ZMP
tmtc2
Ensembl ID:
ZFIN ID:
Description:
transmembrane and TPR repeat-containing protein 2 [Source:RefSeq peptide;Acc:NP_001124075]
Human Orthologue:
TMTC2
Human Description:
transmembrane and tetratricopeptide repeat containing 2 [Source:HGNC Symbol;Acc:25440]
Mouse Orthologue:
Tmtc2
Mouse Description:
transmembrane and tetratricopeptide repeat containing 2 Gene [Source:MGI Symbol;Acc:MGI:1914057]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20223 | Nonsense | Available for shipment | Available now |
sa40235 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33405 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33404 | Essential Splice Site | Available for shipment | Available now |
sa18174 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20223
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 |
---|---|---|---|---|---|
ENSDART00000067261 | Nonsense | 48 | 844 | 2 | 12 |
ENSDART00000146417 | Nonsense | 21 | 817 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 10059629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10996256 |
GRCz11 | 4 | 10995105 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACCAACCAGGACCTCCTACCGGACACCCCATGGACGAACATTCTATA[T/A]GATGACTTCTGGGGCACTTTGCTTACCCACAGCGGCAGCCACAAGTCTTT
Long Flanking Sequence:
AAGCATTAAATTAGAATAAATAAATACATATTTGTTTGTAATAAAACCCACCTGTAATAGATCTGTAAATTATACGATATTATAAATAGTAAATTGATTGTATATTAAATGTATTGCATTATTGTTACTGGTGATTGGTGATGTTTATTCAGTAACAAATGAAATCACTATTGTTTTTTAATTAATTATTCCTTATTAAATAGCACACATATTTCACGTTAGTGTTTGTAAAGTATATTTGTTAAAAAGATTAATGGAATAAGAAAACTTCAGCTGAAGTCCTCCACTACTTAAGGTTATTAATCAACTGAAAATATGCATACATAAACCTTTACGCAAAAAAAAAGAAGTCATATCCTATTCATAAATATCATTCTAAAGGCTGTATTTTTTGCATTTTTTAATCATGTGATTTCCTCATTCTCTCTCCATCTCTGTAGTCGAGCAATCAAAACCAACCAGGACCTCCTACCGGACACCCCATGGACGAACATTCTATA[T/A]GATGACTTCTGGGGCACTTTGCTTACCCACAGCGGCAGCCACAAGTCTTTCCGTCCTCTCTGCACCATCTCTTTCCGCCTCAATTATTTCTTGGGTGGCCTGGATCCCTACGGCTTCCACCTGTTCAACGTGGGCCTTCACTGCTGCGTCACTGCCCTCTTCACTGCATTCTGTCGCCCCTTGCTGGGTGGAGGACCTTGGAGTCTGTTGGCAGGACTGCTCTTCGCCTCTCATCCCATACACACCGAAGCGGTAGCTGGGGTCGTGGGCCGAGCAGATGTTGGAGCAGCCTTTTGCTTCTTATTGTCACTTCTCTGTTATTCCCAATATTGCCGTCTCAGGCATAATGCAGCACACTCGAGTCGGGTTGCGTGGCGTGCTGGATCTTGGCTTGCTGGAAGCCTGGGTGCTGCTGCAGCTGCTTTACTGTGGAAGGAGCAGGGGGTGACTGTTCTGGCTGTTTCAGCTGTTTATGATGTCTGTGTTGTGCATCGGCTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40235
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 |
---|---|---|---|---|---|
ENSDART00000067261 | Essential Splice Site | 502 | 844 | 3 | 12 |
ENSDART00000146417 | Essential Splice Site | 475 | 817 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 10052315)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10988942 |
GRCz11 | 4 | 10987791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGAGGAGATGCTCTACAGATCTGGCATTGCTGTAAATCCTGCTAAAG[G/A]TGGGTTTGGAGAGCGATGATAATAATAAAGCATTATTATTGTATAAATTT
Long Flanking Sequence:
AAACCCACCGCTACAGGCCACTAAAATCAACGAAAGCAATGGAAAATCACATGTGAGCAACGGAAAATATGCAACTAATGGATGCAGTCATAAGCACAATGACAATCACTACAGGGACTTAAACCTAAAAAGTAACGGATATCATAATAAATCCCTCAAAGTTTCTCCAAAAACACTTCCAGCCACAGAGAATGTGGTGGTGTTTTCTCTTGGGCTGCTGGTTTTGCCCTTCATCCCTGCCACTAATTTGTTCTTCTATGTGGGTTTTGTGGTGGCCGAGCGGGTGCTGTATATCCCCAGTATGGGCTTCTGTCTGCTCGTGACCGCCGGGGTGAGGAGCTTGTTTGTCCGTTGCCGGTCAAAAAGCTTCAGAGCTCTCCTGCTGACCTGTACTGCAGGTCTGGTGCTTCTCTACAGCCTGAGGACTGTGAGGAGGAACCAGGACTGGAAGAGTGAGGAGATGCTCTACAGATCTGGCATTGCTGTAAATCCTGCTAAAG[G/A]TGGGTTTGGAGAGCGATGATAATAATAAAGCATTATTATTGTATAAATTTAATATCTAGACAATAAACATTTAATGTAATTTCAAATCTATTGGTAATATACACAGTATATACAGTCAAAATGATTAGCCCTCTTGTGAATTCTTTTTTAAATATTTCCCAAATGATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCTATAATATATTTTTTTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCCAGAATAGAATCAGTTTTTAATTTTCTTAAAATCATTTTAAGGTCAATATTATTAGCCACCTTAAGCAATATTTTTTGCTTGTCTACAGAACAAACCATTGTTATACAATAACTTGTCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTATGCTGAATGCTAGTATCTTGAAGCATATCTAGTCAAATATTATGTACTGCCTTCATGGCAAAGATAAAATAAATTAGTTATTAGAAATGATCGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33405
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 |
---|---|---|---|---|---|
ENSDART00000067261 | Nonsense | 557 | 844 | 5 | 12 |
ENSDART00000146417 | Nonsense | 530 | 817 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 10048968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10985595 |
GRCz11 | 4 | 10984444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGTTTGCTGCTACAGGAGAACGAACGGTTTTCTGAGGCTCTTCACTA[T/G]TATAAACTGGCCATCGGGAGCAGACCGACCCTGGCCTGTGAGTTCAGCTC
Long Flanking Sequence:
AAATAAAATAAACATTAATTTTGCTACTTACATGCTTCCATACAGTAACAATGGAGATAAAATTAATTCTCAATTTAATAGTCATATAACTTCACGGTAATGCTTTAAATCTTGTGCTGTATTTGCAAGCTGCATTTCTCAGAGATGTAATGTCAGACACAATGCACTTGATGAAGCTAGTGACGTCACTGGGAAAAAGCATTGCTTAAAAAGCATTGCATGCGGCTCAGATTGCAACTGCACTTAGTCTGCATCTAGACCCCTCTCAATTAATAAGCTAATATTGTTAGTTAATGGTTTATAAATACTGTGAATTGTAAACAAAAGGCTACCGTATATTGAGCTAATAGCAGTTTGTTAACGGGATGAATTGTGACTTAAATTGTGACCTACTTCAAATCTGACTTCTCATGCTTTAAAACGGTCTGTGTTTTTTTTTTGATTTAACACAGTGGTTTGCTGCTACAGGAGAACGAACGGTTTTCTGAGGCTCTTCACTA[T/G]TATAAACTGGCCATCGGGAGCAGACCGACCCTGGCCTGTGAGTTCAGCTCTAAATATTTCACTTTATTGACCGTCAGAATGAGTCTCTTACTTATTGTCCTATTTCTCACAGCTGCATACTTGAATGTGGGCATCATTCTGGTCTCCCAGGGGAATATTGAAGAGGCCAAGCGGACTTTTCACACATGCGCGGACATCCCAGATGAGAATCTGAAGGACCCTCATGCACACAAAAGCTCTGTGACCAGCTGCTTGTACAACCTTGGCAAACTGCTGCATGATCAGGGCCAGCATGAGGTAGAGCTCAGCTCATTCATTGAGGATTATTGAAGTCTACATGCTCAGTTTAAATTAGATGTGTTTTTGTCATTTGTTTATTATTAAGCAGTTTTCTTATTAGATACAGACAAGCTGATTTTTGTGTGTCATCTACAGGAAGCGCTGTCTGTGTATAAAGAGGCAGTTCGGAAAATGCCACGACAATTCGCACCACAGAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33404
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067261 | Essential Splice Site | 698 | 844 | 8 | 12 |
ENSDART00000146417 | Essential Splice Site | 671 | 817 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 10046798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10983425 |
GRCz11 | 4 | 10982274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCATATTCCTGCCCACCTGACCTATGGAAAGCTACTGTCTATTATGG[T/G]GAGTCAATCTGATTAGAACATTATTGACACGATTGTGTTCATGTTCATAT
Long Flanking Sequence:
AGTGACTTTACTGCCCATTCAAGGCGTACATTAATAGTACATAGGAGATTCTTAGGGAACCAAAGGCATGACCTTGGTTTTGAAAGTTTAACTTGTAGTGTTTTGGTTTCTTTCCTTTCATTAATATTGTATGAAGGAGACTACAGCGGTCTTTTTCAATCTCACAACAGGGTTTACTTTTGATTCTGGACATCAGGCAGTATAAGATCTTTTTTTGTGTTAATGTGTAGTGGTTTTTTGTCTGTGAATCAATTTTGGGAAAATCAATATCTTAAAATGTTTTCAATCACTGTTCAAAATATAACATAGTGATGCATGCCTTTCAGTGCACTTGGATTGTTAACAAGTTTAGGTGATTTTCTGATTTTGGCCTACAGGTGAGGCGTATATGAGGCTGAATATTCTAGAGGAAGCTGGACATTGGTATAGAGAGTCACTAAAGGCCAAACCAGATCATATTCCTGCCCACCTGACCTATGGAAAGCTACTGTCTATTATGG[T/G]GAGTCAATCTGATTAGAACATTATTGACACGATTGTGTTCATGTTCATATTAGTATAATATAATTAGGCTCTTTCATCCATCCATTTATCATTTCTTTTTCCTTTCTGTCCTTTCTATGTGGCCATCCGTCTATTCATCATCCCTTTTTCAATTCATTCTTCAGACAATTACCATCCATCCGTCCATTCATCTAATTATCCATTCATTCATGCATTTTCCTGTCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATTTTCCTGTCCATCCATACATCCATATATCAATCCATTCATCCATTCATTTTCCTGTCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCTTTTTTCTGTCCATCCATCCATTTTCCTGTCCATCCGTCTATCCATCCATCTATCCATCAATTTTCCTGTCTATCCATCCATAAATCCATCCATCCATCCATCCATCCATCTATCCATCCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18174
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067261 | Essential Splice Site | 726 | 844 | 9 | 12 |
ENSDART00000146417 | Essential Splice Site | 699 | 817 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 10044238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10980865 |
GRCz11 | 4 | 10979714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGCRATAGAGCTGGANCCTGCTAGAGGAAACTGCTATATGCATTATGG[T/C]RGGACATTAATTRGAMAACTGTACTCACTTAAAACAGTTGGGTTAATNNT
Long Flanking Sequence:
ATTAAGTATTATAGACCTATACATTTTTGATAAGCGCTTTTGGATGTAGTTGAATGCTTTTCAGCAACCGCAGCCAACGAGAGCATGCAATACTACGGCTTTCCAAGTTATTTCTTTTATCTAAAGTGTTTAGCACAGAAGCGTTCATTGTAGCAAGTCTAATATGACCGCGCTGTTTATGACAAGACTGTTTGCTAAGGTAACACCAACATGGAAGCAATCAGCGCTGAACCATAAAGAAAGTGAGACAACTGCTCATTAAACATGAAGAAACGAGTACACAAGTGCGCTTACTTTCCCACGCTATGATAACATCTAACATCATACGTTGTGCAAATTTAAAGCATCCGTTTACGACCGTGCTTCTTCATTAGTGACGGTGGGTGCGGGCTTAATTGTTTCTTAATTTCTCCACAGGGACAGAAGTCTGAAGCAGAGCGTTACTTCCTGAAGGCGATAGAGCTGGATCCTGCTAGAGGAAACTGCTATATGCATTATGG[T/C]GGGACATTAATTAGACAACTGTACTCACTTAAAACAGTTGGGTTAATAATAACCCAACAGGAAACCCAACAATGTTTTTTTTTTTTTTCTTAAGAACCGCTGTTAGGTTATTTTAATCCAATATATTAGGTTGTTTATGACGATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATGATGATGATGATGATGATGATGATGATAATAATAATACTAACAATAATAATAATAATAATACTAACAATGATAATAATAATAATAATAATAATAATTGTAATAATAATAGTAATAATGATGATAATAATAATAATAATAATAATTGTAATAATAATAATAATAATAATAATAATAATAATAATAATTGTAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAACAACAATAATAATAATAATAATTGTAATAATAATGATAGTAATAATAATAATAATAATAATAATAGTTATTG
Associated Phenotype:
Not determined