ZMP
stk38
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapien STK38, serine/threonine kinase 38 (STK38) [Source:UniProtKB/TrEMBL
Human Orthologue:
STK38
Human Description:
serine/threonine kinase 38 [Source:HGNC Symbol;Acc:17847]
Mouse Orthologue:
Stk38
Mouse Description:
serine/threonine kinase 38 Gene [Source:MGI Symbol;Acc:MGI:2442572]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13697 | Nonsense | Available for shipment | Available now |
sa11837 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13697
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023186 | Nonsense | 264 | 469 | 8 | 12 |
ENSDART00000140588 | Nonsense | 264 | 468 | 9 | 13 |
ENSDART00000023186 | Nonsense | 264 | 469 | 8 | 12 |
ENSDART00000140588 | Nonsense | 264 | 468 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 872805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 875717 |
GRCz11 | 22 | 892615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAATTATGTATTTAATGAACMATTCTCGTAGCGTTTCAGCATATGAACT[C/A]GAAGAGGAAGGCCGAGACATGGAAGAGGAATCGCAGACAGCTRGTCAGTG
Long Flanking Sequence:
TATAACGATAACTACATTAATGCCTACACCAGTGGACGATTACTATATTAGCATTCACACAACCAAACACTAATTGTAACGATAACAATATTAGCATCAAAATAACTATTATTGTCGACACCAGACAACAGTAATAACCATATTAGCTTCAATATATAACATTAACTATTGGTTCATAGCTGTAATAATTACTATATTAGCAATAAGATTAGCAGACAATTACTGTAATAACTTTATTAGCTTTCAGACCAGTTTACGATAATTGTTATGTTAACTTGCATTACGTAAACATTAAAATCCTTAACAGCAGGTGATAACTATTATTATAGCTATAATAGTATCGTTAACAGTGATGTTTCACACACAGCTGTTTCTATGGCAACGCCCTGATGTCATATTAACGCATTTCAATCAAATTCGAAATACGTTTATTTTTCATGTCCACATTTTTAAATTATGTATTTAATGAACCATTCTCGTAGCGTTTCAGCATATGAACT[C/A]GAAGAGGAAGGCCGAGACATGGAAGAGGAATCGCAGACAGCTGGTCAGTGATTTTTCATTTTTATTTAAAATTCTTGCAAACAGGAAGTGATGCGTTACGTTGTTCTGCCTCTTCCAGGCCTTCTCCACAGTGGGAACGCCAGACTACATTGCTCCAGAGGTGTTCATGCAGACCGGATACAACAAGCTCTGTGATTGGTGGAGCCTCGGCGTCATCATGTACGAGATGCTGATTGGTAAGAAACGCTAATTATGCAAATGAGTTGCTTAAATTTGCTGTTAGGATTTGGATATGTATTTATTAACTAAATTATAAAAAATTAATTCTAATAAAAAATGGAAAAAATATGTAAAAAATGATCAAATTTTAGGTGTAATAATTTTCGTAACTTGCACAGTAGCACAATAAAAGTACTAGTAGTTTTTTTTTTTTTCAAAAACGTAAACTAAATTAAATAAAAATAAAAAACATAATGGAAACATGACATTTTAATTATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11837
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023186 | Nonsense | 264 | 469 | 8 | 12 |
ENSDART00000140588 | Nonsense | 264 | 468 | 9 | 13 |
ENSDART00000023186 | Nonsense | 264 | 469 | 8 | 12 |
ENSDART00000140588 | Nonsense | 264 | 468 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 872805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 875717 |
GRCz11 | 22 | 892615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAATTATGTATTTAATGAACMATTCTCGTAGCGTTTCAGCATATGAACT[C/A]GAAGAGGAAGGCCGAGACATGGAAGAGGAATCGCAGACAGCTRGTCAGTG
Long Flanking Sequence:
TATAACGATAACTACATTAATGCCTACACCAGTGGACGATTACTATATTAGCATTCACACAACCAAACACTAATTGTAACGATAACAATATTAGCATCAAAATAACTATTATTGTCGACACCAGACAACAGTAATAACCATATTAGCTTCAATATATAACATTAACTATTGGTTCATAGCTGTAATAATTACTATATTAGCAATAAGATTAGCAGACAATTACTGTAATAACTTTATTAGCTTTCAGACCAGTTTACGATAATTGTTATGTTAACTTGCATTACGTAAACATTAAAATCCTTAACAGCAGGTGATAACTATTATTATAGCTATAATAGTATCGTTAACAGTGATGTTTCACACACAGCTGTTTCTATGGCAACGCCCTGATGTCATATTAACGCATTTCAATCAAATTCGAAATACGTTTATTTTTCATGTCCACATTTTTAAATTATGTATTTAATGAACCATTCTCGTAGCGTTTCAGCATATGAACT[C/A]GAAGAGGAAGGCCGAGACATGGAAGAGGAATCGCAGACAGCTGGTCAGTGATTTTTCATTTTTATTTAAAATTCTTGCAAACAGGAAGTGATGCGTTACGTTGTTCTGCCTCTTCCAGGCCTTCTCCACAGTGGGAACGCCAGACTACATTGCTCCAGAGGTGTTCATGCAGACCGGATACAACAAGCTCTGTGATTGGTGGAGCCTCGGCGTCATCATGTACGAGATGCTGATTGGTAAGAAACGCTAATTATGCAAATGAGTTGCTTAAATTTGCTGTTAGGATTTGGATATGTATTTATTAACTAAATTATAAAAAATTAATTCTAATAAAAAATGGAAAAAATATGTAAAAAATGATCAAATTTTAGGTGTAATAATTTTCGTAACTTGCACAGTAGCACAATAAAAGTACTAGTAGTTTTTTTTTTTTTCAAAAACGTAAACTAAATTAAATAAAAATAAAAAACATAATGGAAACATGACATTTTAATTATTAA
Associated Phenotype:
Not determined