PKHD1L1 (PKHD1 like 1)

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Gene miRNA Gene ontology Other IDs Protein Associated diseases Related genes Diseases linked via similar genes

Gene

• Entrez ID: 93035
• Gene name: PKHD1 like 1
• Gene symbol: PKHD1L1
• Synonyms (NCBI Gene): DFNB124, PKHDL1
• Chromosome: 8
• Chromosome location: 8q23.1-q23.2

miRNA Show/Hide all (29)

miRTarBase ID	miRNA	Experiments	Reference
MIRT019202	hsa-miR-335-5p	Microarray	18185580
MIRT662645	hsa-miR-3675-3p	HITS-CLIP	23824327
MIRT662644	hsa-miR-6887-3p	HITS-CLIP	23824327
MIRT662643	hsa-miR-6892-3p	HITS-CLIP	23824327
MIRT662642	hsa-miR-2276-5p	HITS-CLIP	23824327
MIRT662641	hsa-miR-3183	HITS-CLIP	23824327
MIRT662640	hsa-miR-4723-3p	HITS-CLIP	23824327
MIRT662639	hsa-miR-6769b-3p	HITS-CLIP	23824327
MIRT662638	hsa-miR-4469	HITS-CLIP	23824327
MIRT662637	hsa-miR-6845-3p	HITS-CLIP	23824327
MIRT662636	hsa-miR-642a-5p	HITS-CLIP	23824327
MIRT662645	hsa-miR-3675-3p	HITS-CLIP	23824327
MIRT662644	hsa-miR-6887-3p	HITS-CLIP	23824327
MIRT662643	hsa-miR-6892-3p	HITS-CLIP	23824327
MIRT662642	hsa-miR-2276-5p	HITS-CLIP	23824327
MIRT662641	hsa-miR-3183	HITS-CLIP	23824327
MIRT662640	hsa-miR-4723-3p	HITS-CLIP	23824327
MIRT662639	hsa-miR-6769b-3p	HITS-CLIP	23824327
MIRT662638	hsa-miR-4469	HITS-CLIP	23824327
MIRT662637	hsa-miR-6845-3p	HITS-CLIP	23824327
MIRT662636	hsa-miR-642a-5p	HITS-CLIP	23824327
MIRT1237480	hsa-miR-1244	CLIP-seq
MIRT1237481	hsa-miR-1289	CLIP-seq
MIRT739534	hsa-miR-1323	CLIP-seq
MIRT1237482	hsa-miR-3677-5p	CLIP-seq
MIRT1237483	hsa-miR-370	CLIP-seq
MIRT739536	hsa-miR-3978	CLIP-seq
MIRT739537	hsa-miR-4760-5p	CLIP-seq
MIRT739535	hsa-miR-548o	CLIP-seq

Gene ontology (GO) Show/Hide all (12)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005615	Component	Extracellular space	NAS	12620974
GO:0005829	Component	Cytosol	TAS	21208571
GO:0005886	Component	Plasma membrane	IEA
GO:0006955	Process	Immune response	NAS	12620974
GO:0007605	Process	Sensory perception of sound	IEA
GO:0016020	Component	Membrane	IEA
GO:0016020	Component	Membrane	NAS	12620974
GO:0032426	Component	Stereocilium tip	IEA
GO:0038023	Function	Signaling receptor activity	NAS	12620974
GO:0042995	Component	Cell projection	IEA
GO:0060171	Component	Stereocilium membrane	IEA
GO:0120234	Component	Stereocilium coat	IEA

Other IDs

• MIM: 607843
• HGNC: 20313
• e!Ensembl: ENSG00000205038

Protein

• UniProt ID: Q86WI1
• Protein name: Fibrocystin-L (Polycystic kidney and hepatic disease 1-like protein 1) (PKHD1-like protein 1)
• Protein function: Component of hair-cell stereocilia coat. Required for normal hearing.
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF01833	TIG	146 → 255	IPT/TIG domain	Domain
  PF01833	TIG	1831 → 1910	IPT/TIG domain	Domain
  PF01833	TIG	2091 → 2176	IPT/TIG domain	Domain
  PF01833	TIG	1659 → 1743	IPT/TIG domain	Domain
  PF01833	TIG	1155 → 1236	IPT/TIG domain	Domain
  PF01833	TIG	1999 → 2085	IPT/TIG domain	Domain
  PF01833	TIG	270 → 356	IPT/TIG domain	Domain
  PF01833	TIG	1916 → 1997	IPT/TIG domain	Domain
  PF01833	TIG	1240 → 1325	IPT/TIG domain	Domain
  PF01833	TIG	1566 → 1650	IPT/TIG domain	Domain
  PF01833	TIG	1749 → 1830	IPT/TIG domain	Domain
  PF01833	TIG	1067 → 1151	IPT/TIG domain	Domain
  PF01833	TIG	1330 → 1402	IPT/TIG domain	Domain
  PF01833	TIG	31 → 130	IPT/TIG domain	Domain
  PF07691	PA14	341 → 490	PA14 domain	Domain
  PF10162	G8	2185 → 2303	G8 domain	Domain
  PF10162	G8	3037 → 3173	G8 domain	Domain

• Sequence:

  MGHLWLLGIWGLCGLLLCAADPSTDGSQIIPKVTEIIPKYGSINGATRLTIRGEGFSQAN
  QFNYGVDNAELGNSVQLISSFQSITCDVEKDASHSTQITCYTRAMPEDSYTVRVSVDGVP
  VTENNTCKGHINSWECTFNAKSFRTPTIRSITPLSGTPGTLITIQGRIFTDVYGSNIALS
  SNGKNVRILRVYIGGMPCELLIPQSDNLYGLKLDHPNGDMGSMVCKTTGTFIGHHNVSFI
  LDNDYGRSFPQKMAYFVSSLNKIAMFQTYAEVTMIFPSQGSIRGGTTLTISGRFFDQTDF
  PVRVLVGGEPCDILNVTENSICCKTPPKPHILKTVYPGGRGLKLEVWNNSRPIRLEEILE
  YNEKTPGYMGASWVDSASYIWLMEQDTFVARFSGFLVAPDSDVYRFYIKGDDRYAIYFSQ
  TGLPEDKVRIAYHSANANSYFSSPTQRSDDIHLQKGKEYYIEILLQEYRLSAFVDVGLYQ
  YRNVYTEQQTGDAVNEEQVIKSQSTILQEVQVITLENWETTNAINEVQKIKVTSPCVEAN
  SCSLYQYRLIYNMEKTVFLPADASEFILQSALNDLWSIKPDTVQVIRTQNPQSYVYMVTF
  ISTRGDFDLLGYEVVEGNNVTLDITEQTKGKPNLETFTLNWDGIASKPLTLWSSEAEFQG
  AVEEMVSTKCPPQIANFEEGFVVKYFRDYETDFNLEHINRGQKTAETDAYCGRYSLKNPA
  VLFDSADVKPNRRPYGDILLFPYNQLCLAYKGFLANYIGLKFQYQDNSKITRSTDTQFTY
  NFAYGNNWTYTCIDLLDLVRTKYTGTNVSLQRISLHKASESQSFYVDVVYIGHTSTISTL
  DEMPKRRLPALANKGIFLEHFQVNQTKTNGPTMTNQYSVTMTSYNCSYNIPMMAVSFGQI
  ITHETENEFVYRGNNWPGESKIHIQRIQAASPPLSGSFDIQAYGHILKGLPAAVSAADLQ
  FALQSLEGMGRISVTREGTCAGYAWNIKWRSTCGKQNLLQINDSNIIGEKANMTVTRIKE
  GGLFRQHVLGDLLRTPSQQPQVEVYVNGIPAKCSGDCGFTWDSNITPLVLAISPSQGSYE
  EGTILTIVGSGFSPSSAVTVSVGPVGCSLLSVDEKELKCQILNGSAGHAPVAVSMADVGL
  AQNVGGEEFYFVYQSQISHIWPDSGSIAGGTLLTLSGFGFNENSKVLVGNETCNVIEGDL
  NRITCRTPKKTEGTVDISVTTNGFQATARDAFSYNCLQTPIITDFSPKVRTILGEVNLTI
  KGYNFGNELTQNMAVYVGGKTCQILHWNFTDIRCLLPKLSPGKHDIYVEVRNWGFASTRD
  KLNSSIQYVLEVTSMFPQRGSLFGGTEITIRGFGFSTIPAENTVLLGSIPCNVTSSSENV
  IKCILHSTGNIFRITNNGKDSVHGLGYAWSPPVLNVSVGDTVAWHWQTHPFLRGIGYRIF
  SVSSPGSVIYDGKGFTSGRQKSTSGSFSYQFTSPGIHYYSSGYVDEAHSIFLQGVINVLP
  AETRHIPLHLFVGRSEATYAYGGPENLHLGSSVAGCLATEPLCSLNNTRVKNSKRLLFEV
  SSCFSPSISNITPSTGTVNELITIIGHGFSNLPWANKVTIGSYPCVVEESSEDSITCHID
  PQNSMDVGIRETVTLTVYNLGTAINTLSNEFDRRFVLLPNIDLVLPNAGSTTGMTSVTIK
  GSGFAVSSAGVKVLMGHFPCKVLSVNYTAIECETSPAAQQLVDVDLLIHGVPAQCQGNCT
  FSYLESITPYITGVFPNSVIGSVKVLIEGEGLGTVLEDIAVFIGNQQFRAIEVNENNITA
  LVTPLPVGHHSVSVVVGSKGLALGNLTVSSPPVASLSPTSGSIGGGTTLVITGNGFYPGN
  TTVTIGDEPCQIISINPNEVYCRTPAGTTGMVDVKIFVNTIAYPPLLFTYALEDTPFLRG
  IIPSRGPPGTEIEITGSNFGFEILEISVMINNIQCNVTMANDSVVQCIVGDHAGGTFPVM
  MHHKTKGSAMSTVVFEYPLNIQNINPSQGSFGGGQTMTVTGTGFNPQNSIILVCGSECAI
  DRLRSDYTTLLCEIPSNNGTGAEQACEVSVVNGKDLSQSMTPFTYAVSLTPLITAVSPKR
  GSTAGGTRLTVVGSGFSENMEDVHITIAEAKCDVEYSNKTHIICMTDAHTLSGWAPVCVH
  IRGVGMAKLDNADFLYVDAWSSNFSWGGKSPPEEGSLVVITKGQTILLDQSTPILKMLLI
  QGGTLIFDEADIELQAENILITDGGVLQIGTETSPFQHKAVITLHGHLRSPELPVYGAKT
  LAVREGILDLHGVPVPVTWTRLAHTAKAGERILILQEAVTWKPGDNIVIASTGHRHSQGE
  NEKMTIASVSADGINITLSNPLNYTHLGITVTLPDGTLFEARAEVGILTRNILIRGSDNV
  EWNNKIPACPDGFDTGEFATQTCLQGKFGEEIGSDQFGGCVMFHAPVPGANMVTGRIEYV
  EVFHAGQAFRLGRYPIHWHLLGDLQFKSYVRGCAIHQAYNRAVTIHNTHHLLVERNIIYD
  IKGGAFFIEDGIEHGNILQYNLAVFVQQSTSLLNDDVTPAAFWVTNPNNTIRHNAVAGGT
  HFGFWYRMNNHPDGPSYDRNICQKRVPLGEFFNNTVHSQGWFGMWIFEEYFPMQTGSCTS
  TVPAPAIFNSLTTWNCQKGAEWVNGGALQFHNFVMVNNYEAGIETKRILAPYVGGWGETN
  GAVIKNAKIVGHLDELGMGSAFCTAKGLVLPFSEGLTVSSVHFMNFDRPNCVALGVTSIS
  GVCNDRCGGWSAKFVDVQYSHTPNKAGFRWEHEMVMIDVDGSLTGHKGHTVIPHSSLLDP
  SHCTQEAEWSIGFPGSVCDASVSFHRLAFNQPSPVSLLEKDVVLSDSFGTSIIPFQKKRL
  THMSGWMALIPNANHINWYFKGVDHITNISYTSTFYGFKEEDYVIISHNFTQNPDMFNII
  DMRNGSSNPLNWNTSKNGDWHLEANTSTLYYLVSGRNDLHQSQLISGNLDPDVKDVVINF
  QAYCCILQDCFPVHPPSRKPIPKKRPATYNLWSNDSFWQSSRENNYTVPHPGANVIIPEG
  TWIVADIDMPSMERLIIWGVLELEDKYNVGAAESSYREVVLNATYISLQGGRLIGGWEDN
  PFKGDLKIVLRGNHTTQDWALPEGPNQGAKVLGVFGELDLHGIPHSIYKTKLSETAFAGS
  KVLSLMDAVDWQEGEEIVITTTSYDFHQTETRSIVKILHDHKILILNDSLSYTHFAEKYH
  VPGTGESYTLAADVGILSRNIKIVGEDYPGWSEDSFGARVLVGSFTENMMTFKGNARISN
  VEFYHSGQEGFRDSTDPRYAVTFLNLGQIQEHGSSYIRGCAFHHGFSPAIGVFGTDGLDI
  DDNIIHFTVGEGIRIWGNANRVRGNLIALSVWPGTYQNRKDLSSTLWHAAIEINRGTNTV
  LQNNVVAGFGRAGYRIDGEPCPGQFNPVEKWFDNEAHGGLYGIYMNQDGLPGCSLIQGFT
  IWTCWDYGIYFQTTESVHIYNVTLVDNGMAIFPMIYMPAAISHKISSKNVQIKSSLIVGS
  SPGFNCSDVLTNDDPNIELTAAHRSPRSPSGGRSGICWPTFASAHNMAPRKPHAGIMSYN
  AISGLLDISGSTFVGFKNVCSGETNVIFITNPLNEDLQHPIHVKNIKLVDTTEQSKIFIH
  RPDISKVNPSDCVDMVCDAKRKSFLRDIDGSFLGNAGSVIPQAEYEWDGNSQVGIGDYRI
  PKAMLTFLNGSRIPVTEKAPHKGIIRDSTCKYLPEWQSYQCFGMEYAMMVIESLDPDTET
  RRLSPVAIMGNGYVDLINGPQDHGWCAGYTCQRRLSLFHSIVALNKSYEVYFTGTSPQNL
  RLMLLNVDHNKAVLVGIFFSTLQRLDVYVNNLLVCPKTTIWNAQQKHCELNNHLYKDQFL
  PNLDSTVLGENYFDGTYQMLYLLVKGTIPVEIHTATVIFVSFQLSVATEDDFYTSHNLVK
  NLALFLKIPSDKIRISKIRGKSLRRKRSMGFIIEIEIGDPPIQFISNGTTGQMQLSELQE
  IAGSLGQAVILGNISSILGFNISSMSITNPLPSPSDSGWIKVTAQPVERSAFPVHHVAFV
  SSLLVITQPVAAQPGQPFPQQPSVKATDSDGNCVSVGITALTLRAILKDSNNNQVNGLSG
  NTTIPFSSCWANYTDLTPLRTGKNYKIEFILDNVVGVESRTFSLLAESVSSSGSSSSSNS
  KASTVGTYAQIMTVVISCLVGRMWLLEIFMAAVSTLNITLRSY

• Sequence length: 4243

Associated diseases

Evidence Score:

• ★☆☆☆☆  Gene-disease association found in Text Mining only
• ★★☆☆☆  Found in Text Mining and Unknown/Other Associations
• ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources
• ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
• ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)

Causal
Phenotype Name	Clinical Significance	dbSNP ID	RCV Accession	Evidence Score
Autosomal recessive nonsyndromic hearing loss 124	Pathogenic	rs773702657, rs61745556, rs200149971, rs767753360, rs746243573	RCV004515819 RCV004515820 RCV004515821 RCV004515823 RCV004515824	★★★★★ ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)

Unknown / Other Associations Show/Hide Unknown Diseases (12)
Phenotype Name	Clinical Significance	Source	Reference	Evidence Score
AUTOSOMAL RECESSIVE ISOLATED SENSORINEURAL DEAFNESS TYPE DFNB	—	Disgenet	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DEAFNESS, AUTOSOMAL RECESSIVE	—	Disgenet	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DEAFNESS, AUTOSOMAL RECESSIVE 124	—	Disgenet, HPO Disgenet, HPO	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
FEMALE INFERTILITY	—	GWAS catalog	40229599	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus	Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MULTIPLE SYSTEM ATROPHY	—	GWAS catalog	27629089	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OBESITY	—	GWAS catalog	23251661	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Ovarian serous cystadenocarcinoma	Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
PKHD1L1-related disorder	Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SENSORINEURAL HEARING LOSS OF BILATERAL EARS	—	Disgenet	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Thyroid cancer, nonmedullary, 1	Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine corpus endometrial carcinoma	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining Show/Hide Text Mining Associations (12)
Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Autosomal Recessive Polycystic Kidney Disease	Polycystic kidney disease	BEFREE	31444330, 31452800		★☆☆☆☆ Found in Text Mining only
Colorectal Neoplasms	Colorectal neoplasm	Pubtator	40082818	Associate	★☆☆☆☆ Found in Text Mining only
Lymphatic Metastasis	Lymphatic metastasis	Pubtator	40265473	Associate	★☆☆☆☆ Found in Text Mining only
Malignant neoplasm of thyroid	Thyroid cancer	BEFREE	31452800		★☆☆☆☆ Found in Text Mining only
Melanoma Cutaneous Malignant	Melanoma	Pubtator	38203530	Inhibit	★☆☆☆☆ Found in Text Mining only
Neoplasms	Neoplasms	BEFREE	31452800		★☆☆☆☆ Found in Text Mining only
Papillary thyroid carcinoma	Papillary thyroid carcinoma	BEFREE	31452800		★☆☆☆☆ Found in Text Mining only
T-Cell Large Granular Lymphocyte Leukemia	T-cell Lymphocytic Leukemia	BEFREE	24649974		★☆☆☆☆ Found in Text Mining only
Thyroid Cancer Papillary	Papillary thyroid cancer	Pubtator	40265473	Associate	★☆☆☆☆ Found in Text Mining only
Thyroid carcinoma	Thyroid Carcinoma	BEFREE	31452800		★☆☆☆☆ Found in Text Mining only
Thyroid Carcinoma Anaplastic	Thyroid cancer	Pubtator	39984992	Stimulate	★☆☆☆☆ Found in Text Mining only
Thyroid Neoplasm	Thyroid Neoplasm	BEFREE	31452800		★☆☆☆☆ Found in Text Mining only

Related Genes

Sort by: Blended Diseases Pathways Evidence source

GPR156 3 shared diseasesIsolated sensorineural deafness, Nonsyndromic hearing loss, Deafness 4 shared evidence sourcesDisgenet (Isolated sensorineural deafness), Disgenet (Nonsyndromic hearing loss), Disgenet (Deafness), HPO (Deafness) Related via 3 shared diseases including Isolated sensorineural deafness, Nonsyndromic hearing loss — evidence mostly Disgenet. STX4 3 shared diseasesIsolated sensorineural deafness, Nonsyndromic hearing loss, Deafness 4 shared evidence sourcesDisgenet (Isolated sensorineural deafness), Disgenet (Nonsyndromic hearing loss), Disgenet (Deafness), HPO (Deafness) Related via 3 shared diseases including Isolated sensorineural deafness, Nonsyndromic hearing loss — evidence mostly Disgenet. GIPC3 3 shared diseasesIsolated sensorineural deafness, Nonsyndromic hearing loss, Deafness 5 shared evidence sourcesDisgenet (Isolated sensorineural deafness), Disgenet (Nonsyndromic hearing loss), ClinVar (Nonsyndromic hearing loss), Disgenet (Deafness), HPO (Deafness) Related via 3 shared diseases including Isolated sensorineural deafness, Nonsyndromic hearing loss — evidence mostly Disgenet. CCDC50 3 shared diseasesIsolated sensorineural deafness, Nonsyndromic hearing loss, Deafness 6 shared evidence sourcesDisgenet (Isolated sensorineural deafness), Disgenet (Nonsyndromic hearing loss), ClinVar (Nonsyndromic hearing loss), GenCC (Nonsyndromic hearing loss), Disgenet (Deafness), HPO (Deafness) Related via 3 shared diseases including Isolated sensorineural deafness, Nonsyndromic hearing loss — evidence mostly Disgenet. TMTC4 3 shared diseasesIsolated sensorineural deafness, Nonsyndromic hearing loss, Deafness 4 shared evidence sourcesDisgenet (Isolated sensorineural deafness), Disgenet (Nonsyndromic hearing loss), Disgenet (Deafness), HPO (Deafness) Related via 3 shared diseases including Isolated sensorineural deafness, Nonsyndromic hearing loss — evidence mostly Disgenet.

Related Gene	Shared Diseases	Shared Disease Names	Shared Pathways	Shared Pathway Names	Shared Evidence Sources	Shared Evidence Names
GPR156	3	["Isolated sensorineural deafness","Nonsyndromic hearing loss","Deafness"]	0	[]	4	["Disgenet (Isolated sensorineural deafness)","Disgenet (Nonsyndromic hearing loss)","Disgenet (Deafness)","HPO (Deafness)"]
STX4	3	["Isolated sensorineural deafness","Nonsyndromic hearing loss","Deafness"]	0	[]	4	["Disgenet (Isolated sensorineural deafness)","Disgenet (Nonsyndromic hearing loss)","Disgenet (Deafness)","HPO (Deafness)"]
GIPC3	3	["Isolated sensorineural deafness","Nonsyndromic hearing loss","Deafness"]	0	[]	5	["Disgenet (Isolated sensorineural deafness)","Disgenet (Nonsyndromic hearing loss)","ClinVar (Nonsyndromic hearing loss)","Disgenet (Deafness)","HPO (Deafness)"]
CCDC50	3	["Isolated sensorineural deafness","Nonsyndromic hearing loss","Deafness"]	0	[]	6	["Disgenet (Isolated sensorineural deafness)","Disgenet (Nonsyndromic hearing loss)","ClinVar (Nonsyndromic hearing loss)","GenCC (Nonsyndromic hearing loss)","Disgenet (Deafness)","HPO (Deafness)"]
TMTC4	3	["Isolated sensorineural deafness","Nonsyndromic hearing loss","Deafness"]	0	[]	4	["Disgenet (Isolated sensorineural deafness)","Disgenet (Nonsyndromic hearing loss)","Disgenet (Deafness)","HPO (Deafness)"]

Diseases Linked via Similar Genes

Hearing loss Linked via 4 of 5 related genesGPR156, STX4, GIPC3, TMTC4 Psoriasis Linked via 2 of 5 related genesSTX4, TMTC4 nonsyndromic genetic hearing loss Linked via 2 of 5 related genesGIPC3, CCDC50 Diabetes mellitus type 2 Linked via 1 of 5 related genesSTX4 Alzheimer disease Linked via 1 of 5 related genesGIPC3

Disease	Linked Via (Gene Count)	Linked Via (Gene Names)
Hearing loss	4	["GPR156","STX4","GIPC3","TMTC4"]
Psoriasis	2	["STX4","TMTC4"]
nonsyndromic genetic hearing loss	2	["GIPC3","CCDC50"]
Diabetes mellitus type 2	1	["STX4"]
Alzheimer disease	1	["GIPC3"]