Busch Lab

ZMP

NR_023335.1

Ensembl ID:
ENSDARG00000078604
Description:
wu:fj33d10 (wu:fj33d10), non-coding RNA [Source:RefSeq DNA;Acc:NR_023335]
Human Orthologue:
TBC1D10B
Human Description:
TBC1 domain family, member 10B [Source:HGNC Symbol;Acc:24510]
Mouse Orthologue:
Tbc1d10b
Mouse Description:
TBC1 domain family, member 10b Gene [Source:MGI Symbol;Acc:MGI:1915699]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa26099 Nonsense Mutation detected in F1 DNA Not yet available
sa6036 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa26099
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114217 Nonsense 26 849 1 9
Genomic Location (Zv9):
Chromosome 3 (position 32931856)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32663166
GRCz11 3 32794880
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCCCTCCTGGTATGGGTGAACAACCAGTGCCTGCTCCCTCCAGCCCA[C/T]AGCCTCTCCCCTCAGAAACTCCCATCCCAAAATCCTCTCTCTATGGTGAT
Long Flanking Sequence:
GGTGAAAACTGTTATTTGGAACTTTGATAGTGTTTTTCAAATGACTGTTTACAGTATTTGTGAACATATAAAAGTAACCCAAGGGATCATAGGAGATTTTTTTTTTTCCAAGTTTATTTAAACTTGTCACAGTTTCTGTAAGCGAATAAGAAATGTGTAGACTTTTGCTCAGTAGACTTCTAATGCAAATACAGTTTGTCAATAATTTTTTGGTATCATTTTTCTCATAAGTGACAAAATTATTTTAAATAGTTTTTCTTTCTTGTTTTTTAGGATTTAGATTAATGCATTGTCTCCCACTACATGCATACACTTCAATATATTTCCCCTCATTTATTTTATTTAAAAGGAAAATGTAATGTCAGGCTTGTGATTGTTGTGTTTTTTCTTCTTTTGATCAGCCGTATTACTGAGGAGCAGAAGCTATGGCTGAAATCACCACCATCACTCCCTCCCCTCCTGGTATGGGTGAACAACCAGTGCCTGCTCCCTCCAGCCCA[C/T]AGCCTCTCCCCTCAGAAACTCCCATCCCAAAATCCTCTCTCTATGGTGATCGAGCCGTGATGGGAAACCCTACATTACAGACAGGTGGAAGAAATTCTTCATCTTGGGAGAGCACACCTGGCCAAAACAGTACCTCATCCTCTTCAGTGGGAACTAAGAGCACTGCTGGTCCGCCAGCAGAGGTACTCGCTGCTACACAAGGAGAAACTAATGGGAAAGATGATTTGGTTGAGCAGCACGCTGAATCGCAGAGCTCAGAGCAGGAGCAACAGATGCCGCCATCGCCTGAACTTAATCCCAGTCCTAATCTCTATCCCAATGTTCAAGTCAGCCAGACTTCCAGTCCCGCTCCCCCCATAGACATTCCTCCTCAATCTACACCTCCTCCCCTTCCCAACTCCAACCCGGCCCTCTCTTCGCAAGACTCCAGGCAAACAGAAGCACAAGCAGTCCCGGAGCCCGAACCCAACACTCCAAGCACCACCATGATGACTCATGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6036
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114217 Essential Splice Site 511 849 8 9
Genomic Location (Zv9):
Chromosome 3 (position 32944593)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32675903
GRCz11 3 32807617
KASP Assay ID:
554-3955.1 (used for ordering genotyping assays)
KASP Sequence:
ATTATGTGCCAAATAGAGAGTWTAAATGTATATTTTTGTGTTGTCTGTCA[G/T]GAGTRAAGATCGTGTTTAGGGTGGGTTTGGTGCTCCTCAAGCAGATGTTG
Long Flanking Sequence:
TGTTTCAAGAAAATATCCCTCAAAATGGAGGATGGCAGGATGGATCCATGCTTTCATGTTGTTGACTCCACTGGTTCTCACTTGCGAATGATTCTCACTCTACCATTCAAATGTCGCAGCAAAAATTGAGACTCGTGTATATATATAAGTATATATGTATGTATGTATGTGTGTATGTATGTATTTATATATATTTTTATATATATGTATGTATATATATTTTTTTATATATGTATGTATGTATGTATGTATGTATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATGATAGATGTATATAGATATAGATATGAATTTAAAAGAGTTGTCATTTTAAATGTCAAAAGTGAATTATTATCAGTGTTGAAAACTGTTCAATATTTTGATGGATTGGTTTTAGCATTATGTGCCAAATAGAGAGTATAAATGTATATTTTTGTGTTGTCTGTCA[G/T]GAGTGAAGATCGTGTTTAGGGTGGGTTTGGTGCTCCTCAAGCAGATGTTGGGGTCTGTGGATAAGCTCCGGGAACTGCAGGGCATGTACGAGACTATGGATCGTCTGAGGAATATCCCGCCCGAATCTATTAAGGAGGATGTTCTGGTGCAAGAGGTGTGTGCACAAACTCTCATTTACTGTAGGAGAAGCAGTGGTTGTGTCCACAATATCCTTTCCCATACTTTCTGTTCTGTTTTCAGGTGATCTCTCTGTCTGTGACTGAGGCCCTCATCGAGAGGGAGTGCAGTATTCAGGTGCGTAAGTGGCGGGAATCTCGTGGAGAGTTGACTCACCAGCCGGTGCGCCGTTTGCATGGCACAAGGGCCATCTACGAGCAGAAACAGCGGGCTGCTGCAATCAGCTCTGGTGGGAGCCTGTCATTCCTGGGCGCTCATGTCCCTCCACCTGGGCCTTTACGTGCTTCATCAAGCCTCCTGTCACTTCCTGGACTTAGAAAGT
Associated Phenotype:
Not determined