Nutm2 (NUT family member 2) - Rat Genome Database

Name: Nutm2
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: Nutm2 (NUT family member 2) Mus musculus

Analyze

Symbol:

Nutm2

Name:

NUT family member 2

RGD ID:

1618793

MGI Page

MGI

Description:

Orthologous to several human genes including NUTM2A (NUT family member 2A) and NUTM2B (NUT family member 2B).

Type:

protein-coding

RefSeq Status:

PROVISIONAL

Previously known as:

Fam22; Gm806; hypothetical protein LOC328250; NUT family member Gm806

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Homo sapiens (human):	NUTM2G (NUT family member 2G)	HGNC	Ensembl, Inparanoid, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Pan paniscus (bonobo/pygmy chimpanzee):	LOC117981758 (NUT family member 2G)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Canis lupus familiaris (dog):	LOC119870860 (NUT family member 2G-like)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Sus scrofa (pig):	LOC100514433 (NUT family member 2G)	Transitive Ortholog Pipeline	Transitive Ortholog Pipeline
Other homologs ²
Homo sapiens (human):	NUTM2A (NUT family member 2A)	HGNC	Ensembl, HomoloGene, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Homo sapiens (human):	NUTM2B (NUT family member 2B)	HGNC	Ensembl, HomoloGene, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB
Homo sapiens (human):	NUTM2F (NUT family member 2F)	HGNC	Ensembl, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Homo sapiens (human):	NUTM2D (NUT family member 2D)	HGNC	Ensembl, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Homo sapiens (human):	NUTM2E (NUT family member 2E)	HGNC	Ensembl, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB
Alliance orthologs ³
Homo sapiens (human):	NUTM2F (NUT family member 2F)	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)
Homo sapiens (human):	NUTM2D (NUT family member 2D)	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)
Homo sapiens (human):	NUTM2B (NUT family member 2B)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)
Homo sapiens (human):	NUTM2G (NUT family member 2G)	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)
Homo sapiens (human):	NUTM2E (NUT family member 2E)	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)
Rattus norvegicus (Norway rat):	Nutm2f (NUT family member 2F)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Homo sapiens (human):	NUTM2A (NUT family member 2A)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)

Latest Assembly:

GRCm39 - Mouse Genome Assembly GRCm39

Position:

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	13	50,621,343 - 50,629,391 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	13	50,621,343 - 50,629,391 (+)	Ensembl		GRCm39 Ensembl
GRCm38	13	50,467,307 - 50,475,355 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	13	50,467,307 - 50,475,355 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	13	50,562,676 - 50,570,724 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	13	50,479,804 - 50,487,852 (+)	NCBI		MGSCv36	mm8
Celera	13	51,554,147 - 51,562,195 (+)	NCBI		Celera
Cytogenetic Map	13	A5	NCBI
cM Map	13	25.75	NCBI

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (ISO)

intellectual disability (ISO)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

aristolochic acid A (ISO)

benzo[e]pyrene (ISO)

methapyrilene (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

biological_process (ND)

Cellular Component

cellular_component (ND)

Molecular Function

molecular_function (ND)

protein binding (ISO)

Phenotype Annotations Click to see Annotation Detail View

Mammalian Phenotype

male infertility (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:10349636	PMID:11042159	PMID:11076861	PMID:11217851	PMID:12466851	PMID:16141072	PMID:16141073	PMID:21677750	PMID:27626380	PMID:30973865

Genomics

Comparative Map Data

Nutm2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	13	50,621,343 - 50,629,391 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	13	50,621,343 - 50,629,391 (+)	Ensembl		GRCm39 Ensembl
GRCm38	13	50,467,307 - 50,475,355 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	13	50,467,307 - 50,475,355 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	13	50,562,676 - 50,570,724 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	13	50,479,804 - 50,487,852 (+)	NCBI		MGSCv36	mm8
Celera	13	51,554,147 - 51,562,195 (+)	NCBI		Celera
Cytogenetic Map	13	A5	NCBI
cM Map	13	25.75	NCBI

NUTM2G
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	9	96,928,843 - 96,942,971 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	9	96,928,310 - 96,940,253 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	9	99,691,125 - 99,705,253 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	9	98,730,413 - 98,744,393 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Cytogenetic Map	9	q22.33	NCBI
CHM1_1	9	99,838,303 - 99,851,567 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	9	109,100,632 - 109,114,736 (+)	NCBI		T2T-CHM13v2.0

LOC117981758
(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	11	45,118,423 - 45,132,963 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	9	45,119,171 - 45,136,406 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	9	68,021,404 - 68,032,256 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3

LOC119870860
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ROS_Cfam_1.0	1	98,329,774 - 98,334,945 (+)	NCBI		ROS_Cfam_1.0
UMICH_Zoey_3.1	1	97,954,191 - 97,961,392 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	97,675,541 - 97,679,987 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	98,472,786 - 98,481,155 (-)	NCBI		UU_Cfam_GSD_1.0

LOC100514433
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa10.2	15	155,456,994 - 155,464,476 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

Variants

Variants in Nutm2
181 total Variants

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	133
Count of miRNA genes:	127
Interacting mature miRNAs:	131
Transcripts:	ENSMUST00000096633
Prediction methods:	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.

QTLs in Region (GRCm39)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
26884393	Humsd7_m	humerus midshaft diameter 7, 16 week (mouse)					13	3950000	76048119	Mouse
1558898	Hpi1_m	hapatic PMN infiltration 1 (mouse)			Not determined		13	4414025	53101640	Mouse
1301880	Hypt_m	hypertension (mouse)			Not determined		13	18156792	52156924	Mouse
13463469	Gssq1_m	glomerulosclerosis severity QTL 1 (mouse)					13	19060908	53061050	Mouse
12880423	V25Dq7_m	vitamin D inactive form serum level QTL 7 (mouse)					13	19583983	53583983	Mouse
1301015	Sysbp2_m	systolic blood pressure 2 (mouse)			Not determined		13	20477612	59821605	Mouse
4142147	Mvwf4_m	modifier of von Willebrand factor 4 (mouse)			Not determined			20477612	112898424	Mouse
1357591	Tesq1_m	testis weight QTL 1 (mouse)			Not determined		13	20615512	55720517	Mouse
4142009	Pregq3_m	pregnancy QTL 3 (mouse)			Not determined		13	20615512	72385189	Mouse
10045618	Heal17_m	wound healing/regeneration 17 (mouse)			Not determined		13	20746939	54747056	Mouse
4142489	Ath25_m	atherosclerosis 25 (mouse)			Not determined			25836529	59836529	Mouse
10401111	Pgia40_m	proteoglycan induced arthritis 40 (mouse)			Not determined		13	27918469	61918560	Mouse
1300710	Pcd4ts2_m	p-glycoprotein positive CD4 T cell subset 2 (mouse)			Not determined		13	28210442	62210544	Mouse
1357802	Vtbt15_m	vertebral trabecular bone trait 15 (mouse)			Not determined		13	28217379	62217515	Mouse
10045621	Heal21_m	wound healing/regeneration 21 (mouse)			Not determined		13	28217379	62217515	Mouse
10755533	Chol18_m	cholesterol 18 (mouse)					13	30969467	64969467	Mouse
10755517	Chol15_m	cholesterol 15 (mouse)					13	30969467	64969467	Mouse
12738439	Twq4_m	testis weight QTL 4 (mouse)					13	31129110	65129110	Mouse
14696729	Kidlq2_m	kidney weight, left QTL 2 (mouse)					13	31344736	65344736	Mouse
1301299	Sluc23_m	susceptibility to lung cancer 23 (mouse)			Not determined		13	34921943	68922081	Mouse
10412235	Scgq5_m	spontaneous crescentic glomerulonephritis QTL 5 (mouse)			Not determined		13	36060908	96239162	Mouse
1357587	Pfat3_m	predicted fat percentage 3 (mouse)			Not determined		13	36101530	70101640	Mouse
1301734	Acsns2_m	Angiostrongylus costaricensis nematode susceptibility 2 (mouse)			Not determined		13	36101530	70101640	Mouse
1300561	Heal7_m	wound healing/regeneration 7 (mouse)			Not determined		13	36144820	70144904	Mouse
1300862	Cfbw5_m	cystic fibrosis body weight 5 (mouse)			Not determined		13	38720358	72720517	Mouse
1300985	Bmd13_m	bone mineral density 13 (mouse)			Not determined		13	39629249	73629397	Mouse
1302157	Bwem2_m	body weight day 30 males 2 (mouse)			Not determined		13	39629249	73629397	Mouse
1301801	Cpfd5_m	cerebellum pattern fissures (mouse)			Not determined		13	39629249	73629397	Mouse
15039353	Nmrs35_m	NAFLD-associated magnetic resonance shift 35 (mouse)					13	40588253	74588253	Mouse
1300668	Pas10_m	pulmonary adenoma susceptibility 10 (mouse)			Not determined		13	41489042	75489158	Mouse
12738427	Lfibq24_m	liver fibrosis QTL 24 (mouse)					13	44258107	52758667	Mouse
4142331	Bxs6_m	BXSB/MpJ autoimmune nephritis 6 (mouse)			Not determined			45210442	83744746	Mouse
10412109	Bxs7_m	BXSB/MpJ autoimmune nephritis 7 (mouse)			Not determined		13	45210442	83744746	Mouse
26884396	Humsd4_m	humerus midshaft diameter 4, 10 week (mouse)					13	47853476	73148119	Mouse
4142372	Moo2_m	modifier of Odc2 (mouse)			Not determined		X	50318411	84318559	Mouse
1301666	Eae13_m	susceptibility to experimental allergic encephalomyelitis 13 (mouse)			Not determined		13	50318411	84318559	Mouse
1300573	Elsgp2_m	elevated serum gp70 2 (mouse)			Not determined		13	50616828	84617027	Mouse

Expression

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001033400	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC165366	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK133253	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENSMUST00000096633 ⟹ ENSMUSP00000094390

Type:

CODING

Position:

Mouse Assembly	Chr	Position (strand)	Source
GRCm39 Ensembl	13	50,621,343 - 50,629,391 (+)	Ensembl
GRCm38.p6 Ensembl	13	50,467,307 - 50,475,355 (+)	Ensembl

RefSeq Acc Id:

NM_001033400 ⟹ NP_001028572

RefSeq Status:

PROVISIONAL

Type:

CODING

Position:

Mouse Assembly	Chr	Position (strand)	Source
GRCm39	13	50,621,343 - 50,629,391 (+)	NCBI
GRCm38	13	50,467,307 - 50,475,355 (+)	ENTREZGENE
MGSCv37	13	50,562,676 - 50,570,724 (+)	RGD
Celera	13	51,554,147 - 51,562,195 (+)	RGD
cM Map	13		ENTREZGENE

Sequence:

show sequence

ACTTTCAAACTTTTCTCTCAGCTGTGGCTGGCTCTCTTGAGCATCTGCCATAGATTGGTGACTT
TTGGGTGTGATTTATCCGAATTTTCTCACCATGGACCTGAGCAGACAGACATGGTTACTGTCCA
AGCCTATAGGAATAGTTTCCGAAGCGTCTTCACTGGGACAGAACATGACTATCAACCCTGGTGC
CTCCCTGCCTACATTTGCAACCTTGCCTGTTCTCCCACCTGCCCCCCAGCCAGTACCCCAGTTA
TTTTGGGAGCCCCCAGCACCCCTCGTGACTGCAGGCATCTCTCCCGGGAATCCTTTAGTCTTAT
CTGCCTTGCCTGGGATGCCTTTGGTGGCAGAAGGTGGAAGCACTGCCCTGAGTGCCGCTGTTCC
TCTGAACATTGTACAGCTTGGAACTCTAGGCCAGCCTGTCCAACCTGTGCACAATACCAACATT
GTTCTCACTCAGGTGCCTCTCACTTGTAATATCCCTGGGACCCAAGGTGTGGGTATGGGGTTCA
TGACAACACCTGCTGCAAACAACTTCATAAATACCCGAATTGCTTCGACTGTCCAGCCCCAAGA
AGGAACATGGATCCTGGGTCCTCACCCTCCCACCACACAGCAAGTTGTCCAGCTGGTTCCTGTC
AAGTCTCCAGTGAACTCTGCACAGCCTCCAAAAGGAGCATATGGAGAAAGTGGCCCCGCCAACA
TCCAAACCAACTCCCCAGAAAACTACTTGTCCAAACCAGACAGTGTCTATGGGAATTTCCGGCG
CTGGCAACATATCAAGACACTGGTCCAGAGGCACCTGCCTCAGACCACCGATGTGGCAGCTTTC
TCCTGCTTCCTCATTCCAGTGCTTCGGTCCCTGGCCCGGAGGAAGCCCACCATGAATGTGGAGG
AGGGCCTATGGAGGGGTCTGCAGGAATGGCAGTGTACAAGCAACTATGACCGGATGATCTTCTA
TGAGATGGCAGAAAAGTTCACAGAATTTGAGAGTGCAGAAGAGATGGAGAATTCAAGGCTAGAG
ATAATAAGAAGCATCCAGTACCAAGTTGTTGCAACCATACCAAGGCAAGATCCTCCAAGGCTTC
CAGCTCCTGAGGTGGCTGAGGAACCAGAGTGCACCTCCATGAAGACTGTCCACCAGACTGACCC
TGCCCACCTCCCAGAGCTCAGACCCCAGAAGTTACAGAAGACTGAGACACCCATGGAAATTCCA
CCTGAAGCTGTGCGGGAGTACATGGAGATCATGGACTGGCTGGAGGGGTTTCCTCAGTCATTCA
CGGGAGAGGCCAAGGAAAAGGAGGAAGATGAGAACAATGGACCAGAGCAGGAAGGAGATGACTT
ATACTCAGATGCAGAACTCCTGAGCTACATTGATGAGCTGTGTTCACAGAAACACTTTGTTGAG
CAAGTGGAGGCCATAATCAACCCCCAATTTGTGGCAGAAATCCTATCTACCAAACCAGAAATAG
ACATACTGGCTCTCACCAAGGTGCTGGAGCATGAGGAAGAACTCACTGTTGACCAGCTGCTGGA
GAAGCCCTGCCCAGCTTTGAAGAAGAGGGGAGTTGAGAGAGCACCCCCAAATCCTGGTGCCCCT
CAGATACCTGCCAGTACTTCTGTACCATCTGTTTGCCAAGATGCAGAGAGAGATGAGCATGGTG
TTCAAAGAGGAGCCAGTGCACAAACTGGCTCCTCACGAATGGCTTCCTTAGACCAGCAGTGTCT
TGAAGTCACCAGCGCAGAAATATGGGGGCCTAAGCCTGCTACTGTCTTCCCGAGTAATCAAAGT
TCACCCTCACTGGTAGACGTCAGATACACTGGTATTCCCCGTGGCAGAGGAACATATAACCAAA
GCCCAGGATCCAGATGTGTAAGGAGCTTCAGAGTAGCTTCTGCAATTGAGGACCTCCACAGGTC
ACTGGCCAGAACCATTGAGGACAAGGAAGAGCTCCACAGCCTGTCCTTCCTCCTGGCCTCCCAG
TACAGGCTGGTGCCCTGGAAAGTGCCTCACCAAGTGTGCCCCTATACAGATCTCTCTGACTCTG
AGAGTATCCCCAGCCCGTGCCCAAAGTTAAGGGGCCTTAGCCCTGATCTGTGTTCGATTGCCAA
GTCAAAGAAGCGAGCTCTCTTTGGAAGCTTGGTTCCTATGGCTAAGAGGCCTAACTTAGGACCT
GGTCACGGGGTGTCTGAAGGGCCACTCTCAGCTCTGGAGCTGGCTCACCTCTCACAGCCTCAGA
AAAGGAAGCATGAGCCACTAGGTACCCATAAGAGGAAGAGGAAGAAGAGGCATTGAGCCTCCTG
GGTGATATCCCCTTAAACTGGCCAGAGATTTCACCCTGCCTCTAAACCTAAAACCCCAGAGTGA
GGGGAAAAAAGCAACCAACAGCTCTTGCTCAATCAGGACTGATCCAGCTGCTGCTAAGGATGGA
TCTAGAAGATTAGAGGCACTGGGAAATAAGCACAGGAACGAGGGGTGGGGAAGGGATTGGGAGG
GTGATATCACTTTAGAAGTTTTTAAGTTATGTAAATAAAGACAGCTTCATTG

hide sequence

Protein Sequences


Protein RefSeqs	NP_001028572	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	BAE21581	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSMUSP00000094390
	ENSMUSP00000094390.3
GenBank Protein	Q3V0C3	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_001028572 ⟸ NM_001033400

- UniProtKB:

Q3V0C3 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MDLSRQTWLLSKPIGIVSEASSLGQNMTINPGASLPTFATLPVLPPAPQPVPQLFWEPPAPLVT
AGISPGNPLVLSALPGMPLVAEGGSTALSAAVPLNIVQLGTLGQPVQPVHNTNIVLTQVPLTCN
IPGTQGVGMGFMTTPAANNFINTRIASTVQPQEGTWILGPHPPTTQQVVQLVPVKSPVNSAQPP
KGAYGESGPANIQTNSPENYLSKPDSVYGNFRRWQHIKTLVQRHLPQTTDVAAFSCFLIPVLRS
LARRKPTMNVEEGLWRGLQEWQCTSNYDRMIFYEMAEKFTEFESAEEMENSRLEIIRSIQYQVV
ATIPRQDPPRLPAPEVAEEPECTSMKTVHQTDPAHLPELRPQKLQKTETPMEIPPEAVREYMEI
MDWLEGFPQSFTGEAKEKEEDENNGPEQEGDDLYSDAELLSYIDELCSQKHFVEQVEAIINPQF
VAEILSTKPEIDILALTKVLEHEEELTVDQLLEKPCPALKKRGVERAPPNPGAPQIPASTSVPS
VCQDAERDEHGVQRGASAQTGSSRMASLDQQCLEVTSAEIWGPKPATVFPSNQSSPSLVDVRYT
GIPRGRGTYNQSPGSRCVRSFRVASAIEDLHRSLARTIEDKEELHSLSFLLASQYRLVPWKVPH
QVCPYTDLSDSESIPSPCPKLRGLSPDLCSIAKSKKRALFGSLVPMAKRPNLGPGHGVSEGPLS
ALELAHLSQPQKRKHEPLGTHKRKRKKRH

hide sequence

RefSeq Acc Id:

ENSMUSP00000094390 ⟸ ENSMUST00000096633

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q3V0C3-F1-model_v2	AlphaFold	Q3V0C3	1-733	view protein structure

Promoters

RGD ID:

8680326

Promoter ID:

EPDNEW_M18194

Type:

single initiation site

Name:

Nutm2_1

Description:

Mus musculus NUT family member 2 , mRNA.

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Mouse Assembly	Chr	Position (strand)	Source
GRCm38	13	50,467,307 - 50,467,367	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	MGI:2685652	AgrOrtholog
Ensembl Genes	ENSMUSG00000071909	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENSMUST00000096633	ENTREZGENE
	ENSMUST00000096633.3	UniProtKB/Swiss-Prot
InterPro	NUT	UniProtKB/Swiss-Prot
	NUT_N	UniProtKB/Swiss-Prot
KEGG Report	mmu:328250	UniProtKB/Swiss-Prot
MGD	MGI:2685652	ENTREZGENE
NCBI Gene	328250	ENTREZGENE
PANTHER	NUT FAMILY MEMBER 2A-RELATED	UniProtKB/Swiss-Prot
	PTHR22879	UniProtKB/Swiss-Prot
Pfam	NUT	UniProtKB/Swiss-Prot
PhenoGen	Nutm2	PhenoGen
UniProt	NUTM2_MOUSE	UniProtKB/Swiss-Prot, ENTREZGENE

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2014-12-30	Nutm2	NUT family member 2	Gm806	predicted gene 806	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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Imported Disease Annotations - ClinVar

Mammalian Phenotype