ZMP

wu:fe36b12

Ensembl ID:

ZFIN ID:

Human Orthologues:

PLSCR1, PLSCR2, PLSCR4, PLSCR5

Human Descriptions:

phospholipid scramblase 1 [Source:HGNC Symbol;Acc:9092]
phospholipid scramblase 2 [Source:HGNC Symbol;Acc:16494]
phospholipid scramblase 4 [Source:HGNC Symbol;Acc:16497]
phospholipid scramblase family, member 5 [Source:HGNC Symbol;Acc:19952]

Mouse Orthologues:

1700057G04Rik, Plscr1, Plscr2, Plscr4

Mouse Descriptions:

RIKEN cDNA 1700057G04 gene Gene [Source:MGI Symbol;Acc:MGI:1925709]
phospholipid scramblase 1 Gene [Source:MGI Symbol;Acc:MGI:893575]
phospholipid scramblase 2 Gene [Source:MGI Symbol;Acc:MGI:1270860]
phospholipid scramblase 4 Gene [Source:MGI Symbol;Acc:MGI:2143267]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24439	Essential Splice Site	Available for shipment	Available now
sa25205	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24439

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112607	Essential Splice Site	38	242	1	6

Genomic Location (Zv9):

Chromosome 24 (position 5288633)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	5177126
GRCz11	24	5208913

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAATCCAGGAATACCAGGCTGTCCACCAGGACTGGAGTACCTCACACAGG[T/C]CAGAACACCATCAATACCATATTCAAAATAATAAATATGTATATTGTGAA

Long Flanking Sequence:

TGTTTCTCTGGTCGTGTTCTCATATTAGTCATCTATTGACCGAACACAGACTCAGTATGTTTCCTTTTTGCTTTAAGGGTACACACAATACCAGAAACAGTACATGATTTCAATATCTGTAAGCTATCTGTGTCGGCTGTTCTGTCATGTTGTTGTCCTCTCAGTGGTTGACTATTGCGCTCCTGAAAACATAACTTTATGATTGTAATATAATTTCAGATTTATTGAATAATCATGCATAAGGCTCTAATATGTAAATATTTATTGATAGTGGTCGTGTGTAATATATGTATATTTTTAATAATTAGTTATTGATCTATCAATTAAATTAATTGCGTCATGTGTCCATGCTATTTGTCAATAATGACCTGTAGTTGGTGCTAAAATGTTTTCCTCATCTTCACCACAAGGAAAGGCCACCATGCAGCCTATGAACATGTATATGGTTCCAAATCCAGGAATACCAGGCTGTCCACCAGGACTGGAGTACCTCACACAGG[T/C]CAGAACACCATCAATACCATATTCAAAATAATAAATATGTATATTGTGAAAATTAAAGTTGTCTGTACAAAAAAAAAAATGTAAATAAATAAATGAAATGAAAAAGAAGTCTAAAATGCCATTTAGTGTAACAACAGTTTGTGCACTGAAAATCTTGCAAGGCACATTTAGAAACATATATTTTGTGGACATATTATATATACAGTGCTCAGCATAATTGAGTACACCCCATTTTGAAAGTAAATATTATTCTCCATTTCTCAGTGAATATAGGCAATGTATTTTGGTGCATTGAAACAAAGCAGATTTATCAAACATATTTATTAAAATAATATTTTAGTCACCAAACATTTAGAAATTGAAAGATAATACAATTAAATTTAAGCAAAATATTGCAAAAAAAAAAAAAAAAAAAAAAACAATAAACAATTCAACCTTCAAAATTTCAACAAACTTTTTCCTTTATTTTTGCTTCTCTTGATTTTTCCTCTTTTTAAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25205

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
ENSDART00000112607	Nonsense	201	242	5	6

Genomic Location (Zv9):

Chromosome 24 (position 5293739)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	5182232
GRCz11	24	5214019

KASP Assay ID:

554-7884.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGATGAAGTCAGTATTGGGAAGATCAGCAAACAGTGGACAGGACTCCTG[C/T]GAGAGGTGTTCACAGATTCAGACAACTTTGGCATCCAGTTTCCAATGGAT

Long Flanking Sequence:

GTCCTTGAAAGTGCTTGAATTAAATTTAAAATTACATTTGCTTATGGATTAATTTTTAACAATTGTACTCACTTAAAAACCAAGAAATTCTTAAAATAAAAATCTTAAATTTAATTACTGAACAATAACATTGACAAATGCACATTTTATCAATATTTCAGAAACCAAATTTGAATAATACCAGTATTTAATTCATTTTTTAAATTAAAGTTCTTAAAACATGACTTTTTCAATACTTATTGAAACAGTAAGATTTAGAATTCAATCTTTTCTGTCTATAAATGTCCACTAGGGGGAACTGTTAAGTAGCGGATACAATATTTCAAGTAAATATGCCCGTATATGGATTGATACATTATCGTGCCAAAAAATAAATGATTGAAAACTATAATGTATATCTGTTTTCTATCTTATTTTCAACTTGTCATGCCCTACTGAAGATTCTGACCATGGATGAAGTCAGTATTGGGAAGATCAGCAAACAGTGGACAGGACTCCTG[C/T]GAGAGGTGTTCACAGATTCAGACAACTTTGGCATCCAGTTTCCAATGGATCTGGATGTGAGGATGAAGGCAGTGATGATCGGAGCCTGCTTTCTGATTGTGAGTATAACCTTATGGAGAATATAAAACTGACTGATTGTTTCACAACAATATTATAAAATGACATTACTTTATTGAAATAAATCAATTATATAGGGTGTCTTAAAAAATGTAGGCCCTAAAAAGTTACTTAATTTCACTGAAATTTTGTATTGTAGGTGTTAATTTTAATTTTAAGCCTGTTTATTTTTTTAAGAAGCCATGTCAATAAAGGCAGTTGAACTTTTTCACCTACTTTTTGAGTGCCTTGGATTTTTTTTGCGTATCGACACATCGAATTACCCTTGAAACTCTTTCTGTTTGATTCATCATTAATAAATAATGAACAACTGTACTTGTAAGTAAAAGTCTGAGTCCCAGAATTACTGCTAAATAATCACATAATTAATTTGTTTCAGGACT

Associated Phenotype:

Not determined