330589727222 | 1.0 | FANCB FANCC FANCL | Ocular anterior segment dysgenesis |
| HP:0000582 | 0.00330589727222 | 1.0 | FANCB FANCC FANCL | Upslanted palpebral fissure |
| HP:0100691 | 0.00344756089384 | 1.0 | FANCB FANCC FANCL | Abnormality of the curvature of the cornea |
| HP:0006265 | 0.00409481766341 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia of fingers |
| HP:0001654 | 0.00413522704825 | 1.0 | FANCB FANCC FANCL | Abnormal heart valve morphology |
| HP:0001763 | 0.00417590141266 | 1.0 | FANCB FANCC FANCL | Pes planus |
| HP:0005607 | 0.00425804854398 | 1.0 | FANCB FANCC FANCL | Abnormal tracheobronchial morphology |
| HP:0002032 | 0.00443651401809 | 0.666666666667 | FANCB FANCL | Esophageal atresia |
| HP:0008678 | 0.00459740944144 | 1.0 | FANCB FANCC FANCL | Renal hypoplasia/aplasia |
| HP:0000047 | 0.0046849773967 | 1.0 | FANCB FANCC FANCL | Hypospadias |
| HP:0001824 | 0.00481840327101 | 1.0 | FANCB FANCC FANCL | Weight loss |
| HP:0001384 | 0.00490874658422 | 1.0 | FANCB FANCC FANCL | Abnormal hip joint morphology |
| HP:0000864 | 0.00518653783266 | 1.0 | FANCB FANCC FANCL | Abnormality of the hypothalamus-pituitary axis |
| HP:0000069 | 0.00528141177699 | 1.0 | FANCB FANCC FANCL | Abnormality of the ureter |
| HP:0001643 | 0.00528141177699 | 1.0 | FANCB FANCC FANCL | Patent ductus arteriosus |
| HP:0100627 | 0.0055729611805 | 1.0 | FANCB FANCC FANCL | Displacement of the urethral meatus |
| HP:0001373 | 0.0055729611805 | 1.0 | FANCB FANCC FANCL | Joint dislocation |
| HP:0032076 | 0.00562257211089 | 1.0 | FANCB FANCC FANCL | Abnormal male urethral meatus morphology |
| HP:0001679 | 0.00562257211089 | 1.0 | FANCB FANCC FANCL | Abnormal aortic morphology |
| HP:0000238 | 0.00613496986499 | 1.0 | FANCB FANCC FANCL | Hydrocephalus |
| HP:0001873 | 0.00613496986499 | 1.0 | FANCB FANCC FANCL | Thrombocytopenia |
| HP:0000083 | 0.00618785753624 | 1.0 | FANCB FANCC FANCL | Renal insufficiency |
| HP:0004209 | 0.00634834250104 | 1.0 | FANCB FANCC FANCL | Clinodactyly of the 5th finger |
| HP:0009179 | 0.00640244769281 | 1.0 | FANCB FANCC FANCL | Deviation of the 5th finger |
| HP:0001172 | 0.00640244769281 | 1.0 | FANCB FANCC FANCL | Abnormal thumb morphology |
| HP:0000135 | 0.00645685942958 | 1.0 | FANCB FANCC FANCL | Hypogonadism |
| HP:0002007 | 0.00651157857729 | 1.0 | FANCB FANCC FANCL | Frontal bossing |
| HP:0001159 | 0.00656660600188 | 1.0 | FANCB FANCC FANCL | Syndactyly |
| HP:0011218 | 0.00667758914553 | 1.0 | FANCB FANCC FANCL | Abnormal shape of the frontal region |
| HP:0430000 | 0.00673354659647 | 1.0 | FANCB FANCC FANCL | Abnormal frontal bone morphology |
| HP:0011873 | 0.00767185138664 | 1.0 | FANCB FANCC FANCL | Abnormal platelet count |
| HP:0011875 | 0.00785695607115 | 1.0 | FANCB FANCC FANCL | Abnormal platelet morphology |
| HP:0040019 | 0.00791931286536 | 1.0 | FANCB FANCC FANCL | Finger clinodactyly |
| HP:0410008 | 0.00804501449854 | 1.0 | FANCB FANCC FANCL | Abnormality of the peripheral nervous system |
| HP:0040070 | 0.00823605004937 | 1.0 | FANCB FANCC FANCL | Abnormal upper limb bone morphology |
| HP:0040012 | 0.00841415615575 | 0.666666666667 | FANCL FANCC | Chromosome breakage |
| HP:0000525 | 0.00856112196666 | 1.0 | FANCB FANCC FANCL | Abnormality iris morphology |
| HP:0001560 | 0.00889463686054 | 1.0 | FANCB FANCC FANCL | Abnormality of the amniotic fluid |
| HP:0000008 | 0.00903043109803 | 1.0 | FANCB FANCC FANCL | Abnormal morphology of female internal genitalia |
| HP:0000795 | 0.00909884345483 | 1.0 | FANCB FANCC FANCL | Abnormality of the urethra |
| HP:0001872 | 0.00923670297429 | 1.0 | FANCB FANCC FANCL | Abnormality of thrombocytes |
| WP:WP5316 | 0.00929774738496 | 0.666666666667 | FANCL FANCC | Primary ovarian insufficiency |
| HP:0008056 | 0.00965862232757 | 1.0 | FANCB FANCC FANCL | Aplasia/Hypoplasia affecting the eye |
| HP:0011893 | 0.00980206546887 | 1.0 | FANCB FANCC FANCL | Abnormal leukocyte count |
| HP:0001000 | 0.0107692028076 | 1.0 | FANCB FANCC FANCL | Abnormality of skin pigmentation |
| HP:0004299 | 0.0110010685931 | 1.0 | FANCB FANCC FANCL | Hernia of the abdominal wall |
| HP:0010866 | 0.0112362388299 | 1.0 | FANCB FANCC FANCL | Abdominal wall defect |
| HP:0004207 | 0.0117165861789 | 1.0 | FANCB FANCC FANCL | Abnormal 5th finger morphology |
| HP:0005927 | 0.0128038952176 | 1.0 | FANCB FANCC FANCL | Aplasia/hypoplasia involving bones of the hand |
| HP:0000812 | 0.0128902136124 | 1.0 | FANCB FANCC FANCL | Abnormal internal genitalia |
| HP:0004097 | 0.0129769190851 | 1.0 | FANCB FANCC FANCL | Deviation of finger |
| HP:0011603 | 0.0130640125018 | 1.0 | FANCB FANCC FANCL | Congenital malformation of the great arteries |
| HP:0011004 | 0.0134162829269 | 1.0 | FANCB FANCC FANCL | Abnormal systemic arterial morphology |
| HP:0004298 | 0.0140478920465 | 1.0 | FANCB FANCC FANCL | Abnormality of the abdominal wall |
| HP:0004349 | 0.0141397083344 | 1.0 | FANCB FANCC FANCL | Reduced bone mineral density |
| HP:0000815 | 0.0142438401108 | 0.666666666667 | FANCB FANCC | Hypergonadotropic hypogonadism |
| HP:0001631 | 0.0146990195962 | 1.0 | FANCB FANCC FANCL | Atrial septal defect |
| HP:0011994 | 0.0148886826221 | 1.0 | FANCB FANCC FANCL | Abnormal atrial septum morphology |
| HP:0009484 | 0.0149841228953 | 1.0 | FANCB FANCC FANCL | Deviation of the hand or of fingers of the hand |
| HP:0010460 | 0.0155653417329 | 1.0 | FANCB FANCC FANCL | Abnormality of the female genitalia |
| HP:0030084 | 0.0156636491543 | 1.0 | FANCB FANCC FANCL | Clinodactyly |
| HP:0006496 | 0.0156636491543 | 1.0 | FANCB FANCC FANCL | Aplasia/hypoplasia involving bones of the upper limbs |
| HP:0003272 | 0.0159610532209 | 1.0 | FANCB FANCC FANCL | Abnormal hip bone morphology |
| HP:0001638 | 0.0165671073988 | 1.0 | FANCB FANCC FANCL | Cardiomyopathy |
| HP:0000553 | 0.0173987795596 | 1.0 | FANCB FANCC FANCL | Abnormal uvea morphology |
| HP:0100790 | 0.0180404760879 | 1.0 | FANCB FANCC FANCL | Hernia |
| HP:0001903 | 0.0189203502844 | 1.0 | FANCB FANCC FANCL | Anemia |
| HP:0001637 | 0.0190323050199 | 1.0 | FANCB FANCC FANCL | Abnormal myocardium morphology |
| HP:0000175 | 0.0194845402877 | 1.0 | FANCB FANCC FANCL | Cleft palate |
| HP:0005120 | 0.0200598360525 | 1.0 | FANCB FANCC FANCL | Abnormal cardiac atrium morphology |
| HP:0004348 | 0.0202930882181 | 1.0 | FANCB FANCC FANCL | Abnormality of bone mineral density |
| HP:0001881 | 0.0204103893061 | 1.0 | FANCB FANCC FANCL | Abnormal leukocyte morphology |
| HP:0010987 | 0.0204103893061 | 1.0 | FANCB FANCC FANCL | Abnormal cellular immune system morphology |
| HP:0002921 | 0.0208841138977 | 1.0 | FANCB FANCC FANCL | Abnormal cerebrospinal fluid morphology |
| HP:0000286 | 0.0218534403487 | 1.0 | FANCB FANCC FANCL | Epicanthus |
| HP:0011017 | 0.0218534403487 | 1.0 | FANCB FANCC FANCL | Abnormal cellular physiology |
| HP:0001511 | 0.0218534403487 | 1.0 | FANCB FANCC FANCL | Intrauterine growth retardation |
| HP:0008373 | 0.0219766740349 | 1.0 | FANCB FANCC FANCL | Puberty and gonadal disorders |
| HP:0032251 | 0.0221003701364 | 1.0 | FANCB FANCC FANCL | Abnormal immune system morphology |
| HP:0005528 | 0.022338444757 | 0.666666666667 | FANCL FANCC | Bone marrow hypocellularity |
| HP:0002644 | 0.0223491530492 | 1.0 | FANCB FANCC FANCL | Abnormal pelvic girdle bone morphology |
| HP:0008518 | 0.023863352839 | 0.666666666667 | FANCB FANCL | Aplasia/Hypoplasia involving the vertebral column |
| HP:0000202 | 0.024143102858 | 1.0 | FANCB FANCC FANCL | Orofacial cleft |
| HP:5201015 | 0.0245396066869 | 1.0 | FANCB FANCC FANCL | Craniofacial cleft |
| HP:0001877 | 0.0249404281241 | 1.0 | FANCB FANCC FANCL | Abnormal erythrocyte morphology |
| HP:0025354 | 0.0250749987795 | 1.0 | FANCB FANCC FANCL | Abnormal cellular phenotype |
| HP:0045060 | 0.0264474241065 | 1.0 | FANCB FANCC FANCL | Aplasia/hypoplasia involving bones of the extremities |
| HP:0000036 | 0.0278690351843 | 1.0 | FANCB FANCC FANCL | Abnormal penis morphology |
| HP:0012211 | 0.029641112921 | 1.0 | FANCB FANCC FANCL | Abnormal renal physiology |
| HP:0000539 | 0.0305546473168 | 1.0 | FANCB FANCC FANCL | Abnormality of refraction |
| HP:0011849 | 0.0321185853311 | 1.0 | FANCB FANCC FANCL | Abnormal bone ossification |
| HP:0001780 | 0.0327588054209 | 1.0 | FANCB FANCC FANCL | Abnormal toe morphology |
| HP:0009815 | 0.0332445138436 | 1.0 | FANCB FANCC FANCL | Aplasia/hypoplasia of the extremities |
| HP:0100491 | 0.033570972141 | 1.0 | FANCB FANCC FANCL | Abnormality of lower limb joint |
| HP:0030962 | 0.0337349996922 | 1.0 | FANCB FANCC FANCL | Abnormal morphology of the great vessels |
| HP:0000481 | 0.0338995606663 | 1.0 | FANCB FANCC FANCL | Abnormal cornea morphology |
| HP:0200006 | 0.0371287212398 | 1.0 | FANCB FANCC FANCL | Slanting of the palpebral fissure |
| HP:0011314 | 0.0383682142819 | 1.0 | FANCB FANCC FANCL | Abnormal long bone morphology |
| HP:0002589 | 0.0388502441646 | 0.666666666667 | FANCB FANCL | Gastrointestinal atresia |
| HP:0040069 | 0.0396349906946 | 1.0 | FANCB FANCC FANCL | Abnormal lower limb bone morphology |
| HP:0000508 | 0.0405566996236 | 1.0 | FANCB FANCC FANCL | Ptosis |
| HP:0002242 | 0.0407427395301 | 1.0 | FANCB FANCC FANCL | Abnormal intestine morphology |
| HP:0000028 | 0.0407427395301 | 1.0 | FANCB FANCC FANCL | Cryptorchidism |
| HP:0000080 | 0.0424427653377 | 1.0 | FANCB FANCC FANCL | Abnormality of reproductive system physiology |
| HP:0001671 | 0.0424427653377 | 1.0 | FANCB FANCC FANCL | Abnormal cardiac septum morphology |
| HP:0002119 | 0.043601990352 | 1.0 | FANCB FANCC FANCL | Ventriculomegaly |
| HP:0000218 | 0.0449808704429 | 1.0 | FANCB FANCC FANCL | High palate |
| HP:0003330 | 0.0453801071984 | 1.0 | FANCB FANCC FANCL | Abnormal bone structure |
| HP:0000518 | 0.0490800611352 | 1.0 | FANCB FANCC FANCL | Cataract |
Edges
| Protein 1 | Protein 2 | Score | ProteomeHD | Evidence |
|---|---|---|---|---|
| FANCL | FANCC | 0.994 | bioplex3_WMM bioplex3_HCT116 WMM_only | |
| FANCB | FANCC | 0.993 | bioplex3_WMM bioplex3_HCT116 WMM_only | |
| FANCL | FANCB | 0.991 | 0.226 | hein_WMM bioplex_WMM bioplex3_WMM boldt hein () boldt_WMM |
Related Complexes