ZMP
tmcc3
Ensembl ID:
ZFIN ID:
Description:
transmembrane and coiled-coil domains protein 3 [Source:RefSeq peptide;Acc:NP_001038278]
Human Orthologue:
TMCC3
Human Description:
transmembrane and coiled-coil domain family 3 [Source:HGNC Symbol;Acc:29199]
Mouse Orthologue:
Tmcc3
Mouse Description:
transmembrane and coiled coil domains 3 Gene [Source:MGI Symbol;Acc:MGI:2442900]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13798 | Nonsense | Available for shipment | Available now |
sa33475 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26307 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13798
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 |
---|---|---|---|---|---|
ENSDART00000066946 | Nonsense | 203 | 456 | 2 | 4 |
ENSDART00000122881 | Nonsense | 223 | 476 | 2 | 4 |
ENSDART00000146658 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 4 (position 24846425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25770094 |
GRCz11 | 4 | 25759292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCTGACAACATCGCYCACCTGAAAAGCTCAATGGAGACTGGGTCTGGGT[T/A]GCAGGCGGARGCRGGAGCCCGGATTTTRAGYGGCAGCGCCACAYTGACCC
Long Flanking Sequence:
CGGCCCGCGATCACGATTTGGCCTGGACAGCCTCCAACAAAAGATCCTCAAAGTAAAAGAACAGCTGCGAATTGAGCAAAACCTACAAGATGAGAACGTGGCTGAATATCTTAAACTCATCAACTGTGCAGACAAACAGCAGAGTGGCCGTATTAAACAAGTGTTCGAGAAGAAGAACCAAAAAACTGCCCACAACATCTCCCAACTCCAGAAAAAACTTGAGCAGTATCAGCGCAAGATGAAAGAGTCAGACATCTCCAACGGCACCAAACACGCAACGCCAAAAGACAAAGACAACGACAACCTCAAAGAAACTGTGGTCACCGGAAGCGGACGACATCCACATTTGGACAAAGTCAAAACCATCGGCCCTGGAGTTTCTTTATCTCCGCCGTTCTTCTTTAGCAAGCCCAGGGAAATCGCAAACCTTATTCGCAACAAATTCGGCAGCGCTGACAACATCGCCCACCTGAAAAGCTCAATGGAGACTGGGTCTGGGT[T/A]GCAGGCGGAAGCGGGAGCCCGGATTTTAAGCGGCAGCGCCACATTGACCCCGAAACCTAAATATCCGAGTGATGACGAGTGTTCCACCGAGACGTCAGTTTCTGTGGAAAGTAATGGGCAGGTGACTGGATCGGGCACCACCGGGCAACACAGCGGATCTGCAAGAGAAGCTGAAGTCAATAGCCGACTGCTGGAGGCCTGTGAGGAGATCCGGGAGTTGAGGGAAGCTCAGAGTCTCCTGGCTGACGACATCGAGACACTCAAGAACCAGTTTAAATGTGAAGTGGAGAACATCACGCAGACACTACAAGAGGAGCGATACAGGTCAGTTAATAATTACTGTTGGTGGTCTCGTGAGTGTGGATTCATTTTGGCACATATAGAACTTTAAGAGTTCCCTCTTAGATATTGCTTGATACTGACAGCAGGTTTGGCATGCTGTCCCGGGAGAGAACCCTGAGATAATTGAGCCCAGGGCTCCTGCCTGGTCAATTAGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33475
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066946 | Nonsense | 212 | 456 | 2 | 4 |
ENSDART00000122881 | Nonsense | 232 | 476 | 2 | 4 |
ENSDART00000146658 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 4 (position 24846398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25770067 |
GRCz11 | 4 | 25759265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAATGGAGACTGGGTCTGGGTTGCAGGCGGAAGCGGGAGCCCGGATTT[T/G]AAGCGGCAGCGCCACATTGACCCCGAAACCTAAATATCCGAGTGATGACG
Long Flanking Sequence:
CAGCCTCCAACAAAAGATCCTCAAAGTAAAAGAACAGCTGCGAATTGAGCAAAACCTACAAGATGAGAACGTGGCTGAATATCTTAAACTCATCAACTGTGCAGACAAACAGCAGAGTGGCCGTATTAAACAAGTGTTCGAGAAGAAGAACCAAAAAACTGCCCACAACATCTCCCAACTCCAGAAAAAACTTGAGCAGTATCAGCGCAAGATGAAAGAGTCAGACATCTCCAACGGCACCAAACACGCAACGCCAAAAGACAAAGACAACGACAACCTCAAAGAAACTGTGGTCACCGGAAGCGGACGACATCCACATTTGGACAAAGTCAAAACCATCGGCCCTGGAGTTTCTTTATCTCCGCCGTTCTTCTTTAGCAAGCCCAGGGAAATCGCAAACCTTATTCGCAACAAATTCGGCAGCGCTGACAACATCGCCCACCTGAAAAGCTCAATGGAGACTGGGTCTGGGTTGCAGGCGGAAGCGGGAGCCCGGATTT[T/G]AAGCGGCAGCGCCACATTGACCCCGAAACCTAAATATCCGAGTGATGACGAGTGTTCCACCGAGACGTCAGTTTCTGTGGAAAGTAATGGGCAGGTGACTGGATCGGGCACCACCGGGCAACACAGCGGATCTGCAAGAGAAGCTGAAGTCAATAGCCGACTGCTGGAGGCCTGTGAGGAGATCCGGGAGTTGAGGGAAGCTCAGAGTCTCCTGGCTGACGACATCGAGACACTCAAGAACCAGTTTAAATGTGAAGTGGAGAACATCACGCAGACACTACAAGAGGAGCGATACAGGTCAGTTAATAATTACTGTTGGTGGTCTCGTGAGTGTGGATTCATTTTGGCACATATAGAACTTTAAGAGTTCCCTCTTAGATATTGCTTGATACTGACAGCAGGTTTGGCATGCTGTCCCGGGAGAGAACCCTGAGATAATTGAGCCCAGGGCTCCTGCCTGGTCAATTAGCATGAAAAGAGGTTCTGTGATCAAGTAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26307
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 |
---|---|---|---|---|---|
ENSDART00000066946 | Nonsense | 349 | 456 | 3 | 4 |
ENSDART00000122881 | Nonsense | 369 | 476 | 3 | 4 |
ENSDART00000146658 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 4 (position 24845368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25769037 |
GRCz11 | 4 | 25758235 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAAACAGGAGCTCGCGAGCATCGAGGAGAAGATGGCCTATCAGGCTTA[T/A]GAACGAGCTCGAGATATACAGGTATAATCAAACATGCATGTTCAATAGCA
Long Flanking Sequence:
GGAGATGGGGTGGATGGGGGATTTTTGAAGTAGGGCGAAAATGGGCTATTTATTGTAGGCTAGGATTAATCTGATCGTTGTATCAATGATTGCGGATGAGAGACCAGCCACGATTAATCATATCACATGGCCCTCTTGAAATTAGTTTAAAAAACTTCACTTAGCAGGCATGCGCAATGCACCATATCAGCTATTGGCTAGAAATGTTAACGCTTCTAATGCAATCAAATACTTTTCTTGCCTCTTGAGTCCATTCAAATCCTGATTTATAGATATTTAAAGTATAAACCAATATTAACATTAAAACCTATTACCTAAGATCCTACTAAAAAAAAAAAAACAGCACATTGGCTTAAAGTAAATTTTGATGTTGTTGTTTTTATAAGGTGTGAGCATCTAGAAGACCAGCTGAACGACCTGACAGAGCTCCATCAGAATGAAACCGCAAACCTCAAACAGGAGCTCGCGAGCATCGAGGAGAAGATGGCCTATCAGGCTTA[T/A]GAACGAGCTCGAGATATACAGGTATAATCAAACATGCATGTTCAATAGCACTTCTGGTGCTGACATCATTTTCATTGATCTGGGGCCTGCACTATCCCAGCAAGCACGGAACATTAACATGACGTCAGGTTGACCTTGAACCCCAACGTCGTGGGATGTTGCATTTTTTTTGGAAATAAAGATCAGGTTGATGTCAGGCTGACCTCATGATGTTGTGTGGGCGTTACCAATATGATGTTTATCAGACATTGGATTTTGGTTGCCTTACCTGATGAATAAATGTCAGTATTTGACATCAATATGACGTTGGTTTAAGATTTGGGCTCATGGATTTGGCTCGTGATGTTGGATTTTGGTCACTTTCCAACAGAACCTTAAATCAACTAAAAAACTTGTCATTTGATGTTGTTATTATATGTTAAAAGAACATTGTCTTTAGATGACTGTGACCTAAATCTAACCCAAAATTAACGTCTTATGATGTTGTGTGTCTGCTGGGA
Associated Phenotype:
Not determined