ZMP
ulk1a
Ensembl ID:
ZFIN ID:
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 |
sa17536 | Nonsense | Available for shipment | Available now |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Allele Name:
sa9810
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 |
---|---|---|---|---|---|
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:
sa17536
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 > 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