Busch Lab

ZMP

ulk1a

Ensembl ID:
ENSDARG00000062518
ZFIN ID:
ZDB-GENE-080723-31
Description:
unc-51-like kinase 1a [Source:RefSeq peptide;Acc:NP_001124103]
Human Orthologue:
ULK1
Human Description:
unc-51-like kinase 1 (C. elegans) [Source:HGNC Symbol;Acc:12558]
Mouse Orthologue:
Ulk1
Mouse Description:
Unc-51 like kinase 1 (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1270126]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa13161 Nonsense Available for shipment Available now
sa9810 Nonsense Available for shipment Available now
sa7155 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa25404 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17536 Nonsense Available for shipment Available now
sa34473 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13161
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Nonsense 226 927 9 28
ENSDART00000124641 Nonsense 231 1038 9 32
ENSDART00000142243 None None 558 None 14
ENSDART00000144239 Nonsense 226 271 9 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46378866)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43764623
GRCz11 8 43758042
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTTTTGATTTCTTTAGGCAAGTACTCCTCAGGAAYTRCGGCAGTTYTA[T/G]GAAAGAAACCGGAGCCTCAGTCCCAGGTAAGTGGCCCTGAGCACTGACTG
Long Flanking Sequence:
CAGAGTTTCCTGTTGCATAATAATGTGTGCAAGGGCACAAACTTTAAAGTGGGCGGACGATTTTTTCCTGTGTTGTAGATTTGACATGTAAAGTACCTTTCAAAAGTTTAGGGTCATTGAGTACATTCATGAATTTTGGGTCACACTTTACAATATGGTTCTATTACATAAAAATTTACTATAGAAATACATTTTGTAAAACAGTCATGTTTAGTTTTGTACAAGTATTGTTCTGGGAATTAACAAAATAATTTTTGGGCAAACCTCTGTCCCTTTAAGCCTTGTGTAAACGATTTCCCCTAAACAATTCAGTATCAATCTCCCATGCAATCCAGTTAATGTATTTTGTTTTAGTGAATCAACAATTTCATACTAAATTTAAGTCTGTGATTTAGTTTTGTCCATTAAATGGTTAGATAAGTTAGTTAATAATTTGGTCTCCTTCTGAAATCTTTTTGATTTCTTTAGGCAAGTACTCCTCAGGAACTACGGCAGTTTTA[T/G]GAAAGAAACCGGAGCCTCAGTCCCAGGTAAGTGGCCCTGAGCACTGACTGTTGGTCATCTGTCAACATGATTCAGTGCAATGTGTTTGTGATATAGGGGCAAAGTTCTCTGCTGTTGTAAATTTAGCATTCAAATGAATAGTGCCTTTCAAAAGTTTAGGGTCATTAGGTACACTTATTTAATTACATTTTAAATTGATAAAAGAAAAAAAGACAGTGCAAAATGTCAGAATAGATTTTTGGTTCACACTTTACTACACAGTTCTGCTTGATAATTTACTATAAAACAAAATTTTCTATAAATAATCAAAAACTGTTTTTAAAACAGTCATGTGTCTGTACAACTATTGTTCATTTTAGTACATAAATTAACTGAAACTTAAATTAAAACAGATTTTCGATGGTTTATGTTTTGTCTTCAAATTTACTGTTTGAGCAGAGATGCCCAAAGTAGGGTCCACGGGCCAAAGTTGGCCCATAGTAACCTTTGATTTGGCCCAT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5503
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Essential Splice Site 235 927 10 28
ENSDART00000124641 Essential Splice Site 240 1038 10 32
ENSDART00000142243 None None 558 None 14
ENSDART00000144239 Essential Splice Site 235 271 10 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46380689)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43762800
GRCz11 8 43756219
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTCTGAGTCTTTTCCGTGTTTAAATCGRCACAAAAATTCTTTTTCCA[G/A]TATTCCACGTGAAACTTCCAGTCACTTGAGGCACCTTCTGCTTGGGTTGC
Long Flanking Sequence:
TATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATGTGTGTTGGTGTGTGTGTATGTATGTATGTATGTATGTATTTTTTTTTTTTGACAAATAAATATATTTGCTTTGGTGAGCATATGAGAACAAAACCAACCTCAGACTTTGTAATGGTAGAGTACACAATCGTAGTTCATGTTTATTTATTTTGTGAATGGTGGAGGATTGAGAAGCAAAACCAGTTTCTTTTCTCTCTACCATCTTTCACTTCTTTCCATTATTTAGTGCAAGGCTTTATTTATTTTGTCATTGTTGCAGTGTTTGCATTGATGAGTATCTCCTTTCTGCTATGTCAATCACTGAAAACATCAAGAGCCCAACATAAGATTATAAACATGCACACATAATGGTGAAGCTTCTGAGTCTTTTCCGTGTTTAAATCGGCACAAAAATTCTTTTTCCA[G/A]TATTCCACGTGAAACTTCCAGTCACTTGAGGCACCTTCTGCTTGGGTTGCTGCAGAGAAACCAAAGGGAACGCATAGACTTTGGTCAGTGGACACATGCTTACACACACCTGACTTTACAGTAGTCTGTACACATAAAAAATAATAATAAAGCGACCAATTACAATTCCTTGGAATTACTTATATATATTATTGGTGTCTATTCCAGATGATTTTTTTCACCACCCTTTCCTGGAGGCCAGTACATCTATGAAGAAATGTAAGATTGTGTGTGTATGCATATGTTTCTATGGTCACCATTAACAATAAGGTTGCATTGATGTTAATGTAGTTACTAACATGAACTAATAATGCACAATATTTGTACATCATTCATTAATAGCATCTACTAATTCATTATTACAATCCCAATTCACACTGGTAATGAAGTTAAAATGAAACTAACTTTATAACCAATGACTAATACATCAGACGTTAATACATTACCAAACATTAACTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9810
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Nonsense 461 927 17 28
ENSDART00000124641 Nonsense 487 1038 18 32
ENSDART00000142243 Nonsense 92 558 3 14
ENSDART00000144239 None None 271 None 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46387486)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43756003
GRCz11 8 43749422
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGATGGATCTCCAGCATGTGGGAGAACCGGTGTTTCTCCAGATTCAGGA[G/T]GATCCAGATCGTATTTACCTTCCCCACAGGGWAAAGAAACCAGTTCTTCG
Long Flanking Sequence:
ACACTCTCTGAAGATCACATTCAACAATGGCAGTTGTTCACGTATAACCTGAGAGACAGCTGTCTGAGCTGACATGAGTGGAGAAAGCTAGACTTCTAGAGATAGAAAATAATCCGCAGATCATAAGATTGAACAAATGGTTCAAATGTTTGTTCGAACATGTGGCATGTCAATCATTCACCTATTTTTTTTTCCGCTTTTTTTTTTTAGGCATCTAGAGTCGTGTGGCAGTAGCTACGCTCAGTCTATTCCTGTTCCAGTGCCAACACAAAAGCACAACTACCAGAGGATGGAGCATAATCTACAAGAGTCTGAAAGGTTGGGTTTGTCATCTGACATAATGAGGATGAAGAAATGCATAAAGATTTGCAAGAATGGCCAATTTGTTAACACAACTTCTGTTTTTTATTTTTTATTTCAGGACCTCAGCGTCTGCACATCACTGTTGCTCTGATGGATCTCCAGCATGTGGGAGAACCGGTGTTTCTCCAGATTCAGGA[G/T]GATCCAGATCGTATTTACCTTCCCCACAGGGTAAAGAAACCAGTTCTTCGATGATCTGTTTATGTATTTGCATATTTTCCTTATTGAGGAACAGACTTTAACAGCAGTTTTAAACAGGAAACTGGAAATAACAGATAGCCATTCAGAGTTTGCATATACTGTGTCTGGCATACCCACATGCATTCATATACATTTCATTATGGAAAAAATAATGTCCCTTTAATAACAAAAAAGTAGGGGGGAAAACAGGAAACACTTGACAGAAACTAAAGCAACTTTTTATAAAATGTTTTCAGTGATTAAAATAAATTTGTAATAAAATGTAATTTTTTAATCAACATGATTACAAACATATGTATTCACTTTGCTAAATGTAAAACAGATATAAAATCAAACTAAACTGTAGAGAAAGATTTAAAAAAAAAAAAGAAACCCTGTTTAATCAAACCAAGACACCATGTGGATTCTAAACCTGTTTTTTTCTTTATTTTTTTAGTCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7155
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Essential Splice Site 471 927 None 28
ENSDART00000124641 Essential Splice Site 497 1038 None 32
ENSDART00000142243 Essential Splice Site 102 558 None 14
ENSDART00000144239 None None 271 None 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46387518)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43755971
GRCz11 8 43749390
KASP Assay ID:
554-5342.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTCCAGATTCAGGAGGATCCAGATCGTATTTACCTTCCCCACAGGG[T/A]AAAGAAACCAGTTCTTCGATGATCTGTTTATGTATTTGCATATTTTCCTT
Long Flanking Sequence:
GTTGTTCACGTATAACCTGAGAGACAGCTGTCTGAGCTGACATGAGTGGAGAAAGCTAGACTTCTAGAGATAGAAAATAATCCGCAGATCATAAGATTGAACAAATGGTTCAAATGTTTGTTCGAACATGTGGCATGTCAATCATTCACCTATTTTTTTTTCCGCTTTTTTTTTTTAGGCATCTAGAGTCGTGTGGCAGTAGCTACGCTCAGTCTATTCCTGTTCCAGTGCCAACACAAAAGCACAACTACCAGAGGATGGAGCATAATCTACAAGAGTCTGAAAGGTTGGGTTTGTCATCTGACATAATGAGGATGAAGAAATGCATAAAGATTTGCAAGAATGGCCAATTTGTTAACACAACTTCTGTTTTTTATTTTTTATTTCAGGACCTCAGCGTCTGCACATCACTGTTGCTCTGATGGATCTCCAGCATGTGGGAGAACCGGTGTTTCTCCAGATTCAGGAGGATCCAGATCGTATTTACCTTCCCCACAGGG[T/A]AAAGAAACCAGTTCTTCGATGATCTGTTTATGTATTTGCATATTTTCCTTATTGAGGAACAGACTTTAACAGCAGTTTTAAACAGGAAACTGGAAATAACAGATAGCCATTCAGAGTTTGCATATACTGTGTCTGGCATACCCACATGCATTCATATACATTTCATTATGGAAAAAATAATGTCCCTTTAATAACAAAAAAGTAGGGGGGAAAACAGGAAACACTTGACAGAAACTAAAGCAACTTTTTATAAAATGTTTTCAGTGATTAAAATAAATTTGTAATAAAATGTAATTTTTTAATCAACATGATTACAAACATATGTATTCACTTTGCTAAATGTAAAACAGATATAAAATCAAACTAAACTGTAGAGAAAGATTTAAAAAAAAAAAAGAAACCCTGTTTAATCAAACCAAGACACCATGTGGATTCTAAACCTGTTTTTTTCTTTATTTTTTTAGTCGGAAGCATTCCTGAAACACCCAGTCAGCCTGAAC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa3654
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Splice Site, Nonsense 472 927 18 28
ENSDART00000124641 Nonsense 499 1038 19 32
ENSDART00000142243 Splice Site, Nonsense 103 558 4 14
ENSDART00000144239 None None 271 None 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46387985)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43755504
GRCz11 8 43748923
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGAYACCATGTGGATTCTAAACCTGTTTTTTTCTTTATTTTTTTAGTC[G/T]GAAGCATTCCTGAAACACCCAGTCAGCCTGAACCTGTTGGCAGCAGGACA
Long Flanking Sequence:
AGGATCCAGATCGTATTTACCTTCCCCACAGGGTAAAGAAACCAGTTCTTCGATGATCTGTTTATGTATTTGCATATTTTCCTTATTGAGGAACAGACTTTAACAGCAGTTTTAAACAGGAAACTGGAAATAACAGATAGCCATTCAGAGTTTGCATATACTGTGTCTGGCATACCCACATGCATTCATATACATTTCATTATGGAAAAAATAATGTCCCTTTAATAACAAAAAAGTAGGGGGGAAAACAGGAAACACTTGACAGAAACTAAAGCAACTTTTTATAAAATGTTTTCAGTGATTAAAATAAATTTGTAATAAAATGTAATTTTTTAATCAACATGATTACAAACATATGTATTCACTTTGCTAAATGTAAAACAGATATAAAATCAAACTAAACTGTAGAGAAAGATTTAAAAAAAAAAAAGAAACCCTGTTTAATCAAACCAAGACACCATGTGGATTCTAAACCTGTTTTTTTCTTTATTTTTTTAGTC[G/T]GAAGCATTCCTGAAACACCCAGTCAGCCTGAACCTGTTGGCAGCAGGACAGGGTTTCATGCCACAGGTAAAATATTTTGTTTTACTGTGCACTGATTTGATTTTGTAGACTTGTCCAACTTTCTCTCTCTCTCTCCTTATCTCCCAGATCAACAGCCTGGTCAAGTGTCTCCTCTCTTCACTGACCTCACAGACTTGGACCCAACACTGGCCCAAAGACTCAGAGCTCATCGTCACAGTCTGGATACCATAGTGCACAGGGTGAGTAATTGGGAAGAACTTTTTTTGCTCCACCAATATACAATAGTATTACTGGATCTGGGTTTAAAGCCTCGGATTTGAAAAACGTCTTTGGTAAAGTTTTATAATGAATGAACCAAACCAACCAGTTACTGAATCACATATTACCCATTTAGATTTGATGCACAAAAGTGTATCAAAATCTGACAAAAAGGCAAAGCTACAAAACTGTATTCTAATGAGAGATTAAAACAACATTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25404
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Essential Splice Site 772 927 25 28
ENSDART00000124641 Essential Splice Site 883 1038 29 32
ENSDART00000142243 Essential Splice Site 403 558 11 14
ENSDART00000144239 None None 271 None 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46394773)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43748716
GRCz11 8 43742135
KASP Assay ID:
554-7900.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGATATAAATGTCAAGTACACTGTGGTGACCTGCGTGTGTGTGTGTA[G/A]TTCTGCAGAACAATTGGTTCTCTATATGAAATGTGCTGAGCTGCTGTCTT
Long Flanking Sequence:
GCAATAGACTAAAGCATTTTGTTTTAATTTATTTCATTAGTTTTTTTCATTTTTTTTAAAAAATTTTTTATTATATTTTATTTTATTTTCATACGACTTAAGTAAATGCTAATGTAGTTATCATTATAGCCGGTGTTCTTGGTGAGAACAGCACCAAGTATCATGCCTGCTAGTAGAACTAATTTATCAAAAACATTAGATTTTTATGATGTGATGTCATTTTTTTCATCACCACAGGAGGGACACACGGACTTGCTGAGCCAGCTGCGCTTCGTTCTAGCCTTTTCCCACTGCATAACAGAGCTGGCTGGAACAAAGGACAGCGGGACTGGAAGAAACGTGCCACCTGATGCTTCACTCTTAGAGCAGAGTGTAGTGGCTGACCAGATCAGCCTGCTGAGCCGAGAGTGGAGGTGAAACACTGCTTAATCATACACACACATTATGTGTCTCTGATATAAATGTCAAGTACACTGTGGTGACCTGCGTGTGTGTGTGTA[G/A]TTCTGCAGAACAATTGGTTCTCTATATGAAATGTGCTGAGCTGCTGTCTTCTGCACTACACACAGCGATGGCTGGCATCAAAGAAGGAAAACTCTACCCATCAGGATCTGTGAAACAAGGTAAACCACACACTCCGCTAAAAGCTGTGACACAAAAAGATGATGTCAAAGAACTGACGGTAACTGCGTCTACATCCTAACTTAAAGAAAATCTCCTCAGTCACATTGGTGGAGTTGCTCTTCAGTGTTTTGACTTTTAACAGTGACATTTGCATTACACTTGACTTGACACAATCTACTTCGTAAAAAGTGCTGAAGAAATAAAGATGAATTTAATTTTATCAATTGAAAGTTTGGAAAAACTAAAAGAAGAAGTGAGAATAAAATAGATGATGTTCTTTTAGTAGCTAAAGGAGGTGTTGGTTATCCTCAGTGGTAATTGAAGAACCACAAATGGTCAATTAGTAGCTTTGGTTTAATGTTAGTTACCTCATAATTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17536
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Nonsense 888 927 27 28
ENSDART00000124641 Nonsense 999 1038 31 32
ENSDART00000142243 Nonsense 519 558 13 14
ENSDART00000144239 None None 271 None 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46397112)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43746377
GRCz11 8 43739796
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAGATGTTTCATCAMGGAGAAAGCTCTCTAGAGAGATACCACAAGGCCT[T/G]ACTGCTRATGGAGGGCCTGTCCTTGATTATTACAGAGCCTTCAGACCTAA
Long Flanking Sequence:
TTATTATTATTATTATGTTTAAAACAAATGTTTATTTCTAGAAATTGTTCTACCTTTTATTCAGTAGTTTTGATGGGAAATGTTATAACAATATAAAAGTATTTTACTGTCATTTATGAGACCTTAATTGAGACCTTCATTCTGAGTAGCATGTTGTGTGTGTGTTGCTCTTGCAGTGGTGCGTGAGCTGAATGAGATGTATAAGGAGTGTGTGAACTCCTGTCGTTCTCTGACTGAGAAACTCCAGCACTTCTTCAGCAGCAAACAGAGACTGATGGACCGGATGAACAGCATCACCGCTGAGAGGCTCATCTACGCACACACCATTCAGATGGTAAGAAGGCACACATATAGAGTGTTTCTTATTTTACAAGGAGAAACGTGTTTTAGTTTACAGATTCTGTATGTTTCTCCTCTCTAATGTGATTAGGTACAGACGGCAGCACTGGACGAGATGTTTCATCACGGAGAAAGCTCTCTAGAGAGATACCACAAGGCCT[T/G]ACTGCTGATGGAGGGCCTGTCCTTGATTATTACAGAGCCTTCAGACCTAAACAATGTCAACAAATGTAAGTATGATATGAATAAACTAGCGTTCAAATGGATGGAGTAATTTTTTGTCTTGAAATAAACAAATACTTAAACATTAAATATATTAAAGGAACTATGTAATTTTCAACACTAGTGGGCGCATTTTCACAATAAACAAATATGTGGTTTGATGACGCCCTGACTGAATGTTGATAATAGACCCTTTTCACAATGACGTCACTTTACTTCCCCTCCCCCACCAGCAACGGAGTGTATTTTTAGTTTTGGTTTATTGAATGAACGTGAGACAACTGAAAATATTAACACTGCACATTGTGATTTAAGATTATTCCAGTATTGGGCATGTGTTCAAATGTTTCTCTTTTAATACTGAGCTGCTTTCTGAGTTTGAAAATGCTTCTTTAGGTTATTAAGAGTAGAAGTAAGGTATTGTTTATCTAGGAAAAATATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34473
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090534 Essential Splice Site 909 927 27 28
ENSDART00000124641 Essential Splice Site 1020 1038 31 32
ENSDART00000142243 Essential Splice Site 540 558 13 14
ENSDART00000144239 None None 271 None 11

The following transcripts of ENSDARG00000062518 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46397178)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43746311
GRCz11 8 43739730
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTCCTTGATTATTACAGAGCCTTCAGACCTAAACAATGTCAACAAAT[G/T]TAAGTATGATATGAATAAACTAGCGTTCAAATGGATGGAGTAATTTTTTG
Long Flanking Sequence:
GTTTTGATGGGAAATGTTATAACAATATAAAAGTATTTTACTGTCATTTATGAGACCTTAATTGAGACCTTCATTCTGAGTAGCATGTTGTGTGTGTGTTGCTCTTGCAGTGGTGCGTGAGCTGAATGAGATGTATAAGGAGTGTGTGAACTCCTGTCGTTCTCTGACTGAGAAACTCCAGCACTTCTTCAGCAGCAAACAGAGACTGATGGACCGGATGAACAGCATCACCGCTGAGAGGCTCATCTACGCACACACCATTCAGATGGTAAGAAGGCACACATATAGAGTGTTTCTTATTTTACAAGGAGAAACGTGTTTTAGTTTACAGATTCTGTATGTTTCTCCTCTCTAATGTGATTAGGTACAGACGGCAGCACTGGACGAGATGTTTCATCACGGAGAAAGCTCTCTAGAGAGATACCACAAGGCCTTACTGCTGATGGAGGGCCTGTCCTTGATTATTACAGAGCCTTCAGACCTAAACAATGTCAACAAAT[G/T]TAAGTATGATATGAATAAACTAGCGTTCAAATGGATGGAGTAATTTTTTGTCTTGAAATAAACAAATACTTAAACATTAAATATATTAAAGGAACTATGTAATTTTCAACACTAGTGGGCGCATTTTCACAATAAACAAATATGTGGTTTGATGACGCCCTGACTGAATGTTGATAATAGACCCTTTTCACAATGACGTCACTTTACTTCCCCTCCCCCACCAGCAACGGAGTGTATTTTTAGTTTTGGTTTATTGAATGAACGTGAGACAACTGAAAATATTAACACTGCACATTGTGATTTAAGATTATTCCAGTATTGGGCATGTGTTCAAATGTTTCTCTTTTAATACTGAGCTGCTTTCTGAGTTTGAAAATGCTTCTTTAGGTTATTAAGAGTAGAAGTAAGGTATTGTTTATCTAGGAAAAATATGTTTGCAACCTTTTCACTTATTAATTAAGATTTTTTTCTCAATAATGGATTTATTTTTACTTTGGTGC
Associated Phenotype:
Not determined