ZMP

zgc:153597

Ensembl ID:

ENSDARG00000087868

ZFIN ID:

ZDB-GENE-061027-232

Description:

hypothetical protein LOC768294 [Source:RefSeq peptide;Acc:NP_001070926]

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
sa44052	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa44051	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37786	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44052

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000006065	Essential Splice Site	66	498	2	9

Genomic Location (Zv9):

Chromosome 23 (position 42858578)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	42492381
GRCz11	23	42457877

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTTTTTTAATCATTTACAAACTGAATCTGCTGTAAATGTTTTCCAAACA[G/A]TTGTCTGAATATGGAGGATTGGCCACTGTGTTTATTGGGAGAAAGCCAGC

Long Flanking Sequence:

CAATAATTCAGATTACAGCGATAATGTGGAGAAAATTGATCTTGTGTTGAGCCCAATGAGCCTTACATCTAAAAATAGAGCACGGGTGTTCCTTTAGAGATATCGCTTTGACTCACATGCTGAAAATGGCGGACGTGAAACAACAACCTGAGAATACAGATACGTGCCTGTCAATTAATTTTGGTGGGCGGAGGACCGCACTTCACGTCAAGTTGCAGTCGCTCTGAAAACCGCTCCAATTAGTCCACCGTTTTTCTGTTGTTAAATTGAAAAAAAAGGACTGTGTGTGTTTATATCACCCCAATATGACAGTCTTTACACTATACTTACACACGTCTGTCCAAACAGCTTGAAAAGTAGATTTTTCACAATAAGTGCCCTTTACATAAACTAAAATAAAAAATAAAGTGCAGTTACAACATTTTCAATGGAAAAGTATTACATGTTGTACTTTTTTTAATCATTTACAAACTGAATCTGCTGTAAATGTTTTCCAAACA[G/A]TTGTCTGAATATGGAGGATTGGCCACTGTGTTTATTGGGAGAAAGCCAGCAATAAGCATCAATACAATCCAACTGGCTAAGGAAGCATTAGTACAGGATGTTTTTTCTGGAAGACCTGCTTTGCCTATTTTTGACTGGATATCTCATGGACTCGGTCAGTAACACTTTCATTAACAATACTTTCCAATGAGGATTTAATAGAAATGTAATAAAAAATTAATAATATTGCTGTAAGTTGAAGCATGAATTCATTTCTAATAATTTAAGGGATCAGAGTCAATTATTCTACTTGATGTTCTATATGTTCATAGTTTGCATTTCAAGAAATGTATCTTTAGGTTTGGTAACCATAACACAAGTAGAATAATTGACTCTGATCCATTTAATTATTAGAAATGATTCAATGCTTATAGTTTGCATTTAAAGAAATTCAGTTTTTCTCCCAGACAGCTTGTGTGCAGTACTAGTTTCTCATCTCATCTAAAACATGTTGTATTGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44051

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000006065	Nonsense	151	498	3	9

Genomic Location (Zv9):

Chromosome 23 (position 42856834)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	42494125
GRCz11	23	42459621

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCTGCACACACTCAGAAACTTTGGTCTGGGGAAGAAAACAGTAGAGGAT[C/T]GAGTGTTAGAGGAAAGCCAGTATCTGATTGCTGAAATGCTCAAAGATGAA

Long Flanking Sequence:

CAAGAGGAATAAACTTGAAGGGTTACAGTTTCTTCTTTGTACTTATTAATCCTTACAAGCGTTATTAGTACAACACCTTGTGGCTGTACTAGAGGTGCATCGGAAGAATATTTTGATTGCAACAATGAAATAATTCTCAAGCTAAACATAACAAGAAATAGCCGCCCACCCCCAATAGTTTTAGTTGAATAATTTTAAAAGAATTAACATGTATAAACATCATTTATACATTACTTATTCTAATACTTACTTGAACATTTTAACAATTTTTTTGACTTTTTATCTGTAAAGTGCATGTTATAGTGTGTAATATATGAGAATTGCTTCTGATGGCAGCTACACCATGTAACTATATGCTAAAGATATGTATGTCTGATGGTCTGTTTCTCTCTTTTTTAGGTATAATAATGGTCACATTTAACCACTCTTGGAGGCAGCAGAGACGGTTCGCTCTGCACACACTCAGAAACTTTGGTCTGGGGAAGAAAACAGTAGAGGAT[C/T]GAGTGTTAGAGGAAAGCCAGTATCTGATTGCTGAAATGCTCAAAGATGAAGGTATGAAATGTTCATGCTGGTTTTGGAAACATTTTAAGGTTTGTGATAAAAAGTGTTCTAGTATACTAAAGGTTCAGGCTAATTTTTGCAAATTATTTTGAAAAAAAAATTGTTTCTTTCTTTTCTTTTGTAGGCAAGTCAATGAATCCCCAGCATGCCCTACAGAATGCTGTTTCCAACATTATCTGCTCCATCGTGTTTGGAGATCGCTTTGAGTATGATAACAAACGCTTTGAATACCTTCTGAAAATCCTGAATGAAAACATCATGCTCACAGGGTCAGCTGCAGGACAGGTATGATCAAACTCTTCATTTTTCTTTTTGTGCATCTTCATCCTTATCCTTGTAGTTTTTTTTTTGTTTTTGTTTTTTTTTTTAAATAATTGATTATCTGCCAAAGCCAAAATTTGGTAGAATTTAATTATCAATGCATCCCTTCCATAGCTTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37786

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000006065	Nonsense	191	498	4	9

Genomic Location (Zv9):

Chromosome 23 (position 42856581)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	42494378
GRCz11	23	42459874

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCATGCCCTACAGAATGCTGTTTCCAACATTATCTGCTCCATCGTGTTT[G/T]GAGATCGCTTTGAGTATGATAACAAACGCTTTGAATACCTTCTGAAAATC

Long Flanking Sequence:

AACATTTTAACAATTTTTTTGACTTTTTATCTGTAAAGTGCATGTTATAGTGTGTAATATATGAGAATTGCTTCTGATGGCAGCTACACCATGTAACTATATGCTAAAGATATGTATGTCTGATGGTCTGTTTCTCTCTTTTTTAGGTATAATAATGGTCACATTTAACCACTCTTGGAGGCAGCAGAGACGGTTCGCTCTGCACACACTCAGAAACTTTGGTCTGGGGAAGAAAACAGTAGAGGATCGAGTGTTAGAGGAAAGCCAGTATCTGATTGCTGAAATGCTCAAAGATGAAGGTATGAAATGTTCATGCTGGTTTTGGAAACATTTTAAGGTTTGTGATAAAAAGTGTTCTAGTATACTAAAGGTTCAGGCTAATTTTTGCAAATTATTTTGAAAAAAAAATTGTTTCTTTCTTTTCTTTTGTAGGCAAGTCAATGAATCCCCAGCATGCCCTACAGAATGCTGTTTCCAACATTATCTGCTCCATCGTGTTT[G/T]GAGATCGCTTTGAGTATGATAACAAACGCTTTGAATACCTTCTGAAAATCCTGAATGAAAACATCATGCTCACAGGGTCAGCTGCAGGACAGGTATGATCAAACTCTTCATTTTTCTTTTTGTGCATCTTCATCCTTATCCTTGTAGTTTTTTTTTTGTTTTTGTTTTTTTTTTTAAATAATTGATTATCTGCCAAAGCCAAAATTTGGTAGAATTTAATTATCAATGCATCCCTTCCATAGCTTTATCAGTTGTGTCTGCATTGCCATGAGAAATACCAGAGTAGTGTGTCCTTGATTATAAATTCAAAATGTAAGATGTTATGTATTTGGTATTTCATGTTTTTATTTTGCATTTGATTGCATCATGGGACCTTAATCTTTCTTCAAACAACCTTTAACCTTCGAAAAAGTTATTTTTATTAACATTTTTAATAGTATAAAGTGATATATTGTCTGGGTTGATGTTGTGTATTATGATGTTGTGCTGGAGGCACAGAA

Associated Phenotype:

Not determined