ZMP

zgc:163030

Ensembl ID:

ENSDARG00000069192

ZFIN ID:

ZDB-GENE-060810-77

Description:

hypothetical protein LOC566959 [Source:RefSeq peptide;Acc:NP_001082882]

Human Orthologues:

CST1, CST11, CST2, CST3, CST4, CST5, CST8, CSTL1

Human Descriptions:

cystatin 11 [Source:HGNC Symbol;Acc:15959]
cystatin 8 (cystatin-related epididymal specific) [Source:HGNC Symbol;Acc:2480]
cystatin C [Source:HGNC Symbol;Acc:2475]
cystatin D [Source:HGNC Symbol;Acc:2477]
cystatin S [Source:HGNC Symbol;Acc:2476]
cystatin SA [Source:HGNC Symbol;Acc:2474]
cystatin SN [Source:HGNC Symbol;Acc:2473]
cystatin-like 1 [Source:HGNC Symbol;Acc:15958]

Mouse Orthologues:

Cst10, Cst11, Cst13, Cst3, Cst8, Cstl1

Mouse Descriptions:

cystatin 10 (chondrocytes) Gene [Source:MGI Symbol;Acc:MGI:1930004]
cystatin 11 Gene [Source:MGI Symbol;Acc:MGI:1925490]
cystatin 13 Gene [Source:MGI Symbol;Acc:MGI:1916544]
cystatin 8 (cystatin-related epididymal spermatogenic) Gene [Source:MGI Symbol;Acc:MGI:107161]
cystatin C Gene [Source:MGI Symbol;Acc:MGI:102519]
cystatin-like 1 Gene [Source:MGI Symbol;Acc:MGI:2652834]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa42245	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42245

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
ENSDART00000100504	Nonsense	48	128	1	3
ENSDART00000143945	Nonsense	48	111	1	2

Genomic Location (Zv9):

Chromosome 13 (position 33895964)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	33561944
GRCz11	13	33671489

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACAAAGAATCAAGACAAGCGTTAAAGTTTGCAATGACCCAGTACAACAAA[C/T]AAAACAGAGATGTGTATTTGTGTGATGTCTCTAAAATCATCAAGCTCCAA

Long Flanking Sequence:

AAAAATTGCTAAAAGTAGCAAATTAATATTAAACATTGCTAAACTTGTTAGTCACTTTTTTAAAAATTGCTAAAAGTAGCAAATTAATATTAAACATTGCTAAACTTGTTACCTGGTGCACTTTGGAAAAAATGTTGTAAGGTTAGAATGAAAAGTTGCTATTTTGAGCAACAAAATTGCCAACACTGTAAACGTGTCAAATCCACCTCTCCCTACAACTGCGATTGGTGGACACGTGAAGCCCCGCCCACATTAACAGCGCTTAAAAGTGACGTTTGTTCATTTCAAACCGCAGAATTGATCACGCTTTCGACTTACTGACACAACGAGGAAAGATCAAGACAAATCACTGTTCAAGTATGTTTCTTAAAGCTATTGTGGTGCTTTTTGTGGTGAATTTGACCCTGTCGAGCGCTGGCCTGGTCGGAGGACCAGTGGATGCGAAATTGGACAAAGAATCAAGACAAGCGTTAAAGTTTGCAATGACCCAGTACAACAAA[C/T]AAAACAGAGATGTGTATTTGTGTGATGTCTCTAAAATCATCAAGCTCCAAAAACAAGTAAGTATTTAAACATTTAATTGAGTTATCAGGGAATGTATTTTCATTAGGCTACATCAAGTGTTAAAAGTACATCTTTGAACGCTGTTATGTGTCGTCAAATCTGGTTTAACTGGGTCTGTATTTCTTAAAGTCGTAAGGCTTCACTGTGTGAGTAATGGGTTGTTTAAATTTTTTACATTTTTTTTTTGTTGTTGCTTTTTCCTGTAGAACACGTTTGAGCTTAGTTTGTGTCAGCATTGGCAAACAAATTAAAACATAGTTCAAGTTTAGTAGCCTATAATGAATGGTTATTAGAGGCAAGAATACAAAGGACAATGAATGGGTAAATAAAATGTATGTTAAATTGTGTAAACCGAAAGATGAGTACAATGCTGTTTTAATTTAGAGTAAGTATATTGTAATTTTAATAGTTTCAGTTAGTAGTTTTAATCTTTCATTTTT

Associated Phenotype:

Not determined