ZMP

THSD7B (2 of 2)

Ensembl ID:

ENSDARG00000061497

Description:

thrombospondin, type I, domain containing 7B [Source:HGNC Symbol;Acc:29348]

Human Orthologue:

THSD7B

Human Description:

thrombospondin, type I, domain containing 7B [Source:HGNC Symbol;Acc:29348]

Mouse Orthologue:

Thsd7b

Mouse Description:

thrombospondin, type I, domain containing 7B Gene [Source:MGI Symbol;Acc:MGI:2443925]

Alleles

There are 7 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21942	Nonsense	Available for shipment	Available now
sa31841	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa21942

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087690	Nonsense	209	1573	1	29

Genomic Location (Zv9):

Chromosome 11 (position 34513855)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	33414792
GRCz11	11	33677594
GRCz12tu	11	35966405

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTAAAGGGGTGGCACCTGTTGGGAAAACAACAGTGGATTTTAATTTGGGG[A/T]AAAGTACAGTCAGGACTTCCTATACAATAAAGCGGCACGCGGAAGGTTTT

Long Flanking Sequence:

AGGATCTGTTTGAGTGGCGCTTGTCTCCATGGGGCCCCTGCACTCCGAGTCCTCTCCTCCCAGCCAATCGATGCGTAACCGCTCAACGTGGAGTGCAGAGCCGCAATATGCAGTGTGTGAAGCGTAATAACAACTCCTCGGTGAGCCTACATGTGTGTGAAGCGTTTTCTTCAGCTCCAGAAGGAGAGCAGGCCTGTCTGTTACCTTGTCCGATGGATTGTGTCGTCTCCGCTTTCACCCACTGGTCCACTTGTAGCCGTACATGTGGGTCGGCTCTTCAACAGCGCACACGGGATGTCCTGGCCACACCCCTGTATGGAGGCATGGACTGCCCCAGTTTGACTCAGACACGCCCCTGTAGACATGAGCAAGGCCACCCCGCCCTCTGTCCTTCTGACCAACAGGAATACAGCTACAGTTTGTGGGCGGGGCCTTGGAGCCCTTGCAGAATTAAAGGGGTGGCACCTGTTGGGAAAACAACAGTGGATTTTAATTTGGGG[A/T]AAAGTACAGTCAGGACTTCCTATACAATAAAGCGGCACGCGGAAGGTTTTCATCGTCAAAATCATTACGATGAAAAAGGCTACAAAGTGTCCTGGGAGATCATCATTGGGTACCAGACTAGGCAGCTTCGCTGTTTGAGGAGCGACGGGAAGAACGCTATGCTGAGGTGGGCAGTTATTTTGTCAATAAATGAGTTAATAGACTTTTATAAAGTTGTTCAAGTCATTAAAATCAATCATTTTTATTTTATTTCATAAATTGTTATTATTATTTTACCATATATATTTACAGAACAGTTCTGTCTGGTCCTTGAATCTGATTGGCTGATAGCCATGAGATATTAAAGTAATAATATCAGAATTTTTACAGCCTCCTCACCCTTGCGTATTACTCCGCCCACACAAGTGGCAAGCAGAAGACTACAGTTTGACAAATATTGCAGCTGTATTAAAACAATATACTTTTGAGACACTTTAAGTTGATAATGTAGTTGTTTAGAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa31841

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087690	Essential Splice Site	896	1573	14	29

Genomic Location (Zv9):

Chromosome 11 (position 34576738)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	33477675
GRCz11	11	33740477
GRCz12tu	11	36029438

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCAGCAGTGAAGAGCACTGCTGGACGGCCTTTCATCCAAGGAGTTTTCC[A/G]CCAAGGCCAGAAGGCAGTCCAGGACTGGCGAGGCCTTAGGAGGAGCAGCG

Long Flanking Sequence:

GTCAGTGTCGAGGCTGTGGAAGCTGGCGCACACGCACCCGATCTCTCATAGGTCTCTCTCGATCTCTCATTTTTTACACAATGATGCTTCTTTTATATCATCACATTATCTTTTGGGAGAAGCCTGTGTCACTTTTGATCAAAAATGCCTTGCTTGTTAACTGTAACTGTAACTTTGGGGAATCAATATCAGATCGACCACTTCTTGAAAACTACTAATTTAAAAATCGTTTTTTTGGTCGTTTTTTTATTTATTTTTTGATTGATTGATAAATTATTCTGGGGATGTTTTCTCCTGACTCTGAGCTCTCATTTCCTCCACGCTCTCAGGTCGCAGTAAGAAGCGCTGGCGATGCCAACAGGAGGAGTTGTTTCCTCTGCTGGAGAAAGAAGCTTGTCCTTGTTCTGAATTTCACAGCAGGCCTCAGGGTCCCTGGTCTCCATGTTTACTCTCAGCAGTGAAGAGCACTGCTGGACGGCCTTTCATCCAAGGAGTTTTCC[A/G]CCAAGGCCAGAAGGCAGTCCAGGACTGGCGAGGCCTTAGGAGGAGCAGCGAGTGTGGGCATGGGAGACGCTACAGAGCTCTGGTCTGTCTGGATCATCTGAGACAGCTGGTGGAGCCGGCGCTCTGCAGCAGCCCTGGTGAGGAGAAACACTTCACAAATGAGTTTAAATGTAATGTTAATGTATATAAGTATGTTCACCTAATTGTAATTTTTAATATATAATTAAATTAAATGTAATATTATATAATTATTAATAGACAATCATAATGAATAAGTCATATTTATATTAGGTATGTCCCGATCGATCGGCTGGAGGTCGTTATCAGCCAATGATCACTATTAATGACTTGGTCGGTACTCGTTTATCTGTCAGATCTCATGAACCGATCCTAAATATTTGTCTATGCGTTTATAAGCAGAGGAAGATGCAGCAGCAGCTACTGCATGCATTTAGGCCTTTTTATATAAGAACAGGAAATTTTGTGTTTTGACATTATTT

Associated Phenotype:

Not determined