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