ZMP
LOC100000156
Ensembl ID:
Human Orthologues:
CYP2F1, CYP2S1
Human Descriptions:
cytochrome P450, family 2, subfamily F, polypeptide 1 [Source:HGNC Symbol;Acc:2632]
cytochrome P450, family 2, subfamily S, polypeptide 1 [Source:HGNC Symbol;Acc:15654]
cytochrome P450, family 2, subfamily S, polypeptide 1 [Source:HGNC Symbol;Acc:15654]
Mouse Orthologues:
Cyp2f2, Cyp2s1, Cyp2t4
Mouse Descriptions:
cytochrome P450, family 2, subfamily f, polypeptide 2 Gene [Source:MGI Symbol;Acc:MGI:88608]
cytochrome P450, family 2, subfamily s, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:1921384]
cytochrome P450, family 2, subfamily t, polypeptide 4 Gene [Source:MGI Symbol;Acc:MGI:2686296]
cytochrome P450, family 2, subfamily s, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:1921384]
cytochrome P450, family 2, subfamily t, polypeptide 4 Gene [Source:MGI Symbol;Acc:MGI:2686296]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22559 | Nonsense | Available for shipment | Available now |
sa10284 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22559
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099074 | Nonsense | 215 | 491 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 57727)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 91796 |
GRCz11 | 15 | 19605 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTCCAGATCATCTCTAACCTCATGCGATTTGCAAGCAGCCCTTGGGGA[C/T]AGGTGAGCCACTGAGACAGTGTGGGGCAGGTTTGAGAATGAAGAATGTTT
Long Flanking Sequence:
AATGTGTATACTTGTGAAAGACAGACATTATCGGTATAATGGAGAAGAGTCTAGATTTTGACCGCCTTTACATGTTGGTAGGTCTGATCATCAGCAATGGTGAACGCTGGCGTCAACTGAGGCGGTTCACGCTCACCACACTGAGGGATTTTGGAATGGGACGCAAACGAATGGAGCAGTGGATTCAAGAAGAGAGCAGATACTTGCTCAAGAGTTTTGAAGAAACCAAATGTGAGGGATCAGATTATTCAGCATTTACATCCCATGAGTTCAGTATTAGAGTTGTGGTATAAATGGAGATTCTGGAACTCACAGATGTATAATAAGAGTTTTCTCCTTCAGCCAAACCAGTTGATCCATTATTCTTCATGAGCCGGGCTGTGTCCAACGTCATCTGCTCCCTGGTGTTTGGGCAGCGCTTTGATTATGAAGACAAAAACTTCTTGCAGTTGCTCCAGATCATCTCTAACCTCATGCGATTTGCAAGCAGCCCTTGGGGA[C/T]AGGTGAGCCACTGAGACAGTGTGGGGCAGGTTTGAGAATGAAGAATGTTTTGGAAAAAAAAAAAATTTAAAGTATGGTCGTTATAGTTTCCACAAGACTTATTGTATTGGTTTCAAACCGCCTCCTATCTGTTGGGAAGAAGGAGGTAGAGAACTAAACACGTAACGAATTTATTAAAGGGGAAAAAAACAAACAAACAGCTCCTTACAGAGACTGCCGCTGAACTGAAAACAAACACAATGTAAACGTGTCCAGGCCTGGACTTCTCTCATCCCCCTCTGTAGCCACTCTTATAATCTAGAGCTCCTCCTCGGGACTCGAGGTCGGTGTGTGCCACATGTGCTTCTCGTTCTCACCGGCCTCATTACATTCCCACAGCTCTCAGCCCCGCCCCCTCACCACACCTATATAGATTAAAAGCAAAACAATTGATCAGCTAACTGAGCTTTCAACGCTGCTGTGCTTTTACTAGAGCTGATCAACTCAGTCTTAGCGGTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10284
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099074 | Nonsense | 250 | 491 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 56896)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 90965 |
GRCz11 | 15 | 18774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATKTTWGGAGAGATTGATGATCTCAAATCCTCYATAATGAYAATTATC[A/T]AGGAGCATGAGGAGAATTTGGATYCCAGTGACCCAAAGGACTTTATTGAC
Long Flanking Sequence:
GTGCCACATGTGCTTCTCGTTCTCACCGGCCTCATTACATTCCCACAGCTCTCAGCCCCGCCCCCTCACCACACCTATATAGATTAAAAGCAAAACAATTGATCAGCTAACTGAGCTTTCAACGCTGCTGTGCTTTTACTAGAGCTGATCAACTCAGTCTTAGCGGTGTACTGTCTACAAAGCGGCAACAGTTTGTTTTGGATTAAATCATGTATTCTGTAGAAGGCAGCATGCAGCTATCTCTCTTTAAATCTCACATTCTTCCTCACTGAAGCTAAGCACAGTTGAGTCTGGTTAGTGCCTGAATAGGAAATCACATGGGAAAAAAATACTATAACAATAACAAACTGCAGTTATTATTACTGATATCTCTGGAACTATCTTGTCATTCCTGACAGCTCTACAACATCTTCCCTAAAGTCATGGAGATCTTACCAGGTAGACATCATACCATGTTTGGAGAGATTGATGATCTCAAATCCTCCATAATGACAATTATC[A/T]AGGAGCATGAGGAGAATTTGGATCCCAGTGACCCAAAGGACTTTATTGACTGCTTTCTTATCAGGCTCAATCAGGTATAGAAAGCAAAGAAAAATACACAATTATTGTTCTAGTCTATCTGCAGGTCAATTGCCATATACACATATGCCTTTTCTCCTTTTCTGTTCTCTACAACAGGAGAAACATAATCCTGATACAGAATTCCACAAGGAAAACATGTTTGCCACCTCTTTAAATCTGTTTACAGCTGGTACAGAGACCACCAGCACAACTTTAAGATACGCTCTAATGCTCCTGATCAAGCACCCTCACATTCAGGGTAGGTCCAAAACATTTGTTGGGTGTATGATTGATGTTGTGTTAAGCTCATCTAGCTCTACTCACACACGTCAGTTCTGTGGTGACTGTATTTCACTGCTCTTTATTGTTTGTACAGGGTGCACACATGAAGACTCCAACATATTTTAAACATGTTATTTTAAACAAGTCTGAAACATTTC
Associated Phenotype:
Not determined