ConVarT

Sltm (GeneID: 66660) | Mus musculus

Description:	SAFB-like, transcription modulator [Source:MGI Symbol;Acc:MGI:1913910]
Synonyms:	Met, 130215G10Rik, 5730555F13Rik, 5730455C01Rik
Other ID(s):	MGI:1913910, ENSMUSG00000032212
Protein Accession Numbers:	XP_030100361, NP_001344840, XP_006511418, XP_006511414, XP_030100358, XP_036011075, NP_080613, XP_017169006, XP_030100360, XP_006511417, XP_006511413, XP_030100357, XP_036011074, NP_079966, XP_011241088, XP_006511415, XP_030100359, XP_036011076, XP_006511412, XP_030100356
Statistics:	ClinVar(2) PTM(88)

ClinVar Pathogenicity of Variations

Pathogenic

VUS

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000380516 ENST00000432750 ENST00000492526 ENST00000536328 ENST00000557791 ENST00000557924 ENST00000558486 ENST00000558756 ENST00000559261 ENST00000559305 ENST00000559880 ENST00000560494 ENST00000560682 NP_001013865 NP_079031 ">ENST00000249736 You are here now!

ClinVar Data

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Variation ID	Allele ID	RS Number	Variant Type	Record	Alteration	Clinicial Sig.	Last Update	Phenotypes	Cytogenetic	Review Status	RCV Acc.N.

gnomAD

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Variant ID	Transcript ID	Alteration	Annotation	Allele C.	Allele N.	Allele F.	rsNumber	Flags	Filter
No data available in table

Showing 0 to 0 of 0 entries

Post-translational Modifications (PTMs)

Acetylation

Methylation

Phosphorylation

Sumoylation

Ubiquitination

Show entries

Gene Name	ACC ID	PTM Type	Position	Mod-rsd	Site +/-7 Aa	Mw_kd	Site grpID
SLTM	Q9NWH9	Phosphorylation	1002	S1002-p	tQHssNAsPINRIVQ	117.15	3213960
SLTM	Q9NWH9	Phosphorylation	1011	S1011-p	INRIVQIsGNsMPrG	117.15	36135892
SLTM	Q9NWH9	Phosphorylation	1014	S1014-p	IVQIsGNsMPrGsGs	117.15	3213963
SLTM	Q9NWH9	Methylation	1017	R1017-m1	IsGNsMPrGsGsGFk	117.15	27279695
SLTM	Q9NWH9	Phosphorylation	1019	S1019-p	GNsMPrGsGsGFkPF	117.15	7322876
SLTM	Q9NWH9	Phosphorylation	1021	S1021-p	sMPrGsGsGFkPFkG	117.15	7322879
SLTM	Q9NWH9	Acetylation	1024	K1024-ac	rGsGsGFkPFkGGPP	117.15	475028
SLTM	Q9NWH9	Acetylation	1027	K1027-ac	GsGFkPFkGGPPRRF	117.15	15292605
SLTM	Q9NWH9	Methylation	1027	K1027-m1	GsGFkPFkGGPPRRF	117.15	57990477
SLTM	Q9NWH9	Phosphorylation	126	S126-p	GNDELKDsEEFGENE	117.15	50832264
SLTM	Q9NWH9	Phosphorylation	139	S139-p	NEEENVHskELLsAE	117.15	14580431
SLTM	Q9NWH9	Phosphorylation	14	S14-p	AVAASAAsGQAEGKK	117.15	12668096
SLTM	Q9NWH9	Ubiquitination	140	K140-ub	EEENVHskELLsAEE	117.15	964545424
SLTM	Q9NWH9	Phosphorylation	144	S144-p	VHskELLsAEENKRA	117.15	18015893
SLTM	Q9NWH9	Phosphorylation	170	S170-p	IEKEDIEsQEIEAQE	117.15	14736351
SLTM	Q9NWH9	Phosphorylation	201	S201-p	NEKDIAGsGDGtQEV	117.15	36125906
SLTM	Q9NWH9	Phosphorylation	205	T205-p	IAGsGDGtQEVSKPL	117.15	36127384
SLTM	Q9NWH9	Phosphorylation	214	S214-p	EVSKPLPsEGsLAEA	117.15	56676468
SLTM	Q9NWH9	Phosphorylation	217	S217-p	KPLPsEGsLAEADHt	117.15	7105365
SLTM	Q9NWH9	Phosphorylation	224	T224-p	sLAEADHtAHEEMEA	117.15	36126828

Showing 1 to 20 of 88 entries

Catalogue of Somatic Mutations in Cancer (COSMIC)

Gene Name	Transcript ID	Sample name	Primary Site	Primary Histology	Mutation ID	Mutation CDS	Mutation Aa	Mutation Desc.	FATHMM Prediction	FATHMM Score	Mutation Somatic Status	PUBMED PMID	Tumor Origin	Position

dbSNP

Gene ID	Transcript ID	Consequence	Position	HGVSp	Impact

Protein Domains (PFAM)

Pfam Domain	Domain Name	Description	Positions	Clan	Clan Name	Organism
NO RESULT FOUND
PF00076	RRM_1	RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain)	386-456	CL0221	RRM	Homo sapiens
PF02037	SAP	SAP domain	22-56	CL0306	HeH	Homo sapiens

List of the diseases from DisGeNET

Disease Name	Disease Category	DSI*	DPI**
NO RESULT FOUND
NO RESULT FOUND