Busch Lab

ZMP

tbc1d20

Ensembl ID:
ENSDARG00000032298
ZFIN ID:
ZDB-GENE-050626-61
Description:
TBC1 domain family member 20 [Source:RefSeq peptide;Acc:NP_001020343]
Human Orthologue:
TBC1D20
Human Description:
TBC1 domain family, member 20 [Source:HGNC Symbol;Acc:16133]
Mouse Orthologue:
Tbc1d20
Mouse Description:
TBC1 domain family, member 20 Gene [Source:MGI Symbol;Acc:MGI:1914481]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa24082 Nonsense Available for shipment Available now
sa16338 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24082
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045752 Nonsense 131 397 4 8
Genomic Location (Zv9):
Chromosome 22 (position 10245944)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 10106112
GRCz11 22 10135794
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCGTGAGGGTCTTCAGGAGGAGCTCACCGATATTATTCTGCGTGTTT[T/A]GGTGAAAAACCCTCAGCTGCATTACTATCAGGGTTATCATGACATCGTGG
Long Flanking Sequence:
GGGTGGGCCCACAGAGTTTGTGCTATGCGCTAGTCACTATTAACTGAATGGAGTAGCAGTTCGCAGTTATGTTTTGTTAAATAAGTTGCAGATAAAATTTAAGTTTCAAAACCGCCCAAATTTTGTCAACCCACCTCTGCTATTTTTTACCCACAAAATCTAATTCAAAACCGCCCAATTGGGCAGGAAACCACCCAATCTGGCAACACAGCACAGATCTAAAACCAGTTTTTTGTTTCAGATCCTGTCGATCGAGAAAACAACAAAGACTTTAACCAGGTTCTTCTTGATGTTCAGCGGTCACTTAGACGCTTTCCTCCAGGTCAGCAGACCTATATTTTATTCTATTTTATTTCATAGTATTATATTATCCAGAATGAGCAGCTGCAGTGTTCGTAACTGAAATCCAGTGTTTTGTGTGTGCTTTTGTGCCTCAGGGATGCCGGATGAGCAGCGTGAGGGTCTTCAGGAGGAGCTCACCGATATTATTCTGCGTGTTT[T/A]GGTGAAAAACCCTCAGCTGCATTACTATCAGGGTTATCATGACATCGTGGTCACTTTCCTGCTGGTGCTCGGAGAGAGACTCGCCACTGCCCTCGTGGAGAAACTCTCCACACACCACCTCAGGTCTGAACATATAAATAGAAATTCCTATTCATAAATATAAATGTATATGATTTGTAAAAGCAAATGTGTAGTATCTATTTTTGCCTGTTAGGGGGGGGAAATTTTTTCGTATAATCATTCTCAATTCCTACTAACTACTAGAAATATAAAAAAGTTACGACAGATAGATGGACAGACAGATAGAAAGATAAATAGACAGACAGACAGACAGACTTTCCCAGTAGATATTAGCATGTTGTTAGCATGATTCAAGTATGAATTAGCTTATTTTTTAGTGTTAATGAACATGTTGTTAACATATAATATAAATTAGCATGTTGCTAACATGTTTCTAGTGTGGATTAGCATGTTTTTAGTATGAATTAGCTTGTTTATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16338
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045752 Nonsense 293 397 7 8
Genomic Location (Zv9):
Chromosome 22 (position 10248430)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 10108598
GRCz11 22 10138280
KASP Assay ID:
2261-6448.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCMCGCATCCCAGAGGACCTGCCKTATGAAACGCTGATCAGCCGCGCT[G/T]GAGATCTGYTCGTGCAGTTTCCTCCATCAGAGCTRGCCAGAGAGCGCAGT
Long Flanking Sequence:
CTGTGTTTTCAGGGTGGAATAAATAATTGATACTTTCTATTATGTCGGGACTGTTTGTCCTGATTTTTCTTTCCAGCTACTGTAGTTTTTTTTTATATCTGGAGTTTTGATGTTAGACAAGACTCTTCTTAAACATTAATTACTGAAAATTGCCATTTCTATAATTAGAAGAATACTTTTCTCAATACCGTGGCATAAGGTGAAGTAATATTTCACCTTTAAATGTCACTGTAATTACTATAATGTTAAAAAAGGGGTATTCACTACTGTTATAACACAATTGCTATTTTAAAATGCCATTGTCATTACCGTAATGCAAAGAAGCAATTTCATATTTCTCATTGCTATAGCATACAGTTAATCTGTAAAGTAATTATCTGCAGATCGTGTTGCATCGTGAGGAGGAGGTCTTGGACTGTGAGTGTGACATGGCCATGATGCACCACCTCCTGTCCCGCATCCCAGAGGACCTGCCGTATGAAACGCTGATCAGCCGCGCT[G/T]GAGATCTGTTCGTGCAGTTTCCTCCATCAGAGCTAGCCAGAGAGCGCAGTCAGCAGTGAGTTTCTCTTCGCAGTGATTTTACAGACGCCCTCAAAATCAATGGTTACAAAGATTCGGACATTATAAAATATGCTTTCCATTTAGGGTGAACGAGTTCCAGGTTTTGTATTTGAACCGCATAAACTTTTCCAACACACACACTTTCTGATCTAGATATACAACAGCACGGAGCAGATCATACGCACAAGTCAACGCAAACCTGAATTCTGCACTGCATGCTGTAGTGTGCACTTGGAGAAATGGTGGAAATCATGAATCAGATGTGCTCAATAACACAAGCTCTGATATAAACAACATGCTGCTTGCTATTTTTAATAAGGGGAGGGGCTACCCAATAAGTCCCTCCCTTCCTCTGTTTTTGTGAATATTATGTCACGCATCAAACGCAGCTGCACATTTCACACGGCTTCAGAGCACTGTTGGGGAAGGTTGGCTTTCAT
Associated Phenotype:
Not determined