AiPD: Autoinhibited Protein Database

Q9Y365

Gene name	STARD10 (SDCCAG28, CGI-52)
Protein name	START domain-containing protein 10
Names	StARD10, Antigen NY-CO-28, PCTP-like protein, PCTP-L, Serologically defined colon cancer antigen 28, StAR-related lipid transfer protein 10
Species	Homo sapiens (Human)
KEGG Pathway	hsa:10809
EC number
Protein Class

Descriptions

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

Autoinhibitory domains (AIDs)

244-291 (Predicted disordered autoinhibitory region) PR

Target domain
Relief mechanism
Assay	cis-regPred

AID

244-291 (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

2 structures for Q9Y365

Entry ID	Method	Resolution	Chain	Position	Source
6SER	X-ray	230 A	A	1-291	PDB
AF-Q9Y365-F1	Predicted				AlphaFoldDB

246 variants for Q9Y365

Variant ID(s)	Position	Change	Description	Diseaes Association	Provenance
rs1490595198	1	M>?	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA381781981 rs1266885792	3	K>N		No	ClinGen TOPMed
rs758656594 CA6174723	3	K>R		No	ClinGen ExAC gnomAD
CA224450947 rs955671754	4	L>P		No	ClinGen TOPMed
CA6174722 rs370360543	5	A>E		No	ClinGen ESP ExAC gnomAD
rs370360543 CA381781957	5	A>V		No	ClinGen ESP ExAC gnomAD
rs779879606 CA6174721	7	S>C		No	ClinGen ExAC
rs1433337447 CA381781933	8	T>K		No	ClinGen gnomAD
CA381781920 rs1327460358	10	P>S		No	ClinGen gnomAD
rs997067060 CA224450938	11	Q>*		No	ClinGen TOPMed gnomAD
rs997067060 CA381781915	11	Q>E		No	ClinGen TOPMed gnomAD
rs750273663 CA6174719	11	Q>R		No	ClinGen ExAC gnomAD
CA6174718 rs767515766	12	G>W		No	ClinGen ExAC TOPMed gnomAD
rs962855351 CA381781885	13	P>L		No	ClinGen TOPMed gnomAD
rs962855351 CA224450932	13	P>R		No	ClinGen TOPMed gnomAD
rs1591270771 CA381781887	13	P>S		No	ClinGen Ensembl
CA381781870 rs1424969488	14	R>Q		No	ClinGen TOPMed gnomAD
CA6174716 rs556176957	15	P>A		No	ClinGen 1000Genomes ExAC gnomAD
rs1591270765 CA381781839	16	V>A		No	ClinGen Ensembl
CA6174711 rs759957038	18	G>A		No	ClinGen ExAC gnomAD
rs775994344 CA6174713	18	G>C		No	ClinGen ExAC TOPMed gnomAD
CA6174712 rs759957038	18	G>D		No	ClinGen ExAC gnomAD
CA381781820 rs775994344	18	G>S		No	ClinGen ExAC TOPMed gnomAD
CA6174710 rs776954053	19	R>H		No	ClinGen ExAC gnomAD
CA6174709 rs771499208	20	E>K		No	ClinGen ExAC TOPMed gnomAD
rs747024547 CA6174708	22	V>G		No	ClinGen ExAC gnomAD
rs773325739 CA6174707	23	Q>H		No	ClinGen ExAC gnomAD
rs1363117937 CA381781698	26	D>H		No	ClinGen TOPMed gnomAD
CA381781701 rs1363117937	26	D>N		No	ClinGen TOPMed gnomAD
CA381781702 rs1363117937	26	D>Y		No	ClinGen TOPMed gnomAD
CA6174703 rs369382970	31	R>H		No	ClinGen ESP ExAC TOPMed gnomAD
rs772248657 CA224450904	35	S>*		No	ClinGen ExAC gnomAD
rs781101660 CA6174700	35	S>A		No	ClinGen ExAC TOPMed gnomAD
rs772248657 CA6174699	35	S>L		No	ClinGen ExAC gnomAD
TCGA novel	36	E>V	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs1411430576 CA381781556	38	E>D		No	ClinGen gnomAD
rs1591270709 CA381781552	39	A>D		No	ClinGen Ensembl
rs199692569 CA6174698	39	A>T		No	ClinGen 1000Genomes ExAC gnomAD
rs376885709 CA6174696	47	Y>C		No	ClinGen ESP ExAC TOPMed gnomAD
CA381781468 rs1231344729	48	S>R		No	ClinGen gnomAD
rs759779768 CA6174694	48	S>R		No	ClinGen ExAC gnomAD
rs1591270686 CA381781424	52	V>G		No	ClinGen Ensembl
CA6174693 rs777093879	52	V>L		No	ClinGen ExAC gnomAD
CA381781415 rs1484212002	53	S>F		No	ClinGen gnomAD
CA381781422 rs1355967930	53	S>T		No	ClinGen TOPMed
CA381781407 rs1326197041	54	V>A		No	ClinGen gnomAD
CA224450899 rs772260745	57	Q>R		No	ClinGen gnomAD
rs1591270672 CA381781332	59	V>G		No	ClinGen Ensembl
rs1296065345 CA381781317	60	E>D		No	ClinGen gnomAD
CA224450898 rs78179480	60	E>G		No	ClinGen Ensembl
COSM4146303 CA381781300 rs1370460243	61	M>I	thyroid [Cosmic]	No	ClinGen cosmic curated TOPMed
rs369599250 CA6174690	62	D>N		No	ClinGen ESP ExAC TOPMed gnomAD
rs1354886977 CA381781280	63	R>G		No	ClinGen TOPMed gnomAD
rs1565243898 CA381781276	63	R>P		No	ClinGen Ensembl
rs1565243898 CA381781273	63	R>Q		No	ClinGen Ensembl
CA381781279 rs1354886977	63	R>W		No	ClinGen TOPMed gnomAD
rs1333191577 CA381781262	64	T>M		No	ClinGen gnomAD
CA6174687 rs558713579 COSM4146301	66	H>Q	thyroid [Cosmic]	No	ClinGen cosmic curated 1000Genomes ExAC gnomAD
rs748252119 CA6174688 COSM4146302	66	H>R	thyroid [Cosmic]	No	ClinGen cosmic curated ExAC gnomAD
CA381781220 rs1197786649	68	I>V		No	ClinGen TOPMed gnomAD
CA381777908 rs1386545413	70	C>*		No	ClinGen gnomAD
rs367692859 CA6174657	71	R>Q		No	ClinGen ESP ExAC TOPMed gnomAD
CA224442073 rs898231686	71	R>W		No	ClinGen gnomAD
rs201052442 CA6174656	73	E>D		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA6174655 rs756433640	74	C>S		No	ClinGen ExAC TOPMed gnomAD
rs371842503 CA6174654	75	C>S		No	ClinGen ESP ExAC TOPMed gnomAD
rs1462950561 CA381777871	76	D>H		No	ClinGen TOPMed
rs1241399121 CA381777856	78	P>S		No	ClinGen gnomAD
rs1349042123 CA381777843	80	E>A		No	ClinGen TOPMed
CA381777845 rs1448810251	80	E>Q		No	ClinGen gnomAD
rs762369207 CA6174652	81	T>I		No	ClinGen ExAC gnomAD
rs1357471872 CA381777831	82	L>F		No	ClinGen gnomAD
CA6174650 rs754062872	84	D>N		No	ClinGen ExAC TOPMed gnomAD
CA381777818 rs754062872	84	D>Y		No	ClinGen ExAC TOPMed gnomAD
rs775729949 CA6174648	85	V>I		No	ClinGen ExAC TOPMed gnomAD
rs1431592366 CA381777782	89	I>T		No	ClinGen TOPMed gnomAD
rs771448056 CA224441957	91	Y>*		No	ClinGen Ensembl
CA6174646 rs770170909	92	R>C		No	ClinGen ExAC TOPMed gnomAD
rs760513932 CA6174645	92	R>H		No	ClinGen ExAC TOPMed gnomAD
CA6174644 rs773190837	93	K>R		No	ClinGen ExAC gnomAD
rs772117209 CA6174643	97	S>R		No	ClinGen ExAC gnomAD
rs201257997 CA6174641	99	V>I		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs768152022 CA6174640	100	I>T		No	ClinGen ExAC gnomAD
rs1041347984 CA224441926	100	I>V		No	ClinGen TOPMed
TCGA novel	101	E>Q	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs1489887834 CA381777684	103	F>S		No	ClinGen gnomAD
rs1489490715 CA381777672	104	D>H		No	ClinGen TOPMed gnomAD
CA381777670 rs1489490715	104	D>N		No	ClinGen TOPMed gnomAD
TCGA novel	104	D>Y	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
CA6174639 rs370333254	105	I>V		No	ClinGen ESP ExAC TOPMed gnomAD
rs200273651 CA6174637	106	A>T		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs370883936 CA6174636	107	R>C		No	ClinGen ESP ExAC TOPMed gnomAD
CA224441913 rs376229569	107	R>H		No	ClinGen ESP TOPMed gnomAD
TCGA novel	107	R>L	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs1446101248 CA381777560	111	N>S		No	ClinGen TOPMed
rs757623133 CA6174634	112	A>T	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA gnomAD
COSM271543 rs202222156 CA6174632	114	V>M	large_intestine [Cosmic]	No	ClinGen cosmic curated 1000Genomes ESP ExAC TOPMed gnomAD
rs758462953 CA6174631	115	G>D		No	ClinGen ExAC gnomAD
rs1411484340 CA381777479	116	Y>C		No	ClinGen gnomAD
CA381777488 rs1326534499	116	Y>N		No	ClinGen gnomAD
rs1411484340 CA381777481	116	Y>S		No	ClinGen gnomAD
CA381777312 rs1241959166	120	R>G		No	ClinGen gnomAD
CA6174611 rs752808707	120	R>M		No	ClinGen ExAC gnomAD
CA381777307 rs1378020579	120	R>S		No	ClinGen TOPMed
CA6174610 rs201289203	128	R>C	Variant assessed as Somatic; impact. [NCI-TCGA]	No	ClinGen 1000Genomes ESP ExAC NCI-TCGA TOPMed gnomAD
rs201289203 CA224441413	128	R>G		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA6174609 rs755110131	130	V>I		No	ClinGen ExAC gnomAD
rs754052598 CA6174608	131	I>T		No	ClinGen ExAC TOPMed gnomAD
CA224441398 rs897364971	132	T>N		No	ClinGen TOPMed gnomAD
rs1591263232 CA381777150	132	T>P		No	ClinGen Ensembl
CA6174607 rs199726598	134	R>C		No	ClinGen ESP ExAC TOPMed gnomAD
CA6174605 rs761639628	134	R>H	Variant assessed as Somatic; 4.678e-05 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
CA381777101 rs1433571065	135	S>F		No	ClinGen TOPMed
rs1161536975 CA381777089	136	W>*		No	ClinGen gnomAD
CA381777099 rs1343551250	136	W>R		No	ClinGen gnomAD
rs751362410 CA6174604	138	P>S		No	ClinGen ExAC gnomAD
rs201443300 CA6174603	139	M>V		No	ClinGen ExAC TOPMed
TCGA novel	140	G>D	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs775410490 CA6174601	141	A>T	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	ClinGen ExAC NCI-TCGA TOPMed gnomAD
rs1331462875 CA381777008	142	D>A		No	ClinGen TOPMed
CA381777012 rs1254552598	142	D>H		No	ClinGen TOPMed
CA381776986 rs1247494233	143	Y>C		No	ClinGen TOPMed
rs1209529902 CA381776996	143	Y>D		No	ClinGen TOPMed
CA381776968 rs1195443633	144	I>T		No	ClinGen TOPMed
CA381776963 rs1222192602	145	I>V		No	ClinGen Ensembl
rs369550876 CA224441378	148	Y>*		No	ClinGen ESP ExAC TOPMed gnomAD
CA224441364 rs906302496	151	K>N		No	ClinGen TOPMed
rs1365267268 CA381776789	152	H>L		No	ClinGen TOPMed
CA6174599 rs759069825	152	H>Y		No	ClinGen ExAC TOPMed gnomAD
TCGA novel	153	P>L	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs1186482315 CA381776773	153	P>S		No	ClinGen gnomAD
rs1460818629 CA381775299	154	K>N		No	ClinGen gnomAD
rs371252313 CA6174574	155	Y>*		No	ClinGen ESP ExAC TOPMed gnomAD
rs748545313 CA381775280	155	Y>C		No	ClinGen ExAC TOPMed gnomAD
CA6174575 rs748545313	155	Y>F		No	ClinGen ExAC TOPMed gnomAD
CA381775254 rs769338513	156	P>L		No	ClinGen ExAC TOPMed gnomAD
CA6174573 rs769338513	156	P>Q		No	ClinGen ExAC TOPMed gnomAD
rs749368054 CA6174572	158	R>Q		No	ClinGen ExAC gnomAD
rs1170316626 CA381775228	158	R>W		No	ClinGen gnomAD
rs961581542 CA224440814	159	K>E		No	ClinGen TOPMed
CA6174570 rs756222550	163	R>*		No	ClinGen ExAC TOPMed gnomAD
rs750557441 COSM1475880 CA6174569	163	R>Q	Variant assessed as Somatic; 0.0001856 impact. breast [NCI-TCGA, Cosmic]	No	ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD
CA381775015 rs1479563113	166	S>C		No	ClinGen gnomAD
rs948258163 CA224440800	167	I>V		No	ClinGen Ensembl
CA224440793 rs368968723	168	Q>H		No	ClinGen ESP TOPMed gnomAD
rs1322895969 CA381774962	169	T>A		No	ClinGen gnomAD
rs200600557 CA6174566	169	T>M		No	ClinGen ExAC TOPMed gnomAD
CA381774938 rs1331862703	170	G>S		No	ClinGen gnomAD
CA6174562 rs374927236	179	K>R		No	ClinGen ESP ExAC TOPMed gnomAD
CA6174561 rs760245440	180	S>N		No	ClinGen ExAC TOPMed gnomAD
CA6174560 rs578098555	182	V>I		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA6174559 rs201180158	183	I>V		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs1591262885 CA381774547	184	T>P		No	ClinGen Ensembl
CA224440738 rs935087612	185	Y>C		No	ClinGen Ensembl
CA6174557 rs368273576	189	V>M		No	ClinGen ESP ExAC TOPMed gnomAD
CA381774381 rs1460767494	191	P>T		No	ClinGen gnomAD
rs370159113 CA6174531	193	G>A		No	ClinGen ESP ExAC TOPMed gnomAD
CA6174532 rs370159113	193	G>D		No	ClinGen ESP ExAC TOPMed gnomAD
rs370159113 CA224439234	193	G>V		No	ClinGen ESP ExAC TOPMed gnomAD
rs61740625 CA224439232	194	S>F		No	ClinGen TOPMed gnomAD
CA6174528 rs202137453	196	P>S		No	ClinGen ExAC gnomAD
rs754719737 CA6174527	197	K>T		No	ClinGen ExAC TOPMed gnomAD
CA381773856 rs1411440268	200	V>M		No	ClinGen gnomAD
CA6174523 rs749898399	203	S>F		No	ClinGen ExAC gnomAD
CA6174524 rs756124270	203	S>T		No	ClinGen ExAC gnomAD
rs753643170	204	S>missing	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	NCI-TCGA
rs763874260 CA6174518	210	K>R		No	ClinGen ExAC gnomAD
CA224438501 rs774191373	211	A>=	Variant assessed as Somatic; impact. [NCI-TCGA]	No	ClinGen NCI-TCGA TOPMed
CA381773772 rs1426004821	211	A>S		No	ClinGen TOPMed gnomAD
CA381773742 rs1414929124	214	K>M		No	ClinGen TOPMed
CA224438494 rs996870474	215	M>I		No	ClinGen TOPMed
CA381773726 rs1591261806	216	Y>C		No	ClinGen Ensembl
rs1181884592 CA381773721	217	K>E		No	ClinGen gnomAD
rs767577476 CA6174472	218	A>E		No	ClinGen ExAC TOPMed gnomAD
CA381773696 rs1591261798	220	L>I		No	ClinGen Ensembl
CA6174470 rs180999000	221	K>R		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA381773678 rs1591261788	222	Y>S		No	ClinGen Ensembl
rs1323390476 CA381773639	224	E>A		No	ClinGen gnomAD
COSM931746 rs1454469089 CA381773647	224	E>K	Variant assessed as Somatic; impact. endometrium [NCI-TCGA, Cosmic]	No	ClinGen cosmic curated NCI-TCGA TOPMed
CA381773569 rs1378140734	227	Q>L		No	ClinGen TOPMed
CA381773513 rs1338608222	229	H>P		No	ClinGen gnomAD
rs1280321567 CA381773510	229	H>Q		No	ClinGen gnomAD
rs746873588 CA6174465	230	L>P		No	ClinGen ExAC gnomAD
rs746873588 CA381773485	230	L>Q		No	ClinGen ExAC gnomAD
rs1350949138 CA381773455	231	P>R		No	ClinGen gnomAD
CA224438387 rs1006325347	231	P>S		No	ClinGen TOPMed gnomAD
CA224438381 rs901954295	232	H>Y		No	ClinGen TOPMed gnomAD
CA381773217 rs1591261727	238	H>P		No	ClinGen Ensembl
CA6174463 rs368925280	239	P>L		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
CA381773192 rs1420916329	239	P>T		No	ClinGen gnomAD
rs1266272035 CA381773128	241	Q>H		No	ClinGen TOPMed gnomAD
CA6174461 rs778596394	243	P>L		No	ClinGen ExAC gnomAD
CA381773098 rs778596394	243	P>Q		No	ClinGen ExAC gnomAD
CA381773097 rs778596394	243	P>R		No	ClinGen ExAC gnomAD
rs749638325 CA6174459	245	P>A		No	ClinGen ExAC TOPMed gnomAD
CA381773067 rs1197995601	245	P>L		No	ClinGen gnomAD
rs1197995601 CA381773068	245	P>R		No	ClinGen gnomAD
CA6174456 rs750882418	247	L>V		No	ClinGen ExAC TOPMed gnomAD
rs757329628 CA381773023	248	A>G		No	ClinGen ExAC gnomAD
rs757329628 CA6174454	248	A>V		No	ClinGen ExAC gnomAD
CA381773001 rs1368829776	250	S>L		No	ClinGen TOPMed gnomAD
CA224438294 rs930885906	251	E>A		No	ClinGen Ensembl
CA381772985 rs764367371	253	S>*		No	ClinGen ExAC gnomAD
CA6174452 rs764367371	253	S>L		No	ClinGen ExAC gnomAD
CA381772987 rs1591261691	253	S>P		No	ClinGen Ensembl
TCGA novel	256	H>R	Variant assessed as Somatic; impact. [NCI-TCGA]	No	NCI-TCGA
rs369117140 CA224438259	257	A>G		No	ClinGen ESP ExAC TOPMed gnomAD
rs369117140 CA6174450	257	A>V		No	ClinGen ESP ExAC TOPMed gnomAD
rs146343521 CA6174449	258	D>Y		No	ClinGen 1000Genomes ExAC gnomAD
CA381772916 rs1434672833	260	L>V		No	ClinGen gnomAD
rs766215581 CA6174448	263	I>T		No	ClinGen ExAC gnomAD
rs773157313 CA6174446	265	E>Q		No	ClinGen ExAC gnomAD
rs372636177 CA224438204	266	S>N		No	ClinGen Ensembl
rs1275784497 CA381772810	267	A>T		No	ClinGen TOPMed
rs1312042368 CA381772795	268	V>E		No	ClinGen TOPMed
rs1591261633 CA381772787	269	A>T		No	ClinGen Ensembl
COSM3687804 rs1197797427 CA381772777	270	E>K	large_intestine Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA]	No	ClinGen cosmic curated NCI-TCGA TOPMed gnomAD
rs1193184888 CA381772746	272	R>*		No	ClinGen TOPMed
CA6174442 rs773789120	273	E>G		No	ClinGen ExAC gnomAD
CA381772697 rs1445073446	275	R>W		No	ClinGen gnomAD
CA381772676 rs1191756486	276	M>I		No	ClinGen TOPMed
rs1332687899 CA381772679	276	M>T		No	ClinGen gnomAD
rs1379699130 CA381772688	276	M>V		No	ClinGen gnomAD
CA381772671 rs1391436617	277	G>S		No	ClinGen gnomAD
rs779705766 CA6174439	278	G>D		No	ClinGen ExAC TOPMed gnomAD
rs748883672 CA6174441	278	G>R		No	ClinGen ExAC gnomAD
rs748883672 CA6174440	278	G>S		No	ClinGen ExAC gnomAD
CA6174435 rs371866479	279	A>E		No	ClinGen ESP ExAC TOPMed gnomAD
rs770220463	279	A>missing	Variant assessed as Somatic; 0.0 impact. [NCI-TCGA]	No	NCI-TCGA
rs746271758 CA6174437	279	A>S		No	ClinGen ExAC TOPMed gnomAD
rs746271758 CA381772647	279	A>T		No	ClinGen ExAC TOPMed gnomAD
rs371866479 CA6174436	279	A>V		No	ClinGen ESP ExAC TOPMed gnomAD
CA224438137 rs751656644	281	G>A		No	ClinGen ExAC TOPMed gnomAD
rs751656644 CA381772618	281	G>D		No	ClinGen ExAC TOPMed gnomAD
rs751656644 CA6174433	281	G>V		No	ClinGen ExAC TOPMed gnomAD
rs927178044 CA381772593	282	E>D		No	ClinGen TOPMed gnomAD
rs202089909 CA6174431	282	E>K		No	ClinGen 1000Genomes ExAC TOPMed gnomAD
CA381772540 rs1238402002	284	S>N		No	ClinGen gnomAD
CA381772507 rs1244624340	285	D>E		No	ClinGen TOPMed gnomAD
rs1310627630 CA381772530	285	D>N		No	ClinGen gnomAD
CA224438093 rs374848566 CA381772489	286	D>E		No	ClinGen 1000Genomes ESP ExAC TOPMed gnomAD
rs1042929978 CA224438098	286	D>H		No	ClinGen TOPMed
CA381772458 rs1565237821	288	T>P		No	ClinGen Ensembl
CA381772416 rs1375650745	289	S>L		No	ClinGen TOPMed gnomAD
rs1397292055 CA381772431	289	S>T		No	ClinGen gnomAD
CA381772355 rs1591261555	291	T>P		No	ClinGen Ensembl

No associated diseases with Q9Y365

2 regional properties for Q9Y365

Type	Name	Position	InterPro Accession
domain	START domain	21 - 226	IPR002913
domain	STARD10, START domain	19 - 241	IPR041951

Functions

		Description
EC Number
Subcellular Localization	Cell projection, cilium, flagellum Cytoplasm Membrane	In testis was predominantly detected at the flagella of elongated spermatids, with a strong signal also found at the tail of epididymal sperm (By similarity) Mainly cytosolic
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category	No pathway information available

5 GO annotations of cellular component

Name	Definition
cytosol	The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
intercellular canaliculus	An extremely narrow tubular channel located between adjacent cells. An instance of this is the secretory canaliculi occurring between adjacent parietal cells in the gastric mucosa of vertebrates.
membrane	A lipid bilayer along with all the proteins and protein complexes embedded in it an attached to it.
microvillus	Thin cylindrical membrane-covered projections on the surface of an animal cell containing a core bundle of actin filaments. Present in especially large numbers on the absorptive surface of intestinal cells.
motile cilium	A cilium which may have a variable arrangement of axonemal microtubules and also contains molecular motors. It may beat with a whip-like pattern that promotes cell motility or transport of fluids and other cells across a cell surface, such as on epithelial cells that line the lumenal ducts of various tissues; or they may display a distinct twirling motion that directs fluid flow asymmetrically across the cellular surface to affect asymmetric body plan organization. Motile cilia can be found in single as well as multiple copies per cell.

1 GO annotations of molecular function

Name	Definition
lipid binding	Binding to a lipid.

1 GO annotations of biological process

Name	Definition
lipid transport	The directed movement of lipids into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Lipids are compounds soluble in an organic solvent but not, or sparingly, in an aqueous solvent.

4 homologous proteins in AiPD

UniProt AC	Gene Name	Protein Name	Species	Evidence Code
Q9NQZ5	STARD7	StAR-related lipid transfer protein 7, mitochondrial	Homo sapiens (Human)	PR
Q8R1R3	Stard7	StAR-related lipid transfer protein 7, mitochondrial	Mus musculus (Mouse)	PR
Q9JMD3	Stard10	START domain-containing protein 10	Mus musculus (Mouse)	PR
O17883	strl-1	Steroidogenic acute regulatory-like protein 1	Caenorhabditis elegans	PR

10	20	30	40	50	60
MEKLAASTEP	QGPRPVLGRE	SVQVPDDQDF	RSFRSECEAE	VGWNLTYSRA	GVSVWVQAVE
70	80	90	100	110	120
MDRTLHKIKC	RMECCDVPAE	TLYDVLHDIE	YRKKWDSNVI	ETFDIARLTV	NADVGYYSWR
130	140	150	160	170	180
CPKPLKNRDV	ITLRSWLPMG	ADYIIMNYSV	KHPKYPPRKD	LVRAVSIQTG	YLIQSTGPKS
190	200	210	220	230	240
CVITYLAQVD	PKGSLPKWVV	NKSSQFLAPK	AMKKMYKACL	KYPEWKQKHL	PHFKPWLHPE
250	260	270	280	290
QSPLPSLALS	ELSVQHADSL	ENIDESAVAE	SREERMGGAG	GEGSDDDTSL	T