ZMP

pcyt1bb

Ensembl ID:

ENSDARG00000044456

ZFIN ID:

ZDB-GENE-051120-48

Description:

phosphate cytidylyltransferase 1, choline, beta b [Source:RefSeq peptide;Acc:NP_001032451]

Human Orthologue:

PCYT1B

Human Description:

phosphate cytidylyltransferase 1, choline, beta [Source:HGNC Symbol;Acc:8755]

Mouse Orthologue:

Pcyt1b

Mouse Description:

phosphate cytidylyltransferase 1, choline, beta isoform Gene [Source:MGI Symbol;Acc:MGI:2147987]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38151	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa39499	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38151

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081198	Essential Splice Site	68	359	3	8

Genomic Location (Zv9):

Chromosome Zv9_scaffold3460 (position 54877)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	40601929
GRCz11	21	40624976

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAAAAATGCTGAATCAAAATTGAAAGTACATGTCGTTTGTTTTTGTGC[A/T]GCTCAACGGCCAGTCCGAGTGTACGCCGATGGAATATTTGACCTCTTCCA

Long Flanking Sequence:

AGCGCCTCAGACACCCCTCAAGAAAAAGTGACTTTAGCCCAGGCTCGGCGTGGCACTCCAGGTGAGAGAAACTATTAAGTGTGACAAAGTGAAGATGAAATATTTTGACATTAAATGGTGTATCAGGCGAGCAGTGGTGCTGGTTTTAGCCTCGGCTGGGTCAGCTGACGTTTCTATGTGGAGTTTGCATGTTTTCTCCACGTTCACGTGGGTTTCCTCCGGGCGCTCCGGTTTCCCCCACAGTCCAAAGACATGCAGTACAGGTTAATAGGCTAAATTGTCCATAATGTATGAGGGTGAATGAGTGTGTATGAATGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCCGCTGAGTAAAACAAATGCTGGATAATTTGGCGGTTCATTCCACTGTGGTGACCTCAAATAAATATAGGGACTAAGCCCAAAAGAAAATGAATGAATAAATGAAAAATGCTGAATCAAAATTGAAAGTACATGTCGTTTGTTTTTGTGC[A/T]GCTCAACGGCCAGTCCGAGTGTACGCCGATGGAATATTTGACCTCTTCCATTCGGGTCACGCACGAGCTCTGATGCAGGCCAAGAATTTGTTCCCAAACACACAACTGATTGTTGGCGGTAGGTCACACTGACACCAGTACAGACTCTTTCTGTGCAGTTTTGCAAAAGATAAACAAAAACATCCACGTCACTCGTCCCAAACGCTTAGTAATGACTGCCCTGTACCTTTTGTGTATCTCTGTTAGTATGCAGCGATGCCCTGACGCACAAGTATAAAGGCTACACGGTCATGACGGAGGATGAGCGATATGAAGCCCTCATACACTGTCGTTATGTGGACGAGGTGGTCCGTGACGCTCCCTGGACTCTTACTTCTGAATTCCTAAAAAAACACAGGGTAAATCCATATTCACTTCTTTTATTACAAAGACATTTTGTACTTTGGGCGACGTAGCGGTGCAGTAGGTAGCGCTGTCGCCTCACAGCAAGAAGGTCGCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39499

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081198	Essential Splice Site	158	359	5	8

Genomic Location (Zv9):

Chromosome Zv9_scaffold3460 (position 58437)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	40598369
GRCz11	21	40621416

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTTCATAGTGTCATACTGTACCTAATGTCTTTATTTTCCCATCGTCCTC[A/T]GATTGACTTTGTGGCGCATGATGATATCCCATACACCTCTGCGGGATCAG

Long Flanking Sequence:

ATTGACAGGGAGCGCGCGCGTGATGTGTCTGAGGAGAGATGCGGTGGGGAGGGGTGAGAAGGGTGCACGACGATGCCTATTTGAGGACCGGGAGGGAGACACGAGAATGCCGGGAGATCATCACTCGTTTCCGGGCATCCGGAGACTCGCGAAACTTCCCGCCCTACTCATAATTCTCTCTTTATATAGCCGTATGCCCATTACATATCCATAAAACACTGTGATATAACCGCGCTCGGATCGGATCGCTTTCTCACTGCAACCGAACCGCTCCAAGGTTTGTTTCAATCGAGCCGAGACCACCTCATTCAAGCGATCTCGGAGCGATTACTTTGGCGCGGAACAGATCGCGAATGCCCTGTTCACATATGCCAATAGAACCGCGCTAACTGGGCAAACGAGATACGTTCCGAAACAAAAGTGTAGGTGTGAAAGCACCCTAAGATCCCTGTTTCATAGTGTCATACTGTACCTAATGTCTTTATTTTCCCATCGTCCTC[A/T]GATTGACTTTGTGGCGCATGATGATATCCCATACACCTCTGCGGGATCAGAAGACGTCTACAAACATATCAAAGAAGCAGGTAAAGACTTCACAGCAACCAAACTACACATTTACAGAACTGGCCAGGAACTCATTAAAGCAAACCTCTTCTACATGGCTTATAAGGAATGTTTGTGGCGACTCAGAGAACGGAGGGGATCTCTACCTCTGACATCATCACACGCATCGTTCGAGACTATGACGTCTACGTCAGACGAAACCTGCAGAGAGGATACACGGCACGGGAACTCAACGTTGGCTTCATCAAGGTAATATTGTGTGCTTTTTGTTGGGTTGGGTTGCAATTAGTAATGAATGACTTTTTGAGGTAACTTACCCAATACTGGATTTGAGAAAGGGGAAATGAAGACAGGGTTTACATCTTCATTTGAATGGTTTCAACTCATTTTATTGACAGGAGAAAAAGTATCGTCTGCAACAGCAGGTGGACAGAATGAAG

Associated Phenotype:

Not determined