Busch Lab

ZMP

si:ch211-39i19.4

Ensembl ID:
ENSDARG00000095654
ZFIN ID:
ZDB-GENE-081030-22
Description:
Novel protein similar to the vertebrate tensin family [Source:UniProtKB/TrEMBL;Acc:B8JKC5]
Human Orthologue:
TNS3
Human Description:
tensin 3 [Source:HGNC Symbol;Acc:21616]
Mouse Orthologue:
Tns3
Mouse Description:
tensin 3 Gene [Source:MGI Symbol;Acc:MGI:2443012]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa17437 Essential Splice Site Available for shipment Available now
sa7478 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17437
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000134204 Essential Splice Site 130 290 6 11

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 6667093)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 6572167
GRCz11 20 6562114
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GYATACCATGTTTTGTGTTTCTGACCTGTTTCTTGTTCTYTTGTTTCTCA[G/A]TGAGGAACATGCGTTAGATCTGTATTCCATGAAGAGRTTCTGCAGTGATC
Long Flanking Sequence:
ATGCAAAAATTACATATTGTGATTAAAAATGCATACATAAAGCAATTTAGATTAAATTTATCTTGTAATGGAAGTTAAGACTTCCCCTTTTTTTCCACTATCATGACGTACATCCACTTAACATGGTCCTAAAAAAAAAAAAAAAAAGGAAGGCAGGGCATGATTTTGTCCTTGGATGAAGGCAGAGCTGAAATTAGACACCCCTGATATCCTTGCCCTAAAGGCATTCCATGTGACCAGGAAGTAAAGAAAAGTTGTCTCGAGAGGGCAGGCCTAAGGTATTTGATTTAAGTTTATGAGCTCAAATGGATTTTTACAAAATAATGAAGGGCACTGATACACAGTTTCTAACAAGAGCTACAATACAGACATACAAATCAAAAGGGCACATTTTGATTTTATGGTGACTTAATTGTTTATTGATTTATACAGATTAAATGATCGTATTTGGTATACCATGTTTTGTGTTTCTGACCTGTTTCTTGTTCTCTTGTTTCTCA[G/A]TGAGGAACATGCGTTAGATCTGTATTCCATGAAGAGATTCTGCAGTGATCAAATGGTTAACCTCCTGACTCCATCTCAGAAAAGGCAAGGCTCAGTCTTTAATGCATTAACTTCTTTATTTTCACAATTGTTACTGTACTTACAGTTGAATGAACCTGTGGGTATTACAGAGAATTAATTAACAAGGTTACTTTGATATACTTTACCTCTATACCGAGGGAAGTCATTTATTTGACAGTTAACTAGCCATAACTAGCCAAATTATTTCCATTCTTTAATACATTGGCAGTCCACTTTGTTATATAATAAGTGGATGAGTTTCCATGGACTAAAAGCGAGACATTGTTTGAGATTTGACATTTTGAGATTTTTCAATTATTTGCTTTTCTTACTTACTTTTATATATATATATATATACAGTTGAAGACAAAATTATTAGCCCCCTATAAAATATTTCATTATTTTTCAAATAACTCCCAAGTGCTTTTTAATGGATTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7478
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 > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000134204 Missense 221 290 9 11

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 6675152)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 6580226
GRCz11 20 6570173
KASP Assay ID:
554-4136.1 (used for ordering genotyping assays)
KASP Sequence:
AACTCTCAGTCAGGTTGATGTCGGTCTGATGGACAGAGTGTGTTTTGTTC[T/A]GGATCCTCCTCAGATGATCAAAGGTGATATCATGGTGAGAGACATCTTTY
Long Flanking Sequence:
TGCAATGTAACTTAAATTCAACAAGTAGACCATTAAAATAAAGTATGAGCTAAAAAATATAGGTATCACTTAAATTTAAGGTTTCCTTGTTGCACATGTTCCATGTACTTACTATAGTATTTACAATGATACATAACTGCATGCAATTAACCCCTAACCCGCAGTCTAACCCTAACCATATAGTAAGTACATGTACTTAATTAATATCCTCATGTAATGAGTAGTTACACTGTAACATTTACGCCTTAAAATGAAGTGCAACCAAAATGAATAAAGAAACGTAATATGTTTTTCATATGTGTTTTGTTTTCAGTGTGCCAGCTGTTTATCAGAGTAAATCAAGGCACGCAGACAGCATACACTTCAGGACTGCAGTAGGAACATAAAGATTTTTTAAAGCAATACAAAAGAGCAGAAATTCTGGATTATGTATATTAAGTGCTTGTGTGTAACTCTCAGTCAGGTTGATGTCGGTCTGATGGACAGAGTGTGTTTTGTTC[T/A]GGATCCTCCTCAGATGATCAAAGGTGATATCATGGTGAGAGACATCTTTTCCTGTCTCTTTCACACTGCACGCACATAGACTGCACTGATCTCATGAACGCTGCACAGTGGATCATCTTCTATTCCTCTGTCGCTGCAGATTGTGTGTTATCATAAAAATGTTTCCACGAGGACTCAGGAAACATTGTTTCGTGCTCAGTTTCACACTGCTGCTCTGAGTGCAAAACAATTTGCCTTGCAGAAAGAAGACCTGGATCTGGCCAACAAAGGTAAACCGAAGTGTTTTTAGTAAAGTCATTCACATTATTATAACATATATTAGAACCTTCTTAAGTATATCTAGTTGGCATAACTTATTTTTTTCTAGTTATATTAAACTTTATTTATTATTTATTATTTCTGCAACTTAATACTTTATAGTTACTGGAACTTATTTTTTTTAGGTACAGGAACCTAGTATTTATTGTTATGGCAGCTTATTTTTTCTAGTTCTTCAGCTT
Associated Phenotype:
Not determined