ZMP
tmtc4
Ensembl ID:
ZFIN ID:
Description:
transmembrane and tetratricopeptide repeat containing 4 [Source:RefSeq peptide;Acc:NP_001166973]
Human Orthologue:
TMTC4
Human Description:
transmembrane and tetratricopeptide repeat containing 4 [Source:HGNC Symbol;Acc:25904]
Mouse Orthologue:
Tmtc4
Mouse Description:
transmembrane and tetratricopeptide repeat containing 4 Gene [Source:MGI Symbol;Acc:MGI:1921050]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14987 | Nonsense | Available for shipment | Available now |
sa21512 | Nonsense | Available for shipment | Available now |
sa21511 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14987
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 |
---|---|---|---|---|---|
ENSDART00000078681 | Nonsense | 285 | 739 | 7 | 17 |
ENSDART00000127214 | Nonsense | 285 | 739 | 8 | 18 |
ENSDART00000133427 | None | None | 62 | None | 4 |
ENSDART00000136838 | None | None | 55 | None | 3 |
ENSDART00000142904 | Nonsense | 285 | 299 | 8 | 8 |
ENSDART00000146268 | None | None | 32 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 32549326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 31705272 |
GRCz11 | 9 | 31516018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTTGRCTCTACTCTTTCTTGGTGGTTCCTTACTTATGTACAYGAGATG[G/A]AAAATCATGGGAACTGGACCTCCATCTTTYACMGAGGTGGATAACCCAGC
Long Flanking Sequence:
CAGTTGGTGGCGATAAAAAGTTCTCTGTGTTGTGGATATTTGGCAGCATTCTTCTGTGTGCTGTAGCCATGCTCTGCAAGGAACAAGGCATTACGGCTTTGGTAAGTGAAAATATGTATACAGGTCAAATACAGTAATATAAACACACACAGCATATGCCGTACCTCACATCTGTTTTTAAACTAGCTCCTTCACCATCCATAAAATATCCTTGTTCTTTTTTTTTTTTTTTTGTCTGAAGGGAGTTAATGCTGCTTATGACATTCTCATGGTGTGCAATCTGAACATTTATGAGCTTGCTCACCGGCTGCTGTCCAGGAGAAAATCAGCTGACGTAAGTGTCGGATTCACAGGATGTCACTCTTTATACCCAAACAATCTCTCTAATGGATTTAAACTTTTCTCTTTTGCACCCAGATTGGTGGCTTGCCAAGAAACGGTTTGCTTATGAGGTTGGCTCTACTCTTTCTTGGTGGTTCCTTACTTATGTACACGAGATG[G/A]AAAATCATGGGAACTGGACCTCCATCTTTCACCGAGGTGGATAACCCAGCATCCTTTGCAGAAAATATCATCCTGAGGGTAAGCAGTCCTTTCAGTTTGACAGTTAAAAGTCTACGTAGGGAAAAATGACTTGTTTTTGTAAAGTATGCTTTTAGTAAATTTAAAACAATTATTATTATCATTATTTTCTTAAATTATATTTGTTTTGCTCTAGTTTCAAAGTTAAAAAACAGAAGTCTTACTTGTTGGTATTGAGCGCTTATATATTGGTGTTGTGGTAAACCTAATAAAACTCAATACTTTAAGGGGGAAATGAAGCACTCAGTCAAGTTTGCATTCTTTTGTGCATTGTATTTCACTTTAATAAAAATATATTAAACAAACTTGATTAATGTAACCATTTAGCTGAAAACGGCCTGTTTTACTATAGCTTTTAGACCTAGGGCGCCACCAACTTGGAATGTCGATGTGTCTGACGTCACAGGGTTGGTTTCGTTCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21512
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 |
---|---|---|---|---|---|
ENSDART00000078681 | Nonsense | 359 | 739 | 8 | 17 |
ENSDART00000127214 | Nonsense | 359 | 739 | 9 | 18 |
ENSDART00000133427 | None | None | 62 | None | 4 |
ENSDART00000136838 | None | None | 55 | None | 3 |
ENSDART00000142904 | None | None | 299 | None | 8 |
ENSDART00000146268 | None | None | 32 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 32545772)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 31701718 |
GRCz11 | 9 | 31512464 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATTAGCTCAGCTGCTGATTGGAGGATCGTCTGGCCTGCTGTGCTGTG[G/A]TTCTGTCTGATTGGCTTGGTGAGCCAAGCTCTGTTCTCACAGGACAGTAA
Long Flanking Sequence:
TAGTCCATTACTTTCACTGTATCTGTTTAGCTGAGGGAACAGAACCAACCCTGTGACATCAGGTACAGCAATATTGCAAGATGGAGGCGCCCTAAGTCTAAAATCTATAGTAAAACATGTTGTTTTCTGCTAAATGTTTATTTATTTATCGACTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATGTCCATTTAAGTGGAAATTATTTACAAAACAATGTAAACTTGACTGAGTGCTTCATTTACCCTTTTATAAAAGTGTTGTGGTTACACAGACTGTCATATAGTATATTCTCTGTCATCTTTTCTCAGATTGTGAACTATAATTACTACTACTCTTTGAATGCCTGGTTGCTGCTGTGTCCCTGGTGGCTGTGTTTTGATTGGTCAATGGGCTGTGTGCCTCTGATTAGCTCAGCTGCTGATTGGAGGATCGTCTGGCCTGCTGTGCTGTG[G/A]TTCTGTCTGATTGGCTTGGTGAGCCAAGCTCTGTTCTCACAGGACAGTAATAAAAGAAGGTAAGCACTGTATCAAAATACGACATGCTGTGAGTAGACTTTTGGAAATGGAGACGTTATCTTAAGAAGACAGTCTGATTGTTGTTATCTGAACATTTGTTTCTACACAATTATACTGTCTGTCTATCATACTGCAATACTGCTGTAAGGCAGTCTGGGTTATTCTGCATTTACTGGATTTATTGGGTATGGATTTAAGTAATGTTAATGTCCTTTATTTTATTTTAATATGGTCCAAATTTCAATTAAAATATATATTTTGATCATTTTAGGTTTTCTTTTCCCGGAAATAGCAGTTGGTCAGAATAATAAATAACAATACTACTAATTATAATGTAAAAATAAGTGTTTTTCTACCACTGATGCGACTATATTTTTAATTTCATATGATTCCTTATACAGCATTGATACAATATAATCTGTTAAGTAGACTTAAGCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21511
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078681 | Essential Splice Site | 630 | 739 | 14 | 17 |
ENSDART00000127214 | Essential Splice Site | 630 | 739 | 15 | 18 |
ENSDART00000133427 | None | None | 62 | None | 4 |
ENSDART00000136838 | None | None | 55 | None | 3 |
ENSDART00000142904 | None | None | 299 | None | 8 |
ENSDART00000146268 | None | None | 32 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 32540728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 31696674 |
GRCz11 | 9 | 31507420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCACAGCTTGGCATGGAACAATATGGTCATACTGTTAGACAACACTGG[T/A]AATGTACACCTGATTTTGTTTGTTTGATCAGATTTAAAAGATCAATGAAT
Long Flanking Sequence:
GAATCTTACAGCATGGATTTTTAATGTTTAGCGTGTTTCTTGCATCATTTTATCCACCCTTTCTTTGTAATACAAATCAACATGGGGCAGTTTATAATTAATTAGAGCAAGAAATTGTCTATTCCGCTCTAAATATTGCTCATTATGATGTGTAATAACGTGCTATTTTTGCTGCAATGATGATTTGATTCAAATGCTCCATGAATTATGAACTTCCTAGTGTTTAATATCCTAGTGTTTAATGCACATGCTTTGGATGTGTAGGAAATGCACGTTCAGATTTCCTCAGACCCCATGGTCATTATCTGTGAGAATAAAATGATTAAAACTGGACTGTGCAAAGCATTAAAGAGACATGTTTGTGCTTGTTTGTTTTGCCTTTAGTATGCAGACCTGAACCGTAGCATTGATGCGCTAAATGCCTGGAGGAATGCCACCATGCTGAAGCCTGACCACAGCTTGGCATGGAACAATATGGTCATACTGTTAGACAACACTGG[T/A]AATGTACACCTGATTTTGTTTGTTTGATCAGATTTAAAAGATCAATGAATACTATCATGGGCTGCACAGTGGCGCAGTTGGTAGCACGTTCGCCTCACAGCAAAAAGGTCGCTGGTTCGAGCATTGGCTGGGTCAGTTGGCGTTTCTGTGTGGAGTATGCATATTTTCCTTGTGTTGGCCTGGGTTTCCTCCGGTTTCCCCCACAGTCCAAAGACATTTAGGTGAATTGAATAAGCTAAATTGTCTGTAGTGTATGTGTGTGAATTAGTGTATGCTGGATAAGTTGGTGGTTCATTTCGCTGTGCTGACCCCGGATAAATAAAAGGACAAGCCAAAAAGAAAATGAATGAATAAATGAATACCATCACAAACAGAAAAACTGCAGTGGTCCCTCACTATAACGCAGTTCACCTTTTGCGGCCTTGCATCTACGCAGATTTTTTTAAAAAATTTGACATGCTTTTTTGTGTTCATTGTGTTCTGTGTCCTGATTAGAGCCT
Associated Phenotype:
Not determined