ZMP
tmc4
Ensembl ID:
ZFIN ID:
Human Orthologue:
TMC4
Human Description:
transmembrane channel-like 4 [Source:HGNC Symbol;Acc:22998]
Mouse Orthologue:
Tmc4
Mouse Description:
transmembrane channel-like gene family 4 Gene [Source:MGI Symbol;Acc:MGI:2669035]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42763 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17316 | Nonsense | Available for shipment | Available now |
sa15301 | Nonsense | Available for shipment | Available now |
sa25020 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36188 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9506 | Nonsense | Available for shipment | Available now |
sa18068 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42763
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041054 | Nonsense | 39 | 732 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34348275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32079775 |
GRCz11 | 16 | 32033805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCACCATTCCCTGAGGTTACGGACAGTTGCGGCTCCGGCTCCTGCTCAG[C/T]AGAGCAGCGGAGTTCAGTTTGACTGGGCTTCTCCTCCTCCTGAAGATGCT
Long Flanking Sequence:
GATTTTTCCTTTACCAAACTTGACTGATTTCCGTGAGAATCTTGGGTCCATGTGGGTTACAGTAGGTCTCCTGCAGTAAAATCTACCTTCTGCCACTTTTCTAAATGGTCAACTAGAAGTCAAGTTATTATTTGTTGCTCTAACAAGCAAAAAAAAAAAAAAGTGTTGCTACTTGTTTAAACTACTTGAGCTGAAATAACACAATTTTTTTTTTTTTTGTTTTTCGAGGACAACTTAATTGTTTTATGTTCAATCTAATTTGTATAAACAGTTTGGTTAACTTAATTGACTTGTGTTGGGACAACATGAAGGACTTGTGTGGAACCCAACATTTTTACAGTGAATAAGTCATGTTGCAACTATCCACGCTCTCCTCTGTCATACTTTGTAAAAGTGATTGCTTTCAAAAACATGTGTTTTCACCATCAGACTACCCTAGTCCCGATGTCTCCCACCATTCCCTGAGGTTACGGACAGTTGCGGCTCCGGCTCCTGCTCAG[C/T]AGAGCAGCGGAGTTCAGTTTGACTGGGCTTCTCCTCCTCCTGAAGATGCTGAAGACTCCAGTGAAACACGTAACCTTCGCGAGCTGCCGCTGCACATGAGTCTAAAGAGAGCAGTAAGGTAGACATCCATTATCTTCTTACAGCAACCAACTTTTACATTATCAAAACTGGAATGGAAAGGGAACAGTTAGTCTATTTCTCTGTCCAACGAATTTCTGACAGAAATAATCACAGAAATTCAGTTAAGAAAGTTTTCATATACAGTTGAAGTCAGAAATATTAGACTTCCTGTGTTGTTAGCCCACCCTGTATATATTATTTACATTCTGTTTAATGGAAAGGAGATTTTTTTCAACACATTTATAAACATGATCGTTTTAATAACTCATTTCTTATAACTGATTTATTTTGTCTTTGCCATGATGACAATCAATAATATTTACTAGATATTCTTCAGGATGCTACTATTCAGCTTAAAGTGACAATTAAAGGCTTAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17316
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 |
---|---|---|---|---|---|
ENSDART00000041054 | Nonsense | 152 | 732 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34350787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32082287 |
GRCz11 | 16 | 32036317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCTATTCCTGAGATTTCTGGTGATTCTCAACTTTCTGTCCTCTTTGT[T/A]AATCGCAGCGTTTGTGCTCATTCCCAGCATTGTGTTTCGCTCCTTGAACT
Long Flanking Sequence:
ATGTGGGAAATATAAAAAAAAAAGAATCAAACGTAAGCTAATAATTCTGACTTTGACCTATATGTTTTGTAAAATACAGCAATTTAAATATAGAACATTTTAATTAAAGACAATCAATAAATTGTGAATAATTTACTGCCTTTGTCTGAATGTAAACAATAAAAATGAACTGTAACCCGAGTTTGAGTTTTTCAAAACATGATAAAATCTATTACATATCATTTTTATGACCCAGCACTGTATAAACTATGCACAAAGATATAAAAGTGTTTAATTAAAAACATATGCTGTTCTCATTTAGTACACTGCTCGTCTAGTAAAAGAAGCTCTGGAACATGATAAAATGAAGTTAATAGCAACAATCAAACTAAATGTATTCTCATTTCCCCTTCATTTCCCCTTCCCACTTGTTTTGCTCATAGGTCACTTTGGTGGAGGAGTCCAGTCCTACTTTCTATTCCTGAGATTTCTGGTGATTCTCAACTTTCTGTCCTCTTTGT[T/A]AATCGCAGCGTTTGTGCTCATTCCCAGCATTGTGTTTCGCTCCTTGAACTTCAACTCCACCTCCAACATCACTATAGTCAACACAACAGGTAGGAACACAGTCTCCCTCCCAGACACAAACACAAAGACTGTCACACGTCAGTGCCTCTAATGGGAAGATTCTTGCCGTTTACCGGATACCACAATCCTCTTTGTTTGGCCTGAGATCATTTTGAGTATTCATGAAACCAGCAAAACCAGTCTGGCAACATCCATCTATTTATACTTTACAAAGTCTTTCAAATAAATTAAAAAAACAACAGCACTTATGGCATGTTTTGTTCTGAACCATCGGTTGATCTGGTTAATAATTCATTTCAGTAACTAATCATTAAAAGATAAATCACTTTACAAAGAATTTGACTATTGTGGTTAACAGATTAAATTAGATAATTTCTTCCTTGTTCTAGTAAGTTTTCATTATGTTGAGCAAAATTGATTCTTGCAGTTTGTGATAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15301
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 |
---|---|---|---|---|---|
ENSDART00000041054 | Nonsense | 255 | 732 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34353472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32084972 |
GRCz11 | 16 | 32039002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGCCTACCTGTTGACWGCAGCTTTCTACTTCCTCTTCTGCTTCTTTTG[T/A]ATAAYTATTAGGTGAGTCAGCTTTTGTCAGAGTTGTTAGAACATTGCTST
Long Flanking Sequence:
CTTAACTTAACTTAACTTAACTTAACTTAACTTAACTTAACTTAACTTTAAATGCAAAAATATAACTGATCCCAGACTTTAAATGGTAATGTAAGTGAACTGTATTAAATATGTAGCATTGTCAGCATTTTAGATGCCAGCTTTTACAATTGCTCAACAGCTCTTACAATTTTACAATTATACAACCTTTTCATTTAAACTTAAATGTAAATCAAATTAAAATAAAATGCACAATGTTTTTTTTTACAAAATGTATGCTACAGAAACTACTGTTCCAAGTTTATTTATTCTGACATGTAAGCTGTTTCTTTGTCGGTGAATTATTGCATAATGATCATTACTCATCAATGTCATCTCCTCCATCAGGGTTTTATGGAATATTCATACCTTTTTTATGGCTATTATAATAATACAATGATTGAAAGCGATGGCTTCTCTTACAACATCCCTCTGGCCTACCTGTTGACAGCAGCTTTCTACTTCCTCTTCTGCTTCTTTTG[T/A]ATAATTATTAGGTGAGTCAGCTTTTGTCAGAGTTGTTAGAACATTGCTGTAGAATTAAACTGACGTCTCTGTCTGTCCAACAGAATGGGTGGTACGGCTCGTGTTGTTGTAGAGACGGGTGCAGGAGCAGCCGGGGGTTACTGTATGCTGGTGTTTACAGGATGGGATCACGGTCTTCAAGGAGACCGCGCTGTAAAGCTTAAACAAAACAACGTTCGCTACAGGTTACAGGTCTGTACATGGGAAACCAAAACTAGAAATGAAATGCCCTGAGGTATTTTTTGATGGAATATGGATTGGATCTGCTTAACATTCAACTATCTAATATTTTACCAAATGGATAAAACAAAACATTACAAAATGACAATCTTCAAAGGTGATTTTTGCTATATGATAAGTCTGCTGAGAGGGCCGGTTCTTTTTTTTTCAAAATGTGGACGTTTTTGCAGTTACTCACCTCATTTTCTATTTAACTACAATGTTTAAATATATCATTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25020
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041054 | Nonsense | 427 | 732 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34358001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32089501 |
GRCz11 | 16 | 32043531 |
KASP Assay ID:
554-7544.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTGTAGGGCAGTGTTCTTGCGTTTGGTCAGTTTGGGTGTTTTGCTGTA[C/A]ACTCTATGGGAGCAGATAACCTGTAAAGGAGAGATTGGCAGTGATGACTG
Long Flanking Sequence:
TCTCTTTTTGACTCCTAAGTCTATGAAAACAACAGGATTTACGGGGCTACTGCTGCAGTACTTACCCTCCATGGTCATAACAGCAAGCAATTTTGTGGTGCCTTTACTCTGTGACAAGATTGCATTACTGGAAAAGTATTCCCCCAGTACCACGGTCATCCTAGCCTTGCTCAGGTTTGATCAACACTTGCATCCGCACTGAATGAAGATATCAAAGAGAACAAACAACAGAAATATAATAAGCACTTCTTGTTTAACCTTTGTTAGAGCCCTCGATGAGAGCTCTTTGCAGACCTTCATTAAATAGCTTACAAAAAGATGATTTTAAATGAAACCATGTCATATTCTCTTAACACTCACGCATTGTTCATCCATCCACCGCTCTCTTTGATTTGGTCTTTGTTGTAATTCTATTTTCTGCTCTTGCAATGCTGCTTATTCTCTGTTGTTCGTTGTAGGGCAGTGTTCTTGCGTTTGGTCAGTTTGGGTGTTTTGCTGTA[C/A]ACTCTATGGGAGCAGATAACCTGTAAAGGAGAGATTGGCAGTGATGACTGTAAACTCTGCGGTTATTATTATAACCAATACAAGGTAAACGAAATGTGCACTTATTCATTAATTGTTCAGATCAGATACGCTACCACTAGTTAGCATAAAAAGTCATTGTATAAAAATGGTTTGTTCTTCAGACAATCGAAAAAAATTATACTTAAAAGTGCTAATAATACTGACTTTAAAATGGTGTTAAAAATATTAAAATCTAATTTTGGTATTGCCAAAATAAAACAAATAAGAAGAAAAAATATTATAGGAAATACTGTGTAAATGTCCTTGCTCTGTTAAACGACATTTGGGACATATTTGAAAAAAAACAATTCATAGCAGGGCTAATCATTTTGACTTCACATATTATATTGTAATAAATATTTATATATTATAGTAAATGTCAATAAAGTTACCATATAAAGTCCATATAAAGGATTACATTGTTTGAATTTTAATGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36188
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 |
---|---|---|---|---|---|
ENSDART00000041054 | Essential Splice Site | 549 | 732 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34360247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32091747 |
GRCz11 | 16 | 32045777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCATTTATCAACACCCTCAAATTCGTCATCTTTTATTATTGCAAAAAG[G/A]TACCATGAGCACATCCTTCTCAGATGCACATATAAGTTTTTCAGTCATCT
Long Flanking Sequence:
GAGAAATGAAGAACTTCACACTTTTGAATAGTTTAAGTTTTAGGATTGATATCTTAGTGGTTATTGCCAAAAGTCTCACATTTTTGCAATTTTAGAAATGATTTTAGGTTCAATCCTTCTTTCAATCCTTCTGTTTAGTGCTGGGAGACGCGAGTTGGCCAGGAAATGTATAAATTAACTTTATTTGACTTCCTGATTACCGTTGCTACACTGATCCTGGTAGAGTTTCCACGCAGGTATGTTTCTTTCTTTTGTGTGTGTTGGTTCATACAAGTATTTAGTTAAATATCTAAGTCTGTTACTTTTATATGTTCAGGATCGTGGTGGATCATTGCTCATGCAAACTGAGCCAGCTGGTGGGACGGCAAGAGTTTCTGGTTGCCCCGAATGTTCTTGCTCTCGTTTACAGTCAAACGGTGGTTTGGACTGGAGCTCTTTTCTGTCCATTGCTGCCATTTATCAACACCCTCAAATTCGTCATCTTTTATTATTGCAAAAAG[G/A]TACCATGAGCACATCCTTCTCAGATGCACATATAAGTTTTTCAGTCATCTGCAGTCATTTTTCTTGCTTGTGTCAGATTACTCTCTTCCAAAACTGTCAACCGGCAACAAGAAACTTCAGATCCACCACCTCCAACTTCTTCTTTTTGTTGGTTCTGCTCTTTGGATGGATGTTGGCCAGTGTGGTTCTGCTTTACAGTGTTGCTAAGTGAGTGATTCTCCTCCATAAATGTTGGGAAATATTTCCATCTTCTATGACATCACTGTAAAACCTCAACTTTTGGTTCTTCCTACTGTATGTCAAGATTTATGATGAGTCTGTTTTAGGATCCATCCATCATATGGCTGCGGCCCTTTCCGTCTTGACCCAACTATGTGGGATGCTGTACCACAAGCTGTTAACATGCTAAGCACCACTAGTAGAGCTTTCCTGTTTTACATCGGCTCCCAGAAATGCTCTATTCCACTCTTCATCTTCTCTTGGTTTGTATAAACAGCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9506
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 |
---|---|---|---|---|---|
ENSDART00000041054 | Nonsense | 573 | 732 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34360394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32091894 |
GRCz11 | 16 | 32045924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACCGGCAACAAGAAACTTCAGATCCACCACCTCCAAYTTCTTCTTTY[T/A]GTTGGTTCTGCTCTTTGGATGGATGTTGGCCAGTGTGGTTCTGCTTTACA
Long Flanking Sequence:
ACGCGAGTTGGCCAGGAAATGTATAAATTAACTTTATTTGACTTCCTGATTACCGTTGCTACACTGATCCTGGTAGAGTTTCCACGCAGGTATGTTTCTTTCTTTTGTGTGTGTTGGTTCATACAAGTATTTAGTTAAATATCTAAGTCTGTTACTTTTATATGTTCAGGATCGTGGTGGATCATTGCTCATGCAAACTGAGCCAGCTGGTGGGACGGCAAGAGTTTCTGGTTGCCCCGAATGTTCTTGCTCTCGTTTACAGTCAAACGGTGGTTTGGACTGGAGCTCTTTTCTGTCCATTGCTGCCATTTATCAACACCCTCAAATTCGTCATCTTTTATTATTGCAAAAAGGTACCATGAGCACATCCTTCTCAGATGCACATATAAGTTTTTCAGTCATCTGCAGTCATTTTTCTTGCTTGTGTCAGATTACTCTCTTCCAAAACTGTCAACCGGCAACAAGAAACTTCAGATCCACCACCTCCAACTTCTTCTTTT[T/A]GTTGGTTCTGCTCTTTGGATGGATGTTGGCCAGTGTGGTTCTGCTTTACAGTGTTGCTAAGTGAGTGATTCTCCTCCATAAATGTTGGGAAATATTTCCATCTTCTATGACATCACTGTAAAACCTCAACTTTTGGTTCTTCCTACTGTATGTCAAGATTTATGATGAGTCTGTTTTAGGATCCATCCATCATATGGCTGCGGCCCTTTCCGTCTTGACCCAACTATGTGGGATGCTGTACCACAAGCTGTTAACATGCTAAGCACCACTAGTAGAGCTTTCCTGTTTTACATCGGCTCCCAGAAATGCTCTATTCCACTCTTCATCTTCTCTTGGTTTGTATAAACAGCCCTGCTACATACACTGCTGGTCAAAAGTTTGGGGTCAGTAGGATTTTTAAATGTTTTAAAATAAGCTTATCCTGCTCACCAAGGCTGCATATATATCATCAAAAATACAGTACAAATTGTACAATTGTGAAATTTCATTGCACTATAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18068
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 |
---|---|---|---|---|---|
ENSDART00000041054 | Essential Splice Site | 593 | 732 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34360455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32091955 |
GRCz11 | 16 | 32045985 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTTGGATGGATGTTGGCCAGTGTGGTTCTGCTTTACAGTGTTGCTAA[G/A]TGAGTGATTCTCCTCCATAAATGTTGGGAAATATTTYCATCTTCTATGRC
Long Flanking Sequence:
CACTGATCCTGGTAGAGTTTCCACGCAGGTATGTTTCTTTCTTTTGTGTGTGTTGGTTCATACAAGTATTTAGTTAAATATCTAAGTCTGTTACTTTTATATGTTCAGGATCGTGGTGGATCATTGCTCATGCAAACTGAGCCAGCTGGTGGGACGGCAAGAGTTTCTGGTTGCCCCGAATGTTCTTGCTCTCGTTTACAGTCAAACGGTGGTTTGGACTGGAGCTCTTTTCTGTCCATTGCTGCCATTTATCAACACCCTCAAATTCGTCATCTTTTATTATTGCAAAAAGGTACCATGAGCACATCCTTCTCAGATGCACATATAAGTTTTTCAGTCATCTGCAGTCATTTTTCTTGCTTGTGTCAGATTACTCTCTTCCAAAACTGTCAACCGGCAACAAGAAACTTCAGATCCACCACCTCCAACTTCTTCTTTTTGTTGGTTCTGCTCTTTGGATGGATGTTGGCCAGTGTGGTTCTGCTTTACAGTGTTGCTAA[G/A]TGAGTGATTCTCCTCCATAAATGTTGGGAAATATTTCCATCTTCTATGACATCACTGTAAAACCTCAACTTTTGGTTCTTCCTACTGTATGTCAAGATTTATGATGAGTCTGTTTTAGGATCCATCCATCATATGGCTGCGGCCCTTTCCGTCTTGACCCAACTATGTGGGATGCTGTACCACAAGCTGTTAACATGCTAAGCACCACTAGTAGAGCTTTCCTGTTTTACATCGGCTCCCAGAAATGCTCTATTCCACTCTTCATCTTCTCTTGGTTTGTATAAACAGCCCTGCTACATACACTGCTGGTCAAAAGTTTGGGGTCAGTAGGATTTTTAAATGTTTTAAAATAAGCTTATCCTGCTCACCAAGGCTGCATATATATCATCAAAAATACAGTACAAATTGTACAATTGTGAAATTTCATTGCACTATAAAATAACTGTTCAAAAGTAGATTATAATTGAGTTTATTAATGTATTCCAGTGATTTTAATCATG
Associated Phenotype:
Not determined