NLRP11 (NLR family pyrin domain containing 11)

Gene: NLRP11 (NLR family pyrin domain containing 11) Homo sapiens

Analyze

Symbol:

NLRP11

Name:

NLR family pyrin domain containing 11

RGD ID:

1349443

HGNC Page

HGNC:22945

Description:

Enables RNA binding activity. Predicted to be involved in regulation of inflammatory response. Predicted to be active in cytoplasm.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

CLR19.6; FLJ26273; NACHT, leucine rich repeat and PYD containing 11; NACHT, LRR and PYD containing protein 11; NACHT, LRR and PYD domains-containing protein 11; NALP11; NLR family, pyrin domain containing 11; NOD17; nucleotide-binding oligomerization domain protein 17; nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 11; PAAD- and NACHT-containing protein 10; PAAD- and NACHT-containing protein 10B; PAAD-and NACHT domain-containing protein 10; PAN10; PYPAF6; PYPAF7; PYRIN-containing APAF1-like protein 6

RGD Orthologs

Bonobo

Pig

Green Monkey

Alliance Orthologs

More Info

more info ...

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	19	55,785,399 - 55,836,575 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	55,785,397 - 55,836,800 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	56,296,765 - 56,347,941 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	60,988,577 - 61,035,172 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	60,988,576 - 61,035,166	NCBI
Celera	19	53,341,920 - 53,393,276 (-)	NCBI		Celera
Cytogenetic Map	19	q13.42-q13.43	NCBI
HuRef	19	52,608,953 - 52,660,294 (-)	NCBI		HuRef
CHM1_1	19	56,290,334 - 56,341,701 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	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

aflatoxin B1 (EXP)

benzo[a]pyrene (EXP)

butanal (EXP)

CGP 52608 (EXP)

N-Nitrosopyrrolidine (EXP)

nickel sulfate (EXP)

ozone (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

regulation of inflammatory response (IBA)

Cellular Component

cytoplasm (IBA)

Molecular Function

ATP binding (IEA)

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen (IEA)

RNA binding (HDA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:12019269	PMID:12387869	PMID:12477932	PMID:12563287	PMID:12615073	PMID:14702039	PMID:15489334	PMID:19010793	PMID:19074885	PMID:20403135	PMID:21873635	PMID:22267201
PMID:22658674	PMID:23307926	PMID:23377640	PMID:29097393	PMID:29301940	PMID:30021884	PMID:32832566	PMID:34349018	PMID:36243803	PMID:37478192

Genomics

Comparative Map Data

NLRP11
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	55,785,397 - 55,836,800 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	56,296,765 - 56,347,941 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	60,988,577 - 61,035,172 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	60,988,576 - 61,035,166	NCBI
Celera	19	53,341,920 - 53,393,276 (-)	NCBI		Celera
Cytogenetic Map	19	q13.42-q13.43	NCBI
HuRef	19	52,608,953 - 52,660,294 (-)	NCBI		HuRef
CHM1_1	19	56,290,334 - 56,341,701 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI		T2T-CHM13v2.0

NLRP11
(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	20	62,074,999 - 62,108,834 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	63,865,198 - 63,899,031 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	52,824,237 - 52,858,706 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	61,612,641 - 61,657,497 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	61,612,641 - 61,653,252 (-)	Ensembl	panpan1.1		panPan2

NLRP11
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	6	60,173,139 - 60,217,552 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	60,145,050 - 60,222,936 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	6	55,262,509 - 55,342,266 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

NLRP11
(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	6	48,381,009 - 48,428,934 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	48,381,227 - 48,415,552 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666045	1,051,930 - 1,097,425 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants

Variants in NLRP11
69 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh37/hg19 19q13.42-13.43(chr19:56212463-57191708)x3	copy number gain	See cases [RCV000510179]	Chr19:56212463..57191708 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	copy number gain	See cases [RCV000050883]	Chr19:50191219..58535818 [GRCh38] Chr19:50694476..59047185 [GRCh37] Chr19:55386288..63738997 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	copy number gain	See cases [RCV000052925]	Chr19:49907832..58557889 [GRCh38] Chr19:50411089..59069256 [GRCh37] Chr19:55102901..63761068 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	copy number gain	See cases [RCV000052926]	Chr19:51141518..58539965 [GRCh38] Chr19:51644775..59051332 [GRCh37] Chr19:56336587..63743144 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	copy number gain	See cases [RCV000052914]	Chr19:47908540..58539965 [GRCh38] Chr19:48411797..59051332 [GRCh37] Chr19:53103609..63743144 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	copy number gain	See cases [RCV000052915]	Chr19:47929575..58572206 [GRCh38] Chr19:48432832..59083573 [GRCh37] Chr19:53124644..63775385 [NCBI36] Chr19:19q13.33-13.43	pathogenic
NM_145007.3(NLRP11):c.1993C>T (p.Arg665Cys)	single nucleotide variant	Malignant melanoma [RCV000063641]	Chr19:55807863 [GRCh38] Chr19:56319229 [GRCh37] Chr19:61011041 [NCBI36] Chr19:19q13.43	not provided
NM_134444.5(NLRP4):c.-458G>A	single nucleotide variant	not provided [RCV000089242]	Chr19:55836542 [GRCh38] Chr19:56347908 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.*85A>G	single nucleotide variant	not provided [RCV000089524]	Chr19:55785540 [GRCh38] Chr19:56296906 [GRCh37] Chr19:19q13.42	not provided
NM_145007.3(NLRP11):c.1091A>G (p.Gln364Arg)	single nucleotide variant	Malignant melanoma [RCV000072373]	Chr19:55809519 [GRCh38] Chr19:56320885 [GRCh37] Chr19:61012697 [NCBI36] Chr19:19q13.43	not provided
NM_145007.5(NLRP11):c.-194-7C>T	single nucleotide variant	not provided [RCV000089525]	Chr19:55832101 [GRCh38] Chr19:56343467 [GRCh37] Chr19:19q13.43	not provided
NM_145007.5(NLRP11):c.-284-50A>G	single nucleotide variant	not provided [RCV000089526]	Chr19:55832965 [GRCh38] Chr19:56344331 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.-63+110T>C	single nucleotide variant	not provided [RCV000089527]	Chr19:55831853 [GRCh38] Chr19:56343219 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.150A>G (p.Glu50=)	single nucleotide variant	not provided [RCV000089528]	Chr19:55818025 [GRCh38] Chr19:56329391 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.1841+256A>G	single nucleotide variant	not provided [RCV000089529]	Chr19:55808513 [GRCh38] Chr19:56319879 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.1841+73A>G	single nucleotide variant	not provided [RCV000089530]	Chr19:55808696 [GRCh38] Chr19:56320062 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.1842-128T>C	single nucleotide variant	not provided [RCV000089531]	Chr19:55808142 [GRCh38] Chr19:56319508 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.1842-149C>T	single nucleotide variant	not provided [RCV000089532]	Chr19:55808163 [GRCh38] Chr19:56319529 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.1842-6A>G	single nucleotide variant	not provided [RCV000089533]	Chr19:55808020 [GRCh38] Chr19:56319386 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.2343-32A>G	single nucleotide variant	not provided [RCV000089534]	Chr19:55792503 [GRCh38] Chr19:56303869 [GRCh37] Chr19:19q13.42	not provided
NM_001394894.2(NLRP11):c.2454C>T (p.Tyr818=)	single nucleotide variant	not provided [RCV000089535]	Chr19:55792360 [GRCh38] Chr19:56303726 [GRCh37] Chr19:19q13.42	not provided
NM_001394894.2(NLRP11):c.271+53C>G	single nucleotide variant	not provided [RCV000089536]	Chr19:55817851 [GRCh38] Chr19:56329217 [GRCh37] Chr19:19q13.43	not provided
NM_001394894.2(NLRP11):c.2744C>T (p.Thr915Ile)	single nucleotide variant	not provided [RCV000089537]	Chr19:55788918 [GRCh38] Chr19:56300284 [GRCh37] Chr19:19q13.42	not provided
NM_145007.5(NLRP11):c.-405G>A	single nucleotide variant	not provided [RCV000089241]	Chr19:55836456 [GRCh38] Chr19:56347822 [GRCh37] Chr19:19q13.43	not provided
NM_145007.3(NLRP11):c.2171+1589T>C	single nucleotide variant	Lung cancer [RCV000101321]	Chr19:55799983 [GRCh38] Chr19:56311349 [GRCh37] Chr19:19q13.42	uncertain significance
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	copy number gain	See cases [RCV000134174]	Chr19:52612432..58581203 [GRCh38] Chr19:53115685..59092570 [GRCh37] Chr19:57807497..63784382 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.42-13.43(chr19:55550939-57031576)x1	copy number loss	See cases [RCV000135287]	Chr19:55550939..57031576 [GRCh38] Chr19:56062305..57542944 [GRCh37] Chr19:60754117..62234756 [NCBI36] Chr19:19q13.42-13.43	likely pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	copy number gain	See cases [RCV000135843]	Chr19:50152520..58581203 [GRCh38] Chr19:50655777..59092570 [GRCh37] Chr19:55347589..63784382 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.42-13.43(chr19:55048514-56972458)x3	copy number gain	See cases [RCV000138139]	Chr19:55048514..56972458 [GRCh38] Chr19:55595687..57483826 [GRCh37] Chr19:60251694..62175638 [NCBI36] Chr19:19q13.42-13.43	likely pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	copy number gain	See cases [RCV000142008]	Chr19:52143873..58445521 [GRCh38] Chr19:52647126..58956888 [GRCh37] Chr19:57338938..63648700 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.42-13.43(chr19:55037146-56982033)x3	copy number gain	See cases [RCV000142245]	Chr19:55037146..56982033 [GRCh38] Chr19:55548514..57493401 [GRCh37] Chr19:60240326..62185213 [NCBI36] Chr19:19q13.42-13.43	uncertain significance
GRCh38/hg38 19q13.42(chr19:55066790-55789870)x3	copy number gain	See cases [RCV000142067]	Chr19:55066790..55789870 [GRCh38] Chr19:55578158..56301236 [GRCh37] Chr19:60269970..60993048 [NCBI36] Chr19:19q13.42	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:56200298-57654005)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207313]	Chr19:56200298..57654005 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
chr19:56133299..57648277 complex variant	complex	Breast ductal adenocarcinoma [RCV000207023]	Chr19:56133299..57648277 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55549385-57489784)x3	copy number gain	See cases [RCV000510290]	Chr19:55549385..57489784 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:56286299-56368427)x3	copy number gain	not provided [RCV000752788]	Chr19:56286299..56368427 [GRCh37] Chr19:19q13.42-13.43	benign
GRCh37/hg19 19q13.42-13.43(chr19:54344821-58956888)x3	copy number gain	See cases [RCV000448186]	Chr19:54344821..58956888 [GRCh37] Chr19:19q13.42-13.43	pathogenic
NM_001394894.2(NLRP11):c.625G>A (p.Asp209Asn)	single nucleotide variant	not specified [RCV004319588]	Chr19:55809985 [GRCh38] Chr19:56321351 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.3066G>C (p.Met1022Ile)	single nucleotide variant	not specified [RCV004331833]	Chr19:55785661 [GRCh38] Chr19:56297027 [GRCh37] Chr19:19q13.42	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55844155-57408007)x3	copy number gain	See cases [RCV000511123]	Chr19:55844155..57408007 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
NM_001394894.2(NLRP11):c.223A>G (p.Met75Val)	single nucleotide variant	not specified [RCV004332861]	Chr19:55817952 [GRCh38] Chr19:56329318 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
Single allele	deletion	not provided [RCV000678017]	Chr19:55583239..55929986 [GRCh38] Chr19:56094605..56441352 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55779884-56896574)x1	copy number loss	not provided [RCV000684089]	Chr19:55779884..56896574 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3	copy number gain	not provided [RCV000684095]	Chr19:54196216..58759679 [GRCh37] Chr19:19q13.42-13.43	pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:56246520-56342061)x3	copy number gain	not provided [RCV000752786]	Chr19:56246520..56342061 [GRCh37] Chr19:19q13.42-13.43	benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
NM_001394894.2(NLRP11):c.597G>T (p.Leu199Phe)	single nucleotide variant	not specified [RCV004315107]	Chr19:55810013 [GRCh38] Chr19:56321379 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.3074C>T (p.Ser1025Leu)	single nucleotide variant	not provided [RCV000971969]	Chr19:55785653 [GRCh38] Chr19:56297019 [GRCh37] Chr19:19q13.42	benign
NM_001394894.2(NLRP11):c.2374T>G (p.Cys792Gly)	single nucleotide variant	not provided [RCV000882529]	Chr19:55792440 [GRCh38] Chr19:56303806 [GRCh37] Chr19:19q13.42	benign
GRCh37/hg19 19q13.43(chr19:56309732-56393350)x1	copy number loss	not provided [RCV000849228]	Chr19:56309732..56393350 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:56286280-56321640)x1	copy number loss	not provided [RCV000849480]	Chr19:56286280..56321640 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
NM_001394894.2(NLRP11):c.3004A>G (p.Ile1002Val)	single nucleotide variant	not specified [RCV004301517]	Chr19:55785723 [GRCh38] Chr19:56297089 [GRCh37] Chr19:19q13.42	likely benign
NM_001394894.2(NLRP11):c.252G>C (p.Lys84Asn)	single nucleotide variant	not specified [RCV004288699]	Chr19:55817923 [GRCh38] Chr19:56329289 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2929A>C (p.Ile977Leu)	single nucleotide variant	not provided [RCV000969832]	Chr19:55785798 [GRCh38] Chr19:56297164 [GRCh37] Chr19:19q13.42	benign
GRCh37/hg19 19q13.43(chr19:56332374-56796637)x3	copy number gain	not provided [RCV002472859]	Chr19:56332374..56796637 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	copy number gain	not provided [RCV001259944]	Chr19:48463931..57095254 [GRCh37] Chr19:19q13.33-13.43	pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:56273044-56374621)x1	copy number loss	not provided [RCV001259949]	Chr19:56273044..56374621 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55247893-56503347)x1	copy number loss	not provided [RCV001834407]	Chr19:55247893..56503347 [GRCh37] Chr19:19q13.42-13.43	likely pathogenic
GRCh37/hg19 19q13.43(chr19:56332200-57126728)	copy number gain	not specified [RCV002052691]	Chr19:56332200..57126728 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55434660-56463734)x1	copy number loss	not provided [RCV002279751]	Chr19:55434660..56463734 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
NM_001394894.2(NLRP11):c.2391A>T (p.Arg797Ser)	single nucleotide variant	not specified [RCV004332368]	Chr19:55792423 [GRCh38] Chr19:56303789 [GRCh37] Chr19:19q13.42	uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:56286281-56395259)x1	copy number loss	not provided [RCV002472684]	Chr19:56286281..56395259 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
NM_001394894.2(NLRP11):c.1742C>T (p.Ser581Leu)	single nucleotide variant	not specified [RCV004171366]	Chr19:55808868 [GRCh38] Chr19:56320234 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2450A>T (p.Asn817Ile)	single nucleotide variant	not specified [RCV004077007]	Chr19:55792364 [GRCh38] Chr19:56303730 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.2129A>G (p.His710Arg)	single nucleotide variant	not specified [RCV004107707]	Chr19:55801614 [GRCh38] Chr19:56312980 [GRCh37] Chr19:19q13.43	likely benign
NM_001394894.2(NLRP11):c.2606G>A (p.Ser869Asn)	single nucleotide variant	not specified [RCV004218662]	Chr19:55789307 [GRCh38] Chr19:56300673 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.841C>T (p.Arg281Cys)	single nucleotide variant	not specified [RCV004140690]	Chr19:55809769 [GRCh38] Chr19:56321135 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2143G>A (p.Glu715Lys)	single nucleotide variant	not specified [RCV004132085]	Chr19:55801600 [GRCh38] Chr19:56312966 [GRCh37] Chr19:19q13.43	likely benign
NM_001394894.2(NLRP11):c.2185G>C (p.Asp729His)	single nucleotide variant	not specified [RCV004228595]	Chr19:55796237 [GRCh38] Chr19:56307603 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.617A>T (p.Asp206Val)	single nucleotide variant	not specified [RCV004209423]	Chr19:55809993 [GRCh38] Chr19:56321359 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.535A>G (p.Met179Val)	single nucleotide variant	not specified [RCV004099812]	Chr19:55810075 [GRCh38] Chr19:56321441 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1382C>T (p.Ala461Val)	single nucleotide variant	not specified [RCV004229822]	Chr19:55809228 [GRCh38] Chr19:56320594 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2329C>A (p.Leu777Ile)	single nucleotide variant	not specified [RCV004165315]	Chr19:55796093 [GRCh38] Chr19:56307459 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.1953G>T (p.Arg651Ser)	single nucleotide variant	not specified [RCV004091506]	Chr19:55807903 [GRCh38] Chr19:56319269 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.567C>A (p.His189Gln)	single nucleotide variant	not specified [RCV004185572]	Chr19:55810043 [GRCh38] Chr19:56321409 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2278A>G (p.Ser760Gly)	single nucleotide variant	not specified [RCV004079841]	Chr19:55796144 [GRCh38] Chr19:56307510 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.2906T>C (p.Val969Ala)	single nucleotide variant	not specified [RCV004122349]	Chr19:55785821 [GRCh38] Chr19:56297187 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.103C>A (p.Leu35Ile)	single nucleotide variant	not specified [RCV004112306]	Chr19:55818072 [GRCh38] Chr19:56329438 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2698A>C (p.Met900Leu)	single nucleotide variant	not specified [RCV004225406]	Chr19:55788964 [GRCh38] Chr19:56300330 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.1445G>A (p.Arg482Lys)	single nucleotide variant	not specified [RCV004149787]	Chr19:55809165 [GRCh38] Chr19:56320531 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2060G>A (p.Arg687His)	single nucleotide variant	not specified [RCV004078675]	Chr19:55801683 [GRCh38] Chr19:56313049 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1994G>A (p.Arg665His)	single nucleotide variant	not specified [RCV004069463]	Chr19:55807862 [GRCh38] Chr19:56319228 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.230G>A (p.Arg77His)	single nucleotide variant	not specified [RCV004215854]	Chr19:55817945 [GRCh38] Chr19:56329311 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.841C>G (p.Arg281Gly)	single nucleotide variant	not specified [RCV004125623]	Chr19:55809769 [GRCh38] Chr19:56321135 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2798G>C (p.Gly933Ala)	single nucleotide variant	not specified [RCV004211329]	Chr19:55788864 [GRCh38] Chr19:56300230 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.520G>A (p.Glu174Lys)	single nucleotide variant	not specified [RCV004080258]	Chr19:55810090 [GRCh38] Chr19:56321456 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2830C>T (p.Pro944Ser)	single nucleotide variant	not specified [RCV004180809]	Chr19:55788832 [GRCh38] Chr19:56300198 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.134T>C (p.Ile45Thr)	single nucleotide variant	not specified [RCV004182515]	Chr19:55818041 [GRCh38] Chr19:56329407 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1172T>G (p.Leu391Arg)	single nucleotide variant	not specified [RCV004263255]	Chr19:55809438 [GRCh38] Chr19:56320804 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1253G>C (p.Arg418Thr)	single nucleotide variant	not specified [RCV004265056]	Chr19:55809357 [GRCh38] Chr19:56320723 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2783A>G (p.His928Arg)	single nucleotide variant	not specified [RCV004277852]	Chr19:55788879 [GRCh38] Chr19:56300245 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.1574C>T (p.Ser525Leu)	single nucleotide variant	not specified [RCV004356215]	Chr19:55809036 [GRCh38] Chr19:56320402 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.229C>T (p.Arg77Cys)	single nucleotide variant	not specified [RCV004352189]	Chr19:55817946 [GRCh38] Chr19:56329312 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.370G>A (p.Val124Ile)	single nucleotide variant	not specified [RCV004354846]	Chr19:55810240 [GRCh38] Chr19:56321606 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1023A>T (p.Leu341Phe)	single nucleotide variant	not specified [RCV004351000]	Chr19:55809587 [GRCh38] Chr19:56320953 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	copy number gain	not provided [RCV003485200]	Chr19:49625130..57647352 [GRCh37] Chr19:19q13.33-13.43	likely pathogenic
NM_001394894.2(NLRP11):c.1347A>C (p.Ile449=)	single nucleotide variant	not provided [RCV003415461]	Chr19:55809263 [GRCh38] Chr19:56320629 [GRCh37] Chr19:19q13.43	likely benign
GRCh37/hg19 19q13.42-13.43(chr19:56080158-57672397)x1	copy number loss	not specified [RCV003986104]	Chr19:56080158..57672397 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
NM_001394894.2(NLRP11):c.1906C>T (p.Arg636Trp)	single nucleotide variant	not specified [RCV004495423]	Chr19:55807950 [GRCh38] Chr19:56319316 [GRCh37] Chr19:19q13.43	likely benign
NM_001394894.2(NLRP11):c.591C>A (p.Ser197Arg)	single nucleotide variant	not specified [RCV004495440]	Chr19:55810019 [GRCh38] Chr19:56321385 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1734G>C (p.Met578Ile)	single nucleotide variant	not specified [RCV004495422]	Chr19:55808876 [GRCh38] Chr19:56320242 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2175G>T (p.Leu725Phe)	single nucleotide variant	not specified [RCV004495426]	Chr19:55796247 [GRCh38] Chr19:56307613 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.556C>T (p.Leu186Phe)	single nucleotide variant	not specified [RCV004495438]	Chr19:55810054 [GRCh38] Chr19:56321420 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.602A>G (p.Glu201Gly)	single nucleotide variant	not specified [RCV004495441]	Chr19:55810008 [GRCh38] Chr19:56321374 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1567T>C (p.Trp523Arg)	single nucleotide variant	not specified [RCV004495421]	Chr19:55809043 [GRCh38] Chr19:56320409 [GRCh37] Chr19:19q13.43	likely benign
NM_001394894.2(NLRP11):c.236A>G (p.Glu79Gly)	single nucleotide variant	not specified [RCV004495431]	Chr19:55817939 [GRCh38] Chr19:56329305 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2720G>T (p.Arg907Leu)	single nucleotide variant	not specified [RCV004495433]	Chr19:55788942 [GRCh38] Chr19:56300308 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.2287A>T (p.Met763Leu)	single nucleotide variant	not specified [RCV004495429]	Chr19:55796135 [GRCh38] Chr19:56307501 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.2404A>T (p.Ser802Cys)	single nucleotide variant	not specified [RCV004495432]	Chr19:55792410 [GRCh38] Chr19:56303776 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.3071C>T (p.Thr1024Met)	single nucleotide variant	not specified [RCV004495437]	Chr19:55785656 [GRCh38] Chr19:56297022 [GRCh37] Chr19:19q13.42	likely benign
NM_001394894.2(NLRP11):c.993A>G (p.Ile331Met)	single nucleotide variant	not specified [RCV004495442]	Chr19:55809617 [GRCh38] Chr19:56320983 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.1951A>G (p.Arg651Gly)	single nucleotide variant	not specified [RCV004495425]	Chr19:55807905 [GRCh38] Chr19:56319271 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2311C>A (p.Leu771Ile)	single nucleotide variant	not specified [RCV004495430]	Chr19:55796111 [GRCh38] Chr19:56307477 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.2833G>A (p.Asp945Asn)	single nucleotide variant	not specified [RCV004495435]	Chr19:55788829 [GRCh38] Chr19:56300195 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.2192G>A (p.Arg731Gln)	single nucleotide variant	not specified [RCV004495427]	Chr19:55796230 [GRCh38] Chr19:56307596 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.2723C>A (p.Ser908Tyr)	single nucleotide variant	not specified [RCV004495434]	Chr19:55788939 [GRCh38] Chr19:56300305 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.3010C>T (p.Pro1004Ser)	single nucleotide variant	not specified [RCV004495436]	Chr19:55785717 [GRCh38] Chr19:56297083 [GRCh37] Chr19:19q13.42	uncertain significance
NM_001394894.2(NLRP11):c.1766G>A (p.Cys589Tyr)	single nucleotide variant	not specified [RCV004343688]	Chr19:55808844 [GRCh38] Chr19:56320210 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	copy number gain	See cases [RCV000134139]	Chr19:52955056..58581203 [GRCh38] Chr19:53458309..59092570 [GRCh37] Chr19:58150121..63784382 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	copy number gain	See cases [RCV000445925]	Chr19:50489390..59095359 [GRCh37] Chr19:19q13.33-13.43	pathogenic
NM_001394894.2(NLRP11):c.1511G>A (p.Arg504Lys)	single nucleotide variant	not specified [RCV004322030]	Chr19:55809099 [GRCh38] Chr19:56320465 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3	copy number gain	not provided [RCV000740208]	Chr19:50740074..59097160 [GRCh37] Chr19:19q13.33-13.43	pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:54334195-56434037)x3	copy number gain	not provided [RCV001259948]	Chr19:54334195..56434037 [GRCh37] Chr19:19q13.42-13.43	uncertain significance
NM_001394894.2(NLRP11):c.2333T>C (p.Ile778Thr)	single nucleotide variant	not specified [RCV004181548]	Chr19:55796089 [GRCh38] Chr19:56307455 [GRCh37] Chr19:19q13.42	likely benign
NM_001394894.2(NLRP11):c.1920C>G (p.Ile640Met)	single nucleotide variant	not specified [RCV004273393]	Chr19:55807936 [GRCh38] Chr19:56319302 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001394894.2(NLRP11):c.2236G>A (p.Gly746Arg)	single nucleotide variant	not specified [RCV004256463]	Chr19:55796186 [GRCh38] Chr19:56307552 [GRCh37] Chr19:19q13.42	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	935
Count of miRNA genes:	425
Interacting mature miRNAs:	455
Transcripts:	ENST00000360133, ENST00000443188, ENST00000589093, ENST00000589824, ENST00000590409, ENST00000592953, ENST00000593208, ENST00000593244
Prediction methods:	Microtar, Miranda, Rnahybrid
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

SHGC-153591

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	56,308,407 - 56,308,737	UniSTS	GRCh37
Build 36	19	61,000,219 - 61,000,549	RGD	NCBI36
Celera	19	53,353,565 - 53,353,895	RGD
Cytogenetic Map	19	q13.43	UniSTS
HuRef	19	52,620,594 - 52,620,924	UniSTS
TNG Radiation Hybrid Map	19	19976.0	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

adipose tissue

appendage

entire extraembryonic component

High

Medium

Low

147

140

228

141

510

Below cutoff

1389

1017

1101

388

943

272

1632

906

1907

230

582

798

119

511

1108

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_054722	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001297743	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001385451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001385453	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001394894	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_145007	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_169620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_169621	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_169622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC008749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC012310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK090621	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK129784	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310394	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY095145	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY154466	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY168967	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY168968	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY226382	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC034730	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC036506	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU622142	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000589093 ⟹ ENSP00000466285

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	55,785,399 - 55,831,999 (-)	Ensembl

RefSeq Acc Id:

ENST00000589824 ⟹ ENSP00000468082

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	55,785,397 - 55,818,237 (-)	Ensembl

RefSeq Acc Id:

ENST00000590409 ⟹ ENSP00000466582

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	55,785,404 - 55,836,762 (-)	Ensembl

RefSeq Acc Id:

ENST00000592953 ⟹ ENSP00000468196

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	55,785,404 - 55,831,987 (-)	Ensembl

RefSeq Acc Id:

ENST00000593208 ⟹ ENSP00000468696

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	55,810,236 - 55,836,800 (-)	Ensembl

RefSeq Acc Id:

ENST00000593244 ⟹ ENSP00000467988

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	55,792,370 - 55,836,439 (-)	Ensembl

RefSeq Acc Id:

NM_001297743 ⟹ NP_001284672

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI
CHM1_1	19	56,290,334 - 56,337,032 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI

Sequence:

show sequence

AGCGCTGACTCACCGCTCCACGCCTTCCTGGTCCTTAATGATTGGCGGCTGGAAGCGGGAAGAA
AAGATCCGTGGTGCCATTTGATTGGCCAACGAATTGCTCCCTTGCCATTGGCTCAGAGGGCTTT
TGATGAACAGATCCAGAAAATATGTGAAGCGAAACGCCCACCGCCCCTTGAGGGGCTGTTCTAG
ACCTTTGCTCCTGGTGTCGTATAGAGCGGGGGATATTTCAAGCTGGAGATCCGTTTTCTTGTCC
CAGTGAACAGGTGCACTATGTTGAAATAAGAGTGGTGACGGAGGCCTTGTTTATCTTGTATCTT
ATTGTAAAAGGTCATCAAGAACCCACCTTGGCCAATCAAGAGAGGAGTCAGCTGGCTAATCACC
GGGCAGGCACCGCCTTTTTCTTCCCGCTGCCTAGCTTGTTTGCTTTCGACCAGCCAAGGAGACC
TGGTGGCAGGGTTGGCAATCAGGAGGCATGCAAAGCTGTCATGAGGAGAAAATTCATGCTGCAA
TGGGAAAGTCACACTTTTGGAAAATTTCATTATAAATTTTTTCGTGACGTTTCGTCAGATGTGT
TCTACATACTTCAATTAGCCTATGATTCTACCAGCTATTATTCAGCAAACAATCTCAATGTGTT
CCTGATGGGAGAGAGAGCATCTGGAAAAACTATTGTTATAAATCTGGCTGTGTTGAGGTGGATC
AAGGGTGAGATGTGGCAGAACATGATCTCGTACGTCGTTCACCTCACTGCTCACGAAATAAACC
AGATGACCAACAGCAGCTTGGCTGAGCTAATCGCCAAGGACTGGCCTGACGGCCAGGCTCCCAT
TGCAGACATCCTGTCTGATCCCAAGAAACTCCTTTTCATCCTCGAGGACTTGGACAACATAAGA
TTCGAGTTAAATGTCAATGAAAGTGCTTTGTGTAGTAACAGCACCCAGAAAGTTCCCATTCCAG
TTCTCCTGGTCAGTTTGCTGAAGAGAAAAATGGCTCCAGGCTGCTGGTTCCTCATCTCCTCAAG
GCCCACACGTGGGAATAATGTAAAAACGTTCTTGAAAGAGGTAGATTGCTGCACGACCTTGCAG
CTGTCGAATGGGAAGAGGGAGATATATTTTAACTCTTTCTTTAAAGACCGCCAGAGGGCGTCGG
CAGCCCTCCAGCTTGTACATGAGGATGAAATACTCGTGGGTCTGTGCCGAGTCGCCATCTTATG
CTGGATCACGTGTACTGTCCTGAAGCGGCAGATGGACAAGGGGCGTGACTTCCAGCTCTGCTGC
CAAACACCCACTGATCTACATGCCCACTTTCTTGCTGATGCGTTGACATCAGAGGCTGGACTTA
CTGCCAATCAGTATCACCTAGGTCTCCTAAAACGTCTGTGTTTGCTGGCTGCAGGAGGACTGTT
TCTGAGCACCCTGAATTTCAGTGGTGAAGACCTCAGATGTGTTGGGTTTACTGAGGCTGATGTC
TCTGTGTTGCAGGCCGCGAATATTCTTTTGCCGAGCAACACTCATAAAGACCGTTACAAGTTCA
TACACTTGAACGTCCAGGAGTTTTGTACAGCCATTGCATTTCTGATGGCAGTACCCAACTATCT
GATCCCCTCAGGCAGCAGAGAGTATAAAGAGAAGAGAGAACAATACTCTGACTTTAATCAAGTG
TTTACTTTCATTTTTGGTCTTCTAAATGCAAACAGGAGAAAGATTCTTGAGACATCCTTTGGAT
ACCAGCTACCGATGGTAGACAGCTTCAAGTGGTACTCGGTGGGATACATGAAACATTTGGACCG
TGACCCGGAAAAGTTGACGCACCATATGCCTTTGTTTTACTGTCTCTATGAGAATCGGGAAGAA
GAATTTGTGAAGACGATTGTGGATGCTCTCATGGAGGTTACAGTTTACCTTCAATCAGACAAGG
ATATGATGGTCTCATTATACTGTCTGGATTACTGCTGTCACCTGAGGACACTTAAGTTGAGTGT
TCAGCGCATCTTTCAAAACAAAGAGCCACTTATAAGGCCAACTGCTAGTCAAATGAAGAGCCTT
GTCTACTGGAGAGAGATCTGCTCTCTTTTTTATACAATGGAGAGCCTCCGGGAGCTGCATATCT
TTGACAATGACCTTAATGGTATTTCAGAAAGGATTCTGTCTAAAGCCCTGGAGCATTCTAGCTG
TAAACTTCGCACACTCAAGTTGTCCTATGTCTCGACTGCTTCTGGTTTTGAAGACTTACTCAAG
GCTTTGGCTCGTAATCGGAGCCTGACATACCTGAGTATCAACTGTACGTCCATTTCCCTAAATA
TGTTTTCACTTCTGCATGACATCCTGCACGAGCCCACATGCCAAATAAGTCATCTGAGCTTGAT
GAAATGTGATTTGCGAGCCAGCGAATGTGAAGAAATCGCCTCTCTCCTCATCAGTGGCGGGAGT
CTGAGAAAACTGACCTTATCCAGCAATCCGCTGAGGAGCGACGGGATGAACATACTGTGTGATG
CCTTGCTTCATCCCAACTGCACTCTTATATCACTGGTGTTAGTCTTCTGCTGTCTCACTGAAAA
TTGCTGCAGCGCCCTTGGAAGAGTGCTTCTGTTCAGCCCAACTCTAAGACAACTAGACCTGTGT
GTGAATCGCTTAAAAAATTACGGAGTGTTGCATGTGACGTTTCCCTTGCTGTTTCCAACCTGTC
AGTTAGAGGAGCTTCATCTGTCTGGCTGTTTCTTTAGCAGCGATATCTGTCAATATATTGCCAT
AGTTATTGCTACTAATGAAAAACTGAGGAGCCTGGAGATTGGGAGCAACAAAATAGAAGATGCA
GGAATGCAGCTGCTATGTGGTGGTTTGAGACATCCCAACTGCATGTTGGTGAATATTGGGCTAG
AAGAGTGCATGTTAACCAGTGCCTGCTGTCGATCTCTTGCCTCTGTTCTTACCACCAACAAAAC
ACTAGAAAGACTCAACTTGCTTCAAAATCACTTGGGCAATGATGGAGTTGCAAAACTTCTTGAG
AGCTTGATCAGCCCAGATTGTGTACTTAAGGTAGTTGGGCTTCCATTAACTGGCCTGAACACAC
AAACCCAGCAGTTGCTGATGACTGTAAAGGAAAGAAAACCCAGTTTGATCTTTCTGTCTGAAAC
TTGGTCTTTAAAGGAAGGCAGAGAAATTGGTGTGACACCTGCTTCTCAGCCAGGTTCAATAATA
CCTAATTCTAATTTGGATTACATGTTTTTCAAATTTCCCAGAATGTCTGCAGCCATGAGAACGT
CAAATACAGCATCTAGGCAACCCCTTTGATCATGTTGTACGTAAACAGTATTTATTATAAATTA
CTACCGTGACTGGGATGCAAGAGAATTAGGACTATAATTTTCCTATTTGATGTGTGTGTGTGTG
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACCTTGATCCAGTCAACCACTTCAAATTCCTA
CACTGTCTCAAGAGTATTAAAAGGATTATATGAAGTAATAAAGGATAAAATGCATTGGAAAAA

hide sequence

RefSeq Acc Id:

NM_001385451 ⟹ NP_001372380

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI

Sequence:

show sequence

AGCGCTGACTCACCGCTCCACGCCTTCCTGGTCCTTAATGATTGGCGGCTGGAAGCGGGAAGAA
AAGATCCGTGGTGCCATTTGATTGGCCAACGAATTGCTCCCTTGCCATTGGCTCAGAGGGCTTT
TGATGAACAGATCCAGAAAATATGTGAAGCGAAACGCCCACCGCCCCTTGAGGGGCTGTTCTAG
ACCTTTGCTCCTGGTGTCGTATAGAGCGGGGGATATTTCAAGCTGGAGATCCGTTTTCTTGTCC
CAGTGAACAGGTGCACTATGTTGAAATAAGAGTGGTGACGGAGGCCTTGTTTATCTTGTATCTT
ATTGTAAAAGGTCATCAAGAACCCACCTTGGCCAATCAAGAGAGGAGTCAGCTGGCTAATCACC
GGGCAGGCACCGCCTTTTTCTTCCCGCTGCCTAGCTTGTTTGCTTTCGACCAGCCAAGGAGACC
TGGTGGCAGGGTTGATCTCATATTTCTTGTGCCTCAAAATCCCTTCTCTGAAGTCTGCCTTCCC
TGGAGAAGCAAGATGGCAGAATCGGATTCTACTGACTTTGACCTGCTGTGGTATCTAGAGAATC
TCAGTGACAAGGAATTTCAGAGTTTTAAGAAGTATCTGGCACGCAAGATTCTTGATTTCAAACT
GCCACAGTTTCCACTGATACAGATGACAAAAGAAGAACTGGCTAACGTGTTGCCAATCTCTTAT
GAGGGACAGTATATATGGAATATGCTCTTCAGCATATTTTCAATGATGCGTAAGGAAGATCTTT
GTAGGAAGATCATTGGCAGACGAAACCGCAATCAGGAGGCATGCAAAGCTGTCATGAGGAGAAA
ATTCATGCTGCAATGGGAAAGTCACACTTTTGGAAAATTTCATTATAAATTTTTTCGTGACGTT
TCGTCAGATGTGTTCTACATACTTCAATTAGCCTATGATTCTACCAGCTATTATTCAGCAAACA
ATCTCAATGTGTTCCTGATGGGAGAGAGAGCATCTGGAAAAACTATTGTTATAAATCTGGCTGT
GTTGAGGTGGATCAAGGGTGAGATGTGGCAGAACATGATCTCGTACGTCGTTCACCTCACTGCT
CACGAAATAAACCAGATGACCAACAGCAGCTTGGCTGAGCTAATCGCCAAGGACTGGCCTGACG
GCCAGGCTCCCATTGCAGACATCCTGTCTGATCCCAAGAAACTCCTTTTCATCCTCGAGGACTT
GGACAACATAAGATTCGAGTTAAATGTCAATGAAAGTGCTTTGTGTAGTAACAGCACCCAGAAA
GTTCCCATTCCAGTTCTCCTGGTCAGTTTGCTGAAGAGAAAAATGGCTCCAGGCTGCTGGTTCC
TCATCTCCTCAAGGCCCACACGTGGGAATAATGTAAAAACGTTCTTGAAAGAGGTAGATTGCTG
CACGACCTTGCAGCTGTCGAATGGGAAGAGGGAGATATATTTTAACTCTTTCTTTAAAGACCGC
CAGAGGGCGTCGGCAGCCCTCCAGCTTGTACATGAGGATGAAATACTCGTGGGTCTGTGCCGAG
TCGCCATCTTATGCTGGATCACGTGTACTGTCCTGAAGCGGCAGATGGACAAGGGGCGTGACTT
CCAGCTCTGCTGCCAAACACCCACTGATCTACATGCCCACTTTCTTGCTGATGCGTTGACATCA
GAGGCTGGACTTACTGCCAATCAGTATCACCTAGGTCTCCTAAAACGTCTGTGTTTGCTGGCTG
CAGGAGGACTGTTTCTGAGCACCCTGAATTTCAGTGGTGAAGACCTCAGATGTGTTGGGTTTAC
TGAGGCTGATGTCTCTGTGTTGCAGGCCGCGAATATTCTTTTGCCGAGCAACACTCATAAAGAC
CGTTACAAGTTCATACACTTGAACGTCCAGGAGTTTTGTACAGCCATTGCATTTCTGATGGCAG
TACCCAACTATCTGATCCCCTCAGGCAGCAGAGAGTATAAAGAGAAGAGAGAACAATACTCTGA
CTTTAATCAAGTGTTTACTTTCATTTTTGGTCTTCTAAATGCAAACAGGAGAAAGATTCTTGAG
ACATCCTTTGGATACCAGCTACCGATGGTAGACAGCTTCAAGTGGTACTCGGTGGGATACATGA
AACATTTGGACCGTGACCCGGAAAAGTTGACGCACCATATGCCTTTGTTTTACTGTCTCTATGA
GAATCGGGAAGAAGAATTTGTGAAGACGATTGTGGATGCTCTCATGGAGGTTACAGTTTACCTT
CAATCAGACAAGGATATGATGGTCTCATTATACTGTCTGGATTACTGCTGTCACCTGAGGACAC
TTAAGTTGAGTGTTCAGCGCATCTTTCAAAACAAAGAGCCACTTATAAGGCCAACTGCTAGGTT
GTCCTATGTCTCGACTGCTTCTGGTTTTGAAGACTTACTCAAGGCTTTGGCTCGTAATCGGAGC
CTGACATACCTGAGTATCAACTGTACGTCCATTTCCCTAAATATGTTTTCACTTCTGCATGACA
TCCTGCACGAGCCCACATGCCAAATAAGTCATCTGAGCTTGATGAAATGTGATTTGCGAGCCAG
CGAATGTGAAGAAATCGCCTCTCTCCTCATCAGTGGCGGGAGTCTGAGAAAACTGACCTTATCC
AGCAATCCGCTGAGGAGCGACGGGATGAACATACTGTGTGATGCCTTGCTTCATCCCAACTGCA
CTCTTATATCACTGGTGTTAGTCTTCTGCTGTCTCACTGAAAATTGCTGCAGCGCCCTTGGAAG
AGTGCTTCTGTTCAGCCCAACTCTAAGACAACTAGACCTGTGTGTGAATCGCTTAAAAAATTAC
GGAGTGTTGCATGTGACGTTTCCCTTGCTGTTTCCAACCTGTCAGTTAGAGGAGCTTCATCTGT
CTGGCTGTTTCTTTAGCAGCGATATCTGTCAATATATTGCCATAGTTATTGCTACTAATGAAAA
ACTGAGGAGCCTGGAGATTGGGAGCAACAAAATAGAAGATGCAGGAATGCAGCTGCTATGTGGT
GGTTTGAGACATCCCAACTGCATGTTGGTGAATATTGGGCTAGAAGAGTGCATGTTAACCAGTG
CCTGCTGTCGATCTCTTGCCTCTGTTCTTACCACCAACAAAACACTAGAAAGACTCAACTTGCT
TCAAAATCACTTGGGCAATGATGGAGTTGCAAAACTTCTTGAGAGCTTGATCAGCCCAGATTGT
GTACTTAAGGTAGTTGGGCTTCCATTAACTGGCCTGAACACACAAACCCAGCAGTTGCTGATGA
CTGTAAAGGAAAGAAAACCCAGTTTGATCTTTCTGTCTGAAACTTGGTCTTTAAAGGAAGGCAG
AGAAATTGGTGTGACACCTGCTTCTCAGCCAGGTTCAATAATACCTAATTCTAATTTGGATTAC
ATGTTTTTCAAATTTCCCAGAATGTCTGCAGCCATGAGAACGTCAAATACAGCATCTAGGCAAC
CCCTTTGATCATGTTGTACGTAAACAGTATTTATTATAAATTACTACCGTGACTGGGATGCAAG
AGAATTAGGACTATAATTTTCCTATTTGATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
GTGTGTGTGTGACCTTGATCCAGTCAACCACTTCAAATTCCTACACTGTCTCAAGAGTATTAAA
AGGATTATATGAAGTAATAAAGGATAAAATGCATTGGAAAAA

hide sequence

RefSeq Acc Id:

NM_001385453 ⟹ NP_001372382

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI

Sequence:

show sequence

AGCGCTGACTCACCGCTCCACGCCTTCCTGGTCCTTAATGATTGGCGGCTGGAAGCGGGAAGAA
AAGATCCGTGGTGCCATTTGATTGGCCAACGAATTGCTCCCTTGCCATTGGCTCAGAGGGCTTT
TGATGAACAGATCCAGAAAATATGTGAAGCGAAACGCCCACCGCCCCTTGAGGGGCTGTTCTAG
ACCTTTGCTCCTGGTGTCGTATAGAGCGGGGGATATTTCAAGCTGGAGATCCGTTTTCTTGTCC
CAGTGAACAGGTGCACTATGTTGAAATAAGAGTGGTGACGGAGGCCTTGTTTATCTTGTATCTT
ATTGTAAAAGGTCATCAAGAACCCACCTTGGCCAATCAAGAGAGGAGTCAGCTGGCTAATCACC
GGGCAGGCACCGCCTTTTTCTTCCCGCTGCCTAGCTTGTTTGCTTTCGACCAGCCAAGGAGACC
TGGTGGCAGGGTTGATCTCATATTTCTTGTGCCTCAAAATCCCTTCTCTGAAGTCTGCCTTCCC
TGGAGAAGCAAGATGGCAGAATCGGATTCTACTGACTTTGACCTGCTGTGGTATCTAGAGAATC
TCAGTGACAAGGAATTTCAGAGTTTTAAGAAGTATCTGGCACGCAAGATTCTTGATTTCAAACT
GCCACAGTTTCCACTGATACAGATGACAAAAGAAGAACTGGCTAACGTGTTGCCAATCTCTTAT
GAGGGACAGTATATATGGAATATGCTCTTCAGCATATTTTCAATGATGCGTAAGGAAGATCTTT
GTAGGAAGATCATTGGCAGACGAAACCGCAATCAGGAGGCATGCAAAGCTGTCATGAGGAGAAA
ATTCATGCTGCAATGGGAAAGTCACACTTTTGGAAAATTTCATTATAAATTTTTTCGTGACGTT
TCGTCAGATGTGTTCTACATACTTCAATTAGCCTATGATTCTACCAGCTATTATTCAGCAAACA
ATCTCAATGTGTTCCTGATGGGAGAGAGAGCATCTGGAAAAACTATTGTTATAAATCTGGCTGT
GTTGAGGTGGATCAAGGGTGAGATGTGGCAGAACATGATCTCGTACGTCGTTCACCTCACTGCT
CACGAAATAAACCAGATGACCAACAGCAGCTTGGCTGAGCTAATCGCCAAGGACTGGCCTGACG
GCCAGGCTCCCATTGCAGACATCCTGTCTGATCCCAAGAAACTCCTTTTCATCCTCGAGGACTT
GGACAACATAAGATTCGAGTTAAATGTCAATGAAAGTGCTTTGTGTAGTAACAGCACCCAGAAA
GTTCCCATTCCAGTTCTCCTGGTCAGTTTGCTGAAGAGAAAAATGGCTCCAGGCTGCTGGTTCC
TCATCTCCTCAAGGCCCACACGTGGGAATAATGTAAAAACGTTCTTGAAAGAGGTAGATTGCTG
CACGACCTTGCAGCTGTCGAATGGGAAGAGGGAGATATATTTTAACTCTTTCTTTAAAGACCGC
CAGAGGGCGTCGGCAGCCCTCCAGCTTGTACATGAGGATGAAATACTCGTGGGTCTGTGCCGAG
TCGCCATCTTATGCTGGATCACGTGTACTGTCCTGAAGCGGCAGATGGACAAGGGGCGTGACTT
CCAGCTCTGCTGCCAAACACCCACTGATCTACATGCCCACTTTCTTGCTGATGCGTTGACATCA
GAGGCTGGACTTACTGCCAATCAGTATCACCTAGGTCTCCTAAAACGTCTGTGTTTGCTGGCTG
CAGGAGGACTGTTTCTGAGCACCCTGAATTTCAGTGGTGAAGACCTCAGATGTGTTGGGTTTAC
TGAGGCTGATGTCTCTGTGTTGCAGGCCGCGAATATTCTTTTGCCGAGCAACACTCATAAAGAC
CGTTACAAGTTCATACACTTGAACGTCCAGGAGTTTTGTACAGCCATTGCATTTCTGATGGCAG
TACCCAACTATCTGATCCCCTCAGGCAGCAGAGAGTATAAAGAGAAGAGAGAACAATACTCTGA
CTTTAATCAAGTGTTTACTTTCATTTTTGGTCTTCTAAATGCAAACAGGAGAAAGATTCTTGAG
ACATCCTTTGGATACCAGCTACCGATGGTAGACAGCTTCAAGTGGTACTCGGTGGGATACATGA
AACATTTGGACCGTGACCCGGAAAAGTTGACGCACCATATGCCTTTGTTTTACTGTCTCTATGA
GAATCGGGAAGAAGAATTTGTGAAGACGATTGTGGATGCTCTCATGGAGGTTACAGTTTACCTT
CAATCAGACAAGGATATGATGGTCTCATTATACTGTCTGGATTACTGCTGTCACCTGAGGACAC
TTAAGTTGAGTGTTCAGCGCATCTTTCAAAACAAAGAGCCACTTATAAGGCCAACTGCTAGTCA
AATGAAGAGCCTTGTCTACTGGAGAGAGATCTGCTCTCTTTTTTATACAATGGAGAGCCTCCGG
GAGCTGCATATCTTTGACAATGACCTTAATGGTATTTCAGAAAGGATTCTGTCTAAAGCCCTGG
AGCATTCTAGCTGTAAACTTCGCACACTCAAGTTGTCCTATGTCTCGACTGCTTCTGGTTTTGA
AGACTTACTCAAGGCTTTGGCTCGTAATCGGAGCCTGACATACCTGAGTATCAACTGTACGTCC
ATTTCCCTAAATATGTTTTCACTTCTGCATGACATCCTGCACGAGCCCACATGCCAAATAAGTC
ATCTGAGCTTGATGAAATGTGATTTGCGAGCCAGCGAATGTGAAGAAATCGCCTCTCTCCTCAT
CAGTGGCGGGAGTCTGAGAAAACTGACCTTATCCAGCAATCCGCTGAGGAGCGACGGGATGAAC
ATACTGTGTGATGCCTTGCTTCATCCCAACTGCACTCTTATATCACTGGTGTTAGTCTTCTGCT
GTCTCACTGAAAATTGCTGCAGCGCCCTTGGAAGAGTGCTTCTGTTCAGCCCAACTCTAAGACA
ACTAGACCTGTGTGTGAATCGCTTAAAAAATTACGGAGTGTTGCATGTGACGTTTCCCTTGCTG
TTTCCAACCTGTCAGTTAGAGGAGCTTCAGCTAGAAGAGTGCATGTTAACCAGTGCCTGCTGTC
GATCTCTTGCCTCTGTTCTTACCACCAACAAAACACTAGAAAGACTCAACTTGCTTCAAAATCA
CTTGGGCAATGATGGAGTTGCAAAACTTCTTGAGAGCTTGATCAGCCCAGATTGTGTACTTAAG
GTAGTTGGGCTTCCATTAACTGGCCTGAACACACAAACCCAGCAGTTGCTGATGACTGTAAAGG
AAAGAAAACCCAGTTTGATCTTTCTGTCTGAAACTTGGTCTTTAAAGGAAGGCAGAGAAATTGG
TGTGACACCTGCTTCTCAGCCAGGTTCAATAATACCTAATTCTAATTTGGATTACATGTTTTTC
AAATTTCCCAGAATGTCTGCAGCCATGAGAACGTCAAATACAGCATCTAGGCAACCCCTTTGAT
CATGTTGTACGTAAACAGTATTTATTATAAATTACTACCGTGACTGGGATGCAAGAGAATTAGG
ACTATAATTTTCCTATTTGATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
TGACCTTGATCCAGTCAACCACTTCAAATTCCTACACTGTCTCAAGAGTATTAAAAGGATTATA
TGAAGTAATAAAGGATAAAATGCATTGGAAAAA

hide sequence

RefSeq Acc Id:

NM_001394894 ⟹ NP_001381823

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,831,999 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,931,345 (-)	NCBI

Sequence:

show sequence

GCTTTCGACCAGCCAAGGAGACCTGGTGGCAGGGTTGATCTCATATTTCTTGTGCCTCAAAATC
CCTTCTCTGAAGTCTGCCTTCCCTGGAGAAGCAAGATGGCAGAATCGGATTCTACTGACTTTGA
CCTGCTGTGGTATCTAGAGAATCTCAGTGACAAGGAATTTCAGAGTTTTAAGAAGTATCTGGCA
CGCAAGATTCTTGATTTCAAACTGCCACAGTTTCCACTGATACAGATGACAAAAGAAGAACTGG
CTAACGTGTTGCCAATCTCTTATGAGGGACAGTATATATGGAATATGCTCTTCAGCATATTTTC
AATGATGCGTAAGGAAGATCTTTGTAGGAAGATCATTGGCAGACGAAACCGCAATCAGGAGGCA
TGCAAAGCTGTCATGAGGAGAAAATTCATGCTGCAATGGGAAAGTCACACTTTTGGAAAATTTC
ATTATAAATTTTTTCGTGACGTTTCGTCAGATGTGTTCTACATACTTCAATTAGCCTATGATTC
TACCAGCTATTATTCAGCAAACAATCTCAATGTGTTCCTGATGGGAGAGAGAGCATCTGGAAAA
ACTATTGTTATAAATCTGGCTGTGTTGAGGTGGATCAAGGGTGAGATGTGGCAGAACATGATCT
CGTACGTCGTTCACCTCACTGCTCACGAAATAAACCAGATGACCAACAGCAGCTTGGCTGAGCT
AATCGCCAAGGACTGGCCTGACGGCCAGGCTCCCATTGCAGACATCCTGTCTGATCCCAAGAAA
CTCCTTTTCATCCTCGAGGACTTGGACAACATAAGATTCGAGTTAAATGTCAATGAAAGTGCTT
TGTGTAGTAACAGCACCCAGAAAGTTCCCATTCCAGTTCTCCTGGTCAGTTTGCTGAAGAGAAA
AATGGCTCCAGGCTGCTGGTTCCTCATCTCCTCAAGGCCCACACGTGGGAATAATGTAAAAACG
TTCTTGAAAGAGGTAGATTGCTGCACGACCTTGCAGCTGTCGAATGGGAAGAGGGAGATATATT
TTAACTCTTTCTTTAAAGACCGCCAGAGGGCGTCGGCAGCCCTCCAGCTTGTACATGAGGATGA
AATACTCGTGGGTCTGTGCCGAGTCGCCATCTTATGCTGGATCACGTGTACTGTCCTGAAGCGG
CAGATGGACAAGGGGCGTGACTTCCAGCTCTGCTGCCAAACACCCACTGATCTACATGCCCACT
TTCTTGCTGATGCGTTGACATCAGAGGCTGGACTTACTGCCAATCAGTATCACCTAGGTCTCCT
AAAACGTCTGTGTTTGCTGGCTGCAGGAGGACTGTTTCTGAGCACCCTGAATTTCAGTGGTGAA
GACCTCAGATGTGTTGGGTTTACTGAGGCTGATGTCTCTGTGTTGCAGGCCGCGAATATTCTTT
TGCCGAGCAACACTCATAAAGACCGTTACAAGTTCATACACTTGAACGTCCAGGAGTTTTGTAC
AGCCATTGCATTTCTGATGGCAGTACCCAACTATCTGATCCCCTCAGGCAGCAGAGAGTATAAA
GAGAAGAGAGAACAATACTCTGACTTTAATCAAGTGTTTACTTTCATTTTTGGTCTTCTAAATG
CAAACAGGAGAAAGATTCTTGAGACATCCTTTGGATACCAGCTACCGATGGTAGACAGCTTCAA
GTGGTACTCGGTGGGATACATGAAACATTTGGACCGTGACCCGGAAAAGTTGACGCACCATATG
CCTTTGTTTTACTGTCTCTATGAGAATCGGGAAGAAGAATTTGTGAAGACGATTGTGGATGCTC
TCATGGAGGTTACAGTTTACCTTCAATCAGACAAGGATATGATGGTCTCATTATACTGTCTGGA
TTACTGCTGTCACCTGAGGACACTTAAGTTGAGTGTTCAGCGCATCTTTCAAAACAAAGAGCCA
CTTATAAGGCCAACTGCTAGTCAAATGAAGAGCCTTGTCTACTGGAGAGAGATCTGCTCTCTTT
TTTATACAATGGAGAGCCTCCGGGAGCTGCATATCTTTGACAATGACCTTAATGGTATTTCAGA
AAGGATTCTGTCTAAAGCCCTGGAGCATTCTAGCTGTAAACTTCGCACACTCAAGTTGTCCTAT
GTCTCGACTGCTTCTGGTTTTGAAGACTTACTCAAGGCTTTGGCTCGTAATCGGAGCCTGACAT
ACCTGAGTATCAACTGTACGTCCATTTCCCTAAATATGTTTTCACTTCTGCATGACATCCTGCA
CGAGCCCACATGCCAAATAAGTCATCTGAGCTTGATGAAATGTGATTTGCGAGCCAGCGAATGT
GAAGAAATCGCCTCTCTCCTCATCAGTGGCGGGAGTCTGAGAAAACTGACCTTATCCAGCAATC
CGCTGAGGAGCGACGGGATGAACATACTGTGTGATGCCTTGCTTCATCCCAACTGCACTCTTAT
ATCACTGGTGTTAGTCTTCTGCTGTCTCACTGAAAATTGCTGCAGCGCCCTTGGAAGAGTGCTT
CTGTTCAGCCCAACTCTAAGACAACTAGACCTGTGTGTGAATCGCTTAAAAAATTACGGAGTGT
TGCATGTGACGTTTCCCTTGCTGTTTCCAACCTGTCAGTTAGAGGAGCTTCATCTGTCTGGCTG
TTTCTTTAGCAGCGATATCTGTCAATATATTGCCATAGTTATTGCTACTAATGAAAAACTGAGG
AGCCTGGAGATTGGGAGCAACAAAATAGAAGATGCAGGAATGCAGCTGCTATGTGGTGGTTTGA
GACATCCCAACTGCATGTTGGTGAATATTGGGCTAGAAGAGTGCATGTTAACCAGTGCCTGCTG
TCGATCTCTTGCCTCTGTTCTTACCACCAACAAAACACTAGAAAGACTCAACTTGCTTCAAAAT
CACTTGGGCAATGATGGAGTTGCAAAACTTCTTGAGAGCTTGATCAGCCCAGATTGTGTACTTA
AGGTAGTTGGGCTTCCATTAACTGGCCTGAACACACAAACCCAGCAGTTGCTGATGACTGTAAA
GGAAAGAAAACCCAGTTTGATCTTTCTGTCTGAAACTTGGTCTTTAAAGGAAGGCAGAGAAATT
GGTGTGACACCTGCTTCTCAGCCAGGTTCAATAATACCTAATTCTAATTTGGATTACATGTTTT
TCAAATTTCCCAGAATGTCTGCAGCCATGAGAACGTCAAATACAGCATCTAGGCAACCCCTTTG
ATCATGTTGTACGTAAACAGTATTTATTATAAATTACTACCGTGACTGGGATGCAAGAGAATTA
GGACTATAATTTTCCTATTTGATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
TGTGACCTTGATCCAGTCAACCACTTCAAATTCCTACACTGTCTCAAGAGTATTAAAAGGATTA
TATGAAGTAATAAAGGATAAAATGCA

hide sequence

RefSeq Acc Id:

NM_145007 ⟹ NP_659444

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI
GRCh37	19	56,296,763 - 56,348,128 (-)	RGD
Build 36	19	60,988,577 - 61,035,172 (-)	NCBI Archive
Celera	19	53,341,920 - 53,393,276 (-)	RGD
HuRef	19	52,608,953 - 52,660,294 (-)	ENTREZGENE
CHM1_1	19	56,290,334 - 56,341,701 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI

Sequence:

show sequence

AGCGCTGACTCACCGCTCCACGCCTTCCTGGTCCTTAATGATTGGCGGCTGGAAGCGGGAAGAA
AAGATCCGTGGTGCCATTTGATTGGCCAACGAATTGCTCCCTTGCCATTGGCTCAGAGGGCTTT
TGATGAACAGATCCAGAAAATATGTGAAGCGAAACGCCCACCGCCCCTTGAGGGGCTGTTCTAG
ACCTTTGCTCCTGGTGTCGTATAGAGCGGGGGATATTTCAAGCTGGAGATCCGTTTTCTTGTCC
CAGTGAACAGGTGCACTATGTTGAAATAAGAGTGGTGACGGAGGCCTTGTTTATCTTGTATCTT
ATTGTAAAAGGTCATCAAGAACCCACCTTGGCCAATCAAGAGAGGAGTCAGCTGGCTAATCACC
GGGCAGGCACCGCCTTTTTCTTCCCGCTGCCTAGCTTGTTTGCTTTCGACCAGCCAAGGAGACC
TGGTGGCAGGGTTGATCTCATATTTCTTGTGCCTCAAAATCCCTTCTCTGAAGTCTGCCTTCCC
TGGAGAAGCAAGATGGCAGAATCGGATTCTACTGACTTTGACCTGCTGTGGTATCTAGAGAATC
TCAGTGACAAGGAATTTCAGAGTTTTAAGAAGTATCTGGCACGCAAGATTCTTGATTTCAAACT
GCCACAGTTTCCACTGATACAGATGACAAAAGAAGAACTGGCTAACGTGTTGCCAATCTCTTAT
GAGGGACAGTATATATGGAATATGCTCTTCAGCATATTTTCAATGATGCGTAAGGAAGATCTTT
GTAGGAAGATCATTGGCAGACGAAACCGCAATCAGGAGGCATGCAAAGCTGTCATGAGGAGAAA
ATTCATGCTGCAATGGGAAAGTCACACTTTTGGAAAATTTCATTATAAATTTTTTCGTGACGTT
TCGTCAGATGTGTTCTACATACTTCAATTAGCCTATGATTCTACCAGCTATTATTCAGCAAACA
ATCTCAATGTGTTCCTGATGGGAGAGAGAGCATCTGGAAAAACTATTGTTATAAATCTGGCTGT
GTTGAGGTGGATCAAGGGTGAGATGTGGCAGAACATGATCTCGTACGTCGTTCACCTCACTGCT
CACGAAATAAACCAGATGACCAACAGCAGCTTGGCTGAGCTAATCGCCAAGGACTGGCCTGACG
GCCAGGCTCCCATTGCAGACATCCTGTCTGATCCCAAGAAACTCCTTTTCATCCTCGAGGACTT
GGACAACATAAGATTCGAGTTAAATGTCAATGAAAGTGCTTTGTGTAGTAACAGCACCCAGAAA
GTTCCCATTCCAGTTCTCCTGGTCAGTTTGCTGAAGAGAAAAATGGCTCCAGGCTGCTGGTTCC
TCATCTCCTCAAGGCCCACACGTGGGAATAATGTAAAAACGTTCTTGAAAGAGGTAGATTGCTG
CACGACCTTGCAGCTGTCGAATGGGAAGAGGGAGATATATTTTAACTCTTTCTTTAAAGACCGC
CAGAGGGCGTCGGCAGCCCTCCAGCTTGTACATGAGGATGAAATACTCGTGGGTCTGTGCCGAG
TCGCCATCTTATGCTGGATCACGTGTACTGTCCTGAAGCGGCAGATGGACAAGGGGCGTGACTT
CCAGCTCTGCTGCCAAACACCCACTGATCTACATGCCCACTTTCTTGCTGATGCGTTGACATCA
GAGGCTGGACTTACTGCCAATCAGTATCACCTAGGTCTCCTAAAACGTCTGTGTTTGCTGGCTG
CAGGAGGACTGTTTCTGAGCACCCTGAATTTCAGTGGTGAAGACCTCAGATGTGTTGGGTTTAC
TGAGGCTGATGTCTCTGTGTTGCAGGCCGCGAATATTCTTTTGCCGAGCAACACTCATAAAGAC
CGTTACAAGTTCATACACTTGAACGTCCAGGAGTTTTGTACAGCCATTGCATTTCTGATGGCAG
TACCCAACTATCTGATCCCCTCAGGCAGCAGAGAGTATAAAGAGAAGAGAGAACAATACTCTGA
CTTTAATCAAGTGTTTACTTTCATTTTTGGTCTTCTAAATGCAAACAGGAGAAAGATTCTTGAG
ACATCCTTTGGATACCAGCTACCGATGGTAGACAGCTTCAAGTGGTACTCGGTGGGATACATGA
AACATTTGGACCGTGACCCGGAAAAGTTGACGCACCATATGCCTTTGTTTTACTGTCTCTATGA
GAATCGGGAAGAAGAATTTGTGAAGACGATTGTGGATGCTCTCATGGAGGTTACAGTTTACCTT
CAATCAGACAAGGATATGATGGTCTCATTATACTGTCTGGATTACTGCTGTCACCTGAGGACAC
TTAAGTTGAGTGTTCAGCGCATCTTTCAAAACAAAGAGCCACTTATAAGGCCAACTGCTAGTCA
AATGAAGAGCCTTGTCTACTGGAGAGAGATCTGCTCTCTTTTTTATACAATGGAGAGCCTCCGG
GAGCTGCATATCTTTGACAATGACCTTAATGGTATTTCAGAAAGGATTCTGTCTAAAGCCCTGG
AGCATTCTAGCTGTAAACTTCGCACACTCAAGTTGTCCTATGTCTCGACTGCTTCTGGTTTTGA
AGACTTACTCAAGGCTTTGGCTCGTAATCGGAGCCTGACATACCTGAGTATCAACTGTACGTCC
ATTTCCCTAAATATGTTTTCACTTCTGCATGACATCCTGCACGAGCCCACATGCCAAATAAGTC
ATCTGAGCTTGATGAAATGTGATTTGCGAGCCAGCGAATGTGAAGAAATCGCCTCTCTCCTCAT
CAGTGGCGGGAGTCTGAGAAAACTGACCTTATCCAGCAATCCGCTGAGGAGCGACGGGATGAAC
ATACTGTGTGATGCCTTGCTTCATCCCAACTGCACTCTTATATCACTGGTGTTAGTCTTCTGCT
GTCTCACTGAAAATTGCTGCAGCGCCCTTGGAAGAGTGCTTCTGTTCAGCCCAACTCTAAGACA
ACTAGACCTGTGTGTGAATCGCTTAAAAAATTACGGAGTGTTGCATGTGACGTTTCCCTTGCTG
TTTCCAACCTGTCAGTTAGAGGAGCTTCATCTGTCTGGCTGTTTCTTTAGCAGCGATATCTGTC
AATATATTGCCATAGTTATTGCTACTAATGAAAAACTGAGGAGCCTGGAGATTGGGAGCAACAA
AATAGAAGATGCAGGAATGCAGCTGCTATGTGGTGGTTTGAGACATCCCAACTGCATGTTGGTG
AATATTGGGCTAGAAGAGTGCATGTTAACCAGTGCCTGCTGTCGATCTCTTGCCTCTGTTCTTA
CCACCAACAAAACACTAGAAAGACTCAACTTGCTTCAAAATCACTTGGGCAATGATGGAGTTGC
AAAACTTCTTGAGAGCTTGATCAGCCCAGATTGTGTACTTAAGGTAGTTGGGCTTCCATTAACT
GGCCTGAACACACAAACCCAGCAGTTGCTGATGACTGTAAAGGAAAGAAAACCCAGTTTGATCT
TTCTGTCTGAAACTTGGTCTTTAAAGGAAGGCAGAGAAATTGGTGTGACACCTGCTTCTCAGCC
AGGTTCAATAATACCTAATTCTAATTTGGATTACATGTTTTTCAAATTTCCCAGAATGTCTGCA
GCCATGAGAACGTCAAATACAGCATCTAGGCAACCCCTTTGATCATGTTGTACGTAAACAGTAT
TTATTATAAATTACTACCGTGACTGGGATGCAAGAGAATTAGGACTATAATTTTCCTATTTGAT
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACCTTGATCCAGTCAACCA
CTTCAAATTCCTACACTGTCTCAAGAGTATTAAAAGGATTATATGAAGTAATAAAGGATAAAAT
GCATTGGAAAAA

hide sequence

RefSeq Acc Id:

NR_169620

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI

Sequence:

show sequence

AGCGCTGACTCACCGCTCCACGCCTTCCTGGTCCTTAATGATTGGCGGCTGGAAGCGGGAAGAA
AAGATCCGTGGTGCCATTTGATTGGCCAACGAATTGCTCCCTTGCCATTGGCTCAGAGGGCTTT
TGATGAACAGATCCAGAAAATATGTGAAGCGAAACGCCCACCGCCCCTTGAGGGGCTGTTCTAG
ACCTTTGCTCCTGGTGTCGTATAGAGCGGGGGATATTTCAAGCTGGAGATCCGTTTTCTTGTCC
CAGTGAACAGGTGCACTATGTTGAAATAAGAGTGGTGACGGAGGCCTTGTTTATCTTGTATCTT
ATTGTAAAAGGTCATCAAGAACCCACCTTGGCCAATCAAGAGAGGAGTCAGCTGGCTAATCACC
GGGCAGGCACCGCCTTTTTCTTCCCGCTGCCTAGCTTGTTTGCTTTCGACCAGCCAAGGAGACC
TGGTGGCAGGGTTGGCAATCAGGAGGCATGCAAAGCTGTCATGAGGAGAAAATTCATGCTGCAA
TGGGAAAGTCACACTTTTGGAAAATTTCATTATAAATTTTTTCGTGACGTTTCGTCAGATGTGT
TCTACATACTTCAATTAGCCTATGATTCTACCAGCTATTATTCAGCAAACAATCTCAATGTGTT
CCTGATGGGAGAGAGAGCATCTGGAAAAACTATTGTTATAAATCTGGCTGTGTTGAGGTGGATC
AAGGGTGAGATGTGGCAGAACATGATCTCGTACGTCGTTCACCTCACTGCTCACGAAATAAACC
AGATGACCAACAGCAGCTTGGCTGAGCTAATCGCCAAGGACTGGCCTGACGGCCAGGCTCCCAT
TGCAGACATCCTGTCTGATCCCAAGAAACTCCTTTTCATCCTCGAGGACTTGGACAACATAAGA
TTCGAGTTAAATGTCAATGAAAGTGCTTTGTGTAGTAACAGCACCCAGAAAGTTCCCATTCCAG
TTCTCCTGGTCAGTTTGCTGAAGAGAAAAATGGCTCCAGGCTGCTGGTTCCTCATCTCCTCAAG
GCCCACACGTGGGAATAATGTAAAAACGTTCTTGAAAGAGGTAGATTGCTGCACGACCTTGCAG
CTGTCGAATGGGAAGAGGGAGATATATTTTAACTCTTTCTTTAAAGACCGCCAGAGGGCGTCGG
CAGCCCTCCAGCTTGTACATGAGGATGAAATACTCGTGGGTCTGTGCCGAGTCGCCATCTTATG
CTGGATCACGTGTACTGTCCTGAAGCGGCAGATGGACAAGGGGCGTGACTTCCAGCTCTGCTGC
CAAACACCCACTGATCTACATGCCCACTTTCTTGCTGATGCGTTGACATCAGAGGCTGGACTTA
CTGCCAATCAGTATCACCTAGGTCTCCTAAAACGTCTGTGTTTGCTGGCTGCAGGAGGACTGTT
TCTGAGCACCCTGAATTTCAGTGGTGAAGACCTCAGATGTGTTGGGTTTACTGAGGCTGATGTC
TCTGTGTTGCAGGCCGCGAATATTCTTTTGCCGAGCAACACTCATAAAGACCGTTACAAGTTCA
TACACTTGAACGTCCAGGAGTTTTGTACAGCCATTGCATTTCTGATGGCAGTACCCAACTATCT
GATCCCCTCAGGCAGCAGAGAGTATAAAGAGAAGAGAGAACAATACTCTGACTTTAATCAAGTG
TTTACTTTCATTTTTGGTCTTCTAAATGCAAACAGGAGAAAGATTCTTGAGACATCCTTTGGAT
ACCAGCTACCGATGGTAGACAGCTTCAAGTGGTACTCGGTGGGATACATGAAACATTTGGACCG
TGACCCGGAAAAGTTGACGCACCATATGCCTTTGTTTTACTGTCTCTATGAGAATCGGGAAGAA
GAATTTGTGAAGACGATTGTGGATGCTCTCATGGAGGTTACAGTTTACCTTCAATCAGACAAGG
ATATGATGGTCTCATTATACTGTCTGGATTACTGCTGTCACCTGAGGACACTTAAGTTGAGTGT
TCAGCGCATCTTTCAAAACAAAGAGCCACTTATAAGGCCAACTGCTAGTCAAATGAAGAGCCTT
GTCTACTGGAGAGAGATCTGCTCTCTTTTTTATACAATGGAGAGCCTCCGGGAGCTGCATATCT
TTGACAATGACCTTAATGGTATTTCAGAAAGGATTCTGTCTAAAGCCCTGGAGCATTCTAGCTG
TAAACTTCGCACACTCAAGTTGTCCTATGTCTCGACTGCTTCTGGTTTTGAAGACTTACTCAAG
GCTTTGGCTCGTAATCGGAGCCTGACATACCTGAGTATCAACTGTACGTCCATTTCCCTAAATA
TGTTTTCACTTCTGCATGACATCCTGCACGAGCCCACATGCCAAATAAGTCATCTGAGAATACA
CAGGCCAACGCGACGGCTCACGCCTGGAATCCCAACACTTTGGGAGGCCGAGGCGGGCAGATCA
CCTGAGCTTGATGAAATGTGATTTGCGAGCCAGCGAATGTGAAGAAATCGCCTCTCTCCTCATC
AGTGGCGGGAGTCTGAGAAAACTGACCTTATCCAGCAATCCGCTGAGGAGCGACGGGATGAACA
TACTGTGTGATGCCTTGCTTCATCCCAACTGCACTCTTATATCACTGGTGTTAGTCTTCTGCTG
TCTCACTGAAAATTGCTGCAGCGCCCTTGGAAGAGTGCTTCTGTTCAGCCCAACTCTAAGACAA
CTAGACCTGTGTGTGAATCGCTTAAAAAATTACGGAGTGTTGCATGTGACGTTTCCCTTGCTGT
TTCCAACCTGTCAGTTAGAGGAGCTTCATCTGTCTGGCTGTTTCTTTAGCAGCGATATCTGTCA
ATATATTGCCATAGTTATTGCTACTAATGAAAAACTGAGGAGCCTGGAGATTGGGAGCAACAAA
ATAGAAGATGCAGGAATGCAGCTGCTATGTGGTGGTTTGAGACATCCCAACTGCATGTTGGTGA
ATATTGGGCTAGAAGAGTGCATGTTAACCAGTGCCTGCTGTCGATCTCTTGCCTCTGTTCTTAC
CACCAACAAAACACTAGAAAGACTCAACTTGCTTCAAAATCACTTGGGCAATGATGGAGTTGCA
AAACTTCTTGAGAGCTTGATCAGCCCAGATTGTGTACTTAAGGTAGTTGGGCTTCCATTAACTG
GCCTGAACACACAAACCCAGCAGTTGCTGATGACTGTAAAGGAAAGAAAACCCAGTTTGATCTT
TCTGTCTGAAACTTGGTCTTTAAAGGAAGGCAGAGAAATTGGTGTGACACCTGCTTCTCAGCCA
GGTTCAATAATACCTAATTCTAATTTGGATTACATGTTTTTCAAATTTCCCAGAATGTCTGCAG
CCATGAGAACGTCAAATACAGCATCTAGGCAACCCCTTTGATCATGTTGTACGTAAACAGTATT
TATTATAAATTACTACCGTGACTGGGATGCAAGAGAATTAGGACTATAATTTTCCTATTTGATG
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACCTTGATCCAGTCAACCAC
TTCAAATTCCTACACTGTCTCAAGAGTATTAAAAGGATTATATGAAGTAATAAAGGATAAAATG
CATTGGAAAAA

hide sequence

RefSeq Acc Id:

NR_169621

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI

Sequence:

show sequence

AGCGCTGACTCACCGCTCCACGCCTTCCTGGTCCTTAATGATTGGCGGCTGGAAGCGGGAAGAA
AAGATCCGTGGTGCCATTTGATTGGCCAACGAATTGCTCCCTTGCCATTGGCTCAGAGGGCTTT
TGATGAACAGATCCAGAAAATATGTGAAGCGAAACGCCCACCGCCCCTTGAGGGGCTGTTCTAG
ACCTTTGCTCCTGGTGTCGTATAGAGCGGGGGATATTTCAAGCTGGAGATCCGTTTTCTTGTCC
CAGTGAACAGGTGCACTATGTTGAAATAAGAGTGGTGACGGAGGCCTTGTTTATCTTGTATCTT
ATTGTAAAAGGTCATCAAGAACCCACCTTGGCCAATCAAGAGAGGAGTCAGCTGGCTAATCACC
GGGCAGGCACCGCCTTTTTCTTCCCGCTGCCTAGCTTGTTTGCTTTCGACCAGCCAAGGAGACC
TGGTGGCAGGGTTGATCTCATATTTCTTGTGCCTCAAAATCCCTTCTCTGAAGTCTGCCTTCCC
TGGAGAAGCAAGATGGCAGAATCGGATTCTACTGACTTTGACCTGCTGTGGTATCTAGAGAATC
TCAGTGACAAGGAATTTCAGAGTTTTAAGAAGTATCTGGCACGCAAGATTCTTGATTTCAAACT
GCCACAGTTTCCACTGATACAGATGACAAAAGAAGAACTGGCTAACGTGTTGCCAATCTCTTAT
GAGGGACAGTATATATGGAATATGCTCTTCAGCATATTTTCAATGATGCGTAAGGAAGATCTTT
GTAGGAAGATCATTGGCAGACGAAACCGCAATCAGGAGGCATGCAAAGCTGTCATGAGGAGAAA
ATTCATGCTGCAATGGGAAAGTCACACTTTTGGAAAATTTCATTATAAATTTTTTCGTGACGTT
TCGTCAGATGTGTTCTACATACTTCAATTAGCCTATGATTCTACCAGCTATTATTCAGCAAACA
ATCTCAATGTGTTCCTGATGGGAGAGAGAGCATCTGGAAAAACTATTGTTATAAATCTGGCTGT
GTTGAGGTGGATCAAGGGTGAGATGTGGCAGAACATGATCTCGTACGTCGTTCACCTCACTGCT
CACGAAATAAACCAGATGACCAACAGCAGCTTGGCTGAGCTAATCGCCAAGGACTGGCCTGACG
GCCAGGCTCCCATTGCAGACATCCTGTCTGATCCCAAGAAACTCCTTTTCATCCTCGAGGACTT
GGACAACATAAGATTCGAGTTAAATGTCAATGAAAGTGCTTTGTGTAGTAACAGCACCCAGAAA
GTTCCCATTCCAGTTCTCCTGGTCAGTTTGCTGAAGAGAAAAATGGCTCCAGGCTGCTGGTTCC
TCATCTCCTCAAGGCCCACACGTGGGAATAATGTAAAAACGTTCTTGAAAGAGGTAGATTGCTG
CACGACCTTGCAGCTGTCGAATGGGAAGAGGGAGATATATTTTAACTCTTTCTTTAAAGACCGC
CAGAGGGCGTCGGCAGCCCTCCAGCTTGTACATGAGGATGAAATACTCGTGGGTCTGTGCCGAG
TCGCCATCTTATGCTGGATCACGTGTACTGTCCTGAAGCGGCAGATGGACAAGGGGCGTGACTT
CCAGCTCTGCTGCCAAACACCCACTGATCTACATGCCCACTTTCTTGCTGATGCGTTGACATCA
GAGGCTGGACTTACTGCCAATCAGTATCACCTAGGTCTCCTAAAACGTCTGTGTTTGCTGGCTG
CAGGAGGACTGTTTCTGAGCACCCTGAATTTCAGTGGTGAAGACCTCAGATGTGTTGGGTTTAC
TGAGGCTGATGTCTCTGTGTTGCAGGCCGCGAATATTCTTTTGCCGAGCAACACTCATAAAGAC
CGTTACAAGTTCATACACTTGAACGTCCAGGAGTTTTGTACAGCCATTGCATTTCTGATGGCAG
TACCCAACTATCTGATCCCCTCAGGCAGCAGAGAGTATAAAGAGAAGAGAGAACAATACTCTGA
CTTTAATCAAGTGTTTACTTTCATTTTTGGTCTTCTAAATGCAAACAGGAGAAAGATTCTTGAG
ACATCCTTTGGATACCAGCTACCGATGGTAGACAGCTTCAAGTGGTACTCGGTGGGATACATGA
AACATTTGGACCGTGACCCGGAAAAGTTGACGCACCATATGCCTTTGTTTTACTGTCTCTATGA
GAATCGGGAAGAAGAATTTGTGAAGACGATTGTGGATGCTCTCATGGAGGTTACAGTTTACCTT
CAATCAGACAAGGATATGATGGTCTCATTATACTGTCTGGATTACTGCTGTCACCTGAGGACAC
TTAAGTTGAGTGTTCAGCGCATCTTTCAAAACAAAGAGCCACTTATAAGGCCAACTGCTAGTCA
AATGAAGAGCCTTGTCTACTGGAGAGAGATCTGCTCTCTTTTTTATACAATGGAGAGCCTCCGG
GAGCTGCATATCTTTGACAATGACCTTAATGGTATTTCAGAAAGGATTCTGTCTAAAGCCCTGG
AGCATTCTAGCTGTAAACTTCGCACACTCAAGTTGTCCTATGTCTCGACTGCTTCTGGTTTTGA
AGACTTACTCAAGGCTTTGGCTCGTAATCGGAGCCTGACATACCTGAGTATCAACTGTACGTCC
ATTTCCCTAAATATGTTTTCACTTCTGCATGACATCCTGCACGAGCCCACATGCCAAATAAGTC
ATCTGAGGCCCTCAACGGCTTTCACTTTCATTCCAAATAGAATACACAGGCCAACGCGACGGCT
CACGCCTGGAATCCCAACACTTTGGGAGGCCGAGGCGGGCAGATCACCTGAGCTTGATGAAATG
TGATTTGCGAGCCAGCGAATGTGAAGAAATCGCCTCTCTCCTCATCAGTGGCGGGAGTCTGAGA
AAACTGACCTTATCCAGCAATCCGCTGAGGAGCGACGGGATGAACATACTGTGTGATGCCTTGC
TTCATCCCAACTGCACTCTTATATCACTGGTGTTAGTCTTCTGCTGTCTCACTGAAAATTGCTG
CAGCGCCCTTGGAAGAGTGCTTCTGTTCAGCCCAACTCTAAGACAACTAGACCTGTGTGTGAAT
CGCTTAAAAAATTACGGAGTGTTGCATGTGACGTTTCCCTTGCTGTTTCCAACCTGTCAGTTAG
AGGAGCTTCATCTGTCTGGCTGTTTCTTTAGCAGCGATATCTGTCAATATATTGCCATAGTTAT
TGCTACTAATGAAAAACTGAGGAGCCTGGAGATTGGGAGCAACAAAATAGAAGATGCAGGAATG
CAGCTGCTATGTGGTGGTTTGAGACATCCCAACTGCATGTTGGTGAATATTGGGCTAGAAGAGT
GCATGTTAACCAGTGCCTGCTGTCGATCTCTTGCCTCTGTTCTTACCACCAACAAAACACTAGA
AAGACTCAACTTGCTTCAAAATCACTTGGGCAATGATGGAGTTGCAAAACTTCTTGAGAGCTTG
ATCAGCCCAGATTGTGTACTTAAGGTAGTTGGGCTTCCATTAACTGGCCTGAACACACAAACCC
AGCAGTTGCTGATGACTGTAAAGGAAAGAAAACCCAGTTTGATCTTTCTGTCTGAAACTTGGTC
TTTAAAGGAAGGCAGAGAAATTGGTGTGACACCTGCTTCTCAGCCAGGTTCAATAATACCTAAT
TCTAATTTGGATTACATGTTTTTCAAATTTCCCAGAATGTCTGCAGCCATGAGAACGTCAAATA
CAGCATCTAGGCAACCCCTTTGATCATGTTGTACGTAAACAGTATTTATTATAAATTACTACCG
TGACTGGGATGCAAGAGAATTAGGACTATAATTTTCCTATTTGATGTGTGTGTGTGTGTGTGTG
TGTGTGTGTGTGTGTGTGTGTGTGTGACCTTGATCCAGTCAACCACTTCAAATTCCTACACTGT
CTCAAGAGTATTAAAAGGATTATATGAAGTAATAAAGGATAAAATGCATTGGAAAAA

hide sequence

RefSeq Acc Id:

NR_169622

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,785,399 - 55,836,575 (-)	NCBI
T2T-CHM13v2.0	19	58,884,750 - 58,935,921 (-)	NCBI

Sequence:

show sequence

AGCGCTGACTCACCGCTCCACGCCTTCCTGGTCCTTAATGATTGGCGGCTGGAAGCGGGAAGAA
AAGATCCGTGGTGCCATTTGATTGGCCAACGAATTGCTCCCTTGCCATTGGCTCAGAGGGCTTT
TGATGAACAGATCCAGAAAATATGTGAAGCGAAACGCCCACCGCCCCTTGAGGGGCTGTTCTAG
ACCTTTGCTCCTGGTGTCGTATAGAGCGGGGGATATTTCAAGCTGGAGATCCGTTTTCTTGTCC
CAGTGAACAGGTGCACTATGTTGAAATAAGAGTGGTGACGGAGGCCTTGTTTATCTTGTATCTT
ATTGTAAAAGGTCATCAAGAACCCACCTTGGCCAATCAAGAGAGGAGTCAGCTGGCTAATCACC
GGGCAGGCACCGCCTTTTTCTTCCCGCTGCCTAGCTTGTTTGCTTTCGACCAGCCAAGGAGACC
TGGTGGCAGGGTTGATCTCATATTTCTTGTGCCTCAAAATCCCTTCTCTGAAGTCTGCCTTCCC
TGGAGAAGCAAGATGGCAGAATCGGATTCTACTGACTTTGACCTGCTGTGGTATCTAGAGAATC
TCAGTGACAAGGAATTTCAGAGTTTTAAGAAGTATCTGGCACGCAAGATTCTTGATTTCAAACT
GCCACAGTTTCCACTGATACAGATGACAAAAGAAGAACTGGCTAACGTGTTGCCAATCTCTTAT
GAGGGACAGTATATATGGAATATGCTCTTCAGCATATTTTCAATGATGCGTAAGGAAGATCTTT
GTAGGAAGATCATTGGCAGACGAAACCGTTGTCCTATGTCTCGACTGCTTCTGGTTTTGAAGAC
TTACTCAAGGCTTTGGCTCGTAATCGGAGCCTGACATACCTGAGTATCAACTGTACGTCCATTT
CCCTAAATATGTTTTCACTTCTGCATGACATCCTGCACGAGCCCACATGCCAAATAAGTCATCT
GAGCTTGATGAAATGTGATTTGCGAGCCAGCGAATGTGAAGAAATCGCCTCTCTCCTCATCAGT
GGCGGGAGTCTGAGAAAACTGACCTTATCCAGCAATCCGCTGAGGAGCGACGGGATGAACATAC
TGTGTGATGCCTTGCTTCATCCCAACTGCACTCTTATATCACTGGTGTTAGTCTTCTGCTGTCT
CACTGAAAATTGCTGCAGCGCCCTTGGAAGAGTGCTTCTGTTCAGCCCAACTCTAAGACAACTA
GACCTGTGTGTGAATCGCTTAAAAAATTACGGAGTGTTGCATGTGACGTTTCCCTTGCTGTTTC
CAACCTGTCAGTTAGAGGAGCTTCATCTGTCTGGCTGTTTCTTTAGCAGCGATATCTGTCAATA
TATTGCCATAGTTATTGCTACTAATGAAAAACTGAGGAGCCTGGAGATTGGGAGCAACAAAATA
GAAGATGCAGGAATGCAGCTGCTATGTGGTGGTTTGAGACATCCCAACTGCATGTTGGTGAATA
TTGGGCTAGAAGAGTGCATGTTAACCAGTGCCTGCTGTCGATCTCTTGCCTCTGTTCTTACCAC
CAACAAAACACTAGAAAGACTCAACTTGCTTCAAAATCACTTGGGCAATGATGGAGTTGCAAAA
CTTCTTGAGAGCTTGATCAGCCCAGATTGTGTACTTAAGGTAGTTGGGCTTCCATTAACTGGCC
TGAACACACAAACCCAGCAGTTGCTGATGACTGTAAAGGAAAGAAAACCCAGTTTGATCTTTCT
GTCTGAAACTTGGTCTTTAAAGGAAGGCAGAGAAATTGGTGTGACACCTGCTTCTCAGCCAGGT
TCAATAATACCTAATTCTAATTTGGATTACATGTTTTTCAAATTTCCCAGAATGTCTGCAGCCA
TGAGAACGTCAAATACAGCATCTAGGCAACCCCTTTGATCATGTTGTACGTAAACAGTATTTAT
TATAAATTACTACCGTGACTGGGATGCAAGAGAATTAGGACTATAATTTTCCTATTTGATGTGT
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACCTTGATCCAGTCAACCACTTC
AAATTCCTACACTGTCTCAAGAGTATTAAAAGGATTATATGAAGTAATAAAGGATAAAATGCAT
TGGAAAAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001284672	(Get FASTA)	NCBI Sequence Viewer
	NP_001372380	(Get FASTA)	NCBI Sequence Viewer
	NP_001372382	(Get FASTA)	NCBI Sequence Viewer
	NP_001381823	(Get FASTA)	NCBI Sequence Viewer
	NP_659444	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH34730	(Get FASTA)	NCBI Sequence Viewer
	AAM14632	(Get FASTA)	NCBI Sequence Viewer
	AAO12532	(Get FASTA)	NCBI Sequence Viewer
	AAO12533	(Get FASTA)	NCBI Sequence Viewer
	AAO18162	(Get FASTA)	NCBI Sequence Viewer
	AAO59428	(Get FASTA)	NCBI Sequence Viewer
	BAC03490	(Get FASTA)	NCBI Sequence Viewer
	EAW72415	(Get FASTA)	NCBI Sequence Viewer
	EAW72416	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000466285
	ENSP00000466285.1
	ENSP00000466582.1
	ENSP00000467988.1
	ENSP00000468082
	ENSP00000468082.1
	ENSP00000468196
	ENSP00000468196.1
	ENSP00000468696.1
GenBank Protein	P59045	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_659444 ⟸ NM_145007
- Peptide Label:	isoform 1
- UniProtKB:	Q53ZZ0 (UniProtKB/Swiss-Prot), Q2TV86 (UniProtKB/Swiss-Prot), Q2TV85 (UniProtKB/Swiss-Prot), C9JSF5 (UniProtKB/Swiss-Prot), Q8NBF5 (UniProtKB/Swiss-Prot), P59045 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAESDSTDFDLLWYLENLSDKEFQSFKKYLARKILDFKLPQFPLIQMTKEELANVLPISYEGQY IWNMLFSIFSMMRKEDLCRKIIGRRNRNQEACKAVMRRKFMLQWESHTFGKFHYKFFRDVSSDV FYILQLAYDSTSYYSANNLNVFLMGERASGKTIVINLAVLRWIKGEMWQNMISYVVHLTAHEIN QMTNSSLAELIAKDWPDGQAPIADILSDPKKLLFILEDLDNIRFELNVNESALCSNSTQKVPIP VLLVSLLKRKMAPGCWFLISSRPTRGNNVKTFLKEVDCCTTLQLSNGKREIYFNSFFKDRQRAS AALQLVHEDEILVGLCRVAILCWITCTVLKRQMDKGRDFQLCCQTPTDLHAHFLADALTSEAGL TANQYHLGLLKRLCLLAAGGLFLSTLNFSGEDLRCVGFTEADVSVLQAANILLPSNTHKDRYKF IHLNVQEFCTAIAFLMAVPNYLIPSGSREYKEKREQYSDFNQVFTFIFGLLNANRRKILETSFG YQLPMVDSFKWYSVGYMKHLDRDPEKLTHHMPLFYCLYENREEEFVKTIVDALMEVTVYLQSDK DMMVSLYCLDYCCHLRTLKLSVQRIFQNKEPLIRPTASQMKSLVYWREICSLFYTMESLRELHI FDNDLNGISERILSKALEHSSCKLRTLKLSYVSTASGFEDLLKALARNRSLTYLSINCTSISLN MFSLLHDILHEPTCQISHLSLMKCDLRASECEEIASLLISGGSLRKLTLSSNPLRSDGMNILCD ALLHPNCTLISLVLVFCCLTENCCSALGRVLLFSPTLRQLDLCVNRLKNYGVLHVTFPLLFPTC QLEELHLSGCFFSSDICQYIAIVIATNEKLRSLEIGSNKIEDAGMQLLCGGLRHPNCMLVNIGL EECMLTSACCRSLASVLTTNKTLERLNLLQNHLGNDGVAKLLESLISPDCVLKVVGLPLTGLNT QTQQLLMTVKERKPSLIFLSETWSLKEGREIGVTPASQPGSIIPNSNLDYMFFKFPRMSAAMRT SNTASRQPL hide sequence

RefSeq Acc Id:	NP_001284672 ⟸ NM_001297743
- Peptide Label:	isoform 2
- UniProtKB:	P59045 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRRKFMLQWESHTFGKFHYKFFRDVSSDVFYILQLAYDSTSYYSANNLNVFLMGERASGKTIVI NLAVLRWIKGEMWQNMISYVVHLTAHEINQMTNSSLAELIAKDWPDGQAPIADILSDPKKLLFI LEDLDNIRFELNVNESALCSNSTQKVPIPVLLVSLLKRKMAPGCWFLISSRPTRGNNVKTFLKE VDCCTTLQLSNGKREIYFNSFFKDRQRASAALQLVHEDEILVGLCRVAILCWITCTVLKRQMDK GRDFQLCCQTPTDLHAHFLADALTSEAGLTANQYHLGLLKRLCLLAAGGLFLSTLNFSGEDLRC VGFTEADVSVLQAANILLPSNTHKDRYKFIHLNVQEFCTAIAFLMAVPNYLIPSGSREYKEKRE QYSDFNQVFTFIFGLLNANRRKILETSFGYQLPMVDSFKWYSVGYMKHLDRDPEKLTHHMPLFY CLYENREEEFVKTIVDALMEVTVYLQSDKDMMVSLYCLDYCCHLRTLKLSVQRIFQNKEPLIRP TASQMKSLVYWREICSLFYTMESLRELHIFDNDLNGISERILSKALEHSSCKLRTLKLSYVSTA SGFEDLLKALARNRSLTYLSINCTSISLNMFSLLHDILHEPTCQISHLSLMKCDLRASECEEIA SLLISGGSLRKLTLSSNPLRSDGMNILCDALLHPNCTLISLVLVFCCLTENCCSALGRVLLFSP TLRQLDLCVNRLKNYGVLHVTFPLLFPTCQLEELHLSGCFFSSDICQYIAIVIATNEKLRSLEI GSNKIEDAGMQLLCGGLRHPNCMLVNIGLEECMLTSACCRSLASVLTTNKTLERLNLLQNHLGN DGVAKLLESLISPDCVLKVVGLPLTGLNTQTQQLLMTVKERKPSLIFLSETWSLKEGREIGVTP ASQPGSIIPNSNLDYMFFKFPRMSAAMRTSNTASRQPL hide sequence

RefSeq Acc Id:

ENSP00000466285 ⟸ ENST00000589093

RefSeq Acc Id:

ENSP00000468082 ⟸ ENST00000589824

RefSeq Acc Id:

ENSP00000466582 ⟸ ENST00000590409

RefSeq Acc Id:

ENSP00000468196 ⟸ ENST00000592953

RefSeq Acc Id:

ENSP00000468696 ⟸ ENST00000593208

RefSeq Acc Id:

ENSP00000467988 ⟸ ENST00000593244

RefSeq Acc Id:	NP_001372380 ⟸ NM_001385451
- Peptide Label:	isoform 3

RefSeq Acc Id:	NP_001372382 ⟸ NM_001385453
- Peptide Label:	isoform 4

RefSeq Acc Id:	NP_001381823 ⟸ NM_001394894
- Peptide Label:	isoform 1
- UniProtKB:	Q53ZZ0 (UniProtKB/Swiss-Prot), Q2TV86 (UniProtKB/Swiss-Prot), Q2TV85 (UniProtKB/Swiss-Prot), P59045 (UniProtKB/Swiss-Prot), C9JSF5 (UniProtKB/Swiss-Prot), Q8NBF5 (UniProtKB/Swiss-Prot)

Protein Domains

NACHT Pyrin

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P59045-F1-model_v2	AlphaFold	P59045	1-1033	view protein structure

Promoters

RGD ID:

13205801

Promoter ID:

EPDNEW_H26481

Type:

initiation region

Name:

NLRP11_1

Description:

NLR family pyrin domain containing 11

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26483

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,831,985 - 55,832,045	EPDNEW

RGD ID:

13205805

Promoter ID:

EPDNEW_H26483

Type:

multiple initiation site

Name:

NLRP11_2

Description:

NLR family pyrin domain containing 11

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26481

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	55,836,800 - 55,836,860	EPDNEW

RGD ID:

6795854

Promoter ID:

HG_KWN:31091

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, Lymphoblastoid

Transcripts:

UC002QLZ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	61,012,466 - 61,012,966 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:22945	AgrOrtholog
COSMIC	NLRP11	COSMIC
Ensembl Genes	ENSG00000179873	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000589093	ENTREZGENE
	ENST00000589093.6	UniProtKB/Swiss-Prot
	ENST00000589824	ENTREZGENE
	ENST00000589824.6	UniProtKB/Swiss-Prot
	ENST00000590409	ENTREZGENE
	ENST00000590409.5	UniProtKB/TrEMBL
	ENST00000592953	ENTREZGENE
	ENST00000592953.5	UniProtKB/Swiss-Prot
	ENST00000593208.1	UniProtKB/TrEMBL
	ENST00000593244.5	UniProtKB/TrEMBL
Gene3D-CATH	1.10.533.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	3.40.50.300	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	3.80.10.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000179873	GTEx
HGNC ID	HGNC:22945	ENTREZGENE
Human Proteome Map	NLRP11	Human Proteome Map
InterPro	Cu2_ascorb_mOase_CS-1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DAPIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DEATH-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Leu-rich_rpt	UniProtKB/Swiss-Prot
	LRR_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NACHT_NTPase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NLRC_HD2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NOD2_WH	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	P-loop_NTPase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:204801	UniProtKB/Swiss-Prot
NCBI Gene	204801	ENTREZGENE
OMIM	609664	OMIM
PANTHER	NACHT, LRR AND PYD DOMAINS-CONTAINING PROTEIN 11	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NACHT, LRR AND PYD DOMAINS-CONTAINING PROTEIN 12	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	LRR_6	UniProtKB/Swiss-Prot
	NACHT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NLRC4_HD2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NOD2_WH	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PYRIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA162397841	PharmGKB
PROSITE	CU2_MONOOXYGENASE_1	UniProtKB/TrEMBL
	DAPIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NACHT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	LRR_RI	UniProtKB/Swiss-Prot
	PYRIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	RNI-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF47986	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	C9JSF5	ENTREZGENE
	K7EMN8_HUMAN	UniProtKB/TrEMBL
	K7EQV0_HUMAN	UniProtKB/TrEMBL
	K7ESF9_HUMAN	UniProtKB/TrEMBL
	NAL11_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q2TV85	ENTREZGENE
	Q2TV86	ENTREZGENE
	Q53ZZ0	ENTREZGENE
	Q8NBF5	ENTREZGENE
UniProt Secondary	C9JSF5	UniProtKB/Swiss-Prot
	Q2TV85	UniProtKB/Swiss-Prot
	Q2TV86	UniProtKB/Swiss-Prot
	Q53ZZ0	UniProtKB/Swiss-Prot
	Q8NBF5	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-06-07	NLRP11	NLR family pyrin domain containing 11	NLRP11	NLR family, pyrin domain containing 11	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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