ZMP

si:ch1073-184j22.2

Ensembl ID:

ENSDARG00000078598

ZFIN IDs:

ZDB-GENE-081104-32, ZDB-GENE-090218-31, ZDB-GENE-090218-31

Description:

Novel dual specificity phosphatase catalytic domain containing protein [Source:UniProtKB/TrEMBL;Acc:

Human Orthologues:

DUSP14, DUSP18, DUSP21

Human Descriptions:

dual specificity phosphatase 14 [Source:HGNC Symbol;Acc:17007]
dual specificity phosphatase 18 [Source:HGNC Symbol;Acc:18484]
dual specificity phosphatase 21 [Source:HGNC Symbol;Acc:20476]

Mouse Orthologues:

Dusp14, Dusp18, Dusp21

Mouse Descriptions:

dual specificity phosphatase 14 Gene [Source:MGI Symbol;Acc:MGI:1927168]
dual specificity phosphatase 18 Gene [Source:MGI Symbol;Acc:MGI:1922469]
dual specificity phosphatase 21 Gene [Source:MGI Symbol;Acc:MGI:1920797]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39757	Nonsense	Mutation detected in F1 DNA	Not yet available
sa32834	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39757

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
ENSDART00000114518	Nonsense	99	215	2	2
ENSDART00000132411	Nonsense	78	194	1	1

Genomic Location (Zv9):

Chromosome 2 (position 5041166)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	5486894
GRCz11	2	5398776

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCGACCTTCCAAATGCTCGTCTGGGGGACCACTTTGACCACGTCTCCGCT[C/T]GAATTCACAACAACAGACCTGGAGGAACCCTAGTGCACTGTGCTGCAGGA

Long Flanking Sequence:

TAAATCGCGGTCCGCAGAAATGTCCGCGGGGCTACGTTTCCACAATGAGCCCGGGTTGAATGTATCATTTGCACAATGCAACTTTAAAATACAGTAACATACGGCATTACTGTCCTACAGTAAAATACAGTTCATGTTACAGTTAAATAATTTCGTAAACAGTGTGCAATTACATATTAACACAGCATAGCAGCACAAATTTGGTATAGTAATGGAGTACAGCCTAGTTCAAGTTTATTCAGTTAAAAATGTAACCTTATTTCTATCCTATGTCTGTTTCCAGCGTAATGTCAATATCACAGATAACCCCGACCCTCTTCCTAAGTGGCGCCGATGCGTCAATGAATCAAGCCCTTATGACCCGAAAAGGCATTACACTCATCGTGAACGTGACCCTGTCCCACACCTGCCCTGTCTACCCAGGCGTGGAGTGTATACGTGTGGCAGTGTCCGACCTTCCAAATGCTCGTCTGGGGGACCACTTTGACCACGTCTCCGCT[C/T]GAATTCACAACAACAGACCTGGAGGAACCCTAGTGCACTGTGCTGCAGGAATGAGCCGCTCTCCTGCTGTTATAATGGCATATCTCATGAAGTACAAAGGAGTGACTCTGAGACAGGCGCACAAGTGGGTTAAAGACAGCAGACCATACATTCGCCTTAATGTAGGATTCTGGACCCAGCTTCTGGATTACGAGAGGAAACTCTACGGTAGGAATACTGTGAGAGTGGCTGAACCCGTGGATGCACAGCCAACGCCACAAACACCAAAACTACCCTCCAGGTATAAAATGAGACAGTGTCCTCCGTCTCCAAGAGCGAGCCAACTCAGAAGATTCACCTCCTTTTCATCCTAACCAATGTTTGCAAACTGAGGTCATGAAATATGTTGCATGTACATGGATAACTTCTTTCTACGCCATCACTTTGGATTGGAATCAGTAAGACTTATGAAGTGAAACGAACCAAATAGGCACGTTTTGTTTTACCCCTAGCTTTTATCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32834

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114518	Nonsense	176	215	2	2
ENSDART00000132411	Nonsense	155	194	1	1

Genomic Location (Zv9):

Chromosome 2 (position 5040935)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	5486663
GRCz11	2	5398545

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCTGGATTACGAGAGGAAACTCTACGGTAGGAATACTGTGAGAGTGGCT[G/T]AACCCGTGGATGCACAGCCAACGCCACAAACACCAAAACTACCCTCCAGG

Long Flanking Sequence:

AGTTTATTCAGTTAAAAATGTAACCTTATTTCTATCCTATGTCTGTTTCCAGCGTAATGTCAATATCACAGATAACCCCGACCCTCTTCCTAAGTGGCGCCGATGCGTCAATGAATCAAGCCCTTATGACCCGAAAAGGCATTACACTCATCGTGAACGTGACCCTGTCCCACACCTGCCCTGTCTACCCAGGCGTGGAGTGTATACGTGTGGCAGTGTCCGACCTTCCAAATGCTCGTCTGGGGGACCACTTTGACCACGTCTCCGCTCGAATTCACAACAACAGACCTGGAGGAACCCTAGTGCACTGTGCTGCAGGAATGAGCCGCTCTCCTGCTGTTATAATGGCATATCTCATGAAGTACAAAGGAGTGACTCTGAGACAGGCGCACAAGTGGGTTAAAGACAGCAGACCATACATTCGCCTTAATGTAGGATTCTGGACCCAGCTTCTGGATTACGAGAGGAAACTCTACGGTAGGAATACTGTGAGAGTGGCT[G/T]AACCCGTGGATGCACAGCCAACGCCACAAACACCAAAACTACCCTCCAGGTATAAAATGAGACAGTGTCCTCCGTCTCCAAGAGCGAGCCAACTCAGAAGATTCACCTCCTTTTCATCCTAACCAATGTTTGCAAACTGAGGTCATGAAATATGTTGCATGTACATGGATAACTTCTTTCTACGCCATCACTTTGGATTGGAATCAGTAAGACTTATGAAGTGAAACGAACCAAATAGGCACGTTTTGTTTTACCCCTAGCTTTTATCTTGTGTGTGTGTGTGTGTGTGTATGTTTATTAATGTAATTCTCTTCGTTGGGTGGATAAAACGATGATAATTCATTTCATATTCTGATAACAATATCCACTCACTGGCCACTTTATTAGGTACACCTTATTAGTACCGGTTTGAACCCCCTTTTGCCTTCAGAACTGCCTTAATCCTTTGTGGCATAGATTCAACAGGGTGCTGGAAATATTCCTCAGAGATTTTGGTCCAT

Associated Phenotype:

Not determined