ZMP
cdkn2b
Ensembl ID:
ZFIN ID:
Human Orthologues:
CDKN2A, CDKN2B
Human Descriptions:
cyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4) [Source:HGNC Symbol;Acc:1787]
cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4) [Source:HGNC Symbol;Acc:1788]
cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4) [Source:HGNC Symbol;Acc:1788]
Mouse Orthologues:
Cdkn2a, Cdkn2b
Mouse Descriptions:
cyclin-dependent kinase inhibitor 2A Gene [Source:MGI Symbol;Acc:MGI:104738]
cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4) Gene [Source:MGI Symbol;Acc:MGI:104737]
cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4) Gene [Source:MGI Symbol;Acc:MGI:104737]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25583 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32685 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25583
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 |
---|---|---|---|---|---|
ENSDART00000054209 | Essential Splice Site | 42 | 125 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 25013550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 25437248 |
GRCz11 | 1 | 26130962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGAGTGAATGCCAATGTGGTTAACAAATTTAGAAGAACGCCTATACAG[G/A]TAGGTTTAGACGCGCTTTAAGAATAAACAACGGAAATAAACAAATGCAAA
Long Flanking Sequence:
TGCCAGTTACATTAGCCATAAAACATTAGCAGAACCTAATTTCTGTTTCTCTGCAGCCTCTCCTACTGTGTCGTAAACTCATGTCTTCCTGACTCAGCTGTTGTGCGCAGGCGCAGTATGACAGTACTGCACCACGGTTTTGCTGTGACGTTTATGACAGAGACAAGTCCGAACAAATATCTCGCTACGAAAAATTATTTTAAGACACAACACTTTGATAAACGAGTCAGTTTCGCTTATTTACGCATTATATTGGAACATGTTATTCATGGAGACCGATAAAAATAAATTACAGCGTTGAACTGATTGTTTTCGCAGTATCATCATCATTTGGTTTTACCTGTGAAGCGAATTAATTTCGAAAATCAATAAAGATGATGAACGTCGAGGATGAACTGACCACAGCAGCAGCCACCGGAAACATTTCCCATGTTCAGTTTTTACTTTCTAACGGAGTGAATGCCAATGTGGTTAACAAATTTAGAAGAACGCCTATACAG[G/A]TAGGTTTAGACGCGCTTTAAGAATAAACAACGGAAATAAACAAATGCAAATAAATAAATAAGATTAATTGCAGATATGTAACATTAAATTAGTAACATACAATTCAAAGACTTATTTTGTATTAAAGGTCATATTATTTAACAAATTTAGGCTATTTCATATTTTCACACCTGTTTGACTATATGGGATTTACTTTTCTTTTTTTTTTTTAAATATTAGGCTATTTGTGTATTTATTTTACTCATTTTAGCATGTTTAAGAACCTTTTAGGCTACTTAAACGGCCTGAAACATGTTTACCAATAGCGTGTTATCAACCTATATAATACTAACAACACTTTCTATCTTTTAGTAATGTCATTAATTTTAACATTATAATTTTAACTTATAGCTACATTCTTAGAAATTAGTCCGAAATAAGACAAGGAGTTTTGGATGTATTGTCAAAGTTCAAATTATTCAAAGAAAACTAAAATCTTATTGAAAACGAAAGTCCCAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32685
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054209 | Nonsense | 105 | 125 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 25011706)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 25435404 |
GRCz11 | 1 | 26129118 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAATCCGCTTCGGCGCCGACCCCAATACAAAAGATCACTGCGATTTA[C/T]GACCAGTGGATGTGGCACAACAGACTGGCAACGTAGACGTGGTTGAATTA
Long Flanking Sequence:
TTAAAATGATTATAGGAATCTTCATAATTAATCATATGAAAAATAAGAATTAGCTACAACACAATTTGTTGCATTTAATTGATTTACTGCCCGTGAATAATTTATTGATAGGCTAAAAGAGTAATGCATCATGCACAGCAATGTTCAGTGCCAGCATGTGCACTGCTTTCGTTCCTATTTAACCAAAAAGTATCTACTTTCCAGATTTCGAGTGATGGCAGTAAAATTATTGATTAAACAAACTTCTTTACAGTGACATCATGACGTTACTGGCGTTTATTTTTTCATGAGACAGCAATTTTCCCCCTCTCCAGGTGATGATGATGGGTAACGCACCTTTGGCTCTTGTGCTGCTGGAACAGGGAGCGGACCCTAATGTGCCTGACCCCGACACAGGGAGCACACCTCTGCACGACGCTGCCAGAACCGGATTCATTGACACCGTGCGGCTTTTAATCCGCTTCGGCGCCGACCCCAATACAAAAGATCACTGCGATTTA[C/T]GACCAGTGGATGTGGCACAACAGACTGGCAACGTAGACGTGGTTGAATTACTCAATCGTGTTTAAAATGTTTAAAGACTGCATCACTGCATAGCCTAGGCTACTTTAGGTGGTAACCTTATTAATGCACTCAAGTACTTATAATTCTCAATAGCACATGGTCATTCATGTAGTTTGGAGATTCTAATCATTTAAAATTTTATTTCTGTATCTTTTAAGTTTATTTATTATTATTATTTATTATTAGCTAGTCAATGGGAACTTCAATAAAAGGCTACAGACACAAACCATCATACGCTCATGCTAGCCTATAGTTCGCATAATAAAAAGTGTAGACAGCATTATGTCCAAAGATAAATAAATAATTAAATAACATATCCACCTATTTGTTTTTAACCTGAAAAGCATGGCGACAAACATTGAATCAAATGGCTTGCAACGCAAGGACATCCAATATTTTTGGCGAGCTCTTTCTTTTTTCATTTCTTCCGGTTAAACATG
Associated Phenotype:
Not determined