ZMP

thsd7ba

Ensembl ID:

ENSDARG00000095022

ZFIN ID:

ZDB-GENE-070621-2

Description:

Novel protein similar to human and mouse thrombospondin, type I, domain containing 7B (THSD7B) [Sour

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8510	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa9262	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa8510

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000132123	Essential Splice Site	367	1574	2	26

Genomic Location (Zv9):

Chromosome 9 (position 10575934)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	10379781
GRCz11	9	10351154

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GWAAAGGAGGCCTGCAACATCATTGGAGATCTGCTTCCAAACTGCCCAAG[G/A]TTTCTCTTTCATCCTCCCAATAATAAACTCCTAATGTACATGAATGTGTA

Long Flanking Sequence:

TTTAAAACTGAATTTCAAACTCATCACAGACAAACTCACATACAGACAGAAAACATAAAAGGTTCTTTCCTCCATATCAAACAGCAGTTGAGGAGCAGTTGATGGCATTTATCTCATTATAAAAACAATATGTTCTTTCAACTCTTAAAAAAAAAACGAGGGTGTCTTCTGTTCTTTTTGGCAGAGCTGAAATGTTTGAATATGTTTTCCTCTGCCTCTCATTTTTAATTTATTTGTTTTCTTCCTTATAGCCTTTGTACCCTTGACAACGGCCCTGGCACTTTCCAGTCTTGTGTTATGCCCAGAGACTGCGAGACCTCCGATTGGTCCGTTTGGAGTCCATGTTCAAAGACATGCAGAGCATCAGATATGTCGCCTGGTTTTCGGGTCAGGACTCGAAGCATAACGCACACTCCCATTGGTCAAGGCAAAGGATGCCCTGCTCTTGAAGAAAAGGAGGCCTGCAACATCATTGGAGATCTGCTTCCAAACTGCCCAAG[G/A]TTTCTCTTTCATCCTCCCAATAATAAACTCCTAATGTACATGAATGTGTAAAAAAAAAATACTAAATGATTTTTCGAGTGTTGTGTTCAAGTATTTATTTACTGAACCCCTGTTGCATCTGAGCGTTGTAAAGATTAGAAGCTAATTAATGAGATTAGGTTTTTGATCAATAGAAACAGACTGCTATTTCATTAAAAATGCTGGTTTATGCATCATAACGCTTTGCTTAGTCGATGCATTTTCATTAGTAGATGGTTTCCTACCGGAAAACTGGAAGCTAAGCCTATTAGTATCTTTCAGCGGCAGCTCCCTGTGTCCATTTATCCAATACAACTTTTGAGAGGAGCTCAGCACGATATAATGAGACTAAAGAGCCAAAACAAAAGAAGTGTGTTTCACCACAGCGGGCGCATGCTTTTGTTCTTCAGGTACGTGTGGAAGAGCACCGATTGGGGGGACTGTCAAGTGGCCCCTCTTCTTAGCCAGCAGGACAGAAGGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9262

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000132123	Essential Splice Site	1154	1574	16	26

Genomic Location (Zv9):

Chromosome 9 (position 10424608)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	10228455
GRCz11	9	10199828

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCCTGCATCCTCAACAGCACCTGCTTCAATTACCACTACAATGTYTCCAG[T/C]GGGTCTTACTCATTTTGCTACAACACAACACTGAATGTAACATGAGCTTC

Long Flanking Sequence:

GGTTTCGGTTTTTTGCATAATTGCGAAATGTTCCCAAAAAACCTGGGTGCTCAGATATATGGCAGTAGTCGAAAAGACCTCATGCTGATGATCAGACTCCCCAATAGTCAGATACATGGCCGTGGCCAGCTAGCCGTTTAAAGGGTCTCATTAGCGCCTGACAGTGATGGAGATGCAGATTAGCTGCTGCCTGCAGCCTAACAGCTTCTTACTGTGCATTTAGCATCGCAAGACCATGTGGCTGGGTTTTTTATCTTTTGTGAATTGAACATGTGAGTGTGCACTTTTAAAATAGTGTCGAGACTCATGCGTCAAAGCCATTTTGACATTTTAACTGTATTTTTCTTTTTGTTGTAGCCGTGTGACGAAAACAGCTCGAGGACTAGGACAAGGCACGTGCTGCGCCCCCCGGTGGCTGACAGAGTGTGTCCAGAAAATAATCAGACGGAGCCCTGCATCCTCAACAGCACCTGCTTCAATTACCACTACAATGTTTCCAG[T/C]GGGTCTTACTCATTTTGCTACAACACAACACTGAATGTAACATGAGCTTCTAATGACTATTGCATGACAGACTCTTTTTAACGGTGCAGTGATTCACTTTTTTTTTACTCAAATGCATCTGTTCTCAAATACAATACAGTCCTTGTTAATCGCATTCTAAAAATAACCCGCAAAAGTTAGCTTTTATTTACAATTATTATAGATGTTTTAAGGCTGTAAAACCCTTCACTACACACTATACACTTTTATACATGTTCACACTTTTCTCTTTTGTTAAAGTACTTTCAAAGTTCAAACATCTGTAGAAAAAATGTCCAGTATTATAGAATGAAACCAAAGATCAAAATCTGTTGTCAGGTATAAACATTTATTGCTGTCAGCAAAAGGGCACCGCACGCAGCCACCGACAGTGTGCGTACACTGATATAAACCTATCTTTACAATTCTAAAATGCATGGCACGGTGTGACGAGGCATATTTGGTGTGCGACTCTCTTTACG

Associated Phenotype:

Not determined