ZMP
itga2b
Ensembl ID:
ZFIN ID:
Description:
integrin alpha-IIb [Source:RefSeq peptide;Acc:NP_001003857]
Human Orthologue:
ITGA2B
Human Description:
integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) [Source:HGNC Symbol
Mouse Orthologue:
Itga2b
Mouse Description:
integrin alpha 2b Gene [Source:MGI Symbol;Acc:MGI:96601]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa83 | Essential Splice Site | Confirmed mutation in F2 line | Not yet available |
sa40053 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa19 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa30831 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40052 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10134 | Nonsense | Available for shipment | Available now |
sa40051 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26046 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa83
Status:
Confirmed mutation in F2 line
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016562 | Essential Splice Site | 131 | 1037 | 3 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21592561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21248952 |
GRCz11 | 3 | 21379500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCAGTGGTTGGGTGCTTCAGTTCGAACCTACAACAACTACATCTTGG[T/A]GAGTTACTGTGAGTTCCTTAACCACACTATTCTTCCTGTCAAAGCTGTAT
Long Flanking Sequence:
CATGTCTTTCGACTTCTGAGGGAAACCAGAGCACCCCATGCCAACACCAGGAGAACATGCAAACTCCACACAGAAATGCCAACTGAGCCGACAGTGCTACCCACTGCGCCACCATGCTGCCCCAGATTCCAACATTCTTCATTTATTCCTATGTGTTCAAGAGAACAAACAAATGGGCTTGGAACATGTGAGTACAGGGTGAGTCAATGACAGAATTTTCATTTTAGGCTGAACTGTCATTTTGAATAAAAAACACACAAGAATTGAATCAAAACAAAATGAAAGCTTGCAAATCAGTTACAATTTGATTTTTGTACCCAGTATGTACAGCATATAATGGAATGCCATTTCACATAAAGACATATTGTTCCACACGTTTTTTCTCAATCCATTACTCAAAGGTGATGAAAATATTACATTTGGTAACATGCTCCTAATGGCTCACAAGTCGAACCAGTGGTTGGGTGCTTCAGTTCGAACCTACAACAACTACATCTTGG[T/A]GAGTTACTGTGAGTTCCTTAACCACACTATTCTTCCTGTCAAAGCTGTATATTCATTAGACTGGAGTCTAGTTATTAATAGCATGCATATTAAAGGGCCTTCAGATTTTTTCTCAAGCAATACATGTTTTACATTTAAAATATGGTAAGGTTATTTAGCCTGTTAGCCAATTTTTTTTACTTTTACTCTAGAAATCACTGTTAAACCATGGTTAGTCCAGTAAAAACACTGCTTTGTGGTCACCATAGTTTAAAAGGATTTTTAATTTTACATTTTTAAAAATATGTTTTATAAGATGTTTAATTAGAATTTCTATTTGTCTATCTGTTGTAAAGTGCACACTGCTAGCATTGTTTTTGTGGACAGTGTCCCATAACGAACGGTTTCTGTTTACCTCCTCATGCAAACGGGAGACAGGCCTGTGCCCCATTGTTTCACTGGAACGTCCTCGTGGACCAAGAAGAAGCCATGAACACACCTGTGGGGAACTGTCAGCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40053
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016562 | Essential Splice Site | 287 | 1037 | 9 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21589832)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21246223 |
GRCz11 | 3 | 21376771 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAGATTATGTTGTTGGCGTCCCAAATGATCTGCACACTGCAGGCTCT[G/T]TAAGTGTTCTTGTTACTTGGATAATAATGCACTTCAATTATGGTCTTGCT
Long Flanking Sequence:
TTGTTGGTTGGGTTTAGGGAAGTGGGTGGGTGGGTCAGTCGATCGGTCAGTCAGTCAAACAGTCAGTTGACAGTGGCCTCTGGTGGATTTTTGAGAGAACAGCGGATGGCACTCGCAAGAGAAATTTGAGATCTCAAAAAGACAATTCAATGACAATTAAGAGTTATATTCTGAAATGAACAGAAGACTAAATTATTAATGCTTAACAAATGATTTGTAGTGTGCAGTTTTTATAAAGTGTTACCAAATAAATTATGATGACAAAACAATTCAATGCAGTCACATAATTTTCATTGTAGGATACTCTGTTGCTGCTGGGAAGTTTAATAATGACAACATCCCAGGTAAAAAATAATAATTTTTTTTACACTTTTATTCAGAAACATGCAACTTTTTTTATACAAACCGTAATTGGACATTATTTTCCTGTTGTTCTTTATTTAATGTATATTGCAGATTATGTTGTTGGCGTCCCAAATGATCTGCACACTGCAGGCTCT[G/T]TAAGTGTTCTTGTTACTTGGATAATAATGCACTTCAATTATGGTCTTGCTCAGATAAACAATTGATTAATGATTGGTAAATTGAATGATGATTGGTTGTTTAACTGTGCTTTTTTTAGGTCAAAATAATAAATGGAGCAACCGTGCCTCTACAAATCATGAAGGCAATTAGTGGCACCCAGGTTAAACATTTATTTGTGGTTGCATTTTATTATACAGAAAATGGGTCAGGATGTGATATCTTTAAACTGTTCTCAAATGTGCATCAATAGTTTTTTTTTTTTCATGTGTGTTTATTTTTGTTATTCATTTTATTCCTTTATGAAATATTAAATTCACAAAAATGAAAGAAAAATAATTGCCATGCCTTAATGCCTTCCATCTTCCCACCAGATGAAGTGACTTGATCACTTGGAGATAGTTACATGTCTTTTTTTTTGTCAGTGCTTTAGAGATTGTGATGACTTTTTTAAAACCGATGAGTTGACCAGAAAGTAGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19
Status:
Confirmed mutation in F2 line
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016562 | Nonsense | 355 | 1037 | 12 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21588634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21245025 |
GRCz11 | 3 | 21375573 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGCTGTCCACGCAGAAATTTCGAGAAGTGGGACAGGTGTATGTTTA[C/A]CTGCAAAGAAATGACTTCTCCTTCGCCTCCAGACCCAACCAGATCCTGGC
Long Flanking Sequence:
TAGTGTGGGGTTTTAGCTAATATTTCCAAGACATTATATCACGTAATACACAAACAAACAATTTTATTCAAGAGATAACAATGTATTTTGTTTTGTTATTCAAAACTGTTTTGCTATTTTTTTTATATATATTTTGAAGGTTTATCTTAGAGACACAAAATGTACTCCCAATTCTAGAATCACCGATAAGCTCCTATATGTAAAAATGAACACTAAACATTCTCATGCAGTAATGTTTACTTTTTTTATCTTGTCTCCTGCAGATAGCATCTTATTTTGGACATTCTGTAGCAGTAACAGACATTAACAGAGATGGGTAAGTTATACCTCAGAGACCAGTTGATCCTTCTGGTAGTTCATGAGGTTTTATTAAATGTTTTCTAGATTAATTATACTCCATCTGTGGCCTTCAGGTGGGATGACATCCTGATTGGAGCGCCACTTTTTATGGAGCAGCTGTCCACGCAGAAATTTCGAGAAGTGGGACAGGTGTATGTTTA[C/A]CTGCAAAGAAATGACTTCTCCTTCGCCTCCAGACCCAACCAGATCCTGGCCGGGACATATGCATATGGGCGTTTTGGCAGCGCCATAGCACCTTTGGGAGACCTCGACCATGATGGTTTTAATGGTGAGGGGACATTAGAGCACTTTTAACTGTGAAAATAACACATCTTAATATTTTCATGGATAATTCTGAGCACAAACCACCCACTTCAAATGTCATCACTCAATTGAATGTGTTGTCAGCTAATAGATATGGGCTAGTAGGGGCTGTTATCACCCATCCACATGGTTAATCAGCTATACTAATGAAAAAGACTCCAGATTTGTTTTTACATTACTTTGACGGTTGGGTTTAGGGTTGAGGTAGGGGTAGACATTAATAAAATACAATTAATGGGAAATTTTTATAAATAGTATAAATAATTACTACTACTAGTATTGGGTGTAGAAGGCTACTACTGGCCCATATCTATCACTTGATAACCACTGATAACGTCCAT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa30831
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016562 | Nonsense | 405 | 1037 | 13 | 30 |
ENSDART00000016562 | Nonsense | 405 | 1037 | 13 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21584159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21240550 |
GRCz11 | 3 | 21371098 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCACGTGTATTCATTTCTCCTCAGATGTGGCAGTGGGAGCGCCTGGTT[C/A]AGTTGATGGGGGTAAAGTGTTTATTTACCTGGGTAAGAGTGGTGGTTTGA
Long Flanking Sequence:
CTGTAAAAAAAAAAATCTGTTAATTAACAGTTCGATATTTTGTGATTCACAAGTGTTTTCTACTATTTACGGTTGTGAATTGAATTATGGTACCTCGATCTCTGCTCAGTTGACTTATAAAGTTGAAAATTCAACTTTACAGTTTACCAAAGTTACTTTTATTGACATTTTATTTGTTGGAAACAATATAATGTGAGAAATATTATGTAGAGAAATAAGTCTGTAAAATGTACCAAAAATGTACTGGCAGCTTATTGCAAGGTTTTTGTACCGTAGGTACAACATCAACCCAGACAATATATCACCTTAAACTATTAAAAATGTTGTTGAAAGAAAGACCAAGGTCCCATAAAGCAGAAAAAGCATAAATCCACTTGGTAAACATGGGTAAAATTAAAACATGAATTACAAAATACAGAAAACTGCTCAGTTATGGATATTTTTATAATGTAGCACGTGTATTCATTTCTCCTCAGATGTGGCAGTGGGAGCGCCTGGTT[C/A]AGTTGATGGGGGTAAAGTGTTTATTTACCTGGGTAAGAGTGGTGGTTTGAGCACCCAGTATGTCCAGGTCATCGAGAGCCCATTTCGCAGCCTCATAGATCCTCCAATGTTCGGCTTCAGCATAAGGGGAGGGACAGATATTGATGATAACGGATATCCAGGTACTGTATGTAATACATTGTTTAAAAACCTCTGATGATTTAGTTCTTGTCTCATTCCAGAAATAATGTAAAATGTTTAAATATGATAGGAAACATTTGATTGTCCACACATGACAATGACAGTAAACTTGATTTTACCTGACAGAGTTGACATTGTCAGCCATTTTGTGCTTTAACTCAAAATGCTAAAAAAAATTAGAAGGTTCATGAGAAATTCACTAAAGTATCACAAAAACAGAGTTGAGAAATAATCAATCTATTGATGTATCCTAAACATTTTTTGTACAAATTAATGAAAGAAGAATAATAACATGGACGTAACATGGATAGATAATAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40052
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016562 | Nonsense | 405 | 1037 | 13 | 30 |
ENSDART00000016562 | Nonsense | 405 | 1037 | 13 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21584159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21240550 |
GRCz11 | 3 | 21371098 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCACGTGTATTCATTTCTCCTCAGATGTGGCAGTGGGAGCGCCTGGTT[C/A]AGTTGATGGGGGTAAAGTGTTTATTTACCTGGGTAAGAGTGGTGGTTTGA
Long Flanking Sequence:
CTGTAAAAAAAAAAATCTGTTAATTAACAGTTCGATATTTTGTGATTCACAAGTGTTTTCTACTATTTACGGTTGTGAATTGAATTATGGTACCTCGATCTCTGCTCAGTTGACTTATAAAGTTGAAAATTCAACTTTACAGTTTACCAAAGTTACTTTTATTGACATTTTATTTGTTGGAAACAATATAATGTGAGAAATATTATGTAGAGAAATAAGTCTGTAAAATGTACCAAAAATGTACTGGCAGCTTATTGCAAGGTTTTTGTACCGTAGGTACAACATCAACCCAGACAATATATCACCTTAAACTATTAAAAATGTTGTTGAAAGAAAGACCAAGGTCCCATAAAGCAGAAAAAGCATAAATCCACTTGGTAAACATGGGTAAAATTAAAACATGAATTACAAAATACAGAAAACTGCTCAGTTATGGATATTTTTATAATGTAGCACGTGTATTCATTTCTCCTCAGATGTGGCAGTGGGAGCGCCTGGTT[C/A]AGTTGATGGGGGTAAAGTGTTTATTTACCTGGGTAAGAGTGGTGGTTTGAGCACCCAGTATGTCCAGGTCATCGAGAGCCCATTTCGCAGCCTCATAGATCCTCCAATGTTCGGCTTCAGCATAAGGGGAGGGACAGATATTGATGATAACGGATATCCAGGTACTGTATGTAATACATTGTTTAAAAACCTCTGATGATTTAGTTCTTGTCTCATTCCAGAAATAATGTAAAATGTTTAAATATGATAGGAAACATTTGATTGTCCACACATGACAATGACAGTAAACTTGATTTTACCTGACAGAGTTGACATTGTCAGCCATTTTGTGCTTTAACTCAAAATGCTAAAAAAAATTAGAAGGTTCATGAGAAATTCACTAAAGTATCACAAAAACAGAGTTGAGAAATAATCAATCTATTGATGTATCCTAAACATTTTTTGTACAAATTAATGAAAGAAGAATAATAACATGGACGTAACATGGATAGATAATAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10134
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 |
---|---|---|---|---|---|
ENSDART00000016562 | Nonsense | 616 | 1037 | 19 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21574371)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21230762 |
GRCz11 | 3 | 21361310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACTATTAATTCCCCTAACCTGCTGAAAACTGTTTCTTCTGTTTAGACA[C/T]GAATAATACTAAACTGTGGTCCTGATAATGTCTGTAWTCCAGACCTGCAG
Long Flanking Sequence:
TAATTAATTTTATTTAAATAAACAATTTTTACATAAATAATGGTTTAAATGAATGATTCAGTAACTTACTCATTAAGTCAGACTTCATTATTAGCTTAATCAGTGTTCTTGAATGAACCAATTTAATAAGTGATTCCTTAACAAATTATATGTTAACAGATGCTTTTCCCTCCTATTCATAACAATATAATTAAGTTGCTCTCAAAAGCTTAGAAAAGACAACGGTGATACACCTTAGACATCAATGATAATAGATGTTACCTGTAAACCTTTTTCATAGTACTTCTGTGATAGCTTGACTTTTTGTAACACAGAAATACAATGATCACATATTTTTAAATGTACATCTTCATATTCACAGACAAAGCGCAATAAGCCATTTAGGAATAAAATTGTGTGGGTGTTTTAATTAAGATCACAGTCCTTTAACAATTAATCACCTCATGTAGGCTACTATTAATTCCCCTAACCTGCTGAAAACTGTTTCTTCTGTTTAGACA[C/T]GAATAATACTAAACTGTGGTCCTGATAATGTCTGTATTCCAGACCTGCAGCTGAAGGCAGTAGCGTAAGTTTTGTTAGCTATACAGTAAAAGTTTTAGATTACAGGCATTTATCTCAAACAAGCTATTTTTTTTTCTGAAAACAGGTCAACAGAACCAATCCTGATCGGCGATGAGAATCCAGCGCTGCTGATTATCGAGGCTGAGAATCAGGGAGAAGGAGCCTATGAGACTGAGCTCTATATCAGCCCACCGGCAAACACACACTATCAGGGTGTTTTGAGCAACCATGAGGTGAGGGTTTAGTCACTTCCTGTTTGTTACTGACAGAATCACAAAGTGCAAGATATCAATTTCAATCATGCTGTTGAGTGAAAGAATCTGTTTGGACATTCATATCAAATTGCATGTAAAATAAATGATGGCTTATAGAAAGTAGATTTGAACACATTAAAATGAAAATGGTTGTTAAAACTAACAATACTGATACAAACATTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40051
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 |
---|---|---|---|---|---|
ENSDART00000016562 | Essential Splice Site | 718 | 1037 | 22 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21573424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21229815 |
GRCz11 | 3 | 21360363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTCAGCCCACTGTGGAACATCCCGCTCTCTGTTGTTTTTCTCATTCA[G/A]CTGAAAGCAGGTCTTTACTTCAGCATGGGTGATCTGGAACAGGTGGAGAA
Long Flanking Sequence:
ACATTAAAATGAAAATGGTTGTTAAAACTAACAATACTGATACAAACATTTAAAAAACGTTGCTTTAATTGCATATAATCTTTAAGCTAACATAAGTTAATAGTTAAAAAGTAACCACACAAACCACCCAAGGGTTTGTCTGAACAAGATTTGCATATGAAACTGTCTTTGGTTCGTCAGAAAACTAAATCAGGCCTAACAAATGATATCTGACTGTCCTCTTTCTGTCAGTGCGCTTATTTTATATTCATGCACAAATTAGAGTTATTTCCGGGTCACATACGGTTTAAAATGTGTGGTTGCAGGATTTCAGTGCCTTGGTGTGTGGTCAGAAGAAGGAGAACGGCTCAGTCATTGTGGTCTGCGATCTGGGAAATCCCATGGAGGCCGGACAACAGGTCAGAGTGACATAATGAAGACAAAAACACACCTCAGATGATTTGACCGTTAATTTTCAGCCCACTGTGGAACATCCCGCTCTCTGTTGTTTTTCTCATTCA[G/A]CTGAAAGCAGGTCTTTACTTCAGCATGGGTGATCTGGAACAGGTGGAGAACCACATCACATTTCAAATGCAAATACGAAGGTGTGAACACCCATAAACACACCATCTGTGCTGTTAGCAAAACAAAAACGGCACAAAATGATGTCTCTTTTTTTTCACGGTACATTTTGCTCATGATGACAGTGTTCATTATATTCTTTTGATCTCTTTTATAATTTTTTTTAGTAAGAACAGCCAGAACTCAGATAGCAACCTGGTCCAATTGCAGGTTAATGTAACTGCTGTCGCTTCCCTGGAGATGCGTGGGTTAGTGCCGCTGTCTTTTTCTCATGTCTCTTTGTTTTCCCCCTATTACAAGAGAGAGCATAAAACTGAAAGGAGATAATGACTGGTTGGCTATAAAGAAGTATGCATGTCCATAATCATAAACGAGGATTGTTATTTTCCGCATCACTGTGACAAATCAGGTACAATGTTAAAAGTAAAATTGGTTTGGTTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26046
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 |
---|---|---|---|---|---|
ENSDART00000016562 | Essential Splice Site | 1009 | 1037 | 29 | 30 |
Genomic Location (Zv9):
Chromosome 3 (position 21564562)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 21220953 |
GRCz11 | 3 | 21351501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTCGCTGGACTGCTTCTATTGGCTGCGCTGAGCACCATCTTCTGGAAG[G/A]TACTTCTATGGGTTTAACAGCAGAGGGAGCTATAATTGTCCCTTAAAGAT
Long Flanking Sequence:
TTGATCATTAATAAAATTATCGAGCCCAACTGTTATTAAGATCAAAAAAGTAATACATTTTACAGTTTTTTACATCATAAAACTGAATGTATATTTTTACAGCAAAACAGCCAATCAAAAATAAATAAATAAATAAATATGGCACATTCTGATACAAATTTTGTTTCAATTTTTTAAAGTTCCAATAATAAGCTGGTTATACACAATCTACATTGTGAAAGTGCTATAGAACTAAAGATGATTTGAAGAGAATTTTTTGAGAAAAGCTGCCCCCAATCAGATATTTTAGGCCACACACAAAAAAATATCAAATGATTTCCTGGAAGGACAGCTACTGTAAGCACTGGGCTCGTAATAAAAAAGCTCTATCTATGTAGACTCACACAAAAATAATTTGGCGAAGCCCTGATGGACAAGAGGAGGTACCTTTGTGGTGGATCGTAGTGTCAATCGTCGCTGGACTGCTTCTATTGGCTGCGCTGAGCACCATCTTCTGGAAG[G/A]TACTTCTATGGGTTTAACAGCAGAGGGAGCTATAATTGTCCCTTAAAGATCTGCGAGCTCAGGGGTGGCCAACGCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTGCAACCCATATCAAACACACCTGCCTGTAATTATCACGTGTTGTTCAGGTCCTAATTAATTGATTCAGGTGTGTTTGATATGGGTAGCAACTAAAATCTGCAGGTAAGGGGCTCTCCTGGAACAGGGTTGCCCACCCCTGTACTAGATAAAGATAAACAAACATCTCTGTTAAGTTAACAGATCATGCTTACACCTTGAATCTTCATCCATGTTAACAATATTATAAAACTCTGTATGTTTTAAGATGGGGTTTTTCAAGCGTAACCGTCCTCCATCTGATAATGATGACGATGATGATGATGATGTCACTCAGCAGCTGAATGGAGACTGAAGTCAGACTGCAAATCTTGAGCTTTGTGATGCTGTATGACTTTTAAAATTGTGTTTG
Associated Phenotype:
Not determined