ZMP
zgc:194598
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100170789 [Source:RefSeq peptide;Acc:NP_001124099]
Human Orthologue:
TTC13
Human Description:
tetratricopeptide repeat domain 13 [Source:HGNC Symbol;Acc:26204]
Mouse Orthologue:
Ttc13
Mouse Description:
tetratricopeptide repeat domain 13 Gene [Source:MGI Symbol;Acc:MGI:2384573]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14655 | Nonsense | Available for shipment | Available now |
sa36952 | Essential Splice Site | Available for shipment | Available now |
sa43373 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14655
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092217 | Nonsense | 97 | 825 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 20 (position 4097771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 4040040 |
GRCz11 | 20 | 3991569 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCCTCCCTCTTTCTTTCACMRCAGAATCAGGCAAAGYTGTTTGTCGAA[C/T]AGCGGCGGTTTCCTTWCGCTGTGGACAACCAAAATACCAATGAAGAGCTC
Long Flanking Sequence:
AGATTATTACACCCTGATAGTTATAGTTCATTATAATCTTACTAGTTTCTGGCACGGTTAACTTTTACATTGGAAAATAAGCACAATTTAAATTTTGATCACATTTATCCATTTTATCAATCCGATATTGTACGTTTGTGTTTTTATGGAAGAAAGTCATACAGGTTCTGAAATGACACTACATGAAGGTAATTAAATGATGGCAGAAAATGTGTATTTGTAGCTGAACCCTATCCTTAAACACCTGCATTTAGATCTTAAAACACTGTAAACACACATTGGGATGAGAAGTAGTTTTGACCTAAAACCAAACACTTCCTATGTAGCACAAGCGTTGTTTATCCTCCTCGTCCTCTGTTATTATGGATGTCTTTGCATTGTTTTTTCCATCCACTCTTTGGTTGGATTGATTGTAAGAGGTTGACAGACTTCCTGACATGCTTTCCTTTCTTTCCTCCCTCTTTCTTTCACCGCAGAATCAGGCAAAGTTGTTTGTCGAA[C/T]AGCGGCGGTTTCCTTTCGCTGTGGACAACCAAAATACCAATGAAGAGCTCGGTGTGTGTCAGCTGTGTTTTGTGTTTTTGTGTACTTGTCTGTGTGTAATGAAAGCCTCTAACACTCTTTGTTTGTAATTCAGCCATAGGTTATGTTCTTATTGGAAACGGACTGTATGATGAAGCCATCAAGCACTTCTCCTTACTGCTGCAGGTCAGTTTCATTCAGAATTTATTATATATTTTTTTTTTACATTTAAAGGGTACCTATTATACCCATTTTTACAAGATGTCAAATAAATCTCTGATGTCCCTAGAGTGTGTATGTGAAGTTTCAGCTCACAATACCACATAATTAATGTTTTATAACTCTTTGAATCTGCCCCCTTTAGGCTTTAATCCTAAATATGTCGTTTTGGTCACTGTCGCTTTAAATGCAAATGAGATTATGCTCCCATCTCTCTTTTCAAAAGAAGGCGGAGCTACAGATTCAAAATGCTAGTGGCGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36952
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092217 | Essential Splice Site | 293 | 825 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 20 (position 4105668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 4047347 |
GRCz11 | 20 | 3984551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGTCGGACTTTATAGATGCTTATAAAAGCTTGGGTCAGGCTTACAGG[T/C]AAGGTGACTCTGTCAGTTCTGTCAGATATCTAGATTTTGTCGGATCACAT
Long Flanking Sequence:
ATAGGTTGCCGTGCGTAAGAATTTTAAAAGCAAAATCTGCCAATGACAAACCTGGTTATCCTCTGCCAAGTGCATTTAAAACTCTTTAAAGAACGGCAAACCATTGATTATCCTTGTGCTTTGGTCATTTGCCAAGTTGTAGACAAGTTAAAATTTGTTTTGTTTTTCGCAACGTAATATTTAATAGTATATTTTTCAGTTATGTTAGATCTAGTCTACATTGAGTCAGCGAGAGAGCAAGAGAGATGTTGTGTGCATGTAAATAATACTGACGTCTATCATTTGGTATTTCTGATCTTTTAATCTAATGATGTGAAAACATAATTTAATAATTTACCAGATAAATCAGTCTAAATCTTATTAAAAGTACCACATTAATTAAACATGCTTTGTTTAACATTATTTTCTCCACGCAGGAGGCTATCGAGGTGTTTAAAGAGGCTCTCAAGCTGAAGTCGGACTTTATAGATGCTTATAAAAGCTTGGGTCAGGCTTACAGG[T/C]AAGGTGACTCTGTCAGTTCTGTCAGATATCTAGATTTTGTCGGATCACATGAAACAGGCTTGTGTTTTGATCGATCACTTTAAGTAGGTGAGGGATTTCAACTGGGGTTTAATCTGTTTATTTTTGTCCGCTTGTATTCACGTTCCTGATTTCTTTGAGGCGAGAACCGTTCATAGAAGATGCTGATTGGACACACGAGAAGAACCACCAAAATGTCAATATTGCAAAAGAAACCAAACTGTTAAACATATTATTGTGGAATGCCCTATGTTTTAATGTTTTAAGACAATTTTTTTCTGGAGAAACGTTAAATGAAATAGTTATTAATGTGATTGCTGCTAAAATTGTAACATTTTTATCAAAAGTAAACCTTCAAAACAGTTTTAGATTTTTATCTTATTATCTTTATTATTATTTATGTATTTTACCTTGTGTATTAGTTATTGCTGTTGATGAATTTTAATTGTAAGAATATTTTTATAACTATAGAAAAGTGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43373
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092217 | Essential Splice Site | 451 | 825 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 20 (position 4114100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 4055779 |
GRCz11 | 20 | 3976119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTCATAGAAGACTACGAAGAACAGCCTGGACTTCAGCCGCATATTAA[G/A]TGAGTGTAAAAGACGAGTCTCTTCAGTCTTTTTAGTGTTTGAACATTGTC
Long Flanking Sequence:
TATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAACCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGAATATCTAGTCAAATATTGTTTACTGTCATCATGGCAAAGAGAAAATATTACTTAGAAATTAGTTATTAAAACTATTATGTTAAAAAAATTTCCGTTAAATAGAAATTGTGAAAAAATACACAAGTGGGCTAATACTTCTGACTTCAATAATATATATTACTAAAACTCAATATGATGCATTTTTAACTCTCTAATAAATTATATTATTCATTTTCTGAAACGCCAGTGTTTTTCTCCATCATCTGATAGAATACTCCCGGTATTTACACTCTCATCTGGATGTCCCCGTTGCGGAGTATAATGTCGATCAGGATTTGCCAGGAAATTTTAAGAACCACTGGGCCAAAAATCTCCCCTTCCTCATAGAAGACTACGAAGAACAGCCTGGACTTCAGCCGCATATTAA[G/A]TGAGTGTAAAAGACGAGTCTCTTCAGTCTTTTTAGTGTTTGAACATTGTCTGGATCACATATGAATGAACGAGGAGTTTCCAGCATCATTTGTATGTTTTGTGTATGTGTGTAGAGATGTTCTCCCTCAGAACTTTGACAGTTACTCCGCTGAGGTTCAGAAGCTCATCTGTACAGCAGATCATCTCGGTGCACTGATGCAGTACGACACTTCAGGCTTCTTACCAAACCTCAGAATACACAGAGGTTAGAGTGCTTCTAAAACACTCGAAAATCATGTTTTGTTTTTGCTTTCTCGGCTGTTTTTGTGCATATATAATATAATAATTTATAATAACAGTTTGTTTTACTTTTTCCTCCTAAAAATGTCAAGATGAATTCTGGAATGAAGGACACTCATCCTGAAAGGAGTGTAGTCGAGCGTTGTTTTTTGAGTGTTGTGTCTTGTGTGTTTTGTGTAGCGATGGGTTTGGCCACTATAGAGGTGATGCAGGCCATGCA
Associated Phenotype:
Not determined