ZMP
si:dkey-270k22.4
Ensembl ID:
ZFIN ID:
Description:
LOC564788 protein [Source:UniProtKB/TrEMBL;Acc:A4QP73]
Human Orthologue:
TTC19
Human Description:
tetratricopeptide repeat domain 19 [Source:HGNC Symbol;Acc:26006]
Mouse Orthologue:
Ttc19
Mouse Description:
tetratricopeptide repeat domain 19 Gene [Source:MGI Symbol;Acc:MGI:1920045]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32952 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18336 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32952
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110821 | Nonsense | 17 | 403 | 1 | 10 |
The following transcripts of ENSDARG00000074435 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 32203873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32502780 |
GRCz11 | 2 | 32485998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGGCGCTGCGCTCTTACTGTCGACAACTAGCTGCACAGGTCTTTCGTT[T/A]GAAGCTTTGTGGTAACGAATGTCCGAGAAATGCACCGGGTTGTAGTTTTT
Long Flanking Sequence:
GGACTGGTCCATGATCGACGGTGCGGGACACATTTGTGCAGATATAATAATTACGTTCAAATAAAAAAAACTATTTAATATTTACCTCATAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATAGGAGCAGACATCATTTTAATAAAGTAATAAAATAATAATAATGATAATATATTAAATGGAAAACTGATTAAAATACAACGTAACTACAAATTTAAGTTAAATACACAGAATTAAATACAATGAATGAAAGCAAATCATAGAGCCCGAGCTAGTCACGTGACCACCTCACCTCCAACGCTTGGCTTGCGTCATTGCATAATCACAGAAATATGGCGCTGCGCTCTTACTGTCGACAACTAGCTGCACAGGTCTTTCGTT[T/A]GAAGCTTTGTGGTAACGAATGTCCGAGAAATGCACCGGGTTGTAGTTTTTCTCTTGCGGGAATCAAGTCGCTGCATGAACCGACCGGCGTGCTGGCGCGGTCGAGCCGCTGTGTGAAGCGCTGGCACAGAAGGTCATGGCATCGCTGTGCCAGTCTGCAAATGCCTAGTCAGAAGAGCCACTCGGACACTACAGACTTCAGCAGGTGGACTCTTGCCTGGGGTGCCGTCGGTGAGTTCAGATTCAGGTTGTTTGTGTATCAGAAGAAACAGTTGGTTACATCCTTTGACACATGACGTAACGTGCGTGGTGCTGTCGTAACATTATATGTATGTAATGTTTAAAGCACGTCAAGTCAGATTGACTTCTCTGTGTGTTCATATCAAATGATCTGACGCTCAGATTTGCTTTCACATCAGCCTTTTCGCTTTTTGGAGGCTCAGATGAGAAAACCGAGGAGCAAAAACTTGAGGATGAACTTATTCTGCTCTTGAAGAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18336
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110821 | Nonsense | 109 | 403 | 2 | 10 |
The following transcripts of ENSDARG00000074435 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 32203410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32502317 |
GRCz11 | 2 | 32485535 |
KASP Assay ID:
2259-2220.1 (used for ordering genotyping assays)
KASP Sequence:
CATCAGCCTTTTCGCTTWTTGGAGGCTCAGAKGAGAAAACCGAGGAGCAA[A/T]AACTTGAGGATGAACTTATTCTGCTCTTGAAGAAAGCCAAGGTAAATTAT
Long Flanking Sequence:
TCTTACTGTCGACAACTAGCTGCACAGGTCTTTCGTTTGAAGCTTTGTGGTAACGAATGTCCGAGAAATGCACCGGGTTGTAGTTTTTCTCTTGCGGGAATCAAGTCGCTGCATGAACCGACCGGCGTGCTGGCGCGGTCGAGCCGCTGTGTGAAGCGCTGGCACAGAAGGTCATGGCATCGCTGTGCCAGTCTGCAAATGCCTAGTCAGAAGAGCCACTCGGACACTACAGACTTCAGCAGGTGGACTCTTGCCTGGGGTGCCGTCGGTGAGTTCAGATTCAGGTTGTTTGTGTATCAGAAGAAACAGTTGGTTACATCCTTTGACACATGACGTAACGTGCGTGGTGCTGTCGTAACATTATATGTATGTAATGTTTAAAGCACGTCAAGTCAGATTGACTTCTCTGTGTGTTCATATCAAATGATCTGACGCTCAGATTTGCTTTCACATCAGCCTTTTCGCTTTTTGGAGGCTCAGATGAGAAAACCGAGGAGCAA[A/T]AACTTGAGGATGAACTTATTCTGCTCTTGAAGAAAGCCAAGGTAAATTATGCTGGGATGCTTTCCTGAGAACTCTCAGCACATTAAGAGAGTTTAAGCTAAATTTGTATGCTTTGCTAGCGTAGTCTAAGATAATTCAATCTACACAAATTCAATTAAATTCAAGTTTATTTGTATAGCGGTTTTCACAAATTTATTGTTTCAAAGGAGCTTTACTAAAGGTGCTTATTATTACATTACAGTCAAAGTCAGGAAAATTAAGGTTATTAATTGCCATAACTTTATATTTTTACTAATAGTTTTGTAACTATTACTAATAACTAAATAATTAGTAATTAAACAGTTAAAGTTATATACCTGACTAAAGTCTTGTCGCCTATCCAAGTTTTAGGAGCAACAAATAATCGCTTGACTTCTAGTTGATCATTTTATATCAGAAGTGTCTCATATGACAGGCAAAGGCCTTTAGATTAAGCTTATTTTACCACAATGAAATATGAT
Associated Phenotype:
Not determined