ZMP
tg
Ensembl ID:
ZFIN ID:
Description:
Thyroglobulin [Source:UniProtKB/TrEMBL;Acc:Q2VA53]
Human Orthologue:
TG
Human Description:
thyroglobulin [Source:HGNC Symbol;Acc:11764]
Mouse Orthologue:
Tg
Mouse Description:
thyroglobulin Gene [Source:MGI Symbol;Acc:MGI:98733]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12312 | Nonsense | Available for shipment | Available now |
sa14597 | Nonsense | Available for shipment | Available now |
sa36180 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13796 | Nonsense | Available for shipment | Available now |
sa36179 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30690 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16248 | Nonsense | Available for shipment | Available now |
sa22880 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12312
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 |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 140 | 2733 | 4 | 48 |
ENSDART00000136880 | None | None | 837 | None | 18 |
ENSDART00000137113 | None | None | 134 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33896747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31634647 |
GRCz11 | 16 | 31592574 |
KASP Assay ID:
2260-9889.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGGTGAGTACCAGCAGGTACAGTGTGAWGCGTCTMGCAGCCAGTGCTG[G/A]TGCGTYGACCTAGAGGGCATGGAGATCTATGGAACCAGGCAGAAHGGAAA
Long Flanking Sequence:
CAATGCAGTAGAAAAAAATATTACAGTAAACCTTAATTGCAATCCAATGCATTACTGTTTTTTGTACCTCCAATAAAAAAGTATAAATTACAAAAAAAAAAATTAAAAATAATAATAATCATTAAATAAATAAATTGCAATGTTTGATCACAAGTGTGTTTTCTTTGATTTTTGTTTAAACCAGAAAAATTCCCAATTCTCTAACACTTATATGCTACTAAAAATCAAATCATTATCATCACGTTTAAGTCAATTGCTTCTATTATAAAAATAAATAAAATCATATATGAATCAAAAAAATGGACTGAATTAAAATCAAATGAAGTGACCAGCCCACAATATCCTCTCCTTCCCTCTCTCTCACTCTTCATAGGTTTAACCACCTGCCAGCTCCAGAGACAGCGGGCACTGCAGACTGAAGATGCCACCCTGGTGCCCGTGTGCTTGGACTCAGGTGAGTACCAGCAGGTACAGTGTGATGCGTCTCGCAGCCAGTGCTG[G/A]TGCGTCGACCTAGAGGGCATGGAGATCTATGGAACCAGGCAGAACGGAAAGCCATCCAAATGTAAGTGCACTCATTCAGGGTCATATTTATCCATTTCCCTGGATGCTTTTATTTAGATTATATTCTGAAAGACTTTTATTGCCCTAAAGGGATAGTTCACCTAAAACTGAAATTTCTGTCGTCATTTACTCACTCTTGACTTTTCACAAACCTGTTTGAGTTTCTTTTTTTCCTCTTTACCACAAAATAATTTACTTTGAAAAATGTTGGAAACCTGTAACTATTGGCTTCCATGTTATTTATTTTTCCTACTATAGAAGGCAATGGTTACAGGTTTTCAACATTTTTCAAAATAACTTATTTTGTGTTAAACTGAAAAGGAAATTCAAATATGCAATTGCTTGAGCGTGAGTAAATGGGGAATACATTTTCATTTTTGAATGAACTATCCCTTTTAGTCCAAAATCTTCTGAAGTGGATGTTCTTTGTGATCGGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14597
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 |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 523 | 2733 | 9 | 48 |
ENSDART00000136880 | None | None | 837 | None | 18 |
ENSDART00000137113 | None | None | 134 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33887505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31625405 |
GRCz11 | 16 | 31583332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGTTGGCTAAGACCTTCACAGACAGCTYTGAAAATCTTAATCTAGAC[C/T]AGGAGATCTCTGATGCGTTTGGTCGAYCGGTAAACCTGAAAAACAACAGA
Long Flanking Sequence:
TTTGTGTAGGCACTGGAGTGAAAGACTGCCTGTCTGAGAGGAGACAAGCCCTCTCCAAGCTCTTTTATGGCCCAGCTGGAGACTTCAGCAAGAGCAACGTGTTCTCCTCTTCCAAAGACACCGTCTCTTTTCTTGGTACTTGCAGCCCTGAATTCCAGGAGCTGTTGGCCAACTCCGGTCTTCTGCAGTCATTGCCAGAGTTGGAGCGTCCAAAAGTCACAAACATCCTGGCAGATGTTCTCCAAGGGATGTTTCCCTCTGGCGCTCTTGCCCTGAAGGCTTTAGCTCTCGCCCAGAATCCCAAGAGACTTCAGGAGAATCTTTTTGGAGGGAAATTCCTGAAGAACGCTGGAAATTTCAACTTCTCAGGGACTGTTGGAGACAGTGGCACATTGAGCTTTAGACAAATTTTCAGTCAGGTTGGTCTGACCCAAGTTGTGACAGACTTAATGCAGTTGGCTAAGACCTTCACAGACAGCTCTGAAAATCTTAATCTAGAC[C/T]AGGAGATCTCTGATGCGTTTGGTCGATCGGTAAACCTGAAAAACAACAGAGAAATGATTAAGCTTGTTTCAATGGCTCTTGAGAATACGCATTTTCTTTCTACACTTCGAGTAGCGATCAAACAGTTGAAGGCAGAAGAAACAACCCAGCTGGGTTCATTGTTTCGTGACATTTTCCAGAAATCAGATGTTTGTAAGCCTATGTCTTCCAGCTCAGCTCCATACCTGCCCCAGTGTACTGAGGATGGACTGTACCAGGACGTTCAGTGTCAGGGCTCTGAGTGCTGGTGTGTGGACTCTCGTGGTCTGGAGGTACCAGGTTCTCGCACCACTGGATCCAGGCCGAGATGCCCATCCCAGTGCGAGAAAGAACGTCAGATGGCAATAGCAGTGAAAGCCAGCAGCTCTGCAGGATCTGAGGTCTTCATTCCTAAATGTGAGACTGATGGTGCTTACGTTGCACGGCAGTGTCTTGGCAAAAGTTGTTTCTGCGTGGACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36180
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 |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 684 | 2733 | 9 | 48 |
ENSDART00000136880 | None | None | 837 | None | 18 |
ENSDART00000137113 | None | None | 134 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33887020)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31624920 |
GRCz11 | 16 | 31582847 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAGACTGATGGTGCTTACGTTGCACGGCAGTGTCTTGGCAAAAGTTG[T/A]TTCTGCGTGGACAGATCTGGAACCAAACTCGGCATTCAGAGTTCAGGAAG
Long Flanking Sequence:
AATCTTAATCTAGACCAGGAGATCTCTGATGCGTTTGGTCGATCGGTAAACCTGAAAAACAACAGAGAAATGATTAAGCTTGTTTCAATGGCTCTTGAGAATACGCATTTTCTTTCTACACTTCGAGTAGCGATCAAACAGTTGAAGGCAGAAGAAACAACCCAGCTGGGTTCATTGTTTCGTGACATTTTCCAGAAATCAGATGTTTGTAAGCCTATGTCTTCCAGCTCAGCTCCATACCTGCCCCAGTGTACTGAGGATGGACTGTACCAGGACGTTCAGTGTCAGGGCTCTGAGTGCTGGTGTGTGGACTCTCGTGGTCTGGAGGTACCAGGTTCTCGCACCACTGGATCCAGGCCGAGATGCCCATCCCAGTGCGAGAAAGAACGTCAGATGGCAATAGCAGTGAAAGCCAGCAGCTCTGCAGGATCTGAGGTCTTCATTCCTAAATGTGAGACTGATGGTGCTTACGTTGCACGGCAGTGTCTTGGCAAAAGTTG[T/A]TTCTGCGTGGACAGATCTGGAACCAAACTCGGCATTCAGAGTTCAGGAAGTTCTCTTCAGTGTGAGTCTTGCACGTTAAACACAGATGATTAATTACAGAGCCGGGGAGCATTGTTCCTGTGTTCATACATTTAATTAGGCACACATTTAAATGATCTCACACGTGTGCAATAAACAGTCAAGCAAACATCTCAATGATGCATTCTAGAGACTATGTCTTCTTGTTTAATCGAGCTTAAGTGCTTTTACTTTTCCAAGGCTCTCTGTCAGTAATTTAATTCAAAATAATCATTTATACCTTACAGACTCCTTAAAGGTTAGTATTCTTTAGTAAGACATTTTAAATCATATTTAAAACATTATTAGTTATTAGTTTTCTAATGCAAGTCTGCTTTTGCCTCCATGTTGAAATTTATTTTTTTATATGAAATAAAACTGTCTGGCTAACACATAAATACAGGTTCTGTCTTACAAATGATAAAATATTTGGAAAATGCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13796
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 845 | 2733 | 10 | 48 |
ENSDART00000136880 | None | None | 837 | None | 18 |
ENSDART00000137113 | None | None | 134 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33884612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31622512 |
GRCz11 | 16 | 31580439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGATCTGTTAGACGGGAACAGTGAAGCGGTTTATGGACCATCAGTTTA[C/A]TTRAACCCATTATCCTTATGGCGACTAATCAGATTAGATGATTCTGGTTA
Long Flanking Sequence:
GAAATTATATTAACATATTAAAATAAATCTAAATCTGATAAAAAATAATACTAATAAATCTTCTGATGATCTCTCTTAGGCCCAACCAGCTGCCAGGCCATAGCGATTCAGCAATTCCAGTCTACAATCCGCTCTCTTCTCTCTGATCCACTTTCTGTAACCCAGCTTTCTGAAATATACATTCCTCGATGCTCCTATGATGGCAGCTGGCACCAGATCCAGTGCGATGGACCTCCAGAACAAGCCATTGAGTTCTACCGTGAGTGGGTACGGATCATAAATTTGGGACAAGACCTGCCTGCCTCTGAACTTCTGGGAATTCTACAAACATATGCAAGAAACACACAAGCAATGGCATCATTTAGAGCCTTTGTATCTGAATTGTTCAAAACTGGACACCACAGAGTGTTCCCTGTCCTAGCAAGATTTCAGAAGTTCTCTGATATTCCATCAGATCTGTTAGACGGGAACAGTGAAGCGGTTTATGGACCATCAGTTTA[C/A]TTAAACCCATTATCCTTATGGCGACTAATCAGATTAGATGATTCTGGTTATCCAGGTCTGCTCTCTGACTTCAGCGTTCCTCTTGGAAGCTTTGATCTACGTCAGTGTTGGTGCGTTGATCTTGAAGGAGACATGCTAGCAGGTAGCAAAGCTCCTGTTGGGCAAATCCCAAAATGTGAGTTATGCGTTTATCATATCCACAACACATTTCTTTGTAATCTGTTGAAAGCGTTCTCATTAGATCTCCTCTGTGTGTCTTTTCAGGCCCAGGTCCTTGCTCTGTGGTTCAAAGACAGGTCTCTGAGTTCCTAAAGCAGGCAGAGGAGCTGATCTCTGCCTCAAACAGCACACATGTGCCTGTGGGTTATGGTTTTCTGCTGGCTGAGAGTGTGTATCTGAGCCCTGAGGAGCTGGAGCAGACGAGATCCTCAATGATCCCTGTCACTCAGACTCTTCTGAGCAACACCGACACAGCACTGAGACTCGCAGCTCATTCCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36179
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 |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 857 | 2733 | 10 | 48 |
ENSDART00000136880 | None | None | 837 | None | 18 |
ENSDART00000137113 | None | None | 134 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33884577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31622477 |
GRCz11 | 16 | 31580404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACCATCAGTTTACTTAAACCCATTATCCTTATGGCGACTAATCAGAT[T/A]AGATGATTCTGGTTATCCAGGTCTGCTCTCTGACTTCAGCGTTCCTCTTG
Long Flanking Sequence:
TGATAAAAAATAATACTAATAAATCTTCTGATGATCTCTCTTAGGCCCAACCAGCTGCCAGGCCATAGCGATTCAGCAATTCCAGTCTACAATCCGCTCTCTTCTCTCTGATCCACTTTCTGTAACCCAGCTTTCTGAAATATACATTCCTCGATGCTCCTATGATGGCAGCTGGCACCAGATCCAGTGCGATGGACCTCCAGAACAAGCCATTGAGTTCTACCGTGAGTGGGTACGGATCATAAATTTGGGACAAGACCTGCCTGCCTCTGAACTTCTGGGAATTCTACAAACATATGCAAGAAACACACAAGCAATGGCATCATTTAGAGCCTTTGTATCTGAATTGTTCAAAACTGGACACCACAGAGTGTTCCCTGTCCTAGCAAGATTTCAGAAGTTCTCTGATATTCCATCAGATCTGTTAGACGGGAACAGTGAAGCGGTTTATGGACCATCAGTTTACTTAAACCCATTATCCTTATGGCGACTAATCAGAT[T/A]AGATGATTCTGGTTATCCAGGTCTGCTCTCTGACTTCAGCGTTCCTCTTGGAAGCTTTGATCTACGTCAGTGTTGGTGCGTTGATCTTGAAGGAGACATGCTAGCAGGTAGCAAAGCTCCTGTTGGGCAAATCCCAAAATGTGAGTTATGCGTTTATCATATCCACAACACATTTCTTTGTAATCTGTTGAAAGCGTTCTCATTAGATCTCCTCTGTGTGTCTTTTCAGGCCCAGGTCCTTGCTCTGTGGTTCAAAGACAGGTCTCTGAGTTCCTAAAGCAGGCAGAGGAGCTGATCTCTGCCTCAAACAGCACACATGTGCCTGTGGGTTATGGTTTTCTGCTGGCTGAGAGTGTGTATCTGAGCCCTGAGGAGCTGGAGCAGACGAGATCCTCAATGATCCCTGTCACTCAGACTCTTCTGAGCAACACCGACACAGCACTGAGACTCGCAGCTCATTCCAGTACAGTCTTTGTTTTATCTGTCAGCATAAACATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30690
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 1615 | 2733 | 25 | 48 |
ENSDART00000136880 | None | None | 837 | None | 18 |
ENSDART00000137113 | Nonsense | 77 | 134 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33869575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31607475 |
GRCz11 | 16 | 31565402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTTGTTTGGCCTTGCAGAGCAAAGGATTTCTGGGAAACGACGGCGCT[G/T]AGGCGTTCCAGACTCTCATCTGTGTTCTGAAAATAAAAGGAGATGAACCT
Long Flanking Sequence:
TTCCTACTGAACCAAATTTTTTTGTAGTTTAAATAGATTAAATATTTTTAGAATTATATTAGTTTGAAATATAAATGTTATGTAACATAAATAGCCACATTTAATCAATTAAATGGATGTTTGCTAAGTAAAATAATTAATAAAAGGTCATTAATAATTAAAAATAGAACTATAGTGTACTGTACTACATGCTTTCTCCATTAGCTACTGTATATCGTCACTTTAAATGTACCTGATCATCTCTTCAACATAAATCATAATTGTCCCTCACATAAGCTAATAAATATAATATACATCACATTTTTATTTAAGAAATAATACATAAATCCTATTTAAATGTTATTTCTAGTGTTATATTTGGCATTGGGTCTTTTTTATGTGACTTGATGGCACTCACACCTCCTTTCCCAAAAGTGACATAATTATTGCCAAAGGAGAAAAAAAGTCTTGTGGTTTGTTTGGCCTTGCAGAGCAAAGGATTTCTGGGAAACGACGGCGCT[G/T]AGGCGTTCCAGACTCTCATCTGTGTTCTGAAAATAAAAGGAGATGAACCTGATCTCACAGTGCTGAGAAAGAAAGGTAAAATCATCAGCTATTAGTTACTCACTGCAGTTAAATGTGTTGATACACAGTATGTGTTGTATAGTTTGAACGCGTTCGAGAGGAGAATTAATATTATTAGAAAACAAAGAGTGTGTTTTAATGAAATTAAATCAAAGATAAGTATCAGAATTGAGCCGTGACCTAAAAGATTAAGTTGTGGTTTTGTAAGTAATGATTTTAACTAAGTGGTCTAGTCGTCTGTGGACACAAGAATAAAGCAAATTGTCATAAAAACATTCCTCAGACTTGCTCTGTTAAGAGATAAATATTTTTCCCTGTGAATTAAATGACTTGGTACTTTAAGGCTCTCAGTTTTTGGTTATTTTTGGCGACCCTAAAAGCATTCAGATGCACTTGTGTTTCTTGGCCATGGCATAAAGAACATCGCTGCTTCTTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16248
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 |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 1906 | 2733 | 31 | 48 |
ENSDART00000136880 | Nonsense | 10 | 837 | 1 | 18 |
ENSDART00000137113 | None | None | 134 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33863727)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31601627 |
GRCz11 | 16 | 31559554 |
KASP Assay ID:
2260-9883.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTATATCCTGACACACGTGTGTGCGGAGCWTATGACAAACCTCTCAGA[C/T]AGACATGCAGTTTAGTGATGACACAGAGTCTGCAGACYGCATACCAAAAG
Long Flanking Sequence:
GACGCAGAATAAGATCATACTTTTGTAATGTCTAATATACAGTTAATATCTTAATAATAGGCAGGTAATTATCTAGTAGTTAATAGCATGAATCATGGCCTAAACTAAAGTGTTACCAGCAATTCTTCTGTATTGTCCTCTTAGACTCAGTGAAGGAGGCTTTTGATGTTCTGGACAGTGGCGATGTGAATGTAGACCCTGAGAGAGAACTTCCCAATCAGCTTTACTGGATCTTTAAACACCAGTACTCTTTCCAGGAGGCTCAGCTTTGGTGTCTGAAACGTAGGATGCAAAATTTCATGAGAAACTCTTCACTTGCTACTCTTCACTGTCTTTTTTATGTGTAGGCTGGGCAAGTTTCACTTTCTGATTTGCTTTCAGGATGTGAAGAAGAAGAGCTGTGTCATGTTTCTGACATCCGTGATGAAGGCCCTCTGTATTTTGCATGTGTTTTATATCCTGACACACGTGTGTGCGGAGCATATGACAAACCTCTCAGA[C/T]AGACATGCAGTTTAGTGATGACACAGAGTCTGCAGACCGCATACCAAAAGAAAGGTGAGTCATTTAAACACAAAAAGGCCATGCTTCTCTTTATACAAATAAATGACAAGATTTTTTATAATAAACTAACTGCTGTATGATCATTCTCATTTCTTAGCATTAGCTGTCTGTTTTCAGAGATTTCTTGTGATTGGACAGACGGATGGGTTTTGCATTACCTTTTTCAAATTGCGTGACTGTGGTCTACTGTTAAGTCTGATGTCAGACTCTTAATACCGTCTTTGTGACTGTCTCCTCCTGTAGTTTACTTTATTTGTTTTCAGATGTAATCCTAGCAACTCAACATGGAATGCTGATGATTCAGTGGTTTGTGTAAAAGAAGGCAGACAGATGGTGAAAAGGCAAACAGAGACAATTATGATGGATAAACTATGCCTAGTTTTGAGAGTCTGACTAGTTGTAATTCTGCAGTTTATTATTTCATACAGATCCTGATGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22880
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 |
---|---|---|---|---|---|
ENSDART00000016386 | Nonsense | 2213 | 2733 | 38 | 48 |
ENSDART00000136880 | Nonsense | 317 | 837 | 8 | 18 |
ENSDART00000137113 | None | None | 134 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 33856002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31593902 |
GRCz11 | 16 | 31551829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCCCTTATGCTCGTCCACCAATCGGAGACCTCAGATTCAGCCCCCCA[C/T]AGCCTGCTGACTGGACCGGGACCTGGAACGCCACATTTTCCCGGTGAGCT
Long Flanking Sequence:
GAAAATTAAGAAGAATATTAAGCTGCTATTTACAATACAGATATTTGTGTATGTACTGTGTTCTCATAACTTTTTTTGTATTATAGCCTGTGAGGACAGTGAGTCCTGTTCGGCTGTGTCCATTGATAGCAGAGAGTCAGCTGTGAGATGTGTGATGTATCCAGACACACACACCTGCCTTCCTACGACAAGCGGCCGGCGCTGTTTACTAGTCACCAAAGAGCCTGCTCAATCTGTTTACATCAGAACAGGTGACGCCTCAAAACATTCTTCAGACTAGTCCAAACTGTTTCTGATCCTTTTTCTCTCAAATAACTAAGAGACTTTTCTTTACAGGTGTGCAGCTGGAATTCACCTCTGTGTCCATCCCTGATCATGGCACACTTCTTGGAGAGAGTGAGGTAAAACCGATAACTGGCTCAGATAGCAAGCGTGTGACTTACTTCTTGGGTGTCCCTTATGCTCGTCCACCAATCGGAGACCTCAGATTCAGCCCCCCA[C/T]AGCCTGCTGACTGGACCGGGACCTGGAACGCCACATTTTCCCGGTGAGCTGGCAACTTTGATTGCAGATTGTTAGAGTAGTGTATGAGGTCCAAAACAAGATTGCAGTCAAACCAAAATTATCCCATTATCACAGTTTATTCTGTATAGTTTTGAAACGGTAATAAAATATTGTAAGAAATCTTGCAGTTAAAACTTGTCTGAAAATCATTTGTATTAGTTAACTCTGATAAAAAGGTACAGTTTAATTCATTACTATCAACCAAAAAAATATTTAGATGTTTAGCATGACAGTGTTTACACAACTATCAGTGTTCTCTGTAAAAAAAAAAATGCTGGGTTCCATCAATCAATTTGTGTTGGCACAACATAAAGGAATAAATAAACTAATTAATTTTTATAAATTGTGAATTGAACATAAAACAATTAGATTGTCACAAAAAAACATCAAGAATTGTGTTGTTTCAGCTTATTTGTAAGCCAGTAGTTTGAACAAACAGC
Associated Phenotype:
Not determined