ZMP
tmod4
Ensembl ID:
ZFIN ID:
Description:
tropomodulin-4 [Source:RefSeq peptide;Acc:NP_571271]
Human Orthologue:
TMOD4
Human Description:
tropomodulin 4 (muscle) [Source:HGNC Symbol;Acc:11874]
Mouse Orthologue:
Tmod4
Mouse Description:
tropomodulin 4 Gene [Source:MGI Symbol;Acc:MGI:1355285]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3530 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa18609 | Nonsense | Available for shipment | Available now |
hu3476 | Missense, Splice Site | Confirmed mutation in F2 line | Not yet available |
sa22870 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu3530
Status:
Confirmed mutation in F2 line
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024294 | Nonsense | 88 | 343 | 2 | 9 |
ENSDART00000137153 | Nonsense | 88 | 343 | 3 | 10 |
ENSDART00000024294 | Nonsense | 88 | 343 | 2 | 9 |
ENSDART00000137153 | Nonsense | 88 | 343 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 31913353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29732716 |
GRCz11 | 16 | 29667339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATAGAGCATAAGGATAGAGATGACCTGGTGCCTTTTACAGGGGAGAAG[A/T]GAGGTACCATCACTACTGGACAGATATTATGAACATGATCGTTCATATAT
Long Flanking Sequence:
CTCTGTGGACTGAGCCACCAACTATTCTGGCAAATGTTTTACCCGGCAGATCCAAAACCAATTTAAATGAATTATTGAATGAATAAATAAATGAGTAAGCAAACAAAACAAATGAATGAATGAAACTGTGTGTCTGATGTACAGTGTTCTAATTAAAGTTTTGTCATTGGCCAAGGCTAACATTGTGAAATATTTGACCACTGAAGGCCATGATTGACCAATCAAAAGGAAGTATTCTGTAGTAGCACAACATAAATATTTGCAATACATACTCCTGAATCAGTAATTGGCTGTAAATTTGATTTGTAAATTTTATTGAAAGTTTGTCCACATGTCTTGATTTCCAGAACACTACTCTGCCTGCCGGGTTTCGCCAGCGTGACCAGACCAAGAAGAGTCCCACAGGTCCCTTTGATCGCTTCGCCCTCATGGATTACCTGGAGAAACAAGCCATAGAGCATAAGGATAGAGATGACCTGGTGCCTTTTACAGGGGAGAAG[A/T]GAGGTACCATCACTACTGGACAGATATTATGAACATGATCGTTCATATATCTAATGTCAGAAAAGCCACTCATTCAAAGTCATTATTTGAGATATATATAATATTTATAATTATTTATATATATAAGTATTATATATGGCTATATATCATTTTTCAATTATAATTTTATATTATTTTGTTTATATTATTGCCTTAAATTTGGAATAAAATAAAAGTTGGAATATAATTTTCCCTATACTTGATATCAGTGTGAAATGGTGACAAAACAGGTCCTTGTAAAATGCTTTTTATGTAGATCACAAGGAATCTAATTGGCTCAAACTGCTTTTAGTGAATACTCCATTTAATTCATGAATACAATCAGGGCTTGACATTAACACCCGCCAACCTGCCCAGTAGATTTTAGCGGTGGTGGGTAACACAGACACTACCACTAGCTGGTTGAAAATAATTGTCCTGGAATAATAGTTCTTAAAAGCATGATTCGACCATAAGGGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18609
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 |
---|---|---|---|---|---|
ENSDART00000024294 | Nonsense | 88 | 343 | 2 | 9 |
ENSDART00000137153 | Nonsense | 88 | 343 | 3 | 10 |
ENSDART00000024294 | Nonsense | 88 | 343 | 2 | 9 |
ENSDART00000137153 | Nonsense | 88 | 343 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 31913353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29732716 |
GRCz11 | 16 | 29667339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATAGAGCATAAGGATAGAGATGACCTGGTGCCTTTTACAGGGGAGAAG[A/T]GAGGTACCATCACTAYTGGACMGATATTAWGAAMATGATCGTTCATATAT
Long Flanking Sequence:
CTCTGTGGACTGAGCCACCAACTATTCTGGCAAATGTTTTACCCGGCAGATCCAAAACCAATTTAAATGAATTATTGAATGAATAAATAAATGAGTAAGCAAACAAAACAAATGAATGAATGAAACTGTGTGTCTGATGTACAGTGTTCTAATTAAAGTTTTGTCATTGGCCAAGGCTAACATTGTGAAATATTTGACCACTGAAGGCCATGATTGACCAATCAAAAGGAAGTATTCTGTAGTAGCACAACATAAATATTTGCAATACATACTCCTGAATCAGTAATTGGCTGTAAATTTGATTTGTAAATTTTATTGAAAGTTTGTCCACATGTCTTGATTTCCAGAACACTACTCTGCCTGCCGGGTTTCGCCAGCGTGACCAGACCAAGAAGAGTCCCACAGGTCCCTTTGATCGCTTCGCCCTCATGGATTACCTGGAGAAACAAGCCATAGAGCATAAGGATAGAGATGACCTGGTGCCTTTTACAGGGGAGAAG[A/T]GAGGTACCATCACTACTGGACAGATATTATGAACATGATCGTTCATATATCTAATGTCAGAAAAGCCACTCATTCAAAGTCATTATTTGAGATATATATAATATTTATAATTATTTATATATATAAGTATTATATATGGCTATATATCATTTTTCAATTATAATTTTATATTATTTTGTTTATATTATTGCCTTAAATTTGGAATAAAATAAAAGTTGGAATATAATTTTCCCTATACTTGATATCAGTGTGAAATGGTGACAAAACAGGTCCTTGTAAAATGCTTTTTATGTAGATCACAAGGAATCTAATTGGCTCAAACTGCTTTTAGTGAATACTCCATTTAATTCATGAATACAATCAGGGCTTGACATTAACACCCGCCAACCTGCCCAGTAGATTTTAGCGGTGGTGGGTAACACAGACACTACCACTAGCTGGTTGAAAATAATTGTCCTGGAATAATAGTTCTTAAAAGCATGATTCGACCATAAGGGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu3476
Status:
Confirmed mutation in F2 line
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:
Missense, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024294 | Missense, Splice Site | 89 | 343 | 3 | 9 |
ENSDART00000137153 | Missense, Splice Site | 89 | 343 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 31917221)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29736584 |
GRCz11 | 16 | 29671207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCACGGTAACAACAGTGTGTATCTTTTTTCTCCACTGCTGTCCGTAG[G/A]GAAAGCCTTCGTTCCTAAACCAGGCTCGGGACAAATCCCAGCGGACGAGC
Long Flanking Sequence:
TGGTAGCAGATATCACAGCTTCTGTTACTTTTTACCTTGCACTTTTTTGTTAATATGTATTACTAATTATTTGTTTAGGATATATGTTTTCACATTCTGATTCCTATGCCTATTATTAAATTGTTAAAATGACTATAAATAAATGAAATATACTAAAGAATTAAACATTATATGTTCTATTCTATTCTTTATATGAAAGAGTGTACTTGGATTATGCATATTTATAATGTACATATATAATGAGTGGCATAAAATTATCCTAAAATGACAATAATATCGCTTATCGCAATATATTTTGGTGCAATATATCGTACAACAAAAAATAAATATCGTAATAGGCCTAGGAGAGGACAATAATTTGATAAAAGATTGTGAAAGCACATTAATTAAATAAAATAATGAACCTTTTCTAATATATAAACACTATAAAATTTCTTAAAGCAAATTTTGATTTCACGGTAACAACAGTGTGTATCTTTTTTCTCCACTGCTGTCCGTAG[G/A]GAAAGCCTTCGTTCCTAAACCAGGCTCGGGACAAATCCCAGCGGACGAGCAGATCACTCTGGAACCTGAGCTGGAGGAAGCGCTAAGAAACGCAACAGATGCTGAAATGTGTGACATTGCAGGTAAGCATCACATTTCTAATCTGTTCCTGTTGTTTCTACTCACATGACATCAAACAACTAATGATATCCGGTTCACAATGACTAAAGATAAGCTTTACAACGCTTCGAAGACTAATCTGCACTTCATAACCTGTAATGTCCTGTTACGGCTTTGACTGTAATCCAAAATTTGATCCTTGACTAATCCTTTATTTGCTGTTGTAAACAGGTGATCACAAAAGCTCATGCACAACATCTGTCAATCAAACCCTTTCTAAATTCACCTGTTTTATTTGTGCAGTCAACATACAGCTGTGGAAAAAATGAAGTAGACATTTGAAAATTCTCAGCTTCACTGGGTGTGCTAGATTTACTACAATATGTGTATGTTTGAGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22870
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 |
---|---|---|---|---|---|
ENSDART00000024294 | Nonsense | 171 | 343 | 5 | 9 |
ENSDART00000137153 | Nonsense | 171 | 343 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 31922593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29741956 |
GRCz11 | 16 | 29676579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTTTATTCTCTTTCAGGTGTGGTGAAACCAGATGTGTATAAAATCTA[T/A]CCTGAGGAGCCTCCCAATGACACCAACGTGGAGGAAACTCTCCGCTACAT
Long Flanking Sequence:
TTTGTATTTTGTATTTTTACCCTTTAACTTTCAATAAAAAATAATTTGACCATTTCTTTTTTGGTTAAATTGTGTTCCTGACCACTCTAACTAAACCAATGTTGAGTTTTAATAAAAACCTACGCCCAATATGTCATTTAGGCTGTTACAGTGTTAGTTAAGTGGTTAAAGTTTAAAAGAAATGATATGTTTAATGGAATTATGTTTGTCTCTTCACAGCCATCTTGGGAATGTACACACTCATGAGCAACAAGCAATATTATGATGCCCTGAACACCACCGGCAAGATTGCCAACACAGAAGGCATCAACAGTATGTATACACACATATAACACTGAACCATTTCATGTTAAACAAACATAATAGTTACAACTAATATACTCTATGTGTGTTGTAAGGTCAGTTCCAGTTTTGTATATCCACTGGATTTCTTATAAATCTGAATCATACATGGTTTATTCTCTTTCAGGTGTGGTGAAACCAGATGTGTATAAAATCTA[T/A]CCTGAGGAGCCTCCCAATGACACCAACGTGGAGGAAACTCTCCGCTACATCCAGAAAAATGACAACAGGCTGCAGGAGGTCAACCTCAACAACATCCCGGTAAACATGCTAACTCTGCTACACTCTTTTTAATGTATTGTTCGCTTATACTGTTAGCAATACTTTTACATAAAACAAATCAGGAAGTAACATGATACTTTCTGTCACACACTGTCTAAATAGGTGTGTTGGATTGTTTGAAAGTACACTTTGAAAAGACACACTTTGTCCAGCCATGTGAAATTCTGCATGTATGTTTGACAGTCCTACTTTGTTGATAGATGAGTGCAGTGTAGAACCAGAGGCTGTTAATAAGATATAAAATACATAAATACTGATACTGAACATATTAAACATCTGTAATATAAGACTAAGCAATAGTTACCAAGTAATAAAAACAGTTTGAAACTTTGTGTAGTGGAACATTAATGTAGGATCCAATACAATCAGCAAAGTGCCAT
Associated Phenotype:
Not determined