ZMP
tbc1d22b
Ensembl ID:
ZFIN ID:
Human Orthologue:
TBC1D22B
Human Description:
TBC1 domain family, member 22B [Source:HGNC Symbol;Acc:21602]
Mouse Orthologue:
Tbc1d22b
Mouse Description:
TBC1 domain family, member 22B Gene [Source:MGI Symbol;Acc:MGI:2681867]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31631 | Essential Splice Site | Available for shipment | Available now |
| sa9032 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31631
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098009 | Essential Splice Site | 260 | 399 | 6 | 10 |
| ENSDART00000132253 | Essential Splice Site | 260 | 418 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 10838501)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 10343140 |
| GRCz11 | 8 | 10380869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACAGCCCCTATGTTTTACCTACATGTACCTGTGTGTTTGTCTTCCCT[A/T]GATTCACATCGATATCCCAAGGACGAACCCTTTAATTCCTTTGTTCCAGC
Long Flanking Sequence:
TCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCTGTAGTGTGTGTGTGAATGTGTGTGTGGATGTTTCCCAGAGATGAGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGCTAGATAAGTTGGCGGTTCATTCCACTGTGGCGACCCCGGATTAATAAAGGGACTAAGCTGACAAGAAAATGAATGAATGAATGAATGAATGAATATTTTAATCCTTATTGTTTAGCCCCTTTATAAGACTGAATTTTTATTCTTCATGGTCTTAAAAAGGTCTTAAAGTCTTAAATTTGACTTGGTGAAACCTGCAGAAACCTAGACTTAAACAAATGCATTCAGTTTGTCCTGTGTAATTGTAAAATCGAAATCCATGTCAAATAAATAAAATAGCTATCCTATCAGAAAAAGCACATGAAGTTACTAGGCTTAAACAGCCCCTATGTTTTACCTACATGTACCTGTGTGTTTGTCTTCCCT[A/T]GATTCACATCGATATCCCAAGGACGAACCCTTTAATTCCTTTGTTCCAGCAGCCTTTGGTACAGGAGGTAGGTGATCTCTTTTTTGACAGAAACACCTGACGAGACGTTGCACATCACACACACAGCAGCCGTGGAACGTTTAACCGGATATTTCATGCAAAATTGACATTTTCTGTTAATGTATTTATCCTCAGGCCATTCATAATGTAGGTGATTTTTTTTCTTCTTCTTCAGTAGAACATTAAAGAAAATTATTAGCTGAAACCATGGAACTTCATAAAATGCAAGTTAAAGGCTTCTGGCAATACCCGTAGCTATTGATGATAAATTGAGATCTCATGCAAGAAAATGAACATTATATACTGCATTGTTATCTTTAACAGTCCTGTAACAGAGAGCTTTATTTATATACTGTATACAGTTGAAGTCAGAATTATTAACCCCTTGTTTATTTTTCCCCCAATTTCTGTTTAACGGAGAAAAGATTTTTTCAACACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9032
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098009 | Nonsense | 299 | 399 | 7 | 10 |
| ENSDART00000132253 | Nonsense | 299 | 418 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 10834579)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 10347062 |
| GRCz11 | 8 | 10384791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGAGCGGATTCTGTTCATCTGGGCCATCCGTCACCCYGCTAGCGGATA[C/A]GTGCAGGGCATTAATGACCTGGTCACTCCCTTTTTTGTGGTCTTCCTCTC
Long Flanking Sequence:
TTAAAATGAAGTTATTCTCCTCATGCATCATTTTATATAATAATAAACCAAAACACATCAAGAAAGGCTTCACCACTGCAAGAATTCATCAATAATTTCACTAATGATGTTACCACTGTTCTGGAATGTGTTTTAATGGCTTGCAGAGAGCATGCATTAGTAGAACTGAGCTTTGTGTAATTGGATGCAGACCAGCAGGGGGTGCTGTGGTGTTTTGTCTTATATAGCAGAGCACAACACGAGTAACTCAGAAACCACAAGAAAAAGAGCTCTTGAAATGCAGCCCCGTTTGCAAACCAAGCATCTAAATGAGTGGATCTGTTGGTCTGTTAGGAGTCAATTAAGATTCACCCATTGCCTAAAAGTCAACGATCACATTACCTATGAGAAATTATATTTTTGTGAATCATTGTCTTGTTTTTTTGTCTGTTTGTTTGTGTTTTCCAGGTGTTTGAGCGGATTCTGTTCATCTGGGCCATCCGTCACCCCGCTAGCGGATA[C/A]GTGCAGGGCATTAATGACCTGGTCACTCCCTTTTTTGTGGTCTTCCTCTCTGAATTCGTAGGTAAGTGTCTAATAGTGCATAGATCAGTTGTTCTTTTTATCAAATTTGTCTGCTGTTTGGTCATTCTGTTCAGTCTGTATGTCTATCCTTCTTTTTGTACACTGTTCTATCTATCTATCGTTGTGTGTAATTCTGTTTATCATGTGATATAACTATCAATCCATCCATCGTTCTGTTTGTCAGGTGATTTAACCATCCGTTCATCCATCATATTGTTTATGATGTCATTTAACCATCCATCTATCATTCCATCATTTCATCCATCATTCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCATTCTGTTTATCATGTGATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCACAAG
Associated Phenotype:
Not determined