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Gene: OLFML1 (olfactomedin like 1) Homo sapiens

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Symbol:

OLFML1

Name:

olfactomedin like 1

RGD ID:

1323529

HGNC Page

HGNC:24473

Description:

Predicted to be involved in signal transduction. Predicted to be located in extracellular region. Predicted to be active in extracellular space.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

MVAL564; olfactomedin-like 1; olfactomedin-like protein 1; ONT2; UNQ564

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Olfml1 (olfactomedin-like 1)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OrthoDB, Panther, PhylomeDB
Rattus norvegicus (Norway rat):	Olfml1 (olfactomedin-like 1)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, Panther, PhylomeDB
Chinchilla lanigera (long-tailed chinchilla):	Olfml1 (olfactomedin like 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	OLFML1 (olfactomedin like 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	OLFML1 (olfactomedin like 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Olfml1 (olfactomedin like 1)	NCBI	Ortholog
Sus scrofa (pig):	OLFML1 (olfactomedin like 1)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	OLFML1 (olfactomedin like 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Olfml1 (olfactomedin like 1)	NCBI	Ortholog
Other homologs ²
Canis lupus familiaris (dog):	SYT9 (synaptotagmin 9)	HGNC	Inparanoid
Rattus norvegicus (Norway rat):	Asb1 (ankyrin repeat and SOCS box-containing 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Olfml1 (olfactomedin-like 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Olfml1 (olfactomedin-like 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	olfml1 (olfactomedin-like 1)	Alliance	DIOPT (ZFIN)
Xenopus laevis (African clawed frog):	olfml1.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	olfml1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	7,485,506 - 7,511,377 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	7,485,388 - 7,511,377 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	7,506,737 - 7,532,608 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	7,463,331 - 7,489,140 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	7,463,573 - 7,489,137	NCBI
Celera	11	7,625,730 - 7,651,738 (+)	NCBI		Celera
Cytogenetic Map	11	p15.4	NCBI
HuRef	11	7,165,129 - 7,191,140 (+)	NCBI		HuRef
CHM1_1	11	7,505,519 - 7,531,529 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	7,543,862 - 7,569,737 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

17beta-estradiol (EXP)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

3,3',4,4',5-pentachlorobiphenyl (ISO)

3-chloropropane-1,2-diol (ISO)

3-isobutyl-1-methyl-7H-xanthine (EXP)

4,4'-sulfonyldiphenol (ISO)

4-hydroxyphenyl retinamide (ISO)

6-propyl-2-thiouracil (ISO)

aflatoxin B1 (EXP,ISO)

aldehydo-D-glucose (ISO)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

beta-naphthoflavone (ISO)

bis(2-ethylhexyl) phthalate (EXP,ISO)

bisphenol A (EXP,ISO)

bisphenol F (EXP,ISO)

calcitriol (EXP)

carbon nanotube (ISO)

cyclosporin A (EXP,ISO)

D-glucose (ISO)

dexamethasone (EXP)

dibenz[a,h]anthracene (ISO)

dichloroacetic acid (ISO)

dioxygen (ISO)

diuron (ISO)

dorsomorphin (EXP)

doxorubicin (EXP)

entinostat (EXP)

ethanol (ISO)

folic acid (EXP)

fonofos (EXP)

fructose (ISO)

furan (ISO)

glucose (ISO)

GW 4064 (ISO)

hydroquinone O-beta-D-glucopyranoside (EXP)

indometacin (EXP)

inulin (ISO)

kojic acid (EXP)

mercury dibromide (EXP)

mercury dichloride (ISO)

N-nitrosodiethylamine (ISO)

nickel atom (EXP)

ozone (ISO)

parathion (EXP)

perfluorooctane-1-sulfonic acid (ISO)

phenobarbital (ISO)

phenylmercury acetate (EXP)

pioglitazone (ISO)

pirinixic acid (ISO)

progesterone (EXP)

propiconazole (ISO)

quercetin (EXP)

SB 431542 (EXP)

silicon dioxide (EXP,ISO)

sodium arsenite (ISO)

sulforaphane (EXP)

terbufos (EXP)

tetrachloromethane (ISO)

Triptolide (ISO)

valproic acid (EXP)

XL147 (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

signal transduction (IBA)

Cellular Component

extracellular region (IEA)

extracellular space (IBA)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:12477932	PMID:12975309	PMID:15340161	PMID:15489334	PMID:16344560	PMID:18708057	PMID:21873635	PMID:30266405

Genomics

Comparative Map Data

OLFML1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	7,485,506 - 7,511,377 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	7,485,388 - 7,511,377 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	7,506,737 - 7,532,608 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	7,463,331 - 7,489,140 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	7,463,573 - 7,489,137	NCBI
Celera	11	7,625,730 - 7,651,738 (+)	NCBI		Celera
Cytogenetic Map	11	p15.4	NCBI
HuRef	11	7,165,129 - 7,191,140 (+)	NCBI		HuRef
CHM1_1	11	7,505,519 - 7,531,529 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	7,543,862 - 7,569,737 (+)	NCBI		T2T-CHM13v2.0

Olfml1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	107,166,640 - 107,190,572 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	107,166,653 - 107,190,301 (+)	Ensembl		GRCm39 Ensembl
GRCm38	7	107,567,433 - 107,591,365 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	107,567,446 - 107,591,094 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	114,710,947 - 114,734,879 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	107,358,623 - 107,382,271 (+)	NCBI		MGSCv36	mm8
Celera	7	107,543,398 - 107,567,221 (+)	NCBI		Celera
Cytogenetic Map	7	E3	NCBI
cM Map	7	57.21	NCBI

Olfml1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	170,889,912 - 170,914,300 (+)	NCBI		GRCr8
mRatBN7.2	1	161,478,129 - 161,502,541 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	161,478,242 - 161,502,537 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	169,747,308 - 169,771,491 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	176,933,303 - 176,957,486 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	169,618,081 - 169,642,351 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	171,793,782 - 171,818,074 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	171,793,782 - 171,818,068 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	178,792,340 - 178,816,636 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	164,953,064 - 164,977,360 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	165,048,540 - 165,072,958 (+)	NCBI
Celera	1	159,382,450 - 159,406,508 (+)	NCBI		Celera
Cytogenetic Map	1	q33	NCBI

Olfml1
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955414	23,240,205 - 23,269,620 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955414	23,240,469 - 23,267,380 (+)	NCBI	ChiLan1.0	ChiLan1.0

OLFML1
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	9	9,880,047 - 9,912,924 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	9,843,463 - 9,876,040 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	7,580,561 - 7,606,630 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	7,261,192 - 7,288,514 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	7,261,192 - 7,288,508 (+)	Ensembl	panpan1.1		panPan2

OLFML1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	21	31,136,218 - 31,162,405 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	21	30,986,521 - 31,162,414 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	21	30,706,146 - 30,732,298 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	21	32,001,461 - 32,027,657 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	21	31,737,706 - 32,027,664 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	21	31,273,734 - 31,299,861 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	21	31,436,581 - 31,462,743 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	21	31,732,238 - 31,758,591 (+)	NCBI		UU_Cfam_GSD_1.0

Olfml1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404947	54,340,466 - 54,362,975 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936841	724,386 - 747,592 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936841	724,410 - 747,518 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

OLFML1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1	9	2,145,678 - 2,171,875 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	9	2,617,008 - 2,654,701 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

OLFML1
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	1	57,327,951 - 57,354,150 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	57,329,146 - 57,353,471 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666038	155,059,123 - 155,085,516 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Olfml1
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla 1.0	NW_004624817	9,196,381 - 9,219,125 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in OLFML1
26 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 11p15.4(chr11:3745061-7846057)x3	copy number gain	See cases [RCV000053616]	Chr11:3745061..7846057 [GRCh38] Chr11:3766291..7867604 [GRCh37] Chr11:3722867..7824180 [NCBI36] Chr11:11p15.4	pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3	copy number gain	See cases [RCV000053613]	Chr11:202758..31726224 [GRCh38] Chr11:202758..31747772 [GRCh37] Chr11:192758..31704348 [NCBI36] Chr11:11p15.5-13	pathogenic
GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3	copy number gain	See cases [RCV000133997]	Chr11:446754..18904742 [GRCh38] Chr11:446754..18926289 [GRCh37] Chr11:436754..18882865 [NCBI36] Chr11:11p15.5-15.1	pathogenic
GRCh38/hg38 11p15.4(chr11:7187414-7707594)x3	copy number gain	See cases [RCV000139155]	Chr11:7187414..7707594 [GRCh38] Chr11:7208645..7729141 [GRCh37] Chr11:7165221..7685717 [NCBI36] Chr11:11p15.4	uncertain significance
GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3	copy number gain	See cases [RCV000139987]	Chr11:61793..10727969 [GRCh38] Chr11:61793..10749516 [GRCh37] Chr11:51793..10706092 [NCBI36] Chr11:11p15.5-15.4	pathogenic
GRCh38/hg38 11p15.4(chr11:7359664-7657396)x1	copy number loss	See cases [RCV000141705]	Chr11:7359664..7657396 [GRCh38] Chr11:7380895..7678627 [GRCh37] Chr11:7337471..7635203 [NCBI36] Chr11:11p15.4	uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3	copy number gain	See cases [RCV000511561]	Chr11:230615..37698540 [GRCh37] Chr11:11p15.5-12	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3	copy number gain	See cases [RCV000512225]	Chr11:230615..25584362 [GRCh37] Chr11:11p15.5-14.3	pathogenic
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3	copy number gain	See cases [RCV000512477]	Chr11:230615..31995219 [GRCh37] Chr11:11p15.5-13	pathogenic
GRCh37/hg19 11p15.4(chr11:6969013-9257231)x3	copy number gain	not provided [RCV000683360]	Chr11:6969013..9257231 [GRCh37] Chr11:11p15.4	pathogenic
GRCh37/hg19 11p15.4(chr11:7418934-8308834)x3	copy number gain	not provided [RCV000683352]	Chr11:7418934..8308834 [GRCh37] Chr11:11p15.4	uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:230615-9704511)x3	copy number gain	not provided [RCV000683369]	Chr11:230615..9704511 [GRCh37] Chr11:11p15.5-15.4	pathogenic
GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3	copy number gain	not provided [RCV000683372]	Chr11:230615..17099213 [GRCh37] Chr11:11p15.5-15.1	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136)	copy number gain	Silver-Russell syndrome 1 [RCV000767567]	Chr11:193146..12643136 [GRCh37] Chr11:11p15.5-15.3	pathogenic
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3	copy number gain	not provided [RCV001006372]	Chr11:235934..33826995 [GRCh37] Chr11:11p15.5-13	pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:210300-8664358)x3	copy number gain	Silver-Russell syndrome 1 [RCV001263222]	Chr11:210300..8664358 [GRCh37] Chr11:11p15.5-15.4	pathogenic
GRCh37/hg19 11p15.4(chr11:7502249-7570109)	copy number loss	not specified [RCV002052913]	Chr11:7502249..7570109 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.1102C>T (p.His368Tyr)	single nucleotide variant	not specified [RCV004308744]	Chr11:7510081 [GRCh38] Chr11:7531312 [GRCh37] Chr11:11p15.4	uncertain significance
GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3	copy number gain	See cases [RCV002286351]	Chr11:230615..26881146 [GRCh37] Chr11:11p15.5-14.2	pathogenic
GRCh37/hg19 11p15.4(chr11:7326212-7525985)x3	copy number gain	not provided [RCV002474907]	Chr11:7326212..7525985 [GRCh37] Chr11:11p15.4	uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:230616-8250724)x3	copy number gain	not provided [RCV002472435]	Chr11:230616..8250724 [GRCh37] Chr11:11p15.5-15.4	pathogenic
NM_198474.4(OLFML1):c.848A>G (p.His283Arg)	single nucleotide variant	not specified [RCV004206360]	Chr11:7509827 [GRCh38] Chr11:7531058 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.581C>T (p.Ala194Val)	single nucleotide variant	not specified [RCV004191438]	Chr11:7509560 [GRCh38] Chr11:7530791 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.805T>A (p.Tyr269Asn)	single nucleotide variant	not specified [RCV004225531]	Chr11:7509784 [GRCh38] Chr11:7531015 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.896C>T (p.Pro299Leu)	single nucleotide variant	not specified [RCV004129588]	Chr11:7509875 [GRCh38] Chr11:7531106 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.994A>G (p.Ser332Gly)	single nucleotide variant	not specified [RCV004120120]	Chr11:7509973 [GRCh38] Chr11:7531204 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.401G>A (p.Arg134Gln)	single nucleotide variant	not specified [RCV004154706]	Chr11:7488398 [GRCh38] Chr11:7509629 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.365T>C (p.Met122Thr)	single nucleotide variant	not specified [RCV004136403]	Chr11:7488362 [GRCh38] Chr11:7509593 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.157A>G (p.Thr53Ala)	single nucleotide variant	not specified [RCV004076808]	Chr11:7488154 [GRCh38] Chr11:7509385 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.499G>T (p.Asp167Tyr)	single nucleotide variant	not specified [RCV004187666]	Chr11:7509478 [GRCh38] Chr11:7530709 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.683A>G (p.His228Arg)	single nucleotide variant	not specified [RCV004286810]	Chr11:7509662 [GRCh38] Chr11:7530893 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.280C>A (p.Arg94Ser)	single nucleotide variant	not specified [RCV004279315]	Chr11:7488277 [GRCh38] Chr11:7509508 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.863C>G (p.Thr288Ser)	single nucleotide variant	not specified [RCV004350543]	Chr11:7509842 [GRCh38] Chr11:7531073 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.1155A>C (p.Glu385Asp)	single nucleotide variant	not specified [RCV004341820]	Chr11:7510134 [GRCh38] Chr11:7531365 [GRCh37] Chr11:11p15.4	likely benign
GRCh37/hg19 11p15.5-15.4(chr11:230615-8821443)x3	copy number gain	Russell-Silver syndrome [RCV003444025]	Chr11:230615..8821443 [GRCh37] Chr11:11p15.5-15.4	pathogenic
NM_198474.4(OLFML1):c.691G>A (p.Ala231Thr)	single nucleotide variant	not specified [RCV004499105]	Chr11:7509670 [GRCh38] Chr11:7530901 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.778T>A (p.Leu260Met)	single nucleotide variant	not specified [RCV004499107]	Chr11:7509757 [GRCh38] Chr11:7530988 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.299A>T (p.Asp100Val)	single nucleotide variant	not specified [RCV004499102]	Chr11:7488296 [GRCh38] Chr11:7509527 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.41T>G (p.Leu14Arg)	single nucleotide variant	not specified [RCV004499103]	Chr11:7485916 [GRCh38] Chr11:7507147 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.695C>T (p.Thr232Ile)	single nucleotide variant	not specified [RCV004499106]	Chr11:7509674 [GRCh38] Chr11:7530905 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.809T>C (p.Ile270Thr)	single nucleotide variant	not specified [RCV004499108]	Chr11:7509788 [GRCh38] Chr11:7531019 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.535A>T (p.Ile179Phe)	single nucleotide variant	not specified [RCV004499104]	Chr11:7509514 [GRCh38] Chr11:7530745 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.112C>A (p.Arg38Ser)	single nucleotide variant	not specified [RCV004499101]	Chr11:7485987 [GRCh38] Chr11:7507218 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.1138C>G (p.Leu380Val)	single nucleotide variant	not specified [RCV004655152]	Chr11:7510117 [GRCh38] Chr11:7531348 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.328G>A (p.Glu110Lys)	single nucleotide variant	not specified [RCV004655153]	Chr11:7488325 [GRCh38] Chr11:7509556 [GRCh37] Chr11:11p15.4	uncertain significance
NM_198474.4(OLFML1):c.926A>G (p.Asp309Gly)	single nucleotide variant	not specified [RCV004655154]	Chr11:7509905 [GRCh38] Chr11:7531136 [GRCh37] Chr11:11p15.4	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1362
Count of miRNA genes:	747
Interacting mature miRNAs:	857
Transcripts:	ENST00000329293, ENST00000528308, ENST00000528758, ENST00000530135, ENST00000534244
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
2289313	BW388_H	Body weight QTL 388 (human)	1.57	0.00356	Body fat amount	abdominal	11	4434671	30434671	Human
1559107	SCL32_H	Serum cholesterol level QTL 32 (human)	3.27		Lipid level	LDL cholesterol	11	2892430	28892430	Human
1559113	SCL31_H	Serum cholesterol level QTL 31 (human)	3.72		Lipid level	LDL cholesterol	11	2892430	28892430	Human
597302917	GWAS1398991_H	level of olfactomedin-like protein 3 in blood serum QTL GWAS1398991 (human)		1e-18	level of olfactomedin-like protein 3 in blood serum		11	7494550	7494551	Human

Markers in Region

G62644

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	7,532,133 - 7,532,418	UniSTS	GRCh37
Build 36	11	7,488,709 - 7,488,994	RGD	NCBI36
Celera	11	7,651,267 - 7,651,552	RGD
Cytogenetic Map	11	p15.4	UniSTS
HuRef	11	7,190,665 - 7,190,950	UniSTS
TNG Radiation Hybrid Map	11	3255.0	UniSTS

SHGC-153704

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	7,504,723 - 7,505,016	UniSTS	GRCh37
Build 36	11	7,461,299 - 7,461,592	RGD	NCBI36
Celera	11	7,623,853 - 7,624,146	RGD
Cytogenetic Map	11	p15.4	UniSTS
HuRef	11	7,163,252 - 7,163,545	UniSTS
TNG Radiation Hybrid Map	11	3255.0	UniSTS

RH66484

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	7,531,855 - 7,532,042	UniSTS	GRCh37
Build 36	11	7,488,431 - 7,488,618	RGD	NCBI36
Celera	11	7,650,989 - 7,651,176	RGD
Cytogenetic Map	11	p15.4	UniSTS
HuRef	11	7,190,387 - 7,190,574	UniSTS
GeneMap99-GB4 RH Map	11	41.43	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2347	2788	2243	4864	1713	2205	5	618	1624	457	2210	6876	6135	21	3679	818	1689	1483	165	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001370498	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001370499	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001370500	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001370501	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_198474	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC107884	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298137	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY358591	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC035895	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC092488	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX647908	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB257515	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC397336	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000329293 ⟹ ENSP00000332511

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	7,485,506 - 7,511,377 (+)	Ensembl

Ensembl Acc Id:

ENST00000528308

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	7,485,526 - 7,488,965 (+)	Ensembl

Ensembl Acc Id:

ENST00000528758 ⟹ ENSP00000434813

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	7,485,606 - 7,510,412 (+)	Ensembl

Ensembl Acc Id:

ENST00000530135 ⟹ ENSP00000433455

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	7,485,388 - 7,510,349 (+)	Ensembl

Ensembl Acc Id:

ENST00000534244 ⟹ ENSP00000431558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	7,485,506 - 7,488,206 (+)	Ensembl

RefSeq Acc Id:

NM_001370498 ⟹ NP_001357427

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	7,485,506 - 7,511,377 (+)	NCBI
T2T-CHM13v2.0	11	7,543,862 - 7,569,737 (+)	NCBI

Sequence:

show sequence

ATCTTCACCCCCCACCCCAATGCACACACAATTAAGCCAGGAAGCAGCTTGCAACCACTAGCCT
GGGGAGGGTCCGCATGTGTCAAGGGTGAGGGCAACAGATGCTGGACCCAGGGAGCTCTCTGCCA
CAGGATGATGGTGGCCCTTCGAGGAGCTTCTGCATTGCTGGTTCTGTTCCTTGCAGCTTTTCTG
CCCCCGCCGCAGTGTACCCAGGACCCAGCCATGGTGCATTACATCTACCAGCGCTTTCGAGTCT
TGGAGCAAGGGCTGGAAAAATGTACCCAAGCAACGAGGGCATACATTCAAGAATTCCAAGAGTT
CTCAAAAAATATATCTGTCATGCTGGGAAGATGTCAGACCTACACAAGTGAGTACAAGAGTGCA
GTGGGTAACTTGGCACTGAGAGTTGAACGTGCCCAACGGGAGATTGACTACATACAATACCTTC
GAGAGGCTGACGAGTGCATCGAATCAGAGGACAAGACACTGGCAGAAATGTTGCTCCAAGAAGC
TGAAGAAGAGAAAAAGATCCGGACTCTGCTGAATGCAAGCTGTGACAACATGCTGATGGGCATA
AAGTCTTTGAAAATAGTGAAGAAGATGATGGACACACATGGCTCTTGGATGAAAGATGCTGTCT
ATAACTCTCCAAAGGTGTACTTATTAATTGGATCCAGAAACAACACTGTTTGGGAATTTGCAAA
CATACGGGCATTCATGGAGGATAACACCAAGCCAGCTCCCCGGAAGCAAATCCTAACACTTTCC
TGGCAGGGAACAGGCCAAGTGATCTACAAAGGTTTTCTATTTTTTCATAACCAAGCAACTTCTA
ATGAGATAATCAAATATAACCTGCAGAAGAGGACTGTGGAAGATCGAATGCTGCTCCCAGGAGG
GGTAGGCCGAGCATTGGTTTACCAGCACTCCCCCTCAACTTACATTGACCTGGCTGTGGATGAG
CATGGGCTCTGGGCCATCCACTCTGGGCCAGGCACCCATAGCCATTTGGTTCTCACAAAGATTG
AGCCGGGCACACTGGGAGTGGAGCATTCATGGGATACCCCATGCAGAAGCCAGGATGCTGAAGC
CTCATTCCTCTTGTGTGGGGTTCTCTATGTGGTCTACAGTACTGGGGGCCAGGGCCCTCATCGC
ATCACCTGCATCTATGATCCACTGGGCACTATCAGTGAGGAGGACTTGCCCAACTTGTTCTTCC
CCAAGAGACCAAGAAGTCACTCCATGATCCATTACAACCCCAGAGATAAGCAGCTCTATGCCTG
GAATGAAGGAAACCAGATCATTTACAAACTCCAGACAAAGAGAAAGCTGCCTCTGAAGTAATGC
ATTACAGCTGTGAGAAAGAGCACTGTGGCTTTGGCAGCTGTTCTACAGGACAGTGAGGCTATAG
CCCCTTCACAATATAGTATCCCTCTAATCACACACAGGAAGAGTGTGTAGAAGTGGAAATACGT
ATGCCTCCTTTCCCAAATGTCACTGCCTTAGGTATCTTCCAAGAGCTTAGATGAGAGCATATCA
TCAGGAAAGTTTCAACAATGTCCATTACTCCCCCAAACCTCCTGGCTCTCAAGGATGACCACAT
TCTGATACAGCCTACTTCAAGCCTTTTGTTTTACTGCTCCCCAGCATTTACTGTAACTCTGCCA
TCTTCCCTCCCACAATTAGAGTTGTATGCCAGCCCCTAATATTCACCACTGGCTTTTCTCTCCC
CTGGCCTTTGCTGAAGCTCTTCCCTCTTTTTCAAATGTCTATTGATATTCTCCCATTTTCACTG
CCCAACTAAAATACTATTAATATTTCTTTCTTTTCTTTTCTTTTTTTTGAGACAAGGTCTCACT
ATGTTGCCCAGGCTGGTCTCAAACTCCAGAGCTCAAGAGATCCTCCTGCCTCAGCCTCCTAAGT
ACCTGGGATTACAGGCATGTGCCACCACACCTGGCTTAAAATACTATTTCTTATTGAGGTTTAA
CCTCTATTTCCCCTAGCCCTGTCCTTCCACTAAGCTTGGTAGATGTAATAATAAAGTGAAAATA
TTAACATTTGAATATCGCTTTCCAGGTGTGGAGTGTTTGCACATCATTTAATTCTCGTTTCACC
TTTGTGAAACATGCACAAGTCTTTACAGCTGTCATTCTAGAGTTTAGGTGAGTAACACAATTAC
AAAGTGAAAGATACAGCTAGAAAATACTACAAATCCCATAGTTTTTCCATTGCCCAAGGAAGCA
TCAAATACGTATGTTTGTTCACCTACTCTTATAGTCAATGCGTTCATCGTTTCAGCCTAAAAAT
AATAGTCTGTCCCTTTAGCCAGTTTTCATGTCTGCACAAGACCTTTCAATAGGCCTTTCAAATG
ATAATTCCTCCAGAAAACCAGTCTAAGGGTGAGGACCCCAACTCTAGCCTCCTCTTGTCTTGCT
GTCCTCTGTTTCTCTCTTTCTGCTTTAAATTCAATAAAAGTGACACTGAGCAAATAACCTCATC
AGGTTATATTTGCCCACATACCCTAAGCACAAAA

hide sequence

RefSeq Acc Id:

NM_001370499 ⟹ NP_001357428

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	7,485,766 - 7,511,377 (+)	NCBI
T2T-CHM13v2.0	11	7,544,122 - 7,569,737 (+)	NCBI

Sequence:

show sequence

AGAGGATTTGCCACAGCAGCGGATAGAGCAGGAGAGCACCACCGGAGCCCTTGAGACATCCTTG
AGAAGAGCCACAGCATAAGAGACTGCCCTGCTTGGTGTTTTGCAGGATGATGGTGGCCCTTCGA
GGAGCTTCTGCATTGCTGGTTCTGTTCCTTGCAGCTTTTCTGCCCCCGCCGCAGTGTACCCAGG
ACCCAGCCATGGTGCATTACATCTACCAGCGCTTTCGAGTCTTGGAGCAAGGGCTGGAAAAATG
TACCCAAGCTGTGACAACATGCTGATGGGCATAAAGTCTTTGAAAATAGTGAAGAAGATGATGG
ACACACATGGCTCTTGGATGAAAGATGCTGTCTATAACTCTCCAAAGGTGTACTTATTAATTGG
ATCCAGAAACAACACTGTTTGGGAATTTGCAAACATACGGGCATTCATGGAGGATAACACCAAG
CCAGCTCCCCGGAAGCAAATCCTAACACTTTCCTGGCAGGGAACAGGCCAAGTGATCTACAAAG
GTTTTCTATTTTTTCATAACCAAGCAACTTCTAATGAGATAATCAAATATAACCTGCAGAAGAG
GACTGTGGAAGATCGAATGCTGCTCCCAGGAGGGGTAGGCCGAGCATTGGTTTACCAGCACTCC
CCCTCAACTTACATTGACCTGGCTGTGGATGAGCATGGGCTCTGGGCCATCCACTCTGGGCCAG
GCACCCATAGCCATTTGGTTCTCACAAAGATTGAGCCGGGCACACTGGGAGTGGAGCATTCATG
GGATACCCCATGCAGAAGCCAGGATGCTGAAGCCTCATTCCTCTTGTGTGGGGTTCTCTATGTG
GTCTACAGTACTGGGGGCCAGGGCCCTCATCGCATCACCTGCATCTATGATCCACTGGGCACTA
TCAGTGAGGAGGACTTGCCCAACTTGTTCTTCCCCAAGAGACCAAGAAGTCACTCCATGATCCA
TTACAACCCCAGAGATAAGCAGCTCTATGCCTGGAATGAAGGAAACCAGATCATTTACAAACTC
CAGACAAAGAGAAAGCTGCCTCTGAAGTAATGCATTACAGCTGTGAGAAAGAGCACTGTGGCTT
TGGCAGCTGTTCTACAGGACAGTGAGGCTATAGCCCCTTCACAATATAGTATCCCTCTAATCAC
ACACAGGAAGAGTGTGTAGAAGTGGAAATACGTATGCCTCCTTTCCCAAATGTCACTGCCTTAG
GTATCTTCCAAGAGCTTAGATGAGAGCATATCATCAGGAAAGTTTCAACAATGTCCATTACTCC
CCCAAACCTCCTGGCTCTCAAGGATGACCACATTCTGATACAGCCTACTTCAAGCCTTTTGTTT
TACTGCTCCCCAGCATTTACTGTAACTCTGCCATCTTCCCTCCCACAATTAGAGTTGTATGCCA
GCCCCTAATATTCACCACTGGCTTTTCTCTCCCCTGGCCTTTGCTGAAGCTCTTCCCTCTTTTT
CAAATGTCTATTGATATTCTCCCATTTTCACTGCCCAACTAAAATACTATTAATATTTCTTTCT
TTTCTTTTCTTTTTTTTGAGACAAGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCAGAG
CTCAAGAGATCCTCCTGCCTCAGCCTCCTAAGTACCTGGGATTACAGGCATGTGCCACCACACC
TGGCTTAAAATACTATTTCTTATTGAGGTTTAACCTCTATTTCCCCTAGCCCTGTCCTTCCACT
AAGCTTGGTAGATGTAATAATAAAGTGAAAATATTAACATTTGAATATCGCTTTCCAGGTGTGG
AGTGTTTGCACATCATTTAATTCTCGTTTCACCTTTGTGAAACATGCACAAGTCTTTACAGCTG
TCATTCTAGAGTTTAGGTGAGTAACACAATTACAAAGTGAAAGATACAGCTAGAAAATACTACA
AATCCCATAGTTTTTCCATTGCCCAAGGAAGCATCAAATACGTATGTTTGTTCACCTACTCTTA
TAGTCAATGCGTTCATCGTTTCAGCCTAAAAATAATAGTCTGTCCCTTTAGCCAGTTTTCATGT
CTGCACAAGACCTTTCAATAGGCCTTTCAAATGATAATTCCTCCAGAAAACCAGTCTAAGGGTG
AGGACCCCAACTCTAGCCTCCTCTTGTCTTGCTGTCCTCTGTTTCTCTCTTTCTGCTTTAAATT
CAATAAAAGTGACACTGAGCAAATAACCTCATCAGGTTATATTTGCCCACATACCCTAAGCACA
AAA

hide sequence

RefSeq Acc Id:

NM_001370500 ⟹ NP_001357429

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	7,485,506 - 7,489,024 (+)	NCBI
T2T-CHM13v2.0	11	7,543,862 - 7,547,380 (+)	NCBI

Sequence:

show sequence

ATCTTCACCCCCCACCCCAATGCACACACAATTAAGCCAGGAAGCAGCTTGCAACCACTAGCCT
GGGGAGGGTCCGCATGTGTCAAGGGTGAGGGCAACAGATGCTGGACCCAGGGAGCTCTCTGCCA
CAGGATGATGGTGGCCCTTCGAGGAGCTTCTGCATTGCTGGTTCTGTTCCTTGCAGCTTTTCTG
CCCCCGCCGCAGTGTACCCAGGACCCAGCCATGGTGCATTACATCTACCAGCGCTTTCGAGTCT
TGGAGCAAGGGCTGGAAAAATGTACCCAAGCAACGAGGGCATACATTCAAGAATTCCAAGAGTT
CTCAAAAAATATATCTGTCATGCTGGGAAGATGTCAGACCTACACAAGTGAGTACAAGAGTGCA
GTGGGTAACTTGGCACTGAGAGTTGAACGTGCCCAACGGGAGATTGACTACATACAATACCTTC
GAGAGGCTGACGAGTGCATCGAATCAGAGGACAAGACACTGGCAGAAATGTTGCTCCAAGAAGC
TGAAGAAGAGAAAAAGATCCGGACTCTGCTGAATGCAAGTAAGAAAACTGCATCTTTTCCTAGC
CCTTCTAGGGACTATTATGCTCAGAAACACACAGACTCAGAGCAGTCAGGGAGCATCATAGAGT
AATGAGAGTAAGAATTGGAGGTGTGCTTTTGTGTGCATTGCTGAGAGAGAAAGCTATACAGAGA
ACAGGTGTCCAAAGAGAAATCCATTCTCGCAAAGCCATTCTTTCTTTCACACACAGTGCCTAAA
GCCTCCATAGATGGTGAAGGCTATAGTGCCAAAAGTCAGCCCAAAGAGACTACCTCCTGATAAA
TCTTGGTTTGGTGGAGATGTGTGGTCCCAGATTTTTTCAGGGAAAGTAGCAGTTTGGTGGATTC
TACATCCAGTACCCAGGCTGTAGATAGCATCTGCAAATGTACCAAGAAACAGTCTTAAATTGGA
AATGGCAACAGCCAACCCTCAGGGATGGGAACTGCAGTGAATCACTATTGTGTGTGCTGTCTGA
GATGGTGATATGCATGGGATGTGGTCTAATCTTGTGATCCATCAGAATCACTTCCAAGCCATTA
AGAATAATGTGTAGCAGCTCAAATTATAATAAACAGTATCAGGCAATAAACACACAAATGACAA
AGAAAAA

hide sequence

RefSeq Acc Id:

NM_001370501 ⟹ NP_001357430

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	7,485,766 - 7,489,024 (+)	NCBI
T2T-CHM13v2.0	11	7,544,122 - 7,547,380 (+)	NCBI

Sequence:

show sequence

AGAGGATTTGCCACAGCAGCGGATAGAGCAGGAGAGCACCACCGGAGCCCTTGAGACATCCTTG
AGAAGAGCCACAGCATAAGAGACTGCCCTGCTTGGTGTTTTGCAGGATGATGGTGGCCCTTCGA
GGAGCTTCTGCATTGCTGGTTCTGTTCCTTGCAGCTTTTCTGCCCCCGCCGCAGTGTACCCAGG
ACCCAGCCATGGTGCATTACATCTACCAGCGCTTTCGAGTCTTGGAGCAAGGGCTGGAAAAATG
TACCCAAGCAACGAGGGCATACATTCAAGAATTCCAAGAGTTCTCAAAAAATATATCTGTCATG
CTGGGAAGATGTCAGACCTACACAAGTGAGTACAAGAGTGCAGTGGGTAACTTGGCACTGAGAG
TTGAACGTGCCCAACGGGAGATTGACTACATACAATACCTTCGAGAGGCTGACGAGTGCATCGA
ATCAGAGGACAAGACACTGGCAGAAATGTTGCTCCAAGAAGCTGAAGAAGAGAAAAAGATCCGG
ACTCTGCTGAATGCAAGTAAGAAAACTGCATCTTTTCCTAGCCCTTCTAGGGACTATTATGCTC
AGAAACACACAGACTCAGAGCAGTCAGGGAGCATCATAGAGTAATGAGAGTAAGAATTGGAGGT
GTGCTTTTGTGTGCATTGCTGAGAGAGAAAGCTATACAGAGAACAGGTGTCCAAAGAGAAATCC
ATTCTCGCAAAGCCATTCTTTCTTTCACACACAGTGCCTAAAGCCTCCATAGATGGTGAAGGCT
ATAGTGCCAAAAGTCAGCCCAAAGAGACTACCTCCTGATAAATCTTGGTTTGGTGGAGATGTGT
GGTCCCAGATTTTTTCAGGGAAAGTAGCAGTTTGGTGGATTCTACATCCAGTACCCAGGCTGTA
GATAGCATCTGCAAATGTACCAAGAAACAGTCTTAAATTGGAAATGGCAACAGCCAACCCTCAG
GGATGGGAACTGCAGTGAATCACTATTGTGTGTGCTGTCTGAGATGGTGATATGCATGGGATGT
GGTCTAATCTTGTGATCCATCAGAATCACTTCCAAGCCATTAAGAATAATGTGTAGCAGCTCAA
ATTATAATAAACAGTATCAGGCAATAAACACACAAATGACAAAGAAAAA

hide sequence

RefSeq Acc Id:

NM_198474 ⟹ NP_940876

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	7,485,506 - 7,511,377 (+)	NCBI
GRCh37	11	7,506,600 - 7,533,128 (+)	NCBI
Build 36	11	7,463,331 - 7,489,140 (+)	NCBI Archive
Celera	11	7,625,730 - 7,651,738 (+)	RGD
HuRef	11	7,165,129 - 7,191,140 (+)	RGD
CHM1_1	11	7,505,519 - 7,531,529 (+)	NCBI
T2T-CHM13v2.0	11	7,543,862 - 7,569,737 (+)	NCBI

Sequence:

show sequence

ATCTTCACCCCCCACCCCAATGCACACACAATTAAGCCAGGAAGCAGCTTGCAACCACTAGCCT
GGGGAGGGTCCGCATGTGTCAAGGGTGAGGGCAACAGATGCTGGACCCAGGGAGCTCTCTGCCA
CAGGTCAGTCTACAAGGCCTCAGGGACCAACTTGCCAACAGCTGGACTTGATCACTAGCTGGCA
AACTGAGCTCACGTATCGGGTGGAATAACAAGCGGACTTTGCTCTCTGCTGTGCAAAACGCTGT
TTTTAGAGGATTTGCCACAGCAGCGGATAGAGCAGGAGAGCACCACCGGAGCCCTTGAGACATC
CTTGAGAAGAGCCACAGCATAAGAGACTGCCCTGCTTGGTGTTTTGCAGGATGATGGTGGCCCT
TCGAGGAGCTTCTGCATTGCTGGTTCTGTTCCTTGCAGCTTTTCTGCCCCCGCCGCAGTGTACC
CAGGACCCAGCCATGGTGCATTACATCTACCAGCGCTTTCGAGTCTTGGAGCAAGGGCTGGAAA
AATGTACCCAAGCAACGAGGGCATACATTCAAGAATTCCAAGAGTTCTCAAAAAATATATCTGT
CATGCTGGGAAGATGTCAGACCTACACAAGTGAGTACAAGAGTGCAGTGGGTAACTTGGCACTG
AGAGTTGAACGTGCCCAACGGGAGATTGACTACATACAATACCTTCGAGAGGCTGACGAGTGCA
TCGAATCAGAGGACAAGACACTGGCAGAAATGTTGCTCCAAGAAGCTGAAGAAGAGAAAAAGAT
CCGGACTCTGCTGAATGCAAGCTGTGACAACATGCTGATGGGCATAAAGTCTTTGAAAATAGTG
AAGAAGATGATGGACACACATGGCTCTTGGATGAAAGATGCTGTCTATAACTCTCCAAAGGTGT
ACTTATTAATTGGATCCAGAAACAACACTGTTTGGGAATTTGCAAACATACGGGCATTCATGGA
GGATAACACCAAGCCAGCTCCCCGGAAGCAAATCCTAACACTTTCCTGGCAGGGAACAGGCCAA
GTGATCTACAAAGGTTTTCTATTTTTTCATAACCAAGCAACTTCTAATGAGATAATCAAATATA
ACCTGCAGAAGAGGACTGTGGAAGATCGAATGCTGCTCCCAGGAGGGGTAGGCCGAGCATTGGT
TTACCAGCACTCCCCCTCAACTTACATTGACCTGGCTGTGGATGAGCATGGGCTCTGGGCCATC
CACTCTGGGCCAGGCACCCATAGCCATTTGGTTCTCACAAAGATTGAGCCGGGCACACTGGGAG
TGGAGCATTCATGGGATACCCCATGCAGAAGCCAGGATGCTGAAGCCTCATTCCTCTTGTGTGG
GGTTCTCTATGTGGTCTACAGTACTGGGGGCCAGGGCCCTCATCGCATCACCTGCATCTATGAT
CCACTGGGCACTATCAGTGAGGAGGACTTGCCCAACTTGTTCTTCCCCAAGAGACCAAGAAGTC
ACTCCATGATCCATTACAACCCCAGAGATAAGCAGCTCTATGCCTGGAATGAAGGAAACCAGAT
CATTTACAAACTCCAGACAAAGAGAAAGCTGCCTCTGAAGTAATGCATTACAGCTGTGAGAAAG
AGCACTGTGGCTTTGGCAGCTGTTCTACAGGACAGTGAGGCTATAGCCCCTTCACAATATAGTA
TCCCTCTAATCACACACAGGAAGAGTGTGTAGAAGTGGAAATACGTATGCCTCCTTTCCCAAAT
GTCACTGCCTTAGGTATCTTCCAAGAGCTTAGATGAGAGCATATCATCAGGAAAGTTTCAACAA
TGTCCATTACTCCCCCAAACCTCCTGGCTCTCAAGGATGACCACATTCTGATACAGCCTACTTC
AAGCCTTTTGTTTTACTGCTCCCCAGCATTTACTGTAACTCTGCCATCTTCCCTCCCACAATTA
GAGTTGTATGCCAGCCCCTAATATTCACCACTGGCTTTTCTCTCCCCTGGCCTTTGCTGAAGCT
CTTCCCTCTTTTTCAAATGTCTATTGATATTCTCCCATTTTCACTGCCCAACTAAAATACTATT
AATATTTCTTTCTTTTCTTTTCTTTTTTTTGAGACAAGGTCTCACTATGTTGCCCAGGCTGGTC
TCAAACTCCAGAGCTCAAGAGATCCTCCTGCCTCAGCCTCCTAAGTACCTGGGATTACAGGCAT
GTGCCACCACACCTGGCTTAAAATACTATTTCTTATTGAGGTTTAACCTCTATTTCCCCTAGCC
CTGTCCTTCCACTAAGCTTGGTAGATGTAATAATAAAGTGAAAATATTAACATTTGAATATCGC
TTTCCAGGTGTGGAGTGTTTGCACATCATTTAATTCTCGTTTCACCTTTGTGAAACATGCACAA
GTCTTTACAGCTGTCATTCTAGAGTTTAGGTGAGTAACACAATTACAAAGTGAAAGATACAGCT
AGAAAATACTACAAATCCCATAGTTTTTCCATTGCCCAAGGAAGCATCAAATACGTATGTTTGT
TCACCTACTCTTATAGTCAATGCGTTCATCGTTTCAGCCTAAAAATAATAGTCTGTCCCTTTAG
CCAGTTTTCATGTCTGCACAAGACCTTTCAATAGGCCTTTCAAATGATAATTCCTCCAGAAAAC
CAGTCTAAGGGTGAGGACCCCAACTCTAGCCTCCTCTTGTCTTGCTGTCCTCTGTTTCTCTCTT
TCTGCTTTAAATTCAATAAAAGTGACACTGAGCAAATAACCTCATCAGGTTATATTTGCCCACA
TACCCTAAGCACAAAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001357427	(Get FASTA)	NCBI Sequence Viewer
	NP_001357428	(Get FASTA)	NCBI Sequence Viewer
	NP_001357429	(Get FASTA)	NCBI Sequence Viewer
	NP_001357430	(Get FASTA)	NCBI Sequence Viewer
	NP_940876	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH35895	(Get FASTA)	NCBI Sequence Viewer
	AAH92488	(Get FASTA)	NCBI Sequence Viewer
	AAQ88954	(Get FASTA)	NCBI Sequence Viewer
	BAG60123	(Get FASTA)	NCBI Sequence Viewer
	BAG60415	(Get FASTA)	NCBI Sequence Viewer
	CAI46097	(Get FASTA)	NCBI Sequence Viewer
	EAW68655	(Get FASTA)	NCBI Sequence Viewer
	EAW68656	(Get FASTA)	NCBI Sequence Viewer
	EAW68657	(Get FASTA)	NCBI Sequence Viewer
	EAW68658	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000332511
	ENSP00000332511.3
	ENSP00000431558.1
	ENSP00000433455
	ENSP00000433455.1
	ENSP00000434813.1
GenBank Protein	Q6UWY5	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_940876 ⟸ NM_198474
- Peptide Label:	isoform a precursor
- UniProtKB:	Q6UWY5 (UniProtKB/Swiss-Prot), B4DP03 (UniProtKB/Swiss-Prot), Q569G4 (UniProtKB/Swiss-Prot), Q5HYE3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MMVALRGASALLVLFLAAFLPPPQCTQDPAMVHYIYQRFRVLEQGLEKCTQATRAYIQEFQEFS KNISVMLGRCQTYTSEYKSAVGNLALRVERAQREIDYIQYLREADECIESEDKTLAEMLLQEAE EEKKIRTLLNASCDNMLMGIKSLKIVKKMMDTHGSWMKDAVYNSPKVYLLIGSRNNTVWEFANI RAFMEDNTKPAPRKQILTLSWQGTGQVIYKGFLFFHNQATSNEIIKYNLQKRTVEDRMLLPGGV GRALVYQHSPSTYIDLAVDEHGLWAIHSGPGTHSHLVLTKIEPGTLGVEHSWDTPCRSQDAEAS FLLCGVLYVVYSTGGQGPHRITCIYDPLGTISEEDLPNLFFPKRPRSHSMIHYNPRDKQLYAWN EGNQIIYKLQTKRKLPLK hide sequence

RefSeq Acc Id:	NP_001357427 ⟸ NM_001370498
- Peptide Label:	isoform a precursor
- UniProtKB:	Q6UWY5 (UniProtKB/Swiss-Prot), B4DP03 (UniProtKB/Swiss-Prot), Q569G4 (UniProtKB/Swiss-Prot), Q5HYE3 (UniProtKB/TrEMBL)

RefSeq Acc Id:	NP_001357429 ⟸ NM_001370500
- Peptide Label:	isoform c precursor

RefSeq Acc Id:	NP_001357428 ⟸ NM_001370499
- Peptide Label:	isoform b
- UniProtKB:	B4DN61 (UniProtKB/TrEMBL)

RefSeq Acc Id:	NP_001357430 ⟸ NM_001370501
- Peptide Label:	isoform c precursor

Ensembl Acc Id:

ENSP00000433455 ⟸ ENST00000530135

Ensembl Acc Id:

ENSP00000431558 ⟸ ENST00000534244

Ensembl Acc Id:

ENSP00000332511 ⟸ ENST00000329293

Ensembl Acc Id:

ENSP00000434813 ⟸ ENST00000528758

Protein Domains

Olfactomedin-like

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6UWY5-F1-model_v2	AlphaFold	Q6UWY5	1-402	view protein structure

Promoters

RGD ID:

7219547

Promoter ID:

EPDNEW_H15518

Type:

initiation region

Name:

OLFML1_2

Description:

olfactomedin like 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H15519

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	7,485,359 - 7,485,419	EPDNEW

RGD ID:

7219545

Promoter ID:

EPDNEW_H15519

Type:

initiation region

Name:

OLFML1_1

Description:

olfactomedin like 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H15518

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	7,485,533 - 7,485,593	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:24473	AgrOrtholog
COSMIC	OLFML1	COSMIC
Ensembl Genes	ENSG00000183801	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000329293	ENTREZGENE
	ENST00000329293.4	UniProtKB/Swiss-Prot
	ENST00000528758.1	UniProtKB/TrEMBL
	ENST00000530135	ENTREZGENE
	ENST00000530135.5	UniProtKB/Swiss-Prot
	ENST00000534244.1	UniProtKB/TrEMBL
GTEx	ENSG00000183801	GTEx
HGNC ID	HGNC:24473	ENTREZGENE
Human Proteome Map	OLFML1	Human Proteome Map
InterPro	Olfac-like_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Olfactomedin-like_domain	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:283298	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	283298	ENTREZGENE
PANTHER	OLFACTOMEDIN-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR23192:SF13	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	OLF	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134904379	PharmGKB
PROSITE	OLF	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	OLF	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	B4DN61	ENTREZGENE, UniProtKB/TrEMBL
	B4DP03	ENTREZGENE
	E9PKN7_HUMAN	UniProtKB/TrEMBL
	E9PN44_HUMAN	UniProtKB/TrEMBL
	OLFL1_HUMAN	UniProtKB/Swiss-Prot
	Q569G4	ENTREZGENE
	Q5HYE3	ENTREZGENE, UniProtKB/TrEMBL
	Q6UWY5	ENTREZGENE
UniProt Secondary	B4DP03	UniProtKB/Swiss-Prot
	Q569G4	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-11-17	OLFML1	olfactomedin like 1		olfactomedin-like 1	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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