zgc:103559

Ensembl ID:

ENSDARG00000038293

ZFIN ID:

ZDB-GENE-041212-22

Description:

hypothetical protein LOC494056 [Source:RefSeq peptide;Acc:NP_001008599]

Human Orthologues:

CRMP1, DPYS, DPYSL2, DPYSL3, DPYSL4, DPYSL5

Human Descriptions:

collapsin response mediator protein 1 [Source:HGNC Symbol;Acc:2365]
dihydropyrimidinase [Source:HGNC Symbol;Acc:3013]
dihydropyrimidinase-like 2 [Source:HGNC Symbol;Acc:3014]
dihydropyrimidinase-like 3 [Source:HGNC Symbol;Acc:3015]
dihydropyrimidinase-like 4 [Source:HGNC Symbol;Acc:3016]
dihydropyrimidinase-like 5 [Source:HGNC Symbol;Acc:20637]

Mouse Orthologues:

Crmp1, Dpys, Dpysl2, Dpysl3, Dpysl4, Dpysl5

Mouse Descriptions:

collapsin response mediator protein 1 Gene [Source:MGI Symbol;Acc:MGI:107793]
dihydropyrimidinase Gene [Source:MGI Symbol;Acc:MGI:1928679]
dihydropyrimidinase-like 2 Gene [Source:MGI Symbol;Acc:MGI:1349763]
dihydropyrimidinase-like 3 Gene [Source:MGI Symbol;Acc:MGI:1349762]
dihydropyrimidinase-like 4 Gene [Source:MGI Symbol;Acc:MGI:1349764]
dihydropyrimidinase-like 5 Gene [Source:MGI Symbol;Acc:MGI:1929772]

Allele Name	Consequence	Status	Availability
sa38551	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa25338	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa20703	Nonsense	Available for shipment	Available now

Allele Name:

sa38551

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
ENSDART00000055848	Essential Splice Site	50	459	2	11

Genomic Location (Zv9):

Chromosome 6 (position 26845782)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	27146993
GRCz11	6	27137554

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATTAACAGATTACTTCAATAGTTTGATAATACAACAGCATCTTTATAAC[A/T]GGTACTGGATGTGGGTGACAGTCTGATAATGCCAGGTATAGTGGACAGTC

Long Flanking Sequence:

AATGCAGTGAACTGCGAAACTTCAGCAATGTCAAAAATACTATAGCAATTTAGAGTAAATACTATCATTTTTTACCCTTTCTATAATAAAGTACTTGAGCTAACCTGTTGTGGTAATTATAGTTGCTTTAGTAACACAACAACTATAGTTACTGAAATTAAACTACTGTGGTTTTCTACAGCTATACATAAATATTATACTACTCTTAACCACAGTGTACTGTAGTAAAACTAAATCACACTACATTATTTGTTACAGTTTATCATCAGTTCACTTTAGTTAATACAACAGCAACCTCTGGCATTTGTAACAAGTTGTAAATGCAATACCATACAGTGAAATACACTTAATGGTTTAAAACACTATAGTAATTGTATAAATTACTATTGTATTTTTTTCATGTGGGCAGGTTTAATTAATAGTATATAAATTAATCAATAGATTCAAATCTATTAACAGATTACTTCAATAGTTTGATAATACAACAGCATCTTTATAAC[A/T]GGTACTGGATGTGGGTGACAGTCTGATAATGCCAGGTATAGTGGACAGTCATGTCCATGTAAATGAACCAGGTCGCACTGACTGGGAAGGGTACTGGACCGCCACACGAGCAGCTGCTGCTGGAGGCATCACCACCATTGCAGACATGCCACTGTGAGTACCCTTAAAATCTACAGACTGAAGCGACAATCCATTTACAACAGACTGTAGAATTAGACAAACTGACAAGTTGTTGTTTTATTTATTCCTCCTTCCATACCTCCACAGAAACACAATCCCACCAACTACTACTCTTAGAAACTTTAATGAGAAGCTGTGTGCTGCTACAGGGCAGTGCTTCGTAGACACTGCTTTTTGGGGAGGAGTCATTCCTGGCAACCAGGTACTTGCTTTATATACTACAAATTGTTAATTAAGGGATACTTTTTACAGTACACACTCTCAGAAATAAGGTACAAATTTGTAAAAGGTACAAATTTGTACCTAAAAGGTCCATATTA

Associated Phenotype:

Not determined

Allele Name:

sa25338

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
ENSDART00000055848	Essential Splice Site	139	459	4	11

Genomic Location (Zv9):

Chromosome 6 (position 26844823)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	27146034
GRCz11	6	27136595

KASP Assay ID:

554-7541.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTAAAACTTGCCTTTTTCTGCCCATCATATTGTTTTTTTTTTTCTGTCAC[A/T]GATGGAGTTAAAGCCGATGTGCCAAGCTGGTGTGGCTGGATTTAAGTGCT

Long Flanking Sequence:

ATTTGTAAAAGGTACAAATTTGTACCTAAAAGGTCCATATTAATACCGCAAGGGTACTTATTGGTACCGAAAAAGTACAAAAGTGTTCCTCTTAGTACTAATATATACGTCTGAGGTACCAGTATGAACCCTTCAAGCACAAATGTGTACCTTTTGAAAAGGTAACACCCCAGTGACAGCTCTCGTACCTTTATTTCTGAGAGTGTAGTTGACAGTTCGTTACTATCCACAAGGCAGGTAAGATGTTGAGACAGATAATCATGTATACAAAAGATATGCTATGTTAGTGTAATGAGTGATGATTAATCAGAATGATGACAGCTGTAGATGGTAGATTGGCACAATGCATAATGGGAAGTGTAGTCCGGGTGAAAGGCAGAGGTGATATTTGGAGTGGCCCCTAGTGAGTCTTATGGGCACTCCAGCTAGAACTCAAAACATTAACAAAGACTAAAACTTGCCTTTTTCTGCCCATCATATTGTTTTTTTTTTTCTGTCAC[A/T]GATGGAGTTAAAGCCGATGTGCCAAGCTGGTGTGGCTGGATTTAAGTGCTTTCTGATCCACAGTGGAGTAGAGGAGTTTCCTCATGTAACCGATGCTGATTTGCATGCAGCTATGAAACAGCTCCAGGGCACGAACAGCGTTCTGCTGGTAAGCTTATTTATTTTCTGCTCACCCCAATTTTTTTAGCTTGGTATCAGATTTCATGGAACATTTCTGCCACAATGAATATCTCACATCACTGTCCACCAATGTTAAAGTGGGGCAATATTAAGGCTTAACCGTCAATGAAATCCTTTTTTTTTTTTTTTTTTTTTGCTTAATTTGTTGTTTTTTTTCTTGGCTTTTCAAGAAATTCCACTATACAACTGTTATCTCCCAGTAGTTAATTTGTTTCCTCAACATTTCTGGCATGATGTGTAACTCACTTCACTGAACCAATATTGGGGTATAATTGTCAATGAAATCAGGTAGAAACATATCTTAGTATGCAACAATAAAC

Associated Phenotype:

Not determined

Allele Name:

sa20703

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000055848	Nonsense	283	459	7	11

Genomic Location (Zv9):

Chromosome 6 (position 26841521)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	27142732
GRCz11	6	27133293

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCCACCACTACCTTAACCTGTCAGCAGAGGACATTCCAGGACGGGCCACT[C/T]AATTCAAATGCTGCCCCCCGATACGGGGCACGGCCAACCAGGTGTCCAAA

Long Flanking Sequence:

ACGATACATCAATAGAATGCTCATTTAATCAATTTTCAGGCTGGTTTTGTGGTTCAGGGTCACATATTTAGCATTCATTAGACCTCTAATCAAAATCATGAACATTTCTTAATTTAAAACAAATGTTTTGGTTTTTCTCTTGTTATGCAGATCCGCAGGAATATTCCACCTTCCTAAAGTCCAGACCTGACATTATGGAGCTTGAGGCCATCCATACAGTCATTGAGTTCTGCTTACAGTATCAGTATGTTATGCTTGATAAAGTCTTAAAGTCTCAATTATCTGATGGCTGTTTCGACATATCAGAGCAGCCAATCCAGAGATGAAGGGTCACATGTTCTGTTCTTATAATCAGAGTGCGATGCCACATTGTGCACCTGTCATCTGCTGAGCCTCTAGAGCTCATTAGAGCAGCGAAGCAAGCTGGAGCTCCATTGACAGTGGAGACCACCCACCACTACCTTAACCTGTCAGCAGAGGACATTCCAGGACGGGCCACT[C/T]AATTCAAATGCTGCCCCCCGATACGGGGCACGGCCAACCAGGTGTCCAAAAACACACACTAAAACAGACCGAATTTTTATTTTATTCAAATCAAAATGTCAGATTTTTTTTACAAATTGGGCATCACTATAAGCAACTTAATTCATGAGTTTAAATACTTTTAATATTGTTTTGTTTTCTTTAATTATTATTAGTGACCCAGGGCCACAAATATATTATATTTTAGAAGTCCTAATAGGCCACGGATTCGAATATTATTTTCTCTCTTGTTTTCTTGTGATAACGACTTAATTATCTTGTGATTTCGACATAACTCATTTAGTAGTGATCTCGACATAACAAAACGTTGTTTTCTCATTATCATGACATAATTTTTTCATTATCTCAGTGTAACAAAAGTTTACAACTTATTTTTTCGGCTAATACAATGTTAGATGCATATCATATAGTTTGCAGCTTTCACTTTTTAAAATAATTGTAAATTACTGGAAACGGTAGAA

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details