ZMP

zgc:92407

Ensembl ID:

ENSDARG00000057714

ZFIN ID:

ZDB-GENE-040704-33

Description:

Cytidine monophosphate-N-acetylneuraminic acid hydroxylase [Source:UniProtKB/Swiss-Prot;Acc:Q6GML1]

Human Orthologues:

AL133268.1, CMAH

Human Descriptions:

Putative cytidine monophosphate-N-acetylneuraminic acid hydroxylase-like protein [Source:UniProtKB/S
cytidine monophosphate-N-acetylneuraminic acid hydroxylase (CMP-N-acetylneuraminate monooxygenase) p

Mouse Orthologue:

Cmah

Mouse Description:

cytidine monophospho-N-acetylneuraminic acid hydroxylase Gene [Source:MGI Symbol;Acc:MGI:103227]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa40200	Nonsense	Mutation detected in F1 DNA	Not yet available
sa33356	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa40200

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080439	Nonsense	79	591	2	14

Genomic Location (Zv9):

Chromosome 4 (position 2094932)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	2384639
GRCz11	4	2233952

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAATTGTGTGTTCGTTACAGAACAGTTCGGTGTACCAAACACTACTGG[A/T]AACTCAACGTGGCCACTATGCAGTACGTCAATCCACCAGACAGCTTCATG

Long Flanking Sequence:

TAAGTTAGCCTGATTGGGTAACTATACTTGAACAAAGGAAAATTAAGACCTGTTTAACAAAGTTTTAAAGGTTTTAAAGACCTACAACACAATATTTCAGTCAATTTAAGGCCCAGAATTTTCTTTTTGAGATTAAAGATATTACAAGACTTTTTAAGACCCCGCGGACACCCTGATTTACATATATATTCCAGCCAAACTAAAAGAATTACAACTTTCTCCAGAGAATAAACATAATAGGAAATATTGTGAAAATTTGATTTGCTCTGTCAAACAGCACTTGGGAAACATTTGTAAAAAAACAAACAAAATTCACAACCATTTGTGGCTAATAACTGCATCTTTAACTGTTCATTTCACTGATATTTTATACTGTGCAAAATGTGTTACTCTTACTTTAGGTTTTGAGCAAGATTTACAAATGCCGTACTGTAGAAATTATTGTAAATAATGAATTGTGTGTTCGTTACAGAACAGTTCGGTGTACCAAACACTACTGG[A/T]AACTCAACGTGGCCACTATGCAGTACGTCAATCCACCAGACAGCTTCATGCAGGATGAACTCGGTAAGATCCCTCAAACGTTTGTTTTTGTAAATGAAGCAATGATGACAACATTGACAAGAGTCTTTACGGCTTCAGTGGATTCACCAAGAAGCTACAACAACTAATGCATCTTTCTTTTCTAACTTTAGATTTCTGGAAGTAAATCTGCCTCTGTATTACTGCAAGCTTTTCTTACATGGAGTTTTTGTCTTGTTTTTAGTCCCAATGTCTAGAAATTCCTAAATCAAGAAGCACTTTCTATACAACTAGCGCATAATGTGTTGTTTTCAGAAATAATAAGTCCAAATTAAGTGAGTTTTTCTTTAAAAAAAAGCAAAATAATTAACCAATGTGATAAGTTAAACAAGTTAAATAAGTTATTTATTTAAGGGGCTCTATCATACACCCGGTGCAATAAGGCACAAAACGTGTATGGCGCGATTTGTTGCTATTTTCAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33356

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080439	Nonsense	434	591	11	14

Genomic Location (Zv9):

Chromosome 4 (position 2106940)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	2396647
GRCz11	4	2245960

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTGCCATCACTGATCCGCCTCATGGCACAAAGATCTACAAGGACAACT[G/A]GGAGTTTGACCTGTATTTGAATCAATTGAACGCCTCCATTTCAGCTGAAA

Long Flanking Sequence:

AAGCTAAAACATGAATTATTTATAGCAATGTCTGGTGATGCTAGAATGTTGTCTGCAACATGCTAATTCATGCTAGTTACAGATGAACAAAATGTTGTCATATTGCTAAAATATTTATCATGTTTTATTACATGGCTAACATGATTTAGCATGTTGCTATTAGCATAAATGAACATGCTAAACACTAATCACTGTTGTTGCATGTTTTAGCATGTTGTTAACAGAATTTAGCATGCTAAAATATTTCCCATGCATGGCTAGCAAGAAAATTGCTGAAGATGTTAATTCATGAAAACATGTGCTGGCTATACTAGAATCTTGCAGAATCTAGTGACGTATTAGCCATGTGCTAACAAGCAAAAGAAGCATGTTAAGATCACATCTGAGTAAATTAGCATGCCACACATCCGTCATTTCTGTTTTTCCATCTGCTTGATTTTCTCTTTGCAGAACTGCCATCACTGATCCGCCTCATGGCACAAAGATCTACAAGGACAACT[G/A]GGAGTTTGACCTGTATTTGAATCAATTGAACGCCTCCATTTCAGCTGAAATCTTCAAACACAAGCACTGGATCCAGTATTATTATAACTGGGCAGGATTCAGAAACTACAATCTGGTCATCCGGGTAATTAACTCACATTGATTACCTATTTTATTATGCTAACCCTTACTAAACACATTAGCCATGCAGAAAAACATAACAGCCATGAAAAAACAGAAATGTTTAAACAAACCGTGCTTAACATGGACAGCCACATGGTATAAGTATCAATAACATCCTCATTTATGCTCACTAAATATTACAAATGTCTTAAACATAAAGCTAATTTATGCAAGCAACAAGTTAAAACATGTTAGCTCTGCATGATAAATATTCTAACATGCTATTTCTCGCTAAAAACGTTAAAAAATACAAGCCATCTTCTTAAACAATAATAAAACTTTTTTAGGAAGATGTTCATTTATGCTAGCAACATAGCAATGCATGTTAGCCTGCACTA

Associated Phenotype:

Not determined