Is(In8B2-8B3.1;6C1)1Tshir (Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1)

Gene: Is(In8B2-8B3.1;6C1)1Tshir (Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1) Mus musculus

Analyze

Symbol:

Is(In8B2-8B3.1;6C1)1Tshir

Name:

Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1

RGD ID:

15038936

MGI Page

MGI

Description:

ASSOCIATED WITH abnormal ankle joint morphology; abnormal cervical vertebrae morphology; abnormal craniofacial morphology; ASSOCIATED WITH chromosomal duplication syndrome

Type:

protein-coding

Previously known as:

recombination induced mutation 4; Ri; Rim4

Latest Assembly:

GRCm39 - Mouse Genome Assembly GRCm39

NCBI Annotation Information:

Genome Annotation Status: not in current annotation release

Position:

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Cytogenetic Map	6		NCBI

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

chromosomal duplication syndrome (IAGP)

Phenotype Annotations Click to see Annotation Detail View

Mammalian Phenotype

abnormal ankle joint morphology (IAGP)

abnormal cervical vertebrae morphology (IAGP)

abnormal craniofacial morphology (IAGP)

abnormal limb development (IAGP)

abnormal lumbar vertebrae morphology (IAGP)

abnormal pollex morphology (IAGP)

abnormal skeleton morphology (IAGP)

abnormal tibia morphology (IAGP)

abnormal vertebral transverse process morphology (IAGP)

abnormal zone of polarizing activity morphology (IAGP)

absent vertebral spinous process (IAGP)

brachydactyly (IAGP)

clavicle hypoplasia (IAGP)

clinodactyly (IAGP)

domed cranium (IAGP)

hemimelia (IAGP)

microcephaly (IAGP)

patent ductus arteriosus (IAGP)

polydactyly (IAGP)

postnatal growth retardation (IAGP)

preaxial polydactyly (IAGP)

premature death (IAGP)

sacral vertebral transformation (IAGP)

scoliosis (IAGP)

short tibia (IAGP)

syndactyly (IAGP)

triphalangia (IAGP)

ventricular septal defect (IAGP)

zygomatic bone hypoplasia (IAGP)

References

Additional References at PubMed

PMID:7628698	PMID:9073443	PMID:23449628

Genomics

Expression

Sequence

Nucleotide Sequences

Additional Information

External Database Links

Database	Acc Id	Source(s)
MGD	MGI:97926	ENTREZGENE
NCBI Gene	Is(In8B2-8B3.1;6C1)1Tshir	ENTREZGENE
PhenoGen	Is(In8B2-8B3.1;6C1)1Tshir	PhenoGen

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 - MGI

Mammalian Phenotype