hu.MAP 3.0: Complex View

Human Protein Complex Map

Complex: huMAP3_08282.1

Complex Portal: CPX-17044

Confidence: High

Genename	Protein Name	Uniprot Annotation Score	Links
B9D2	B9 domain-containing protein 2 (MKS1-related protein 2)	5	UniProt NCBI
TMEM231	Transmembrane protein 231	5	UniProt NCBI
CC2D2A	Coiled-coil and C2 domain-containing protein 2A	5	UniProt NCBI
ASIC2	Acid-sensing ion channel 2 (ASIC2) (Amiloride-sensitive brain sodium channel) (Amiloride-sensitive cation channel 1, neuronal) (Amiloride-sensitive cation channel neuronal 1) (Brain sodium channel 1) (BNC1) (BNaC1) (Mammalian degenerin homolog) (MDEG)	5	UniProt NCBI
TMEM17	Transmembrane protein 17	4	UniProt NCBI
CHRNA3	Neuronal acetylcholine receptor subunit alpha-3	5	UniProt NCBI
TCTN1	Tectonic-1	5	UniProt NCBI

Enrichments

Term ID	Corrected Pval	Fraction Complex Coverage	Proteins	Term Name
GO:0036038	8.73008139488e-11	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	MKS complex
WP:WP4656	4.42656222522e-09	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	Joubert syndrome
HP:0010459	1.55991449867e-08	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	True hermaphroditism
HP:0100732	6.0352262497e-08	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Pancreatic fibrosis
HP:0006870	7.54279269726e-08	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Lobar holoprosencephaly
HP:0000068	9.31603571786e-08	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Urethral atresia
WP:WP4803	2.42970001794e-07	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	Ciliopathies
GO:0035869	3.22197042001e-07	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	ciliary transition zone
HP:0010295	4.2594549796e-07	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia of the tongue
HP:0001737	4.2594549796e-07	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Pancreatic cysts
HP:0000037	4.88968098733e-07	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Male pseudohermaphroditism
HP:0001747	4.88968098733e-07	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Accessory spleen
HP:0002323	4.88968098733e-07	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Anencephaly
HP:0002419	7.20330405503e-07	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Molar tooth sign on MRI
HP:0006706	1.02533089038e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Cystic liver disease
HP:0000221	1.14576950689e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Furrowed tongue
HP:0002612	1.27650452211e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Congenital hepatic fibrosis
HP:0000073	1.41810497204e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Ureteral duplication
HP:0000647	2.10507139526e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Sclerocornea
HP:0001177	4.53407225409e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Preaxial hand polydactyly
WP:WP4536	5.93407064908e-06	0.571428571429	TMEM17 TCTN1 TMEM231 CC2D2A	Genes related to primary cilium development based on CRISPR
HP:0004422	6.11226645085e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Biparietal narrowing
HP:0000528	9.20803618222e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Anophthalmia
HP:0001830	9.20803618222e-06	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Postaxial foot polydactyly
HP:0001746	1.18407584274e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Asplenia
HP:0001360	1.2578732756e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Holoprosencephaly
HP:0002418	1.33506082231e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal midbrain morphology
HP:0010451	1.58798920487e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia of the spleen
HP:0009799	1.77546377933e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Supernumerary spleens
HP:0100258	1.77546377933e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Preaxial polydactyly
HP:0001162	2.56425880234e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Postaxial hand polydactyly
HP:0010322	2.56425880234e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal fifth toe morphology
HP:0002270	2.63746333121e-05	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormality of the autonomic nervous system
HP:0000003	2.83131938786e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Multicystic kidney dysplasia
HP:0002789	2.83131938786e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Tachypnea
HP:0012090	2.97239508873e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal pancreas morphology
HP:0001696	4.49117687237e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Situs inversus totalis
HP:0011534	4.89535719988e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal spatial orientation of the cardiac segments
HP:0000657	5.55187626829e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Oculomotor apraxia
HP:0000457	6.27212522551e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Depressed nasal ridge
HP:0000062	6.52705278452e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Ambiguous genitalia
HP:0011815	7.06007150711e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Cephalocele
HP:0002084	7.06007150711e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Encephalocele
HP:0001651	9.18503706207e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Dextrocardia
HP:0004307	9.52365056635e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal anatomic location of the heart
HP:0008055	9.87151173709e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia affecting the uvea
HP:0008053	9.87151173709e-05	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia of the iris
HP:0000069	0.000102178728737	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormality of the ureter
HP:0000482	0.000109722436777	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Microcornea
HP:0001829	0.000113587650454	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Foot polydactyly
HP:0009136	0.000130074791482	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Duplication involving bones of the feet
HP:0008062	0.000134461885723	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia affecting the anterior segment of the eye
HP:0001305	0.000148288378179	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Dandy-Walker malformation
HP:0000293	0.000148288378179	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Full cheeks
HP:0100259	0.000153124982188	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Postaxial polydactyly
HP:0001395	0.000153124982188	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Hepatic fibrosis
HP:0034237	0.000158078526287	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Open neural tube defect
HP:0004362	0.000190360293174	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal enteric ganglion morphology
HP:0002251	0.000190360293174	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aganglionic megacolon
HP:0012331	0.000196185092441	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal autonomic nervous system morphology
HP:0025633	0.000196185092441	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal ureter morphology
HP:0025028	0.000196185092441	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal enteric nervous system morphology
HP:0410008	0.000205269133442	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormality of the peripheral nervous system
HP:0000532	0.000233978474571	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal chorioretinal morphology
HP:0000795	0.000251676380995	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormality of the urethra
HP:0010950	0.000262030622668	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal fourth ventricle morphology
HP:0002198	0.000262030622668	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Dilated fourth ventricle
HP:0002350	0.000300541855379	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Cerebellar cyst
HP:0001120	0.000361370005107	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of corneal size
HP:0002085	0.000370752622358	0.428571428571	B9D2 TMEM231 CC2D2A	Occipital encephalocele
HP:0001161	0.000370756208707	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Hand polydactyly
HP:0001562	0.000410132544577	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Oligohydramnios
HP:0000612	0.000410132544577	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Iris coloboma
HP:0000340	0.000474946842546	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Sloping forehead
HP:0000610	0.000474946842546	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal choroid morphology
HP:0005445	0.00051007992158	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Enlarged posterior fossa
HP:0002553	0.000613260790757	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Highly arched eyebrow
HP:0010576	0.00074713218725	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Intracranial cystic lesion
HP:0002186	0.000763247638573	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Apraxia
HP:0030724	0.000779621016095	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Central nervous system cyst
HP:0000932	0.000847748000294	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal posterior cranial fossa morphology
HP:0002876	0.00104065814502	0.428571428571	B9D2 CC2D2A TCTN1	Episodic tachypnea
HP:0009997	0.00105804081098	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Duplication of phalanx of hand
HP:0004275	0.00107891730228	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Duplication of hand bones
HP:0009142	0.00107891730228	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Duplication of bones involving the upper extremities
HP:0002104	0.00110009942968	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Apnea
HP:0002693	0.00110009942968	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal skull base morphology
HP:0000426	0.00116550894293	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Prominent nasal bridge
HP:0011119	0.00128091308142	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal nasal dorsum morphology
HP:0000368	0.0013049791219	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Low-set, posteriorly rotated ears
HP:0000589	0.00148300663271	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Coloboma
HP:0004426	0.00153703909149	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal cheek morphology
REAC:R-HSA-5620912	0.0016610504278	0.428571428571	B9D2 CC2D2A TCTN1	Anchoring of the basal body to the plasma membrane
HP:0010442	0.00167853607728	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Polydactyly
HP:0000276	0.00170796088405	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Long face
HP:0002438	0.00179854424952	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Cerebellar malformation
HP:0007957	0.00195740944778	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Corneal opacity
HPA:0060873	0.00217633465067	0.428571428571	B9D2 TMEM231 CC2D2A	bronchus; ciliated cells (ciliary rootlets)[High]
HP:0000107	0.00219709409919	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Renal cyst
HP:0000568	0.00223303835962	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Microphthalmia
GO:0060271	0.00227446778994	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	cilium assembly
HP:0006487	0.00230623880941	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Bowing of the long bones
HP:0100729	0.00249705480857	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Large face
HP:0001320	0.00253658569138	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Cerebellar vermis hypoplasia
HP:0410043	0.00282649713289	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal neural tube morphology
HP:0045005	0.00282649713289	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Neural tube defect
HP:0001732	0.0030940278937	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of the pancreas
GO:0044782	0.00323554146091	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	cilium organization
HP:0000940	0.00333099705828	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal diaphysis morphology
HP:0100887	0.00342946822114	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of globe size
HP:0006817	0.00358121595245	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia of the cerebellar vermis
HP:0007700	0.00401031404951	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Ocular anterior segment dysgenesis
HP:0010936	0.00554811459408	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormality of the lower urinary tract
HP:0030809	0.005744599238	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal tongue morphology
HP:0002334	0.00643050545945	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal cerebellar vermis morphology
HP:0000864	0.00726204381131	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of the hypothalamus-pituitary axis
HP:0000238	0.00905879972047	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Hydrocephalus
HP:0001172	0.00958196122438	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal thumb morphology
HPA:0210873	0.00981112959854	0.428571428571	B9D2 TMEM231 CC2D2A	fallopian tube; ciliated cells (ciliary rootlets)[High]
HP:0000157	0.0129372325986	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of the tongue
REAC:R-HSA-5617833	0.01389705158	0.428571428571	B9D2 CC2D2A TCTN1	Cilium Assembly
HP:0000525	0.0140382017336	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality iris morphology
HP:0001560	0.0147606689523	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of the amniotic fluid
HP:0000358	0.0150572374866	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Posteriorly rotated ears
GO:0120031	0.0154131050819	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	plasma membrane bounded cell projection assembly
HP:0001883	0.0162878804703	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Talipes
HP:0008056	0.0164467892795	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia affecting the eye
HP:0001321	0.016606844302	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Cerebellar hypoplasia
HP:0005656	0.016930414323	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Positional foot deformity
HP:0000463	0.0170939400162	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Anteverted nares
GO:0030031	0.017418204933	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	cell projection assembly
HP:0002269	0.0186188605393	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of neuronal migration
HP:0012210	0.0188789462622	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormal renal morphology
HP:0005288	0.0196899667773	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal nostril morphology
HP:0000032	0.0198654308581	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormal male external genitalia morphology
HP:0004207	0.0211882801616	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal 5th finger morphology
GO:0005929	0.0230843069002	0.714285714286	B9D2 TCTN1 TMEM231 TMEM17 CC2D2A	cilium
HP:0000811	0.0243441930823	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormal external genitalia
HP:0010461	0.0244625952771	0.714285714286	B9D2 CHRNA3 TMEM231 TCTN1 CC2D2A	Abnormality of the male genitalia
HPA:0320872	0.0245180774371	0.428571428571	B9D2 TMEM231 CC2D2A	nasopharynx; ciliated cells (ciliary rootlets)[>=Medium]
GO:0120036	0.0268095067638	0.857142857143	CC2D2A TMEM17 CHRNA3 TCTN1 B9D2 TMEM231	plasma membrane bounded cell projection organization
GO:0030030	0.0290357560482	0.857142857143	CC2D2A TMEM17 CHRNA3 TCTN1 B9D2 TMEM231	cell projection organization
HP:0007360	0.0292411387003	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Aplasia/Hypoplasia of the cerebellum
HP:0025408	0.0297325816248	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal spleen morphology
HP:0000553	0.0355505847959	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal uvea morphology
HP:0001743	0.0361182340875	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormality of the spleen
HP:0000429	0.0366925546754	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal morphology of the nasal alae
HPA:0320871	0.0396586841496	0.428571428571	B9D2 TMEM231 CC2D2A	nasopharynx; ciliated cells (ciliary rootlets)[>=Low]
HPA:0060872	0.0400108894602	0.428571428571	B9D2 TMEM231 CC2D2A	bronchus; ciliated cells (ciliary rootlets)[>=Medium]
HP:0000175	0.0412176875551	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Cleft palate
HP:0012622	0.0412791464602	0.428571428571	CHRNA3 TMEM231 CC2D2A	Chronic kidney disease
REAC:R-HSA-1852241	0.0422635503964	0.428571428571	B9D2 CC2D2A TCTN1	Organelle biogenesis and maintenance
HP:0000648	0.0437930719501	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Optic atrophy
HP:0002921	0.0451244081745	0.571428571429	B9D2 TCTN1 TMEM231 CC2D2A	Abnormal cerebrospinal fluid morphology

Edges

Protein 1	Protein 2	Score	ProteomeHD	Evidence
B9D2	TMEM231	0.999		bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM boldt bioplex3_HCT116 boldt_WMM
CC2D2A	TCTN1	0.999		bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM bioplex3_HCT116
B9D2	TCTN1	0.999		bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM bioplex3_HCT116
TMEM231	TCTN1	0.997		bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM boldt bioplex3_HCT116 boldt_WMM
B9D2	CC2D2A	0.997		bioplex3_HEK293 bioplex_WMM bioplex3_WMM gupta () bioplex3_HCT116
ASIC2	TMEM231	0.989		bioplex3_WMM bioplex3_HCT116 WMM_only
TMEM231	TMEM17	0.988		bioplex3_WMM bioplex3_HCT116 WMM_only
TMEM231	CC2D2A	0.984	0.074	bioplex_WMM bioplex3_WMM bioplex3_HCT116 WMM_only
CHRNA3	TMEM231	0.967		bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM
B9D2	TMEM17	0.902		bioplex3_WMM gupta ()
CC2D2A	TMEM17	0.902		bioplex3_WMM WMM_only
TMEM17	TCTN1	0.607		bioplex3_WMM WMM_only

Related Complexes

Genename	Complexes
B9D2	huMAP3_03061.1 huMAP3_08282.1 huMAP3_09116.1 huMAP3_11588.1 huMAP3_14119.1 huMAP3_15177.1
TMEM231	huMAP3_03061.1 huMAP3_07211.1 huMAP3_08282.1 huMAP3_09416.1 huMAP3_11588.1 huMAP3_14119.1 huMAP3_14700.1
CC2D2A	huMAP3_03061.1 huMAP3_08282.1 huMAP3_09116.1 huMAP3_11588.1 huMAP3_14119.1 huMAP3_15177.1
ASIC2	huMAP3_00129.1 huMAP3_02656.1 huMAP3_02911.1 huMAP3_03061.1 huMAP3_08031.1 huMAP3_08282.1 huMAP3_09416.1 huMAP3_10530.1 huMAP3_11089.1 huMAP3_11588.1 huMAP3_11974.1 huMAP3_12482.1 huMAP3_14990.1
TMEM17	huMAP3_03061.1 huMAP3_08282.1 huMAP3_09416.1 huMAP3_11588.1 huMAP3_14119.1 huMAP3_15177.1
CHRNA3	huMAP3_01325.1 huMAP3_03061.1 huMAP3_08075.1 huMAP3_08282.1 huMAP3_09416.1 huMAP3_11420.1 huMAP3_13682.1 huMAP3_15126.1
TCTN1	huMAP3_03061.1 huMAP3_08282.1 huMAP3_09116.1

hu.MAP 3.0: Complex View

Search for a protein

Complex: huMAP3_08282.1

Complex Portal: CPX-17044