ZMP

zgc:92041

Ensembl ID:

ENSDARG00000017314

ZFIN ID:

ZDB-GENE-040808-55

Description:

hypothetical protein LOC445282 [Source:RefSeq peptide;Acc:NP_001003737]

Human Orthologue:

CELA1

Human Description:

chymotrypsin-like elastase family, member 1 [Source:HGNC Symbol;Acc:3308]

Mouse Orthologue:

Cela1

Mouse Description:

chymotrypsin-like elastase family, member 1 Gene [Source:MGI Symbol;Acc:MGI:95314]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43764	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37421	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43764

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
ENSDART00000021594	Nonsense	176	266	6	8
ENSDART00000063389	None	None	120	None	4

The following transcripts of ENSDARG00000017314 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 22 (position 7481586)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	7413863
GRCz11	22	7443709

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACTTTATTTCTCTCCTGCAGCTGGTGGCTCCCTCTCCGCTCAGCTGAAA[C/T]AGGCCTATCTGCCCGTGGTCGACTACAATACCTGCTCTCGTGGTGACTGG

Long Flanking Sequence:

TAAAAAAATGTAAATAAAACAAATAAATATAAATTAATCATGTTTCAAATGTTAGCTTACTTTAGTTCCATCAAACATTTGGCCAAAATTCAGAAAAAGTTTGCAGTTACCATGATTTTACTACTTATTTTATCAACCCATAATAATATTAAACATTTTCTAAAGGTTATAGCGCCCCCTAGCTTCCAACACGAGCGAAATGTGTGTTTTAAACTGTTTTTACTCTCAGATATGATATTGCTCTTCTGCGCCTGTCCTCCAACGCCTCCCTGAACACATACGTGCAGTTGGGCACTCTTCCCCCCTCTGGACAGGTTCTGCCCCACAACAACGCCTGCTACATCACTGGCTGGGGCCTCACTTCCAGTAACGTTGACTTATGTTTTTTTTAAATGACTCATGTGTTGCCAGAAATGATTGATGTTTGCTGATTCCTGAAGCGTTTCTTTCTACTTTATTTCTCTCCTGCAGCTGGTGGCTCCCTCTCCGCTCAGCTGAAA[C/T]AGGCCTATCTGCCCGTGGTCGACTACAATACCTGCTCTCGTGGTGACTGGTGGGGAAGCACCGTGAAGAACACCATGGTTTGCGCTGGTGGCGGAAGCCTGTCTGGATGCCAGGTGACCATCTAAAAAAACAGTCTAAAACTATTTGGTATTGAAGTACAGAGTGTAATTCTTGTTATGTTTTTTTTATAGGGTGACTCTGGCGGTCCTCTGAACTGTCAGGTCAGCGGTCAGTACGTCGTCCACGGTGTGACCAGCTTTGTGTCTTCATCCGGTTGTAACGCCTACCAGAAGCCAACCGTCTTCACTCGCGTCTCTGCCTACATCAGCTGGATTAATGGCGTAAGTGCAATTTATGAATTTATATAGTCGTTAAAATAAAGCAATGATGATAAGAATATCTTTTAACACCCTGTTTTCGTTTCAGATTGCTAAATAAGCTGAACAATCAGAGAAGAAGAGAGACTAACATCCTCGGGAATGCCAACATTTAACATCTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37421

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000021594	Essential Splice Site	263	266	7	8
ENSDART00000063389	None	None	120	None	4

The following transcripts of ENSDARG00000017314 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 22 (position 7481928)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	7414205
GRCz11	22	7444051

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCCAACCGTCTTCACTCGCGTCTCTGCCTACATCAGCTGGATTAATGGC[G/A]TAAGTGCAATTTATGAATTTATATAGTCGTTAAAATAAAGCAATGATGAT

Long Flanking Sequence:

TCACTGGCTGGGGCCTCACTTCCAGTAACGTTGACTTATGTTTTTTTTAAATGACTCATGTGTTGCCAGAAATGATTGATGTTTGCTGATTCCTGAAGCGTTTCTTTCTACTTTATTTCTCTCCTGCAGCTGGTGGCTCCCTCTCCGCTCAGCTGAAACAGGCCTATCTGCCCGTGGTCGACTACAATACCTGCTCTCGTGGTGACTGGTGGGGAAGCACCGTGAAGAACACCATGGTTTGCGCTGGTGGCGGAAGCCTGTCTGGATGCCAGGTGACCATCTAAAAAAACAGTCTAAAACTATTTGGTATTGAAGTACAGAGTGTAATTCTTGTTATGTTTTTTTTATAGGGTGACTCTGGCGGTCCTCTGAACTGTCAGGTCAGCGGTCAGTACGTCGTCCACGGTGTGACCAGCTTTGTGTCTTCATCCGGTTGTAACGCCTACCAGAAGCCAACCGTCTTCACTCGCGTCTCTGCCTACATCAGCTGGATTAATGGC[G/A]TAAGTGCAATTTATGAATTTATATAGTCGTTAAAATAAAGCAATGATGATAAGAATATCTTTTAACACCCTGTTTTCGTTTCAGATTGCTAAATAAGCTGAACAATCAGAGAAGAAGAGAGACTAACATCCTCGGGAATGCCAACATTTAACATCTGTAAAGGCCAAATATACTTCAATAAACTTTACATGTTGAGCTGAAGCAGTTTAAAGATTATTTGTGTCTTAATTTAATCCAGTTTGATCAAAAAATGATCTTCAGTTGAAAACCTAAATGTTTTTTTATACTTAAGGTGGATAATTTAAGTATTTTATTGAATTCAGATTTGCTTTTTAAACAAGTTAGTACAGAGAATGGAGCTCGCAACTGTGTTAAATATACAATATACAAAGCAAAACACTTCTACCATAAACATATCAAACCTCAACAAAGTAAGGCAATTTTTAAAAAAAATTTGCATAAAGTCTAAACACAGATGACTAAAATATTTCAGATACCCA

Associated Phenotype:

Not determined