Busch Lab

ZMP

tekt2

Ensembl ID:
ENSDARG00000028973
ZFIN ID:
ZDB-GENE-040113-1
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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