Busch Lab

ZMP

si:dkey-12m15.4

Ensembl ID:
ENSDARG00000002981
ZFIN IDs:
ZDB-GENE-040625-72, ZDB-GENE-100922-21
Description:
hypothetical protein LOC415182 [Source:RefSeq peptide;Acc:NP_001002092]
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]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa24408 Essential Splice Site Available for shipment Available now
sa44053 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24408
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045049 Essential Splice Site 116 499 2 9
ENSDART00000050571 None None 69 None 1
ENSDART00000102944 Essential Splice Site 42 425 2 9
Genomic Location (Zv9):
Chromosome 23 (position 42953663)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 42397296
GRCz11 23 42362792
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGGAAGACCATGTCTGCCGGTTATAGACTGGACTTCTAATGGATGCG[G/A]TCAGTAACACTTTTCTTAATCAAGCTCCAAAAAATAATTCTCAAAGAACC
Long Flanking Sequence:
CTCCTCCCTCTGTTATAAAGCTCCTGACCCTCTGCTGCTGTTGTGTTTGTCCTGAACTCAATCTGTCATCATGTTTGGGGCTCTTGTAAAGTTAGACCTTTCCTCTGTGGGCTTGACTCTGTTGCTGGGCTTGATTCTTCTGGTTCTGTTTGAGATCTTCAGGATTCATTCTTACAAAAGTCGATTTCCGCCTGGTCCAACACCTCTGCCTTTTGTGGGAAACCTACCACATTTATTGAGGGACCCGATGGGCTTCAACAGATTAGTAAGTTGTTGCTGTTTTCTCTCATTGTGAAGCTCTGCTGCTGTATTCTGAACAATACTGCTGTAAATGTTCTCTAAACAGATGGCTCAATATGGAGAAATGTCCACTATGTATCTTGGGAAAAAGCCAGCGATAGTCCTCAATACAATCCAGGTGGCTAAGGAAGCCCTGGTTCAGGAAGCTTTTGCTGGAAGACCATGTCTGCCGGTTATAGACTGGACTTCTAATGGATGCG[G/A]TCAGTAACACTTTTCTTAATCAAGCTCCAAAAAATAATTCTCAAAGAACCTTTCAGTAAACAGATCAGAATCAGTTTATGGGCCCTATCATACACCCGGCGCAATGTGGCGCAAGGCACACGCAATACTCTTTTGCTTGTTTTAGCTCGGCGCAAGGGTCATTTTGAGGTGTTGCGCCACGCTGTTTAAATAGCAAATGCATTTGCGCTCAAATGTGCGCCCATAGGCTTTCTGGTCTAAAAAAAGCAGGCGTGTTTTGGCGCGTTGGTATTTTGAAAAACTGTAAATAGTCTGATTTTTAGACCAGAACAAAGTCGGTCTATTGTCTGGCGCGAAGTGCGCCTGGCTTACACACTACACACAAGATGTAGAGCAATACGCAAATATCTTTACATATGAAAAATATATAATATCTTAAGGATATATATAAAATAAGGATATATACAGGATATAAATATAAATAATTAAAATATTACAAAACATATTAATTTCTAGCCTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44053
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045049 Nonsense 484 499 9 9
ENSDART00000050571 None None 69 None 1
ENSDART00000102944 None None 425 None 9
Genomic Location (Zv9):
Chromosome 23 (position 42944168)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 42406791
GRCz11 23 42372287
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGATGCAAAGCCCTTAGACATGGATGGCATCGTGGGTATAGTCCGCTA[T/A]CCTCAAACCTTTAGCATCATCTGCTGCAGTAGAGACAGCAAAAAGTGACC
Long Flanking Sequence:
GGTTCGGGCTAAAATGCAAGCCTCTAACCATGAACTCCTGCATTGGGGTGTATGTTTGTTCACACTTATTTTTAAAATCAGCATGTACTGCATTTCTACATACCCAAAACATACTATGTATGCCCATGACGTCTTTGTTTTTCAAAGATTTCCGCATTTTGTGTTTACATGGAAGCAATAACTGTGCCTTTTTCAAAAACTTGCACTTTTCCCAATATACATTTTCAGTCTCCATTGTTGTGAAAACGACAGAAAATGCATTAAAAGTTGACAGTTTTTGACTGAATCGTTGTTGTGTTAAATGCCCCCTAAAGCACAGGCAGTAGTCACTGGATTGATCTGTGTGCTTGTTTTTCAGGGCTGAGGGCCTGTATAGGTGAGTCACTAGTGAGGACGGAGCTCTTCTTGTTCGCCACTGTTCTCCTACAGAGGATTCATTTCTCTTGGCCGCCTGATGCAAAGCCCTTAGACATGGATGGCATCGTGGGTATAGTCCGCTA[T/A]CCTCAAACCTTTAGCATCATCTGCTGCAGTAGAGACAGCAAAAAGTGACCCGAAACACATCAAGCCATAACATACAAAGGAAAAACAATAACAGCACAGCCGTTGAGCGCAGAAGAGCACTTTGGCTCATCTATATCATGTATAATTCACAGTTCTCAGGTAACTCAGATAATAAAAAGAAGAGTGTGTATTATTCTTTGCATTGATGCTTCTTAACATGTTTGAACATTTAAGCAGTTTTTTAATCTTCATGCAATCAAAAATTGAATAGTTTTTACCCTTTGTTTTGACTTTATTCTAATTATTTTATTCTGATTATTGTACTGTAATGATCTTTCATTAAATAAAGAATTAATGAAATAAATAAAGTCATTTTTTAAAGACTCAGGGCTGCCATTTCATTGTTTTTAGCTTCAACTACCCATTTTGCATGGAAATCACTGGCTAATTGACTCTTCACTAAGCCCCGCCCTGCTTAGTTACTGTTCTTACACATGTTA
Associated Phenotype:
Not determined