Busch Lab

ZMP

lmo7b

Ensembl ID:
ENSDARG00000053535
ZFIN ID:
ZDB-GENE-060825-242
Description:
Novel protein similar to H.sapiens LMO7, LIM domain 7 (LMO7, zgc:152922) [Source:UniProtKB/TrEMBL;Ac
Human Orthologue:
LMO7
Human Description:
LIM domain 7 [Source:HGNC Symbol;Acc:6646]
Mouse Orthologue:
Lmo7
Mouse Description:
LIM domain only 7 Gene [Source:MGI Symbol;Acc:MGI:1353586]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa19525 Essential Splice Site Available for shipment Available now
sa19524 Essential Splice Site Available for shipment Available now
sa16373 Nonsense Available for shipment Available now
sa12998 Nonsense Available for shipment Available now
sa38276 Nonsense Mutation detected in F1 DNA Not yet available
sa31214 Nonsense Available for shipment Available now
sa10064 Nonsense Available for shipment Available now
sa10684 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa19525
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075577 None None 1188 None 27
ENSDART00000083736 Essential Splice Site None 161 None 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 None None 227 None 8
ENSDART00000143048 None None 822 None 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34083007)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33717758
GRCz11 1 34450326
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGTAGCCGCGGGAAGCAAATACACGTAATTGAAAGAAGGGCTTGCAGG[T/A]AAGTTTAGACTTGTTGCATTTGTGTTTTCTTGTGTGGTGGCACAGGTGTG
Long Flanking Sequence:
TTGGGTGAACTAACGACAGATATGACTAGTGAAAAATGTCTTACCTGACTTGGACAGTTAACAAACAGCAACGTTTTTGAAGTGATATTTGTCTCCATCTGCTGGTCAATGTGGCTAAAGCCCGCGAATCCTCTCCGACACTTTTTATATAGCAGCAGGGGGCGTGGCATATATTTAAACAACTCATCATCATCTTCTCTACCTATGCACTTGTCTCTGCAAACGCAGCAGCTGTTCTCCGCGTTTTCCGTTTGTCTCATCACTGAACATGGATGTTTCAGTTCCTGCTTACGAGTAGTTTGGTGAAAGGTGGCGGCTGACTTGAGGAATCCTGCAAGGTGTTCATGCTGTGCATTTGAAAAGGAGTGTTTGCAAAAGTTGAAGAAAGTTGGAGACGCGCACTGGTAGCGGGAAACACCTTGCGCTTTCGCCTCGAGACATCTGGGAAGTGAAGTAGCCGCGGGAAGCAAATACACGTAATTGAAAGAAGGGCTTGCAGG[T/A]AAGTTTAGACTTGTTGCATTTGTGTTTTCTTGTGTGGTGGCACAGGTGTGCGGGGTTCTGAATCACCATCTTTTAAGGTGGCAAACATGAAGGTGATGGAAGTTCCTGTTAACCTTTTCATATTGAGGTAAAGTTGGTTCTATATTCACACAATTTCCCACCGAATGCCATGGTAAAAATGTCAAATTATCACTGAACGTTTATGCGAATATAAAACCACCTTTTCTTTAATCCTGTTTATTACAGTGGACGTCACTTTATGCTAAACAAGATAAAATTATATGTGCAACCGTTGTTATTTGAAATTAATATAAAGGGGTCCCATTACTAAATCATAATGTCTGGATTTTTTCCTTAATGTAAAAAAGGTGTACTTTACTACAGCAATACAGCTAGGTGTGCTGTACAAACATTAGTAAATCATTTTGGTTATTTTTTTCTACGCTTTTCTTTAAACATGTTCATAATGTTGTGACATCTTTTTCTTTTTTCTTTTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19524
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
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075577 Essential Splice Site 106 1188 5 27
ENSDART00000083736 Essential Splice Site 106 161 6 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 Essential Splice Site 91 227 5 8
ENSDART00000143048 None None 822 None 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34065500)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33700251
GRCz11 1 34432819
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGATCTGTGTCTGTTCATTTCATTTAACCTGCTTCTTTTCTTCTGCTT[A/T]GACGTGAAGAGACAAACAGAAGACTAAAAAATGTAAGTTTTATTTTTTAT
Long Flanking Sequence:
TTTCACTTAATAACCACAGAACTATTACATCAAATGTTCCTCCTTAACCTGTCTAGTTTGTTTAACATAACATGACTGTTTAATGAGCATTAGGGACTTAAATGGTTGCATTTGTCTGCAAAAACATGTTTGCTAGTTCATAGTGCTAAACAGATGGCTCGCATGTCCAATGTCAGCACACACAAGCATGCACCCCTGTCAGACTGATTACTGTTTTGTGTGTGTGTGTGTGTGTGTGTGTTTGCTTATGTGACGAAAAGGATGATTGTTCTTGTTATAATAAGCAGTTTTGTATGGAATTCTTGTTTGTTGATTTGTTAATATATTTACCAGTGTACATGATTTGTGACTTATGTGACATATACAGTAGTCGGTCCATTTATAGCAGTGACTTAATTTTATTGGATGGTAGGAATGGATTTAGTTGCTTGCGCTGTATAGGGTGCAGGAACTGATCTGTGTCTGTTCATTTCATTTAACCTGCTTCTTTTCTTCTGCTT[A/T]GACGTGAAGAGACAAACAGAAGACTAAAAAATGTAAGTTTTATTTTTTATGCTATTGCTATCTTGTTTTATCACCGACAAATGACTTCTGTTGAATGACTTAAGTGTCTGTGCATGGTATAGTATGTCTTTGCAGAGTGAATTTGGCCTTTGACTCTTTATTTTGCATACCCAACAAGCTGATTTGTAATTGTATCTCATTACAGTCGTCTAGTGAAGTGTTGTTTAGAATTGGACATTTAAAGCCACTTTGCATGCTTTATAGATTAAGGACTCCGATGCAGATACATATGAACAGTGTTCTTTTTTTCTTTAACTTTGTTTTGTAATAATACATATTTAAAATGGTTTAATTTGGCGATAGCAGTTTCATTTCTGCTAGAGTCATGAGAATTAATGTAAATTCAGTGTAATTGAACGGGTTGTTTATTAACAATGACCATAATATTTGTAGGAAACTTTTTGGTAAAAAAAAAAGGCCAAATGTATGGTTTCTGCAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16373
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075577 Nonsense 657 1188 13 27
ENSDART00000083736 None None 161 None 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 None None 227 None 8
ENSDART00000143048 Nonsense 291 822 4 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34029447)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33664198
GRCz11 1 34396766
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCGGGAGAGACTTTGGATTCAAGGCTCACTGGGACTCAGTTGGTGCTTA[T/A]GTKAAATCTGTTCAAGCAGGTAAGACTTAATGGTTKCTGTGAAGTGGTCR
Long Flanking Sequence:
TGCTGTTTTATGGAGAGAAATGTCAAGACACTGTTAAGCTTAATAGTTTATTCTGTTGCCAATTGAAAAAAAAAATATATATATATGAAGGGGTATAATATTATTACCTTAAAAAATATTTTAAATTAAATAAAAACAGCTTTTACTCCAGCCAAGCTAAAATAAATAAGACTTTCCCTGTAGAAAAATGTAGACTAGATAAACGCTGTGAAAATGTCCTTGCTCTGTTAAACATCACTTGGGAATTATTTGAAAAATAATTCACTGGAGGGCCTAATCGTTTTGCCTTCAACTCTATGTACTGAACGGTTTGTGTTATACAGACTGAAGCAGATTTCCCGAGGAAGAAGGTGTCATGGGATCCTCAGGTGTCACATTCTCTCTCTGTATCTCTCTCTCTTTCAGGTGGGTCAAAGTGAAATGCGAGTCTGCTTGAATCAGAAGCCTAACAGCGGGAGAGACTTTGGATTCAAGGCTCACTGGGACTCAGTTGGTGCTTA[T/A]GTTAAATCTGTTCAAGCAGGTAAGACTTAATGGTTTCTGTGAAGTGGTCGCTTTAGATGTATATGGATGTTTCTCCGTGTTTTGAGAAATACGGTGCAGCTTTGGAGAGGTGTATGTTTACTCGCGAATGACTATATGAATAGAAGAGAACTGCGTTTAGGATTTATTTAAGGCTGATAGGCTGTTTTTGCTTCCAATTACAATACATGTATGTAGCATTTGGGATCTCTGTTTGCATACTCTTGTAGCTTTTAGAGTTTGTGGATGTTTATGTATCCCACTGTGTCCTTGAAAGATCTATTTGTAGCTTCTTTGAATTTTGAGTGGTGTTTGTGTATTGCTAAGAATGTTTCTGTTCAGCTGAAGTTTTTTTATTCTTGGGATTCTGGAGAGAGACTGAGATGCTGAATGATTTATAGAGAACAGTGAAGGTGTTTTACTCTGCATTAGTCTGATTGGTTAAACTGAAGAAGTCTTGGAACCTGTCCTCTAGACAGTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12998
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075577 Nonsense 736 1188 15 27
ENSDART00000083736 None None 161 None 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 None None 227 None 8
ENSDART00000143048 Nonsense 370 822 6 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34021807)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33656558
GRCz11 1 34389126
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCAGTGGCCAACCTTCCCTACCATACCAGAGCCATAAGATAATCAATT[T/A]GACAAGTGCCACTTCAACACTTATAGGGCGACCTGAGCACTTTRTYCCCA
Long Flanking Sequence:
TCCTTTATATCTATTATTAATCATACATTGTATTGTTTCAAACTACTAAAATGTCAATAAAAGTCATTTAGTTATACTGCTGCATTCAATTTTGAACATCAAAAGTAGACAAAGTGGAGATCAAGGTCATTAAATACAATTCATAACCATAAAAAATGGAAAACAGTCGACGAATCACAAGATAAGAATACCTTAATTAACCGATATTTACAGTATGTATTAATATAGTTGTATAAAGACCTGCAGCTTCATGGGTTTTCACAATTGCACCAGTAATCTTTCTTCATCATTTAAATATAGGCACAGTTAATTTCAATAATCACACATGATTTTACACAAACAATGGTCAATTCTGGTTAAAATCCTGATGTACGTCACTGACAAGTTCACTCATTTGTGTCCTTGACGTTTCTTAATTGCTGATGTATGTTTTGGGTACTGGACAGACTGGGGCAGTGGCCAACCTTCCCTACCATACCAGAGCCATAAGATAATCAATT[T/A]GACAAGTGCCACTTCAACACTTATAGGGCGACCTGAGCACTTTGTCCCCATCAACACAAGCTCAAACTCTTCAGTGGAGACTGTGGGGAAGACACAGGTCAACGGACAGCCTGCCAATGTGAGTCAGCACAATGTAATCTGTCTAATCTAATGAATGTGGGAAATTAGTGAGTTTAACTGTATGTGTATGTCTTTCTGTGGTAATTTATATTCTAGCTTGTGCAGTGAATATTAAATGGTAGGCAGTAATTAAACCGGATTAATGATGCCTTTTGTATATAAATTAATTAATCAGAAGATTGCAACTTATCAATTAAAATTAGCAGTAAAGACATCATAATGTTACTAGAGGTTTTTATTTACAGCTATAAAAAAATCCTTAAAACTGTTTACAGCATGGAAAGTGGAAAAATGGGGATGCAAACTTGCATGCATGAACTGAAGGATTTTGAGAAATAATGTTGCAATGAACATTATAAAAATGTATCTTTGCCATCATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38276
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075577 Nonsense 901 1188 20 27
ENSDART00000083736 None None 161 None 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 None None 227 None 8
ENSDART00000143048 Nonsense 535 822 11 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34012374)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33647125
GRCz11 1 34379693
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCCCTCATAATTCACCTCCCTTCTACAACCAGTCGAGTGCCACCTTTT[C/A]AGTGACGTTTAATGAGAATGTGGCAGCAGCACAGAACAGACAGGCCTGTG
Long Flanking Sequence:
AACGTCAGGAAATTTTAAAAAAGAGACTTGCTGGGTTTATATCACTCCAATATGATTGTGGACACACTATACCTACACACAGTTCTGTCCAAACAGCTTACAAACGTAGATTTTTATCATAGGTGCCCTTTAATGATGCACACTTTAGTCAAATAAATGCAAATAACATGCCTGCTCTTTAAATAGTCAAAAGTCAGTGGTTTCTATGGTTCTGAGCTTATGCATATTATGATTTCATGAGCTATGGTTTATCTGTAAAATTGCCTGAAATTGTAACCACATTGTAAGGGCAGCATGCTAATCTTTCTCATTTTTTCAACAGTGCTTTCATTTATCGTTATATTCTGCAACTGCTAACTACAGTATGAATGGTGAATGGTTAACATTGTTGTTCATCTCCTGTTGCTATTAGGAGCAGAAAACCCTTGACGTGCTGTCCAATGGAAACCCTGCCCCTCATAATTCACCTCCCTTCTACAACCAGTCGAGTGCCACCTTTT[C/A]AGTGACGTTTAATGAGAATGTGGCAGCAGCACAGAACAGACAGGCCTGTGTGCAAACAGCAGCAGGACACCAGTCAATAAAAGCAGAAGACAAGTGTGATTCACCCACAAAGACTCTGTGGTAAGAAATCAGCCAAGCACAGTTGCAAAATATATTTGATGCATTGCTGAAAATATTGTAAATGCCTTTTTGGTTAAAAACTGTATCTTTTAACTGTTTTCAAATACAATACCTCAAATGACTATAATAATTTTAGTAGAGGCATTCAAAGGATTAACATTTGAGAACCGTGGCACCGTCTGCACATGTAATCTTAATAACATTAATAGTTGTGCCACTTAGAGATGCATGTTTGAAACATTTGGATCCACATTAATTATATGTATGATAAAAATAATACCACCTGTAAATATTGTAACTGCCTTATATTGTGCTTTTGTAGACCATGAAAACCATATACTGTATGACTTCACATACAGTAGTTAACAGTAGCTTATGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31214
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
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075577 Nonsense 1100 1188 24 27
ENSDART00000083736 None None 161 None 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 None None 227 None 8
ENSDART00000143048 Nonsense 734 822 15 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34006991)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33641742
GRCz11 1 34374310
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGTAAAACTGAACTCAAACACAACTACTCCTGAACCGCCGGGCCTC[G/T]AGTCCCGTCCAAACTCTCAGCAGCAGGGCAGGTATGGACTATTCATGTGT
Long Flanking Sequence:
AGATAAATAAAAATCAAATATAGCAGTGCAACAGGAATTATGTTTGATGCTTCTTTTTTTTTTTGTAAACCAACATTGCTGTTTAGTGTAAACCATTATTTAAAGCAGTCATTCTTTAAATACCTTTAACAGCCCTTATTTAAAACAGTCAAAATATAGTCAACCATTTGGTATAGCAGGCAGTTAAAGGGCTAGTATACATTTTTTATAATATACAATTTTTAGGCTAAAAGAACACTCCTACTGTGAAGTTCCAGTAATATTTATTATCTCAAACTGTGTCTCTTTGTTACAGATATGAATCTATGGACAATCTCCACACAACTAACTCGTGGTCCAGGCAGTCGTACACTTCCGGTTTGTCCAGCAGACCTCATTCTGCATTAGGAAGCAGTGGCTCTTACAGAAGTGGACGCAGCAGCCTGGGCCCCGGATCAGCCATCTTCTCTACTGGAGTAAAACTGAACTCAAACACAACTACTCCTGAACCGCCGGGCCTC[G/T]AGTCCCGTCCAAACTCTCAGCAGCAGGGCAGGTATGGACTATTCATGTGTGGAAGTCATGTTTTTACATTTAAATAATACTTTTAATTTTCCCTTTCCTTTTATTCAGTAAATGTATTTTCAGTTTAAACACTTTGAAGTGAATGTTAAGTGCAGCTCTTTTTTTATTTGTTTTTCCTAAAGAAGGATCTCACTCTACCATACATTTAACCCCAGGTATTTTTGCAGTCAGTGGCTGTGTTTTATACGCAGAACACTGGTACTCCATTTTGAGTATATACTGTAGTGTATACTGAGTACAATTTAAAAGTATATATGCATGAGACGGTATGCTGCTTTTCATATTGTTTACAAAAATCGTACTCTACAAAACCTATATTAATAAAATGTGTAATTAGTGATGCACTGAAATGAACAAACATTTAGGATGCAGTTAATAGGCAAATAGGGTATAAAGCATAACATTCATTTAATACTCAAATTTGTAAAACATAACTGCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10064
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
ENSDART00000075577 Nonsense 1107 1188 24 27
ENSDART00000083736 None None 161 None 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 None None 227 None 8
ENSDART00000143048 Nonsense 741 822 15 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34006970)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33641721
GRCz11 1 34374289
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACAACTACWCCTGAACCGMCGGGCCTCGAGTCCCGTCCAAACTCTCAG[C/T]AGCAGGGCAGGTATGGACTATTCATGTGTGRAAGTCATGTYTTTACATTT
Long Flanking Sequence:
AGCAGTGCAACAGGAATTATGTTTGATGCTTCTTTTTTTTTTTGTAAACCAACATTGCTGTTTAGTGTAAACCATTATTTAAAGCAGTCATTCTTTAAATACCTTTAACAGCCCTTATTTAAAACAGTCAAAATATAGTCAACCATTTGGTATAGCAGGCAGTTAAAGGGCTAGTATACATTTTTTATAATATACAATTTTTAGGCTAAAAGAACACTCCTACTGTGAAGTTCCAGTAATATTTATTATCTCAAACTGTGTCTCTTTGTTACAGATATGAATCTATGGACAATCTCCACACAACTAACTCGTGGTCCAGGCAGTCGTACACTTCCGGTTTGTCCAGCAGACCTCATTCTGCATTAGGAAGCAGTGGCTCTTACAGAAGTGGACGCAGCAGCCTGGGCCCCGGATCAGCCATCTTCTCTACTGGAGTAAAACTGAACTCAAACACAACTACTCCTGAACCGCCGGGCCTCGAGTCCCGTCCAAACTCTCAG[C/T]AGCAGGGCAGGTATGGACTATTCATGTGTGGAAGTCATGTTTTTACATTTAAATAATACTTTTAATTTTCCCTTTCCTTTTATTCAGTAAATGTATTTTCAGTTTAAACACTTTGAAGTGAATGTTAAGTGCAGCTCTTTTTTTATTTGTTTTTCCTAAAGAAGGATCTCACTCTACCATACATTTAACCCCAGGTATTTTTGCAGTCAGTGGCTGTGTTTTATACGCAGAACACTGGTACTCCATTTTGAGTATATACTGTAGTGTATACTGAGTACAATTTAAAAGTATATATGCATGAGACGGTATGCTGCTTTTCATATTGTTTACAAAAATCGTACTCTACAAAACCTATATTAATAAAATGTGTAATTAGTGATGCACTGAAATGAACAAACATTTAGGATGCAGTTAATAGGCAAATAGGGTATAAAGCATAACATTCATTTAATACTCAAATTTGTAAAACATAACTGCGATGTGTTTAAATGGCACAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10684
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075577 Essential Splice Site 1146 1188 25 27
ENSDART00000083736 None None 161 None 8
ENSDART00000135351 None None 178 None 2
ENSDART00000140515 None None 227 None 8
ENSDART00000143048 Essential Splice Site 780 822 16 18

The following transcripts of ENSDARG00000053535 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 34005140)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 33639891
GRCz11 1 34372459
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGGTCATCGATTCCCTGGAGCTCTGCTTTCACATTGGCTGCTTCAAG[G/A]TGAGGCCGGAGGTCACCTGAAACTGAGAGAACTGGCCATCCATGGACATG
Long Flanking Sequence:
TAATCCAAATAAGCACTATAGACTAAAAAAAGAAGACCTTATATTAATAGTCCTGCATAAGTGTGTCAACAGCTGACATGTTTACCTGCTGTTTATCCAAATTGTCTGCATAAAAGAAACTGATACCTCACATAAGAAATGGTAATAAAATCTGCCCATTTCAGCTGATGAAATTTCAGTGCATCACTAGTGAAAATTGTTATTGTGTGTGTTTACATATACTGTATAGGCCAATATGGCTATTCCATTGATAATATAAAAGTTACTCTGTTCAGTATACATGCAGTATAGTAAGGTATTAAACTATTTGTCCGCCGCCAACCCTCTCTGGTAAATGAAGTGGACTGAGGCAGAGGTCTTTTGTGTGACATTGAGCATGTGGTGCCTGTAGGCTGGTCAGTGGCAGGCGGATGTGCTCGAGGTGCGAGCAGCCGCTGGGGAAGGGAGCTGCCATGGTCATCGATTCCCTGGAGCTCTGCTTTCACATTGGCTGCTTCAAG[G/A]TGAGGCCGGAGGTCACCTGAAACTGAGAGAACTGGCCATCCATGGACATGCCTGGGGTTTTAATCTTCATCATCTGGGGAAATGGGAGAGAATTAGCCACTACTCTTTTGGTGAAGGCAATCAGATTGCAAGCATGCAGGACAAATTAGAAATGCTGTCTTAAATTGATCTAAAACTGTCTTAAAATGCTGTCTTAAATCTAAAACTGATAAAATATAACAATTTCAGTAATGCTTTGTTTTAGGGTGTGTATAAGTTTGGCAGGTTTGGTTTTATTCAAACTGAAAAAAAAATCACGGCTTGAATTCAAGCATATAGCATTTAGAAGTTTGTAACTATGTTTGCAAAATAAATGCCTTTTTTGGTATATTTGGATTTGGTTTTTGAAGCGACAGTGAATTCTAAAGTATGCTAAAAAACACACCCTTAATTTAAACATCCACATGATCACACCGGTGTGATTTAGAACATTAAGTGCATGACATAATTGGTTGTTAAAT
Associated Phenotype:
Not determined