ZMP
zgc:110749
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC541440 [Source:RefSeq peptide;Acc:NP_001013583]
Human Orthologues:
AC008537.2, CYP2A7P1
Human Description:
cytochrome P450, family 2, subfamily A, polypeptide 7 pseudogene 1 [Source:HGNC Symbol;Acc:2612]
Mouse Orthologues:
Cyp2ab1, Cyp2j13
Mouse Descriptions:
cytochrome P450, family 2, subfamily ab, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:3644957]
cytochrome P450, family 2, subfamily j, polypeptide 13 Gene [Source:MGI Symbol;Acc:MGI:2385197]
cytochrome P450, family 2, subfamily j, polypeptide 13 Gene [Source:MGI Symbol;Acc:MGI:2385197]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44265 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30231 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16848 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44265
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064591 | Nonsense | 93 | 491 | 2 | 9 |
ENSDART00000110692 | Nonsense | 107 | 461 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 17723946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 17270787 |
GRCz11 | 25 | 17367187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTTTGCAGTTATTAAAGAAGCTCTGGTTACCAAAGCTCAAGACTTTT[C/A]AGGACGACCTCAAGACTTCATGATCAGTCACGCCACAGAGAATAAAGGTA
Long Flanking Sequence:
ATATTGAACCAATCACCTTATCAGATGGTGGTTGTAGCCATTAGAGAATGTAGCAAGATCTAAGAGAAAGGTGTTGCTATATAAAAAGCTCCAGGAAGACCTGTCTACTACTCAAGCTTGTTTTGTGACTGCAGCTGGACAACAGTAAGCATGTTGGGTTCTTCTCTTCTTGTTGTAATATGCATTTTGCTCATCTTCTTCCTCATAAGGGTCAAGAAGCCAAAGAATTTTCCTCCAGGACCTCCTCCAGTTCCTATATTTGGAAATCTGCTTCAGCTCAACCTAGCTAATCCTTTAAAGGATTTTGAAAAAGTATGGTTTACTACTTCTCATCTTGAGTCAAAACTATTTTTTTCTGTACAATAATTGTCCGCTTTTTTTAAAGTTTGCAGAAAAATACGGGGAAATATTCAGCCTGTATACTGGATCGAGGCCAGCAGTCATTCTGAACAGTTTTGCAGTTATTAAAGAAGCTCTGGTTACCAAAGCTCAAGACTTTT[C/A]AGGACGACCTCAAGACTTCATGATCAGTCACGCCACAGAGAATAAAGGTAACTCCCAATAACAGTCCCAGATGTCAAATCGGCATTAAAATTGCAATCTAGGAAATTAAATTGCTTAGACAACAAAATTGCTTTTTTGACATTTCAGCTGCTAATGAAAAAAGTTCAAGCAAGGTTAATATTAAATGTGCTTTCTGAATGAGTTTAGAATCGTTTAATGAATGACTCAAGACAGTGAAGTCAAGATGGAGGAAATCAGGTTCTACAAAAGTAAACCCGTAGCTGATTAGTGATAATTGTATCAAAGGTTACCCAATATATTTATTCCACTTTGATTGTGTGAGCTGTGATTCCACTTTACTTGTTTTCACTAAAACAGCTGCATCAACCTAAAGCTAATTACCTTGATTTAACACTGTAAAAAATACTGGGTTGCACACAATCGATTTGTGTTGAGCCAACATAAAGGAATAAAGTTAACCTTTTAGTTTTTACAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30231
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 |
---|---|---|---|---|---|
ENSDART00000064591 | Nonsense | 95 | 491 | 2 | 9 |
ENSDART00000110692 | Nonsense | 109 | 461 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 17723941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 17270782 |
GRCz11 | 25 | 17367182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAGTTATTAAAGAAGCTCTGGTTACCAAAGCTCAAGACTTTTCAGGA[C/T]GACCTCAAGACTTCATGATCAGTCACGCCACAGAGAATAAAGGTAACTCC
Long Flanking Sequence:
GAACCAATCACCTTATCAGATGGTGGTTGTAGCCATTAGAGAATGTAGCAAGATCTAAGAGAAAGGTGTTGCTATATAAAAAGCTCCAGGAAGACCTGTCTACTACTCAAGCTTGTTTTGTGACTGCAGCTGGACAACAGTAAGCATGTTGGGTTCTTCTCTTCTTGTTGTAATATGCATTTTGCTCATCTTCTTCCTCATAAGGGTCAAGAAGCCAAAGAATTTTCCTCCAGGACCTCCTCCAGTTCCTATATTTGGAAATCTGCTTCAGCTCAACCTAGCTAATCCTTTAAAGGATTTTGAAAAAGTATGGTTTACTACTTCTCATCTTGAGTCAAAACTATTTTTTTCTGTACAATAATTGTCCGCTTTTTTTAAAGTTTGCAGAAAAATACGGGGAAATATTCAGCCTGTATACTGGATCGAGGCCAGCAGTCATTCTGAACAGTTTTGCAGTTATTAAAGAAGCTCTGGTTACCAAAGCTCAAGACTTTTCAGGA[C/T]GACCTCAAGACTTCATGATCAGTCACGCCACAGAGAATAAAGGTAACTCCCAATAACAGTCCCAGATGTCAAATCGGCATTAAAATTGCAATCTAGGAAATTAAATTGCTTAGACAACAAAATTGCTTTTTTGACATTTCAGCTGCTAATGAAAAAAGTTCAAGCAAGGTTAATATTAAATGTGCTTTCTGAATGAGTTTAGAATCGTTTAATGAATGACTCAAGACAGTGAAGTCAAGATGGAGGAAATCAGGTTCTACAAAAGTAAACCCGTAGCTGATTAGTGATAATTGTATCAAAGGTTACCCAATATATTTATTCCACTTTGATTGTGTGAGCTGTGATTCCACTTTACTTGTTTTCACTAAAACAGCTGCATCAACCTAAAGCTAATTACCTTGATTTAACACTGTAAAAAATACTGGGTTGCACACAATCGATTTGTGTTGAGCCAACATAAAGGAATAAAGTTAACCTTTTAGTTTTTACAAATGTATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16848
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 |
---|---|---|---|---|---|
ENSDART00000064591 | Nonsense | 402 | 491 | 8 | 9 |
ENSDART00000110692 | Nonsense | 416 | 461 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 17719892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 17266733 |
GRCz11 | 25 | 17363133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YCCAACCTTACYAGKGTGCTAAAAGAAGAAGGTCAGTGGAAGTTTCCTYA[T/G]GAGTTCAACCCAGCAAACTTYCTGAATGAGCAGGGCCAGTTTGAGAAGCC
Long Flanking Sequence:
ACAGTTTTTATGTGTACTTTGCACCGAAGAAGCTAAATGTGTGATGTTTTTTCATTACTGTTTTGCATATGTTAAGTTTTCAAAACTTTCAGAAGGATGTTAGCATTTTAGCAAAGCTAGCATGTCAAAAGAAACTTGAACATTCAAACACAGCCTTGTTTTCTAACCAGTAAAATGCCAGCAAGAGATTGATGATGTTCTGGAGGGTAAAGATCAGGTGATGTATGAAGACAGACACAATATGCCGTACACACTGGCTGTGATTCATGAGGTTCAGCGTGTCGCTAACACTGTACCGCTAAGTGTGTTTCACTCCACCACACGAGACACAGAGCTAATGGGCTACAGCATCCCAAAGGTGAGGAAACATTTGGAGCGACTTAAAGACTATTATACTTCAAAATAAACTGTAATCAATTGTTTCTTGTTTGTCAGGGAACTATAATCATTCCCAACCTTACCAGGGTGCTAAAAGAAGAAGGTCAGTGGAAGTTTCCTTA[T/G]GAGTTCAACCCAGCAAACTTCCTGAATGAGCAGGGCCAGTTTGAGAAGCCTGAGGCTTTCATACCCTTCTCCACAGGTAACAGTTTTAAGTATTCAAGCACAGCATGAAACTGTTGTAGTTGCTATCATTTTTATACACTCTTTATTAGGTACACCTGTCCTAGTTTAATCAACCAATCATATGGCAGAAACTCAATGCATTTAGGCATGTAGACATGGTAAAGACGATCTGCTGCAGTTCAAACTGACCATCAGAATGGTGAAGAAAGGTGACTTAAGTAACTTTGAACATGGCATGGTTGTTGGTGCCAGTCGAGCTGGTCTGAATATTTCAGAAACTGCAGATCTACTGGGATTGTCATGCACAACCATCTCTAGGGTTCACAAAGAATGGTCCTAAAAAGAGAAAATATCCAGTGAGCAGCAGTTCTGTGGGCGCAAATGCCTTGTTGATGGCAGAGGTCAGAGGAGAATGGCCAGACTGGGTTGAGCTGATAGAA
Associated Phenotype:
Not determined