ZMP
ttc21b
Ensembl ID:
ZFIN ID:
Description:
tetratricopeptide repeat protein 21B [Source:RefSeq peptide;Acc:NP_001121730]
Human Orthologue:
TTC21B
Human Description:
tetratricopeptide repeat domain 21B [Source:HGNC Symbol;Acc:25660]
Mouse Orthologue:
Ttc21b
Mouse Description:
tetratricopeptide repeat domain 21B Gene [Source:MGI Symbol;Acc:MGI:1920918]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34770 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31749 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34770
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044270 | Essential Splice Site | 400 | 1321 | 10 | 29 |
| ENSDART00000138937 | None | None | 189 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 51033132)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 50148093 |
| GRCz11 | 9 | 49845484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACTGGAGTTTCTCACAGAGATCCAGCAGTCCATTGGCAAATCAGGGG[T/C]GAGAAAAAATTTATGTGCCCTACTATCTTCATTCATTCATGTTCTTTTTG
Long Flanking Sequence:
ACAAATAATTTAATTAAGTAGATTTTACAAAAACAAAACAAATTAACATTCATTCATTATGAAACTCATTCTTTGAATTCATTCAAACTCCACACAGAAATGCCAACTGGCCCAGCCAGTACTCGAACCAGCCACCTTTTTGCTGTGAGGCGACAGTTCTAACCACTGAGCCACCGTAGTGCCCCCAATAAATTTGCATAGTTAATATTAATAGTATATAGATAATTGTAGTGCAGTACTTAATAGTAATATAATAATTACTAATAGAACATAGACAGTAATATAGACAATAATAGTATATAAATGCTGAAATTACACTGTTTAGGATGCCTGACTAAAATTAGCATGATTATTAAACCACATTTTGATTTTTTTATTTGTGTATTGTTGTGTTTGTACAGGTATCATCAGGTGTCAGCTAATAGAAGGACACATAGAAGATGCAGAACAGCAACTGGAGTTTCTCACAGAGATCCAGCAGTCCATTGGCAAATCAGGGG[T/C]GAGAAAAAATTTATGTGCCCTACTATCTTCATTCATTCATGTTCTTTTTGGCTTAGTCTCTTTATTAATCTGGGGTCGCCACACCGGAATGAACCGCCAACTTATCCAGCGCTGGGAAACATCCATACACACTCATTCACACACATACACTACGGACAATTTAGCTTACTCAATTCACCTATACGGCATGTTTGGATTGTGAGGAAAACCGGAGCACCCAGAAGGAACCCACGCCAACACGGGGAGAACATGCAAACTCCACATTCAATCGAGCGACCTTCTTGCTATGAGGCGAATGTGCTACTCACTGCGTCACCGTGCAGCCCGACCTACTATCTTACTTAAAAAAAATCTAGATGATTTCTTATAGGAAGATTCACAGACTTTTCCCAATAATAAAGTATTTTATGTCGAATAAAGTCTGCCATTTGATTCAGATTCTGCAGAGACTTGGTTCATTAATCCACTTATGCTGTGTTTACCTCTTGAGTCATCCACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31749
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044270 | Essential Splice Site | 1234 | 1321 | 27 | 29 |
| ENSDART00000138937 | None | None | 189 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 51067481)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 50113744 |
| GRCz11 | 9 | 49811135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCCTTTTTGGTAACTGTGCTATGCTGATGTTTTAACATGTTCAACACT[A/C]GTCCTGCTGTAAGGCGTATGAGTACATGGGCTACATTATGGAGAAAGAGC
Long Flanking Sequence:
TACATAATTATTATTCTAATAATTATTAAAGTTATTATTATTAATTATAATAATGTATATCATTATTTTCATTTACAATATTTATAATAATAATAATAATTATTATTATTATTATTATTATTATTATTATTATTATTTAAAAATCTGCATTTTCTAAAAATAATAAAATACAAAATTAAATACAAATATTAAAATAATTAAAAATAATAAAAAAGGAATACTAATTTTTGGTAGTTATAATCAGGGCTATTAAAATGTCAATATACAGATAATCCAATGATGACATCTGTGTGACTTAATTTTTTAATTGACAAAATATGGTAAATATTAGTTATTAAATTGCATCTTTTTATTGCTACATTGTTTTAGCAGATGGTATTTTGTTATAAGCAAAATTACATTTGGATTAATAATTACTTTGTTTGTAAATGCTCAGTTCATGTTGTCTAAAGTCCTTTTTGGTAACTGTGCTATGCTGATGTTTTAACATGTTCAACACT[A/C]GTCCTGCTGTAAGGCGTATGAGTACATGGGCTACATTATGGAGAAAGAGCAGTCTTTCAGAGATGCTGCTATGAATTATGAAATGGCCTGGAAGTACAGCAATCAAACCAACCCTACGATCGGTGAGATTACAGCTGCTCTTGAACCATCCTCATGTGTGTTTACAATCACATCACTCACTAACACTCACTGCGTCATCTTTGTTTACCAGGCTACAAGCTTGCCTTCAACTACCTGAAGGCCAAAAGACACGTGGATGCTATAGATGTGTGCCATAAAGTGAGTATAAAAGAATAACTGCGGCAAATATAAATATATCTTATTAAATAAATACTATACTGAGACAAGCAGTCATATTACAGAAGTAAAAGCATGTTTCCATGTCAATCACATTTTTACATATCTTTTCAGACAAAAATACCTTGAGCTAAACTTCATTTACAGTTGAAGTCAGAATTATTAGCCCCCTTTTGAAATTTTTTTCTTTTTTAAATATTTCC
Associated Phenotype:
Not determined