ZMP
sptb
Ensembl ID:
ZFIN ID:
Description:
spectrin beta chain, erythrocyte [Source:RefSeq peptide;Acc:NP_571600]
Human Orthologue:
SPTB
Human Description:
spectrin, beta, erythrocytic [Source:HGNC Symbol;Acc:11274]
Mouse Orthologue:
Spnb1
Mouse Description:
spectrin beta 1 Gene [Source:MGI Symbol;Acc:MGI:98387]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42981 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32168 | Nonsense | Available for shipment | Available now |
sa12908 | Nonsense | Available for shipment | Available now |
sa13819 | Nonsense | Available for shipment | Available now |
sa17671 | Nonsense | Available for shipment | Available now |
sa36485 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23143 | Nonsense | Available for shipment | Available now |
sa1326 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42981
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 49 | 2357 | 1 | 36 |
ENSDART00000145147 | Nonsense | 49 | 2357 | 1 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38741166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38626063 |
GRCz11 | 17 | 38573648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTGACAATGACAACAGCTCAGCCAGACTCTTTGAGCGCTCACGCATT[A/T]AAGCTCTTGCAGGTGAGTCGCCTCAAGTTACATCAAACTGAGCACATGTT
Long Flanking Sequence:
GCCATACATACTTCTGCCAACGTAATTCGCAATCTCCAGAAAAGTATTTAGGGCTACGCTTTCAGAATGAGCCTATGTTGAATTTTCTAGAAACTGGTTGTTTTTTTCTGAAGCACACAGAGAGGATTGCCACTTTAAGACTTTTTTAAGACATTTGAATATTTATAACATATTATATAATATATGTATAAAAAGAATATGTATTATTGATTGATTAAATATTTTAAAGATAAATATGCAGTTAAACCCATCCTTGATTGTCTTTCATCCTTCAGATCAACCACCTCTGGATTCCACTGTCTTGTCATCGTGTGGCACGCTGAGGTGTCTGGCCCCTTTCATCTCTTTGCATCTTGATGGCAACTATGACCTCCACCACAGACTATGACAACGCTGAAATCACTCAGCAGTACAGCCGTATCAACACTCGCTTCGAACTGTCTGATGAAGAACTTGACAATGACAACAGCTCAGCCAGACTCTTTGAGCGCTCACGCATT[A/T]AAGCTCTTGCAGGTGAGTCGCCTCAAGTTACATCAAACTGAGCACATGTTGCTTTGGCTTAGATATACAGACATACATTTACAGACATACTGTATAGGCAGCTGAACCCTATCCTCTCCTGCCCCTTCAACCAGCCGGGATCATTTGCACATACCCAGCGTGCTTCAGTATGACTGAGCTGGACAGCTGCCCGTCTGTGCCCATATCATAGATCACTGGAATAGCTGCAGGAGCTTGTAATTTTTGGCACACCTGTGAGGTTTGCGGTTCTCAGCGACAGCAGGTTTTAAATAGCAATTTCACAATCAGACCTACAAGCACCTTTCCAGGGAAAAGGCAATCCACGCATGACAGTTATGAAAAAAGAGACAGCATACATTTCTTTTCTGATGCTTTGTGTTGCAACCGGTCCTAATTTTTGGATTTGTTGCAGATCTGATCATGTTACATGCATCTAAATAACAAGAACACATATCTAGCGTAATCTATTTGAATCCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32168
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 |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 787 | 2357 | 13 | 36 |
ENSDART00000145147 | Nonsense | 787 | 2357 | 13 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38755646)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38640543 |
GRCz11 | 17 | 38588128 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGAGACAGATGAGCAGTGACGATGTTGGGCATGATGAGTACACTACA[C/T]AGCGACTGCTCAAGAAACACCGTGACTTAAGAGATGAGGCTGCTAAGAAT
Long Flanking Sequence:
TACAGCATTTGGACCTGTGCTACCAGGAGTTGTGTGCACTGGCAGCTCAAAGAAAAGCACGCCTTGAGCAGTCACGGCGCCTTTGGAACTTTTTATGGGAGATAGCAGAGCTGGAAAGCTGGATTCGTGAAAGGGAGCAAATATTTTCCTCTCTTGACTATGGTAAGGACCTGACCAGTGTGTTGATACTGCAAAGCAAACACAGTGTCTTTGAGGATGAGCTTGCAGCAAGACGGGACAACTTGAAGCAGGTGATGGACGAGGGAGAGAGCATGATCCAGATCAAGCACTTGGGTTCCCCCAAAGTGCAGCAACGCATGAATGATGTACAAAGACAGTGGCAACAACTGGAGGAACTGGCTGCATTCCGTAAACAGAATCTGCAAGACACCCAACGTTTCTTCCAGTTTCAGGGTGATGCTGATGACCTCAAGGCTTGGCTGGTCGATGCAATGAGACAGATGAGCAGTGACGATGTTGGGCATGATGAGTACACTACA[C/T]AGCGACTGCTCAAGAAACACCGTGACTTAAGAGATGAGGCTGCTAAGAATGGAGCCACCATTGATGCTCTATCCAAACAGGCCAATGCACTTCCTGAAGAACTACGGAATACCCCTGACATCCAGGGCCGTCTGAATGATATACGGGATATGTATATTGAGCTTCTGACCCTCTCTGATTTGAGGCAGAAGAAACTGGATGACACCATGGCTCTTTACACTATCTTCAGTGAGACAGATGCTTGTGAGCTCTGGATGGGCCAGAAAGAGACCTGGCTGGTTGGGTTAGAGACACCTGAGAATTTGGAAGATCTAGAAATTGTACAAAACAGGTATGGCAATTATTTTTATGAACCCAGAGACAGAACTTTAAGAATTTTTCATAAACTCCATAAAATTCTCATCTGTTTATTGGTAGGCTAAGCATTCTTGCTCAAGAAATGGGTAATATGCAGACTCGAGTTGATAACGTTAATAAAGCAGCCAAGCAACTTGAAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12908
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 799 | 2357 | 13 | 36 |
ENSDART00000145147 | Nonsense | 799 | 2357 | 13 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38755682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38640579 |
GRCz11 | 17 | 38588164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AHGAGTACACTACACAGCGACTGCTCAAGAAACACCGTGACTTAAGAGAT[G/T]AGGCTGCTAAGAATGGAGCCACCATTGATGCTCTATCCAAACAGGCCAAW
Long Flanking Sequence:
CACTGGCAGCTCAAAGAAAAGCACGCCTTGAGCAGTCACGGCGCCTTTGGAACTTTTTATGGGAGATAGCAGAGCTGGAAAGCTGGATTCGTGAAAGGGAGCAAATATTTTCCTCTCTTGACTATGGTAAGGACCTGACCAGTGTGTTGATACTGCAAAGCAAACACAGTGTCTTTGAGGATGAGCTTGCAGCAAGACGGGACAACTTGAAGCAGGTGATGGACGAGGGAGAGAGCATGATCCAGATCAAGCACTTGGGTTCCCCCAAAGTGCAGCAACGCATGAATGATGTACAAAGACAGTGGCAACAACTGGAGGAACTGGCTGCATTCCGTAAACAGAATCTGCAAGACACCCAACGTTTCTTCCAGTTTCAGGGTGATGCTGATGACCTCAAGGCTTGGCTGGTCGATGCAATGAGACAGATGAGCAGTGACGATGTTGGGCATGATGAGTACACTACACAGCGACTGCTCAAGAAACACCGTGACTTAAGAGAT[G/T]AGGCTGCTAAGAATGGAGCCACCATTGATGCTCTATCCAAACAGGCCAATGCACTTCCTGAAGAACTACGGAATACCCCTGACATCCAGGGCCGTCTGAATGATATACGGGATATGTATATTGAGCTTCTGACCCTCTCTGATTTGAGGCAGAAGAAACTGGATGACACCATGGCTCTTTACACTATCTTCAGTGAGACAGATGCTTGTGAGCTCTGGATGGGCCAGAAAGAGACCTGGCTGGTTGGGTTAGAGACACCTGAGAATTTGGAAGATCTAGAAATTGTACAAAACAGGTATGGCAATTATTTTTATGAACCCAGAGACAGAACTTTAAGAATTTTTCATAAACTCCATAAAATTCTCATCTGTTTATTGGTAGGCTAAGCATTCTTGCTCAAGAAATGGGTAATATGCAGACTCGAGTTGATAACGTTAATAAAGCAGCCAAGCAACTTGAAGACAGCAGACATCCACAAACAAAACAAGTGAAAGACTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13819
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 |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 929 | 2357 | 14 | 36 |
ENSDART00000145147 | Nonsense | 929 | 2357 | 14 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38756158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38641055 |
GRCz11 | 17 | 38588640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGATAACGTTAATAAAGCAGCCAAGCAACTYGAAGACAGCAGACATCCA[C/T]AAACAAAACAAGTGAAAGACTGTCAAATTCGTCTCAATAAGAGGTAAGAT
Long Flanking Sequence:
AAGAAACACCGTGACTTAAGAGATGAGGCTGCTAAGAATGGAGCCACCATTGATGCTCTATCCAAACAGGCCAATGCACTTCCTGAAGAACTACGGAATACCCCTGACATCCAGGGCCGTCTGAATGATATACGGGATATGTATATTGAGCTTCTGACCCTCTCTGATTTGAGGCAGAAGAAACTGGATGACACCATGGCTCTTTACACTATCTTCAGTGAGACAGATGCTTGTGAGCTCTGGATGGGCCAGAAAGAGACCTGGCTGGTTGGGTTAGAGACACCTGAGAATTTGGAAGATCTAGAAATTGTACAAAACAGGTATGGCAATTATTTTTATGAACCCAGAGACAGAACTTTAAGAATTTTTCATAAACTCCATAAAATTCTCATCTGTTTATTGGTAGGCTAAGCATTCTTGCTCAAGAAATGGGTAATATGCAGACTCGAGTTGATAACGTTAATAAAGCAGCCAAGCAACTTGAAGACAGCAGACATCCA[C/T]AAACAAAACAAGTGAAAGACTGTCAAATTCGTCTCAATAAGAGGTAAGATTTAAACAGTATTCCTAAATGTAAATATATAAAATATTTATGAATGATCTGCAATGTTACTTTTTCTATTCTCACAGATGGGAGGCTTTTAAAGCAATGGTCGAAGATAAGAAACATAGGGTAGATTCTGCTCTTAGCCTACATAACTATGATCTTGATTGTGATGAGACAGAATCATGGATAAAAGAAAAGACGAGAGTCATTGAGTCTACACAGGATCTTGGGAATGACCTTGCTGCTGTCATTACTATTCAAAGGAAGCTTTTTGGCATGGAAAGAGACCTTGCTGCCATCCAAGATAAGTTGGATTCCCTGCGTGACGAGGCCCAGAAGCTTGTAAAGGAGCACCCAGAAAATGCTTCTGATATACTTGCCAGACAGGAAGAGTTGGATGCAGCATGGGACACCTTGAAACGTACCCTGAAAGACCGTGAAGACTCTCTTGGGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17671
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 |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 1101 | 2357 | 15 | 36 |
ENSDART00000145147 | Nonsense | 1101 | 2357 | 15 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38756758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38641655 |
GRCz11 | 17 | 38589240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTTCAAGTCACAGAAGGCTGTTGCTTCTGAAGATATGCCAGATGGTT[T/A]ACCAGAGGCTGAGCAACTCCTGAATCTCCATRATGCTTTGAGGCATGATA
Long Flanking Sequence:
GCAATGTTACTTTTTCTATTCTCACAGATGGGAGGCTTTTAAAGCAATGGTCGAAGATAAGAAACATAGGGTAGATTCTGCTCTTAGCCTACATAACTATGATCTTGATTGTGATGAGACAGAATCATGGATAAAAGAAAAGACGAGAGTCATTGAGTCTACACAGGATCTTGGGAATGACCTTGCTGCTGTCATTACTATTCAAAGGAAGCTTTTTGGCATGGAAAGAGACCTTGCTGCCATCCAAGATAAGTTGGATTCCCTGCGTGACGAGGCCCAGAAGCTTGTAAAGGAGCACCCAGAAAATGCTTCTGATATACTTGCCAGACAGGAAGAGTTGGATGCAGCATGGGACACCTTGAAACGTACCCTGAAAGACCGTGAAGACTCTCTTGGGGAGGTCAGCAAGCTGCAGACCTTCTTACAGGACATGGACGATTTTCAAGCTTGGTTGTTCAAGTCACAGAAGGCTGTTGCTTCTGAAGATATGCCAGATGGTT[T/A]ACCAGAGGCTGAGCAACTCCTGAATCTCCATGATGCTTTGAGGCATGATATGGATGGCCATGAGGAAGACTACCATCGTGTGAAAGACACAGGAGCTGCTGTTATTCAAGGTCAAGAAGATGATCCTCAGTACCAGCAACTGGAACAGAGGCTGGAGGGTCTTGATAAGGGCTGGGGTGAGCTTCACAAAATGTGGGACAGTCGCAAGAACTTCCTAGATCAGGGTCTCGGTTTCCAACAATTCATGAGAGATGCCAAACAGGCTGATGCCATCTTAAATAATCAGGTATATATGCAGAGACTTTTTCATTTATTGAATCAAAATAGATGTAGTTTAGCTTTCTTTTCATTAAAAAGAGTAATTTTAAGGAAACCATACCATGGTAAATTCCAAAACAAAGTGGCTAATATTCTTTGCTAATGATCTTTAATTGCCAATTACACTTTTATACCCATTTAAAACGCTATATCTCTTTTTTTGTGTTTTTTAATTTTACTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36485
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 1444 | 2357 | 20 | 36 |
ENSDART00000145147 | Nonsense | 1444 | 2357 | 20 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38759345)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38644242 |
GRCz11 | 17 | 38591827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTCTATTCCTCCCTAGATAACAGAGAATCAGGTTCGGGACCGTGCA[C/T]GAGAGCTTGAAGAACTTCAGGAGGCTGTAGAGCAGCATGGTTCTCTTAGA
Long Flanking Sequence:
CCCCTTCTACTTTGTACCATAATTTCAGTACCATGTTCTTGCATTTAGGAGGGACAGGAACTGATGGAATCCAAGCCTGAGTTTGAGCCTATTGTTAAGGATCGCCTTGCCAAGCTTCATGAACTATGGGATAAGCTGGAGAGCACCACACAAGAAAAGGCTCGGCTACTGTTTGATGCAAACCGTTCTGAGCTGTTCGATCAGAGCCTAGCTGACCTAAAGAAATGGTTAGCTGAATTGCAGCAGCAACTTCAGGGTGATGTGGAAGAAGAAGTTAAGGATCTTACCAGTGCCAACATCCTGCTAAAGAAACATCAGGTGTGACAGTAAATTTGATATTTTGTCATTGTGTTGTTTTTGAGACAATTCTACAGTAGACTACTTCAGTTGAAGTTAATTATGATCTCTGCACTGTCCTTTCATGTCGAAGTTTATAGTACAGTGCAAAAATCTTCTCTATTCCTCCCTAGATAACAGAGAATCAGGTTCGGGACCGTGCA[C/T]GAGAGCTTGAAGAACTTCAGGAGGCTGTAGAGCAGCATGGTTCTCTTAGAGAGGACCAGCCTGAGCTTGAGATTGAGCAACAAAATCTTCAGAGAGATTTCCAGAAGCTCCTCACACCTTTATCACAACGCAAGGGAAAGCTGGAGGCTGCTAAGGCAGTGCACCAGTTCTTTAGAGATCTTGCTGATGAAATAGTATGTACATACCTGAGCATACCCATATACAGCTTTTCAGAATGCATATAGTTTTAATGAATGATTTTCTTGATTTTCTCCTCAGCTCTGGGTTAATGAAAGGTTACCAATGGCTATGTCAGATGATCATGGTAACAATCTTCAGACTGTCCAACTTTTGCTTAAGAAGAACCAAGTAAGTTTGTTCCCACTTTCCCCCCACAGATATTCATTATCATTCATTATCATGTATCCTTTTATATACCTCATCCACCCCTTTCATAAACACTGTGCATGTCCTGTGCAGTCCTTACAAAAAGAGATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23143
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 |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 1510 | 2357 | 21 | 36 |
ENSDART00000145147 | Nonsense | 1510 | 2357 | 21 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38759629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38644526 |
GRCz11 | 17 | 38592111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGCATATAGTTTTAATGAATGATTTTCTTGATTTTCTCCTCAGCTCT[G/A]GGTTAATGAAAGGTTACCAATGGCTATGTCAGATGATCATGGTAACAATC
Long Flanking Sequence:
TACCAGTGCCAACATCCTGCTAAAGAAACATCAGGTGTGACAGTAAATTTGATATTTTGTCATTGTGTTGTTTTTGAGACAATTCTACAGTAGACTACTTCAGTTGAAGTTAATTATGATCTCTGCACTGTCCTTTCATGTCGAAGTTTATAGTACAGTGCAAAAATCTTCTCTATTCCTCCCTAGATAACAGAGAATCAGGTTCGGGACCGTGCACGAGAGCTTGAAGAACTTCAGGAGGCTGTAGAGCAGCATGGTTCTCTTAGAGAGGACCAGCCTGAGCTTGAGATTGAGCAACAAAATCTTCAGAGAGATTTCCAGAAGCTCCTCACACCTTTATCACAACGCAAGGGAAAGCTGGAGGCTGCTAAGGCAGTGCACCAGTTCTTTAGAGATCTTGCTGATGAAATAGTATGTACATACCTGAGCATACCCATATACAGCTTTTCAGAATGCATATAGTTTTAATGAATGATTTTCTTGATTTTCTCCTCAGCTCT[G/A]GGTTAATGAAAGGTTACCAATGGCTATGTCAGATGATCATGGTAACAATCTTCAGACTGTCCAACTTTTGCTTAAGAAGAACCAAGTAAGTTTGTTCCCACTTTCCCCCCACAGATATTCATTATCATTCATTATCATGTATCCTTTTATATACCTCATCCACCCCTTTCATAAACACTGTGCATGTCCTGTGCAGTCCTTACAAAAAGAGATTGATGGTCATCAACCACGCATTGATGAAGTGTTAGAGCGGGGTCGGCGAATGGCAGCAGCAGCAGAGGGCAGTCCAGAGGAAGAACGCATGTCTGAGGAGATGAAGAAGCTTCAGGTGGTGTGGGCACAGCTACAGGAAGAGATGGCAAAACGAAGAGAACGGCTTTATGGCTCTAATGAGGCCCAACAGTATTACAATGATGCAGATGATTCTGAGGCCTGGATAGGTGAACAAGAACTCTACATGATTGCTGATGAGATGGCAAAGGTAAGACTGTGAAGACTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1326
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 |
---|---|---|---|---|---|
ENSDART00000040627 | Nonsense | 1917 | 2357 | 27 | 36 |
ENSDART00000145147 | Nonsense | 1917 | 2357 | 27 | 36 |
Genomic Location (Zv9):
Chromosome 17 (position 38763326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38648223 |
GRCz11 | 17 | 38595808 |
KASP Assay ID:
554-1240.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTTGAGGCCTGGAAGGGTCTGTTGGATGCTTGTGCGGGTAGGAGGAAA[C/T]AGCTGGAGGAGACAGCAGACAAATTCCGCTTTTTCACCATGGTGAGAGAC
Long Flanking Sequence:
GTATGGGGTTGAGAATTAAAAAATAAAATATTTTTTACAATCGTCTGTGAATTTTGTTAGGTATTTTTATGATGGAAAAGAGCTGGTTGGTCACATTGAGGAAAAGAAGAATGAACTTCCTGAAGACTTGGGAGAAGACTTCAGCAAAGCAGAATCATTCCACCGAATGCATGCTGCATTTGAGAGGGATATCAGCTCCTTGGGCAAACAGGCAAGGGCACATCAAATAAAAAATGGTTGTCATTCACATCAAATTACTGTGCCTTGAACATATTTATAGGTTTGCATAGAAAATCCCAAAATGTTATGCCTTAAATTCTTAAGGCTTAAATTATTAAGTTTTTTTTTTTCTCTTCATGCAGGTAAAACAGTTCCAGGAGACAGCAGCTAGATTGCATGCCCAGTATGCAGGAGATCAGGCTACTGCCATTCAAGCAACTGAAAAAGAGGTTGTTGAGGCCTGGAAGGGTCTGTTGGATGCTTGTGCGGGTAGGAGGAAA[C/T]AGCTGGAGGAGACAGCAGACAAATTCCGCTTTTTCACCATGGTGAGAGACCTAATGGCCTGGATGGAAAGCATCCTTCAACAGATAGAGACACAGGAAAAACCAAGGTAAGAAAATGAGTGGAATCGCTGTGGTCATAAAATTAGATATCCATTTTTCTCTGTAATAAAGTTTGTCTCTTGTTGTCCACTGAAGAGACGTCTCCTCAGTGGAGCTTCTGATGAAGTATCATCAAGGGATCCGTGCTGAAATTGAGACCCGTGGGCCAAAGTTTAATCAGTGTGTGCAACTTGGACAGGCTCTCCTGGAACGCAAGCACAAGGACTCTGCAGAGGTATCCATTCCTAGGAAGCAACAAGCACAACAGTTTGCCAGTGTCCAGATTGTGTTTATTTACACTTTTTCTCCTCACAGATTAAAGAGAAGCTGATGCAACTGGTAGAGAAGAGAAAAGAGATGATGCTCAAATGGGATGATCGATGGGACTGGCTCAGACTTTGT
Associated Phenotype:
Not determined