LMBR1L (limb development membrane protein 1 like)

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Gene: LMBR1L (limb development membrane protein 1 like) Homo sapiens

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Symbol:

LMBR1L

Name:

limb development membrane protein 1 like

RGD ID:

1603995

HGNC Page

HGNC:18268

Description:

Enables transmembrane signaling receptor activity. Involved in receptor-mediated endocytosis and signal transduction. Located in endoplasmic reticulum membrane and plasma membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ10494; FLJ36251; KIAA1174; limb development membrane protein 1 like-protein; limb development membrane protein 1-like; limb region 1 homolog-like; limb region 1 protein homolog-like; limb region 1-like protein -like; LIMR; lipocalin-1 interacting membrane receptor; lipocalin-1-interacting membrane receptor; lipocalin-interacting membrane receptor

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):	Lmbr1l (limb region 1 like)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Lmbr1l (limb development membrane protein 1-like)	HGNC	Ensembl, NCBI, Panther
Chinchilla lanigera (long-tailed chinchilla):	Lmbr1l (limb development membrane protein 1 like)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	LMBR1L (limb development membrane protein 1 like)	NCBI	Ortholog
Canis lupus familiaris (dog):	LMBR1L (limb development membrane protein 1 like)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoMCL, Panther, PhylomeDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Lmbr1l (limb development membrane protein 1 like)	NCBI	Ortholog
Sus scrofa (pig):	LMBR1L (limb development membrane protein 1 like)	HGNC	Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	LMBR1L (limb development membrane protein 1 like)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Lmbr1l (limb development membrane protein 1 like)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Lmbr1l (limb development membrane protein 1-like)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Lmbr1l (limb region 1 like)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	lmbr1l (limb development membrane protein 1-like)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Caenorhabditis elegans (roundworm):	R05D3.2	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	lili	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus tropicalis (tropical clawed frog):	lmbr1l	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	lmbr1l.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	lmbr1l.S	Alliance	DIOPT (Xenbase)

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	12	49,097,139 - 49,110,847 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	49,097,136 - 49,110,900 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	49,490,922 - 49,504,630 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	47,777,189 - 47,790,947 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	12	48,285,709 - 48,299,467 (-)	NCBI		Celera
Cytogenetic Map	12	q13.12	NCBI
HuRef	12	46,521,993 - 46,535,753 (-)	NCBI		HuRef
CHM1_1	12	49,456,235 - 49,470,132 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	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

1,2-dimethylhydrazine (ISO)

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

3,4-methylenedioxymethamphetamine (ISO)

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

4,4'-sulfonyldiphenol (ISO)

acrylamide (ISO)

all-trans-retinoic acid (EXP)

apigenin (ISO)

Benoxacor (ISO)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP,ISO)

cadmium atom (ISO)

cadmium dichloride (ISO)

carbon nanotube (ISO)

chlorpyrifos (ISO)

ciguatoxin CTX1B (ISO)

clofibrate (ISO)

decabromodiphenyl ether (ISO)

dexamethasone (EXP)

Dibutyl phosphate (EXP)

folic acid (ISO)

fulvestrant (EXP)

indometacin (EXP)

ozone (EXP,ISO)

paracetamol (ISO)

pirinixic acid (EXP)

sodium arsenite (EXP)

titanium dioxide (ISO)

triphenyl phosphate (EXP)

triptonide (ISO)

triticonazole (ISO)

urethane (EXP)

valproic acid (ISO)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

endocytosis (IEA)

hematopoietic stem cell differentiation (IEA,ISS)

negative regulation of canonical Wnt signaling pathway (IEA,ISS)

receptor-mediated endocytosis (IBA,IMP)

signal transduction (IBA,IDA)

T cell apoptotic process (IEA,ISS)

T cell differentiation (IEA,ISS)

T cell proliferation (IEA,ISS)

Wnt signaling pathway (IEA)

Cellular Component

endomembrane system (IEA)

endoplasmic reticulum (IEA)

endoplasmic reticulum membrane (IDA,IEA)

membrane (IEA)

plasma membrane (IBA,IDA,IEA)

Molecular Function

protein binding (IPI)

transmembrane signaling receptor activity (IBA,IDA)

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:10574461	PMID:11287427	PMID:12477932	PMID:12591932	PMID:12975309	PMID:14702039	PMID:15489334	PMID:16344560	PMID:16423471	PMID:17991420	PMID:19136951	PMID:20446115
PMID:21516116	PMID:21791187	PMID:21873635	PMID:23964685	PMID:26638075	PMID:26871637	PMID:27432908	PMID:31073040	PMID:32513696	PMID:33961781	PMID:35146515	PMID:35156780

Genomics

Comparative Map Data

LMBR1L
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	49,097,136 - 49,110,900 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	49,490,922 - 49,504,630 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	47,777,189 - 47,790,947 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	12	48,285,709 - 48,299,467 (-)	NCBI		Celera
Cytogenetic Map	12	q13.12	NCBI
HuRef	12	46,521,993 - 46,535,753 (-)	NCBI		HuRef
CHM1_1	12	49,456,235 - 49,470,132 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI		T2T-CHM13v2.0

Lmbr1l
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	15	98,801,798 - 98,815,944 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	15	98,801,798 - 98,816,112 (-)	Ensembl		GRCm39 Ensembl
GRCm38	15	98,903,918 - 98,918,098 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	15	98,903,917 - 98,918,231 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	15	98,734,352 - 98,748,529 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	15	98,731,955 - 98,746,132 (-)	NCBI		MGSCv36	mm8
Celera	15	101,053,500 - 101,067,677 (-)	NCBI		Celera
Cytogenetic Map	15	F1	NCBI
cM Map	15	55.1	NCBI

Lmbr1l
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	7	131,940,081 - 131,958,832 (-)	NCBI		GRCr8
mRatBN7.2	7	130,061,136 - 130,078,101 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	7	130,061,136 - 130,076,381 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	7	131,866,544 - 131,881,784 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	7	134,092,106 - 134,107,346 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	7	134,004,617 - 134,019,857 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	7	140,585,512 - 140,600,797 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	7	140,585,832 - 140,600,818 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	X	115,090,815 - 115,107,826 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	7	137,683,441 - 137,692,537 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	7	137,759,902 - 137,768,974 (-)	NCBI
Celera	7	126,552,541 - 126,561,639 (-)	NCBI		Celera
Cytogenetic Map	7	q36	NCBI

Lmbr1l
(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_004955500	7,921,233 - 7,934,538 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955500	7,922,422 - 7,934,538 (-)	NCBI	ChiLan1.0	ChiLan1.0

LMBR1L
(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	10	45,073,683 - 45,088,075 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	12	45,070,444 - 45,084,836 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	12	39,639,957 - 39,653,736 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	12	40,519,746 - 40,533,435 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	12	40,519,746 - 40,533,435 (+)	Ensembl	panpan1.1		panPan2

LMBR1L
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	27	5,475,632 - 5,488,456 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	27	5,475,658 - 5,487,978 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	27	40,769,055 - 40,781,876 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	27	5,526,748 - 5,539,570 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	27	5,526,933 - 5,539,567 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	27	5,490,998 - 5,503,814 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	27	5,480,920 - 5,493,521 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	27	41,161,667 - 41,174,498 (-)	NCBI		UU_Cfam_GSD_1.0

Lmbr1l
(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_024404945	66,254,281 - 66,272,032 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936512	6,892,801 - 6,910,576 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936512	6,892,798 - 6,910,576 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

LMBR1L
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	5	15,121,554 - 15,135,252 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	5	15,121,550 - 15,137,625 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	5	15,480,564 - 15,494,714 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

LMBR1L
(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	11	45,338,090 - 45,355,551 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	11	45,337,977 - 45,355,812 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666037	200,790,166 - 200,803,727 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Lmbr1l
(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_female_1.0 Ensembl	NW_004624816	3,078,152 - 3,094,252 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624816	3,078,299 - 3,094,010 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in LMBR1L
30 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	copy number gain	See cases [RCV000139555]	Chr12:121271..133196807 [GRCh38] Chr12:282465..133773393 [GRCh37] Chr12:100698..132283466 [NCBI36] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	copy number gain	See cases [RCV000258805]	Chr12:1..133851895 [GRCh37] Chr12:12p13.33-q24.33	pathogenic\|likely pathogenic
GRCh37/hg19 12p11.21-q13.12(chr12:31886971-50360461)x3	copy number gain	See cases [RCV000207454]	Chr12:31886971..50360461 [GRCh37] Chr12:12p11.21-q13.12	pathogenic
GRCh37/hg19 12q11-13.12(chr12:37857750-49791459)x3	copy number gain	See cases [RCV000448835]	Chr12:37857750..49791459 [GRCh37] Chr12:12q11-13.12	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	copy number gain	See cases [RCV000510482]	Chr12:173787..133777902 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	copy number gain	See cases [RCV000511643]	Chr12:173787..133777902 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
NM_018113.4(LMBR1L):c.15C>A (p.Asp5Glu)	single nucleotide variant	not specified [RCV004301821]	Chr12:49110541 [GRCh38] Chr12:49504324 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.667G>A (p.Val223Ile)	single nucleotide variant	not specified [RCV004331802]	Chr12:49102916 [GRCh38] Chr12:49496699 [GRCh37] Chr12:12q13.12	uncertain significance
GRCh37/hg19 12q13.12(chr12:49191810-49630201)x3	copy number gain	not provided [RCV000683434]	Chr12:49191810..49630201 [GRCh37] Chr12:12q13.12	uncertain significance
NC_000012.11:g.26370251_54361538inv	inversion	not specified [RCV000714265]	Chr12:26370251..54361538 [GRCh37] Chr12:12p12.1-q13.13	uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3	copy number gain	not provided [RCV000750246]	Chr12:191619..133777645 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3	copy number gain	not provided [RCV000750253]	Chr12:621220..133779118 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
NM_018113.4(LMBR1L):c.947T>C (p.Ile316Thr)	single nucleotide variant	not specified [RCV004296233]	Chr12:49101533 [GRCh38] Chr12:49495316 [GRCh37] Chr12:12q13.12	uncertain significance
GRCh37/hg19 12q13.11-13.12(chr12:49024019-50299974)x3	copy number gain	not provided [RCV001259140]	Chr12:49024019..50299974 [GRCh37] Chr12:12q13.11-13.12	uncertain significance
GRCh37/hg19 12q11-13.12(chr12:37873948-49578619)x3	copy number gain	See cases [RCV001353185]	Chr12:37873948..49578619 [GRCh37] Chr12:12q11-13.12	likely pathogenic
NM_018113.4(LMBR1L):c.863G>A (p.Arg288Gln)	single nucleotide variant	DSD incomplete virilization [RCV001849542]	Chr12:49102187 [GRCh38] Chr12:49495970 [GRCh37] Chr12:12q13.12	likely pathogenic
NM_018113.4(LMBR1L):c.862C>T (p.Arg288Trp)	single nucleotide variant	DSD incomplete virilization [RCV001849543]	Chr12:49102188 [GRCh38] Chr12:49495971 [GRCh37] Chr12:12q13.12	likely pathogenic
NM_018113.4(LMBR1L):c.115A>G (p.Ile39Val)	single nucleotide variant	DSD incomplete virilization [RCV001849544]	Chr12:49107003 [GRCh38] Chr12:49500786 [GRCh37] Chr12:12q13.12	uncertain significance
GRCh37/hg19 12q11-13.12(chr12:37857750-49791459)	copy number gain	not specified [RCV002052988]	Chr12:37857750..49791459 [GRCh37] Chr12:12q11-13.12	pathogenic
NM_018113.4(LMBR1L):c.1336C>T (p.Leu446Phe)	single nucleotide variant	not specified [RCV004082481]	Chr12:49098010 [GRCh38] Chr12:49491793 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1169C>T (p.Thr390Met)	single nucleotide variant	not specified [RCV004205551]	Chr12:49100560 [GRCh38] Chr12:49494343 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1432G>A (p.Gly478Ser)	single nucleotide variant	not specified [RCV004233369]	Chr12:49097710 [GRCh38] Chr12:49491493 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1156G>A (p.Asp386Asn)	single nucleotide variant	not specified [RCV004187633]	Chr12:49100573 [GRCh38] Chr12:49494356 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.190G>A (p.Ala64Thr)	single nucleotide variant	not specified [RCV004097009]	Chr12:49105925 [GRCh38] Chr12:49499708 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1103T>C (p.Val368Ala)	single nucleotide variant	not specified [RCV004095551]	Chr12:49100626 [GRCh38] Chr12:49494409 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.946A>G (p.Ile316Val)	single nucleotide variant	not specified [RCV004076380]	Chr12:49101534 [GRCh38] Chr12:49495317 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.434A>G (p.Lys145Arg)	single nucleotide variant	not specified [RCV004136551]	Chr12:49104449 [GRCh38] Chr12:49498232 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.242T>G (p.Leu81Arg)	single nucleotide variant	not specified [RCV004123510]	Chr12:49104835 [GRCh38] Chr12:49498618 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.64G>C (p.Glu22Gln)	single nucleotide variant	not specified [RCV004077778]	Chr12:49110492 [GRCh38] Chr12:49504275 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.719A>G (p.Gln240Arg)	single nucleotide variant	not specified [RCV004273440]	Chr12:49102518 [GRCh38] Chr12:49496301 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.64G>A (p.Glu22Lys)	single nucleotide variant	not specified [RCV004286941]	Chr12:49110492 [GRCh38] Chr12:49504275 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.155C>T (p.Thr52Ile)	single nucleotide variant	not specified [RCV004253216]	Chr12:49106963 [GRCh38] Chr12:49500746 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.359C>T (p.Ser120Phe)	single nucleotide variant	not specified [RCV004276773]	Chr12:49104524 [GRCh38] Chr12:49498307 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1150T>A (p.Trp384Arg)	single nucleotide variant	not specified [RCV004351320]	Chr12:49100579 [GRCh38] Chr12:49494362 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.998G>A (p.Arg333Gln)	single nucleotide variant	not specified [RCV004363495]	Chr12:49101482 [GRCh38] Chr12:49495265 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1378C>T (p.Arg460Trp)	single nucleotide variant	not specified [RCV004342646]	Chr12:49097968 [GRCh38] Chr12:49491751 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1414C>G (p.Leu472Val)	single nucleotide variant	not specified [RCV004365441]	Chr12:49097728 [GRCh38] Chr12:49491511 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1209C>G (p.Ser403Arg)	single nucleotide variant	not specified [RCV004407578]	Chr12:49100419 [GRCh38] Chr12:49494202 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1229C>T (p.Ser410Phe)	single nucleotide variant	not specified [RCV004407579]	Chr12:49100399 [GRCh38] Chr12:49494182 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.1437C>A (p.Phe479Leu)	single nucleotide variant	not specified [RCV004407580]	Chr12:49097705 [GRCh38] Chr12:49491488 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.925C>G (p.Leu309Val)	single nucleotide variant	not specified [RCV004407583]	Chr12:49102125 [GRCh38] Chr12:49495908 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.476T>C (p.Met159Thr)	single nucleotide variant	not specified [RCV004407581]	Chr12:49103773 [GRCh38] Chr12:49497556 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.757C>T (p.Arg253Cys)	single nucleotide variant	not specified [RCV004407582]	Chr12:49102480 [GRCh38] Chr12:49496263 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.578A>G (p.Tyr193Cys)	single nucleotide variant	not specified [RCV004637195]	Chr12:49103144 [GRCh38] Chr12:49496927 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.241C>T (p.Leu81Phe)	single nucleotide variant	not specified [RCV004637196]	Chr12:49104836 [GRCh38] Chr12:49498619 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.208T>C (p.Phe70Leu)	single nucleotide variant	not specified [RCV004634028]	Chr12:49104869 [GRCh38] Chr12:49498652 [GRCh37] Chr12:12q13.12	uncertain significance
NM_018113.4(LMBR1L):c.389T>C (p.Phe130Ser)	single nucleotide variant	not specified [RCV004634029]	Chr12:49104494 [GRCh38] Chr12:49498277 [GRCh37] Chr12:12q13.12	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	10256
Count of miRNA genes:	1231
Interacting mature miRNAs:	1628
Transcripts:	ENST00000267102, ENST00000395141, ENST00000417750, ENST00000457164, ENST00000547382, ENST00000547670, ENST00000547675, ENST00000547698, ENST00000547813, ENST00000548983, ENST00000549296, ENST00000549429, ENST00000549587, ENST00000549730, ENST00000550137, ENST00000550815, ENST00000550867, ENST00000551115, ENST00000551143, ENST00000551169, ENST00000551272, ENST00000551535, ENST00000551782, ENST00000551854, ENST00000552141, ENST00000552153, ENST00000552449, ENST00000552577, ENST00000552879, ENST00000553040, ENST00000553204
Prediction methods:	Microtar, 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.

Markers in Region

RH93826

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	49,490,995 - 49,491,134	UniSTS	GRCh37
Build 36	12	47,777,262 - 47,777,401	RGD	NCBI36
Celera	12	48,285,782 - 48,285,921	RGD
Cytogenetic Map	12	q13.12	UniSTS
HuRef	12	46,522,066 - 46,522,205	UniSTS
GeneMap99-GB4 RH Map	12	218.85	UniSTS

LIMR__7410

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	49,490,805 - 49,491,477	UniSTS	GRCh37
Build 36	12	47,777,072 - 47,777,744	RGD	NCBI36
Celera	12	48,285,592 - 48,286,264	RGD
HuRef	12	46,521,876 - 46,522,548	UniSTS

MARC_14539-14540:1008957287:5

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	49,497,498 - 49,498,300	UniSTS	GRCh37
Build 36	12	47,783,765 - 47,784,567	RGD	NCBI36
Celera	12	48,292,285 - 48,293,087	RGD
HuRef	12	46,528,571 - 46,529,373	UniSTS

RH103359

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	12	q13.12	UniSTS
GeneMap99-GB4 RH Map	12	218.92	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	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2253	4973	1726	2351	6	624	1950	465	2269	7305	6471	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001300750	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001300751	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352161	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352162	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352163	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352164	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352165	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352166	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352167	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352168	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_018113	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019626	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019631	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449047	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449048	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449049	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449050	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449051	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449052	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449054	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429139	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429142	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429143	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372530	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372531	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372532	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372533	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372534	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372535	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_002957350	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008488640	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_245944	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB033000	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC011603	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF260728	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF351620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK001356	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK001651	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK093570	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298026	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298859	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310674	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL137599	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL556633	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY358572	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC008337	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC015015	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031550	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471111	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA012883	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178712	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU178715	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MW841072	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MW841073	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000267102 ⟹ ENSP00000267102

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,139 - 49,110,847 (-)	Ensembl

Ensembl Acc Id:

ENST00000417750 ⟹ ENSP00000394677

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,136 - 49,110,681 (-)	Ensembl

Ensembl Acc Id:

ENST00000457164 ⟹ ENSP00000413785

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,102,353 - 49,110,850 (-)	Ensembl

Ensembl Acc Id:

ENST00000547382 ⟹ ENSP00000447329

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,142 - 49,110,850 (-)	Ensembl

Ensembl Acc Id:

ENST00000547670 ⟹ ENSP00000446718

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,700 - 49,110,877 (-)	Ensembl

Ensembl Acc Id:

ENST00000547675 ⟹ ENSP00000447240

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,102,476 - 49,110,675 (-)	Ensembl

Ensembl Acc Id:

ENST00000547698 ⟹ ENSP00000448821

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,145 - 49,101,549 (-)	Ensembl

Ensembl Acc Id:

ENST00000547813

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,327 - 49,101,658 (-)	Ensembl

Ensembl Acc Id:

ENST00000548983

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,106,691 - 49,110,847 (-)	Ensembl

Ensembl Acc Id:

ENST00000549296 ⟹ ENSP00000450032

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,104,499 - 49,110,850 (-)	Ensembl

Ensembl Acc Id:

ENST00000549429

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,100,759 - 49,101,501 (-)	Ensembl

Ensembl Acc Id:

ENST00000549587

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,104,494 - 49,105,232 (-)	Ensembl

Ensembl Acc Id:

ENST00000549730

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,103,103 - 49,106,080 (-)	Ensembl

Ensembl Acc Id:

ENST00000550137 ⟹ ENSP00000449103

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,104,470 - 49,110,845 (-)	Ensembl

Ensembl Acc Id:

ENST00000550815 ⟹ ENSP00000448973

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,104,751 - 49,110,677 (-)	Ensembl

Ensembl Acc Id:

ENST00000550867

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,158 - 49,110,667 (-)	Ensembl

Ensembl Acc Id:

ENST00000551115

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,106,423 - 49,110,884 (-)	Ensembl

Ensembl Acc Id:

ENST00000551143

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,098,002 - 49,102,343 (-)	Ensembl

Ensembl Acc Id:

ENST00000551169 ⟹ ENSP00000448128

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,103,081 - 49,107,011 (-)	Ensembl

Ensembl Acc Id:

ENST00000551272

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,674 - 49,100,732 (-)	Ensembl

Ensembl Acc Id:

ENST00000551535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,106,589 - 49,110,900 (-)	Ensembl

Ensembl Acc Id:

ENST00000551782 ⟹ ENSP00000449633

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,104,503 - 49,110,886 (-)	Ensembl

Ensembl Acc Id:

ENST00000551854 ⟹ ENSP00000446641

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,104,474 - 49,110,205 (-)	Ensembl

Ensembl Acc Id:

ENST00000552141

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,101,920 - 49,103,778 (-)	Ensembl

Ensembl Acc Id:

ENST00000552153

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,103,687 - 49,110,871 (-)	Ensembl

Ensembl Acc Id:

ENST00000552449 ⟹ ENSP00000450362

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,100,600 - 49,102,176 (-)	Ensembl

Ensembl Acc Id:

ENST00000552577

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,137 - 49,104,379 (-)	Ensembl

Ensembl Acc Id:

ENST00000552879

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,101,103 - 49,103,120 (-)	Ensembl

Ensembl Acc Id:

ENST00000553040 ⟹ ENSP00000448147

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,097,157 - 49,102,196 (-)	Ensembl

Ensembl Acc Id:

ENST00000553204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	49,103,701 - 49,110,693 (-)	Ensembl

RefSeq Acc Id:

NM_001300750 ⟹ NP_001287679

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
CHM1_1	12	49,456,235 - 49,470,135 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GTTTCATCCTACAAAATGGGCGTAACAATGTCTACCTACTCCATTGTGTGGACCAAAGGAGATG
GTTAATGTGAAAGCCCTTTGTGAACCTGAAGTGAGCAACTGCTGGATGAATGTCATTACGGGCA
CAGGCTCTGTGTCATCTCCTCTCCTAGTGCTTCCACAGCCAGGACCAGAGACCTCCCTGATGAC
TGGGGAACCTGTGGATGATGAAGATGCCACCGTCAACAAGATTGCGCTCGAGCTGTGCACCTTT
ACCCTGGCAATTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTCCATCATCAGCAATGAGGTGC
TGCTCTCCCTGCCTCGGAACTACTACATCCAGTGGCTCAACGGCTCCCTCATCCATGGCCTCTG
GAACCTTGTTTTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCATGCCCTTTGCATATTTCTTC
ACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGGCCGGGTCTATGAGACAGTGG
TGATGTTGATGCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGGGTGGCATCAGCCATTGTGGA
CAAGAACAAGGCCAACAGAGAGTCACTCTATGACTTTTGGGAGTACTATCTCCCCTACCTCTAC
TCATGCATCTCCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTACTCCACTGGGTCTCGCCCGCA
TGTTCTCCGTCACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTGGAAGACCTGGAGGAGCAGCT
GTACTGCTCAGCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTGTAATCCTACTTCCTGCTGG
CTGCCTTTAGACATGGAGCTGCTACACAGACAGGTCCTGGCTCTGCAGACACAGAGGGTCCTGC
TGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCTACCCCCTGGCTATGCTGTG
CTTGCTGGTGCTGACGGGCCTGTCTGTGCTCATTGTGGCCATCCACATCCTGGAGCTGCTCATC
GATGAGGCTGCCATGCCCCGAGGCATGCAGGGTACCTCCTTAGGCCAGGTCTCCTTCTCCAAGC
TGGGCTCCTTTGGTGCCGTCATTCAGGTTGTACTCATCTTTTACCTAATGGTGTCCTCAGTTGT
GGGCTTCTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATGGCACGACACTGCCATGACG
CAGATAATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTTCTCTCGAA
CCCTGGGGCTCACTCGCTTTGACCTGCTGGGTGACTTTGGACGCTTCAACTGGCTGGGCAATTT
CTACATTGTGTTCCTCTACAACGCAGCCTTTGCAGGCCTCACCACACTCTGTCTGGTGAAGACC
TTCACTGCAGCTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTGGACAGACTGCCGCTGCCCG
TCTCCGGTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGGAA
GGAAAAAACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGACC
TCAGGACCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCATA
ATCTGAGCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCATG
GGGTAGGGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCCTC
ACTGCTGTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGGTA
GGGGCAGGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGGCC
CAGCAGAGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGGAT
AGGGAGGAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTTAA
A

hide sequence

RefSeq Acc Id:

NM_001300751 ⟹ NP_001287680

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
CHM1_1	12	49,456,235 - 49,470,135 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GTGGATGATGAAGATGCCACCGTCAACAAGATTGCGCTCGAGCTGTGCACCTTTACCCTGGCAA
TTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTCCATCATCAGCAATGAGGTGCTGCTCTCCCT
GCCTCGGAACTACTACATCCAGTGGCTCAACGGCTCCCTCATCCATGGCCTCTGGAACCTTGTT
TTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCATGCCCTTTGCATATTTCTTCACTGAGTCTG
AGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGGCCGGGTCTATGAGACAGTGGTGATGTTGAT
GCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGGGTGGCATCAGCCATTGTGGACAAGAACAAG
GCCAACAGAGAGTCACTCTATGACTTTTGGGAGTACTATCTCCCCTACCTCTACTCATGCATCT
CCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTACTCCACTGGGTCTCGCCCGCATGTTCTCCGT
CACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTGGAAGACCTGGAGGAGCAGCTGTACTGCTCA
GCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTGTAATCCTACTTCCTGCTGGCTGCCTTTAG
ACATGGAGCTGCTACACAGACAGGTCCTGGCTCTGCAGACACAGAGGGTCCTGCTGGAGAAGAG
GCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCTACCCCCTGGCTATGCTGTGCTTGCTGGTG
CTGACGGGCCTGTCTGTGCTCATTGTGGCCATCCACATCCTGGAGCTGCTCATCGATGAGGCTG
CCATGCCCCGAGGCATGCAGGTTGTACTCATCTTTTACCTAATGGTGTCCTCAGTTGTGGGCTT
CTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATGGCACGACACTGCCATGACGCAGATA
ATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTTCTCTCGAACCCTGG
GGCTCACTCGCTTTGACCTGCTGGGTGACTTTGGACGCTTCAACTGGCTGGGCAATTTCTACAT
TGTGTTCCTCTACAACGCAGCCTTTGCAGGCCTCACCACACTCTGTCTGGTGAAGACCTTCACT
GCAGCTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTGGACAGACTGCCGCTGCCCGTCTCCG
GTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGGAAGGAAAA
AACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGACCTCAGGA
CCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCATAATCTGA
GCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCATGGGGTAG
GGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCCTCACTGCT
GTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGGTAGGGGCA
GGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGGCCCAGCAG
AGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGGATAGGGAG
GAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_001352161 ⟹ NP_001339090

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GTGGATGATGAAGATGCCACCGTCAACAAGATTGCGCTCGAGCTGTGCACCTTTACCCTGGCAA
TTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTCCATCATCAGCAATGAGGTGCTGCTCTCCCT
GCCTCGGAACTACTACATCCAGTGGCTCAACGGCTCCCTCATCCATGGCCTCTGGAACCTTGTT
TTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCATGCCCTTTGCATATTTCTTCACTGAGTCTG
AGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGGCCGGGTCTATGAGACAGTGGTGATGTTGAT
GCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGGGTGGCATCAGCCATTGTGGACAAGAACAAG
GCCAACAGAGAGTCACTCTATGACTTTTGGGAGTACTATCTCCCCTACCTCTACTCATGCATCT
CCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTACTCCACTGGGTCTCGCCCGCATGTTCTCCGT
CACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTGGAAGACCTGGAGGAGCAGCTGTACTGCTCA
GCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTGTAATCCTACTTCCTGCTGGCTGCCTTTAG
ACATGGAGCTGCTACACAGACAGGTCCTGGCTCTGCAGACACAGAGGGTCCTGCTGGAGAAGAG
GCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCTACCCCCTGGCTATGCTGTGCTTGCTGGTG
CTGACGGGCCTGTCTGTGCTCATTGTGGCCATCCACATCCTGGAGCTGCTCATCGATGAGGCTG
CCATGCCCCGAGGCATGCAGGTTGTACTCATCTTGTATCCTTCTGGAAACCCATCATTGCCTCT
GTTCAGCAAACCTGTCTCCTGGGACTCTAGACCGAGCACTTCTTGGACTTTTTACCTAATGGTG
TCCTCAGTTGTGGGCTTCTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATGGCACGACA
CTGCCATGACGCAGATAATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCACTTCCTGT
CTTCTCTCGAACCCTGGGGCTCACTCGCTTTGACCTGCTGGGTGACTTTGGACGCTTCAACTGG
CTGGGCAATTTCTACATTGTGTTCCTCTACAACGCAGCCTTTGCAGGCCTCACCACACTCTGTC
TGGTGAAGACCTTCACTGCAGCTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTGGACAGACT
GCCGCTGCCCGTCTCCGGTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCT
GGGGGTGGGAAGGAAAAAACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGG
CTACTTGGACCTCAGGACCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGC
ACTATTGCATAATCTGAGCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTG
GCCTCAGCATGGGGTAGGGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACAT
CAATCTGCCTCACTGCTGTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAAT
AGGGTGGGGTAGGGGCAGGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCT
TGCCTCTGGCCCAGCAGAGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAG
ACCAAGGGGATAGGGAGGAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTT
TGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_001352162 ⟹ NP_001339091

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GGCCTCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCATGCCCTTTGCAT
ATTTCTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGGCCGGGTCTATGA
GACAGTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGGGTGGCATCAGCC
ATTGTGGACAAGAACAAGGCCAACAGAGAGTCACTCTATGACTTTTGGGAGTACTATCTCCCCT
ACCTCTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTACTCCACTGGGTCT
CGCCCGCATGTTCTCCGTCACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTGGAAGACCTGGAG
GAGCAGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTGTAATCCTACTT
CCTGCTGGCTGCCTTTAGACATGGAGCTGCTACACAGACAGGTCCTGGCTCTGCAGACACAGAG
GGTCCTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCTACCCCCTGGCT
ATGCTGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCATTGTGGCCATCCACATCCTGGAGC
TGCTCATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGGTACCTCCTTAGGCCAGGTCTCCTT
CTCCAAGCTGGGCTCCTTTGGTGCCGTCATTCAGGTTGTACTCATCTTTTACCTAATGGTGTCC
TCAGTTGTGGGCTTCTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATGGCACGACACTG
CCATGACGCAGATAATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTT
CTCTCGAACCCTGGGGCTCACTCGCTTTGACCTGCTGGGTGACTTTGGACGCTTCAACTGGCTG
GGCAATTTCTACATTGTGTTCCTCTACAACGCAGCCTTTGCAGGCCTCACCACACTCTGTCTGG
TGAAGACCTTCACTGCAGCTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTGGACAGACTGCC
GCTGCCCGTCTCCGGTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGG
GGTGGGAAGGAAAAAACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTA
CTTGGACCTCAGGACCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACT
ATTGCATAATCTGAGCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCC
TCAGCATGGGGTAGGGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAA
TCTGCCTCACTGCTGTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGG
GTGGGGTAGGGGCAGGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGC
CTCTGGCCCAGCAGAGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACC
AAGGGGATAGGGAGGAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGT
TTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_001352163 ⟹ NP_001339092

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GGCTCGAGCTGTGCACCTTTACCCTGGCAATTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTC
CATCATCAGCAATGAGGTGCTGCTCTCCCTGCCTCGGAACTACTACATCCAGTGGCTCAACGGC
TCCCTCATCCATGGCCTCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCA
TGCCCTTTGCATATTTCTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGG
CCGGGTCTATGAGACAGTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGG
GTGGCATCAGCCATTGTGGACAAGAACAAGGCCAACAGAGAGTCACTCTATGACTTTTGGGAGT
ACTATCTCCCCTACCTCTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTAC
TCCACTGGGTCTCGCCCGCATGTTCTCCGTCACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTG
GAAGACCTGGAGGAGCAGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCT
GTAATCCTACTTCCTGCTGGCTGCCTTTAGACATGGAGCTGCTACACAGACAGGTCCTGGCTCT
GCAGACACAGAGGGTCCTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGC
TACCCCCTGGCTATGCTGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCATTGTGGCCATCC
ACATCCTGGAGCTGCTCATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGTTGTACTCATCTT
GTATCCTTCTGGAAACCCATCATTGCCTCTGTTCAGCAAACCTGTCTCCTGGGACTCTAGACCG
AGCACTTCTTGGACTTTTTACCTAATGGTGTCCTCAGTTGTGGGCTTCTATAGCTCTCCACTCT
TCCGGAGCCTGCGGCCCAGATGGCACGACACTGCCATGACGCAGATAATTGGGAACTGTGTCTG
TCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTTCTCTCGAACCCTGGGGCTCACTCGCTTTGAC
CTGCTGGGTGACTTTGGACGCTTCAACTGGCTGGGCAATTTCTACATTGTGTTCCTCTACAACG
CAGCCTTTGCAGGCCTCACCACACTCTGTCTGGTGAAGACCTTCACTGCAGCTGTGCGGGCAGA
GCTGATCCGGGCCTTTGGGCTGGACAGACTGCCGCTGCCCGTCTCCGGTTTCCCCCAGGCATCT
AGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGGAAGGAAAAAACTGGACACTGCCATC
TGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGACCTCAGGACCTGGAATCTGAGAGGG
TGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCATAATCTGAGCCAGAGTTTGGGACCA
GGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCATGGGGTAGGGCTGGGTGACTGGGTC
TAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCCTCACTGCTGTTCTGGGCCATCCCCA
TAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGGTAGGGGCAGGGAAAGGACTGGGCCA
GGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGGCCCAGCAGAGCCTAAGCACTGTGCT
ATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGGATAGGGAGGAGGAGGCTTCAGCCAT
CAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_001352164 ⟹ NP_001339093

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GGCTCGAGCTGTGCACCTTTACCCTGGCAATTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTC
CATCATCAGCAATGAGGTGCTGCTCTCCCTGCCTCGGAACTACTACATCCAGTGGCTCAACGGC
TCCCTCATCCATGGCCTCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCA
TGCCCTTTGCATATTTCTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGG
CCGGGTCTATGAGACAGTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGG
GTGGCATCAGCCATTGTGGACAAGAACAAGGCCAACAGAGAGTCACTCTATGACTTTTGGGAGT
ACTATCTCCCCTACCTCTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTAC
TCCACTGGGTCTCGCCCGCATGTTCTCCGTCACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTG
GAAGACCTGGAGGAGCAGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCT
GTAATCCTACTTCCTGCTGGCTGCCTTTAGACATGGAGCTGCTACACAGACAGGTCCTGGCTCT
GCAGACACAGAGGGTCCTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGC
TACCCCCTGGCTATGCTGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCATTGTGGCCATCC
ACATCCTGGAGCTGCTCATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGTTGTACTCATCTT
TTACCTAATGGTGTCCTCAGTTGTGGGCTTCTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCC
AGATGGCACGACACTGCCATGACGCAGATAATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCT
CAGCACTTCCTGTCTTCTCTCGAACCCTGGGGCTGGACAGACTGCCGCTGCCCGTCTCCGGTTT
CCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGGAAGGAAAAAACT
GGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGACCTCAGGACCTG
GAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCATAATCTGAGCCA
GAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCATGGGGTAGGGCT
GGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCCTCACTGCTGTTC
TGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGGTAGGGGCAGGGA
AAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGGCCCAGCAGAGCC
TAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGGATAGGGAGGAGG
AGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_001352165 ⟹ NP_001339094

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGCTGCGAGGAAAGGCCCCTAGGCTGGGTC
TGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCCCAGAGGCACCTCGGCT
TCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTATCCGTGCGAGAACAGCT
ATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGCAACACTGTACATCCTC
TGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACAGGCTCGAGCTGTGCAC
CTTTACCCTGGCAATTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTCCATCATCAGCAATGAG
GTGCTGCTCTCCCTGCCTCGGAACTACTACATCCAGTGGCTCAACGGCTCCCTCATCCATGGCC
TCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCATGCCCTTTGCATATTT
CTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGGCCGGGTCTATGAGACA
GTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGGGTGGCATCAGCCATTG
TGGACAAGAACAAGGCCAACAGAGAGTCACTCTATGACTTTTGGGAGTACTATCTCCCCTACCT
CTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTACTCCACTGGGTCTCGCC
CGCATGTTCTCCGTCACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTGGAAGACCTGGAGGAGC
AGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTGTAATCCTACTTCCTG
CTGGCTGCCTTTAGACATGGAGCTGCTACACAGACAGGTCCTGGCTCTGCAGACACAGAGGGTC
CTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCTACCCCCTGGCTATGC
TGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCATTGTGGCCATCCACATCCTGGAGCTGCT
CATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGGTACCTCCTTAGGCCAGGTCTCCTTCTCC
AAGCTGGGCTCCTTTGGTGCCGTCATTCAGGTTGTACTCATCTTTTACCTAATGGTGTCCTCAG
TTGTGGGCTTCTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATGGCACGACACTGCCAT
GACGCAGATAATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTTCTCT
CGAACCCTGGGGCTCACTCGCTTTGACCTGCTGGGTGACTTTGGACGCTTCAACTGGCTGGGCA
ATTTCTACATTGTGTTCCTCTACAACGCAGCCTTTGCAGGCCTCACCACACTCTGTCTGGTGAA
GACCTTCACTGCAGCTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTGGACAGACTGCCGCTG
CCCGTCTCCGGTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTG
GGAAGGAAAAAACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTG
GACCTCAGGACCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTG
CATAATCTGAGCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAG
CATGGGGTAGGGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTG
CCTCACTGCTGTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGG
GGTAGGGGCAGGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCT
GGCCCAGCAGAGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGG
GGATAGGGAGGAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTT
TTAAA

hide sequence

RefSeq Acc Id:

NM_001352166 ⟹ NP_001339095

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GGCTCGAGCTGTGCACCTTTACCCTGGCAATTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTC
CATCATCAGCAATGAGGTGCTGCTCTCCCTGCCTCGGAACTACTACATCCAGTGGCTCAACGGC
TCCCTCATCCATGGCCTCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCA
TGCCCTTTGCATATTTCTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGG
CCGGGTCTATGAGACAGTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGG
GTGGCATCAGCCATTGTGGACAAGAACAAGGCCAACAGAGAGTCACTCTATGACTTTTGGGAGT
ACTATCTCCCCTACCTCTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTAC
TCCACTGGGTCTCGCCCGCATGTTCTCCGTCACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTG
GAAGACCTGGAGGAGCAGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCT
GTAATCCTACTTCCTGCTGGCTGCCTTTAGACATGGAGCTGCTACACAGACAGGTCCTGGCTCT
GCAGACACAGAGGGTCCTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGC
TACCCCCTGGCTATGCTGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCATTGTGGCCATCC
ACATCCTGGAGCTGCTCATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGGTACCTCCTTAGG
CCAGGTCTCCTTCTCCAAGCTGGGCTCCTTTGGTGCCGTCATTCAGGTTGTACTCATCTTTTAC
CTAATGGTGTCCTCAGTTGTGGGCTTCTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGAT
GGCACGACACTGCCATGACGCAGATAATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGC
ACTTCCTGTCTTCTCTCGAACCCTGGGGCTCACTCGCTTTGACCTGCTGGGTGACTTTGGACGC
TTCAACTGGCTGGGCAATTTCTACATTGTGTTCCTCTACAACGCAGCCTTTGCAGGCCTCACCA
CACTCTGTCTGGTGAAGACCTTCACTGCAGCTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCT
GGACAGACTGCCGCTGCCCGTCTCCGGTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGA
CCTCCAGCTGGGGGTGGGAAGGAAAAAACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGA
AGCCCAAGGCTACTTGGACCTCAGGACCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGA
GCCATCTGCACTATTGCATAATCTGAGCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATAC
TTAACTGTGGCCTCAGCATGGGGTAGGGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTG
TTTACACATCAATCTGCCTCACTGCTGTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTG
ATGTGCAATAGGGTGGGGTAGGGGCAGGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGAT
TGTCTCCCTTGCCTCTGGCCCAGCAGAGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACC
ACCTGAAAGACCAAGGGGATAGGGAGGAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAG
GGTTTGCTTTGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_001352167 ⟹ NP_001339096

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GGCTCGAGCTGTGCACCTTTACCCTGGCAATTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTC
CATCATCAGCAATGAGGTGCTGCTCTCCCTGCCTCGGAACTACTACATCCAGTGGCTCAACGGC
TCCCTCATCCATGGCCTCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCA
TGCCCTTTGCATATTTCTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGG
CCGGGTCTATGAGACAGTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGG
GTGGCATCAGCCATTGTGGACAAGAACAAGGCCAACAGAGAGTCACTCTATGACTTTTGGGAGT
ACTATCTCCCCTACCTCTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCTCCTGGCTGCTGG
AAGACCTGGAGGAGCAGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTG
TAATCCTACTTCCTGCTGGCTGCCTTTAGACATGGAGCTGCTACACAGACAGGTCCTGGCTCTG
CAGACACAGAGGGTCCTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCT
ACCCCCTGGCTATGCTGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCATTGTGGCCATCCA
CATCCTGGAGCTGCTCATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGGTACCTCCTTAGGC
CAGGTCTCCTTCTCCAAGCTGGGCTCCTTTGGTGCCGTCATTCAGGTTGTACTCATCTTTTACC
TAATGGTGTCCTCAGTTGTGGGCTTCTATAGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATG
GCACGACACTGCCATGACGCAGATAATTGGGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCA
CTTCCTGTCTTCTCTCGAACCCTGGGGCTCACTCGCTTTGACCTGCTGGGTGACTTTGGACGCT
TCAACTGGCTGGGCAATTTCTACATTGTGTTCCTCTACAACGCAGCCTTTGCAGGCCTCACCAC
ACTCTGTCTGGTGAAGACCTTCACTGCAGCTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTG
GACAGACTGCCGCTGCCCGTCTCCGGTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGAC
CTCCAGCTGGGGGTGGGAAGGAAAAAACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAA
GCCCAAGGCTACTTGGACCTCAGGACCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAG
CCATCTGCACTATTGCATAATCTGAGCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATACT
TAACTGTGGCCTCAGCATGGGGTAGGGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGT
TTACACATCAATCTGCCTCACTGCTGTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTGA
TGTGCAATAGGGTGGGGTAGGGGCAGGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATT
GTCTCCCTTGCCTCTGGCCCAGCAGAGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCA
CCTGAAAGACCAAGGGGATAGGGAGGAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGG
GTTTGCTTTGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_001352168 ⟹ NP_001339097

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GTGGATGATGAAGATGCCACCGTCAACAAGATTGCGCTCGAGCTGTGCACCTTTACCCTGGCAA
TTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTCCATCATCAGCAATGAGGTGCTGCTCTCCCT
GCCTCGGAACTACTACATCCAGTGGCTCAACGGCTCCCTCATCCATGGCCTCTGGAACCTTGTT
TTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCATGCCCTTTGCATATTTCTTCACTGAGTCTG
AGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGGCCGGGTCTATGAGACAGTGGTGATGTTGAT
GCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGGGTGGCATCAGCCATTGTGGACAAGAACAAG
GCCAACAGAGAGTCACTCTATGACTTTTGGGAGTACTATCTCCCCTACCTCTACTCATGCATCT
CCTTCCTTGGGGTTCTGCTGCTCCTGGCTGCTGGAAGACCTGGAGGAGCAGCTGTACTGCTCAG
CCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTGTAATCCTACTTCCTGCTGGCTGCCTTTAGA
CATGGAGCTGCTACACAGACAGGTCCTGGCTCTGCAGACACAGAGGGTCCTGCTGGAGAAGAGG
CGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCTACCCCCTGGCTATGCTGTGCTTGCTGGTGC
TGACGGGCCTGTCTGTGCTCATTGTGGCCATCCACATCCTGGAGCTGCTCATCGATGAGGCTGC
CATGCCCCGAGGCATGCAGGGTACCTCCTTAGGCCAGGTCTCCTTCTCCAAGCTGGGCTCCTTT
GGTGCCGTCATTCAGGTTGTACTCATCTTTTACCTAATGGTGTCCTCAGTTGTGGGCTTCTATA
GCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATGGCACGACACTGCCATGACGCAGATAATTGG
GAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTTCTCTCGAACCCTGGGGCTC
ACTCGCTTTGACCTGCTGGGTGACTTTGGACGCTTCAACTGGCTGGGCAATTTCTACATTGTGT
TCCTCTACAACGCAGCCTTTGCAGGCCTCACCACACTCTGTCTGGTGAAGACCTTCACTGCAGC
TGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTGGACAGACTGCCGCTGCCCGTCTCCGGTTTC
CCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGGAAGGAAAAAACTG
GACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGACCTCAGGACCTGG
AATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCATAATCTGAGCCAG
AGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCATGGGGTAGGGCTG
GGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCCTCACTGCTGTTCT
GGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGGTAGGGGCAGGGAA
AGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGGCCCAGCAGAGCCT
AAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGGATAGGGAGGAGGA
GGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

NM_018113 ⟹ NP_060583

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI
GRCh37	12	49,490,334 - 49,504,683 (-)	NCBI
Build 36	12	47,777,189 - 47,790,947 (-)	NCBI Archive
Celera	12	48,285,709 - 48,299,467 (-)	RGD
HuRef	12	46,521,993 - 46,535,753 (-)	RGD
CHM1_1	12	49,456,235 - 49,470,135 (-)	NCBI
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

Sequence:

show sequence

GTAGCGAGCCTAGTGGCGGGTGTTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGG
GAGCAAAGGGAGGACAGAGCCCTTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGG
CGTCCGGACGACTGTATCTGAGCCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAG
GCCCCTAGGCTGGGTCTGGGTGCTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCC
CAGAGGCACCTCGGCTTCAGTCATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTAT
CCGTGCGAGAACAGCTATTCCACGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGC
AACACTGTACATCCTCTGCCACATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACA
GTGGATGATGAAGATGCCACCGTCAACAAGATTGCGCTCGAGCTGTGCACCTTTACCCTGGCAA
TTGCCCTGGGTGCTGTCCTGCTCCTGCCCTTCTCCATCATCAGCAATGAGGTGCTGCTCTCCCT
GCCTCGGAACTACTACATCCAGTGGCTCAACGGCTCCCTCATCCATGGCCTCTGGAACCTTGTT
TTTCTCTTCTCCAACCTGTCCCTCATCTTCCTCATGCCCTTTGCATATTTCTTCACTGAGTCTG
AGGGCTTTGCTGGCTCCAGAAAGGGTGTCCTGGGCCGGGTCTATGAGACAGTGGTGATGTTGAT
GCTCCTCACTCTGCTGGTGCTAGGTATGGTGTGGGTGGCATCAGCCATTGTGGACAAGAACAAG
GCCAACAGAGAGTCACTCTATGACTTTTGGGAGTACTATCTCCCCTACCTCTACTCATGCATCT
CCTTCCTTGGGGTTCTGCTGCTCCTGGTGTGTACTCCACTGGGTCTCGCCCGCATGTTCTCCGT
CACTGGGAAGCTGCTAGTCAAGCCCCGGCTGCTGGAAGACCTGGAGGAGCAGCTGTACTGCTCA
GCCTTTGAGGAGGCAGCCCTGACCCGCAGGATCTGTAATCCTACTTCCTGCTGGCTGCCTTTAG
ACATGGAGCTGCTACACAGACAGGTCCTGGCTCTGCAGACACAGAGGGTCCTGCTGGAGAAGAG
GCGGAAGGCTTCAGCCTGGCAACGGAACCTGGGCTACCCCCTGGCTATGCTGTGCTTGCTGGTG
CTGACGGGCCTGTCTGTGCTCATTGTGGCCATCCACATCCTGGAGCTGCTCATCGATGAGGCTG
CCATGCCCCGAGGCATGCAGGGTACCTCCTTAGGCCAGGTCTCCTTCTCCAAGCTGGGCTCCTT
TGGTGCCGTCATTCAGGTTGTACTCATCTTTTACCTAATGGTGTCCTCAGTTGTGGGCTTCTAT
AGCTCTCCACTCTTCCGGAGCCTGCGGCCCAGATGGCACGACACTGCCATGACGCAGATAATTG
GGAACTGTGTCTGTCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTTCTCTCGAACCCTGGGGCT
CACTCGCTTTGACCTGCTGGGTGACTTTGGACGCTTCAACTGGCTGGGCAATTTCTACATTGTG
TTCCTCTACAACGCAGCCTTTGCAGGCCTCACCACACTCTGTCTGGTGAAGACCTTCACTGCAG
CTGTGCGGGCAGAGCTGATCCGGGCCTTTGGGCTGGACAGACTGCCGCTGCCCGTCTCCGGTTT
CCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGGAAGGAAAAAACT
GGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGACCTCAGGACCTG
GAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCATAATCTGAGCCA
GAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCATGGGGTAGGGCT
GGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCCTCACTGCTGTTC
TGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGGTAGGGGCAGGGA
AAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGGCCCAGCAGAGCC
TAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGGATAGGGAGGAGG
AGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTTAAA

hide sequence

RefSeq Acc Id:

XM_024449053 ⟹ XP_024304821

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI

Sequence:

show sequence

ACTAGATCTCTTAAAAAGATGGACCCTCAGCGGCGCTTCCTCGTAGCGAGCCTAGTGGCGGGTG
TTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGGGAGCAAAGGGAGGACAGAGCCC
TTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGGCGTCCGGACGACTGTATCTGAG
CCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAGGCCCCTAGGCTGGGTCTGGGTG
CTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCCCAGAGGCACCTCGGCTTCAGTC
ATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTATCCGTGCGAGAACAGCTATTCCA
CGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGCAACACTGTACATCCTCTGCCAC
ATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACAGTGGATGATGAAGATGCCACCG
TCAACAAGATTGCGCTCGAGCTGTGCACCTTTACCCTGGCAATTGCCCTGGGTGCTGTCCTGCT
CCTGCCCTTCTCCATCATCAGCAATGAGGTGCTGCTCTCCCTGCCTCGGAACTACTACATCCAG
TGGCTCAACGGCTCCCTCATCCATGGCCTCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCC
TCATCTTCCTCATGCCCTTTGCATATTTCTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAA
GGGTGTCCTGGGCCGGGTCTATGAGACAGTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTA
GGTATGGTGTGGGTGGCATCAGCCATTGTGGACAAGAACAAGGCCAACAGAGAGTCACTCTATG
ACTTTTGGGAGTACTATCTCCCCTACCTCTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCT
CCTGGTGTGTACTCCACTGGGTCTCGCCCGCATGTTCTCCGTCACTGGGAAGCTGCTAGTCAAG
CCCCGGCTGCTGGAAGACCTGGAGGAGCAGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGA
CCCGCAGGATCTGTAATCCTACTTCCTGCTGGCTGCCTTTAGACATGGAGCTGCTACACAGACA
GGTCCTGGCTCTGCAGACACAGAGGGTCCTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAA
CGGAACCTGGGCTACCCCCTGGCTATGCTGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCA
TTGTGGCCATCCACATCCTGGAGCTGCTCATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGT
TGTACTCATCTTTTACCTAATGGTGTCCTCAGTTGTGGGCTTCTATAGCTCTCCACTCTTCCGG
AGCCTGCGGCCCAGATGGCACGACACTGCCATGACGCAGATAATTGGGAACTGTGTCTGTCTCC
TGGTCCTAAGCTCAGCACTTCCTGTCTTCTCTCGAACCCTGGGGCTGGACAGACTGCCGCTGCC
CGTCTCCGGTTTCCCCCAGGCATCTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGG
AAGGAAAAAACTGGACACTGCCATCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGA
CCTCAGGACCTGGAATCTGAGAGGGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCA
TAATCTGAGCCAGAGTTTGGGACCAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCA
TGGGGTAGGGCTGGGTGACTGGGTCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCC
TCACTGCTGTTCTGGGCCATCCCCATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGG
TAGGGGCAGGGAAAGGACTGGGCCAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGG
CCCAGCAGAGCCTAAGCACTGTGCTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGG
ATAGGGAGGAGGAGGCTTCAGCCATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTT
AAAGCACCTGTCTCTGTGTATATTTGAACAGCCTTGCTCCCACCAGCCCGGCGTCTGCCCAGTA
AGAGAAGCAGAGGGGTCCTGCCCACCATCCTTTTCCTTCCCCTTCATCTATATTATTACCATCC
TTTGGGGACTTGGATCTGGTGTTAGGCCATGCAGTTGGGCAGTGGGAAACTCCTCCATCCTCAG
TCTTGCTTAAAGCTGGCTTGTCCCCTGACTCCTCCTTATATTCATGGCCTTGTTTCTGTACCTT
GAGTATTGGGGGTAGGACATGGGCATAGGAGTAGGCTAACCTCCCCGATACACTCATACCTTCA
GCCCTATCCTCCCTGGCTTAACTATTGGATATAGAGTAAAATAAGTGGCTGGCTGACAAGGATT
TTCATTTCCTACCTGAGAGAAGAATCTAGCTTTTTACTAGAGGCCATCAGTTTCTTGAAAAGCC
CATGTGCTATGTTGGGAGTAAGAGCGCAAAACTTAGGCTTATACAGATTGTGTATTGCACAGCT
TCCAGGGACACCATTCACCTCATAGTCATTGTGTGGATAGTTACTATGATAGTTTTCTAATAAA
TGTCAGTCATCTTGA

hide sequence

RefSeq Acc Id:

XM_047429139 ⟹ XP_047285095

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,107,044 (-)	NCBI

RefSeq Acc Id:

XM_047429140 ⟹ XP_047285096

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,110,847 (-)	NCBI

RefSeq Acc Id:

XM_047429141 ⟹ XP_047285097

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,101,010 - 49,110,847 (-)	NCBI

RefSeq Acc Id:

XM_047429142 ⟹ XP_047285098

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,109,786 (-)	NCBI

RefSeq Acc Id:

XM_047429143 ⟹ XP_047285099

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,097,139 - 49,104,546 (-)	NCBI

RefSeq Acc Id:

XM_054372530 ⟹ XP_054228505

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	49,059,322 - 49,069,227 (-)	NCBI

RefSeq Acc Id:

XM_054372531 ⟹ XP_054228506

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

RefSeq Acc Id:

XM_054372532 ⟹ XP_054228507

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	49,059,322 - 49,073,030 (-)	NCBI

RefSeq Acc Id:

XM_054372533 ⟹ XP_054228508

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	49,063,193 - 49,073,030 (-)	NCBI

RefSeq Acc Id:

XM_054372534 ⟹ XP_054228509

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	49,059,322 - 49,071,969 (-)	NCBI

RefSeq Acc Id:

XM_054372535 ⟹ XP_054228510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	49,059,322 - 49,066,729 (-)	NCBI

RefSeq Acc Id:

XR_008488640

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	49,062,571 - 49,073,030 (-)	NCBI

RefSeq Acc Id:

XR_245944

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,100,388 - 49,110,847 (-)	NCBI
GRCh37	12	49,490,334 - 49,504,683 (-)	NCBI

Sequence:

show sequence

ACTAGATCTCTTAAAAAGATGGACCCTCAGCGGCGCTTCCTCGTAGCGAGCCTAGTGGCGGGTG
TTTGCATTGAAACGTGAGCGCGACCCGACCTTAAAGAGTGGGGAGCAAAGGGAGGACAGAGCCC
TTTAAAACGAGGCGGGTGGTGCCTGCCCCTTTAAGGGCGGGGCGTCCGGACGACTGTATCTGAG
CCCCAGACTGCCCCGAGTTTCTGTCGCAGGCTGCGAGGAAAGGCCCCTAGGCTGGGTCTGGGTG
CTTGGCGGCGGCGGCTTCCTCCCCGCTCGTCCTCCCCGGGCCCAGAGGCACCTCGGCTTCAGTC
ATGCTGAGCAGAGTATGGAAGCACCTGACTACGAAGTGCTATCCGTGCGAGAACAGCTATTCCA
CGAGAGGATCCGCGAGTGTATTATATCAACACTTCTGTTTGCAACACTGTACATCCTCTGCCAC
ATCTTCCTGACCCGCTTCAAGAAGCCTGCTGAGTTCACCACAGTGGATGATGAAGATGCCACCG
TCAACAAGATTGCGCTCGAGCTGTGCACCTTTACCCTGGCAATTGCCCTGGGTGCTGTCCTGCT
CCTGCCCTTCTCCATCATCAGCAATGAGGTGCTGCTCTCCCTGCCTCGGAACTACTACATCCAG
TGGCTCAACGGCTCCCTCATCCATGGCCTCTGGAACCTTGTTTTTCTCTTCTCCAACCTGTCCC
TCATCTTCCTCATGCCCTTTGCATATTTCTTCACTGAGTCTGAGGGCTTTGCTGGCTCCAGAAA
GGGTGTCCTGGGCCGGGTCTATGAGACAGTGGTGATGTTGATGCTCCTCACTCTGCTGGTGCTA
GGTATGGTGTGGGTGGCATCAGCCATTGTGGACAAGAACAAGGCCAACAGAGAGTCACTCTATG
ACTTTTGGGAGTACTATCTCCCCTACCTCTACTCATGCATCTCCTTCCTTGGGGTTCTGCTGCT
CCTGGTGTGTACTCCACTGGGTCTCGCCCGCATGTTCTCCGTCACTGGGAAGCTGCTAGTCAAG
CCCCGGCTGCTGGAAGACCTGGAGGAGCAGCTGTACTGCTCAGCCTTTGAGGAGGCAGCCCTGA
CCCGCAGGATCTGTAATCCTACTTCCTGCTGGCTGCCTTTAGACATGGAGCTGCTACACAGACA
GGTCCTGGCTCTGCAGACACAGAGGGTCCTGCTGGAGAAGAGGCGGAAGGCTTCAGCCTGGCAA
CGGAACCTGGGCTACCCCCTGGCTATGCTGTGCTTGCTGGTGCTGACGGGCCTGTCTGTGCTCA
TTGTGGCCATCCACATCCTGGAGCTGCTCATCGATGAGGCTGCCATGCCCCGAGGCATGCAGGT
ACCAGGCTGCCCTCCCACCTTACCTAATGGTGTCCTCAGTTGTGGGCTTCTATAGCTCTCCACT
CTTCCGGAGCCTGCGGCCCAGATGGCACGACACTGCCATGACGCAGATAATTGGGAACTGTGTC
TGTCTCCTGGTCCTAAGCTCAGCACTTCCTGTCTTCTCTCGAACCCTGGGGCTCACTCGCTTTG
ACCTGCTGGGTGACTTTGGACGCTTCAACTGGCTGGGCAATTTCTACATTGTGTTCCTCTACAA
CGCAGCCTTTGCAGGCCTCACCACACTCTGTCTGGTGAAGACCTTCACTGCAGCTGTGCGGGCA
GAGCTGATCCGGGCCTTTGGGCTGGACAGACTGCCGCTGCCCGTCTCCGGTTTCCCCCAGGCAT
CTAGGAAGACCCAGCACCAGTGACCTCCAGCTGGGGGTGGGAAGGAAAAAACTGGACACTGCCA
TCTGCTGCCTAGGCCTGGAGGGAAGCCCAAGGCTACTTGGACCTCAGGACCTGGAATCTGAGAG
GGTGGGTGGCAGAGGGGAGCAGAGCCATCTGCACTATTGCATAATCTGAGCCAGAGTTTGGGAC
CAGGACCTCCTGCTTTTCCATACTTAACTGTGGCCTCAGCATGGGGTAGGGCTGGGTGACTGGG
TCTAGCCCCTGATCCCAAATCTGTTTACACATCAATCTGCCTCACTGCTGTTCTGGGCCATCCC
CATAGCCATGTTTACATGATTTGATGTGCAATAGGGTGGGGTAGGGGCAGGGAAAGGACTGGGC
CAGGGCAGGCTCGGGAGATAGATTGTCTCCCTTGCCTCTGGCCCAGCAGAGCCTAAGCACTGTG
CTATCCTGGAGGGGCTTTGGACCACCTGAAAGACCAAGGGGATAGGGAGGAGGAGGCTTCAGCC
ATCAGCAATAAAGTTGATCCCAGGGTTTGCTTTGTTTTTTTAAAGCACCTGTCTCTGTGTATAT
TTGAACAGCCTTGCTCCCACCAGCCCGGCGTCTGCCCAGTAAGAGAAGCAGAGGGGTCCTGCCC
ACCATCCTTTTCCTTCCCCTTCATCTATATTATTACCATCCTTTGGGGACTTGGATCTGGTGTT
AGGCCATGCAGTTGGGCAGTGGGAAACTCCTCCATCCTCAGTCTTGCTTAAAGCTGGCTTGTCC
CCTGACTCCTCCTTATATTCATGGCCTTGTTTCTGTACCTTGAGTATTGGGGGTAGGACATGGG
CATAGGAGTAGGCTAACCTCCCCGATACACTCATACCTTCAGCCCTATCCTCCCTGGCTTAACT
ATTGGATATAGAGTAAAATAAGTGGCTGGCTGACAAGGATTTTCATTTCCTACCTGAGAGAAGA
ATCTAGCTTTTTACTAGAGGCCATCAGTTTCTTGAAAAGCCCATGTGCTATGTTGGGAGTAAGA
GCGCAAAACTTAGGCTTATACAGATTGTGTATTGCACAGCTTCCAGGGACACCATTCACCTCAT
AGTCATTGTGTGGATAGTTACTATGATAGTTTTCTAATAAATGTCAGTCATCTTGA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001287679	(Get FASTA)	NCBI Sequence Viewer
	NP_001287680	(Get FASTA)	NCBI Sequence Viewer
	NP_001339090	(Get FASTA)	NCBI Sequence Viewer
	NP_001339091	(Get FASTA)	NCBI Sequence Viewer
	NP_001339092	(Get FASTA)	NCBI Sequence Viewer
	NP_001339093	(Get FASTA)	NCBI Sequence Viewer
	NP_001339094	(Get FASTA)	NCBI Sequence Viewer
	NP_001339095	(Get FASTA)	NCBI Sequence Viewer
	NP_001339096	(Get FASTA)	NCBI Sequence Viewer
	NP_001339097	(Get FASTA)	NCBI Sequence Viewer
	NP_060583	(Get FASTA)	NCBI Sequence Viewer
	XP_024304821	(Get FASTA)	NCBI Sequence Viewer
	XP_047285095	(Get FASTA)	NCBI Sequence Viewer
	XP_047285096	(Get FASTA)	NCBI Sequence Viewer
	XP_047285097	(Get FASTA)	NCBI Sequence Viewer
	XP_047285098	(Get FASTA)	NCBI Sequence Viewer
	XP_047285099	(Get FASTA)	NCBI Sequence Viewer
	XP_054228505	(Get FASTA)	NCBI Sequence Viewer
	XP_054228506	(Get FASTA)	NCBI Sequence Viewer
	XP_054228507	(Get FASTA)	NCBI Sequence Viewer
	XP_054228508	(Get FASTA)	NCBI Sequence Viewer
	XP_054228509	(Get FASTA)	NCBI Sequence Viewer
	XP_054228510	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH08337	(Get FASTA)	NCBI Sequence Viewer
	AAH15015	(Get FASTA)	NCBI Sequence Viewer
	AAH31550	(Get FASTA)	NCBI Sequence Viewer
	AAK60600	(Get FASTA)	NCBI Sequence Viewer
	AAK63067	(Get FASTA)	NCBI Sequence Viewer
	AAQ88935	(Get FASTA)	NCBI Sequence Viewer
	ALQ34169	(Get FASTA)	NCBI Sequence Viewer
	ALQ34170	(Get FASTA)	NCBI Sequence Viewer
	ALQ34171	(Get FASTA)	NCBI Sequence Viewer
	ALQ34172	(Get FASTA)	NCBI Sequence Viewer
	ALQ34173	(Get FASTA)	NCBI Sequence Viewer
	BAA86488	(Get FASTA)	NCBI Sequence Viewer
	BAA91646	(Get FASTA)	NCBI Sequence Viewer
	BAA91811	(Get FASTA)	NCBI Sequence Viewer
	BAG60328	(Get FASTA)	NCBI Sequence Viewer
	BAG60981	(Get FASTA)	NCBI Sequence Viewer
	CAB70835	(Get FASTA)	NCBI Sequence Viewer
	EAW58040	(Get FASTA)	NCBI Sequence Viewer
	EAW58041	(Get FASTA)	NCBI Sequence Viewer
	EAW58042	(Get FASTA)	NCBI Sequence Viewer
	EAW58043	(Get FASTA)	NCBI Sequence Viewer
	EAW58044	(Get FASTA)	NCBI Sequence Viewer
	EAW58045	(Get FASTA)	NCBI Sequence Viewer
	EAW58046	(Get FASTA)	NCBI Sequence Viewer
	EAW58047	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000267102
	ENSP00000267102.8
	ENSP00000394677.1
	ENSP00000413785.2
	ENSP00000446641.1
	ENSP00000446718.1
	ENSP00000447240.1
	ENSP00000447329
	ENSP00000447329.1
	ENSP00000448128.1
	ENSP00000448147.1
	ENSP00000448821.1
	ENSP00000448973.1
	ENSP00000449103.1
	ENSP00000449633.1
	ENSP00000450032.1
	ENSP00000450362.1
GenBank Protein	Q6UX01	(Get FASTA)	NCBI Sequence Viewer
	QVG59798	(Get FASTA)	NCBI Sequence Viewer
	QVG59799	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_060583 ⟸ NM_018113
- Peptide Label:	isoform 1
- UniProtKB:	Q9NVU9 (UniProtKB/Swiss-Prot), Q9NVE1 (UniProtKB/Swiss-Prot), Q9NT09 (UniProtKB/Swiss-Prot), Q96HN8 (UniProtKB/Swiss-Prot), Q96BY8 (UniProtKB/Swiss-Prot), Q969J4 (UniProtKB/Swiss-Prot), Q9ULP6 (UniProtKB/Swiss-Prot), Q6UX01 (UniProtKB/Swiss-Prot), A0A024R0Y9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEAPDYEVLSVREQLFHERIRECIISTLLFATLYILCHIFLTRFKKPAEFTTVDDEDATVNKIA LELCTFTLAIALGAVLLLPFSIISNEVLLSLPRNYYIQWLNGSLIHGLWNLVFLFSNLSLIFLM PFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWEY YLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRIC NPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAIH ILELLIDEAAMPRGMQGTSLGQVSFSKLGSFGAVIQVVLIFYLMVSSVVGFYSSPLFRSLRPRW HDTAMTQIIGNCVCLLVLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAAFAGLTT LCLVKTFTAAVRAELIRAFGLDRLPLPVSGFPQASRKTQHQ hide sequence

RefSeq Acc Id:	NP_001287680 ⟸ NM_001300751
- Peptide Label:	isoform 3
- UniProtKB:	A0A0S2Z6E3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEAPDYEVLSVREQLFHERIRECIISTLLFATLYILCHIFLTRFKKPAEFTTVDDEDATVNKIA LELCTFTLAIALGAVLLLPFSIISNEVLLSLPRNYYIQWLNGSLIHGLWNLVFLFSNLSLIFLM PFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWEY YLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRIC NPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAIH ILELLIDEAAMPRGMQVVLIFYLMVSSVVGFYSSPLFRSLRPRWHDTAMTQIIGNCVCLLVLSS ALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAAFAGLTTLCLVKTFTAAVRAELIRAFG LDRLPLPVSGFPQASRKTQHQ hide sequence

RefSeq Acc Id:

NP_001287679 ⟸ NM_001300750

- Peptide Label:

isoform 2

- Sequence:

show sequence

MVNVKALCEPEVSNCWMNVITGTGSVSSPLLVLPQPGPETSLMTGEPVDDEDATVNKIALELCT
FTLAIALGAVLLLPFSIISNEVLLSLPRNYYIQWLNGSLIHGLWNLVFLFSNLSLIFLMPFAYF
FTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWEYYLPYL
YSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRICNPTSC
WLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAIHILELL
IDEAAMPRGMQGTSLGQVSFSKLGSFGAVIQVVLIFYLMVSSVVGFYSSPLFRSLRPRWHDTAM
TQIIGNCVCLLVLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAAFAGLTTLCLVK
TFTAAVRAELIRAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:	XP_024304821 ⟸ XM_024449053
- Peptide Label:	isoform X3
- UniProtKB:	A0A0S2Z5S6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEAPDYEVLSVREQLFHERIRECIISTLLFATLYILCHIFLTRFKKPAEFTTVDDEDATVNKIA LELCTFTLAIALGAVLLLPFSIISNEVLLSLPRNYYIQWLNGSLIHGLWNLVFLFSNLSLIFLM PFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWEY YLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRIC NPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAIH ILELLIDEAAMPRGMQVVLIFYLMVSSVVGFYSSPLFRSLRPRWHDTAMTQIIGNCVCLLVLSS ALPVFSRTLGLDRLPLPVSGFPQASRKTQHQ hide sequence

RefSeq Acc Id:

NP_001339094 ⟸ NM_001352165

- Peptide Label:

isoform 8

- Sequence:

show sequence

MPFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWE
YYLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRI
CNPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAI
HILELLIDEAAMPRGMQGTSLGQVSFSKLGSFGAVIQVVLIFYLMVSSVVGFYSSPLFRSLRPR
WHDTAMTQIIGNCVCLLVLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAAFAGLT
TLCLVKTFTAAVRAELIRAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:

NP_001339091 ⟸ NM_001352162

- Peptide Label:

isoform 5

- Sequence:

show sequence

MEAPDYEVLSVREQLFHERIRECIISTLLFATLYILCHIFLTRFKKPAEFTTGLWNLVFLFSNL
SLIFLMPFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESL
YDFWEYYLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAA
LTRRICNPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSV
LIVAIHILELLIDEAAMPRGMQGTSLGQVSFSKLGSFGAVIQVVLIFYLMVSSVVGFYSSPLFR
SLRPRWHDTAMTQIIGNCVCLLVLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAA
FAGLTTLCLVKTFTAAVRAELIRAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:

NP_001339096 ⟸ NM_001352167

- Peptide Label:

isoform 9

- Sequence:

show sequence

MTFGSTISPTSTHASPSLGFCCSWLLEDLEEQLYCSAFEEAALTRRICNPTSCWLPLDMELLHR
QVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAIHILELLIDEAAMPRGMQ
GTSLGQVSFSKLGSFGAVIQVVLIFYLMVSSVVGFYSSPLFRSLRPRWHDTAMTQIIGNCVCLL
VLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAAFAGLTTLCLVKTFTAAVRAELI
RAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:

NP_001339093 ⟸ NM_001352164

- Peptide Label:

isoform 7

- Sequence:

show sequence

MPFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWE
YYLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRI
CNPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAI
HILELLIDEAAMPRGMQVVLIFYLMVSSVVGFYSSPLFRSLRPRWHDTAMTQIIGNCVCLLVLS
SALPVFSRTLGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:

NP_001339092 ⟸ NM_001352163

- Peptide Label:

isoform 6

- Sequence:

show sequence

MPFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWE
YYLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRI
CNPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAI
HILELLIDEAAMPRGMQVVLILYPSGNPSLPLFSKPVSWDSRPSTSWTFYLMVSSVVGFYSSPL
FRSLRPRWHDTAMTQIIGNCVCLLVLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYN
AAFAGLTTLCLVKTFTAAVRAELIRAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:

NP_001339095 ⟸ NM_001352166

- Peptide Label:

isoform 8

- Sequence:

show sequence

MPFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWE
YYLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRI
CNPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAI
HILELLIDEAAMPRGMQGTSLGQVSFSKLGSFGAVIQVVLIFYLMVSSVVGFYSSPLFRSLRPR
WHDTAMTQIIGNCVCLLVLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAAFAGLT
TLCLVKTFTAAVRAELIRAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:

NP_001339097 ⟸ NM_001352168

- Peptide Label:

isoform 9

- Sequence:

show sequence

MTFGSTISPTSTHASPSLGFCCSWLLEDLEEQLYCSAFEEAALTRRICNPTSCWLPLDMELLHR
QVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAIHILELLIDEAAMPRGMQ
GTSLGQVSFSKLGSFGAVIQVVLIFYLMVSSVVGFYSSPLFRSLRPRWHDTAMTQIIGNCVCLL
VLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNAAFAGLTTLCLVKTFTAAVRAELI
RAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

RefSeq Acc Id:

NP_001339090 ⟸ NM_001352161

- Peptide Label:

isoform 4

- Sequence:

show sequence

MEAPDYEVLSVREQLFHERIRECIISTLLFATLYILCHIFLTRFKKPAEFTTVDDEDATVNKIA
LELCTFTLAIALGAVLLLPFSIISNEVLLSLPRNYYIQWLNGSLIHGLWNLVFLFSNLSLIFLM
PFAYFFTESEGFAGSRKGVLGRVYETVVMLMLLTLLVLGMVWVASAIVDKNKANRESLYDFWEY
YLPYLYSCISFLGVLLLLVCTPLGLARMFSVTGKLLVKPRLLEDLEEQLYCSAFEEAALTRRIC
NPTSCWLPLDMELLHRQVLALQTQRVLLEKRRKASAWQRNLGYPLAMLCLLVLTGLSVLIVAIH
ILELLIDEAAMPRGMQVVLILYPSGNPSLPLFSKPVSWDSRPSTSWTFYLMVSSVVGFYSSPLF
RSLRPRWHDTAMTQIIGNCVCLLVLSSALPVFSRTLGLTRFDLLGDFGRFNWLGNFYIVFLYNA
AFAGLTTLCLVKTFTAAVRAELIRAFGLDRLPLPVSGFPQASRKTQHQ

hide sequence

Ensembl Acc Id:

ENSP00000267102 ⟸ ENST00000267102

Ensembl Acc Id:

ENSP00000447329 ⟸ ENST00000547382

Ensembl Acc Id:

ENSP00000448821 ⟸ ENST00000547698

Ensembl Acc Id:

ENSP00000447240 ⟸ ENST00000547675

Ensembl Acc Id:

ENSP00000446718 ⟸ ENST00000547670

Ensembl Acc Id:

ENSP00000450032 ⟸ ENST00000549296

Ensembl Acc Id:

ENSP00000394677 ⟸ ENST00000417750

Ensembl Acc Id:

ENSP00000413785 ⟸ ENST00000457164

Ensembl Acc Id:

ENSP00000448973 ⟸ ENST00000550815

Ensembl Acc Id:

ENSP00000449103 ⟸ ENST00000550137

Ensembl Acc Id:

ENSP00000448128 ⟸ ENST00000551169

Ensembl Acc Id:

ENSP00000446641 ⟸ ENST00000551854

Ensembl Acc Id:

ENSP00000449633 ⟸ ENST00000551782

Ensembl Acc Id:

ENSP00000450362 ⟸ ENST00000552449

Ensembl Acc Id:

ENSP00000448147 ⟸ ENST00000553040

RefSeq Acc Id:	XP_047285096 ⟸ XM_047429140
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047285098 ⟸ XM_047429142
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047285095 ⟸ XM_047429139
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047285099 ⟸ XM_047429143
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047285097 ⟸ XM_047429141
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054228507 ⟸ XM_054372532
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054228506 ⟸ XM_054372531
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054228509 ⟸ XM_054372534
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054228505 ⟸ XM_054372530
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054228510 ⟸ XM_054372535
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054228508 ⟸ XM_054372533
- Peptide Label:	isoform X4

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6UX01-F1-model_v2	AlphaFold	Q6UX01	1-489	view protein structure

Promoters

RGD ID:

6790208

Promoter ID:

HG_KWN:15545

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000318696, UC001RTG.2, UC001RTI.2, UC009ZLD.1, UC009ZLE.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	47,790,534 - 47,791,034 (-)	MPROMDB

RGD ID:

6850744

Promoter ID:

EP73166

Type:

initiation region

Name:

HS_LIMR

Description:

Lipocalin-interacting membrane receptor.

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

NEDO full length human cDNA sequencing project.; Oligo-capping

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	47,790,725 - 47,790,785	EPD

RGD ID:

7223805

Promoter ID:

EPDNEW_H17647

Type:

initiation region

Name:

LMBR1L_2

Description:

limb development membrane protein 1 like

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H17648

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,110,675 - 49,110,735	EPDNEW

RGD ID:

7223803

Promoter ID:

EPDNEW_H17648

Type:

initiation region

Name:

LMBR1L_1

Description:

limb development membrane protein 1 like

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H17647

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	49,110,847 - 49,110,907	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:18268	AgrOrtholog
COSMIC	LMBR1L	COSMIC
Ensembl Genes	ENSG00000139636	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000267102	ENTREZGENE
	ENST00000267102.13	UniProtKB/Swiss-Prot
	ENST00000417750.5	UniProtKB/TrEMBL
	ENST00000457164.6	UniProtKB/TrEMBL
	ENST00000547382	ENTREZGENE
	ENST00000547382.5	UniProtKB/Swiss-Prot
	ENST00000547670.5	UniProtKB/TrEMBL
	ENST00000547675.5	UniProtKB/TrEMBL
	ENST00000547698.5	UniProtKB/TrEMBL
	ENST00000549296.1	UniProtKB/TrEMBL
	ENST00000550137.5	UniProtKB/TrEMBL
	ENST00000550815.1	UniProtKB/TrEMBL
	ENST00000551169.5	UniProtKB/TrEMBL
	ENST00000551782.5	UniProtKB/TrEMBL
	ENST00000551854.5	UniProtKB/TrEMBL
	ENST00000552449.1	UniProtKB/TrEMBL
	ENST00000552577	ENTREZGENE
	ENST00000553040.5	UniProtKB/TrEMBL
GTEx	ENSG00000139636	GTEx
HGNC ID	HGNC:18268	ENTREZGENE
Human Proteome Map	LMBR1L	Human Proteome Map
InterPro	LIMR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	LMBR1-like_membr_prot	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:55716	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	55716	ENTREZGENE
OMIM	610007	OMIM
PANTHER	PROTEIN LMBR1L	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR12625	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	LMBR1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA142671545	PharmGKB
PRINTS	LIPOCALINIMR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A024R0Y9	ENTREZGENE, UniProtKB/TrEMBL
	A0A0S2Z5F8_HUMAN	UniProtKB/TrEMBL
	A0A0S2Z5M5_HUMAN	UniProtKB/TrEMBL
	A0A0S2Z5S6	ENTREZGENE, UniProtKB/TrEMBL
	A0A0S2Z6E3	ENTREZGENE, UniProtKB/TrEMBL
	E7ESX7_HUMAN	UniProtKB/TrEMBL
	F8VPB1_HUMAN	UniProtKB/TrEMBL
	F8VVE2_HUMAN	UniProtKB/TrEMBL
	F8VYZ9_HUMAN	UniProtKB/TrEMBL
	F8VZU8_HUMAN	UniProtKB/TrEMBL
	F8W054_HUMAN	UniProtKB/TrEMBL
	F8W0N6_HUMAN	UniProtKB/TrEMBL
	F8WE63_HUMAN	UniProtKB/TrEMBL
	H0YHY8_HUMAN	UniProtKB/TrEMBL
	H0YHZ2_HUMAN	UniProtKB/TrEMBL
	H0YI83_HUMAN	UniProtKB/TrEMBL
	H0YIX2_HUMAN	UniProtKB/TrEMBL
	LMBRL_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q969J4	ENTREZGENE
	Q96BY8	ENTREZGENE
	Q96HN8	ENTREZGENE
	Q9NT09	ENTREZGENE
	Q9NVE1	ENTREZGENE
	Q9NVU9	ENTREZGENE
	Q9ULP6	ENTREZGENE
UniProt Secondary	Q969J4	UniProtKB/Swiss-Prot
	Q96BY8	UniProtKB/Swiss-Prot
	Q96HN8	UniProtKB/Swiss-Prot
	Q9NT09	UniProtKB/Swiss-Prot
	Q9NVE1	UniProtKB/Swiss-Prot
	Q9NVU9	UniProtKB/Swiss-Prot
	Q9ULP6	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-03-14	LMBR1L	limb development membrane protein 1 like		limb development membrane protein 1-like	Symbol and/or name change	5135510	APPROVED
2013-08-13	LMBR1L	limb development membrane protein 1-like		limb region 1 homolog (mouse)-like	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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