ZMP
ENSDARG00000058556
Ensembl ID:
Human Orthologues:
MUC5AC, MUC6
Human Descriptions:
mucin 5AC, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7515]
mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7517]
mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7517]
Mouse Orthologues:
Muc5ac, Muc5b, Muc6
Mouse Descriptions:
mucin 5, subtype B, tracheobronchial Gene [Source:MGI Symbol;Acc:MGI:1921430]
mucin 5, subtypes A and C, tracheobronchial/gastric Gene [Source:MGI Symbol;Acc:MGI:104697]
mucin 6, gastric Gene [Source:MGI Symbol;Acc:MGI:2663233]
mucin 5, subtypes A and C, tracheobronchial/gastric Gene [Source:MGI Symbol;Acc:MGI:104697]
mucin 6, gastric Gene [Source:MGI Symbol;Acc:MGI:2663233]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa927 | Nonsense | Available for shipment | Available now |
sa44237 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38012 | Nonsense | Available for shipment | Available now |
sa25223 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44238 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7537 | Missense | Mutation detected in F1 DNA | Not yet available |
sa44239 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24614 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa927
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 |
---|---|---|---|---|---|
ENSDART00000081428 | Nonsense | 231 | 1989 | 5 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8624003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8338908 |
GRCz11 | 25 | 8415976 |
KASP Assay ID:
554-0832.1 (used for ordering genotyping assays)
KASP Sequence:
AATGTTACGGCAGCCATGACTGTCTGTGCAACACGCTAACAGAGATCTCA[C/T]GACAATGCACACATGCTGGAGGACAACCAGGAACATGGAGGACAGAACAG
Long Flanking Sequence:
AGTTTTCTAAGTACATTTTTGGGTACCTTTCAAGGCTTCCTAAATCCCTTTAATAAATTTGAAGCAATGGGTTTACTTACTTATTTAAGTACAGTCAACTAATTCAAAACAATGGCTTTATTCACTTATGTAAGTAAATTCGACTAAACTGTGATGTTTTACCAACTAAATCCTCAGGTCCAGCCACATGGAAGATCTCAACACCAACTGAATCCTGTGAAGACGTTATACTTCCACCCAAGGATCAGTGTGACCAGGTATTAGCCAAAATCGTGAGCATTTTAAAATGGAAATTTTGATGCTCGCAATTGAACGTTTGACCAATTTTCCATTTTTTTTTTCAGAACACAATGGTTTGCCAGCAGTACCTCAGCAGTCCAGGGTTTAGTGGCTGTTATGATGTGATGGACATGAAAATATTTGAAAAAGCCTGTGTGAGCGACATGTGCCAATGTTACGGCAGCCATGACTGTCTGTGCAACACGCTAACAGAGATCTCA[C/T]GACAATGCACACATGCTGGAGGACAACCAGGAACATGGAGGACAGAACAGCTCTGCCGTGAGTATCACTTCTAAAAAATAATGAAAAAGAAGGCATAAAATTTCATGTTTACATCGATTATAATCCTTACCCATTAAAACTATACTAGCATGACTTATTATCTGGTCATTTTAACACATTTAATACAAGACTAATTGTCTTATTTTGTGGAGCAGCAAAGATGTGTCCTATAAACCTGCAATACATGGAGTGTGGAGGTCCGTGTAAGAGCACTTGCTCTGATCCAACTGCACATCTAATGTGTAAAGATCACTGTGTGGATGGCTGCTTCTGCCCTGAAGGTAATTTTATGCAATATCAAGTGACTTTTTGTGCTTGTGAATAAAATATTATTAACTAAATTGCACCATCTGTTCTTTTTGTAAAGGGACCGTTGAAGACGACATTGGTCAGGGTGGTTGTGTTCCTGTAAACGAGTGTCCATGTGTGCATGATGGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44237
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081428 | Essential Splice Site | 561 | 1989 | 12 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8626021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8340926 |
GRCz11 | 25 | 8417994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCTTTTCTGCATGTCATTCAGAAATATGCCCAAAGATTTACTATGAAG[T/C]GAGTTCTTTTGTATATTTCCTTTTGAAATGAACTATATACAGTATTTATA
Long Flanking Sequence:
TATTCATATAAACTGTGTAATAAAAATGTATATGACTACTTTATTAAAGAAACAATACAATATATCAGTGGAGATAAAAGCATGAACCTAACTACTTACCTTTCTTTCTGCTTCTTTAAGGACTGTGTGGAAACTACAATGATGTCCAATCAGATGACTTTAAAACAGATTTGGGTATCACAGAGGGCACAGCGATATCTTTTGCCAACTTTTGGAAGAAAACCCCATATAGTTGTCCTGATCTTGAAAACACATTTGACAACCCCTGTAGCCTGAGTGTGGACACAGGTATATGAAGTATTACAATAAACGGTTTTAAATAGTAATAACTAATTAATGGTATTCGCAAATGCATATGTTGCAAACTTTACAGAACTATGTCGAATCTTTATTATTTTATTCAGAGAAACTTGCTAAAGACTGGTGTTCCCGTCTGACTAACCAAAGTGGAGCCTTTTCTGCATGTCATTCAGAAATATGCCCAAAGATTTACTATGAAG[T/C]GAGTTCTTTTGTATATTTCCTTTTGAAATGAACTATATACAGTATTTATAGCAGACGCATTATCATTTTGTCACATCTGGGATTCATTGTCTGCAGAGGTGCGTCTATGACACCTGCAAGTGTGCAGATATCAGGAAGTGCATCTGTGCGGCTGTGTCCACTTATGCCCATGCTTGTGCTGCAAGAGGAATCATTCTCCAAGGCTGGATGGATTCAGACCCTTGTGGTATTATCTATATTATCTATTTGAATAACGTTCTGTTGATTTGGGGAAAAATAAACAATTCGTAATAAGTGTTCATTCTATGCATAGAATCTGAGTGTTCAGAGAACATGAAGCACTCCTACGGTATGACTGGCTGTGGCCTCACCTGCCGTTCTCTCAGTGGACAAGAAAACACCTGCCAAGGGTCCTTCACGCCTGTAGATGGCTGTGTTTGTTCTGAGGGAACCTACCTTAATGAAGAAGGCATCTGTGTGCCTGCTGACCAGTGTCCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38012
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 |
---|---|---|---|---|---|
ENSDART00000081428 | Nonsense | 636 | 1989 | 14 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8626427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8341332 |
GRCz11 | 25 | 8418400 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTGTGGCCTCACCTGCCGTTCTCTCAGTGGACAAGAAAACACCTGC[C/T]AAGGGTCCTTCACGCCTGTAGATGGCTGTGTTTGTTCTGAGGGAACCTAC
Long Flanking Sequence:
AAACTTGCTAAAGACTGGTGTTCCCGTCTGACTAACCAAAGTGGAGCCTTTTCTGCATGTCATTCAGAAATATGCCCAAAGATTTACTATGAAGTGAGTTCTTTTGTATATTTCCTTTTGAAATGAACTATATACAGTATTTATAGCAGACGCATTATCATTTTGTCACATCTGGGATTCATTGTCTGCAGAGGTGCGTCTATGACACCTGCAAGTGTGCAGATATCAGGAAGTGCATCTGTGCGGCTGTGTCCACTTATGCCCATGCTTGTGCTGCAAGAGGAATCATTCTCCAAGGCTGGATGGATTCAGACCCTTGTGGTATTATCTATATTATCTATTTGAATAACGTTCTGTTGATTTGGGGAAAAATAAACAATTCGTAATAAGTGTTCATTCTATGCATAGAATCTGAGTGTTCAGAGAACATGAAGCACTCCTACGGTATGACTGGCTGTGGCCTCACCTGCCGTTCTCTCAGTGGACAAGAAAACACCTGC[C/T]AAGGGTCCTTCACGCCTGTAGATGGCTGTGTTTGTTCTGAGGGAACCTACCTTAATGAAGAAGGCATCTGTGTGCCTGCTGACCAGTGTCCTTGTTACAGCGGTGACCAGGTCACAAAACCTTCGGAAGTATCCCACGTAGATGGTCTAACATGGTAAGTTCCTCAATTAACATCCAATGCATTGACGATAGTTTCCCAGAGATGGGTTGTGGCTGTAAGGGCATCCGCTGCGTAAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCTGACAAGAGAATGAATGAATGAATGCATTGACGATAGAATACCAATGCAACCATTAGTAACTCCTGATTTGCACAATTTTACAGCACCTGTAAACTTGGCAAACTGCACTGCTCCAATCCTGAAAGTAAGTTTCAACGTTTTTTATTCTGCAATTCCACCAGTCAAATTCCGACTTTAATCATCACTTGTGCAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25223
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081428 | Essential Splice Site | 790 | 1989 | 18 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8627475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8342380 |
GRCz11 | 25 | 8419448 |
KASP Assay ID:
554-7465.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGTGCAAACCATTAAAAGGCTGAATCTATGAATTATGTCTATATTAC[A/G]GCACATGCAGAAATGGGATGTGGGATTGCACGGAAAAAGAGTGTTACGGC
Long Flanking Sequence:
GGTGCTCTTCAAATGCTCAAATTATGAACCAGGAAAAAAGGGCACAGAGTGTCAGAGAACATGCCAGAAACAAGACATTAACAATTGTGTAAGTTTTAGAAATTTACACATTATTTTGGCCACAAAAAATTGTGCAGGTCTCAGCTAAGAAGAAATGAGGATTACCAATGCTAAACCTTTCTGGGTTTTTGTTTTGGCTGTAGGTGAGCACAGGGTGTGTATCAGGGTGTATGTGTCCAGATAACCTTCTGGCTGATGGACAAGGTGGATGTGTGGAGAGGGAAAAATGTCCCTGTGTCCACAATGGAGTTACCTATTCATCTGGAGAACAAGTTCAAGAGGACTGTAACACCTGGTGAGCCAGCGTTATTAGCAATAGGAAATAAATGACAAATATATCATCACATGTGCACTTAAGTAATATTATGAGATTCCCTATATAGGTGGTAAATTGGTGCAAACCATTAAAAGGCTGAATCTATGAATTATGTCTATATTAC[A/G]GCACATGCAGAAATGGGATGTGGGATTGCACGGAAAAAGAGTGTTACGGCACCTGCACCATCTATGGTGAAGGTCATTTCATGACATTTGATGGCAAGAAATATTCTTTCCATGGAGACTGTGAACAAATCTTAGTCCATGTATGTTTTGCATCAATTTTGGCCTTTCCAAGTTAGAAAGAAAATTAGATTACAACCTTATTACAATCTTACAATTTGTTTGGTTTCTCTAGGATTACTGCAATACAGACCAGAGTCCATACTCTTTACGCCTTGTCACAGAGAACATCCCATGTGGCACCTCTGGAACCATTTGCTCCAAGTCCATCAATCTTTTCTTTGGGGTGAGGATACATCTTAGCTAAAAGTCAGCTTGAGTATGCAAGCAGCATATATCATGAGAAAAGACTGTTCAATTATTAATTCTGTTGATGGATACCTTTCTAACTGACTATTTCAATACTGCAGAGATACAAACTGATTTTATCAGAGGAGAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44238
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 |
---|---|---|---|---|---|
ENSDART00000081428 | Essential Splice Site | 836 | 1989 | 18 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8627616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8342521 |
GRCz11 | 25 | 8419589 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCAAGAAATATTCTTTCCATGGAGACTGTGAACAAATCTTAGTCCAT[G/A]TATGTTTTGCATCAATTTTGGCCTTTCCAAGTTAGAAAGAAAATTAGATT
Long Flanking Sequence:
CAGCTAAGAAGAAATGAGGATTACCAATGCTAAACCTTTCTGGGTTTTTGTTTTGGCTGTAGGTGAGCACAGGGTGTGTATCAGGGTGTATGTGTCCAGATAACCTTCTGGCTGATGGACAAGGTGGATGTGTGGAGAGGGAAAAATGTCCCTGTGTCCACAATGGAGTTACCTATTCATCTGGAGAACAAGTTCAAGAGGACTGTAACACCTGGTGAGCCAGCGTTATTAGCAATAGGAAATAAATGACAAATATATCATCACATGTGCACTTAAGTAATATTATGAGATTCCCTATATAGGTGGTAAATTGGTGCAAACCATTAAAAGGCTGAATCTATGAATTATGTCTATATTACAGCACATGCAGAAATGGGATGTGGGATTGCACGGAAAAAGAGTGTTACGGCACCTGCACCATCTATGGTGAAGGTCATTTCATGACATTTGATGGCAAGAAATATTCTTTCCATGGAGACTGTGAACAAATCTTAGTCCAT[G/A]TATGTTTTGCATCAATTTTGGCCTTTCCAAGTTAGAAAGAAAATTAGATTACAACCTTATTACAATCTTACAATTTGTTTGGTTTCTCTAGGATTACTGCAATACAGACCAGAGTCCATACTCTTTACGCCTTGTCACAGAGAACATCCCATGTGGCACCTCTGGAACCATTTGCTCCAAGTCCATCAATCTTTTCTTTGGGGTGAGGATACATCTTAGCTAAAAGTCAGCTTGAGTATGCAAGCAGCATATATCATGAGAAAAGACTGTTCAATTATTAATTCTGTTGATGGATACCTTTCTAACTGACTATTTCAATACTGCAGAGATACAAACTGATTTTATCAGAGGAGAAAGAAATTCAAGTTGTTGAAAGCAATGGCACAGATTACCAATACCAAATCCATACTGCTGGGATATACAATGTCATTGAGGTCAAAGGTCTGTTGAACTTAATCTGGGACAGTAAAACAAGTGTGATGCTCCAACTGCATCCCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7537
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:
A > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081428 | Missense | 1762 | 1989 | 38 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8648479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8363384 |
GRCz11 | 25 | 8440452 |
KASP Assay ID:
554-4050.1 (used for ordering genotyping assays)
KASP Sequence:
TTTSTTCTGTCTAGTGCCGAAAGACGTTTGTGTGCACAATAACACTGAGT[A/G]TCAGGTGAGTTGYTGAGTTTATASTAACTAGTAACACCAACAGTAAAATG
Long Flanking Sequence:
TCTAAACCTTTATGAATGTATTTTTTCTCTTGAACACAAAACAAGATGTTCTGAAGATTGGTGGAAAAATAGCATCCACCGACATGCAAAAAACTAATGTCATTGAATTGACAAGTAAAGTCAGTGGCTGTTTTTTCCAACATTCACTCTAACAAATGCTGGGTTCAACACAATTCCCTAATGTTATCCCAAAACAAATCGATTAAGTTAACTTAATCATTCTTACAAATTTAAGTGGATTGAACATAAAACAATTAAGTTGTTCCCAAAAAAAAAATACTAAGAATTGTGTTGTTTTAATTCATTTTAGATAAGTAGTTTAAACAAGCAGCAAATGTCATTTTTTGAGTGTAATTCAACAGAAGAAACTGGTTTGGAACAAGTGGCAGATGATGACAGAACTTTTATTTTTGAGAGAACTATGCCTTAAGCAATTTCTGACACTGTATATTTCTTCTGTCTAGTGCCGAAAGACGTTTGTGTGCACAATAACACTGAGT[A/G]TCAGGTGAGTTGCTGAGTTTATACTAACTAGTAACACCAACAGTAAAATGTTCTCTAATAATGAGTTTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTTTTGTAGCCTGGAGTTAAAATCCCCACAGAGCCTTGTATGGAATGTCACTGTCATATGGATAAGGATAAAGATATGGATGAAGACAGACATAGTAAACTACACACTGTGACTTGTGTTAAAAAAGTCTGTACACCTTGCTCTGAGGTAATCATTTCAACTGATGTTAGTGATTAAAATACATTGGGAAAGATTTATATTCTGAATTCCAACAGTAATTTTTGAGTTCTGAAGCATACACATCATAAGCTCCTACATTCAATGTTTCCAAATGATTGAGTAAAATTTGATTGAATCTTTTTTGTGCTCCAAGGGCTTTGAGCTTGTGGAACAAGAAGGAGAGTGTTGTGGAACGTGCAAGCAGAAGTCCTGTATTTATACAGCGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44239
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 |
---|---|---|---|---|---|
ENSDART00000081428 | Nonsense | 1827 | 1989 | 40 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8648970)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8363875 |
GRCz11 | 25 | 8440943 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACAAGAAGGAGAGTGTTGTGGAACGTGCAAGCAGAAGTCCTGTATTTA[T/A]ACAGCGCCAGATAACACCACTCACACTCTTCAGGTACAAACCTTTCTTCA
Long Flanking Sequence:
ACACTGAGTATCAGGTGAGTTGCTGAGTTTATACTAACTAGTAACACCAACAGTAAAATGTTCTCTAATAATGAGTTTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTTTTGTAGCCTGGAGTTAAAATCCCCACAGAGCCTTGTATGGAATGTCACTGTCATATGGATAAGGATAAAGATATGGATGAAGACAGACATAGTAAACTACACACTGTGACTTGTGTTAAAAAAGTCTGTACACCTTGCTCTGAGGTAATCATTTCAACTGATGTTAGTGATTAAAATACATTGGGAAAGATTTATATTCTGAATTCCAACAGTAATTTTTGAGTTCTGAAGCATACACATCATAAGCTCCTACATTCAATGTTTCCAAATGATTGAGTAAAATTTGATTGAATCTTTTTTGTGCTCCAAGGGCTTTGAGCTTGTGGAACAAGAAGGAGAGTGTTGTGGAACGTGCAAGCAGAAGTCCTGTATTTA[T/A]ACAGCGCCAGATAACACCACTCACACTCTTCAGGTACAAACCTTTCTTCATTTGTCTACGCATTTATTCAAACAAACCTTCTTTATTTGTTCTGCAGTACTTATTTCAGCCTATATCTCCCTTTAATTCTTTTAGCCTGGAGAGGTCAAAAGTCATCACAAATGTGAGACTCTTACCTGTCGTGAAATTGATGGTGTGTTTGTGACAGAGAAGATCAAACCTAAATGCCCTGACTTTAATCCTGATGACTGTGAGGCTGTAAGTAGTGGTTGATAAGATATTACCATTAATCAAATTTCCACTTTGTTTGCTGTTATATGTACTCTTCATGAATATGTATTAACTCAAGTTCTCAAAGAATATAGTCAAATTTCACTCAACCCAATTCTTAAGTAATCTTTATACAATTAAGTGAAGTTTATTTATAAACTAATTTCGAGAGGATCACGTTTGCTTGCAGCCGGTCCCGCATTATACAATTTCTGATTCGCCGATCAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24614
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081428 | Essential Splice Site | 1879 | 1989 | 41 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8649229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8364134 |
GRCz11 | 25 | 8441202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGATCAAACCTAAATGCCCTGACTTTAATCCTGATGACTGTGAGGCT[G/T]TAAGTAGTGGTTGATAAGATATTACCATTAATCAAATTTCCACTTTGTTT
Long Flanking Sequence:
TTGCTCTGAGGTAATCATTTCAACTGATGTTAGTGATTAAAATACATTGGGAAAGATTTATATTCTGAATTCCAACAGTAATTTTTGAGTTCTGAAGCATACACATCATAAGCTCCTACATTCAATGTTTCCAAATGATTGAGTAAAATTTGATTGAATCTTTTTTGTGCTCCAAGGGCTTTGAGCTTGTGGAACAAGAAGGAGAGTGTTGTGGAACGTGCAAGCAGAAGTCCTGTATTTATACAGCGCCAGATAACACCACTCACACTCTTCAGGTACAAACCTTTCTTCATTTGTCTACGCATTTATTCAAACAAACCTTCTTTATTTGTTCTGCAGTACTTATTTCAGCCTATATCTCCCTTTAATTCTTTTAGCCTGGAGAGGTCAAAAGTCATCACAAATGTGAGACTCTTACCTGTCGTGAAATTGATGGTGTGTTTGTGACAGAGAAGATCAAACCTAAATGCCCTGACTTTAATCCTGATGACTGTGAGGCT[G/T]TAAGTAGTGGTTGATAAGATATTACCATTAATCAAATTTCCACTTTGTTTGCTGTTATATGTACTCTTCATGAATATGTATTAACTCAAGTTCTCAAAGAATATAGTCAAATTTCACTCAACCCAATTCTTAAGTAATCTTTATACAATTAAGTGAAGTTTATTTATAAACTAATTTCGAGAGGATCACGTTTGCTTGCAGCCGGTCCCGCATTATACAATTTCTGATTCGCCGATCAGACGATTCCTAAGCCACTATAAATACCCTAAGTTCCATATAATAGCCATATTCTAGGGATGTAACGGTATCAGAATTTCACGGTACGATAATACCTCGGTATGAATGGCACGGTACGGTATTTATTGAATAATTTACAGGAAAAAACAAAACTAATGAAAAGACTCGAAAAAAGTGCCAAAAGTGTTTATTTACCTTAGCACTGAACATATCAATGACATACAAATCAGCCATCTATCTGTAAGTTTCAAAACAGGAACTTC
Associated Phenotype:
Not determined