ZMP
zgc:73220
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393726 [Source:RefSeq peptide;Acc:NP_957047]
Human Orthologue:
TBCEL
Human Description:
tubulin folding cofactor E-like [Source:HGNC Symbol;Acc:28115]
Mouse Orthologue:
Tbcel
Mouse Description:
tubulin folding cofactor E-like Gene [Source:MGI Symbol;Acc:MGI:1925543]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22626 | Nonsense | Available for shipment | Available now |
| sa15855 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22626
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006910 | None | None | 176 | None | 4 |
| ENSDART00000124092 | Nonsense | 266 | 448 | 6 | 8 |
| ENSDART00000135770 | Nonsense | 266 | 448 | 7 | 9 |
| ENSDART00000138166 | Nonsense | 24 | 206 | 1 | 3 |
The following transcripts of ENSDARG00000002682 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 19909752)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 21012378 |
| GRCz11 | 15 | 20948110 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTGTTACCTTTTTTCTGATCATTTTATGTGAATCAGGACTTAATCGAT[G/A]GGAGGATATTGAGAAGCTAACCTTTCTGCCTAAGCTGGAAGAGGTGAGGT
Long Flanking Sequence:
GTTTTTTTATGTTTTGTTTTGTATATTTTGTTTAACAGTAACAATGTATGAGCGTCTCAAACATTCTTGTTTTTGCACTAAATAGTTTATCCGCAAAGTGTCAACACTGAACAAGGCCTTTGTTTCAGAGTTGGAAAAGAACAACATCATACATCTGAAGATGGCATAAACAGTAGATGTACTTTAAAGGGCTGTGTATTTACTGTGCATGTATGTAAAAAAAAAAACACCTGTACTTTTAGCTTAAATTATTATTATGTGTCAGTTTTAATTTAGCGTTTTTTGCTATTTGAGTACAATATAAGTACATATCCTTATACTTTTGGTTACTTTATTTTGAGTCACTGAGTTAATAAACTACCTGGACTTAATTGTATGGGTAGGAGGAAGGTTAAGTTTAGCATTTGTTGCATGTAGTAGTTGTAGTTGCATGGAGAATGTTTTAAATGATAGTGTTACCTTTTTTCTGATCATTTTATGTGAATCAGGACTTAATCGAT[G/A]GGAGGATATTGAGAAGCTAACCTTTCTGCCTAAGCTGGAAGAGGTGAGGTTGCAAGGCATTCCTCTACTGCAGACTTACACAAGCACGGAGCGGCGCAGTCTGATGATAGCCCAGTAAGTCTGATGTATCTGACAGAGGAAATTCACACAAAAGTGGAAATTCTGTCATCCCTTTGGCCCTGCTTCAAACTTGTGGTTACATGCATTTTCAGCGATCTGAACATCTGAGATGCAGCACTATTGCATGCTGTATCTCCTTAATGCTGTAATTAGTGCAAAAGGTGGCCCAACAAAGTACCGAGGACATAATACAGTACATCAACACACTTTTCAGAAGGCCAACATATATTTAAGATTATTTTTTTATTGGTCACATAAAATATTTTAATTTTGTGAAATACTGGATTTAGGATTTTTCATCTTCTAAAATCTGTTTTTTTTTCATCTTTTAAAATATTTGACTTTGTGTATAGTGAACTAATATAACACACAAGTTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15855
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006910 | None | None | 176 | None | 4 |
| ENSDART00000124092 | Nonsense | 430 | 448 | 8 | 8 |
| ENSDART00000135770 | Nonsense | 430 | 448 | 9 | 9 |
| ENSDART00000138166 | Nonsense | 188 | 206 | 3 | 3 |
The following transcripts of ENSDARG00000002682 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 19906469)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 21009095 |
| GRCz11 | 15 | 20944827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGGGCACTGCCTATGGCCCYGATGAGCTCAAATACAGTGCACGGGCCT[T/A]GCACTCCTACAGCATTCAAGATGGGGATGAGATCCTGGTAGTTCCAAAAG
Long Flanking Sequence:
CACATGGTCTGTTTTAAGGATGTTTTTGGTACCTTTCTGAACTATTAATGAGTCAGGGACCTTGCTTTATAGGGAGGATGTGGGATCTAAAATATCATCATTTTGCTATTATGAGGTATTAGTGATGGAATTTTTTCATTTTTTGTGTGAACTGCCCCTTTAAAAGTTATTGGTAGTATTTTGACACTCTATTTGTTTAAATGGCTGAATGAGGTTAAAGTTCTTGTATTTTCTTTGGAGATATCACTGTTTGGTGACCAAATATGGGAAACTGGCTCCTCTGGCTGAGATCGACCTGAGACCACGTTTCCATGCCAAAGTAGAGGTGCGCTTTGAGGACAAAGTCGAGCAGGTGAGCATCCGTTTGGACCAGACCGTGGCCGAGCTCAAGAAGCAGCTGAAGACTGTAGTACAGCTTCCTACCAACAACATGCGTCTTTACTACATAGACAAGGGCACTGCCTATGGCCCCGATGAGCTCAAATACAGTGCACGGGCCT[T/A]GCACTCCTACAGCATTCAAGATGGGGATGAGATCCTGGTAGTTCCAAAAGCAAAATAACCTACTTTTTTCCTCCACCACCAGAAACACAGAAAGCTACATTTAAATTACCAAACCCACTTTGAACTAGTGCTGCCTATGCTCCACAGAGTGAATGGGACTATCTTTCAGGGAAAAAAAAAACATTTAAGGACTTGCTGGAGCTTATGTCACGTATCACATGTGTTGCCAGTAGTAAAGGTTTAATTTTTGACTTCACAAGCACCCCGGTATTTTCAAAGGCCTGTTTCTTCAAGAGTAAAGCACAGTGGAAAGATGTGCGTTTTACCATTCTTAAGACAATCACCCATAGCTGACAGAAAATGTTGCACTGCACTGATGTCTTAAAGAAGAAATTGTGGAAACCCATTGCCTGCTGATGTGTGTCATATGCTGTCAGCCATTTATTACATGCAAAAGACTCTCAGGCCTTATATTCTGTATGGGCAGTGCTAGCTTCACA
Associated Phenotype:
Not determined