ZMP
tekt2
Ensembl ID:
ZFIN ID:
Description:
tektin 2 [Source:RefSeq peptide;Acc:NP_001017432]
Human Orthologue:
TEKT2
Human Description:
tektin 2 (testicular) [Source:HGNC Symbol;Acc:11725]
Mouse Orthologue:
Tekt2
Mouse Description:
tektin 2 Gene [Source:MGI Symbol;Acc:MGI:1346335]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13527 | Nonsense | Available for shipment | Available now |
sa23460 | Nonsense | Available for shipment | Available now |
sa25088 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13214 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13527
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 |
---|---|---|---|---|---|
ENSDART00000046527 | Nonsense | 17 | 429 | 2 | 11 |
ENSDART00000059358 | Nonsense | 17 | 425 | 2 | 10 |
ENSDART00000135102 | None | None | 284 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 11268602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10727831 |
GRCz11 | 19 | 10646756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGGCCACCTTAAGCTCGAAGCCRGCCTCACGCTACAGTGTTTCTGACT[G/A]GGCAACWAACAATAAGCAAATSTCAGATACTGCTGAACACAAACGCAATG
Long Flanking Sequence:
AAATAGAGTGGATTTCTATGGAAGACTTGGCTGCTATATGTCTGTAGCCATTAATATAAAATCAAAATGCTTTCCAGAGCACGAAGCACACAAGTTTGGACATTATTCATTGTAGCATTAAACATTTAGTGTAAATAAACTGGAGGTAATGGATTCTGGTAATCTTTAATTCTGCCTTGTCAAATTTGTTCACCTAGTGTCTCTCTGTGTCTGTTCAAATACAACTGTTCACATTATTTTCTAAAATACTGGAGACTATAGTGTAGACATCAGAATAATTAACCGAATAAGCATTACTGACAGTTTGATCAATAATAATAATATGAGTGAAAAATAACTGAATAGTAAAGCACATAGAATCAGAAAGCTAACCTTGTTTTTGTTTACCAGAACTATTTTTTTTTCTTCATGTTGTCTTGTTTCTATGGCATCAGATACTGTGTCAGCAAACATGGCCACCTTAAGCTCGAAGCCAGCCTCACGCTACAGTGTTTCTGACT[G/A]GGCAACTAACAATAAGCAAATGTCAGATACTGCTGAACACAAACGCAATGTTTCACACGAGATACGACAGGAAGGAAGAGCTCTGCGTAACGAAACGACCAATAAGGTAATGTTATTAAAGGGATAGTTCACCCCAAAATTAAAATTTACTCACCATTTACTCGCAGTCAATTGGTTCTCAAAATTTACGCTATATAGTTTTATAAATATAGCGTATTTTATAATAGTCTTCTTTTAAACACAAAATACATCCAATAATACTACAGAAGTCAATTTCCATTATTCTTCAGGATATATTCCTTTGTGTTCAACATTAGAAAGAAACTTAAACAGGATTTGAACAAGTGGAGGATGAATAAATTATTGTAGAATGTTCCTTTTGGCTGAACTATCCCTTTAGGATGAGGGTGGGAAGTTGTTTGGCAGAATAAAAAAGGATGTATCAAACAAATTTTTTGCATGACAGACAAGCTGGAATGAGTATGACAGCACCCGGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23460
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046527 | Nonsense | 161 | 429 | 4 | 11 |
ENSDART00000059358 | Nonsense | 161 | 425 | 4 | 10 |
ENSDART00000135102 | None | 16 | 284 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 11265925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10725154 |
GRCz11 | 19 | 10644079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGATGGAGCACAACGTGTCCTTCAACAGTGCATCGATCAGGCCTTTGAA[C/T]AGCTGTGGTAAGAACATTCAGATTTCAGGTTGGAAGCCCTCACTAGTTTG
Long Flanking Sequence:
TTTGATTTATGTGCGCACAAAAGACTTTTTGTTGAATGATAATATTCTAATTGAACCACTGACGACTTATGGTCTATATTCAGAATGTTTTTTGGTATTGTTCTTGAATTTGAATGAGTCAGGAACATTGTTGTTTATGGAGGATGAGGGAGCTCTCAGATATCATTTAAAATATCTTAATTTGTGTTCTGAATATGAACGAATGTCTCAGGGGTTTGGAAAGACATGAGGTGAGTAATTAATAACAATTTTCACTCAAAGAGAAAGATAATACCTCCTCCTCATTTCACAAAATTGTTAAGTCCAAGGAGGAGATGGAACGAGCCCTTGCAGCCACAGTTCTGCCTCTTGAAGTGACCGCCGAGTGCTTGAACCTGAGGGAAGGCCGTCGTGGGAAGGAGCTGGTCAGTGACCCAGTAGAAGCTGAACTTAAGAAAGAAGTTGAGGTGATTGATGGAGCACAACGTGTCCTTCAACAGTGCATCGATCAGGCCTTTGAA[C/T]AGCTGTGGTAAGAACATTCAGATTTCAGGTTGGAAGCCCTCACTAGTTTGAAGATTAGCTCAATTATAAACCCAATATTAAACTTAAAAACAGCTTGTTTAAAATGAGTTGAAACAACACAATTCTTAGTTTTTTTGAGGTGAACAACTTAATTTAATTTGTAAAATGATTAAGTTAACTTTTGGGACAACATGAAGTGTTAGGACAATGGTTTGTGTTCAGACAACATGAAGAATTGGTGTGGAACCCAGAATTTTATACAGTGTACACTCAAAAACTACTTTAAGGTACGGTACTTTAAACCCCTGCTACCCCTTCAGGTGGTGGGCCTGCAGGAAAATGGTCCCACGTCTCTTCTTTGGACTAAGCTCTCACCAGGGAGCTCGAGGGTTCTTGGGAGTATGCCCAACCAGTCCACATGTGTCTTGTGGACTTGGAGAAGGCATTCAATTGTGTCCCTCGTGGCATTCTGTGGAAGGGACTCTGGGGTCAAAGGCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25088
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 |
---|---|---|---|---|---|
ENSDART00000046527 | Essential Splice Site | 215 | 429 | 6 | 11 |
ENSDART00000059358 | Essential Splice Site | 211 | 425 | 5 | 10 |
ENSDART00000135102 | Essential Splice Site | 70 | 284 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 11264072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10723301 |
GRCz11 | 19 | 10642226 |
KASP Assay ID:
554-7445.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATCACCTGAGATCTCACTGAAGCCTAACCCTACAAGAGTGCCCCCTGG[G/A]TGAGTTTATGAGTAAACTATAAGCAAACATGCTATCTTTGCTTAATATTG
Long Flanking Sequence:
TCGGCTGGCCTGGCAATGCCTCGGGAACACCCCTGGAGAAGCTGGACGAAGTGTCTGGGGAGAGGGAAGTCTGGGGTTCTCTCCTGAGACTGCTGCCTTCACGACGCGGCCCTGGTAAAGCGGTTGAAAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGATTAAGTTAACTTTGTTTTAACAATTTTGCTTTAACAAAATTTTAGCAATTTAATTAATTTGTGTTGAGACAATATAAAGGATTTATGTGAAACCCAGCATTTTTTACAGTGTACTTGACCTTTGACTGTTGAAATATGATGAAAATAAGCTTGTTGCTAATCTCAGCAGATCTTCTCAGTCGTCTACAGGAAGCTCGGCAACAGCTGACCATTGACCTTCAGGATAAAATAGAGGCCCTCGATGTGGATATGTCATGCTTATCTCTTACTATACAATCACCTGAGATCTCACTGAAGCCTAACCCTACAAGAGTGCCCCCTGG[G/A]TGAGTTTATGAGTAAACTATAAGCAAACATGCTATCTTTGCTTAATATTGTTTAAAAAAAAACAACAACAATAAACAAGTTATTTATCTGGGATTTTGTCGTCTTTTTTTGCAGTTCCACCAATCCCCAGCAGTGGGAGCAGTTCAGCCGGTACAATATTAGCCGGGCAAGGGAAGAGATGCAGGTCTCAGTGCAGATAAGAGAAAATAACAGCATCACAAGAGCACAGGTGCAAGACCTGGCCTACAGATTTAAATTCAACATGTTTACGCATTTTAAAGCTCAGTTTGAAGGAACTTTTAGGTTAGAACCAGTGTTGGGTGTTATTAGTTACAAAGTAGTTACTAGTCACTGTAATTAAATTACTCATCCATTGAAAAATATAAGCAGTGGTCATTTTTAGGGTCAGTGAGTTGAAGTTACTTATATACTTGCCTTTTAATTGCTATAAATAAAATCAATGGTTCTGTAAAATTAGAGAAGCCAATAATTTAGTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13214
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046527 | Essential Splice Site | 290 | 429 | 9 | 11 |
ENSDART00000059358 | Essential Splice Site | 286 | 425 | 8 | 10 |
ENSDART00000135102 | Essential Splice Site | 145 | 284 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 11260340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10719569 |
GRCz11 | 19 | 10638494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAATGTTTATTTATTTGTTGATATTTCGATATGTGGGCYSATATGTTTC[A/T]GACTCAAGATGAGATTGCTGAGCTGGAGAAGGATATCATTGGCYTGGAGG
Long Flanking Sequence:
GATATTTTCCCTTGTTCTGTCCATTCTATGGTAAATCTAGAGATCATTGTGTGTGAAAATCCCAGTAGATCAGTAGTTTCTGACGTAAACAAGACCAGCCAATCTGGTACCAACAACCATGGTAACTTTCTAAGTCATTTACATCACTTTTCTACCACATTGCAATGGTCAGTTTTATAGTCTTGAGCATGGGTGTAGAAACATGTGCTTGGAGGGCCTATGCTTCAACTAATTGTAAGATGAATTTAGAGAACAGTGGACCTGCAAAGTAGGATTTGTCACCCAATATCTAGCGCCAATGTGATTGGCTGATTAGATATTTCCATTAATAAGCAATGAAAGTTGTTTTTAATAAGAGTGGTGTTCATTATAATGCAGTGTAGGTCATTGTTCAAAATATCTGCCAATCAGAATCAAGAATTCCAGTGCGTTGTGAGATAATGGATTAATAGAATGTTTATTTATTTGTTGATATTTCGATATGTGGGCTCATATGTTTC[A/T]GACTCAAGATGAGATTGCTGAGCTGGAGAAGGATATCATTGGCCTGGAGGAGGACCTGCAGGCTAAGACAGCGCCTCTAAAGCTGGTCCACACCCGTCTGGAGAACAGGATAAAGAGACCTGGCATGGACTTGTGCCGAGATGAGGTAACATCACAACCAGTTGGTTGGTTACAGTACCTTACACAGTGGTTTGGTCAAATTCTGGAAATTTGGCATGCAAAAAAAGGCAATGTCTATTGACAACAGTGTTGCGATGTATGATATAAACTAAATACACACAAACTACTTTCAAACCAAACAGATAATCTTTCAGCCTCACATGAGATTCCTGATTGAATGGCTTCTGAACCATCTTTTAACTGTGCTCAACTTGTTAAATCCAGTTAATTGTGTGATTGGACTGTACATGTATTTAGGTTTGTAATGCTTCATGTTAATCATGTAAATGATTGACTGTCAATATGCAGTTTGTCTTTCATTATATAAAATATCTACAAAA
Associated Phenotype:
Not determined