ZMP
ttc14
Ensembl ID:
ZFIN ID:
Description:
tetratricopeptide repeat protein 14 [Source:RefSeq peptide;Acc:NP_001014336]
Human Orthologue:
TTC14
Human Description:
tetratricopeptide repeat domain 14 [Source:HGNC Symbol;Acc:24697]
Mouse Orthologue:
Ttc14
Mouse Description:
tetratricopeptide repeat domain 14 Gene [Source:MGI Symbol;Acc:MGI:1914370]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12653 | Nonsense | Available for shipment | Available now |
sa12660 | Nonsense | Available for shipment | Available now |
sa17378 | Essential Splice Site | Available for shipment | Available now |
sa37571 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11411 | Nonsense | Available for shipment | Available now |
sa15413 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12653
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 |
---|---|---|---|---|---|
ENSDART00000028085 | Nonsense | 7 | 665 | 1 | 12 |
ENSDART00000028085 | Nonsense | 7 | 665 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 40596979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37676355 |
GRCz11 | 22 | 37611273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGTAAATATGTGTGTTTGCAGACMCTGAAGATGGACAGAGATTTACTC[C/T]GACAGTCTGTGTCGTTTCACGGGGAAAACCTGCTGTCGCTGTTGAAATGT
Long Flanking Sequence:
GACTTTTATTTTGGAAAACCTGCTAGTTTTTAGTCGGTGACTTTAATTTTGAAAACAAGACAACAACAAGCCGTTTCACGCTAACCGCCGCCTCTCGTGCTTTCTTGTTTGTCTTGTGCTCTTGTCGAGTTTAAACAAACTGAATTCAGACTATCACATTTAATACATTGCTGAAGAATAAAACTAATATAATGTTTTAGTAATTTCCGAAGTGGTTAAACGCTTTTTTTCCGGTTAGCTTCCGGTTTCCACGTCTCCCATTTGGCTTTAGCACGTTTACGTTTGCAGCTATTTCTGCAAGAATTCAGACACTTTTATAACTTCTTTAGCGTTTGAGAGAATAAACAAACGATCAACATATCTCCTATTACTTATCTACTGATTACTATTACTTATTCAGTCAGTTCTGAGTCTTTACTCGACGTCTGTGGTGGTATTGCAGCACACAGGGGTGTAAATATGTGTGTTTGCAGACACTGAAGATGGACAGAGATTTACTC[C/T]GACAGTCTGTGTCGTTTCACGGGGAAAACCTGCTGTCGCTGTTGAAATGTGAACAGAATGAAAACCCAGACTTTAAACATTTGGCCTCTGATCTCTACAAAAGCCTTAACCAAAGGTAAGAGGAGTTCACAACTGCTGCACGTGGCTATTTTTTATCCCTCATGCCTGCGCTGTGTTGACAAAACTCAAGACTCCTGAAATAACCCATAAAGCACAACTGAAGTCAAGAAAAACATATCGCATGACTTCATTGATTCGTAGTATTTCTGTGTAATGTAATTCTGTATATTCTAGATAAATAATATAAATATTTACACTTTAGAGTCTATATATAATATTATATAATAAGTGTGTGTGTGTGTTTGTTTGAGAATGACCCAGTACCCCAAGACCTACTGTAAGTGTCAATTTGTTTGGATATTAGATTTCTATATTATCTAAAAGCTAAAATAAGCCACATAAAATAGAGGTAACGTTGGTTTTATATTTGCACATTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12660
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 |
---|---|---|---|---|---|
ENSDART00000028085 | Nonsense | 7 | 665 | 1 | 12 |
ENSDART00000028085 | Nonsense | 7 | 665 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 40596979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37676355 |
GRCz11 | 22 | 37611273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGTAAATATGTGTGTTTGCAGACMCTGAAGATGGACAGAGATTTACTC[C/T]GACAGTCTGTGTCGTTTCACGGGGAAAACCTGCTGTCGCTGTTGAAATGT
Long Flanking Sequence:
GACTTTTATTTTGGAAAACCTGCTAGTTTTTAGTCGGTGACTTTAATTTTGAAAACAAGACAACAACAAGCCGTTTCACGCTAACCGCCGCCTCTCGTGCTTTCTTGTTTGTCTTGTGCTCTTGTCGAGTTTAAACAAACTGAATTCAGACTATCACATTTAATACATTGCTGAAGAATAAAACTAATATAATGTTTTAGTAATTTCCGAAGTGGTTAAACGCTTTTTTTCCGGTTAGCTTCCGGTTTCCACGTCTCCCATTTGGCTTTAGCACGTTTACGTTTGCAGCTATTTCTGCAAGAATTCAGACACTTTTATAACTTCTTTAGCGTTTGAGAGAATAAACAAACGATCAACATATCTCCTATTACTTATCTACTGATTACTATTACTTATTCAGTCAGTTCTGAGTCTTTACTCGACGTCTGTGGTGGTATTGCAGCACACAGGGGTGTAAATATGTGTGTTTGCAGACACTGAAGATGGACAGAGATTTACTC[C/T]GACAGTCTGTGTCGTTTCACGGGGAAAACCTGCTGTCGCTGTTGAAATGTGAACAGAATGAAAACCCAGACTTTAAACATTTGGCCTCTGATCTCTACAAAAGCCTTAACCAAAGGTAAGAGGAGTTCACAACTGCTGCACGTGGCTATTTTTTATCCCTCATGCCTGCGCTGTGTTGACAAAACTCAAGACTCCTGAAATAACCCATAAAGCACAACTGAAGTCAAGAAAAACATATCGCATGACTTCATTGATTCGTAGTATTTCTGTGTAATGTAATTCTGTATATTCTAGATAAATAATATAAATATTTACACTTTAGAGTCTATATATAATATTATATAATAAGTGTGTGTGTGTGTTTGTTTGAGAATGACCCAGTACCCCAAGACCTACTGTAAGTGTCAATTTGTTTGGATATTAGATTTCTATATTATCTAAAAGCTAAAATAAGCCACATAAAATAGAGGTAACGTTGGTTTTATATTTGCACATTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17378
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028085 | Essential Splice Site | 151 | 665 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 40594059)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37673435 |
GRCz11 | 22 | 37608353 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCACYRCTGGTGGACTGAARAGAGACATTGAGGAWCTTGAGATYAAG[G/A]TGTGCTTGCATAGTTKGTCTCTTTATTGTTGTRSCTATTTATTAGACATT
Long Flanking Sequence:
TTTTTAAAAAGTCATTGATAATAATACCTGTGTATGAGTGGACTTATAGAGTATAAAGGATGAGCAAAGGATTCATACGGTCCTAGAAAGCCTGGAAAATGCCTTGTCAAAACTCCAGCACTTTTCCAGATTTTCTAGGACCGTATGAACCCTGTGCTCGTCATTTACTCTCTTGGAAATAACGTCATCATTCAGCGTTCACCATGTGCATGTAGACGTATAACATGACTGAATATTTACCTGAAAGTAATGGGATTTTAGTAGTAAAAATGTGTCTGAAATATTGTGCTGCTGTTTCAGAGGCGTTTGCCGTCATGCCTCCGCTGGAGCAGTTCATGGAGGTGTCGTTCGAGGAGAGACGCGAGCTCTTCTACCGAGATGTGGAGCGCGGAGACATGGTCATCGGCAGAATCAATTCAGTGCGAGACTTCGGCTTATTCGTGACGCTGCTCTGCACCGCTGGTGGACTGAAGAGAGACATTGAGGATCTTGAGATCAAG[G/A]TGTGCTTGCATAGTTTGTCTCTTTATTGTTGTACCTATTTATTAGACATTCTGACTATATGATGATCTCACAATATTGTGATTTCCACTCTAAGATATGCTCTTTTTAAATGTCTGGGTAAAAACACAACTACCCCCCCCCCCATTTAACACAATATATTTTATTTTAAAGGGCACATAGGTTACCCCTATTTTCATATTTATTATAAGTCTTTTGTGTCTAGTATTTGTACACCTCTAACGCACCATTCACACGGGGCGTCAGCGTCAACGCTTCCCATTCACTTTGAATGGGTGATGTCAGGCGTTGCCGAACTGCATTGTGGTTCCGCCGGTGCCGCTTCAGAGGCGTTGCTCGCTGCAGAAGTTGGGACTAGCTCAACTTTTCAAGCGCCAATGCAAGCATCAACCAATCAGATCGCTGTATGCAAATACATTAACTAGACAGTGGCCTATTGCTGACTGAATTTCATTGGTTGATGCTGCTATGACGATCGCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37571
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028085 | Essential Splice Site | 299 | 665 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 40587853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37667229 |
GRCz11 | 22 | 37602147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTACGACTATCAGAAAGAAGCAGTCTGTTTCCTGGGCCTTAAAATGG[T/A]TTGTTTTTAATCTGCTTTTCTACATGATTTTCAATTAGATCATTATTTTA
Long Flanking Sequence:
TTGCTTTCTATTGCTTTTAAATGATGTATGCTGCTTCTTATACCTTCATATATATGGGGTGAAATGGTTGACACATTCGTCACTTGGATGTTTGTGCTTTCTCATCTTCAGTCGAGGTGAAATCGTTTCCTCTGACAGCAACGAGACCTTCGAGAAGCTCCTGGACGATTCACTGGGTTTGTCGAACCCGTTAAACGTGGATTTCCTTCTGGGCAAACTGGGAATCAGTGACACACAGACTCCTTCACTCATGAGGGGTTTGCAGAGGTGTGTGTTTGGCCTTTATAGATGCTTTTATTTCAGTTAAGCTGGTTTATATATGGTTGAAGTTGGAATTATTAGCTCTCCTGAATATAGAGAGGATTTTCTCAACACATTTCTAAACGTAATAGTTTTAATAACTCATTTCTAATATGTCTGTTCACAGTAAGCGCTTTAAAGAGGAGGATTTTGCTACGACTATCAGAAAGAAGCAGTCTGTTTCCTGGGCCTTAAAATGG[T/A]TTGTTTTTAATCTGCTTTTCTACATGATTTTCAATTAGATCATTATTTTATCGATTGACTGGATTTTTTTGCTTACATTTTTACTTTACATTTTGTCATAAAGTAACTTTTAGACATAGTTTTATGAGACAGAATGAATCCTATAGAAGCAAAAAAAAAATCCAAAACAAAGTTTTTATAACCTTGCTTCTCTAATGTGAGACGTTGCTCTACTTTGTGTCTTTAAAGACTTGTTTTTAGTGGTCGACGGGTTATTAAAACTTGGTTTTGGATTTATTTAGCTTGTCTGCTTTACATTTTGTCACATAGTGAGACACTGCTTTAATTATTTATATTTGTCAGAAATGACAAGAAGGCAAGTTTTTATGATCTTCGTTCTCTAATATGTAAGGGTATCATGATCCTCCAAATCCTCGATTCGATTACATTTTCAATTCTAAAGGCTTGATTCGATTTTCGATTATGAATAATTAATTAATTAATGACCAATTAATTATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11411
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 |
---|---|---|---|---|---|
ENSDART00000028085 | Nonsense | 380 | 665 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 40583550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37662926 |
GRCz11 | 22 | 37597844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGAAACGCTAAGAAATACCTGTGCCAGACGCTGGTGGARCGCGGAGGA[C/T]AGTACGTCTGTTTATTCCCGCTTTACATCTTTTATACCTCACCAAACACA
Long Flanking Sequence:
AGTAAAAAGAACGCTAGAACCGTATGAGCACCGGCAAGAGCTTTCATTTGAGCTATAACTTGTTCATGTGTCATATGAAAAATATGAAAATGAACCAATGCTCAATACCCAGCTCGGGTATTCAAAATACTGTGTATTTAAGTGTAAATAACTTTTGTACAGTAGATTAAAAACCAAAGTGATGCATATGTGCATAAAATATAGATTCTACACGTTCAAACGAAACCACTTACAGGGGTCTGGTGCAATGCAGCCCTTTAAATCTGAAAGCGAAAGTCGATGACGTCACAGACCTGGTACCGGGTCTGCAGAGTTTAACTGGTTAAAGGGTTAAAACATAAATTAATAAGTGGCTGAAAGTGTGTTTTTTTTTTCTCAGATACGCCACCAAAGGCAGTCTGGTGAAGGCGATTGAGGACTTTGAGCTGGCTCTGGAGAACTGCCCCACACACAGAAACGCTAAGAAATACCTGTGCCAGACGCTGGTGGAGCGCGGAGGA[C/T]AGTACGTCTGTTTATTCCCGCTTTACATCTTTTATACCTCACCAAACACAGCAGAAGATACGATTTACAGTCACTTCATTTACGCTAAATTACACTGAATCATTCTGCTTTCTTTAAATATATAGTCAAAACACTACTATCATTAATAATGCTATAGCCCAGCATGCCATGCTATCGAGTCATAATATTTATATGTCTTTCTTTTTTTTGATACTGTATATTTTTAGATGTGATGCAGATGAGTTTATGAAATCTTGCAGCCTATAATGACTGATTTTACAGCAACTTTTCTCAACCTTTGTGGAATTTCTAGTATGATTTGCTGTAAAAATGCACAAAATAAGCTTATAATATTAATGTTTTGACCCACTGTATATATTTTTAGACCTGATTCTGACAAGTCATAGTTTTTGCATGTCTGTCTTTACATTTAATGAATTTTGGCGTGCAAAAACATCAAATTTTGCAGAGACTTTTCCAAAATTTGTGCATTTTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15413
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 |
---|---|---|---|---|---|
ENSDART00000028085 | Nonsense | 415 | 665 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 40582515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37661891 |
GRCz11 | 22 | 37596809 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTTTTAGACGACACGTTTAAAGAGGCGGCAGAGGYTCTGGAGAAACTG[C/T]AGATCCGCATCCAGGTGAGCTGGAGAAACCTGTCCGCCAGTCCGCATTCA
Long Flanking Sequence:
TTTTACTTTTTTAATGCAGATTTTTTTACAATTTTCTGCATTTTCAGTGTAATTTGATGTAAAAATACAGAAAATAATCTCAATATTTTTCTTTCTTTGTATGTACTTCATATTATTAAAGTGATGCTGATTAATCATAGCTATTACAATGATGTTACACAATACCTGAAAAGTGACTAACTTCCCTGCATTCTGTTTTAAATAGATACGGTAAGTAAATGTGTTCTGTCACAAATGTCTCCATTAGGCTTGATAATATATTGTTTTAGCTAGAGCCCTGCATTTGAGTCCCTCCTTTTTTAAACCCCTAGTGCCGGGTTTTAACTTAATGAAATGATTGAGAACATTCAAACTTGCTTATATGTGTTTTGCTATCTCTCTGATGATTTCTGCACAGAGTTGAGGAAGAAGAGAAGCTAGTGACGGCAGAGAGTCTCTATAAAAGAGCCCTGGTTTTAGACGACACGTTTAAAGAGGCGGCAGAGGTTCTGGAGAAACTG[C/T]AGATCCGCATCCAGGTGAGCTGGAGAAACCTGTCCGCCAGTCCGCATTCACTCAGACAGTCAGCTTCTGGTATGCCTCAATTTAGGCACAGGCTGTACTGTATCTCTTGGTTAACACAGGGTTCCCACACTTCTTGAATTTCAGACATGTGGATTCAAGGCCTGGAAAGAACTTAAGCGCAAATAGTGCTGGAATTAAATTCATTTTATTATTTCAATAACTGTACTTAATTGTCTAAAACTGATTGGAAAAATGCAGAAATTCCTAAACTGAAAATCTTAAAGGTGCTTTATGTAAGTTTCTGACTTTTCTAAAGTATAAAAACACCATAATATGTTTGCAGATATTTCAGAAGCATGCTCAGTGAACATTCTTGTTTATCAAAAAAACATGGCTGATGTCCAATATTCTGCTTTGAACGTGCTTTCTGTGCCAGAATGGTTGTTTTTGTTTTGGCCATTTAACCCGCCCAATGCCAGTTTAGCCAATTATATTTAAGC
Associated Phenotype:
Not determined