AiPD: Autoinhibited Protein Database

Q86UD1

Gene name	OAF (NS5ATP13TP2)
Protein name	Out at first protein homolog
Names	HCV NS5A-transactivated protein 13 target protein 2
Species	Homo sapiens (Human)
KEGG Pathway	hsa:220323
EC number
Protein Class

Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

1-86 (Predicted disordered autoinhibitory region) PR

Target domain
Relief mechanism
Assay	cis-regPred

AID

1-86 (Predicted disordered autoinhibitory region)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

References

Yeon JH et al. (2016) "Systems-wide Identification of cis-Regulatory Elements in Proteins", Cell Systems, 2, 89-100

Autoinhibited structure

Activated structure

1 structures for Q86UD1

Entry ID	Method	Resolution	Chain	Position	Source
AF-Q86UD1-F1	Predicted				AlphaFoldDB

250 variants for Q86UD1

Variant ID(s)	Position	Change	Description	Diseaes Association	Provenance
rs1393353919 CA382987733	2	R>S		No	ClinGen gnomAD
rs1471720941 CA382987742	3	L>H		No	ClinGen TOPMed
rs1410847616 CA382987747	4	P>S		No	ClinGen TOPMed gnomAD
rs1488164224 CA382987767	7	P>H		No	ClinGen TOPMed
rs1307843989 CA382987763	7	P>T		No	ClinGen gnomAD
rs1335222390 CA382987782	10	R>C		No	ClinGen TOPMed gnomAD
CA382987780 rs1335222390	10	R>S		No	ClinGen TOPMed gnomAD
CA6322931 rs776338575	12	A>S		No	ClinGen ExAC gnomAD
CA382987792 rs776338575	12	A>T		No	ClinGen ExAC gnomAD
CA382987814 rs1395739814	16	L>Q		No	ClinGen TOPMed
TCGA novel	17	L>V	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA382987825 rs1303142798	18	P>L		No	ClinGen TOPMed gnomAD
rs950503738 CA229702962	20	L>F		No	ClinGen TOPMed gnomAD
rs1591356583 CA382987843	21	A>V		No	ClinGen Ensembl
CA382987847 rs1360716538	22	P>Q		No	ClinGen TOPMed gnomAD
CA6322934 rs376205535	26	T>K		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA382987870 rs376205535	26	T>M		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
rs1211446065 CA382987872	27	G>C		No	ClinGen gnomAD
rs538541142 CA6322935	27	G>V		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
rs1479857230 CA382987876	28	A>T		No	ClinGen gnomAD
rs1463335170 CA382987881	28	A>V		No	ClinGen TOPMed
CA382987885 rs1269655072	29	P>L		No	ClinGen TOPMed
rs1311149738 CA382987896	31	E>*		No	ClinGen TOPMed
CA229702998 rs367611125	31	E>D		No	ClinGen Ensembl
CA382987907 rs1250579176	33	R>W		No	ClinGen gnomAD
rs1422446026 CA382987919	35	R>C		No	ClinGen gnomAD
rs1413778080 CA382987920	35	R>H		No	ClinGen gnomAD
rs1422446026 CA382987917	35	R>S		No	ClinGen gnomAD
rs1407733720 CA382987926	36	V>G		No	ClinGen gnomAD
CA6322937 rs763181491	36	V>L		No	ClinGen ExAC gnomAD
CA6322938 rs763181491	36	V>M		No	ClinGen ExAC gnomAD
rs751704055 CA6322939	37	R>Q		No	ClinGen ExAC gnomAD
CA382987934 rs1351289165	38	L>P		No	ClinGen gnomAD
rs532033758 CA229703030	39	P>A		No	ClinGen Ensembl
CA6322940 rs550463179	39	P>L		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA382987939 rs550463179	39	P>R		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA6322941 rs568473213	40	D>Y		No	ClinGen 1000Genomes ExAC gnomAD
TCGA novel	41	G>S	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs752703302 CA6322942	42	Q>R		No	ClinGen ExAC TOPMed gnomAD
rs1340720551 CA382987962	43	V>M		No	ClinGen TOPMed gnomAD
rs1038972926 CA229703062	45	E>G		No	ClinGen TOPMed
CA382987973 rs1289709935	45	E>K	Variant assessed as Somatic; impact. [NCI-TCGA]	No	ClinGen NCI-TCGA TOPMed
CA382988001 rs1183912757	49	Q>E		No	ClinGen TOPMed gnomAD
CA382988002 rs1183912757	49	Q>K		No	ClinGen TOPMed gnomAD
rs1187801329 CA382988011	50	A>E		No	ClinGen TOPMed
CA382988014 rs1477405493	51	D>N		No	ClinGen gnomAD
rs1591356644 CA382988032	53	D>Y		No	ClinGen Ensembl
rs758096188 CA6322947	54	A>V		No	ClinGen ExAC gnomAD
rs1591356647 CA382988046	55	D>G		No	ClinGen Ensembl
CA382988056 rs1167686631	56	S>I		No	ClinGen gnomAD
rs1167686631 CA382988054	56	S>N		No	ClinGen gnomAD
CA229703128 rs1042767814	56	S>R		No	ClinGen Ensembl
rs1591356658 CA382988069	58	S>N		No	ClinGen Ensembl
rs746646677 CA6322949	58	S>R		No	ClinGen ExAC gnomAD
CA382988070 rs1431801348	58	S>R		No	ClinGen gnomAD
CA382988089 rs1321817550	61	L>P		No	ClinGen gnomAD
rs1321817550 CA382988088	61	L>Q		No	ClinGen gnomAD
rs768490831 CA6322950	62	R>C		No	ClinGen ExAC TOPMed gnomAD
rs768490831 CA382988091	62	R>S		No	ClinGen ExAC TOPMed gnomAD
CA382988096 rs1298982093	63	K>Q		No	ClinGen TOPMed gnomAD
rs776429214 CA6322951	64	P>S		No	ClinGen ExAC gnomAD
rs1363588918 CA382988115	65	D>E		No	ClinGen gnomAD
CA6322952 rs747605497	66	G>S		No	ClinGen ExAC gnomAD
CA6322953 rs769370556	67	T>S		No	ClinGen ExAC TOPMed gnomAD
rs773555799 CA6322954	69	V>I		No	ClinGen ExAC gnomAD
CA229703186 rs761869786	73	A>T		No	ClinGen Ensembl
CA6322959 rs186811345	74	D>N		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA6322960 rs558880898	75	F>L		No	ClinGen 1000Genomes ExAC gnomAD
rs1390774916 CA382988182	76	K>R		No	ClinGen gnomAD
CA382988412 rs1421507207	79	V>L		No	ClinGen gnomAD
CA382988435 rs1431057802	81	V>I		No	ClinGen TOPMed
rs1341459465 CA382988448	82	F>L		No	ClinGen TOPMed gnomAD
rs896667803 CA229715429	83	R>Q	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen NCI-TCGA TOPMed gnomAD
rs141895960 CA6322977	83	R>W		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA6322979 rs775722950	84	A>T		No	ClinGen ExAC TOPMed gnomAD
rs565827586 CA6322980	85	L>R		No	ClinGen 1000Genomes ExAC gnomAD
rs766480346 CA6322984	94	Q>H		No	ClinGen ExAC TOPMed gnomAD
CA6322983 rs761793474	94	Q>R		No	ClinGen ExAC TOPMed gnomAD
rs751518135 CA6322985	95	S>R		No	ClinGen ExAC gnomAD
CA6322986 rs150612328	96	Q>R		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs781090802 CA6322987	98	Q>*		No	ClinGen ExAC gnomAD
CA382988635 rs1464940239	99	A>G		No	ClinGen gnomAD
TCGA novel	101	C>*	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA382988648 rs1172480901	101	C>F		No	ClinGen gnomAD
CA382988646 rs1172480901	101	C>Y		No	ClinGen gnomAD
rs752417239 CA6322988	103	V>I		No	ClinGen ExAC TOPMed gnomAD
rs1348173628 CA382988666	104	T>A		No	ClinGen gnomAD
CA6322989 rs367715451	104	T>I		No	ClinGen ESP ExAC TOPMed gnomAD
CA382988675 rs1406882492	105	Q>H		No	ClinGen gnomAD
rs777291216 CA6322990	106	L>M		No	ClinGen ExAC TOPMed gnomAD
rs1591360665 CA382988688	107	Q>R		No	ClinGen Ensembl
rs1230493594 CA382988717	109	N>T		No	ClinGen gnomAD
rs1255338346 CA382988739 CA382988737	110	E>D		No	ClinGen gnomAD
rs371279928 CA6322991	111	I>V		No	ClinGen ESP ExAC gnomAD
CA229715583 rs886759316	112	I>V	Variant assessed as Somatic; impact. [NCI-TCGA]	No	ClinGen NCI-TCGA TOPMed
CA382988785 rs1272217553	114	S>N		No	ClinGen gnomAD
rs779439439 CA6322993	114	S>R		No	ClinGen ExAC gnomAD
rs1183187871 CA382988810	116	A>G		No	ClinGen gnomAD
CA229715613 rs1003874844	116	A>T		No	ClinGen TOPMed
CA382988812 rs1183187871	116	A>V	Variant assessed as Somatic; impact. [NCI-TCGA]	No	ClinGen NCI-TCGA gnomAD
CA382988828 rs1252984657	117	M>I		No	ClinGen gnomAD
CA229715644 rs1015665240	117	M>T		No	ClinGen Ensembl
CA382988843 rs1335346508	119	K>E		No	ClinGen gnomAD
CA382988864 rs1431478862	120	L>P		No	ClinGen gnomAD
CA6322996 rs376270711	121	R>Q	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen 1000Genomes ESP ExAC NCI-TCGA TOPMed gnomAD
rs749392944 CA6322995	121	R>W		No	ClinGen ExAC TOPMed gnomAD
rs1167025965 CA382988885	122	Q>R		No	ClinGen gnomAD
rs1173971800 CA382989045	124	N>S		No	ClinGen TOPMed
rs776950790 CA6323020	125	P>S	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
CA6323023 rs773363476	126	R>Q	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
rs147440018 CA6323022 COSM1351921	126	R>W	large_intestine [Cosmic]	No	ClinGen cosmic curated ESP ExAC TOPMed gnomAD
rs767623985 CA6323025	127	A>E		No	ClinGen ExAC gnomAD
CA6323024 rs759546390	127	A>P		No	ClinGen ExAC gnomAD
CA382989065 rs1421638275	128	V>A		No	ClinGen gnomAD
rs1418172517 CA382989069	129	R>P		No	ClinGen TOPMed gnomAD
rs1418172517 CA382989068	129	R>Q	Variant assessed as Somatic; 9.371e-05 impact. [NCI-TCGA]	No	ClinGen NCI-TCGA TOPMed gnomAD
rs200957652 CA6323027	129	R>W		No	ClinGen ExAC TOPMed gnomAD
CA6323028 rs879007742	131	A>G		No	ClinGen TOPMed gnomAD
CA6323029 rs879007742	131	A>V		No	ClinGen TOPMed gnomAD
rs756846378 CA6323033	132	E>G		No	ClinGen ExAC gnomAD
CA6323032 rs753552892	132	E>K		No	ClinGen ExAC gnomAD
CA382989092 rs764731731	133	E>A		No	ClinGen ExAC TOPMed gnomAD
rs1327564480 CA382989094	133	E>D		No	ClinGen TOPMed
rs764731731 CA6323035	133	E>G		No	ClinGen ExAC TOPMed gnomAD
rs750002128 CA6323036	134	V>F		No	ClinGen ExAC
CA6323037 rs757890745	134	V>G		No	ClinGen ExAC gnomAD
rs747441332 CA6323039	135	R>Q		No	ClinGen ExAC TOPMed gnomAD
CA6323038 rs145186688	135	R>W		No	ClinGen ESP ExAC TOPMed gnomAD
rs1226591355 CA382989111	136	G>D		No	ClinGen TOPMed gnomAD
CA382989107 rs1226591355	136	G>V		No	ClinGen TOPMed gnomAD
rs1330379864 CA382989120	137	L>P		No	ClinGen gnomAD
CA6323042 rs559289815	139	H>R		No	ClinGen 1000Genomes ExAC gnomAD
TCGA novel	140	L>M	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs770071046 CA6323043	142	M>I		No	ClinGen ExAC TOPMed gnomAD
rs1432103988 CA382989182	142	M>V	Variant assessed as Somatic; impact. [NCI-TCGA]	No	ClinGen NCI-TCGA TOPMed gnomAD
CA229716958 rs904668889	143	D>V		No	ClinGen Ensembl
CA6323045 rs749433430	145	A>S		No	ClinGen ExAC TOPMed gnomAD
rs749433430 CA229716973	145	A>T		No	ClinGen ExAC TOPMed gnomAD
CA6323047 rs775531621	147	N>S		No	ClinGen ExAC TOPMed gnomAD
CA6323048 rs775531621	147	N>T		No	ClinGen ExAC TOPMed gnomAD
CA6323049 rs113497939	148	F>C		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA382989247 rs113497939	148	F>S		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
TCGA novel	152	A>G	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
TCGA novel	152	A>P	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs776223244 CA6323050	152	A>S		No	ClinGen ExAC gnomAD
CA6323051 rs761591936	154	L>P		No	ClinGen ExAC gnomAD
rs772065124 CA382989300	157	H>N		No	ClinGen ExAC TOPMed gnomAD
CA6323054 rs757941904	157	H>Q		No	ClinGen ExAC TOPMed gnomAD
CA382989304 rs1357535253	157	H>R		No	ClinGen gnomAD
rs772065124 CA6323053	157	H>Y		No	ClinGen ExAC TOPMed gnomAD
CA6323055 rs765765008	159	H>P		No	ClinGen ExAC gnomAD
CA229717044 rs747799548	160	N>S		No	ClinGen Ensembl
CA6323057 rs375967354	161	V>M		No	ClinGen ExAC TOPMed gnomAD
rs1277114075 CA382989334	162	C>Y		No	ClinGen gnomAD
CA229717054 rs1024562348	163	A>P		No	ClinGen Ensembl
rs748586285 CA6323059	164	E>K	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
CA229717101 rs867204745	165	A>V		No	ClinGen Ensembl
CA6323061 rs778184167	166	V>M		No	ClinGen ExAC TOPMed gnomAD
rs1178493294 CA382989395	171	T>I		No	ClinGen gnomAD
CA382989390 rs1470197969	171	T>P		No	ClinGen gnomAD
CA6323062 rs140254492	172	R>C		No	ClinGen ESP ExAC TOPMed gnomAD
CA6323063 rs771067831	172	R>H	Variant assessed as Somatic; 9.344e-05 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA gnomAD
CA382989413 rs1377070600	174	E>V		No	ClinGen TOPMed gnomAD
CA6323066 rs768543253	177	R>Q		No	ClinGen ExAC TOPMed gnomAD
CA6323065 rs200189572	177	R>W		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs1462020438 CA382989688	185	D>G		No	ClinGen gnomAD
rs1167213794 CA382989693	186	S>G		No	ClinGen gnomAD
rs1282105771 CA382989709	188	V>E		No	ClinGen TOPMed gnomAD
CA382989719 rs1435055718	189	F>L		No	ClinGen TOPMed gnomAD
CA6323089 rs745994132	190	E>K		No	ClinGen ExAC gnomAD
rs745994132 CA382989721	190	E>Q		No	ClinGen ExAC gnomAD
CA382989728 rs1565344283	191	A>P		No	ClinGen Ensembl
rs1437674138 CA382989748	194	K>R		No	ClinGen TOPMed
rs1591361646 CA382989754	195	A>T		No	ClinGen Ensembl
rs372887924 CA6323091	199	A>V	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ESP ExAC NCI-TCGA gnomAD
rs1219619461 CA382989788	200	E>A		No	ClinGen gnomAD
rs769597846 CA6323093	203	R>C		No	ClinGen ExAC TOPMed gnomAD
CA6323094 rs772930917	207	V>G		No	ClinGen ExAC gnomAD
CA229719000 rs377006820	207	V>M		No	ClinGen ESP gnomAD
CA6323095 rs762669044	208	G>W		No	ClinGen ExAC
rs1591361666 CA382989845	209	D>G		No	ClinGen Ensembl
CA382989841 rs770552269	209	D>N		No	ClinGen ExAC gnomAD
CA6323096 rs770552269	209	D>Y		No	ClinGen ExAC gnomAD
CA382989852 rs2508489	210	H>L		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs1185224365 CA382989848	210	H>N		No	ClinGen gnomAD
rs2508489 CA382989851	210	H>P		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
VAR_032993 rs2508489 CA6323097	210	H>R		No	ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD
TCGA novel	210	H>Y	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs759011534 CA6323098	211	G>R		No	ClinGen ExAC gnomAD
rs759011534 CA382989856	211	G>W		No	ClinGen ExAC gnomAD
rs767017386 CA6323099	212	K>N	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA gnomAD
CA6323100 rs753281905	213	P>L		No	ClinGen ExAC gnomAD
CA6323102 rs149920245	214	C>*		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA6323103 rs138294086	215	V>I		No	ClinGen ESP ExAC TOPMed gnomAD
CA6323105 rs546311468	217	R>C		No	ClinGen 1000Genomes ExAC gnomAD
VAR_032994 rs2508490 CA6323106	217	R>H		No	ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD
CA6323104 rs546311468	217	R>S		No	ClinGen 1000Genomes ExAC gnomAD
CA382989906 rs1415050037	218	Y>C		No	ClinGen TOPMed gnomAD
rs758438096 CA6323107	218	Y>H		No	ClinGen ExAC TOPMed gnomAD
CA382989915 rs375396320	219	G>C		No	ClinGen gnomAD
CA229719133 rs375396320	219	G>S		No	ClinGen gnomAD
rs1237751649 CA382989941	221	S>N		No	ClinGen gnomAD
rs1164691031 CA382989956	223	A>P		No	ClinGen gnomAD
rs1591361706 CA382989990	225	Y>S		No	ClinGen Ensembl
rs538405203 CA229719143	226	P>A		No	ClinGen 1000Genomes
TCGA novel	226	P>L	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA229719144 rs901706274	228	M>I		No	ClinGen TOPMed
CA382990083 rs748088964	231	Y>*		No	ClinGen ExAC TOPMed gnomAD
rs755975922 CA6323111	234	S>G		No	ClinGen ExAC gnomAD
TCGA novel	234	S>I	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA229719181 rs766616644	235	R>C		No	ClinGen TOPMed gnomAD
CA6323112 rs777680684	235	R>H	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
rs770734523 CA6323114	236	D>H		No	ClinGen ExAC TOPMed gnomAD
rs770734523 CA382990142	236	D>N		No	ClinGen ExAC TOPMed gnomAD
rs745479682 CA6323116	237	R>Q	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
CA6323115 COSM3935343 rs368374827	237	R>W	oesophagus [Cosmic]	No	ClinGen cosmic curated ESP ExAC TOPMed gnomAD
rs1440884895 CA382990177	239	T>A		No	ClinGen TOPMed
rs771724362 CA6323117	239	T>M		No	ClinGen ExAC gnomAD
rs1591361731 CA382990203	241	Y>C		No	ClinGen Ensembl
rs760258411 CA6323119	241	Y>H		No	ClinGen ExAC gnomAD
rs139019085 CA6323120	242	K>E		No	ClinGen ESP ExAC gnomAD
rs1218721011 CA382990218	242	K>R		No	ClinGen TOPMed
rs142969345 CA6323123	246	R>C		No	ClinGen ESP ExAC gnomAD
rs750630893 CA6323124	246	R>H		No	ClinGen ExAC TOPMed gnomAD
rs1290104864 CA382990316	249	Q>R		No	ClinGen TOPMed
rs867444448 CA229719245	250	K>Q		No	ClinGen Ensembl
CA229719246 rs1011955810	250	K>R		No	ClinGen TOPMed
rs758586410 CA382990358	252	Y>D		No	ClinGen ExAC TOPMed gnomAD
CA6323125 rs758586410	252	Y>H		No	ClinGen ExAC TOPMed gnomAD
rs751702862 CA6323127	255	D>N		No	ClinGen ExAC TOPMed gnomAD
rs11545299 CA382990435	257	Y>C	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen NCI-TCGA gnomAD
CA229719256 rs11545299	257	Y>F		No	ClinGen gnomAD
rs11545299 CA382990434	257	Y>S		No	ClinGen gnomAD
rs1480438394 CA382990443	258	V>L		No	ClinGen gnomAD
rs1480438394 CA382990439	258	V>M		No	ClinGen gnomAD
CA382990454 rs749212923	259	P>S		No	ClinGen ExAC TOPMed gnomAD
rs749212923 CA6323130	259	P>T		No	ClinGen ExAC TOPMed gnomAD
CA6323133 rs745514310	260	Q>H		No	ClinGen ExAC TOPMed gnomAD
rs778714800 CA6323132	260	Q>R		No	ClinGen ExAC gnomAD
rs1396249004 CA382990491	262	Q>K		No	ClinGen gnomAD
rs143774863 CA6323135	263	L>R		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs1298207929 CA382990549	266	W>*		No	ClinGen gnomAD
rs1461202729 CA382990540	266	W>R		No	ClinGen gnomAD
rs768251643 CA6323137	267	D>G		No	ClinGen ExAC TOPMed gnomAD
rs768251643 CA382990559	267	D>V		No	ClinGen ExAC TOPMed gnomAD
rs1438131967 COSM1171754 CA382990565	268	E>K	oesophagus [Cosmic]	No	ClinGen cosmic curated gnomAD
rs1371716800 CA382990592	269	D>E		No	ClinGen TOPMed gnomAD
TCGA novel	269	D>V	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA382990583 rs1325133880	269	D>Y		No	ClinGen gnomAD
rs777035631 CA6323138	272	P>R		No	ClinGen ExAC gnomAD

No associated diseases with Q86UD1

No regional properties for Q86UD1

Type	Name	Position	InterPro Accession
No domain, repeats, and functional sites for Q86UD1

Functions

		Description
EC Number
Subcellular Localization
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category	No pathway information available

No GO annotations of cellular component

Name	Definition
No GO annotations for cellular component

No GO annotations of molecular function

Name	Definition
No GO annotations for molecular function

No GO annotations of biological process

Name	Definition
No GO annotations for biological process

1 homologous proteins in AiPD

UniProt AC	Gene Name	Protein Name	Species	Evidence Code
Q6AYE5	Oaf	Out at first protein homolog	Rattus norvegicus (Rat)	PR

10	20	30	40	50	60
MRLPGVPLAR	PALLLLLPLL	APLLGTGAPA	ELRVRVRLPD	GQVTEESLQA	DSDADSISLE
70	80	90	100	110	120
LRKPDGTLVS	FTADFKKDVK	VFRALILGEL	EKGQSQFQAL	CFVTQLQHNE	IIPSEAMAKL
130	140	150	160	170	180
RQKNPRAVRQ	AEEVRGLEHL	HMDVAVNFSQ	GALLSPHLHN	VCAEAVDAIY	TRQEDVRFWL
190	200	210	220	230	240
EQGVDSSVFE	ALPKASEQAE	LPRCRQVGDH	GKPCVCRYGL	SLAWYPCMLK	YCHSRDRPTP
250	260	270
YKCGIRSCQK	SYSFDFYVPQ	RQLCLWDEDP	YPG